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http://www.europrise.org
The European HIV Prevention R&D Network
Europrise SCIENCE UPDATE
Issued on every Monday - The Companion to the EUROPRISE NEWS (issued on every Friday) - Sources: NCBI
(NLM/NIH) – MIS (Medical Intelligence Solutions) - Scope: S&T information of interest to any organisation
involved in HIV/AIDS PREVENTION RESEARCH AND INNOVATION – i.e. research re science, technology,
strategies and policies - Distribution: free Search Term: “HIV” Selection ratio: +/- 65/100 -
This bulletin includes references of articles that are already printed as well as e-publications (ahead of print)
----------------------------------------------------------------------------------------------------INTENDED FOR WIDE DISTRIBUTION: TELL YOUR FRIENDS!
EUROPRISE SCIENCE UPDATE N° 10-17
INCLUDING
SELECTED TITLES FROM RECENT ( BANFF, ETC.) CONFERENCES
2266 A
Apprriill 22001100
W
WEEEEK
K 1100--1177
M
Maaiinn H
Heeaaddiinnggss
Microbicides............................................................................................................ 17
Diagnosis ................................................................................................................ 18
Epidemiology .......................................................................................................... 23
Health economics ................................................................................................... 36
Immunology ............................................................................................................ 38
Pathology ................................................................................................................ 54
Recommendations & Policies ............................................................................... 64
Therapy, others ....................................................................................................... 70
Vaccines, clinical .................................................................................................... 71
Vaccines, research ................................................................................................. 72
Virology ................................................................................................................... 74
Selected from Recent Conferences (Source: MIS) .............................................. 81
------------------------------------------------------------------------------------------------------------------------------------Free for Distribution to any interested reader - EUROPRISE contact: [email protected]
Searching within this issue use EDIT / SEARCH function of MS Word
Accuracy of information depends on reliability of sources
The Europrise members do not necessarily share the opinions expressed in the reported items
EUROPRISE SCIENCE UPDATE 10-17
CONTENTS
To go to item please click on page number in this table
To go to PubMed click on link below the abstract
When you have a subscription to the concerned source you can also access the
complete article from PubMed by clicking on source in the window
Please check with your library for copyright compliance in so doing
Microbicides............................................................................................................ 17
Acceptability and Adherence of a Candidate Microbicide Gel Among High-Risk
Women in Africa and India .............................................................................................17
Magnetic Resonance Imaging of Topical Microbicide Formulations in the Pigtailed
Macaque: Product Distribution and Transport ..............................................................18
Diagnosis ................................................................................................................ 18
Use of the Rapid HIV Test in the Newborn and Cord Blood .........................................18
Easier Said Than Done: HIV Screening in Pediatric Primary Care ..............................18
Patterns of HIV Testing in Adolescent Couples ............................................................18
Implementation of Opt-Out Oral Rapid HIV Screening in the Pediatric Emergency
Department in an Urban Area With High Prevalence of HIV Infection .........................19
SPiral Isothermal DNA Replication (SPIDR): A Novel Method for Nucleic Acid
Amplification and Role in Rapid Infectious Disease Diagnostics ................................19
An Integrated, Self-Contained Microfluidic Cassette for Isolation, Amplification, and
Detection of Nucleic Acids .............................................................................................19
Need for Point-of-Care HIV Molecular Diagnostic Technologies in Resource-Limited
Settings. Proceedings From the Workshop "Novel Technologies in Rapid HIV-1 Viral
Detection" ........................................................................................................................20
Highly Variable Use of Diagnostic Methods for Sexually Transmitted Infections Results of a Nationwide Survey, Germany 2005 ...........................................................20
The Role of HIV-DNA Testing in Clinical Practice .........................................................21
Need for Point-of-Care HIV Molecular Diagnostic Technologies in Resource-Limited
Settings. Proceedings From the Workshop "Novel Technologies in Rapid HIV-1 Viral
Detection" ........................................................................................................................21
A Simple Fluorescence Based Assay for Quantification of Human Immunodeficiency
Virus Particle Release .....................................................................................................22
Epidemiology .......................................................................................................... 23
HIV Risk Behavior in Treatment-Seeking Opioid-Dependent Youth: Results From a
NIDA Clinical Trials Network Multisite Study ................................................................23
[Epidemiology of HIV. Update] .......................................................................................23
Sexual Behavior and Knowledge of Sexually Transmitted Infections Among
University Students in Sao Paulo, Brazil .......................................................................24
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EUROPRISE SCIENCE UPDATE 10-17
Prevalence and Pattern of Disclosure of HIV Status in HIV-Infected Children in
Ghana...............................................................................................................................25
Practice of Feeding Premasticated Food to Infants Among HIV-Infected Mothers ....25
Trends in Pediatric HIV Hospitalizations .......................................................................25
PRBC Transfusion and Infection Risk: What Have We Learned From Hepatitis and
HIV, and What Might the Future Hold? ..........................................................................25
Love, Trust and Condom Use in Serious Teen Relationships .....................................26
Change Over Time in the HIV/AIDS Risk Perceptions of South African Youth ...........26
Sugar Daddies Syndrome: Elderly Sexual Behaviour and Implications for the Spread
of HIV/AIDS in Nigeria .....................................................................................................26
Community HIV Prevalence and Parity Progression ....................................................26
Environmental Change, Risky Sexual Behavior, and the HIV/AIDS Pandemic:
Exploring Linkages Through Livelihoods in Rural Haiti...............................................26
Using Population Policies and Non-Governmental Organizations to Explain HIV/AIDS
Outcomes in Sub-Saharan Africa...................................................................................27
Perceptions of Risk and Sexual Behavior Change Following Adult Male Circumcision
in Urban Swaziland .........................................................................................................27
Gender, Family, and HIV/AIDS in Lesotho .....................................................................27
Risky Sexual Behavior, Substance Abuse and Sexually Transmitted Infections
Among Street Adolescents in India ...............................................................................27
Community Factors Shaping the Sexual Behavior of Married Males in 8 African
Countries .........................................................................................................................28
Nepali College Students' Susceptibility to HIV .............................................................28
Condom Use Negotiation and Practice Among Married Women in Vietnam ..............28
In Search of the Holy Grail: Improving Assessments of Sexual Activity in Population
Surveys Through Collecting Biomarkers ......................................................................28
Non Use of Condoms by Men in Marital Unions in Cameroon .....................................28
Global Trends in AIDS Mortality .....................................................................................29
Sexual Concurrency in Uganda, Zambia and Zimbabwe: The Role of Gender,
Economic Status, and Migration ....................................................................................29
Transactional Sex and Sexually Transmitted Infections Among Women in Uganda .29
Frequency of HIV Type 2 Infections Among Blood Donor Population From India: a
10-Year Experience .........................................................................................................29
Next Steps for Ukraine Abolition of HIV Registries, Implementation of Routine
Human Immunodeficiency Virus Testing and Expansion of Services.........................30
Impact of Injecting Drug Use on Mortality in Danish HIV-Infected Patients: a NationWide Population-Based Cohort Study ...........................................................................30
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Pregnancy and HIV Infection in Young Women in North Carolina ..............................31
Sexual and Drug Use Risk Behaviors of Long-Haul Truck Drivers and Their
Commercial Sex Contacts in New Mexico .....................................................................32
The Situation of Romanian HIV-Positive Adolescents: Results From the First
National Representative Survey .....................................................................................32
Sex Frequency and Sex Planning Among Men Who Have Sex With Men in Bangkok,
Thailand: Implications for Pre- and Post-Exposure Prophylaxis Against HIV Infection
..........................................................................................................................................33
Recording of Maternal Deaths in an East African University Hospital ........................34
Human Immunodeficiency Virus Risk Behavior Among Female Substance Abusers
..........................................................................................................................................34
HIV Transmission Risk Through Anal Intercourse: Systematic Review, Meta-Analysis
and Implications for HIV Prevention ..............................................................................35
Impulsive SUI Epidemic Model for HIV/AIDS With Chronological Age and Infection
Age ...................................................................................................................................36
Health economics ................................................................................................... 36
Patient Costs of Accessing Collaborative Tuberculosis and Human
Immunodeficiency Virus Interventions in Ethiopia .......................................................36
HIV-Related Deaths and Economic Shocks: Does Survivors' Consumption Recover
Over Time in Kwazulu-Natal? .........................................................................................37
Health Financing in Brazil, Russia and India: What Role Does the International
Community Play? ............................................................................................................37
Immunology ............................................................................................................ 38
A Novel Polymorphism in ABCB1 Gene, CYP2B6*6 and Sex Predict Single-Dose
Efavirenz Population Pharmacokinetics in Ugandans .................................................38
Oxidant/Antioxidant Status in Patients With Chronic HIV Infection ............................38
Caveolin-1 Modulates HIV-1 Envelope Induced Bystander Apoptosis Through Gp41
..........................................................................................................................................39
Protein Kinase A Phosphorylation Activates Vpr-Induced Cell Cycle Arrest During
Human Immunodeficiency Virus Type-1 Infection ........................................................40
Live Cell Co-Imaging of the Genomic RNAs and Gag Proteins of Two Lentiviruses .40
HIV-1 Nef Associates With P22-Phox, a Component of the NADPH Oxidase Protein
Complex ...........................................................................................................................41
First-Year Lymphocyte T CD4+ Response to Antiretroviral Therapy According to the
HIV Type in the IeDEA West Africa Collaboration .........................................................41
Induction of Systemic HIV-1-Specific Cellular Immune Responses by Oral Exposure
in the Uninfected Partner of Discordant Couples .........................................................42
CXCR4 in Clinical Hematology .......................................................................................43
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EUROPRISE SCIENCE UPDATE 10-17
Abundant Expression of HIV Target Cells and C-Type Lectin Receptors in the
Foreskin Tissue of Young Kenyan Men .........................................................................44
FoxP3 Overexpression and CD1a(+) and CD3(+) Depletion in Anal Tissue As
Possible Mechanisms for Increased Risk of Human Papillomavirus-Related Anal
Carcinoma in HIV Infection .............................................................................................44
Innate Inhibitory Activity of Amniotic Fluid Against HIV-1: A Potential Role in
Prevention of In Utero Transmission .............................................................................45
Defining Immune Abnormalities and Their Consequences in the HIV Exposed but
Uninfected Child..............................................................................................................45
Determinants of the Interpersonal Variation in Treatment Response to Anti-HlV
Nucleoside Analogs ........................................................................................................46
Establishment of Hematologic and Immunologic Reference Values for Healthy
Tanzanian Children in the Kilimanjaro Region..............................................................46
Sevi, A Natural Enhancer of Hiv Infection, As A Novel Target to Prevent Hiv
Transmission ...................................................................................................................46
The Role of Ferritin Heavy Chain and Opiates in Neuroaids: A Systematic in Vivo
Analysis of A Novel Cxcr4 Regulator Within the Human Cortex .................................47
The Hiv Glycoprotein Gp120 Impairs Fast Axonal Transport by A Mechanism
Involving Activation of Selected Phosphotransferases ...............................................47
Genital Secretions From Hiv Infected Women Exhibit Decreased Activity Against
Hsv-2 ................................................................................................................................47
Cocaine Use Predicts Lack of Virologic Control Based on A Rapid Screening Tool
for Adherence and Active Substance Abuse in An Outpatient Hiv Clinic ...................47
Monocyte Dysregulation Is Induced by Nef Exosome Endocytosis ............................48
EBV, Lymphoma-Risk and the Potential Role of HIV-Infection for IBD Patients
Undergoing Immunosuppression ..................................................................................48
Modularity in Protein Interaction Network Hubs Predicts Viral Host-Pathogen
Interactions......................................................................................................................48
Comparative Host-Pathogen Interactome Mapping for HIV and HTLV Retroviruses:
Unraveling New Therapeutic Opportunities for Retroviral Associated Diseases .......48
Functional Insights From Protein-Protein and Genetic Interaction Maps ...................49
Neoepitope Antibodies to Monitor Proteolytic Networks .............................................49
Generation of a Family-Specific Phage Library of Llama Single Chain Antibody
Fragments That Neutralize HIV-1 ...................................................................................49
Prognostic Value of Peripheral Blood Mononuclear Cell-Associated HIV-1 DNA for
Virological Outcome in Asymptomatic HIV-1 Chronic Infection ..................................50
CCR2 Plays a Critical Role in Dendritic Cell Maturation: Possible Role of CCL2 and
NF-{Kappa}B ....................................................................................................................51
Mhc Haplotype M3 Is Associated With Early Control of SHIVsbg Infection in
Mauritian Cynomolgus Macaques..................................................................................51
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EUROPRISE SCIENCE UPDATE 10-17
HIV+ Elite Controllers Have Low HIV-Specific T-Cell Activation Yet Maintain Strong,
Polyfunctional T-Cell Responses ...................................................................................52
Kinetics of Interaction of HIV Fusion Protein (Gp41) With Lipid Membranes Studied
by Real-Time AFM Imaging.............................................................................................53
Antibodies: Beyond Neutralization ................................................................................53
Inhibition of DC-SIGN-Mediated Transmission of Human Immunodeficiency Virus
Type 1 by Toll-Like Receptor 3 Signalling in Breast Milk Macrophages .....................53
Pathology ................................................................................................................ 54
Sporothrix Schenckii Meningitis in AIDS During Immune Reconstitution Syndrome 54
Incidence of Tuberculosis in People Living With the Human Immunodeficiency Virus
in Saudi Arabia ................................................................................................................55
The Association Between Cervical Human Papillomavirus Infection and HIV
Acquisition Among Women in Zimbabwe .....................................................................55
HIV-Associated Neurocognitive Disorder: Pathogenesis and Therapeutic
Opportunities...................................................................................................................56
Tuberculosis Rates Among HIV-Infected Persons in New York City, 2001-2005 ........57
HIV-Associated Lymphoma ............................................................................................57
Higher Mortality in HIV-2/HTLV-1 Co-Infected Patients With Pulmonary Tuberculosis
in Guinea-Bissau, West Africa, Compared to HIV-2-Positive HTLV-1-Negative
Patients ............................................................................................................................57
Global Health Lessons From HIV and Hepatitis Co-Infection in China .......................58
Colonization With Staphylococcus Aureus (SA) in HIV-Infected Children and
Adolescents in Brooklyn, NY .........................................................................................58
HIV Subtype A Is Associated With Poorer Neuropsychological Performance
Compared to Subtype D in ART-Naïve Ugandan Children ...........................................59
Morbidities of Late Preterm Infants Born From 1993-2007 in a Tertiary Care Center.59
Increased Risk of Myocardial Infarction in HIV-Infected Patients in France, Relative
to the General Population ...............................................................................................59
[Diagnosis, Treatment and Prevention of Renal Diseases in HIV Infected Patients.
Recommendations of the Spanish AIDS Study Group/National AIDS Plan.] ..............60
Seroprevalence Of Common Vaccine-Preventable Viral Infections In Hiv-Positive
Adults ...............................................................................................................................60
Beta-Chemokine Production by Neural and Glial Progenitor Cells Is Enhanced by
HIV-1 Tat: Effects on Microglial Migration .....................................................................61
Memantine for AIDS Dementia Complex: Open-Label Report of ACTG 301 ...............62
HIV-1 and Kidney Cells: Better Understanding of Viral Interaction .............................62
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Septicaemia in a Population-Based HIV Clinical Cohort in Rural Uganda, 1996-2007:
Incidence, Aetiology, Antimicrobial Drug Resistance and Impact of Antiretroviral
Therapy ............................................................................................................................63
Recommendations & Policies ............................................................................... 64
Impact of Introducing Human Immunodeficiency Virus Testing, Treatment and Care
in a Tuberculosis Clinic in Rural Kenya ........................................................................64
Doubts Remain, Risks Persist: HIV Prevention Knowledge and HIV Testing Among
Drug Users in Rio De Janeiro, Brazil .............................................................................65
Senegalese Religious Leaders' Perceptions of HIV/AIDS and Implications for
Challenging Stigma and Discrimination ........................................................................65
Meanings of Sex, Concepts of Risk and Sexual Practices Among Migrant Coal
Miners in Quang Ninh, Vietnam......................................................................................66
Assessment of Safety and Toxicity Following Maternal Antiretroviral Exposure in
Infants Born to HIV-1-Infected Women Enrolled in Antiretroviral Treatment Protocols
in Diverse Areas of the World. Six Month Results of AIDS Clinical Trials Group
(ACTG) Study 5190/Pediatric AIDS Clinical Trials Group (PACTG) 1054 ....................66
Relative Efficacy of an HIV Prevention Intervention Among Diverse High-Risk Youth
in San Diego, California ..................................................................................................67
Pediatricians' Attitudes and Counseling Practices Regarding Neonatal Male
Circumcisions .................................................................................................................67
Men's Labor Migration and Women's Informal Communication on HIV/AIDS in
Mozambique ....................................................................................................................67
Women Who Know: The Relationship Between Risk and HIV Testing........................67
Circumcision, Information, and HIV Prevention ............................................................68
Best Practices in Global STI/HIV Prevention .................................................................68
HIV/AIDS in the Slums Of Nairobi: The Capacity of the Private Health Sector to
Respond to the High Disease Burden............................................................................68
The Context of Condom Use Among Young Adults in the Philippines: Implications
for HIV Risk Prevention ..................................................................................................68
Addressing Comprehensive Knowledge As a Strategy to Mitigate HIV Related Risk
Behavior Among Young Men in India ............................................................................68
Media Exposure on Condom Use Among Adolescents Age 12 - 19 in Ghana:
Application of the TPB Model .........................................................................................69
Formative Work Towards Utilization of Networks to Build Upon Existing Hiv
Prevention Programs for High Risk Men in India ..........................................................69
Information and Communication: a Library's Local Response to HIV/AIDS in Zambia
..........................................................................................................................................69
Findings in Humanized-Mouse Model Suggest Benefit of Further Studies in HIV PreExposure Prophylaxis.....................................................................................................70
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Therapy, others ....................................................................................................... 70
Associations With Virologic Treatment Failure in Adults on Antiretroviral Therapy in
South Africa .....................................................................................................................70
Is It Time to Treat HIV Elite Controllers With Combined Antiretroviral Therapy?.......71
Vaccines, clinical .................................................................................................... 71
Heterologous Prime-Boost HIV-1 Vaccination Regimens in Pre-Clinical and Clinical
Trials ................................................................................................................................71
Vaccines, research ................................................................................................. 72
Antibody-Mediated Protection Against Mucosal SHIV Challenge of Macaques
Immunized With Alphavirus Replicon Particles and Boosted With Trimeric Envelope
Glycoprotein in MF59 Adjuvant ......................................................................................72
Selection of a Rare Neutralization-Resistant Variant Following Passive Transfer of
Convalescent Immune Plasma in EIAV-Challenged SCID Horses ...............................73
Increased Sensitivity of HIV Variants Selected by Attachment Inhibitors to Broadly
Neutralizing Antibodies ..................................................................................................73
Virology ................................................................................................................... 74
Mannose-Rich Glycosylation Patterns on HIV-1 Subtype C Gp120 and Sensitivity to
the Lectins, Griffithsin, Cyanovirin-N and Scytovirin ...................................................74
Prevalence of Transmitted Drug Resistance Associated Mutations and HIV-1
Subtypes in New HIV-1 Diagnoses, U.S.-2006 ...............................................................75
Simultaneous Detection of Human Immunodeficiency Virus Type-1 Drug Resistant
Minority Genotypes by a Multiplex Oligonucleotide Ligation Assay ...........................75
HIV Classification Using Coalescent Theory.................................................................76
Characterization and Frequency of a Newly Identified HIV-1 BF1 Intersubtype
Circulating Recombinant Form in Sao Paulo, Brazil ....................................................76
[The Results of a Study of HIV-1 Resistance in the Area of Yamal and the
Comparison of the Frequency of Mutations With Different Score Values] .................77
HIV-1 Subtype C-Infected Individuals Maintaining High Viral Load As Potential
Targets for the "Test-and-Treat" Approach to Reduce HIV Transmission ..................78
Human Immunodeficiency Virus Type 1 (HIV-1) Protease Codon 36 Polymorphisms
and the Differential Development of Resistance to Nelfinavir, Lopinavir and
Atazanavir in Different HIV-1 Subtypes .........................................................................79
The HIV-1 Matrix Protein P17 Activates the Transcription Factors C-Myc and CREB in
Human B Cells .................................................................................................................79
HIV-1 Subtype C Transmission Network: The Phylogenetic Reconstruction Strongly
Supports the Epidemiological Data ...............................................................................80
[Human Immunodeficiency Virus (HIV) Type 1 With R5 Tropism Among HIV-1
Antiretroviral-Experienced Patients in Spain.] ..............................................................80
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EUROPRISE SCIENCE UPDATE 10-17
[The Results of a Study of HIV-1 Resistance in the Area of Yamal and the
Comparison of the Frequency of Mutations With Different Score Values] .................81
Selected from Recent Conferences (Source: MIS) .............................................. 81
Microbicides ....................................................................................................................81
Development and In Vitro Evaluation of Gel-Formulated Saquinavir As Vaginal Microbicide: AntiHIV-1 Activity and Phar-Maceutical Availability in Biorelevant Media ............................................ 81
Diagnosis .........................................................................................................................82
The Roche CAP/CTM V2.0 and the Abbott ReaITime HIV-1 Assays Perform Equally for
Quantification of Viral Load in HIV-1 B and Non-B Subtypes ........................................................ 82
Epidemiology...................................................................................................................82
Trends in HIV-1 Epidemic Among MSM in Israel ........................................................................... 82
Mother to Child Transmission of Hiv Infected Pregnant Women From 2000 to 2007 in Catalonia
(Spain): the Nenexp Project ........................................................................................................... 82
Health economics ...........................................................................................................82
Raltegravir - Could a Lower Dose Improve Access for People With HIV in Developing Countries?
........................................................................................................................................................ 82
Immunology .....................................................................................................................83
Discordant Immunodominant Patterns of HIV-Specific CD8 T Cells Defined by Cytokine
Production or Proliferative Capacity in HIV Elite Controllers ......................................................... 83
Discordant Immunodominant Patterns of HIV-Specific CD8 T Cells Defined by Cytokine
Production or Proliferative Capacity in HIV Elite Controllers ......................................................... 83
CTL-Escape Nef Variants Influence CCR5 Down-Regulation and HIV Superinfection Susceptibility
........................................................................................................................................................ 83
Genetic Testing for HLA-B*5701 in HIV-Infected Patients: Candidates for Abacavir Therapy ...... 83
Investigating Pro-and Anti-Inflammatory Cytokine Levels in Patients With Advanced HIV-1
Infection, Characterised by the Presence of Opportunistic Infections ........................................... 84
Susceptibility of Cells From the Female Upper Reproductive Tract to Infection by
Transmitted/Founder HIV-1 ............................................................................................................ 84
Secretion of MHC Class I Chain-Related Protein A in Chronic HIV-1 Infection Leads to Impaired
Control of HIV-1 Replication ........................................................................................................... 84
How Does Neutralization Breadth Develop in HIV Infection? ........................................................ 84
Regulatory T Cells Control HIV Replication in Activated T Cells Through Contact-Dependent and
Independent Pathways ................................................................................................................... 85
A Large-Scale Analysis of Immunoglobulin Sequences Derived From Plasmablasts/Plasma Cells
in Acute HIV-1 Infection Subjects ................................................................................................... 85
Myeloid Dendritic Cells During the Chronic Stage of HIV Infection Upregulate LPS-Responsive
Genes ............................................................................................................................................. 85
The Cross-Reactive Capacity of HIV-Specific CTLs Towards HIV Variant Antigens Is Dependent
on Their Cognate Peptides ............................................................................................................ 85
Combined Blockade of the PD-1 and IL-10 Pathways Synergistically Enhance HIV-Specific CD4 T
Cell Functions ................................................................................................................................. 85
IL-16 DCs Loaded With Complement-Opsonised HIV Efficiently Induce Expansion of Naive
CD8+T Cells .................................................................................................................................... 86
FCGR Genetics in HIV Disease ..................................................................................................... 86
Changes in Host Microrna Expression in Monocyte-Derived Dendritic Cells Following HIV-1
Infection .......................................................................................................................................... 86
Integrative Genomic Analysis of HIV-Specific CD8+ T Cells Reveal That BATF Is a Key Regulator
of T Cell Exhaustion ....................................................................................................................... 86
HIV-1 Neutralization in Primary Cells Is Less Efficient When Infection Is Mediated by Cell-Cell
Interaction ....................................................................................................................................... 87
Differential NK Cell Subset Involvement in ADCC or Respond to MHC Class 1 Negative Target
Cells................................................................................................................................................ 87
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Prevalence of Vaccine-Preventable Infections Among Hiv-Infected Children in the Uk and Ireland
Over 12 Years, 1996-2007 ............................................................................................................. 87
Interleukin (IL)-21, but Not IL-2, Induces Antiviral Activity and Costimulatory Molecules in CD8 T
Cells Without Promoting HIV Replication ....................................................................................... 87
Maintaining CD28 Expression Prevents Replicative Senescence in Human CD 8 T Cells ........... 87
Impact of GB Virus C (Hepatitis G Virus) in HIV-1 Pathogenesis .................................................. 88
Host Determinants of HIV-1 Control in African Americans ............................................................ 88
APOBEC3G Expression Is Induced in Highly HIV Susceptible CD4+CCR6+T Cells by CCR6
Ligands ........................................................................................................................................... 88
A Chinese Rhesus Macaque Model for Testing "Live" Microbicides ............................................. 88
Phenotypical and Functional Studies of CD1d-Restricted NKT Cells and NK Cells in Patients With
Primary HIV-1 Infection Treated With Interleukin-2 ....................................................................... 89
Low Levels of Varicella-Specific Antibodies in Treated Hiv-Infected Children Results From Failure
to Reactivate Anti-Vzv Memory Responses, Rather Than Lower Initial Responses Or Accelerated
Antibody Loss ................................................................................................................................. 89
Human NK Inhibitory Receptor KIR3DL1 Recognition of Conserved Regions of HLA-B .............. 89
Innate Sensing of HIV-Infected Cells ............................................................................................. 89
Mathematical Models of Persistent Infections ................................................................................ 90
Differences in the Frameshift-Regulating P1-Site in Treatment-Naive and PIresistant HIV Isolates
........................................................................................................................................................ 90
The Role of Adapter Protein-1 in MHC-I Trafficking in Antigen Presenting Cells .......................... 90
Multiparametric Flow Analysis of HIV-Specific CD8 T-Cell Mediated Virus Inhibition ................... 90
MHC Haplotype M3 Is Associated With Early Control of SHIVsbg Infection in Mauritian
Cynomolgus Macaques .................................................................................................................. 90
Characterization of A4ß7 Integrin Expression on Cervical T Lymphocytes ................................... 91
SIVmac251infection of Rhesus Macaques Destroys Secondary Lymphoid Tissue Architecture and
Depletes Naïve T Cell Populations ................................................................................................ 91
Early Selection for Escape Mutation in an SIV Nef Epitope Following Adoptive Transfer of VirusSpecific CD8+ Tcell Clones During Acute Infection ....................................................................... 91
Protective Effects of Monomeric and Dimeric Forms of the 2G12 Neutralizing Antibody Against
HIV-1 Infection in a Modified Humanized Mouse Model ................................................................ 91
Setting Up Multiple Barricades Along the HIV Infection Pathway-Learning From Genetic Pathway
Profile of HIV Resistant Sexworkers .............................................................................................. 92
Evaluation of Solid Matrix Transport Device (SampleTanker®) for Transport of Plasma Between
Clinical Sites for HIV-1 Resistance and Antibody Testing ............................................................. 92
HLA-B35-Cw4 Increases Both Vertical HIV Transmission and Progression ................................. 92
Recognition of Cryptic Epitopes Is a Ubiquitous Feature of AIDS Virus Infection ......................... 92
Differences in HIV Entry and Trafficking in Primary Lymphocytes Versus Epithelial Cell Line
Models: Implications for the Assessment of HIV-1 Neutralizing Antibodies .................................. 92
Estimating HIV Stoichiometries ...................................................................................................... 93
Cd8 T Cell Responses to a Novel, Highly Conserved HLA-A*0201(A2) Epitope in HIV Gag ....... 93
The Role of NK/DC Cross-Talk in HIV Pathogenesis .................................................................... 93
An Investigation into the Role of a CD4 Polymorphism in Susceptibility to HIV-1 Infection in an
African Female Sex Worker Cohort ............................................................................................... 93
Loss of Polyclonal Memory B-Cells During Chronic HIV Infection Is Driven by FOX03a-and
TRAIL-Mediated Apoptosis and Is Rescued by IL-2 ...................................................................... 93
Role of IL-7 and Type I IFN in Immune Activation of T Cells in HIV Infection ............................... 94
Antigen Processing Influences HIV-Specific Cytotoxic T Lymphocyte Immunodominance .......... 94
Molecular Architecture of Trimeric SIV and HIV-1 Envelope Glycoproteins .................................. 94
Extensive HLA-Driven Viral Diversity Following a Narrow-Source HIV-1 Outbreak in Rural China
........................................................................................................................................................ 94
Receptors and Pathways Utilized by Dendritic Cells for Antigen Presentation of Free and
Complement Opsonized HIV .......................................................................................................... 95
Antibody VRC01: To Be or Not To Be Like CD4 ............................................................................ 95
A Multiparametric FACS Assay to Assess HIV-1 Tropism on T Cell Subsets ............................... 95
Vaccinating Hiv-Positive Children in the West Midlands ................................................................ 95
Diversity of the CD8+T Cell Repertoire Responding to an Immunodominant Epitope Does Not
Depend on the Context of Infection ................................................................................................ 95
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Co-Localization of Antigen Processing and Receptor Binding Sites in HIV Gp120: A Mechanism to
Explain the Difficulty in Eliciting Broadly Neutralizing Antibodies .................................................. 96
Cytotoxic T Lymphocytes, Virus Strategies and Sterilising Immunity ............................................ 96
CD4+ T Cell Mediated B Cell Activation in Response to Inactivated HIV-1 Is Highly Correlated
With the Level of HIV-1 Viremia ..................................................................................................... 96
T Regulatory Cells in HIV-2 Infections Are Significantly Lower Than HIV-1 and Positively
Correlate With Immune Activation and Viral Loads ....................................................................... 96
Gut-Homing Potential of and Th17 Profiles of HIV-Specific CD4+ and CD8+ T-Cells in HIVInfected Subjects With Slow Disease Progression ........................................................................ 97
HIV Controller CD4+ T Cells Respond to Minimal Amounts of Gag Antigen Due to High TCR
Avidity ............................................................................................................................................. 97
Early Genital Tract Compartmentalization During Acute SIV Infection .......................................... 97
Synergistic Effect of Bacterial LPS and HIV Virions on Memory B Cell Death .............................. 97
Prevalent HLA Class I Allele Combinations Result in a Lack of HIV-1-Specific CD8+ T Cell
Responses and Higher Viral Set Point ........................................................................................... 98
HIV-1 Control After Treatment Interruption Is Associated to Low Levels of HIV-1 DNA ............... 98
Elite Controllers Recognize A Novel Subdominant Epitope in HIV Gag P24 ................................ 98
Regulation of IRF-1 Expression and Responsiveness to IFN-Gamma in Kenyan Women Resistant
to HIV-1 Infection Involves NF-KappaB Binding and Epigenetic Controls Via HDAC2 Recruitment
........................................................................................................................................................ 98
Comprehensive Analysis of Frequency and Phenotvpe of T Regulatory Cells in HIV Infection:
CD39 Expression on FoxP3+T Regulatory Cells in HIV Infection Correlates With Disease
Progression .................................................................................................................................... 99
Dynamics of CTL Epitope Escape and Reversion in an African Subtype C Cohort ...................... 99
Synthesis of Novel CADA Analog Prodrugs Designed As Down- Modulators of the CD4 Receptor
........................................................................................................................................................ 99
Memory Phenotypes of Polyfunctional HIV-Specific CD8+ T Cell Responses .............................. 99
Vaginal Langerhans Cells Resist Genomic Integration of HIV-1 but Transmit Endocytosed Virions
to Susceptible Target Cells .......................................................................................................... 100
Exploring HIV-1 Envelope Glycoprotein Trimer Stability .............................................................. 100
Induction of PD-1 Ligands on Primary Human Macrophages by HIV-1 Virions........................... 100
Patient Specific Transcriptional Profiling of Early Acute HIV-1 Infection ..................................... 100
Nonpathogenic Natural SIV Infection ........................................................................................... 101
Identification and Characterization of Early Founder Populations in Rhesus Macaques Vaginally
Infected With SIVmac251 ............................................................................................................. 101
Rapid Degranulation of NK Cells Following Activation by HIV-Specific Antibodies ..................... 101
Immunological and Viral Evolution on Failing Dual Boosted Protease Inhibitor Regimen in HIV-1Infected Salvage Patients ............................................................................................................ 101
Prediction of Neutralization Breadth by a HIV-1 Broadly Neutralizing Antibody .......................... 101
A Systems Biology Approach for Immune Monitoring in HIV Resistant Sex Workers From Nairobi,
Kenya ........................................................................................................................................... 102
Mucosal Immune Responses to HIV Infection ............................................................................. 102
Analysis of HIV-1 Gag Epitopes of Two HLA Class I Alleles Associated With Different Outcomes
of HIV-1 Infection in the Pumwani Sex Worker Cohort ................................................................ 102
Influence of HLA-G Polymorphisms on Human Immunodeficiency Virus Infection and Hepatitis C
Virus Co-Infection in Brazilian Patients ........................................................................................ 102
The Presence of Neutralizing and Non-Neutralizing Anti-HIV Antibodies Inhibits the Mobility of the
Virus in Cervical Mucus ................................................................................................................ 103
Regulatory T Cells and Immune Activation in the Rectal Mucosa of HIV+ Subjects ................... 103
Rapid Progression of Disease in HIV-2 Related to HLA-B15 Genotype...................................... 103
Performance Evaluation of Two Multiplex Technologies for the Measurement of Serum Cytokines
in HIV-Infected Individuals ........................................................................................................... 103
Spread of HIV Through T Cell Virological Synapses Enhances Multiplicity of Infection .............. 103
Does Increased Expression of HLA-C Allow Better Control of HIV-1 Viral Load? ....................... 104
Exploring Antibody Recognition of the V3 Region on HIV-1 ........................................................ 104
Multiple, Distinct Regulatory T Cell Populations Control Peripheral Blood and Liver Immunity to
Human Hepatitis C Virus Infections ............................................................................................. 104
CTL Responses to HIV-1 During Acute and Chronic Infection .................................................... 104
Soluble IL-7Ra (CD127) Decreases IL-7 Activity and Is Increased in HIV Infection ................... 105
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Unravelling CD4 T Cell Dysfunction During Chronic Infection ..................................................... 105
NK/DC Crosstalk and Regulation of Adaptive Immunity .............................................................. 105
Damaged Intestinal Epithelial Integrity and Tissue Macrophage Dysfunction Underlie Microbial
Translocation in Simian Immunodeficiency Virus Infections ........................................................ 105
Altered Sema4D Expression During HIV-1 Infection Is Associated With Decreased HIV-Specific T
Cell Responses ............................................................................................................................ 106
Significant Impairment in Innate Immune Cells Recruitment by Chronic Untreated Antibodies to
Mediate ADCC ............................................................................................................................. 106
Association of HLA-DRB1*0101 Exon 2 Mutations With HIV Progression .................................. 106
Neutralization of HIV-1 by Breast Milk in a Fc ? Receptor Expressing Cell Line ......................... 106
Type I Interferon Increases the Sensitivity of Human Immunodeficiency Virus (HIV)-Specific CD8+
T Lymphocytes to CD95/Fas-Mediated Apoptosis ....................................................................... 106
Absent Correlation Between Cross-Reactive HIV-1 Specific Neutralizing Activity in Serum and the
Clinical Course of HIV-1 Infection ................................................................................................ 107
Immunodominant HIV-Specific CD8+ T-Cell Responses Are Common to Blood and Rectal
Mucosa, and Gag-Specific Mucosal Responses Dominate in HIV Controllers............................ 107
Recently Transmitted HIV and the Early Neutralizing Antibody Response ................................. 107
Role of PI3K and Autophagy in Virus-Stimulated IFN-a Production by Human Plasmacytoid
Dendritic Cells .............................................................................................................................. 107
Viral Regulation of a TLR/RLR-Independent Program of Host Cell Recognition of HIV Infection 108
Investigation of the Sensitivity of Acute-Phase HIV-1 Isolates to Type I Interferons ................... 108
HIV-1 Infection Sensitizes CD4+ T Cells to Cell Death Induced by TNF-Alpha .......................... 108
B Cells Diversify the HIV Env Genes and Promote Anti-Env Immunity ....................................... 108
Concurrent Up-Regulation of Activation/Maturation Receptors and IFN-a by Plasmacytoid
Dendritic Cells in Response to HSV and HIV .............................................................................. 108
Induction and Maintenance of Systemic IL10 in Chronic LCMV Infection ................................... 109
Identification of an IL-7 Responsive CD4+ Lymphoid Tissue Inducer Cell From Adult Human
Blood ............................................................................................................................................ 109
Higher Peripheral Treg Frequencies and T Cell Activation but Lower Absolute Treg Numbers in
HIV-1 Chronic Progressors Compared to Elite Controllers .......................................................... 109
HLA-B*5701 in HIV Infected Patients: Relevance for Abacavir Hypersensitivity ......................... 109
HLA Allelic Distribution in HIV-1 Monoinfected Patients and HIV-1/HCV Coinfected Patients in Rio
De Janeiro, Brazil ......................................................................................................................... 109
The Antiviral Factor APOBEC3G Improves CTL Recognition of HIV-Infected T Cells: Linking
Intrinsic and Adaptive Immune Responses .................................................................................. 110
Bioinformatical Analvsis of Epitope Repertoire of HLA Class I Alleles Associated With Different
Outcomes of HIV-1 Infection ........................................................................................................ 110
Natural Killer Cell Function and Disease Progression in Portuguese Patients With HIV - an
Immunogenetic Perspective ......................................................................................................... 110
Loss of TRAF1 From Ag-Specific T Cells During Persistent Viral Infection Leads to
Desensitization of the 4-1BB Signaling Pathway ......................................................................... 110
Contribution of Siglec-1 to HIV-1 Infection of Macrophages ........................................................ 111
Isolation of Cross-Clade HIV-Neutralizing Human Antibodies From Memory B Cell Repertoires
Using Short Term Culture and High-Throuehput Primarv Neutralization Screens ...................... 111
An Analysis of Genital Tract Derived HIV From Heterosexual Transmission Pairs ..................... 111
HLA Class I Associations With Viral Variation Predicts a New HIV RT-Specific T-Cell Epitope in a
Single-Source HIV-1 Outbreak in Rural China ............................................................................. 111
IL-2 Induces Perforin Mediated Cytotoxicity in CD4 Cells Via STAT5 Signaling ......................... 112
Adaptation of HIV-1 Envelope Glycoprotein to Humoral Immunity at a Population Level ........... 112
Reduced Replication Capacity of Recombinant Viruses Encoding Acute/Early HIV-1 GagProtease Sequences From Individuals Expressing Protective HLA Class I Alleles..................... 112
Temporal Analysis of SlVmac239 Infection and Evolution in 12 Cynomolgous Macaques ......... 112
Altered NK Cell Differentiation of CD56bright/CD16-NK Cells With Down-Regulation of CCR7 Is
Associated With Increased Viral Load in HIV-1 Infection............................................................. 113
Evidence That GC1qR and DC-SIGN Associate on the Surface of Immature Dendritic Cells .... 113
PD-1 Is Upregulated on Natural Killer Cells in Chronic HIV-1 Infection ....................................... 113
Comprehensive Analysis of Escape Mutation From HIV-1-Specific Cytotoxic T Cells Restricted by
Asian Allele HLA-B*5401 ............................................................................................................. 113
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HIV-1 Up-Regulates Type 1 Long-Interspersed Nuclear Elements Retrotransposition by Vif and
Vpr ................................................................................................................................................ 114
Viral Load in HIV+ Partner Associates With Exposed Uninfected Partners' Capacity to Neutralize
HIV-1 in Vitro ................................................................................................................................ 114
Development of Neutralizing Antibodies Against Heterologous HIV Viruses Is Common and
Correlated With Viral Evolution to Escape Neutralizing Antibodies ............................................. 114
HLA-B*57 and -B*58 Fail to Control HIV Clade AE in Thailand ................................................... 114
Effect of Antiretroviral Therapy Initiation on Mucosal T-Cells in HIV Infection............................. 115
Influence of HLA-Bw4 Alleles Protective for HIV on NK Cell Polyfunctional Potential ................ 115
Pathogenic SIVmac251 Infection Induces a Striking Acute-Phase Systemic Cytokine Response
Similar to That Observed in Acute HIV-1 Infection ...................................................................... 115
Genetic Determinants of HIV-1 Infection and Progression to AIDS: Indian Experience .............. 115
Systemic Cytokine Levels Correlate With Disease Outcome in Chronic HIV Infection ............... 116
Immunoregulatory Properties of HLA-G in HIV-1 Infection .......................................................... 116
HLA B *08 FLK T Cell Clones From Chronic HIV Infection With the Same T Cell Receptor Have
Unique Polyfunctional Cytokine Profiles ...................................................................................... 116
CD4 Naïve Phenotype T Cells Are Recruited into the Proliferating T Cell Pool Mainly As a
Homeostatic Response to HIV Induced CD4 T Cell Depletion .................................................... 116
Analysis of T-Cell Subsets by the FluoroSpot Assay ................................................................... 117
HIV Disease Progression in Early Infection Varies by Infecting HIV-1 Subtype in Sub Saharan
Africa ............................................................................................................................................ 117
Yeast-Elicited Cross-Reactive Antibodies to HIV Env Glycans Recognize Monomeric Gp120 but
Bind Trimeric Env Poorly .............................................................................................................. 117
Differential MHC Class I Allele Expression in Distinct Lymphocyte Subsets ............................... 117
HIV-1 Replication Activates CD4+T Cells With Specificities for Persistent Herpes Viruses ........ 118
Pathology.......................................................................................................................118
Fungal Infections in Hiv Infected Patients .................................................................................... 118
Increased Cholesteryl Ester in HDL Along With Increased Triglyceride in HDL and LDL of HIV
Patients Suggests That a Defect in Reverse Cholesterol Transport Contributes to HIV
Dyslipedemia ................................................................................................................................ 118
Recommendations & Policies ......................................................................................118
Review of the Revisions to the World Health Organization (WHO) Guidelines for Antiretroviral
Treatment ..................................................................................................................................... 118
Vaccines, clinical ..........................................................................................................119
Screening for Help: CD4 T Cells in the Step Trial ........................................................................ 119
HIV-1 Subtype Distribution in HIV-1 Positive Volunteers Prior and During the Phase III PrimeBoost HIV-1 Vaccine Trial in Thailand (RV144) ........................................................................... 119
RV 144 Update: Vaccination With ALVAC and AIDSVAX to Prevent HIV-1 Infection in Thai Adults
...................................................................................................................................................... 119
Serological Immunity to Adenovirus Serotype 5 Is Not Associated With Risk of HIV Infection ... 120
Immunogenicity of the Thai Phase III (RV144) HIV Vaccine Regimen ........................................ 120
Increased HIV-Specific Immunity in HIV-Infected Individuals Vaccinated With a DNA Prime, RAd5
Boost Regimen ............................................................................................................................. 120
Population Epitope Maps of the Step and HVTN 054 HIV Vaccine Trials Reveal Vaccine-Induced
Epitope Hotspots .......................................................................................................................... 120
Induction of Viral Inhibition in Clinical HIV Vaccine Trials of Diverse Immunogens .................... 121
Comparison of T Cell Responses Elicited Bv CD40L Adjuvanted ALVAC Prime-Boost and DNA
Prime-ALVAC Boost HIV-1 Vaccine Regimen ............................................................................. 121
Vaccines, research ........................................................................................................121
Systemic Innate Immune Responses to a DNA/MVA Candidate HIV Vaccine ............................ 121
Glucopyranosyl Lipid A (GLA), a Synthetic TLR4 Vaccine Adjuvant, Induces Potent Th1Promoting Immune Responses .................................................................................................... 122
HIV Subtype A and B Vaccines Based on Envelope Quasispecies ............................................ 122
Transient but Recurrent CD4+ T Cell Activation, Hexon-Specific T Cell Immunity and Neutralizing
Antibody Responses After Ad5 Infection of Rhesus Macaques .................................................. 122
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Enhanced Expression of HIV Antigens and Improved Antigen Presentation After Infection With
Replication Competent Attenuated Vaccinia Virus in Vitro .......................................................... 122
A DNA Vaccine Encoding Conserved HIV CD4 Epitopes Induces Broad and Polyfunctional
Responses in BALB/c and HLA Class II-Transgenic Mice........................................................... 123
Vaccine-Elicited Non-Neutralizing Envelope Antibodies in Sera and Mucosal Secretions
Contribute to Protection Against SHIV89.6Pin Rhesus Macaques ................................................. 123
GB Virus C Envelope Protein E2 Elicits Antibodies That React With a Conserved Antigen on HIV1 Particles and That Broadly Neutralize HIV-1 Infectivity ............................................................ 123
Prevention of Systemic Infection by a Multigenic Recombinant Protein Vaccine After Heterologous
R5 Clade C SHIV Challenge: Correlates of Protection ................................................................ 123
Engineering the CD4+ T-Cell Response for Improved Immunity ................................................. 124
Lentiviral Vector-Based Anti-HIV-1 Vaccination in Macaques Induces Strong T-Cell and Antibody
Responses Post-Immunization, Significant Recall Responses Post-SIVmac251 Challenge and
Controls Viral Replication During Setpoint and Chronic Phases ................................................. 124
Future Directions in AIDS Vaccine Development ........................................................................ 124
Electroporation of an HIV-1 DNA Vaccine Based on an Alphavirus Replicon Vector Has a DoseSparing Effect ............................................................................................................................... 124
Conserved Elements Vaccine for HIV-1 P24gag Is Immunogenic in Mice and Macaques ......... 125
Enhanced Level and Quality of Memory T Cells Elicited by a Replicating Ad-HIVenv and -HIVtat
Prime/Protein Boost Regimen Compared to Tat- or Env-Only Regimens ................................... 125
Vaccine Antigen Designs to Address HIV Variability ................................................................... 125
RAd Prime/RLCMV Boost Vaccination Induces Long-Lasting HIV-1 Specific Humoral and Cellular
Immune Responses in Mice ......................................................................................................... 125
Cytotoxic Capacity of SIV-Specific-CD8+T Cells From SIV-Infected Rhesus Macaques Measured
Against Primary Autologous CD4+T Cells .................................................................................... 126
Vaccine Design: Lessons From Acute HIV-1 Infection ................................................................ 126
GB Virus C Envelope Protein E2 Elicits Polyvalent Antibodies That Cross-React With HIV-1 Gp41
MPER (T-20) and Lipids ............................................................................................................... 126
Cross-Reactive Anti-HIV Neutralizing Antibody Responses During Acute / Early HIV Infection . 126
Adjuvant Effect on the Induction of Glycan-Specific Antibodies Against HIV Env Using Single
Yeast Glycoproteins ..................................................................................................................... 127
HIV Fragment Vaccine Induces Broader T Cell Response in Mice ............................................. 127
The Antiviral Efficacy of HIV-Specific CD8+ Tcells to a Conserved Epitope Is Heavily Dependent
on the Infecting HIV-1 Isolate ....................................................................................................... 127
HIV/SIV Vaccine Efficacy Dependent on the Dose of SIVmac251 Challenge Exposure in
Macaques ..................................................................................................................................... 127
TSLP, a Promising New Mucosal Adjuvant for Intranasal Immunisation With Gp140 ................. 128
Innate and Adaptive Immune Correlates of Vaccine-Induced Control of Mucosal Transmission of
SIV in Macaques .......................................................................................................................... 128
Deciphering HIV Epitope Production: Implications for Immunogen Design ................................. 128
Biochemical, Biophysical Characterization and Immunogenicity of HIV Envelopes Derived From
Clade C Primary Early Isolates .................................................................................................... 128
AS01, an Adjuvant System Potentiating Vaccines Against Complex Pathogens ........................ 129
The Effect of Vaccine-Induced SIV-Specific Immune Response on Viral Acquisition and
Replication .................................................................................................................................... 129
Oral Vaccination With Lipid Vehicle-Entrapped Multivalent HIV Peptides Enhances Specific
Immune Responses ..................................................................................................................... 129
VSV Vectors Expressing Chimeric SIV Envelope Proteins Direct Antibody Response Against
Gp41 ............................................................................................................................................. 129
Macaques Vaccinated With SlVmac239?Nef Delay Acquisition and Control Replication After
Repeated Low Dose Heterologous SIV Challenge ...................................................................... 129
Strong Protection Against SIVsmE660 Mucosal Challenge Conferred by a Novel, Heterologous,
Prime-Boost Vaccine Regimen .................................................................................................... 130
HIV-Specific Antibodies Mediate Rapid Antibody-Dependent Cellular Cytotoxicity Against Primary
HIV-Infected CD4+ T Cells ........................................................................................................... 130
HIV-1 Epidemic in India: Deciding the Decisive Lmmunogenetic Correlates for Designing Vaccine
Strategies ..................................................................................................................................... 130
Characterization of Neutralizing Quaternary Epitope Exposure on Soluble HIV-1 Env Constructs
...................................................................................................................................................... 130
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HIV-1 Peptides Expressed by Recombinant Modified Vaccinia Virus Ankara Activate Natural Killer
Cells Capable of Controlling HIV Infection in Dendritic Cells In Vitro .......................................... 131
Induction of Distinct Clonotypes by Overlapping HLA-A2-Restricted HIV Gag-Epitopes May
Contribute to Their Subdominant Status ...................................................................................... 131
Targeting HIV Peptides to HIV Patient Dendritic Cells Via CD40 Elicits Expansion of Multi-Epitope
Polyfunctional CD4+ and CD8+T Cells ......................................................................................... 131
Live Attenuated SIV: Characterising the Role of Vaccine Persistence in Protection ................... 132
Complement As an Endogenous Adjuvant for Dendritic Cell-Mediated Induction of RetrovirusSpecific CTLs ............................................................................................................................... 132
Enhanced Mucosal and Systemic Humoral Responses Following Intranasal Immunization With
HIV-1 Gp140 Combined With TLR-4 and Chitosan Adjuvants .................................................... 132
Isolation of Cross-Clade HIV-Neutralizing Human Antibodies From Memory B Cell Repertoires
Using Short Term Culture and High-Throughput Primary Neutralization Screens ...................... 132
A High Throughput Screen for Small Molecule Haptens Binding to an HIV-1 Neutralizing Antibody
Yields Vaccine Leads ................................................................................................................... 133
Comparison of Intravenous and Low-Dose Rectal SIVmac251 Challenge Models in the Setting of
Adenovirus-Based Immunization ................................................................................................. 133
Recombinant Yellow Fever Vaccine Virus 17D Expressing SlVmac239 Gag Induces SIV-Specific
CD8+ T Cell Responses in Rhesus Macaques ............................................................................ 133
HIV-1 Envelope-CD4 Receptor Complexes Elicit Broad T- and Bcell Immune Responses As Well
As Cross-Reactive Neutralizing Antibodies in Rhesus Macaques ............................................... 134
Ultra-Deep Sequencing During Acute HIV Infection Reveals the Earliest Adaptive Changes to
Host Selection Pressures ............................................................................................................. 134
Characterization of HIV Epitope-Specific CD8+ T Cell Clonal Repertoires After Vaccination ..... 134
Direct Comparison of Soluble Multimeric Forms of CD40L, CD27L, 4-1 BBL, and BAFF to IL-12
and IL-15 As HIV DNA Vaccine Adjuvants .................................................................................. 135
Characterization of Simian Adenoviruses As the Base for a New Generation OfAdenovirus
Vaccine Vectors ........................................................................................................................... 135
Design of Improved CD4bs Mimetics for HIV-1 Immunization ..................................................... 135
Immunosafety Assessment of CD4 MAB-Based Bifunctional HIV Entry Inhibitor (CD4-BFFI) Using
In Vitro Immunoassays ................................................................................................................. 135
Improved Immunogenicity Conferred by Activated but Not Resting Apoptotic Lymphocytes ...... 135
Comparison of Antibody Responses Induced by a Virus-Like Particle-Based Vaccine Upon
Intramuscular, Pulmonary, and Vaginal Delivery ......................................................................... 136
Novel VLPs Rapidly Induce High Titer Neutralizing Antibodies When Combined With DNA
Vaccines in Rabbits ...................................................................................................................... 136
Comparative Analysis of Rare Adenovirus Serotypes and Their Effects on Human Dendritic Cells
...................................................................................................................................................... 136
Antibodies Elicited by a Heterologous Glycoprotein Mediate a Broad Neutralization of HIV ...... 136
Lessons Learned From Live Attenuated SIV ............................................................................... 137
Targeting the Vaginal Mucosa With Human Papilloma Virus Psudovirions Delivering SIV DNA
Vaccines ....................................................................................................................................... 137
NSG-Hu Mice Generate HIV Specific Human Immune Responses After Gp96 Vaccination ...... 137
Immune Activation of Human and Macaque Dendritic Cells and Macrophages Upon Infection by
HIV and Single Cycle SIV Viruses Encoding TRAF- Mediated Activation Domains .................... 137
Virology..........................................................................................................................138
Molecular Epidemiology of the Transmission of HIV-1 Between Couples in the Central Area of
Portugal ........................................................................................................................................ 138
Study of the Mutations Associated to Integrase Inhibitor Resistance in Subtype B and Non-B
Human Immunodeficiency Virus Type 1 ...................................................................................... 138
Predictors of Immunological Failure Among Adult Patients Receiving Antiretroviral Therapy (ART)
at an HIV/AIDS Program in Uganda ............................................................................................. 138
Diversity of HIV-1 Subtype C Strains Isolated in Romania: a Phylogenetic Analysis .................. 138
Resistance Levels in Patients Failing Initial PI or NNRTI Combination Therapy in Greece ........ 139
S/GSK1349572, a Next Generation Integrase Inhibitor (INI), Has Potential for a High Genetic
Barrier to Resistance Based on in Vitro Passage Study .............................................................. 139
The Role of HIV Recombination In Shaping the Current HIV Epidemic ...................................... 139
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EUROPRISE SCIENCE UPDATE 10-17
Structure-Guided Approach for the Development of Molecular-Targeting Agents for AIDS Therapy
...................................................................................................................................................... 140
Molecular Epidemiology of HIV-1 Subtypes Circulating in Russia Based on Analysis of Pol
Sequences in Plasma Samples Collected in 2007- 2009 ............................................................ 140
Pyrosequencing of HIV-1 Reverse Transcriptase to Reveal Minority Populations of Resistant
Virus Before Start of a NNRTI-Based Regimen ........................................................................... 140
HIV-Infected Patients With Positive MT-2 Cultures May Need More Frequent Monitoring and/or
HAART Initiation at Higher CD4 Counts ...................................................................................... 140
Detection of Predicted CXCR4-Using HIV-1 Variants in Longitudinally Obtained Paired Plasma
and PBMC Samples Using 454-Sequencing ............................................................................... 141
HIV-1 Integrase Mutation E157Q Has Low Impact on Integrase Inhibitor Resistance: a Case
Report ........................................................................................................................................... 141
HIV Drug Resistance in Children With Treatment Failure to First-Line Regimens in Ho Chi Minh
City, Vietnam ................................................................................................................................ 141
Determinants of Virological Response to Raltegravir (RAL)-Containing Regimens and Prevalence
of RAL-Resistance Associated Mutations at Failure in ARCA ..................................................... 141
Evaluation of Drug Resistance Among HIV-1 B, C and F Subtypes Drug-Treated Patients
Followed in Central Italy ............................................................................................................... 142
Characterisation of HIV-1 From Patients With Virological Failure to a Boosted Protease Inhibitor
Regimen ....................................................................................................................................... 142
Raltegravir Genetic Resistance Patterns in HIV-2 Infected Patients Failing Raltegravir-Containing
Regimen ....................................................................................................................................... 142
Severe Immune Suppression in Patients Exclusively Infected With HIV-1 R5 Variants Is
Associated With a Higher Net Charge in Gp120 Variable Regions ............................................. 142
Consecutive Increase of HIV-1 Transmitted Drug Resistance Rate in Poland ............................ 143
HIV-1 Tropism and Drug Resistance Mutations in Subtype C-Infected Patients From KwaZulu
Natal ............................................................................................................................................. 143
Primary Resistance to Maraviroc in a Large Set of V3 Sequences From Recent Seroconverters,
Drug-Naïve, and Antiretroviral-Experienced HIV+ Patients ......................................................... 143
Polymorphisms in the Integrase Gene of Antiretroviral Therapy Naïve Patients Infected With HIV1 Non-B Subtypes: The SnoB Study ............................................................................................ 143
Transmission of Drug Resistance, X4 Variants and Non-B Subtypes in a Large Cohort of HIV
Recent Seroconverters in Spain .................................................................................................. 144
Phylogenetic Analysis of HIV-1 B and Non-B Subtypes in Newly Diagnosed Individuals in Ireland
...................................................................................................................................................... 144
Declining Prevalence of HIV 1 Transmitted Drug Resistance in Ireland 2004- 2008 .................. 144
Dynamic Escape of Pre-Existing Raltegravir-Resistant HIV-1 From Raltegravir Pressure ......... 145
Resistance Mutations and HIV-1 Genetic Diversity Among Newly Diagnosed Patients in Two
Different Geographical Areas of Spain......................................................................................... 145
Trends, Along a Decade, of Antiretroviral Resistance in a Newly Diagnosed HIV-1 Cohort of From
Galicia, Spain, Including Diverse Genetic Forms ......................................................................... 145
Sudden Viral Load Increase As an Indicator of HIV-1 Superinfection in HAART-Naive HIVInfected Patients ........................................................................................................................... 146
Emergence of Resistance to the New Drug Classes in an Italian National Database: 2007-2009
...................................................................................................................................................... 146
Faster HIV-1 Disease Progression Among Brazilian Recently Infected Individual Harboring
CXCR4 Using Strains ................................................................................................................... 146
Evaluation of Hiv-1 Genetic Diversity in Infected Mothers From Two Regions of Portugal Enrolled
in A Study of Mother-To-Child Transmission ............................................................................... 147
ARV Resistance in HIV-1 From Drug-Naive and Treated Patients in Bulgaria............................ 147
Rega 8: An Improved Genotypic Interpretation System That Significantly Predicts HIV-Therapy
Response for B and Non-B Subtypes .......................................................................................... 147
Prevalence of HIV-1 Subtypes and Drug Resistance Mutations in ResRIS, the National Drug
Resistance Database of the Spanish AIDS Research Network ................................................... 147
Identification of a New HIV-1 Circulating Recombinant Form (CRF44-DB) in Spain .................. 148
HIV-1 Diversity Among Different Risk Groups in Bulgaria ........................................................... 148
Transmitted Drug Resistance in HIV-1 CRF06_Cpx Infected Patients in Estonia in 2008 .......... 148
Mutations at the C-Terminal Domain of RT in HIV-1+ Patients Failing Nevirapine or Efavirenz Do
Not Display Strong Impact on Etravirine Susceptibility ................................................................ 148
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EUROPRISE SCIENCE UPDATE 10-17
Impact of Baseline HIV-1 Integrase Polymorphisms With Virological Outcome in Patients Starting
a Raltegravir-Containing Regimen ............................................................................................... 149
Drug Resistance Mutations in HIV-1+ Non-B Subtypes in Spain - More Frequent and No
Preferential Selection of K65R in Clade C Than in Other Subtypes ............................................ 149
Decreasing Prevalence and 5-Year Incidence of Major NRTI-, NNRTI- and PI-Mutations in ARTExperienced HIV-Patients in Stockholm, Sweden ....................................................................... 149
The Influence of PCR Amplification Variation on the Ability of Population-Based PCR to Detect
Non-R5 HIV .................................................................................................................................. 150
Integrase Inhibitor Resistance-Associated Mutations Have No Impact on Performance of the
Abbott ReaITime HIV-1 Assay ..................................................................................................... 150
HIV Drug Resistance Patterns of Maternal HAART Cohorts to Prevent HIV Postnatal Mother-toChild Transmission in Rwanda ..................................................................................................... 150
Development of Resistance to the Natural HIV-1 Entry Virus Inhibitory Peptide (VIRIP) ............ 150
Residual Activity of Raltegravir Despite Multiple N155H Pathway Resistance Mutations ........... 151
Differences in Susceptibility to Darunavir and Etravirine Reported by Two Genotypic Interpretation
Systems ........................................................................................................................................ 151
Resistance Patterns in HIV+ Patients Failing Raltegravir Outside Clinical Trials - the Spanish
Integrase Resistance (SINRES) Group........................................................................................ 151
Resistance Mutations in the Viral Protease Alter the in Vitro Resistance Profiles of Bevirimat .. 151
Temporal Changes in HIV Drug Resistant Prevalences Across the World. Review ................... 152
-------------------------------------------------------------
Microbicides
Acceptability and Adherence of a Candidate Microbicide Gel Among
High-Risk Women in Africa and India
GREENE E., Batona, G., Hallad, J., Johnson, S., Neema, S., and Tolley, E. E.
Cult.Health Sex. 1 ,2010
AD - Family Health International, Research Triangle Park, North Carolina, USA
ENG
Vaginal microbicides currently under development are substances that may prevent the
transmission of HIV. Qualitative, in-depth post-trial interview data from a Phase III clinical
trial of 6% Cellulose Sulfate microbicide gel in two sites in Africa (Uganda and Benin) and
two in India (Chennai and Bagalkot) were examined in order to better understand factors
that influence microbicide acceptability and adherence in a clinical trial setting. Women
found the gel relatively easy to use with partners with whom there were no expectations of
fidelity, in situations where they had access to private space and at times when they were
expecting to engage in sexual intercourse. Adherence to gel seemed significantly more
difficult with primary partners due to decreased perceptions of risk, inconvenience or fear of
partner disapproval. Findings suggest that women in a variety of settings may find a
microbicide gel to be highly acceptable for its lubricant qualities and protective benefits but
that adherence and consistent use may depend greatly on contextual and partner-related
factors. These findings have important implications for future trial designs, predicting
determinants of microbicide use and acceptability and marketing and educational efforts
should a safe and efficacious microbicide be found
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20397080
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HIV/Microbicides
Magnetic Resonance Imaging of Topical Microbicide Formulations
in the Pigtailed Macaque: Product Distribution and Transport
PATTON D.
,Rancho Mirage, CA; USA, P-32 ,2010
Source: Conference (MIS)
------------------------------------------------------
Diagnosis
Use of the Rapid HIV Test in the Newborn and Cord Blood
MALAGA L., Rajbhandari, P., Purswani, J., Hagmann, S., Dunne, J., and Purswani, M.
,Vancouver, BC; Canada, 2870.585 ,2010
Bronx-Lebanon Hospital Center, Bronx, NY; Irvington High School, Irvington, NY
Source: Conference (MIS)
-----------------------------------------------------HIV/Diagnosis
Easier Said Than Done: HIV Screening in Pediatric Primary Care
RELLOSA N., White, K., Fogel, B., Levy, C., and Freedman, A.
,Vancouver, BC; Canada, 1477.270 ,2010
Infectious Diseases, Children's National Medical Center, Washington, DC; General
Pediatrics, Nemours/A.I.duPont Hospital for Children, Wilmington, DE; General Pediatrics,
The Children's Hospital of Philadelphia, Philadelphia, PA; Infectious Diseases,
Nemours/A.I.duPont Hospital for Children, Wilmington, DE
Source: Conference (MIS)
-----------------------------------------------------HIV/Diagnosis
Patterns of HIV Testing in Adolescent Couples
WELLS C., Watnick, D., and Bauman, L.
,Vancouver, BC; Canada, 2842.163 ,2010
Stanford School of Medicine, Stanford, CA; Pediatrics, Albert Einstein College of Medicine,
Bronx, NY
Source: Conference (MIS)
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EUROPRISE SCIENCE UPDATE 10-17
HIV/Diagnosis
Implementation of Opt-Out Oral Rapid HIV Screening in the
Pediatric Emergency Department in an Urban Area With High
Prevalence of HIV Infection
BAGHDASSARIAN A., Walkoff, L., Khan, M., Kingsnorth, J., Sathe, N., Johnson, B.,
Chamberlain, J., Sill, A., Teach, S., and Rakhmanina, N.
,Vancouver, BC; Canada, 1494.462 ,2010
Pediatrics, The George Washington University, Washington, DC; Emergency Medicine,
Children's National Medical Center, Washington, DC; Infectious Diseases, Children's
National Medical Center, Washington, DC; Biostatistics and Informatics, Children's National
Medical Center, Washington, DC
Source: Conference (MIS)
-----------------------------------------------------HIV/Diagnosis
SPiral Isothermal DNA Replication (SPIDR): A Novel Method for
Nucleic Acid Amplification and Role in Rapid Infectious Disease
Diagnostics
DHAMNE N., Ishwad, C., Mead, D., Ross, T., Wadowsky, R., and Vats, A.
,Vancouver, BC; Canada, 2868.551 ,2010
Childrens Hospital of Pittsburgh, Pittsburgh, PA; Lucigen Corp, Middleton, WI; University
of Pittsburgh, Pittsburgh, PA
Source: Conference (MIS)
-----------------------------------------------------HIV/Diagnosis
An Integrated, Self-Contained Microfluidic Cassette for Isolation,
Amplification, and Detection of Nucleic Acids
CHEN D., Mauk, M., Qiu, X., Liu, C., Kim, J., Ramprasad, S., Ongagna, S., Abrams, W. R.,
Malamud, D., Corstjens, P. L., and Bau, H. H.
Biomed.Microdevices. 2010
AD - Department of Mechanical Engineering and Applied Mechanics, University of
Pennsylvania,
Philadelphia,
PA,
19104,
USA
ENG
A self-contained, integrated, disposable, sample-to-answer, polycarbonate microfluidic
cassette for nucleic acid-based detection of pathogens at the point of care was designed,
constructed, and tested. The cassette comprises on-chip sample lysis, nucleic acid isolation,
enzymatic amplification (polymerase chain reaction and, when needed, reverse
transcription), amplicon labeling, and detection. On-chip pouches and valves facilitate fluid
flow control. All the liquids and dry reagents needed for the various reactions are pre-stored
in the cassette. The liquid reagents are stored in flexible pouches formed on the chip surface.
Dry (RT-)PCR reagents are pre-stored in the thermal cycling, reaction chamber. The process
operations include sample introduction; lysis of cells and viruses; solid-phase extraction,
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EUROPRISE SCIENCE UPDATE 10-17
concentration, and purification of nucleic acids from the lysate; elution of the nucleic acids
into a thermal cycling chamber and mixing with pre-stored (RT-)PCR dry reagents; thermal
cycling; and detection. The PCR amplicons are labeled with digoxigenin and biotin and
transmitted onto a lateral flow strip, where the target analytes bind to a test line consisting of
immobilized avidin-D. The immobilized nucleic acids are labeled with up-converting
phosphor (UCP) reporter particles. The operation of the cassette is automatically controlled
by an analyzer that provides pouch and valve actuation with electrical motors and heating
for the thermal cycling. The functionality of the device is demonstrated by detecting the
presence of bacterial B.Cereus, viral armored RNA HIV, and HIV I virus in saliva samples.
The cassette and actuator described here can be used to detect other diseases as well as the
presence of bacterial and viral pathogens in the water supply and other fluids
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20401537
-----------------------------------------------------HIV/Diagnosis
Need for Point-of-Care HIV Molecular Diagnostic Technologies in
Resource-Limited Settings. Proceedings From the Workshop
"Novel Technologies in Rapid HIV-1 Viral Detection"
J.Infect.Dis. 201 Suppl 1:S1-84., S1-84 ,2010
engLink
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20225953
-----------------------------------------------------HIV/Diagnosis
Highly Variable Use of Diagnostic Methods for Sexually Transmitted
Infections - Results of a Nationwide Survey, Germany 2005
GILSDORF A., Hofmann, A., Hamouda, O., and Bremer, V.
BMC.Infect.Dis. 10 (1), 98 ,2010
ENG
ABSTRACT: BACKGROUND: Sexual transmitted infections (STIs) have increased in
Germany and other countries in Europe since the mid-nineties. To obtain a better picture of
diagnostic methods used in STI testing institutions in Germany, we performed a nationwide
survey amongst STI specialists in order to evaluate the quality of STI reports and provide
recommendations to harmonize and possibly improve STI diagnostics in Germany.
METHODS: We asked sentinel physicians and randomly chosen gynaecologists, urologists
and dermato-venerologists, about the diagnostic methods used in 2005 to diagnose HIV,
chlamydia (CT), gonorrhoea (GO) and syphilis (SY) in a national cross-sectional survey in
order to recognize potential problems and provide recommendations. RESULTS: A total of
739/2287 (32%) physicians participated. Of all participants, 80% offered tests for HIV, 84%
for CT, 83% for GO and 83% for SY. Of all participants who performed HIV testing, 90%
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EUROPRISE SCIENCE UPDATE 10-17
requested an antibody test, 3% a rapid test and 1% a nucleic acid amplification test (NAAT).
For CT testing, NAAT was used in 33% and rapid tests in 34% of participants. GO resistance
testing was performed by 31% of the participants. SY testing was performed in 98% by
serology. CONCLUSIONS: Diagnostic methods for STI vary highly among the participants.
Diagnostic guidelines should be reviewed and harmonised to ensure consistent use of the
optimal STI diagnostic methods
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20403184
-----------------------------------------------------HIV/Diagnosis
The Role of HIV-DNA Testing in Clinical Practice
D'ETTORRE G., Zaffiri, L., Ceccarelli, G., Mastroianni, C. M., and Vullo, V.
New Microbiol. 33 (1), 1-11 ,2010
AD - Department of Tropical and Infectious Diseases, "La Sapienza" University of Rome,
Italy
gabrielladettorre@uniroma1it
eng
HIV-1 RNA levels and CD4+T lymphocyte counts are currently the standard markers used
in clinical practice for the management of HIV infection. Nowadays it is also possible to
monitor the evolution of HIV infection by measuring HIV-DNA. This measurement is a
useful new clinical marker mainly been used to date in experimental evaluations. HIV-DNA
can be detected in lymphoid tissues and in PBMC even during powerful and prolonged
antiretroviral therapy. Understanding the HIV-DNA marker, together with all the other
standard markers used in clinical practice, is now essential in monitoring the progression of
the infection. Furthermore, the measurement of the levels of HIV-DNA in different stages
could indicate the spread of the infection reflecting the ability of antiretroviral therapy to
purge reservoirs. This review highlights the importance of evaluating the HIV-DNA load
which could provide an indirect estimate of the quantity of reservoirs. This is an important
factor in establishing the progression of infection, sequencing therapy and predicting the
failure of antiretroviral therapy at a early stage
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20402409
-----------------------------------------------------HIV/Diagnosis
Need for Point-of-Care HIV Molecular Diagnostic Technologies in
Resource-Limited Settings. Proceedings From the Workshop
"Novel Technologies in Rapid HIV-1 Viral Detection"
J.Infect.Dis. 201 Suppl 1:S1-84., S1-84 ,2010
engLink
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20225953
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21 / 152
EUROPRISE SCIENCE UPDATE 10-17
-----------------------------------------------------HIV/Diagnosis
A Simple Fluorescence Based Assay for Quantification of Human
Immunodeficiency Virus Particle Release
HERMLE J., Anders, M., Heuser, A. M., and Mueller, B.
BMC.Biotechnol. 10 (1), 32 ,2010
ENG
ABSTRACT: BACKGROUND: The assembly and release of human immunodeficiency virus
(HIV) particles from infected cells represent attractive, but not yet exploited targets for
antiretroviral therapy. The availability of simple methods to measure the efficiency of these
replication steps in tissue culture would facilitate the identification of host factors essential
for these processes as well as the screening for lead compounds acting as specific inhibitors
of particle formation. We describe here the development of a rapid cell based assay for
quantification of human immunodeficiency virus type 1 (HIV-1) particle assembly and/or
release. RESULTS: Using a fluorescently labelled HIV-derivative, which carries an eYFP
domain within the main viral structural protein Gag in the complete viral protein context,
the release of virus like particles could be monitored by directly measuring the fluorescence
intensity of the tissue culture supernatant. Intracellular Gag was quantitated in parallel by
direct fluorescence analysis of cell lysates, allowing us to normalize for Gag expression
efficiency. The assay was validated by comparison with p24 capsid ELISA measurements, a
standard method for quantifying HIV-1 particles. Optimization of conditions allowed the
robust detection of particle amounts corresponding to 25 ng p24/ml in medium by
fluorescence spectroscopy. Further adaptation to a multi-well format rendered the assay
suitable for medium or high throughput screening of siRNA libraries to identify host cell
factors involved in late stages of HIV replication, as well as for random screening approaches
to search for potential inhibitors of HIV-1 assembly or release. CONCLUSIONS: The fast and
simple fluorescence based quantification of HIV particle release yielded reproducible results
which were comparable to the well established ELISA measurements, while in addition
allowing the parallel determination of intracellular Gag expression. The protocols described
here can be used for screening of siRNA libraries or chemical compounds, respectively, for
inhibition of HIV in a 96-well format
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20406458
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EUROPRISE SCIENCE UPDATE 10-17
Epidemiology
HIV Risk Behavior in Treatment-Seeking Opioid-Dependent Youth:
Results From a NIDA Clinical Trials Network Multisite Study
MEADE C. S., Weiss, R. D., Fitzmaurice, G. M., Poole, S. A., Subramaniam, G. A., Patkar, A.
A., Connery, H. S., and Woody, G. E.
J.Acquir.Immune.Defic.Syndr. 2010
AD - From the *Department of Psychiatry and Behavioral Sciences, Duke University Medical
Center, Durham, NC; daggerDepartment of Psychiatry, Harvard Medical School and
McLean Hospital, Belmont, MA; double daggerDepartment of Psychiatry, University of
Pennsylvania and Treatment Research Institute, Philadelphia, PA; and section signDivision
of Clinical Neuroscience and Behavioral Research, National Institute on Drug Abuse,
Bethesda,
MD
ENG
OBJECTIVE:: To assess baseline rates of and changes in HIV drug and sexual risk behavior as
a function of gender and treatment in opioid-dependent youth. METHODS:: One hundred
fifty participants were randomly assigned to extended buprenorphine/naloxone therapy
(BUP) for 12 weeks or detoxification for 2 weeks; all received drug counseling for 12 weeks.
HIV risk was assessed at baseline and 4-week, 8-week, and 12-week follow-ups. Behavioral
change was examined using generalized estimating equations. RESULTS:: Baseline rates of
past-month HIV risk for females/males were 51%/45% for injection drug use (IDU) (ns),
77%/35% for injection risk (P < 0.001), 82%/74% for sexual activity (ns), 14%/24% for
multiple partners (ns), and 68%/65% for unprotected intercourse (ns). IDU decreased over
time (P < 0.001), with greater decreases in BUP versus detoxification (P < 0.001) and females
versus males in BUP (P < 0.05). Injection risk did not change for persistent injectors. Sexual
activity decreased in both genders and conditions (P < 0.01), but sexual risk did not.
CONCLUSIONS:: Overall, IDU and sexual activity decreased markedly, particularly in BUP
patients and females, but injection and sexual risk behaviors persisted. Although extended
BUP seems to have favorable effects on HIV risk behavior in opioid-dependent youth, risk
reduction counseling may be necessary to extend its benefits
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20393347
-----------------------------------------------------HIV/Epidemiology
[Epidemiology of HIV. Update]
DORRUCCI M.
Recenti Prog.Med. 101 (1), 12-15 ,2010
AD - Dipartimento di Malattie Infettive, Parassitarie e Immunomediate, Reparto di
Epidemiologia,
Istituto
Superiore
di
Sanita,
Roma
mariadorrucci@issit
ita
In this decade, the global prevalence of HIV-1 infection stabilized at 0.8% (range: 0.7-0.9%).
However, important regional differences in trends and mode of transmission: Sub-Saharan
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EUROPRISE SCIENCE UPDATE 10-17
Africa is the most affected by HIV. Since 2001, the number of people with HIV in Eastern
Europe and Central Asia increased from 650,000 to 1,5 million in 2007. Overall trends were
stable in Central and Western Europe. Heterosexual and homosexual transmission accounts
for the largest proportion in these regions. Transmission among injecting drug users has
decreased. Similar trends have been observed in Italy: in 2007, there were 1,679 new
diagnoses, equivalent to an incidence of 6,0 per 100,000 population. Over the years there has
been a progressive increase in the proportion of diagnoses among women and in the median
age at diagnosis, as well as changes in the exposure categories (i.e. a decrease in the
proportion of injecting drug users and an increase in infections attributed to homosexual and
heterosexual contacts). The era of combination antiretroviral therapy (cART) has resulted in
a reduction of morbidity and mortality. Before the advent of cART in 1996, the main causes
of morbidity and mortality in people with HIV were the opportunistic infections and
malignancies AIDS associated
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20391681
-----------------------------------------------------HIV/Epidemiology
Sexual Behavior and Knowledge of Sexually Transmitted Infections
Among University Students in Sao Paulo, Brazil
CAETANO M. E., Linhares, I. M., Pinotti, J. A., Maggio da, Fonseca A., Wojitani, M. D., and
Giraldo, P. C.
Int.J.Gynaecol.Obstet. 2010
AD - Department of Gynecology and Obstetrics, University of Sao Paulo Medical School,
Hospital
das
Clinicas,
Sao
Paulo,
Brazil
ENG
OBJECTIVE: To investigate the sexual behavior and knowledge about sexually transmitted
infections (STIs) among undergraduate students in Sao Paulo, Brazil. METHODS: Selfreported questionnaires were used. RESULTS: Most of the 447 students in the study were
single (97.3%), in their first year of university (87.7%), and the mean ages were 20.4years
(males) and 19.8years (females). Vaginal intercourse was practiced by 69.7% of males and
48.4% of females, oral sex by 64.5% of males and 43.7% of females, and anal sex by 18.4% of
males and 14.1% of females. Use of a condom during vaginal sex was practiced by 80.4% of
males and 74.8% of females and during anal sex by 47.8% of males and 30.0% of females.
Knowledge of transmission of STIs was greater than 90% for HIV, syphilis, genital herpes,
and gonorrhea; 63%-76% for HPV and genital warts; 30%-34% for Trichomonas and only
16% for Chlamydia. Only 25%-34% knew that HIV was transmitted by breastfeeding; 56%60% knew that HIV was transmitted by anal sex. CONCLUSION: Many students engage in
high-risk sexual behavior with multiple partners and use condoms inconsistently.
Knowledge of the acquisition and modes of sexual and vertical transmission of HIV are
strikingly deficient
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20394925
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EUROPRISE SCIENCE UPDATE 10-17
HIV/Epidemiology
Prevalence and Pattern of Disclosure of HIV Status in HIV-Infected
Children in Ghana
KALLEM S., Renner, L., Ghebremichael, M., and Paintsil, E.
,Vancouver, BC; Canada, 2870.584 ,2010
Yale University School of Medicine, New Haven, CT; University of Ghana Medical School,
Accra, Ghana; Harvard University, Cambridge, MA
Source: Conference (MIS)
-----------------------------------------------------HIV/Epidemiology
Practice of Feeding Premasticated Food to Infants Among HIVInfected Mothers
SALAMI O., Hafeez, S., Maldonado, M., Alvarado, M., Purswani, M., and Hagmann, S.
,Vancouver, BC; Canada, 443 ,2010
Department of Pediatrics, Albert-Einstein College of Medicine, Bronx-Lebanon Hospital
Center, Bronx, NY; Division of Pediatric Infectious Diseases, Albert-Einstein College of
Medicine, Bronx-Lebanon Hospital Center, Bronx, NY
Source: Conference (MIS)
-----------------------------------------------------HIV/Epidemiology
Trends in Pediatric HIV Hospitalizations
RAUCH D.
,Vancouver, BC; Canada, 2870.578A ,2010
Pediatrics, Mt. Sinai School of Medicine/Elmhurst Hospital Center, Elmhurst, NY
Source: Conference (MIS)
-----------------------------------------------------HIV/Epidemiology
PRBC Transfusion and Infection Risk: What Have We Learned From
Hepatitis and HIV, and What Might the Future Hold?
KLEINMAN S., Caplan, M., and Carlo, W.
,Vancouver, BC; Canada ,2010
1) University of British Columbia, Vancouver, BC, Canada; 2) Northshore University Health
System, Evanston, IL; 3) University of Alabama at Birmingham, Birmingham, AL
Source: Conference (MIS)
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EUROPRISE SCIENCE UPDATE 10-17
HIV/Epidemiology
Love, Trust and Condom Use in Serious Teen Relationships
BAUMAN L., Watnick, D., and Silver, E.
,Vancouver, BC; Canada, 2765.6 ,2010
Pediatrics, Albert Einstein College of Medicine, Bronx, NY
Source: Conference (MIS)
-----------------------------------------------------HIV/Epidemiology
Change Over Time in the HIV/AIDS Risk Perceptions of South
African Youth
ANDERSON K. and Beutel, A.
,Dallas, TX; USA ,2010
University of Oklahoma
Source: Conference (MIS)
-----------------------------------------------------HIV/Epidemiology
Sugar Daddies Syndrome: Elderly Sexual Behaviour and
Implications for the Spread of HIV/AIDS in Nigeria
WAHAB E.
,Dallas, TX; USA ,2010
Lagos State University
Source: Conference (MIS)
-----------------------------------------------------HIV/Epidemiology
Community HIV Prevalence and Parity Progression
DEROSE L.
,Dallas, TX; USA ,2010
University of Maryland
Source: Conference (MIS)
-----------------------------------------------------HIV/Epidemiology
Environmental Change, Risky Sexual Behavior, and the HIV/AIDS
Pandemic: Exploring Linkages Through Livelihoods in Rural Haiti
HUNTER L., Reid-Hresko, J., and Dickinson, T.
,Dallas, TX; USA ,2010
University of Colorado, Boulder
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EUROPRISE SCIENCE UPDATE 10-17
Source: Conference (MIS)
-----------------------------------------------------HIV/Epidemiology
Using Population Policies and Non-Governmental Organizations to
Explain HIV/AIDS Outcomes in Sub-Saharan Africa
ROBINSON R.
,Dallas, TX; USA ,2010
American University
Source: Conference (MIS)
-----------------------------------------------------HIV/Epidemiology
Perceptions of Risk and Sexual Behavior Change Following Adult
Male Circumcision in Urban Swaziland
GRUND J. and Hennink, M.
,Dallas, TX; USA ,2010
Emory University
Source: Conference (MIS)
-----------------------------------------------------HIV/Epidemiology
Gender, Family, and HIV/AIDS in Lesotho
HARRISON A., Short, S., Tuoane-Nkhasi, M., and Hlabana, T.
,Dallas, TX; USA ,2010
1) Brown University; 2) Statistics South Africa
Source: Conference (MIS)
-----------------------------------------------------HIV/Epidemiology
Risky Sexual Behavior, Substance Abuse and Sexually Transmitted
Infections Among Street Adolescents in India
GHOSH A. and Ladusingh, L.
,Dallas, TX; USA ,2010
International Institute for Population Sciences (IIPS)
Source: Conference (MIS)
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HIV/Epidemiology
Community Factors Shaping the Sexual Behavior of Married Males
in 8 African Countries
STEPHENSON R.
,Dallas, TX; USA ,2010
Emory University
Source: Conference (MIS)
-----------------------------------------------------HIV/Epidemiology
Nepali College Students' Susceptibility to HIV
ADHIKARI R.
,Dallas, TX; USA ,2010
Tribhuvan University, Nepal
Source: Conference (MIS)
-----------------------------------------------------HIV/Epidemiology
Condom Use Negotiation and Practice Among Married Women in
Vietnam
MAI DO
,Dallas, TX; USA ,2010
Tulane University
Source: Conference (MIS)
-----------------------------------------------------HIV/Epidemiology
In Search of the Holy Grail: Improving Assessments of Sexual
Activity in Population Surveys Through Collecting Biomarkers
KULCZYCKI A.
,Dallas, TX; USA ,2010
University of Alabama, Birmingham
Source: Conference (MIS)
-----------------------------------------------------HIV/Epidemiology
Non Use of Condoms by Men in Marital Unions in Cameroon
NKOMA M.
,Dallas, TX; USA ,2010
Ministry of Economy, Cameroon
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EUROPRISE SCIENCE UPDATE 10-17
Source: Conference (MIS)
-----------------------------------------------------HIV/Epidemiology
Global Trends in AIDS Mortality
BONGAARTS J., Pelletier, F., and Gerland, P.
,Dallas, TX; USA ,2010
1) Population Council; 2) United Nations Population Division
Source: Conference (MIS)
-----------------------------------------------------HIV/Epidemiology
Sexual Concurrency in Uganda, Zambia and Zimbabwe: The Role of
Gender, Economic Status, and Migration
KLEIN HATTORI M., Braun, S., Chapman, H., Chuong, C., Morales, M., and Wagley, S.
,Dallas, TX; USA ,2010
1) Brown University; 2) Columbia University School of Social Work
Source: Conference (MIS)
-----------------------------------------------------HIV/Epidemiology
Transactional Sex and Sexually Transmitted Infections Among
Women in Uganda
NANKINGA O. and Kabagenyi, A.
,Dallas, TX; USA ,2010
Makerere University
Source: Conference (MIS)
-----------------------------------------------------HIV/Epidemiology
Frequency of HIV Type 2 Infections Among Blood Donor Population
From India: a 10-Year Experience
KANNANGAI R., Nair, S. C., Sridharan, G., Prasannakumar, S., and Daniel, D.
Indian J.Med.Microbiol. 28 (2), 111-113 ,2010
AD - Department of Immunohaematology and Transfusion Medicine, Christian Medical
College,
Vellore
632
004,
India
eng
PURPOSE: In India, HIV-2 epidemic is alongside with HIV-1. Blood banks are introducing
nucleic acid testing (NAT) for screening. The limitation of NAT systems is the inability to
detect HIV-2. MATERIALS AND METHOD: An analysis of HIV screening of a blood bank at
a tertiary care center from 1998 to 2007 was carried out. RESULTS: A total of 175026 donors
were screened by serological assays and 789 were reactive for HIV antibody. Only 478 (61%)
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EUROPRISE SCIENCE UPDATE 10-17
were confirmed positive by Western blot/immunoblot. There were 465 (97.2%) donations
positive for HIV-1, 6 (1.3%) for HIV-2 (monotypic infection) and 7 (1.5%) for HIV-1 and HIV2 (dual infection). CONCLUSION: We show the presence of HIV-2 infection among the
blood donors and the need for incorporating HIV-2 detection also in the NAT systems
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20404454
-----------------------------------------------------HIV/Epidemiology
Next Steps for Ukraine Abolition of HIV Registries, Implementation
of Routine Human Immunodeficiency Virus Testing and Expansion
of Services
IZENBERG J. M. and Altice, F. L.
Addiction. 105 (3), 569-570 ,2010
engLink
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20403006
-----------------------------------------------------HIV/Epidemiology
Impact of Injecting Drug Use on Mortality in Danish HIV-Infected
Patients: a Nation-Wide Population-Based Cohort Study
LARSEN M. V., Omland, L. H., Gerstoft, J., Larsen, C. S., Jensen, J., Obel, N., and Kronborg,
G.
Addiction. 105 (3), 529-535 ,2010
AD - Department of Infectious Diseases, Copenhagen University Hospital, DK - 2650
Hvidovre,
Denmark
mvlarsen@dadlnetdk
eng
OBJECTIVES: To estimate the impact of injecting drug use (IDU) on mortality in HIVinfected patients in the highly active antiretroviral therapy (HAART) era. DESIGN:
Population-based, nation-wide prospective cohort study in Denmark (the Danish HIV
Cohort Study). METHODS: A total of 4578 HIV-infected patients were followed from 1
January 1997 or date of HIV diagnosis. We calculated mortality rates stratified on IDU. One-,
5- and 10-year survival probabilities were estimated by Kaplan-Meier methods, and Cox
regression analyses were used to estimate mortality rate ratios (MRR). RESULTS: Of the
patients, 484 (10.6%) were categorized as IDUs and 4094 (89.4%) as non-IDUs. IDUs were
more likely to be women, Caucasian, hepatitis C virus (HCV) co-infected and younger at
baseline; 753 patients died during observation (206 IDUs and 547 non-IDUs). The estimated
10-year survival probabilities were 53.2% [95% confidence interval (CI): 48.1-58.3] in the IDU
group and 82.1% (95% CI: 80.7-83.6) in the non-IDU group. IDU as route of HIV infection
more than tripled the mortality in HIV-infected patients (MRR: 3.2; 95% CI: 2.7-3.8).
Adjusting for potential confounders did not change this estimate substantially. The risk of
HIV-related death was not increased in IDUs compared to non-IDUs (MRR 1.1; 95% CI 0.7--------------------------------------------------------------------------------------------------------------
30 / 152
EUROPRISE SCIENCE UPDATE 10-17
1.7). CONCLUSIONS: Although Denmark's health care system is tax paid and antiretroviral
therapy is provided free of charge, HIV-infected IDUs still suffer from substantially
increased mortality in the HAART era. The increased risk of death seems to be non-HIVrelated and is due probably to the well-known risk factors associated with intravenous drug
abuse
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20402997
-----------------------------------------------------HIV/Epidemiology
Pregnancy and HIV Infection in Young Women in North Carolina
TORRONE E. A., Wright, J., Leone, P. A., and Hightow-Weidman, L. B.
Public Health Rep. 125 (1), 96-102 ,2010
AD - University of North Carolina at Chapel Hill, Gillings School of Global Public Health,
Department of Epidemiology, CB# 7435, Chapel Hill, NC 27599, USA torrone@emailuncedu
eng
OBJECTIVES: We described young women in North Carolina (NC) who were pregnant at
the time of diagnosis with human immunodeficiency virus (HIV) infection to identify an atrisk population that could be targeted for increased HIV screening. We investigated the
combined effect of partner counseling and referral services (PCRS) and comprehensive
prenatal HIV screening. METHODS: We conducted a retrospective review of PCRS charts on
young women newly diagnosed with HIV in NC between 2002 and 2005. We determined the
prevalence of pregnancy in the study sample and conducted bivariate analyses to assess
predictors of pregnancy at the time of HIV diagnosis, calculating prevalence ratios (PRs)
with 95% confidence intervals (CIs). We analyzed results of partner notification efforts,
including timing and stage of diagnosis of HIV-positive partners. RESULTS: During the fouryear period, 551 women aged 18-30 years were newly diagnosed with HIV; 30% were
pregnant at the time of HIV diagnosis. Pregnant women were more likely to be Hispanic
(PR=1.58, 95% CI 1.15, 2.17) and not report typical risk factors. Fourteen percent of pregnant
women's partners had an undiagnosed infection compared with slightly more than 8% of
nonpregnant women's partners (p<0.01). CONCLUSIONS: Ethnic differences in co-diagnosis
of pregnancy and HIV suggest that young Hispanic women may have differential access to
and acceptance of routine HIV screening. Comprehensive prenatal screening combined with
partner notification can be effective in reaching infected male partners who are undiagnosed
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20402201
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HIV/Epidemiology
Sexual and Drug Use Risk Behaviors of Long-Haul Truck Drivers
and Their Commercial Sex Contacts in New Mexico
MCCREE D. H., Cosgrove, S., Stratford, D., Valway, S., Keller, N., Vega-Hernandez, J., and
Jenison, S. A.
Public Health Rep. 125 (1), 52-60 ,2010
AD - Centers for Disease Control and Prevention, 1600 Clifton Rd NE, MS E-37, Atlanta, GA
30333,
USA
zyr1@cdcgov
eng
OBJECTIVES: Long-haul truck drivers and their commercial sex contacts (CCs) have been
associated with the spread of sexually transmitted infections (STIs) in the developing world.
However, there is a paucity of information about the STI risk behaviors of these populations
in the U.S. We conducted a qualitative phase of a two-phase study to gather information
about STI-related risk behaviors in drivers and their CCs in New Mexico. METHODS:
Between July and September 2004, we conducted face-to-face unstructured and
semistructured qualitative interviews at trucking venues, health department facilities, and a
community-based organization to solicit information on sexual behavior and condom and
illicit drug use. The interviews were audiotaped, transcribed, reviewed for quality control,
and then coded and analyzed for emerging themes using NVivo software. RESULTS: Thirtythree long-haul truck drivers and 15 CCs completed the interview. The truck drivers were
mostly male and non-Hispanic white with a mean age of 41 years. The majority of the CCs
were female, the largest percentage was Hispanic, and the mean age was 36 years. Data
suggested risky sexual behavior and drug use (i.e., inconsistent condom use, illicit drug use
including intravenous drug use, and the exchange of sex for drugs) that could facilitate
STI/human immunodeficiency virus (HIV) and hepatitis virus transmission. Results also
showed a low knowledge about STIs and lack of access to general health care for both
populations. CONCLUSIONS: Additional studies are needed to further assess risk and
inform the development of prevention interventions and methods to provide STI/HIV and
other medical services to these populations
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20402196
-----------------------------------------------------HIV/Epidemiology
The Situation of Romanian HIV-Positive Adolescents: Results From
the First National Representative Survey
BUZDUCEA D., Lazar, F., and Mardare, E. I.
AIDS Care. 1-8 ,2010
AD - Faculty of Sociology and Social Work, University of Bucharest, Romania
ENG
Young people are one of the groups most affected by HIV/AIDS worldwide. For over a
decade after the fall of the Communism, Romania accounted for over 50% of the total
pediatric cases in Europe (Buzducea & Lazar, 2008; Mardarescu, 2008) with an estimated
10,000 children infected in hospital settings (nosocomial) between 1986 and 1992. Although
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about 3000 of these children died of AIDS, many of them have survived almost 20 years. This
paper presents the methodology and the results of the first representative research on
adolescents living with HIV/AIDS registered with medical services in Romania (N=534
subjects) attending the nine Regional Centers for HIV/AIDS Surveillance (August-October
2006). The general objective of the research was to assess the situation of 15-19 year-old
young people living with HIV/AIDS (PLWHA) from Romania and the dynamics of their risk
behaviors in respect to virus transmission (O'Leary, 2002). Based on the research findings,
the implications for practice are discussed and specific interventions are recommended to
better respond the needs of young PLWHA
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20401766
-----------------------------------------------------HIV/Epidemiology
Sex Frequency and Sex Planning Among Men Who Have Sex With
Men in Bangkok, Thailand: Implications for Pre- and Post-Exposure
Prophylaxis Against HIV Infection
VAN GRIENSVEN F., Thienkrua, W., Sukwicha, W., Wimonsate, W., Chaikummao, S.,
Varangrat, A., and Mock, P.
J.Int.AIDS Soc. 13 (1), 13 ,2010
ENG
ABSTRACT: OBJECTIVE: Daily HIV anti-retroviral pre-exposure prophylaxis (PrEP) is being
evaluated in clinical trials among men who have sex with men (MSM). However, daily PrEP
may not be congruent with sexual exposure profiles of MSM. Here we investigate sex
frequency and sex planning to identify and inform appropriate PrEP strategies for MSM.
METHODS: We evaluated sex frequency and sex planning in a cohort HIV-negative MSM in
Bangkok, Thailand. chi2 test was used to compare reports of sex on different weekdays;
logistic regression was used to identify predictors of sex frequency and sex planning.
RESULTS: Of 823 MSM (mean age 28.3 yrs) 86% reported sex on 2 days per week or less and
65% reported their last sex to have been planned. Sex on the weekend (~30%) was more often
reported than sex on weekdays (~23%). In multivariate analysis, use of alcohol, erectile
dysfunction drugs, group sex, sex with a foreigner, buying and selling sex and a history of
HIV testing were associated with having sex on 3 days per week or more; age 22 to 29 years,
not identifying as homosexual, receptive anal intercourse and not engaging in group sex
were associated with unplanned sex. CONCLUSION: Intermittently dosed PrEP (as opposed
to daily) may be a feasible HIV prevention strategy and should be considered for evaluation
in clinical trials. Predictors of sex frequency and sex planning may help to identify those in
need for daily PrEP and those who may not be able to take a timely pre-exposure dose
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20398261
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HIV/Epidemiology
Recording of Maternal Deaths in an East African University Hospital
BERGSJO P., Vangen, S., Lie, R. T., Lyatuu, R., Lie-Nielsen, E., and Oneko, O.
Acta Obstet.Gynecol.Scand. 2010
AD - Norwegian Institute of Public Health, Division of Epidemiology, Oslo, Norway
ENG
Abstract Objective. To trace all maternal deaths at a tertiary East African university hospital
with a systematic registration of all births. Design. Descriptive study. Sample. One hundred
and nineteen cases of maternal death which occurred in the period from 2000 to 2007
(including). Methods. Identification through the birth registry and separate manual tracing
of all case records. Account of practical problems concerning identification of cases and
analysis of time trends, mothers' domicile, occurrence by phase of pregnancy, birth and
puerperium, and diagnoses. Results. There was considerable under-reporting of deaths in
the medical birth registry. Twenty of 119 mothers died before 23 weeks' gestational age, most
of them of unsafe abortion. Other prevalent direct causes of death were hemorrhage,
eclampsia and other hypertensive complications. HIV/AIDS was primary cause in 20 cases.
Conclusion. Even with relatively complete ascertainment of births, single hospital-based
medical birth registries have limitations in studies of maternal deaths. They may identify
risks among women who arrive for delivery at the hospital, but are not be well suited for
estimation of total maternal mortality within the hospital walls. This would require
additional data. Extending the birth registry monitoring system to all health institutions with
obstetrical services in a region will give more reliable estimates to be followed over time and
serve as a basis for regular auditing, to the benefit of mothers and their children
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20397762
-----------------------------------------------------HIV/Epidemiology
Human Immunodeficiency Virus Risk Behavior Among Female
Substance Abusers
RAMSEY S. E., Bell, K. M., and Engler, P. A.
J.Addict.Dis. 29 (2), 192-199 ,2010
AD - The Warren Alpert Medical School of Brown University, Providence, RI, USA
Susan_Ramsey@Brownedu
eng
HIV is an increasingly critical and costly health problem for American women. Substance
use plays a major role in human immunodeficiency virus (HIV) infection in women. There
are several plausible explanations for the association between substance use and HIV risk
behavior. Pregnant substance abusers are a population deserving special attention given the
prevalence of risk behavior in this population and the added risk of perinatal transmission of
HIV. Current guidelines for the screening and treatment of HIV among pregnant women
and their infants are delineated. Substance abuse treatment has a limited impact on HIV risk
behavior in female substance abusers. Similarly, traditional knowledge-based and skill-based
HIV risk reduction interventions have modest efficacy in this population. Hence, there is a
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need to develop new interventions that directly target sex-related and drug-related HIV risk
behavior among female substance abusers. Recent work suggests that the incorporation of
motivational interviewing components into traditional HIV risk reduction interventions may
be a promising new direction for the field
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20407976
-----------------------------------------------------HIV/Epidemiology
HIV Transmission Risk Through Anal Intercourse: Systematic
Review, Meta-Analysis and Implications for HIV Prevention
BAGGALEY R. F., White, R. G., and Boily, M. C.
Int.J.Epidemiol. 2010
AD - Department of Infectious Disease Epidemiology, MRC Centre for Outbreak Analysis
and Modelling, Faculty of Medicine, Imperial College London, London, UK, Centre for the
Mathematical Modelling of Infectious Disease, Infectious Disease Epidemiology Unit,
Department of Epidemiology and Population Health, London School of Hygiene and
Tropical Medicine, London, UK, Department of Infectious Disease Epidemiology, Faculty of
Medicine, Imperial College London, London, UK and URESP, Centre de recherche FRSQ du
CHA
universitaire
de
Quebec,
Quebec,
Canada
ENG
BACKGROUND: The human immunodeficiency virus (HIV) infectiousness of anal
intercourse (AI) has not been systematically reviewed, despite its role driving HIV epidemics
among men who have sex with men (MSM) and its potential contribution to heterosexual
spread. We assessed the per-act and per-partner HIV transmission risk from AI exposure for
heterosexuals and MSM and its implications for HIV prevention. METHODS: Systematic
review and meta-analysis of the literature on HIV-1 infectiousness through AI was
conducted. PubMed was searched to September 2008. A binomial model explored the
individual risk of HIV infection with and without highly active antiretroviral therapy
(HAART). RESULTS: A total of 62 643 titles were searched; four publications reporting peract and 12 reporting per-partner transmission estimates were included. Overall, random
effects model summary estimates were 1.4% [95% confidence interval (CI) 0.2-2.5)] and 40.4%
(95% CI 6.0-74.9) for per-act and per-partner unprotected receptive AI (URAI), respectively.
There was no significant difference between per-act risks of URAI for heterosexuals and
MSM. Per-partner unprotected insertive AI (UIAI) and combined URAI-UIAI risk were
21.7% (95% CI 0.2-43.3) and 39.9% (95% CI 22.5-57.4), respectively, with no available per-act
estimates. Per-partner combined URAI-UIAI summary estimates, which adjusted for
additional exposures other than AI with a 'main' partner [7.9% (95% CI 1.2-14.5)], were lower
than crude (unadjusted) estimates [48.1% (95% CI 35.3-60.8)]. Our modelling demonstrated
that it would require unreasonably low numbers of AI HIV exposures per partnership to
reconcile the summary per-act and per-partner estimates, suggesting considerable variability
in AI infectiousness between and within partnerships over time. AI may substantially
increase HIV transmission risk even if the infected partner is receiving HAART; however,
predictions are highly sensitive to infectiousness assumptions based on viral load.
CONCLUSIONS: Unprotected AI is a high-risk practice for HIV transmission, probably with
substantial variation in infectiousness. The significant heterogeneity between infectiousness
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estimates means that pooled AI HIV transmission probabilities should be used with caution.
Recent reported rises in AI among heterosexuals suggest a greater understanding of the role
AI plays in heterosexual sex lives may be increasingly important for HIV prevention
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20406794
-----------------------------------------------------HIV/Epidemiology
Impulsive SUI Epidemic Model for HIV/AIDS With Chronological Age
and Infection Age
YAN P.
J.Theor.Biol. 2010
AD - School of Science, Anhui Agricultural University, HeFei, 230036, PR China; College of
Mathematics and System Science, Xinjiang University, Urumqi, 830046, PR China
ENG
This paper develops an impulsive SUI model of Human Immunodeficiency Virus/Acquired
Immunodeficiency Syndrome(HIV/AIDS) epidemic for the first time to study the dynamic
behavior of this model. The SUI model is described by impulsive partial differential
equations. First, the well-posedness of the model is attained by the method of characteristic
lines and iterative method. Secondly, the basic reproduction number R(0)(q, T) of the
epidemic which depends on the impulsive HIV-finding period T and the HIV-finding
proportion q is obtained by mathematical analysis. Our result shows that HIV/AIDS
epidemic can be theoretically eradicated if we can have the suitable HIV-finding proportion
q and the impulsive HIV-finding period T such that R(0)(q, T) < 1. We also conjecture that
the infection-free periodic solution of the SUI model is unstable when R(0)(q, T) > 1
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20406648
------------------------------------------------------
Health economics
Patient Costs of Accessing Collaborative Tuberculosis and Human
Immunodeficiency Virus Interventions in Ethiopia
VASSALL A., Seme, A., Compernolle, P., and Meheus, F.
Int.J.Tuberc.Lung Dis. 14 (5), 604-610 ,2010
AD - Department of Development Policy and Practice, Royal Tropical Institute, Amsterdam,
The
Netherlands
annavassall@lshtmacuk
eng
OBJECTIVE: To measure the patient costs of tuberculosis and human immunodeficiency
virus (TB-HIV) services from hospital-based pilot sites for collaborative TB-HIV
interventions in Ethiopia. METHODS: Costs of pre-treatment and treatment for a range of
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TB-HIV services provided as part of a collaborative TB-HIV programme in Ethiopia were
estimated. RESULTS: Patient costs were found to be substantial compared to income levels.
Pre-treatment costs were 35% of annual household income for TB patients (with no HIV),
33% for those with TB and HIV and 40% for those with HIV (with no TB). Pre-treatment
direct costs were particularly significant. Patient costs during treatment for TB range
between 49% and 71% of annual household income. Patient costs in the first year of
antiretroviral treatment were 21% of annual household income. Costs fell as treatment
progressed. CONCLUSION: Our results highlight the need to mitigate the economic impact
on patients of treatment for TB and HIV/AIDS (acquired immune-deficiency syndrome) in
low-income countries. Collaborative TB-HIV services may provide an opportunity to reduce
pre-treatment costs by providing an additional channel for the early diagnosis of HIV. Costs
may be further reduced by ensuring that diagnostics are provided free of charge, providing
social support at the start of treatment and bringing services closer to the patient
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20392354
-----------------------------------------------------HIV/Health economics
HIV-Related Deaths and Economic Shocks: Does Survivors'
Consumption Recover Over Time in Kwazulu-Natal?
GARBERO A. and Timaeus, I.
,Dallas, TX; USA ,2010
London School of Hygiene and Tropical Medicine (LSHTM)
Source: Conference (MIS)
-----------------------------------------------------HIV/Health economics
Health Financing in Brazil, Russia and India: What Role Does the
International Community Play?
SRIDHAR D. and Gomez, E. J.
Health Policy Plan. 2010
AD - All Souls College, Oxford, UK and Rutgers University, New Jersey, USA
ENG
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20400535
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Immunology
A Novel Polymorphism in ABCB1 Gene, CYP2B6*6 and Sex Predict
Single-Dose Efavirenz Population Pharmacokinetics in Ugandans
MUKONZO J. K., Roshammar, D., Waako, P., Andersson, M., Fukasawa, T., Milani, L.,
Svensson, J. O., Ogwal-Okeng, J., Gustafsson, L. L., and Aklillu, E.
Br.J.Clin.Pharmacol. 68 (5), 690-699 ,2009
AD - Division of Clinical Pharmacology, Department of Laboratory Medicine, Karolinska
University
Hospital-Huddinge,
Karolinska
Institutet,
Stockholm,
Sweden
eng
AIMS: Efavirenz exhibits pharmacokinetic variability causing varied clinical response. The
aim was to develop an integrated population pharmacokinetic/pharmacogenetic model and
investigate the impact of genetic variations, sex, demographic and biochemical variables on
single-dose efavirenz pharmacokinetics among Ugandan subjects, using NONMEM.
METHODS: Efavirenz plasma concentrations (n = 402) from 121 healthy subjects were
quantified by high-performance liquid chromatography. Subjects were genotyped for 30
single nucleotide polymorphisms (SNPs), of which six were novel SNPs in CYP2B6, CYP3A5
and ABCB1. The efavirenz pharmacokinetics was described by a two-compartment model
with zero- followed by first-order absorption. RESULTS: Apparent oral clearance (95%
confidence interval) was 4 l h l(-1) (3.5, 4.5) in extensive metabolizers. In the final model,
incorporating multiple covariates, statistical significance was found only for CYP2B6*6 and
CYP2B6*11 on apparent oral clearance as well as ABCB1 (rs3842) on the relative
bioavailability. Subjects homozygous for CYP2B6*6 (G516T, A785G) and *11 displayed 21
and 20% lower apparent oral clearance, respectively. Efavirenz relative bioavailability was
26% higher in subjects homozygous for ABCB1 (rs3842). The apparent peripheral volume of
distribution was twofold higher in women compared with men. CONCLUSIONS: The model
identified the four factors CYP2B6*6, CYP2B6*11, a novel variant allele in ABCB1 (rs3842)
and sex as major predictors of efavirenz plasma exposure in a healthy Ugandan population
after single-dose administration. Use of mixed-effects modelling allowed the analysis and
integration of multiple pharmacogenetic and demographic covariates in a pharmacokinetic
population model
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=19916993
-----------------------------------------------------HIV/Immunology
Oxidant/Antioxidant Status in Patients With Chronic HIV Infection
COACCIOLI S., Crapa, G., Fantera, M., Del, Giorno R., Lavagna, A., Standoli, M. L.,
Frongillo, R., Biondi, R., and Puxeddu, A.
Clin.Ter. 161 (1), 55-58 ,2010
AD - Dept of Internal Medicine, Perugia University School of Medicine, Didactic and
Scientific District of Terni Santa Maria General Hospital, Italy scoaccioli@tinit
<scoaccioli@tinit>
eng
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The infection caused by HIV leads to an activation of the immune system, which involves
local and systemic oxidative stress. In HIV-positive (HIV+) patients, oxidative damage is the
result of HIV infection and its progression through the replication of the virus. We have
examined 52 subjects: 26 HIV+ patients, and 26 healthy subjects (NC). Analysis of the
parameters of the oxidant/antioxidant status (total antioxidant capacity (TAC),
hydroperoxides (free radicals, PRO), thiols as thiolic capacity, TC) was carried out by means
of the OXY-Absorbent test, the d-Rom test, and the -SHp test, respectively. Healthy subjects
presented the following values: TAC (micromol/ml) 259.5+/-40.5; TC (micromol/l)
434.09+/-18.31; PRO (mg/dl) 54.09+/-7.3; CD4+ cells (cells/ml) 850+/-333. Values of HIV+
patients were the following: TAC 218.73+/-18.55 (ns vs NC; TC 250.88+/-93.11 (p 0.001 vs
NC); PRO 110.5+/-23.61 (p 0.0005 vs NC); CD4+ cells 354+/-323.35 (p 0.0005 vs NC). The
statistical analysis shows a direct correlation between TAC vs CD4+ cells; an indirect
correlation between hydroperoxides vs CD4+ cells; not significant result between thiolic
capacity vs CD4+ cells; finally, good correlations between TAC, hydroperoxides, and thiolic
capacity vs HIV-RNA. The data obtained have proven that HIV+ patients present a condition
of important oxidative stress. We may affi rm that this disease concurs with an increase of
extreme stress; a condition in which the antioxidant defences are present, but are insufficient
in neutralising the damaging actions of reactive species of oxygen, thus contributing to an
acceleration in the natural history of HIV infections
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20393680
-----------------------------------------------------HIV/Immunology
Caveolin-1 Modulates HIV-1 Envelope Induced Bystander Apoptosis
Through Gp41
WANG X. M., Nadeau, P. E., Lo, Y. T., and Mergia, A.
J.Virol. 2010
AD - Department of Infectious Disease and Pathology, College of Veterinary Medicine,
University
of
Florida,
Gainesville,
FL
32611,
USA
ENG
Human immunodeficiency virus (HIV) envelope (Env) mediated bystander apoptosis is
known to cause the progressive, severe, and irreversible loss of CD4+ T cells in HIV-1
infected patients. Env-induced bystander apoptosis has been shown to be gp41 dependent
and related to the membrane hemifusion between envelope expressing cells and target cells.
Caveolin-1 (Cav-1), the scaffold protein of a specific membrane lipid raft called caveolae, has
been reported to interact with gp41. However, the underlying pathological or physiological
meaning of this robust interaction remains unclear. In this report, we examine the interaction
of cellular Cav-1 and HIV gp41 within the lipid rafts and show that Cav-1 modulates Envinduced bystander apoptosis through the interaction with gp41 in SupT1 cells and CD4+ T
lymphocytes isolated from human peripheral blood. Cav-1 significantly suppressed Envinduced membrane hemifusion, caspase-3 activation and augmented Hsp70 upregulation.
Moreover, a peptide containing the Cav-1 scaffold domain sequence markedly inhibited
bystander apoptosis and apoptotic signal pathways. Our studies shed new light on the
potential role of Cav-1 in limiting HIV pathogenesis and the development of a novel
therapeutic strategy in treating HIV-1 infected patients
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Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20392844
-----------------------------------------------------HIV/Immunology
Protein Kinase A Phosphorylation Activates Vpr-Induced Cell Cycle
Arrest During Human Immunodeficiency Virus Type-1 Infection
BARNITZ R. A., Wan, F., Tripuraneni, V., Bolton, D. L., and Lenardo, M. J.
J.Virol. 2010
AD - Laboratory of Immunology, National Institute of Allergy and Infectious Diseases,
National Institutes of Health, Bethesda, MD 20892, USA; Immunology Graduate Group,
University
of
Pennsylvania,
Philadelphia,
PA
19104,
USA
ENG
Infection with human immunodeficiency virus type 1 (HIV-1) causes an inexorable depletion
of CD4(+) T cells. The loss of these cells is particularly pronounced in the mucosal immune
system during acute infection, and the data suggest that direct viral cytopathicity is a major
factor. Cell cycle arrest caused by the HIV-1 accessory protein Vpr is strongly correlated with
virus-induced cell death, and phosphorylation of Vpr serine 79 (S79) is required to activate
G2,M cell cycle blockade. However, the kinase responsible for phosphorylating Vpr remains
unknown. Our bioinformatic analyses revealed that S79 is part of a putative phosphorylation
site recognized by Protein Kinase A (PKA). We show that PKA interacts with Vpr and
directly phosphorylates S79. Inhibition of PKA activity during HIV-1 infection abrogates Vpr
cell cycle arrest. These findings provide new insight into the signaling event that activates
Vpr cell cycle arrest, ultimately leading to the death of infected T cells
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20392842
-----------------------------------------------------HIV/Immunology
Live Cell Co-Imaging of the Genomic RNAs and Gag Proteins of
Two Lentiviruses
KEMLER I., Meehan, A., and Poeschla, E. M.
J.Virol. 2010
AD - Department of Molecular Medicine and Division of Infectious Diseases, Mayo Clinic
College
of
Medicine,
Rochester,
MN
ENG
HIV-1 Gag and genomic RNA determinants required for encapsidation are well established
but where and when encapsidation occurs in the cell is unknown. We constructed MS2
phage coat protein labeling systems to track spatial dynamics of primate and nonprimate
lentiviral genomic RNAs (HIV-1, FIV) vis-a-vis their Gag proteins in live cells. Genomic
RNAs of both lentiviral genera were observed to traffic into the cytoplasm and this was Revdependent. In transit, FIV Gag and genomic RNA accumulated independently of each other
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at the nuclear envelope and focal co-localizations of psi(+) genomic RNA and Gag were
observed to extend outward from the cytoplasmic face. In contrast, although HIV-1 genomic
RNA was detected at the nuclear envelope, HIV-1 Gag was not. For both lentiviruses,
genomic RNAs were seen at the plasma membrane if and only if Gag was present and psi
was intact. In addition, HIV-1 and FIV genomes accumulated with Gag in late endosomal
foci, again only psi-dependently. Thus, lentiviral genomic RNAs require specific Gag
binding to accumulate at the plasma membrane, packaged genomes co-internalize with Gag
into the endosomal pathway, and plasma membrane RNA incorporation by Gag does not
trigger committed lentiviral particle egress from the cell. Based on the FIV results, we
hypothesize that Gag-genome association may initiate at the nuclear envelope
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20392841
-----------------------------------------------------HIV/Immunology
HIV-1 Nef Associates With P22-Phox, a Component of the NADPH
Oxidase Protein Complex
SALMEN S., Colmenares, M., Peterson, D. L., Reyes, E., Rosales, J. D., and Berrueta, L.
Cell Immunol. 2010
AD - Institute of Clinical Immunology, University of Los Andes, Merida, Venezuela
ENG
Altered neutrophil function may contribute to the development of AIDS during the course of
HIV infection. It has been described that Nef, a regulatory protein from HIV, can modulate
superoxide production in other cells, therefore altered superoxide production in neutrophils
from HIV infected patients, could be secondary to a direct effect of Nef on components of the
NADPH oxidase complex. In this work, we describe that Nef, was capable of increasing
superoxide production in human neutrophils. Furthermore, a specific association between
Nef and p22-phox, a membrane component of the NADPH oxidase complex, was found. We
propose that this association may reflect a capability of Nef to modulate by direct
association, the enzymatic complex responsible for one of the most efficient innate defense
mechanisms in phagocytes, contributing to the pathogenesis of the disease
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20392440
-----------------------------------------------------HIV/Immunology
First-Year Lymphocyte T CD4+ Response to Antiretroviral Therapy
According to the HIV Type in the IeDEA West Africa Collaboration
DRYLEWICZ J., Eholie, S., Maiga, M., Zannou, D. M., Sow, P. S., Ekouevi, D. K., Peterson, K.,
Bissagnene, E., Dabis, F., and Thiebaut, R.
AIDS. 24 (7), 1043-1050 ,2010
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EUROPRISE SCIENCE UPDATE 10-17
AD
INSERM
U897,
France
eng
OBJECTIVE: To compare the lymphocyte T CD4+ (CD4) response to combinations of
antiretroviral therapy (ART) in HIV-1, HIV-2 and dually positive patients in West Africa.
DESIGN AND SETTING: Collaboration of 12 prospective cohorts of HIV-infected adults
followed in Senegal (2), Gambia (1), Mali (2), Benin (1) and Cote d'Ivoire (6). Subjects: Nine
thousand, four hundred and eighty-two patients infected by HIV-1 only, 270 by HIV-2 only
and 321 dually positive, who initiated an ART. OUTCOME MEASURES: CD4 change over a
12-month period. RESULTS: Observed CD4 cell counts at treatment initiation were similar in
the three groups [overall median 155, interquartile range (IQR) 68; 249 cells/microl). In HIV1 patients, the most common ART regimen was two nucleoside reverse transcriptase
inhibitors (NRTIs) and one non-nucleoside reverse transcriptase inhibitor (NNRTI; N = 7714)
as well as for dually positive patients (N = 135). HIV-2 patients were most often treated with
a protease inhibitor-based regimen (N = 193) but 45 of them were treated with an NNRTIcontaining ART. In those treated with a NNRTI-containing regimen, the estimated mean
CD4 change between 3 and 12 months was significantly lower in HIV-2 (-41 cells/microl per
year) and dually positive patients (+12 cells/microl per year) compared to HIV-1 patients
(+69 cells/microl per year, overall P value 0.01). The response in HIV-2 and dually positive
patients treated by another regimen (triple NRTIs or protease inhibitor-containing ART) was
not significantly different than the response obtained in HIV-1-only patients (all P values
>0.30). CONCLUSION: An optimal CD4 response to ART in West Africa requires
determining HIV type prior to initiation of antiretroviral drugs. NNRTIs are the mainstay of
first-line ART in West Africa but are not adapted to the treatment of HIV-2 and dually
positive patients
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20397306
-----------------------------------------------------HIV/Immunology
Induction of Systemic HIV-1-Specific Cellular Immune Responses
by Oral Exposure in the Uninfected Partner of Discordant Couples
PEREZ C. L., Hasselrot, K., Bratt, G., Broliden, K., and Karlsson, A. C.
AIDS. 24 (7), 969-974 ,2010
AD - Department of Virology, Swedish Institute for Infectious Disease Control, and
Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Sweden
eng
OBJECTIVES: Previous studies have identified HIV-specific T-cell responses in HIV-exposed
uninfected individuals (EUI). However, so far no study has investigated exposure through
oral sex. Our aim was to investigate whether oral exposure is enough to induce a systemic
HIV-specific T-cell response. DESIGN: Peripheral blood mononuclear cells were collected
from 25 EUI living with a HIV-positive partner. Sexual behavior was described by the EUI in
self-reported questionnaires. All clinical data of the infected partners were well documented.
METHODS: Peripheral blood mononuclear cells were stimulated with five different HIV
peptide pools and HIV-specific T-cell responses were detected using the interferon-[gamma]
enzyme-linked immunospot assay. Multiple cytokine production was studied longitudinally
using flow cytometry intracellular cytokine assay. RESULTS: The majority of the discordant
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EUROPRISE SCIENCE UPDATE 10-17
couples reported having protected anal intercourse but unprotected oral sex. Three of the 23
tested EUI with evaluable results had HIV-Gag or Nef-specific T-cell responses. Two of the
responders reported unprotected oral sex as the only route of exposure. The HIV-specific
CD4+ and CD8+ T cells in the Gag-responder showed production of multiple cytokines. The
magnitude of the responses decreased over time when the level of exposure, determined by
the viral load in the partner, declined. CONCLUSION: HIV exposure through oral sex is
sufficient to induce systemic HIV-specific CD4+ and CD8+ T-cell immune responses in some
uninfected individuals. Further investigation is needed to determine whether these
responses have any protective role against HIV infection, or are merely evidence of exposure
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20397304
-----------------------------------------------------HIV/Immunology
CXCR4 in Clinical Hematology
CALANDRA G., Bridger, G., and Fricker, S.
Curr.Top.Microbiol.Immunol. 2010
AD - Private Consultant, 50 Wyndham Hills, Cresco, PA, 18326, USA, calandra@sunlinknet
ENG
Pharmacological manipulation of CXCR4 has proven clinically useful for mobilization of
stem and progenitor cells and in several preclinical models of disease. It is a key component
in the localization of leukocytes and stem cells. For patients with multiple myeloma and nonHodgkin's Lymphoma, treatment with plerixafor, an inhibitor of CXCL12 binding to CXCR4,
plus G-CSF mobilizes stem cells for autologous transplantation to a greater degree than the
treatment with G-CSF alone, and in some cases when patients could not be mobilized with
cytokines, chemotherapy, or the combination. Stem cells from healthy donors mobilized with
single agent plerixafor have been used for allogeneic transplantation in acute myelogenous
leukemia (AML) patients, although this is still in the early phase of clinical development.
Plerixafor is also undergoing evaluation to mobilize tumor cells in patients with AML and
chronic lymphocytic leukemia (CLL) to enhance the effectiveness of chemotherapy regimens.
Plerixafor's effect on neutrophils may also restore circulating neutrophil counts to normal
levels in patients with chronic neutropenias such as in WHIMs syndrome. Other areas where
inhibition of CXCR4 may be useful based upon preclinical or clinical data include peripheral
vascular disease, autoimmune diseases such as rheumatoid arthritis, pulmonary
inflammation, and HIV
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20397073
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HIV/Immunology
Abundant Expression of HIV Target Cells and C-Type Lectin
Receptors in the Foreskin Tissue of Young Kenyan Men
HIRBOD T., Bailey, R. C., Agot, K., Moses, S., Ndinya-Achola, J., Murugu, R., Andersson, J.,
Nilsson, J., and Broliden, K.
Am.J.Pathol. 2010
AD - From the Department of Medicine, Center for Molecular Medicine,* Infectious Disease
Unit, Solna, Karolinska Institutet, Stockholm, Sweden; Division of Epidemiology, School of
Public Health, University of Illinois at Chicago, Chicago, Illinois; the Impact Research and
Development Organization, Kisumu, Kenya; the Departments of Medical Microbiology,
Community Health Sciences, and Medicine, University of Manitoba, Winnipeg, Canada; the
Department of Medical Microbiology, University of Nairobi, Nairobi, Kenya; and the
Department of Medicine, Huddinge, Karolinska Institutet, Stockholm, Sweden
ENG
A biological explanation for the reduction in HIV-1 (HIV) acquisition after male circumcision
may be that removal of the foreskin reduces the number of target cells for HIV. The
expression of potential HIV target cells and C-type lectin receptors in foreskin tissue of men
at risk of HIV infection were thus analyzed. Thirty-three foreskin tissue samples, stratified by
Herpes simplex virus type 2 status, were obtained from a randomized, controlled trial
conducted in Kenya. The samples were analyzed by confocal in situ imaging microscopy and
mRNA quantification by quantitative RT-qPCR. The presence and location of T cells
(CD3(+)CD4(+)), Langerhans cells (CD1a(+)Langerin/CD207(+)), macrophages (CD68(+) or
CD14(+)), and submucosal dendritic cells (CD123(+)BDCA-2(+) or CD11c(+)DC-SIGN(+))
were defined. C-type lectin receptor expressing cells were detected in both the epithelium
and submucosa, and distinct lymphoid aggregates densely populated with CD3(+)CD4(+) T
cells were identified in the submucosa. Although the presence of lymphoid aggregates and
mRNA expression of selected markers varied between study subjects, Herpes simplex virus
type 2 serostatus was not the major determinant for the detected differences. The detection of
abundant and superficially present potential HIV target cells and submucosal lymphoid
aggregates in foreskin mucosa from a highly relevant HIV risk group demonstrate a possible
anatomical explanation that may contribute to the protective effect of male circumcision on
HIV transmission
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20395432
-----------------------------------------------------HIV/Immunology
FoxP3 Overexpression and CD1a(+) and CD3(+) Depletion in Anal
Tissue As Possible Mechanisms for Increased Risk of Human
Papillomavirus-Related Anal Carcinoma in HIV Infection
YAGHOOBI M., Le, Gouvello S., Aloulou, N., Duprez-Dutreuil, C., Walker, F., and Sobhani,
I.
Colorectal Dis. 2010
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EUROPRISE SCIENCE UPDATE 10-17
AD - Department of Medicine, University of Toronto, Toronto, Ontario, Canada
ENG
Abstract Aim: Human papillomavirus (HPV) is a main risk factor for anal cancer. We
analyzed local cellular and humoral immunity factors in the anal mucosa in an attempt to
explain how HIV infection increases the risk of anal cancer in HPV-infected patients.
Method: HIV-positive cases and matched HIV-negative controls with less than one
recurrence of condylomas were included in a prospective study following treatment of the
initial lesions. Patients were followed every 3 to 6 months for the development of anal
intraepithelial neoplasia (AIN3) and cancer for up to 60 months. Tissue CD1a(+), CD3(+),
CD4(+), CD8(+) cells and mRNAs of selected cytokines and chemokines were quantified and
compared in patients with or without AIN3 or cancer using morphometric or
immunohistochemistric analysis and qRT-PCR. Results: Sixty six individuals (22 patients and
44 controls) were included. In case group, CD1a(+) and CD3(+) cell counts were significantly
lower in biopsies from AIN3 and cancer specimens compared with those from AIN1-2 or
normal biopsies (p< 0.0001). A CD1a(+) count of less than 10/mm was predictive of AIN3
and cancer (Odds ratio= 9.4, 95% CI: 5.4-18.3, p <0.0001). IL-8 and IL23 levels were
significantly higher in cancer than in non-cancer tissues regardless of HIV status (p=0.02).
FoxP3 expression was significantly higher in HIV-infected cases than in controls with
AIN3/cancer (p< 0.04). Conclusion: Depletion of CD1a(+) and CD3(+) cells and over
expression of FoxP3 in the anal mucosa appears likely to contribute to the risk of HPVrelated anal cancer in HIV-infected patients. Furthermore, over expression of IL-8 and IL-23
in the anal mucosa might be responsible for the development of this cancer regardless of HIV
status
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20394639
-----------------------------------------------------HIV/Immunology
Innate Inhibitory Activity of Amniotic Fluid Against HIV-1: A
Potential Role in Prevention of In Utero Transmission
FARZIN A., Ank, B., Boyer, P., Nielsen, K., and Bryson, Y.
,Vancouver, BC; Canada, 4413.447 ,2010
University of California, Los Angeles, Los Angeles, CA
Source: Conference (MIS)
-----------------------------------------------------HIV/Immunology
Defining Immune Abnormalities and Their Consequences in the HIV
Exposed but Uninfected Child
REIKIE B., Adams, R., Cotton, M., Speert, D., de, Beer C., Fortuno, E., Esser, M., and
Kollmann, T.
,Vancouver, BC; Canada, 442 ,2010
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EUROPRISE SCIENCE UPDATE 10-17
Pediatrics, University of British Columbia, Vancouver, BC, Canada; Pathology, University of
Stellenbosch, Stellenbosch, South Africa; Pediatrics, Tygerberg Hospital, Tygerberg, South
Africa
Source: Conference (MIS)
-----------------------------------------------------HIV/Immunology
Determinants of the Interpersonal Variation in Treatment Response
to Anti-HlV Nucleoside Analogs
PAINTSIL E., Dutschman, G., Rong, Hu, and Cheng, Y.
,Vancouver, BC; Canada, 2870.580 ,2010
Pediatrics, Yale University, New Haven, CT; Pharmacology, Yale University, New Haven,
CT
Source: Conference (MIS)
-----------------------------------------------------HIV/Immunology
Establishment of Hematologic and Immunologic Reference Values
for Healthy Tanzanian Children in the Kilimanjaro Region
BUCHANAN A., Muro, F., Gratz, J., Crump, J., Musyoka, A., Sichangi, M., Morrissey, A.,
M'rimberia, J., Njau, B., Msuya, L., Bartlett, J., and Cunningham, C.
,Vancouver, BC; Canada, 1492.380 ,2010
Division of Pediatric Infectious Diseases, Department of Pediatrics, Duke University Medical
Center, Durham, NC; Kilimanjaro Christian Medical Centre, Moshi, Tanzania, United
Republic of; Kilimanjaro Christian Medical College, Tumaini University, Moshi, Tanzania,
United Republic of; Division of Infectious Diseases and International Health, Department of
Medicine, Duke University Medical Center, Durham, NC; Duke Global Health Institute,
Duke University, Durham, NC
Source: Conference (MIS)
-----------------------------------------------------HIV/Immunology
Sevi, A Natural Enhancer of Hiv Infection, As A Novel Target to
Prevent Hiv Transmission
TOUGER OLSEN J. and Dewhurst, S.
,Chicago, IL; USA, 141 ,2010
University of Rochester, Rochester NY
Source: Conference (MIS)
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HIV/Immunology
The Role of Ferritin Heavy Chain and Opiates in Neuroaids: A
Systematic in Vivo Analysis of A Novel Cxcr4 Regulator Within the
Human Cortex
PITCHER J., Shimizu, S., and Meucci, O.
,Chicago, IL; USA, 156 ,2010
Drexel University College of Medicine, Philadelphia, PA
Source: Conference (MIS)
-----------------------------------------------------HIV/Immunology
The Hiv Glycoprotein Gp120 Impairs Fast Axonal Transport by A
Mechanism Involving Activation of Selected Phosphotransferases
BERTH S., Sarma, T., Morfini, G., and Brady, S.
,Chicago, IL; USA, 4 ,2010
University of Illinois at Chicago, Chicago, IL
Source: Conference (MIS)
-----------------------------------------------------HIV/Immunology
Genital Secretions From Hiv Infected Women Exhibit Decreased
Activity Against Hsv-2
MADAN R., Torres, M., Kim, M., Keller, M., and Herold, B.
,Washington, DC; USA, A-239 ,2010
Albert Einstein College of Medicine, Bronx, NY, United States
Source: Conference (MIS)
-----------------------------------------------------HIV/Immunology
Cocaine Use Predicts Lack of Virologic Control Based on A Rapid
Screening Tool for Adherence and Active Substance Abuse in An
Outpatient Hiv Clinic
DESRUISSEAU A., Stinnette, S., Kheshti, A., and Qian, H.
,Washington, DC; USA, A-133 ,2010
1) Meharry Medical College, Nashville, TN, United States; 2) Comprehensive Care Center
(Vanderbilt University), Nashville,TN, United States
Source: Conference (MIS)
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HIV/Immunology
Monocyte Dysregulation Is Induced by Nef Exosome Endocytosis
JOHNSON K., Bo-Huang, M., Ali, S., Roth, B., Shelton, M., Powell, M., and Bond, V.
,Washington, DC; USA, A-224 ,2010
Morehouse School of Medicine, Atlanta, GA, United States
Source: Conference (MIS)
-----------------------------------------------------HIV/Immunology
EBV, Lymphoma-Risk and the Potential Role of HIV-Infection for
IBD Patients Undergoing Immunosuppression
WEINSTOCK D.
,Miami, FL; USA ,2010
Dana-Farber Cancer Institute and Harvard Medical School, 44 Binney Street, Dana 510B,
Boston, MA 02115, USA
Source: Conference (MIS)
-----------------------------------------------------HIV/Immunology
Modularity in Protein Interaction Network Hubs Predicts Viral HostPathogen Interactions
EVANS P., Dampier, W., Tozeren, A., and Ungar, L.
,Quebec; Canada, 119 ,2010
1) Genomics and Computational Biology, University of Pennsylvania, Philadelphia, PA
19104, USA; 2) School of Biomedical Engineering, Drexel University, Philadelphia, PA 19104,
USA
Source: Conference (MIS)
-----------------------------------------------------HIV/Immunology
Comparative Host-Pathogen Interactome Mapping for HIV and HTLV
Retroviruses: Unraveling New Therapeutic Opportunities for
Retroviral Associated Diseases
TWIZERE J., Simonis, N., Rual, J., Lemmens, I., Hirozane-Kishikawa, T., Dricot, A., Tong,
Hao, Boxus, M., Dewulf, J., Legros, S., Klitgord, N., Martin, M., Smolyar, A., Willaert, J.,
Dequiedt, F., Navratil, V., Cusick, M., Burny, A., Hill, D., Tavernier, J., Vidal, M., and
Kettmann, R.
,Quebec; Canada, 243 ,2010
1) Center for Cellular and Molecular Biology, Gembloux University (FUSAGx), 13 avenue
Marechal Juin, 5030 Gembloux, Belgium; 2) Center for Cancer Systems Biology and
Department of Cancer Biology (CCSB), Dana-Farber Cancer Institute, and Department of
Genetics, Harvard Medical School, 44 Binney Street, Boston, MA 02115, USA; 3) Laboratoire
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EUROPRISE SCIENCE UPDATE 10-17
de Bioinformatique des Génomes et des Réseaux (BiGRe), Université Libre de Bruxelles,
Campus Plaine, CP 263, Boulevard du Triomphe, 1050 Bruxelles, Belgium; 4) Department of
Medical Protein Research, VIB, Ghent University, 9000 Ghent, Belgium; 5) Ecole Nationale
Vétérinaire de Lyon, Université de Lyon, INRA, UMR754, and INSERM, U851, 21 avenue
Tony Garnier, Lyon, 69007, France
Source: Conference (MIS)
-----------------------------------------------------HIV/Immunology
Functional Insights From Protein-Protein and Genetic Interaction
Maps
KROGAN N.
,Quebec; Canada ,2010
Cellular and Molecular Pharmacology/California Institute for Quantitative Biomedical
Sciences, University of California, San Francisco, CA, 94158
Source: Conference (MIS)
-----------------------------------------------------HIV/Immunology
Neoepitope Antibodies to Monitor Proteolytic Networks
KOERBER J., Sidhu, S., and Wells, J.
,Quebec; Canada, 237 ,2010
Department of Cellular and Molecular Pharmacology, University of California - San
Francisco, San Francisco, CA 94158, USA
Source: Conference (MIS)
-----------------------------------------------------HIV/Immunology
Generation of a Family-Specific Phage Library of Llama Single
Chain Antibody Fragments That Neutralize HIV-1
KOH W. W., Steffensen, S., Gonzalez, M., Hoorelbeke, B., Gorlani, A., Szynol, A., Forsman,
A., asa-Chapman, M. M., de, Haard H., Verrips, T., and Weiss, R. A.
J.Biol.Chem. 2010
AD
University
College
London,
United
Kingdom;
ENG
Recently we described llama antibodies fragments (VHH) that neutralize human
immunodeficiency virus type 1 (HIV-1). These VHH were obtained after selective elution of
phages carrying an immune library raised against gp120 of HIV-1 subtype B/C CN54 with
soluble CD4. We describe here a new, family-specific approach to obtain the largest possible
diversity of related VHH that compete with soluble CD4 for binding to the HIV-1 envelope
glycoprotein. The creation of this family-specific library of homologous VHH has enabled us
to isolate phages carrying similar nucleotide sequences as the parental VHH. These VHH
displayed varying binding affinities and neutralisation phenotypes to a panel of different
strains and subtypes of HIV-1. Sequence analysis of the homologues showed that the C--------------------------------------------------------------------------------------------------------------
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EUROPRISE SCIENCE UPDATE 10-17
terminal 3 amino acids of the CDR3 loop were crucial in determining the specificity of these
VHH for different subtype C HIV-1 strains. There was a correlation between affinity of VHH
binding to gp120 of HIV-1 IIIB and breadth of neutralization of diverse HIV-1 envelopes. The
family-specific approach has therefore allowed us to better understand the interaction of
CD4 binding site antibodies with virus strain specificity, and has potential use for the
bioengineering of antibodies and HIV-1 vaccine development
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20400507
-----------------------------------------------------HIV/Immunology
Prognostic Value of Peripheral Blood Mononuclear Cell-Associated
HIV-1 DNA for Virological Outcome in Asymptomatic HIV-1 Chronic
Infection
RODRIGUEZ-SAINZ C., Ramos, R., Valor, L., Lopez, F., Santamaria, B., Hernandez, D. C.,
Cruz, J. S., Navarro, J., Modrego, J., Alecsandru, D., and Fernandez-Cruz, E.
J.Clin.Virol. 2010
AD - Clinical Immunology Division, Hospital General Universitario Gregorio Maranon,
Microbiology Department, Universidad Complutense de Madrid, Madrid, Spain
ENG
BACKGROUND: Studies in primary HIV-1 infection and advanced HIV-1 disease have
demonstrated that HIV-1 DNA associated with peripheral blood mononuclear cells (PBMC
HIV-1 DNA) has predictive value for disease progression. OBJECTIVES: To analyse in
asymptomatic HIV-1 chronic infection the predictive value of PBMC HIV-1 DNA for
virological failure. STUDY DESIGN: In 115 individuals who had previously participated in
study STIR-2102, we retrospectively analysed the PBMC HIV-1 DNA by quantitative realtime PCR. Antiretroviral naive patients (baseline pre-ART) received 6 weeks of ART prior to
randomisation (baseline post-ART). The predictive value of PBMC HIV-1 DNA, HIV-1 RNA
in plasma and CD4(+) T cells, at baselines pre-ART and post-ART, was determined by
Kaplan-Meier and Proportional Hazards Regression analyses. RESULTS: At baseline postART, 82% of patients showed suppression of HIV-1 RNA, however they maintained
significant amounts of HIV-1 DNA (geometric mean: 690copies/10(6) PBMC). Pre-ART and
post-ART levels of HIV-1 DNA and pre-ART levels of HIV-1 RNA showed predictive value
(Log-Rank test: p<0.001, p<0.001, p=0.003, respectively). In a multivariate model post-ART
PBMC HIV-1 DNA was the stronger predictive variable (adjusted HR, 2.51 [95% CI, 1.334.73, p=0.004]) independently of HIV-1 RNA (HR 1.74 [95% CI, 1.16-2.61, p=0.007]).
CONCLUSIONS: PBMC HIV-1 DNA is an effective prognostic marker for virological
outcome in individuals with asymptomatic HIV-1 chronic infection
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20399705
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HIV/Immunology
CCR2 Plays a Critical Role in Dendritic Cell Maturation: Possible
Role of CCL2 and NF-{Kappa}B
JIMENEZ F., Quinones, M. P., Martinez, H. G., Estrada, C. A., Clark, K., Garavito, E., Ibarra,
J., Melby, P. C., and Ahuja, S. S.
J.Immunol. 2010
AD - Audie L Murphy Division, Veterans Administration Center for Research on AIDS and
HIV-1
Infection,
South
Texas
Veterans
Health
Care
System
ENG
We postulated that CCR2-driven activation of the transcription factor NF-kappaB plays a
critical role in dendritic cell (DC) maturation (e.g., migration, costimulation, and IL-12p70
production), necessary for the generation of protective immune responses against the
intracellular pathogen Leishmania major. Supporting this notion, we found that CCR2, its
ligand CCL2, and NF-kappaB were required for CCL19 production and adequate
Langerhans cell (LC) migration both ex vivo and in vivo. Furthermore, a role for CCR2 in
upregulating costimulatory molecules was indicated by the reduced expression of CD80,
CD86, and CD40 in Ccr2(-/-) bone marrow-derived dendritic cells (BMDCs) compared with
wild-type (WT) BMDCs. Four lines of evidence suggested that CCR2 plays a critical role in
the induction of protective immunity against L. major by regulating IL-12p70 production and
migration of DC populations such as LCs. First, compared with WT, Ccr2(-/-) lymph node
cells, splenocytes, BMDCs, and LCs produced lower levels of IL-12p70 following stimulation
with LPS/IFN-gamma or L. major. Second, a reduced number of LCs carried L. major from
the skin to the draining lymph nodes in Ccr2(-/-) mice compared with WT mice. Third, early
treatment with exogenous IL-12 reversed the susceptibility to L. major infection in Ccr2(-/-)
mice. Finally, disruption of IL-12p70 in radioresistant cells, such as LCs, but not in BMDCs
resulted in the inability to mount a fully protective immune response in bone marrow
chimeric mice. Collectively, our data point to an important role for CCR2-driven activation
of NF-kappaB in the regulation of DC/LC maturation processes that regulate protective
immunity against intracellular pathogens
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20404272
-----------------------------------------------------HIV/Immunology
Mhc Haplotype M3 Is Associated With Early Control of SHIVsbg
Infection in Mauritian Cynomolgus Macaques
MEE E. T., Berry, N., Ham, C., Aubertin, A., Lines, J., Hall, J., Stebbings, R., Page, M.,
Almond, N., and Rose, N. J.
Tissue Antigens. 2010
AD - Division of Retrovirology, National Institute for Biological Standards and Control,
Health
Protection
Agency,
Hertfordshire,
UK
ENG
The restricted major histocompatibilty complex of Mauritian cynomolgus macaques confers
exceptional potential on this species in human immunodeficiency virus (HIV) vaccine
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EUROPRISE SCIENCE UPDATE 10-17
development. However, knowledge of the effects of Mhc genetics on commonly used simian
immunodeficiency virus (SIV) and simian/human immunodeficiency virus (SHIV) stocks is
incomplete. We determined the effect of Mhc haplotypes on SHIVsbg replication kinetics in a
cohort of 25 naive cynomolgus macaques. Haplotype M3 was associated with a 1.58log(10)
reduction in viraemia at day 28 post infection (p.i.). Haplotype M6 was associated with
elevated SHIVsbg viraemia at days 28 and 56. No significant effect of Mhc class II haplotypes
on viral replication was observed. These data emphasise the importance of genetic
characterisation of experimental macaques and advance our understanding of host genetic
effects in SIV/SHIV models of HIV infection
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20403147
-----------------------------------------------------HIV/Immunology
HIV+ Elite Controllers Have Low HIV-Specific T-Cell Activation Yet
Maintain Strong, Polyfunctional T-Cell Responses
OWEN R. E., Heitman, J. W., Hirschkorn, D. F., Lanteri, M. C., Biswas, H. H., Martin, J. N.,
Krone, M. R., Deeks, S. G., and Norris, P. J.
AIDS. 2010
AD - aBlood Systems Research Institute, USA bDepartments of Laboratory Medicine, USA
cEpidemiology and Biostatistics, USA dMedicine, University of California, San Francisco,
California,
USA
ENG
OBJECTIVE:: HIV elite controllers are a unique group of rare individuals who maintain
undetectable viral loads in the absence of antiretroviral therapy. We studied immune
responses in these individuals to inform vaccine development, with the goal of identifying
the immune correlates of protection from HIV. METHODS:: We compared markers of
cellular activation, HIV-specific immune responses and regulatory T (Treg) cell frequencies
in four groups of individuals: HIV-negative healthy controls, elite controllers (HIV RNA
level <75 copies/ml), individuals on HAART and individuals with HIV RNA level more
than 10 000 copies/ml (noncontrollers). RESULTS:: Elite controllers possessed significantly
lower levels of activated HIV-specific CD8 T cells and of recently divided HIV-specific CD4
T cells than noncontrollers, whereas these differences were not seen in the respective
cytomegalovirus-specific T-cell populations. Elite controllers also mounted a stronger and
broader cytokine and chemokine response following HIV-specific stimulation than
individuals on HAART and noncontrollers. Finally, we found that HAART-suppressed
individuals had elevated Treg cell frequencies, whereas elite controllers and noncontrollers
maintained normal percentages of Treg cells. CONCLUSION:: Elite controllers maintain high
levels of HIV-specific immune responses with low levels of HIV-specific T-cell activation and
do not have elevated Treg cell levels. Based on these data an ideal HIV vaccine would induce
strong HIV-specific immune responses whereas minimizing HIV-specific T-cell activation
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20400885
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HIV/Immunology
Kinetics of Interaction of HIV Fusion Protein (Gp41) With Lipid
Membranes Studied by Real-Time AFM Imaging
BITLER A., Lev, N., Fridmann-Sirkis, Y., Blank, L., Cohen, S. R., and Shai, Y.
Ultramicroscopy. 2010
AD
Department
of
Chemical
Research
Support,
Israel
ENG
One of the most important steps in the process of viral infection is a fusion between cell
membrane and virus, which is mediated by the viral envelope glycoprotein. The study of
activity of the glycoprotein in the post-fusion state is important for understanding the
progression of infection. Here we present a first real-time kinetic study of the activity of gp41
(the viral envelope glycoprotein of human immunodeficiency virus-HIV) and its two
mutants in the post-fusion state with nanometer resolution by atomic force microscopy
(AFM). Tracking the changes in the phosphatidylcholine (PC) and phosphatidylcholinephosphatidylserine (PC:PS) membrane integrity over one hour by a set of AFM images
revealed differences in the interaction of the three types of protein with zwitterionic and
negatively charged membranes. A quantitative analysis of the slow kinetics of hole
formation in the negatively charged lipid bilayer is presented. Specifically, analysis of the
rate of roughness change for the three types of proteins suggests that they exhibit different
types of kinetic behavior
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20399563
-----------------------------------------------------HIV/Immunology
Antibodies: Beyond Neutralization
VON BUBNOFF A.
IAVI.Rep. 14 (1), 8-12 ,2010
engLink
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20349583
-----------------------------------------------------HIV/Immunology
Inhibition of DC-SIGN-Mediated Transmission of Human
Immunodeficiency Virus Type 1 by Toll-Like Receptor 3 Signalling
in Breast Milk Macrophages
YAGI Y., Watanabe, E., Watari, E., Shinya, E., Satomi, M., Takeshita, T., and Takahashi, H.
Immunology. 2010
AD - Department of Microbiology and Immunology, Nippon Medical School, Tokyo, Japan
ENG
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Summary The majority of cells in early/colostrum milk are breast milk macrophages
(BrMMo) expressing dendritic cell (DC)-specific intercellular adhesion molecule 3 (ICAM3)
grabbing nonintegrin (DC-SIGN), and the expression level of DC-SIGN on BrMMo will
determine cell-to-cell human immunodeficiency virus type 1 (HIV-1) transmissibility. Thus,
one of the strategies to prevent vertical transmission of HIV-1 through breast-feeding is to
find a way to suppress DC-SIGN expression on BrMMo. As for the expression of Toll-like
receptors (TLRs) in BrMMo, TLR3 was always seen in BrMMo but not in peripheral blood
monocytes (PBMo). Also, the expression of TLR3 was slightly enhanced in BrMMo when the
cells were treated with interleukin (IL)-4. Moreover, when TLR3 was stimulated with its
specific ligand, the double-stranded RNA (dsRNA) poly(I:C), DC-SIGN expression on
BrMMo was reduced even in the IL-4-mediated enhanced state. Some reduction may be
caused by type I interferons (IFNs), such as IFN-alpha/beta, secreted from BrMMo. Indeed,
both IFNs, particularly IFN-beta, showed a strong capacity to suppress the enhancement of
DC-SIGN expression on IL-4-treated BrMMo and such TLR3-mediated DC-SIGN
suppression was partially abrogated by the addition of anti-IFN-alpha/beta-receptor-specific
antibodies. As expected, DC-SIGN-mediated HIV-1 transmission to CD4-positive cells by
BrMMo was inhibited by either poly(I:C) stimulation or by treatment with type I IFNs. These
findings suggest a possible strategy for preventing mother-to-child transmission (MTCT) of
HIV-1 via breast-feeding through TLR3 signalling
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20406303
------------------------------------------------------
Pathology
Sporothrix Schenckii Meningitis in AIDS During Immune
Reconstitution Syndrome
GALHARDO M. C., Silva, M. T., Lima, M. A., Nunes, E. P., Schettini, L. E., de Freitas, R. F.,
de Almeida, Paes R., Neves, E. D., and do Valle, A. C.
J.Neurol.Neurosurg.Psychiatry. 2010
AD - Evandro Chagas Clinical Research Institute (IPEC), Oswaldo Cruz Foundation
(FIOCRUZ),
Avenida
Brasil,
Rio
de
Janeiro,
Brazil
ENG
Sporotrichosis is a fungal disease usually restricted to the cutaneous and lymphatic systems.
Visceral involvement is unusual. To date, only 21 cases of sporotrichosis meningitis have
been reported, some of these associated with immunosuppression. According to the reported
cases, difficulty establishing the correct diagnosis is almost the rule which, undoubtedly, is
associated with a worse prognosis. In this report, two HIV infected patients are described
who developed meningitis due to Sporothrix schenckii associated with immune
reconstitution inflammatory syndrome. This is the first report of sporotrichosis meningitis
associated with immune reconstitution inflammatory syndrome in AIDS patients
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20392979
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EUROPRISE SCIENCE UPDATE 10-17
-----------------------------------------------------HIV/Pathology
Incidence of Tuberculosis in People Living With the Human
Immunodeficiency Virus in Saudi Arabia
OMAIR M. A., Al-Ghamdi, A. A., and Alrajhi, A. A.
Int.J.Tuberc.Lung Dis. 14 (5), 600-603 ,2010
AD - Section of Infectious Diseases, Department of Medicine, King Faisal Specialist Hospital
and
Research
Centre,
Riyadh,
Saudi
Arabia
eng
OBJECTIVE: To identify the incidence of tuberculosis (TB) in people living with the human
immunodeficiency virus (HIV) (PLWH) followed at an HIV referral and care facility.
DESIGN: Observational longitudinal cohort. METHODS: Data were collected longitudinally
as patients were admitted to the HIV programme and included demographics, TB diagnosis
and treatment, CD4+ T lymphocyte count and TB treatment outcomes. The TB-free follow-up
period of all patients was used to calculate TB incidence rates. RESULTS: Between 1997 and
2007, 217 new adult patients joined the HIV programme. TB was diagnosed in 16 patients
(7.4%), all of whom had acquired immune-deficiency syndrome at the time of TB diagnosis.
Seven developed extra-pulmonary disease (44%), six had pulmonary TB (37%), while three
had both (19%). The TB incidence rate was 1354 per 100,000 person-years (py) among the
HIV-infected cohort. The incidence rate of pulmonary TB was 762/100,000 py and for extrapulmonary TB it was 592/100,000 py. Seven patients (44%) died despite early diagnosis and
treatment for TB. CONCLUSION: Among PLWH in Saudi Arabia, TB incidence is 30 times
higher than in the general population, with significant mortality despite early diagnosis,
treatment and tertiary care support
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20392353
-----------------------------------------------------HIV/Pathology
The Association Between Cervical Human Papillomavirus Infection
and HIV Acquisition Among Women in Zimbabwe
AVERBACH S. H., Gravitt, P. E., Nowak, R. G., Celentano, D. D., Dunbar, M. S., Morrison, C.
S., Grimes, B., and Padian, N. S.
AIDS. 24 (7), 1035-1042 ,2010
AD - University of California, San Francisco School of Medicine, San Francisco, California,
USA
eng
BACKGROUND: The prevalence of human papillomavirus (HPV) is higher among HIVpositive women, but the prevalence of HPV prior to HIV acquisition has not been carefully
evaluated. OBJECTIVE: This study evaluated whether HPV infection is independently
associated with heterosexual HIV acquisition in a cohort of Zimbabwean women. DESIGN:
Case-control study nested within a large multicenter cohort study (HC-HIV). METHODS:
Cases consisted of Zimbabwean women with incident HIV infection observed during follow--------------------------------------------------------------------------------------------------------------
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up (n = 145). HIV-uninfected controls were selected and matched to cases (n = 446). The
prevalence of cervical HPV infections was compared at the visit prior to HIV infection in the
cases and at the same follow-up visit in the matched controls. RESULTS: The odds of
acquiring HIV were 2.4 times higher in women with prior cervical HPV infection after
adjustment for behavioral and biologic risk factors. There was no statistically significant
difference in the risk of HIV acquisition between women infected with high-risk vs. low-risk
HPV types. Loss of detection of at least one HPV DNA type was significantly associated with
HIV acquisition [odd ratio = 5.4 (95% confidence interval 2.9-9.9)] (P < .0001). Conclusion:
Cervical HPV infection is associated with HIV acquisition among women residing in a
region with a high prevalence of both infections. Further studies are required to evaluate
whether the observed association is causal
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20397287
-----------------------------------------------------HIV/Pathology
HIV-Associated Neurocognitive Disorder: Pathogenesis and
Therapeutic Opportunities
LINDL K. A., Marks, D. R., Kolson, D. L., and Jordan-Sciutto, K. L.
J.Neuroimmune.Pharmacol. 2010
AD - Department of Pathology, School of Dental Medicine, University of Pennsylvania, 240 S
40th St, Room 312 Levy Building, Philadelphia, PA, 19104-6030, USA
ENG
Human immunodeficiency virus type 1 (HIV) infection presently affects more that 40 million
people worldwide, and is associated with central nervous system (CNS) disruption in at least
30% of infected individuals. The use of highly active antiretroviral therapy has lessened the
incidence, but not the prevalence of mild impairment of higher cognitive and cortical
functions (HIV-associated neurocognitive disorders) as well as substantially reduced a more
severe form dementia (HIV-associated dementia). Furthermore, improving neurological
outcomes will require novel, adjunctive therapies that are targeted towards mechanisms of
HIV-induced neurodegeneration. Identifying such molecular and pharmacological targets
requires an understanding of the events preceding irreversible neuronal damage in the CNS,
such as actions of neurotoxins (HIV proteins and cellular factors), disruption of ion channel
properties, synaptic damage, and loss of adult neurogenesis. By considering the specific
mechanisms and consequences of HIV neuropathogenesis, unified approaches for
neuroprotection will likely emerge using a tailored, combined, and non-invasive approach
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20396973
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EUROPRISE SCIENCE UPDATE 10-17
HIV/Pathology
Tuberculosis Rates Among HIV-Infected Persons in New York City,
2001-2005
TRIEU L., Li, J., Hanna, D. B., and Harris, T. G.
Am.J.Public Health. 2010
AD
New
York
City
Dept
of
Health
and
Mental
Hygiene
ENG
We calculated population-based tuberculosis (TB) rates among HIV-infected persons in New
York City from 2001 through 2005 using data from the city's TB and HIV/AIDS surveillance
registries, and we examined those rates using linear trend tests and incidence rate ratios
(IRRs). HIV-infected individuals had 16 times the TB rate of a "non-HIV" population (HIV
status negative or unknown; IRR=16.0; 95% confidence interval=14.9, 17.2). TB rates declined
significantly among the US-born HIV-infected population (Ptrend<.001) but not among the
foreign-born HIV-infected population (Ptrend=.355). Such disparities must be addressed if
further declines are to be achieved
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20395574
-----------------------------------------------------HIV/Pathology
HIV-Associated Lymphoma
LEVINE A. M.
Blood. 115 (15), 2986-2987 ,2010
AD
City
of
Hope
National
Medical
Center,
USA
engLink
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20395421
-----------------------------------------------------HIV/Pathology
Higher Mortality in HIV-2/HTLV-1 Co-Infected Patients With
Pulmonary Tuberculosis in Guinea-Bissau, West Africa, Compared
to HIV-2-Positive HTLV-1-Negative Patients
NORRGREN H., Bamba, S., Da Silva, Z. J., Koivula, T., and Andersson, S.
Int.J.Infect.Dis. 2010
AD - Department of Clinical Sciences, Division of Infection Medicine, Lund University, 221
85
Lund,
Sweden
ENG
OBJECTIVES: To investigate the effect of human T-lymphotropic virus type 1 (HTLV-1) on
CD4 counts and mortality in tuberculosis (TB) patients with or without human
immunodeficiency virus (HIV). METHODS: A prospective study on 280 hospitalized
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patients with pulmonary TB was performed in Guinea-Bissau, 1994-1997, including HIV,
CD4 counts and clinical outcome. We compared the CD4 count levels at the time of inclusion
between HIV-negative and HIV-positive patients, with or without HTLV-1. Mortality was
determined while patients were on treatment for TB. RESULTS: Median CD4% was
significantly higher in HIV-positive subjects co-infected with HTLV-1 compared to HTLV-1negative patients. Two hundred thirty-three individuals were included in the analysis of
mortality, and among HIV-negative subjects the mortality was 18.6/100 person-years . In
HIV-2-positive HTLV-1-negative subjects the mortality was 39.5/100 person-years and in
HIV-2/HTLV-1 co-infected patients it was 113.6/100 person-years (adjusted mortality rate
ratio 4.7, 95% CI 1.5-14.4; p < 0.01). When all HIV-positive patients were analyzed together,
corresponding mortality rates were 53.5/100 person-years and 104.8/100 person-years ,
respectively (not significant). CONCLUSIONS: HIV/HTLV-1 co-infected patients
hospitalized for pulmonary TB had a high mortality and had significantly higher CD4%
compared to only HIV-positive subjects. This may imply that HTLV-1 has an adverse effect
on the immune system in HIV-infected subjects, independently of the CD4 count, that makes
co-infected subjects more vulnerable to TB
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20395161
-----------------------------------------------------HIV/Pathology
Global Health Lessons From HIV and Hepatitis Co-Infection in China
SHERER R.
Hepatol.Res. 40 (3), 248-250 ,2010
AD - Professor of Medicine Section of Infectious Diseases and Global Health University of
Chicago
Chicago
IL,
USA
engLink
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20394673
-----------------------------------------------------HIV/Pathology
Colonization With Staphylococcus Aureus (SA) in HIV-Infected
Children and Adolescents in Brooklyn, NY
NATHAWAD R., Mendez, H., Cambridge, R., Gesner, M., Desai, N., and Hammerschlag, M.
,Vancouver, BC; Canada, 2864.523 ,2010
Pediatrics, SUNY Downstate Medical Center, Brooklyn, NY; Pediatrics, Kings County
Hospital Center, Brooklyn, NY
Source: Conference (MIS)
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HIV/Pathology
HIV Subtype A Is Associated With Poorer Neuropsychological
Performance Compared to Subtype D in ART-Naïve Ugandan
Children
BOIVIN M., Ruel, T., Boal, H., Bangirana, P., and Wong, J.
,Vancouver, BC; Canada, 2870.581 ,2010
Psychiatry & Neurology, Michigan State University, East Lansing, MI; Pediatrics, University
of California, San Francisco, San Francisco, CA; Pediatrics, University of Washington, Seattle,
WA; Psychiatry, Makerere University, Kampala, Uganda
Source: Conference (MIS)
-----------------------------------------------------HIV/Pathology
Morbidities of Late Preterm Infants Born From 1993-2007 in a
Tertiary Care Center
REZAIE K., Bui, K., Barton, L., and Ramanathan, R.
,Vancouver, BC; Canada, 573 ,2010
Division of Neonatal Medicine, University of Southern California, Los Angles, CA
Source: Conference (MIS)
-----------------------------------------------------HIV/Pathology
Increased Risk of Myocardial Infarction in HIV-Infected Patients in
France, Relative to the General Population
LANG S., Mary-Krause, M., Cotte, L., Gilquin, J., Partisani, M., Simon, A., Boccara, F.,
Bingham, A., and Costagliola, D.
AIDS. 2010
AD - aINSERM U943, France bUPMC Univ-Paris 6, UMR S943, Paris, France cHospice Civil
de Lyon, Hotel Dieu, service d'hepatologie, Lyon, France dAPHP, Hopital Necker, Service
des Maladies Infectieuses et Tropicales, Paris, France eHopitaux Universitaires de
Strasbourg, Hopital de jour du COREVIH, Strasbourg, France fAPHP, Hopital PitieSalpetriere, Service de Medecine Interne I, France gAPHP, Hopital Saint-Antoine, Service de
Cardiologie, France hINSERM U970, Paris Cardiovascular Research Center_PARCC, France
iUniversite Paris Descartes, UMR S970, France jAPHP, Hopital Pitie-Salpetriere, Service des
Maladies
Infectieuses
et
Tropicales,
Paris,
France
ENG
The incidence of myocardial infarction (MI) is lower in France than in English-speaking and
northern European countries. We estimated the incidence of MI in the HIV-infected
population in France, on the basis of the data from the FHDH-ANRS CO4 cohort, by
comparison with the general population. The sex- and age-standardized morbidity ratio was
estimated as 1.5 [95% confidence interval (CI) 1.3-1.7] overall, 1.4 (95% CI 1.3-1.6) in men and
2.7 (95% CI 1.8-3.9) in women
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Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20400883
-----------------------------------------------------HIV/Pathology
[Diagnosis, Treatment and Prevention of Renal Diseases in HIV
Infected Patients. Recommendations of the Spanish AIDS Study
Group/National AIDS Plan.]
GUTIERREZ F. and Polo, R.
Enferm.Infecc.Microbiol.Clin. 2010
AD - Unidad de Enfermedades Infecciosas, Hospital General Universitario de Elche,
Alicante,
Espana
SPA
The incidence of opportunistic infections and tumours in HIV-infected patients has sharply
declined in the HAART era. At the same time there has been a growing increase of other
diseases not directly linked to immunodeficiency. Renal diseases are an increasing cause of
morbidity and mortality among HIV-infected patients. In the general population, chronic
renal failure has considerable multiorgan repercussions that have particular implications in
patients with HIV infection. The detection of occult or subclinical chronic kidney disease is
crucial since effective measures for delaying progression exist. Furthermore, the
deterioration in glomerular filtration should prompt clinicians to adjust doses of some
antiretroviral agents and other drugs used for treating associated comorbidities. Suppression
of viral replication, strict control of blood pressure, dyslipidemia and diabetes mellitus, and
avoidance of nephrotoxic drugs in certain patients are fundamental components of programs
aimed to prevent renal damage and delaying progression of chronic kidney disease in
patients with HIV. Renal transplantation and dialysis have also special implications in HIVinfected patients. In this article, we summarise the updated clinical practice guidelines for
the evaluation, management and prevention of renal diseases in HIV-infected patients from a
panel of experts in HIV and nephrologists on behalf of the Spanish AIDS Study Group
(GESIDA) and the National AIDS Plan
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20399541
-----------------------------------------------------HIV/Pathology
Seroprevalence Of Common Vaccine-Preventable Viral Infections In
Hiv-Positive Adults
MOLTON J., Smith, C., Chaytor, S., Maple, P., Brown, K., Johnson, M., and Geretti, A. M.
J.Infect. 2010
AD
Department
of
Virology
ENG
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OBJECTIVES: Guidelines recommend a proactive approach for offering vaccination to
susceptible HIV-infected patients. The size of the HIV-positive population that remains
susceptible to vaccine-preventable infections is largely unknown. The study determined
serostatus and recalled infection and vaccination history for measles, mumps, rubella,
varicella-zoster virus (VZV), hepatitis A, and hepatitis B among HIV-positive adults
accessing routine care. METHODS: The study recruited 200 consecutive patients with a
median CD4 count of 461 (interquartile range 326, 641) cells/mm(3); 62.5% were on
suppressive antiretroviral therapy. Patients underwent serological testing and completed a
questionnaire about recalled infection and vaccination history. RESULTS: Seronegativity
rates were 7.0% [95% confidence interval 3.9-11.5%] for measles, 12.0% [7.5-16.5%] for
mumps, 5.0% [2.4-9.0%] for rubella, 1.5% [0.3-4.3%] for VZV, 19.5% [14.0-25.0%] for hepatitis
A, and 22.5% [16.7-28.3%] for hepatitis B. For hepatitis B, seropositivity rates were 6.5% [3.510.9%] for surface antigen, 38.0% [31.3-44.7%] for anti-core antibody, and 33.0% [26.5-39.5%]
for anti-surface antibody alone. While patients who recalled a history of infection were
generally seropositive, up to 50.5% of patients were unsure of their vaccination history.
CONCLUSIONS: A proportion of HIV-positive adults lack evidence of immunity against
common, vaccine-preventable viral infections. Efforts are needed to improve knowledge and
records of vaccination history
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20403382
-----------------------------------------------------HIV/Pathology
Beta-Chemokine Production by Neural and Glial Progenitor Cells Is
Enhanced by HIV-1 Tat: Effects on Microglial Migration
HAHN Y. K., Vo, P., Fitting, S., Block, M. L., Hauser, K. F., and Knapp, P. E.
J.Neurochem. 2010
AD - Department of Anatomy and Neurobiology, Virginia Commonwealth University,
Richmond,
VA
23298
USA
ENG
Abstract HIV-1 neuropathology results from collective effects of viral proteins and
inflammatory mediators on several cell types. Significant damage is mediated indirectly
through inflammatory conditions promulgated by glial cells, including microglia that are
productively infected by HIV-1, and astroglia. Neural and glial progenitors exist in both
developing and adult brains. To determine whether progenitors are targets of HIV-1, a
multi-plex assay was performed to assess chemokine/cytokine expression after treatment
with viral proteins Tat or gp120. In the initial screen, ten analytes were basally released by
murine striatal progenitors. The beta-chemokines CCL5/RANTES, CCL3/MIP-1alpha, and
CCL4/MIP-1beta were increased by 12 h exposure to HIV-1 Tat. Secreted factors from Tattreated progenitors were chemoattractive towards microglia, an effect blocked by 2D7 antiCCR5 antibody pretreatment. Tat and opiates have interactive effects on astroglial
chemokine secretion, but this interaction did not occur in progenitors. gp120 did not affect
chemokine/cytokine release, although both CCR5 and CXCR4, which serve as gp120 coreceptors, were detected in progenitors. We postulate that chemokine production by
progenitors may be a normal, adaptive process that encourages immune inspection of newly
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generated cells. Pathogens such as HIV might usurp this function to create a maladaptive
state, especially during development or regeneration, when progenitors are numerous
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20403075
-----------------------------------------------------HIV/Pathology
Memantine for AIDS Dementia Complex: Open-Label Report of
ACTG 301
ZHAO Y., Navia, B. A., Marra, C. M., Singer, E. J., Chang, L., Berger, J., Ellis, R. J., Kolson, D.
L., Simpson, D., Miller, E. N., Lipton, S. A., Evans, S. R., Schifitto, G., and Adult Aids Clinical
Trial Group
HIV.Clin.Trials. 11 (1), 59-67 ,2010
AD
Harvard
School
of
Public
Health,
Boston,
Massachusetts,
USA
ENG
Objective: To evaluate the long-term safety and efficacy of memantine use as treatment of
HIV-associated cognitive impairment.Background: The results of a 20-week, randomized,
double-blind, placebo-controlled trial of memantine in HIV-infected participants with
cognitive impairment (ACTG 301) were previously reported. We report the results of the upto-60-week open-label phase following the double-blind phase.Method: Participants received
open-label memantine and were escalated to a 40 mg/day dose or their maximum tolerated
dose in the double- blind phase. Adverse experiences were used to evaluate safety, and
changes in the mean of eight neuropsychological test scores (NPZ-8) were used to evaluate
efficacy.Results: Ninety-nine participants entered the initial 12-week openlabel phase and 45
in the additional 48-week extension. Twenty-seven participants reported severe adverse
experiences. During the initial 12-week open-label phase, participants randomized to
memantine in the double-blind phase had a statistically significant higher improvement in
NPZ-8 compared to those randomized to placebo in the double-blind phase. No statistically
significant NPZ-8 changes were detected during the 48-week extension.Conclusion: Longterm use of memantine appears safe and tolerable. Future randomized studies with longer
follow-up are necessary to establish efficacy of memantine for the treatment of HIVassociated cognitive impairment
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20400412
-----------------------------------------------------HIV/Pathology
HIV-1 and Kidney Cells: Better Understanding of Viral Interaction
MIKULAK J. and Singhal, P. C.
Nephron Exp.Nephrol. 115 (2), e15-e21 ,2010
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AD - Feinstein Institute for Medical Research and Long Island Jewish Medical Center, New
Hyde
Park,
NY,
USA
ENG
HIV-associated nephropathy (HIVAN) is the most common disease affecting untreated
seropositive patients of African descent. Besides genetic (African descent) and HIV-1
infection (environmental), specific host factors such as activation of renin-angiotensinaldosterone system (RAAS) have also been demonstrated to play a role in the manifestation
of HIVAN. The recent identification of MYH9 as susceptible allele is a key step forward in
our understanding for the pathogenesis of focal glomerulosclerosis in people of AfricanAmerican descent. HIV-1 transgenic models have significantly advanced our knowledge
base in terms of role of HIV-1 genes in general and individual gene in particular in the
development of renal lesions mimicking HIVAN. These studies suggest that viral replication
is not needed for the development of renal lesions. Renal biopsy data from HIVAN patients
suggest that renal epithelial cells express HIV-1 genes and thus it may be sufficient to invoke
HIVAN phenotype in the presence of specific host and genetic factors. On the other hand,
immune response to infection may be required to induce HIV-1 associated immune complex
kidney disease (HIVICK). Since renal cell lack conventional HIV-1 receptors, HIV-1 entry
into renal cells has been a mystery. Recently, non-conventional pathways have been
demonstrated to facilitate HIV-1 entry into renal cells in in vitro studies. These include
presence of DEC-205 receptors in renal tubular cells and lipid rafts in podocytes. However,
HIV-1 entry through these pathways only allows non-productive infection. It appears that
the presence of specific genetic and host factors in in vivo conditions may be facilitating the
development of the productive HIV-1 infection in kidney cells
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20407278
-----------------------------------------------------HIV/Pathology
Septicaemia in a Population-Based HIV Clinical Cohort in Rural
Uganda, 1996-2007: Incidence, Aetiology, Antimicrobial Drug
Resistance and Impact of Antiretroviral Therapy
MAYANJA B. N., Todd, J., Hughes, P., Van der, Paal L., Mugisha, J. O., Atuhumuza, E.,
Tabuga, P., Maher, D., and Grosskurth, H.
Trop.Med.Int.Health. 2010
AD - MRC/UVRI Uganda Research Unit on AIDS, Entebbe, Uganda
ENG
Summary Objectives To describe the incidence and aetiology of septicaemia, and
antimicrobial drug resistance in HIV-infected and uninfected individuals, and the impact of
antiretroviral therapy (ART) on septicaemia. Methods Between 1996 and 2007, we followed
up a rural population-based cohort of HIV-infected and uninfected participants. The
aetiology and incidence of septicaemia, and antimicrobial drug resistances were determined.
ART became available in 2004, and its impact on the incidence of septicaemia was examined.
Results The overall septicaemia incidence (per 1000 pyrs) was 32.4 (95% CI 26.2-40.6) but was
only 2.6 (95% CI 1.3-6.2) in HIV-negative patients and 67.1 (95% CI 53.4-85.4) in HIV-positive
patients not on ART. Among those on ART, the overall incidence was 71.5 (95% CI 47.1114.3), although it was 121.4 (95%CI 77.9-200.4) in the first year on ART and 37.4 (95%CI 18.9--------------------------------------------------------------------------------------------------------------
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85.2) in the subsequent period. Septicaemia incidence was significantly associated with lower
CD4 counts. The commonest isolates were Streptococcus pneumoniae (SPN, n = 68) and
Non-typhi salmonellae (NTS, n = 42). Most SPN isolates were susceptible to ceftriaxone and
erythromycin, while resistance to cotrimoxazole and penicillin was common. All NTS
isolates were susceptible to ciprofloxacin, but resistance to cotrimoxazole and
chloramphenicol was common. Conclusions Septicaemia incidence was higher in HIVinfected than in HIV-uninfected participants, and it remained high for some time among
those who started ART. Starting ART earlier at higher CD4 counts is likely to lead to lower
septicaemia incidence. Both SPN and NTS, the commonest isolates, were resistant to most
commonly available antimicrobials. Blood culture laboratory surveillance systems to monitor
antibiotic susceptibility and inform treatment guidelines are needed in Africa
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20406428
------------------------------------------------------
Recommendations & Policies
Impact of Introducing Human Immunodeficiency Virus Testing,
Treatment and Care in a Tuberculosis Clinic in Rural Kenya
HUERGA H., Spillane, H., Guerrero, W., Odongo, A., and Varaine, F.
Int.J.Tuberc.Lung Dis. 14 (5), 611-615 ,2010
AD - Medecins Sans Frontieres, Nairobi, Kenya helenahuerga@parismsforg
eng
SETTING: In July 2005, Medecins Sans Frontieres and the Ministry of Health, Kenya,
implemented an integrated tuberculosis-human immunodeficiency virus (TB-HIV)
programme in western Kenya. OBJECTIVE: To evaluate the impact of an integrated TB-HIV
programme on patient care and TB programme outcomes. DESIGN: Retrospective
evaluation of three time periods: before (January-June 2005), shortly after (January-June
2006) and medium term after (January-December 2007) the implementation of the integrated
programme. RESULTS: Respectively 79% and 91% of TB patients were HIV tested shortly
and at medium term after service integration. The HIV-positive rate varied from 96% before
the intervention to respectively 88% (305/347) and 74% (301/405) after. The estimated
number of HIV-positive cases was respectively 303, 323 and 331 in the three periods. The
proportion of patients receiving cotrimoxazole prophylaxis increased significantly from 47%
(142/303) to 94% (303/323) and 86% (285/331, P < 0.05). Before the intervention, 87%
(171/197) of the TB-HIV patients would have been missed when initiating antiretroviral
treatment, compared to respectively 29% (60/210) and 36% (78/215) after the integration.
The TB programme success rate increased from 56% (230/409) to 71% (319/447) in the third
period (P < 0.05); however, there was no significant decrease in the default rate: 20% to 22%
(P = 0.66) and 18% (P = 0.37). CONCLUSION: Integrated TB-HIV care has a very positive
impact on the management of TB-HIV patients and on TB treatment outcomes
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20392355
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-----------------------------------------------------HIV/Recommendations & Policies
Doubts Remain, Risks Persist: HIV Prevention Knowledge and HIV
Testing Among Drug Users in Rio De Janeiro, Brazil
SINGER M., Clair, S., Malta, M., Bastos, F. I., Bertoni, N., and Santelices, C.
Subst.Use.Misuse. 2010
AD - Department of Anthropology, University of Connecticut, Storrs, Connecticut, USA
ENG
Brazil has been recognized for being the first developing country to provide universal AIDS
treatment. Brazil also implemented a comprehensive prevention initiative. These efforts have
been successful, with about half the number of HIV/AIDS cases forecast in 1992 developing
by 2000 . However, HIV/AIDS continues to spread, including among not-in-treatment drug
users. Questions have been raised about gaps in existing prevention efforts. Based on
qualitative research in 2006 -2008 with street drug users in Rio de Janeiro (focus groups, N =
24; a pile sort, N = 108; open-ended interviews, N = 34), this paper examines enduring gaps
in HIV knowledge and prevailing risk patterns and proposes strategies for strengthening
prevention
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20392169
-----------------------------------------------------HIV/Recommendations & Policies
Senegalese Religious Leaders' Perceptions of HIV/AIDS and
Implications for Challenging Stigma and Discrimination
ANSARI D. A. and Gaestel, A.
Cult.Health Sex. 1 ,2010
AD - Institute of Social Psychology, The London School of Economics and Political Science,
London,
UK
ENG
Senegal has been heralded as a model country in the fight against HIV/AIDS because of the
low prevalence in the general population and concerted prevention efforts since the start of
the epidemic. Despite its success, stigma and discrimination remain a reality for people
living with HIV/AIDS as HIV transmission remains linked to lifestyle and perceived
morality. Because religious teaching and the participation of religious leaders in HIV
prevention is reported as partially responsible for Senegal's success, the present study seeks
to deepen the understanding of their role in psychosocial aspects of care and support of
people living with HIV/AIDS. Interviews were conducted with 87 religious leaders. Muslim,
Catholic and Protestant leaders differ in their involvement in HIV/AIDS education, their
opinions of condom use and their counselling techniques for people living with HIV/AIDS.
Most religious leaders in each group believed that addressing the HIV/AIDS epidemic and
the reduction of HIV/AIDS-related stigma and discrimination are priorities, yet some
leaders still hold beliefs about HIV/AIDS that may ostracise people living with HIV/AIDS.
Organisations working to sensitise religious leaders on HIV/AIDS should focus more on the
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everyday experience of people living with HIV/AIDS, promote the value of condom use,
even if solely among married couples, and reinforce religious leaders' roles as spiritual
counsellors
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20397082
-----------------------------------------------------HIV/Recommendations & Policies
Meanings of Sex, Concepts of Risk and Sexual Practices Among
Migrant Coal Miners in Quang Ninh, Vietnam
VAN TUAN T.
Cult.Health Sex. 1 ,2010
AD
ActionAid
Vietnam,
Hanoi,
Viet
Nam
ENG
The study explores the meanings of sex among migrant coal miners in Vietnam and
identifies contextual factors influencing engagement in unsafe sexual practices. Findings
reveal that sex carries a number of social meanings in the lives of migrant miners: sex is
relaxation and reward for their risk and hard work; access to sex is an incentive for miners to
continue working in the mine; sex strengthens identity and social networks; sex helps miners
to affirm manhood, group membership and masculinity; and sex workers are confidants
with whom they can share their problems. Facing accidents at work on a daily basis, miners
are less inclined to worry about the long-term risks of HIV infection. In addition, being
excluded from access to relevant information, miners feel distant from HIV infection.
Findings suggest that interventions on sexual behaviour and practices should be sensitive to
the concepts of risk and meanings of sex among migrant groups such as coal miners
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20397081
-----------------------------------------------------HIV/Recommendations & Policies
Assessment of Safety and Toxicity Following Maternal
Antiretroviral Exposure in Infants Born to HIV-1-Infected Women
Enrolled in Antiretroviral Treatment Protocols in Diverse Areas of
the World. Six Month Results of AIDS Clinical Trials Group (ACTG)
Study 5190/Pediatric AIDS Clinical Trials Group (PACTG) 1054
NIELSEN-SAINES K., Komarow, L., Cu-Uvin, S., Jourdain, G., Klingman, K., Shapiro, D.,
Mofenson, L., Campbell, T., Hitti, J., and Currier, J.
,Vancouver, BC; Canada, 2870.577 ,2010
Pediatrics, David Geffen UCLA School of Medicine, Los Angeles, CA; SDAC, Harvard
School of Public Health, Boston, MA; Obstetrics and Gynecology, Brown University,
Providence, RI; Pediatrics, Institut de Recherche Pour le Developpement, Chiang Mai,
Thailand; NIAID, National Institutes of Health-NIH, Bethesda, MD; Infectious Diseases,
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EUROPRISE SCIENCE UPDATE 10-17
University of Colorado, Denver, CO; Obstetrics, University of Washington, Seattle, WA;
Internal Medicine, David Geffen UCLA School of Medicine, Los Angeles, CA
Source: Conference (MIS)
-----------------------------------------------------HIV/Recommendations & Policies
Relative Efficacy of an HIV Prevention Intervention Among Diverse
High-Risk Youth in San Diego, California
BLANCO E., Lindsay, S., Lemus, H., Ojeda, N., and Zuniga, M.
,Vancouver, BC; Canada, 2 ,2010
Pediatrics, UC San Diego, La Jolla, CA; Graduate School of Public Health, San Diego State
University, San Diego, CA; Sociology, San Diego State University, San Diego, CA; Medicine,
UC San Diego, La Jolla, CA
Source: Conference (MIS)
-----------------------------------------------------HIV/Recommendations & Policies
Pediatricians' Attitudes and Counseling Practices Regarding
Neonatal Male Circumcisions
DIEKEMA D., Carlo, W., Zimmerman, E., and O'Conner, K.
,Vancouver, BC; Canada, 4402.145 ,2010
Pediatrics, University of Washington, Seattle, WA; Neonatology, University of Alabama at
Birmingham, Birmingham, AL; Practice, American Academy of Pediatrics, Elk Grove Village,
IL; Research, American Academy of Pediatrics, Elk Grove Village, IL
Source: Conference (MIS)
-----------------------------------------------------HIV/Recommendations & Policies
Men's Labor Migration and Women's Informal Communication on
HIV/AIDS in Mozambique
AGADJANIAN V.
,Dallas, TX; USA ,2010
Arizona State University
Source: Conference (MIS)
-----------------------------------------------------HIV/Recommendations & Policies
Women Who Know: The Relationship Between Risk and HIV Testing
HOWDEN L.
,Dallas, TX; USA ,2010
Texas A&M University
Source: Conference (MIS)
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-----------------------------------------------------HIV/Recommendations & Policies
Circumcision, Information, and HIV Prevention
THORNTON R., Munthali, A., and Godlonton, S.
,Dallas, TX; USA ,2010
University of Michigan
Source: Conference (MIS)
-----------------------------------------------------HIV/Recommendations & Policies
Best Practices in Global STI/HIV Prevention
KIMUNA S. and Burke, S.
,Dallas, TX; USA ,2010
East Carolina University
Source: Conference (MIS)
-----------------------------------------------------HIV/Recommendations & Policies
HIV/AIDS in the Slums Of Nairobi: The Capacity of the Private
Health Sector to Respond to the High Disease Burden
MGOMELLA G., Ekirapa, A., and Kyobutungi, C.
,Dallas, TX; USA ,2010
African Population and Health Research Center (APHRC)
Source: Conference (MIS)
-----------------------------------------------------HIV/Recommendations & Policies
The Context of Condom Use Among Young Adults in the
Philippines: Implications for HIV Risk Prevention
LUCEA M., Rose, L., and Kub, J.
,Dallas, TX; USA ,2010
Johns Hopkins University
Source: Conference (MIS)
-----------------------------------------------------HIV/Recommendations & Policies
Addressing Comprehensive Knowledge As a Strategy to Mitigate
HIV Related Risk Behavior Among Young Men in India
PANDEY V.
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,Dallas, TX; USA ,2010
International Institute for Population Sciences (IIPS)
Source: Conference (MIS)
-----------------------------------------------------HIV/Recommendations & Policies
Media Exposure on Condom Use Among Adolescents Age 12 - 19 in
Ghana: Application of the TPB Model
ACOSTA P. and Belue, R.
,Dallas, TX; USA ,2010
Pennsylvania State University
Source: Conference (MIS)
-----------------------------------------------------HIV/Recommendations & Policies
Formative Work Towards Utilization of Networks to Build Upon
Existing Hiv Prevention Programs for High Risk Men in India
SCHNEIDER J., Kumar, P., Laumann, E., Yeldandi, V., Dandona, L., and Mayer, K.
,Washington, DC; USA, A-040 ,2010
1) University of Chicago, Chicago, IL, United States; 2) Public Health Foundation of India,
Hyderabad, India; 3) Brown University, Providence, RI, United States; 4) SHARE-India,
Hyderabad, India
Source: Conference (MIS)
-----------------------------------------------------HIV/Recommendations & Policies
Information and Communication: a Library's Local Response to
HIV/AIDS in Zambia
KANYENGO C. W.
Health Info.Libr.J. 27 (1), 57-65 ,2010
AD - University of Zambia Library, Lusaka, Zambia ckanyengo@yahoocom
eng
OBJECTIVE: To document and describe the University of Zambia Medical library's responses
to the fight against HIV/AIDS in Zambia. METHODS: The methodology adopted was a case
study approach combined with an analysis of the literature such as annual reports and
official documents. This was augmented by personal reflections of the author having worked
at the Medical Library. RESULTS: The University of Zambia Medical library has over the
years instituted and implemented HIV/AIDS information provision programmes that
include the provision of information in various formats -- print or electronic and, in addition,
capacity building in HIV/AIDS information literacy skills. CONCLUSION: A library's social
responsibility calls for it to be part of national responses to crises that arise in society. As
HIV/AIDS has affected every aspect of Zambian society prevention, treatment, care and
support there is an understanding that the library's role should be using the critical and
strategic resource at its disposal - information -- as part of their contribution to the fight
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EUROPRISE SCIENCE UPDATE 10-17
against HIV/AIDS. In this context, libraries should source, collect, organize and disseminate
information on HIV/AIDS in a way that is easily accessible to researchers, HIV/AIDS
programme implementation agencies and the ordinary public
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20402805
-----------------------------------------------------HIV/Recommendations & Policies
Findings in Humanized-Mouse Model Suggest Benefit of Further
Studies in HIV Pre-Exposure Prophylaxis
Expert.Rev.Clin.Immunol. 6 (2), 186 ,2010
engLink
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20402380
------------------------------------------------------
Therapy, others
Associations With Virologic Treatment Failure in Adults on
Antiretroviral Therapy in South Africa
DATAY M. I., Boulle, A., Mant, D., and Yudkin, P.
J.Acquir.Immune.Defic.Syndr. 2010
AD - From the *Department of Primary Health Care, University of Oxford, Oxford, United
Kingdom; and daggerSchool of Public Health and Family Medicine, University of Cape
Town,
Cape
Town,
South
Africa
ENG
OBJECTIVES:: Highly active antiretroviral therapy (HAART) has been available in
government facilities in the Western Cape Province of South Africa since 2001. We aimed to
investigate factors associated with virologic treatment failure in this setting. DESIGN:: Casecontrol study, matched on facility and on starting date and duration of HAART. METHODS::
Cases and controls were identified from clinic registers from May 2001 to June 2006. Cases
were patients who switched to second-line therapy after confirmed virologic failure (2
consecutive viral loads above 1000 copies/mL). Controls were on first-line treatment with
viral load <400 copies per milliliter at the time of case incidence. RESULTS:: One hundred
thirty cases and 238 controls were selected from 8 clinics (median 16.6 months on HAART,
interquartile range: 12.2-24.6). Treatment interruptions [adjusted odds ratio (AOR) 8.6, 95%
confidence interval: 3.6 to 20.8], prior nevirapine-based prevention of mother-to-child
transmission (PMTCT) treatment (AOR: 9.6, 95% confidence interval: 2.9 to 32.2), a baseline
CD4 count less than 50 cells per microliter or from 50-150 cells per microliter (AOR: 6.6, 95%
confidence interval: 2.3 to 18.8 and AOR: 5.8, 95% confidence interval: 2.1 to 16.3 compared
with a baseline CD4 count of more than 150 cells/muL), and the use of nevirapine in the
initial regimen (AOR: 2.5, 95% confidence interval: 1.4 to 4.7) were all independently
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EUROPRISE SCIENCE UPDATE 10-17
associated with virologic treatment failure. CONCLUSIONS:: In this setting, nevirapine in
the initial HAART regimen or for PMTCT treatment is associated with virologic treatment
failure, together with low CD4 count at ART initiation. Earlier initiation of HAART and
access to improved triple therapy and PMTCT regimens are priorities for HIV programs in
Southern Africa
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20395870
-----------------------------------------------------HIV/Therapy, others
Is It Time to Treat HIV Elite Controllers With Combined Antiretroviral
Therapy?
TORRE D.
Clin.Infect.Dis. 50 (10), 1425-1426 ,2010
engLink
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20397932
------------------------------------------------------
Vaccines, clinical
Heterologous Prime-Boost HIV-1 Vaccination Regimens in PreClinical and Clinical Trials
BROWN S. A., Surman, S. L., Sealy, R., Jones, B. G., Slobod, K. S., Branum, K., Lockey, T. D.,
Howlett, N., Freiden, P., Flynn, P., and Hurwitz, J. L.
Viruses. 2 (2), 435-467 ,2010
AD - Department of Immunology, St Jude Children's Research Hospital, 262 Danny Thomas
Place,
Memphis,
TN,
USA;
scottbrown@stjudeorg
ENG
Currently, there are more than 30 million people infected with HIV-1 and thousands more
are infected each day. Vaccination is the single most effective mechanism for prevention of
viral disease, and after more than 25 years of research, one vaccine has shown somewhat
encouraging results in an advanced clinical efficacy trial. A modified intent-to-treat analysis
of trial results showed that infection was approximately 30% lower in the vaccine group
compared to the placebo group. The vaccine was administered using a heterologous primeboost regimen in which both target antigens and delivery vehicles were changed during the
course of inoculations. Here we examine the complexity of heterologous prime-boost
immunizations. We show that the use of different delivery vehicles in prime and boost
inoculations can help to avert the inhibitory effects caused by vector-specific immune
responses. We also show that the introduction of new antigens into boost inoculations can be
advantageous, demonstrating that the effect of ;original antigenic sin' is not absolute. Preclinical and clinical studies are reviewed, including our own work with a three-vector
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EUROPRISE SCIENCE UPDATE 10-17
vaccination regimen using recombinant DNA, virus (Sendai virus or vaccinia virus) and
protein. Promising preliminary results suggest that the heterologous prime-boost strategy
may possibly provide a foundation for the future prevention of HIV-1 infections in humans
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20407589
------------------------------------------------------
Vaccines, research
Antibody-Mediated Protection Against Mucosal SHIV Challenge of
Macaques Immunized With Alphavirus Replicon Particles and
Boosted With Trimeric Envelope Glycoprotein in MF59 Adjuvant
BARNETT S. W., Burke, B., Sun, Y., Kan, E., Legg, H., Lian, Y., Bost, K., Zhou, F., Goodsell,
A., Zur, Megede J., Polo, J., Donnelly, J., Ulmer, J., Otten, G. R., Miller, C. J., Vajdy, M., and
Srivastava, I. K.
J.Virol. 2010
AD - Novartis Vaccines and Diagnostics, 350 Massachusetts Avenue, Cambridge, MA 02139;
California National Primate Research Center, University of California, Davis, CA
ENG
We have previously shown that rhesus macaques were partially protected against high dose
intravenous challenge with SHIVSF162P4 following sequential immunization with chimeric
recombinant VEE/SIN alphavirus replicon particles (VRP) encoding HIV-1SF162
gp140DeltaV2 envelope (Env) and trimeric Env protein in MF59 adjuvant (Xu, R., I. K.
Srivastava, C. E. Greer, I. Zarkikh, Z. Kraft, L. Kuller, J. M. Polo, S. W. Barnett, and L.
Stamatatos. 2006. AIDS Res. Human Retro. 22:1022-1030). The protection did not require T
cell immune responses directed toward SIV Gag. We extend those findings here to
demonstrate antibody-mediated protection against mucosal challenge in macaques using
prime-boost regimens incorporating both intramuscular and mucosal routes of delivery.
Vaccination groups were primed with VRP followed by boosting with Env protein in MF59
adjuvant, or given VRP intramuscular immunizations alone followed by intrarectal challenge
with SHIVSF162P4. Results demonstrated that these vaccines were able to effectively protect,
in varying degrees, against subsequent mucosal SHIV challenge, but most noteworthy, all
macaques that received the intramuscular VRP prime plus Env protein boost were
completely protected. A statistically significant association was observed between the titer of
virus neutralizing and binding antibodies as well as the avidity of anti-Env antibodies
measured pre-challenge and protection from infection. These results highlight the merit of
the alphavirus replicon vector prime plus Env protein boost vaccine approach for the
induction of protective antibody responses and are of particular relevance to advancing our
understanding of the potential correlates of immune protection against HIV infection at a
relevant mucosal portal of entry
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20392857
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HIV/Vaccines, research
Selection of a Rare Neutralization-Resistant Variant Following
Passive Transfer of Convalescent Immune Plasma in EIAVChallenged SCID Horses
TAYLOR S. D., Leib, S. R., Carpenter, S., and Mealey, R. H.
J.Virol. 2010
AD - Department of Veterinary Microbiology and Pathology, Washington State University,
Pullman, Washington 99164-7040; Department of Animal Science, Iowa State University,
Ames,
Iowa
50011
ENG
Vaccines preventing HIV-1 infection will likely elicit antibodies that neutralize diverse
strains. However, the capacity for lentiviruses to escape broadly neutralizing antibodies
(nAbs) is not completely understood, nor is it known whether nAbs alone can control
heterologous infection. Here, we determined that convalescent immune plasma from a horse
persistently infected with equine infectious anemia virus (EIAV) neutralized homologous
virus and several envelope variants containing heterologous principal neutralizing domains
(PND). Plasma was infused into young horses (foals) affected with severe combined
immunodeficiency (SCID), followed by challenge with a homologous EIAV stock. Treated
SCID foals were protected against clinical disease, with complete prevention of infection
occurring in one foal. In three SCID foals, a novel neutralization-resistant variant arose that
was found to pre-exist at a low frequency in the challenge inoculum. In contrast, SCID foals
infused with non-immune plasma developed acute disease associated with high levels of the
predominant challenge virus. Following transfer to an immunocompetent horse, the
neutralization-resistant variant induced a single febrile episode and was subsequently
controlled in the absence of type-specific nAb. Long term control was associated with the
presence of cytotoxic T lymphocytes (CTL). Our results demonstrate that immune plasma
with neutralizing activity against heterologous PND variants can prevent lentivirus infection
and clinical disease in the complete absence of T cells. Importantly however, rare
neutralization-resistant envelope variants can replicate in vivo under relatively broad
selection pressure, highlighting the need for protective lentivirus vaccines to elicit nAb
responses with increased breadth and potency and/or CTL that target conserved epitopes
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20392850
-----------------------------------------------------HIV/Vaccines, research
Increased Sensitivity of HIV Variants Selected by Attachment
Inhibitors to Broadly Neutralizing Antibodies
ZHOU N., Fan, L., Ho, H. T., Nowicka-Sans, B., Sun, Y., Zhu, Y., Hu, Y., McAuliffe, B., Rose,
B., Fang, H., Wang, T., Kadow, J., Krystal, M., Alexander, L., Colonno, R., and Lin, P. F.
Virology. 2010
AD - Department of Virology, 5 Department of Research Parkway, Wallingford, CT 06498,
USA
ENG
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Treatment with HIV attachment inhibitors (AIs) can select for escape mutants throughout the
viral envelope. We report on three such mutations: F423Y (gp120 CD4 binding pocket) and
I595F and K655E (gp41 ectodomain). Each displayed decreased sensitivity to the AI BMS488043 and earlier generation AIs, along with increased sensitivity to the broadly
neutralizing antibodies 2F5 and 4E10, without affecting the rate of viral entry or sensitivity to
the entry inhibitors AMD-3100 and Enfuvirtide. We also observed that I595F did not
substantially increase envelope sensitivity to HIV-infected patient sera. Based on these
observations, we propose that although F423Y, I595F and K655E may all affect the
presentation of the 2F5 and 4E10 epitopes, natural immune mimicry is rare only for the I595F
effect. Thus, it seems that in addition to restricting AI resistance development, incorporation
of I595F into an appropriate vehicle could elicit a novel antiviral response to improve vaccine
efficacy
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20400170
------------------------------------------------------
Virology
Mannose-Rich Glycosylation Patterns on HIV-1 Subtype C Gp120
and Sensitivity to the Lectins, Griffithsin, Cyanovirin-N and
Scytovirin
ALEXANDRE K. B., Gray, E. S., Lambson, B. E., Moore, P. L., Choge, I. A., Mlisana, K.,
Karim, S. S., McMahon, J., O'Keefe, B., Chikwamba, R., and Morris, L.
Virology. 2010
AD - National Institute for Communicable Diseases, Johannesburg, South Africa
ENG
Griffithsin (GRFT), Cyanovirin-N (CV-N) and Scytovirin (SVN) are lectins that inhibit HIV-1
infection by binding to multiple mannose-rich glycans on the HIV-1 envelope glycoproteins
(Env). Here we show that these lectins neutralize subtype C primary virus isolates in
addition to Env-pseudotyped viruses obtained from plasma and cervical vaginal lavages.
Among 15 subtype C pseudoviruses, the median IC(50) values were 0.4, 1.8 and 20.1nM for
GRFT, CV-N and SVN, respectively, similar to what was found for subtype B and A.
Analysis of Env sequences suggested that concomitant lack of glycans at positions 234 and
295 resulted in natural resistance to these compounds, which was confirmed by site-directed
mutagenesis. Furthermore, the binding sites for these lectins overlapped that of the 2G12
monoclonal antibody epitope, which is generally absent on subtype C Env. This data support
further research on these lectins as potential microbicides in the context of HIV-1 subtype C
infection
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20392471
------------------------------------------------------
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HIV/Virology
Prevalence of Transmitted Drug Resistance Associated Mutations
and HIV-1 Subtypes in New HIV-1 Diagnoses, U.S.-2006
WHEELER W. H., Ziebell, R. A., Zabina, H., Pieniazek, D., Prejean, J., Bodnar, U. R., Mahle,
K. C., Heneine, W., Johnson, J. A., and Hall, H. I.
AIDS. 2010
AD - aDivision of HIV/AIDS Prevention, National Center for HIV, Viral Hepatitis, STD and
TB Prevention, Centers for Disease Control and Prevention, Atlanta, USA bThe Ginn Group
Inc, Peachtree City, USA cBusiness Computer Applications, Atlanta, Georgia, USA dUnited
States Department of Health and Human Services, Washington, DC, USA *The members of
the Variant, Atypical, and Resistant HIV Surveillance are listed in the Acknowledgements
ENG
OBJECTIVE:: To determine the distribution of HIV-1 subtypes and the prevalence of
transmitted drug resistance-associated mutations (TDRM) among persons newly diagnosed
with HIV-1 infection in the United States. METHODS:: We used sequence data from Variant,
Atypical, and Resistant HIV Surveillance (VARHS) collected from newly diagnosed persons
in 10 states and 1 county health department in 2006. To evaluate TDRM, we used a mutation
list for surveillance of TDRM appropriate for the primarily subtype B HIV epidemic in the
United States. RESULTS:: Sequences were obtained from 2030 of 10 860 persons newly
diagnosed with HIV in 11 surveillance areas. Mutations associated with transmitted drug
resistance occurred in 292 (14.6%) persons; TDRM associated with a specific drug class
occurred in 156 (7.8%) for non-nucleoside reverse transcriptase inhibitors, 111 (5.6%) for
nucleoside reverse transcriptase inhibitors and 90 (4.5%) for protease inhibitors. There were
no significant differences in prevalence of TDRM by demographic characteristic. The HIV-1
subtype B was the most prevalent subtype occurring in 1922 (96.2%) persons; subtype C
(1.3%) was the most prevalent non-B subtype. CONCLUSION:: We presented a clade Boptimized mutation list for evaluating surveillance of TDRM in the United States and
analyzed the largest collection of sequence data obtained from individuals newly diagnosed
with HIV. The prevalence of TDRM in persons newly diagnosed with HIV is higher than in
previous U.S. studies; however, this is not necessarily a significant trend. Continued
reporting of sequence data for public health purposes from all sources will improve
representativeness and accuracy in analyzing trends in transmitted drug resistance and
genetic diversity
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20395786
-----------------------------------------------------HIV/Virology
Simultaneous Detection of Human Immunodeficiency Virus Type-1
Drug Resistant Minority Genotypes by a Multiplex Oligonucleotide
Ligation Assay
ELLIS N., Vaz, L., Koth, A., and Frenkel, L.
,Vancouver, BC; Canada, 2870.573 ,2010
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Seattle Children's Hospital, Seattle, WA; Loma Linda University, Loma Linda, CA;
University of Washington, Seattle, WA
Source: Conference (MIS)
-----------------------------------------------------HIV/Virology
HIV Classification Using Coalescent Theory
BULLA I., Schultz, A. K., Schreiber, F., Zhang, M., Leitner, T., Korber, B., Morgenstern, B.,
and Stanke, M.
Bioinformatics. 2010
AD - Abteilung Bioinformatik, Institut fur Mikrobiologie und Genetik, Georg-AugustUniversitat
Gattingen,
Goldschmidtstr
1,
37077
Gattingen,
Germany
ENG
MOTIVATION: Existing coalescent models and phylogenetic tools based on them are not
designed for studying the genealogy of sequences like those of HIV since in HIV
recombinants with multiple cross-over points between the parental strains frequently arise.
Hence, ambiguous cases in the classification of HIV sequences into subtypes and Circulating
Recombinant Forms (CRFs) have been treated with ad hoc methods in lack of tools based on
a comprehensive coalescent model accounting for complex recombination patterns.
RESULTS: We developed the program ARGUS that scores classifications of sequences into
subtypes and recombinant forms. It reconstructs Ancestral Recombination Graphs (ARGs)
that reflect the genealogy of the input sequences given a classification hypothesis. An ARG
with maximal probability is approximated using a Markov Chain Monte Carlo approach.
ARGUS was able to distinguish the correct classification with a low error rate from plausible
alternative classifications in simulation studies with realistic parameters. We applied our
algorithm to decide between two recently debated alternatives in the classification of CRF02
of HIV-1 and find that CRF02 is indeed a recombinant of subtypes A and G. AVAILABILITY:
ARGUS is implemented in C++ and the source code is available at
http://gobics.de/software. CONTACT: [email protected] SUPPLEMENTARY
INFORMATION: Details of the algorithm and its testing are described in the online
supplementary material
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20400454
-----------------------------------------------------HIV/Virology
Characterization and Frequency of a Newly Identified HIV-1 BF1
Intersubtype Circulating Recombinant Form in Sao Paulo, Brazil
SANABANI S. S., Pastena, E. R., Neto, W. K., Martinez, V. P., and Sabino, E. C.
Virol.J. 7 (1), 74 ,2010
ENG
ABSTRACT: BACKGROUND: HIV circulating recombinant forms (CRFs) play an important
role in the global and regional HIV epidemics, particularly in regions where multiple
subtypes are circulating. To date, several (>40) CRFs are recognized worldwide with five
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EUROPRISE SCIENCE UPDATE 10-17
currently circulating in Brazil. Here, we report the characterization of near full-length
genome sequences (NFLG) of six phylogenetically related HIV-1 BF1 intersubtype
recombinants (five from this study and one from other published sequences) representing
CRF46_BF1. METHODS: Initially, we selected 36 samples from 888 adult patients residing in
Sao Paulo who had previously been diagnosed as being infected with subclade F1 based on
pol subgenomic fragment sequencing. Proviral DNA integrated in peripheral blood
mononuclear cells (PBMC) was amplified from the purified genomic DNA of all 36-blood
samples by five overlapping PCR fragments followed by direct sequencing. Sequence data
were obtained from the five fragments that showed identical genomic structure and
phylogenetic trees were constructed and compared with previously published sequences.
Genuine subclade F1 sequences and any other sequences that exhibited unique mosaic
structures were omitted from further analysis. RESULTS: Of the 36 samples analyzed, only
six sequences, inferred from the pol region as subclade F1, displayed BF1 identical mosaic
genomes with a single intersubtype breakpoint identified at the nef-U3 overlap (HXB2
position 9347-9365; LTR region). Five of these isolates formed a rigid cluster in phylogentic
trees from different subclade F1 fragment regions, which we can now designate as
CRF46_BF1. According to our estimate, the new CRF accounts for 0.56% of the HIV-1
circulating strains in Sao Paulo. Comparison with previously published sequences revealed
an additional five isolates that share an identical mosaic structure with those reported in our
study. Despite sharing a similar recombinant structure, only one sequence appeared to
originate from the same CRF46_BF1 ancestor. CONCLUSION: We identified a new
circulating recombinant form with a single intersubtype breakpoint identified at the nef-LTR
U3 overlap and designated CRF46_BF1.Given the biological importance of the LTR U3
region, intersubtype recombination in this region could play an important role in HIV
evolution with critical consequences for the development of efficient genetic vaccines
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20398371
-----------------------------------------------------HIV/Virology
[The Results of a Study of HIV-1 Resistance in the Area of Yamal
and the Comparison of the Frequency of Mutations With Different
Score Values]
Klin.Lab Diagn. (2), 43-46 ,2010
rus
The amino acid sequence of the known strain HXB-2 belonging to subtype B is used as a
reference strain matrix to determine HIV genotypic resistance by the sequencing technique.
However, numerous studies have ascertained that HIV non-B subtypes have been widely
accepted in Russia. The authors' data show that the significance of low score mutations in the
Russian populations of HIV-1 is yet to be explained, unquestionably, arouses great scientific
interest, and calls for further study
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20397579
-------------------------------------------------------------------------------------------------------------------------------------------------------------------
77 / 152
EUROPRISE SCIENCE UPDATE 10-17
HIV/Virology
HIV-1 Subtype C-Infected Individuals Maintaining High Viral Load
As Potential Targets for the "Test-and-Treat" Approach to Reduce
HIV Transmission
NOVITSKY V., Wang, R., Bussmann, H., Lockman, S., Baum, M., Shapiro, R., Thior, I.,
Wester, C., Wester, C. W., Ogwu, A., Asmelash, A., Musonda, R., Campa, A., Moyo, S., van,
Widenfelt E., Mine, M., Moffat, C., Mmalane, M., Makhema, J., Marlink, R., Gilbert, P., Seage,
G. R., III, DeGruttola, V., and Essex, M.
PLoS.One. 5 (4), e10148 ,2010
AD - Harvard School of Public Health AIDS Initiative, Department of Immunology and
Infectious Diseases, Harvard School of Public Health, Boston, Massachusetts, United States
of
America
eng
The first aim of the study is to assess the distribution of HIV-1 RNA levels in subtype C
infection. Among 4,348 drug-naive HIV-positive individuals participating in clinical studies
in Botswana, the median baseline plasma HIV-1 RNA levels differed between the general
population cohorts (4.1-4.2 log(10)) and cART-initiating cohorts (5.1-5.3 log(10)) by about one
log(10). The proportion of individuals with high (> or = 50,000 (4.7 log(10)) copies/ml) HIV-1
RNA levels ranged from 24%-28% in the general HIV-positive population cohorts to 65%83% in cART-initiating cohorts. The second aim is to estimate the proportion of individuals
who maintain high HIV-1 RNA levels for an extended time and the duration of this period.
For this analysis, we estimate the proportion of individuals who could be identified by
repeated 6- vs. 12-month-interval HIV testing, as well as the potential reduction of HIV
transmission time that can be achieved by testing and ARV treating. Longitudinal analysis of
42 seroconverters revealed that 33% (95% CI: 20%-50%) of individuals maintain high HIV-1
RNA levels for at least 180 days post seroconversion (p/s) and the median duration of high
viral load period was 350 (269; 428) days p/s. We found that it would be possible to identify
all HIV-infected individuals with viral load > or = 50,000 (4.7 log(10)) copies/ml using
repeated six-month-interval HIV testing. Assuming individuals with high viral load initiate
cART after being identified, the period of high transmissibility due to high viral load can
potentially be reduced by 77% (95% CI: 71%-82%). Therefore, if HIV-infected individuals
maintaining high levels of plasma HIV-1 RNA for extended period of time contribute
disproportionally to HIV transmission, a modified "test-and-treat" strategy targeting such
individuals by repeated HIV testing (followed by initiation of cART) might be a useful public
health strategy for mitigating the HIV epidemic in some communities
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20405044
------------------------------------------------------
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EUROPRISE SCIENCE UPDATE 10-17
HIV/Virology
Human Immunodeficiency Virus Type 1 (HIV-1) Protease Codon 36
Polymorphisms and the Differential Development of Resistance to
Nelfinavir, Lopinavir and Atazanavir in Different HIV-1 Subtypes
LISOVSKY I., Schader, S. M., Martinez-Cajas, J. L., Oliveira, M., Moisi, D., and Wainberg, M.
A.
Antimicrob.Agents Chemother. 2010
AD - McGill University AIDS Centre, Lady Davis Institute, Jewish General Hospital,
Montreal QC, Canada; Division of Experimental Medicine, McGill University, Montreal, QC,
Canada; Department of Microbiology and Immunology, McGill University, Montreal QC,
Canada; Infectious Diseases Division, Department of Medicine, Queen's University, Kingston
ON,
Canada
ENG
Amino acid 36 of the human immunodeficiency virus type 1 (HIV-1) protease differs among
various viral subtypes in that methionine is usually found in subtype B viruses but
isoleucine is common in other subtypes. This polymorphism is associated with higher rates
of treatment failure involving protease inhibitors (PIs) in non-subtype B infected patients. To
investigate this, we generated genetically homogeneous wild-type viruses from subtype B, C
and CRF02_AG full-length molecular clones and showed that subtype C and CRF02_AG I36
viruses exhibited higher levels of resistance to various PIs relative to their respective M36
counterparts, while the opposite was observed for subtype B viruses. Selections for resistance
with each variant were performed with Nelfinavir (NFV), Lopinavir (LPV) and Atazanavir
(ATV). Sequence analysis of the protease gene at week 35 revealed that the major NFV
resistance mutation D30N emerged in NFV-selected subtype B and in I36 subtype C viruses
despite polymorphic variation. A unique mutational pattern developed in subtype C M36
viruses selected with NFV or ATV. The presence of I47A in LPV-selected I36 CRF02_AG
conferred higher level resistance than L76V in LPV-selected M36 CRF02_AG. Phenotypic
analysis revealed a >1000-fold increase in NFV resistance in I36 subtype C NFV-selected
virus with no apparent impact on viral replication capacity. Thus, the position 36
polymorphism in PR appears to have a differential effect on both drug susceptibility and
viral replication capacity depending on both viral subtype and the drug being evaluated
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20404123
-----------------------------------------------------HIV/Virology
The HIV-1 Matrix Protein P17 Activates the Transcription Factors CMyc and CREB in Human B Cells
LI S., Bozzo, L., Wu, Z., Lu, W., and Romerio, F.
New Microbiol. 33 (1), 13-24 ,2010
AD - Institute of Human Virology, University of Maryland, School of Medicine, Baltimore
21201,
USA
eng
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79 / 152
EUROPRISE SCIENCE UPDATE 10-17
The human immunodeficiency virus matrix protein p17 plays a critical role in many steps of
the virus life cycle. In addition, p17 displays biological activities outside infected cells.
Indeed, virus-neutralizing antibodies against p17 in plasma of infected patients correlate
with slower disease progression, and p17 has been shown to interact with an as yet
unidentified cell surface receptor expressed on peripheral blood B cells. The present study
investigated intracellular signaling pathways triggered following this interaction. Using
protein/DNA arrays, we show that p17 increases phosphorylation and the DNA-binding
activity of CREB and c-Myc through the time- and dose-dependent activation of the
cAMP/PKA and MEK/ERK signaling pathways. Interestingly, we found that both signaling
pathways are synergistically activated upon co-stimulation through the CD19 receptor. As
both CREB and c-Myc are involved in the regulation of cell proliferation, differentiation, and
survival, our findings might suggest a potential mechanism of B cell lymphomagenesis
during HIV-1 infection
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20402410
-----------------------------------------------------HIV/Virology
HIV-1 Subtype C Transmission Network: The Phylogenetic
Reconstruction Strongly Supports the Epidemiological Data
BON I., Ciccozzi, M., Zehender, G., Biagetti, C., Verrucchi, G., Lai, A., Presti, A. L., Gibellini,
D., and Re, M. C.
J.Clin.Virol. 2010
AD - Microbiology Section of the Department of Haematology and Oncologic Sciences,
University
of
Bologna,
Via
Massarenti,
9-40138
Bologna,
Italy
ENG
The sequence and times of the transmission events was reported after a hospital accident by
a phylodynamic reconstruction of transmission network among four subjects. The dated tree
allowed to date the transmission events with good approximation, the time point and
direction of each transmission, estimated on the basis of the phylogeny, and agreed with the
presumptive time of infection on the basis of clinical history-taking
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20400369
-----------------------------------------------------HIV/Virology
[Human Immunodeficiency Virus (HIV) Type 1 With R5 Tropism
Among HIV-1 Antiretroviral-Experienced Patients in Spain.]
ARRIBAS J. R., Rivero, A., Leal, M., and Sanchez-de la, Rosa R.
Enferm.Infecc.Microbiol.Clin. 2010
AD
Hospital
Universitario
La
Paz,
SPALink
Madrid,
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80 / 152
Espana
:
EUROPRISE SCIENCE UPDATE 10-17
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20400209
-----------------------------------------------------HIV/Virology
[The Results of a Study of HIV-1 Resistance in the Area of Yamal
and the Comparison of the Frequency of Mutations With Different
Score Values]
Klin.Lab Diagn. (2), 43-46 ,2010
rus
The amino acid sequence of the known strain HXB-2 belonging to subtype B is used as a
reference strain matrix to determine HIV genotypic resistance by the sequencing technique.
However, numerous studies have ascertained that HIV non-B subtypes have been widely
accepted in Russia. The authors' data show that the significance of low score mutations in the
Russian populations of HIV-1 is yet to be explained, unquestionably, arouses great scientific
interest, and calls for further study
Link
:
http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=Citation&li
st_uids=20397579
------------------------------------------------------
Selected from Recent Conferences (Source: MIS)
Microbicides
Development and In Vitro Evaluation of Gel-Formulated Saquinavir As Vaginal
Microbicide: Anti-HIV-1 Activity and Phar-Maceutical Availability in Biorelevant
Media
VERMEIRE K., Brouwers, J., Augustijns, P., and Schols, D.
,San Francisco, CA; USA, 106 ,2010
1) Rega Institute for Medical Research, Katholieke Universiteit Leuven, Leuven, Belgium; 2)
Laboratory for Pharmacotechnology and Biopharmacy, Katholieke Universiteit Leuven,
Leuven,
Belgium
------------------------------------------------------
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81 / 152
EUROPRISE SCIENCE UPDATE 10-17
Diagnosis
The Roche CAP/CTM V2.0 and the Abbott ReaITime HIV-1 Assays Perform
Equally for Quantification of Viral Load in HIV-1 B and Non-B Subtypes
DEVAUX C., Karasi, J., Dziezuk, F., Quennety, L., Thamke, D., Münch-Garthoff, S., Kirpach,
P., Hemmer, R., Stockinget, H., and Schmit, J.
,Sorrento; Italy, 40 ,2010
1) CRP-Santé, Retrovirology Laboratory, Luxembourg, Luxembourg; 2) Centre Hospitalier
de Luxembourg, Microbiology Laboratory, Luxembourg, Luxembourg; 3) Roche Diagnostics
Ltd, Roche Molecular Diagnostics Development, Rotkreuz, Switzerland; 4) Roche
Diagnostics
Ltd,
Marketing,
Mannheim,
Germany
------------------------------------------------------
Epidemiology
Trends in HIV-1 Epidemic Among MSM in Israel
GROSSMAN Z., Riesenberg, K., Chowers, M., Pollack, S., Kra-Oz, Z., Maayan, S., Mor, Z.,
Elbirt, D., Sthoeger, Z., Ram, D., Rudich, H., Leshem, E., and Levy, I.
,Sorrento; Italy, 75 ,2010
1) Sheba Medical Center and Tel Aviv University, National HIV Reference Lab Central
Virology PHL and School of public Health, Tel Aviv, Israel; 2) Soroka Medical Center,
Infectious Diseases, Beer-Sheva, Israel; 3) Meir Medical Center, Infectious Diseases, KfarSaba, Israel; 4) Rambam Medical Center, Immunology, Haifa, Israel; 5) Rambam Medical
Center, Virology, Haifa, Israel; 6) Hadassah Medical Center, Infectious Diseases, Jerusalem,
Israel; 7) Ministry of Health, Tuberculosis and AIDS, Jerusalem, Israel; 8) Kaplan Medical
Center, Neve-Or, Rehovot, Israel; 9) Sheba Medical Center, National HIV Reference Lab PHL
MOH, Ramat Gan, Israel; 10) Sheba Medical Center, Infectious Diseases, Ramat Gan, Israel
-----------------------------------------------------HIV/Epidemiology
Mother to Child Transmission of Hiv Infected Pregnant Women From 2000 to
2007 in Catalonia (Spain): the Nenexp Project
FRICK A., Carnicer-Pont, D., Noguera, A., Murtra-Garrell, N., Masip, J., and Nenexp Study
Group
,Nice; France ,2010
1)
Barcelona;
2)
Badalona;
3)
Esplugues
de
Llobregat,
Spain
------------------------------------------------------
Health economics
Raltegravir - Could a Lower Dose Improve Access for People With HIV in
Developing Countries?
HILL A. and Calmy, A.
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EUROPRISE SCIENCE UPDATE 10-17
,Sorrento; Italy, 54 ,2010
1) University of Liverpool, Pharmacology Research Laboratories, Liverpool, United
Kingdom; 2) Medecins Sans Frontieres, Treatment Access Campaign, Geneva, Switzerland
------------------------------------------------------
Immunology
Discordant Immunodominant Patterns of HIV-Specific CD8 T Cells Defined by
Cytokine Production or Proliferative Capacity in HIV Elite Controllers
NDHLOVU Z., Proudfoot, J., Kaufmann, D., and Walker, B.
,Baltimore, MD; USA, 39.4 ,2010
Infectious diseases, Ragon Institute of MGH, MIT and Harvard, Charlestown, MA, United
States
-----------------------------------------------------HIV/Immunology
Discordant Immunodominant Patterns of HIV-Specific CD8 T Cells Defined by
Cytokine Production or Proliferative Capacity in HIV Elite Controllers
NDHLOVU Z., Proudfoot, J., Kaufmann, D., and Walker, B.
,Banff, AB; Canada, 319 ,2010
Ragon Institute of MGH, MIT and Harvard, Charlestown
------------------------------------------------------
MA
02129,
USA
HIV/Immunology
CTL-Escape Nef Variants Influence CCR5 Down-Regulation and HIV
Superinfection Susceptibility
MWIMANZI P., Takiguchi, M., and Ueno, T.
,Banff, AB; Canada, 316 ,2010
Center
for
AIDS
Research,
Kumamoto
------------------------------------------------------
University,
Kumamoto,
Japan
HIV/Immunology
Genetic Testing for HLA-B*5701 in HIV-Infected Patients: Candidates for
Abacavir Therapy
NARDI G., Massi, L., Onorina, Paci O., Grazioli, M., and Gaspari, P.
,Florence; Italy, P291 ,2010
Ospedale
Mazzoni,
Ascoli
Piceno,
------------------------------------------------------
--------------------------------------------------------------------------------------------------------------
83 / 152
Italy
EUROPRISE SCIENCE UPDATE 10-17
HIV/Immunology
Investigating Pro-and Anti-Inflammatory Cytokine Levels in Patients With
Advanced HIV-1 Infection, Characterised by the Presence of Opportunistic
Infections
OSAKWE C., Bleotu, C., Chifiriuc, M., Otelea, D., Paraschiv, S., Dragiceanou, R., StrainuCercel, A., and Lazar, V.
,Banff, AB; Canada, 368 ,2010
1) University of Bucharest, Faculty of Biology; 2) Institute of Virology, S. Nicolau; 3) National
Institute
of
Infectious
Diseases,
Prof.
Matei
Bals
-----------------------------------------------------HIV/Immunology
Susceptibility of Cells From the Female Upper Reproductive Tract to Infection
by Transmitted/Founder HIV-1
OCHSENBAUER C., Gosh, M., Fahey, J., Zheng, Shen, Patel, M., Ochiel, D., Haitao, Ding,
Spurgin, J., Smith, K., Kappes, J., and Wira, C.
,Banff, AB; Canada, 323 ,2010
1) University of Alabama at Birmingham, Birmingham, AL, USA; 2) Dartmouth Medical
School,
Lebanon,
NH,
USA
-----------------------------------------------------HIV/Immunology
Secretion of MHC Class I Chain-Related Protein A in Chronic HIV-1 Infection
Leads to Impaired Control of HIV-1 Replication
NOLTING A., Luteijn, R., Dugast, A., Carrington, M., Rihn, S., Kane, K., Jost, S., Toth, I.,
Faetkenheuer, G., Hartmann, P., Altfeld, M., and Alter, G.
,Banff, AB; Canada, 321 ,2010
1) Ragon Institute of MGH, MIT, and Harvard (formerly Partners AIDS Research Center)
and Infectious Disease Unit, Massachusetts General Hospital and Division of AIDS, Harvard
Medical School, Boston, MA; 2) Infectious Diseases Department of the University Hospital of
Cologne,
Germany
-----------------------------------------------------HIV/Immunology
How Does Neutralization Breadth Develop in HIV Infection?
MORRIS L., Gray, E., Moore, P., Madiga, M., Mlisana, K., and Salim, Abdool Karim
,Banff, AB; Canada, 013 ,2010
National Institute for Communicable Diseases, Sandringham, Johannesburg, South Africa;
CAPRISA,
University
of
KwaZulu
Natal,
Durban,
South
Africa
------------------------------------------------------
--------------------------------------------------------------------------------------------------------------
84 / 152
EUROPRISE SCIENCE UPDATE 10-17
HIV/Immunology
Regulatory T Cells Control HIV Replication in Activated T Cells Through
Contact-Dependent and Independent Pathways
MORENO-FERNANDEZ M., Rueda, C., and Chougnet, C.
,Banff, AB; Canada, 326 ,2010
1) Cincinnati Children's Hospital, OH, USA; 2) Grupo Inmunovirologia, Universidad de
Antioquia,
Medellin,
Colombia
-----------------------------------------------------HIV/Immunology
A Large-Scale Analysis of Immunoglobulin Sequences Derived From
Plasmablasts/Plasma Cells in Acute HIV-1 Infection Subjects
MUNSHAW S., Liao, H., Dixon, A., Xi, Chen, Derosa, K., Nagel, A., Parks, R., Whitesides, J.,
Marshall, D., Amos, J., Yi, Yang, Feng, Gao, Tomaras, G., Moody, A., Kelsoe, G., Shea, T.,
Margolis, D., Markowitz, M., Goepfert, P., Shaw, G., Haynes, B., and Kepler, T.
,Banff, AB; Canada, 315 ,2010
1) Center for Computational Immunology, Duke University; 2) Duke Human Vaccine
Institute, Duke University Medical Center, Durham; 3) University of North Carolina-Chapel
Hill, Chapel Hill, NC; 4) Aaron Diamond AIDS Research Center, Rockefeller University,
New
York,
NY;
5)
University
of
Alabama,
Birmingham
AL
-----------------------------------------------------HIV/Immunology
Myeloid Dendritic Cells During the Chronic Stage of HIV Infection Upregulate
LPS-Responsive Genes
MURRAY S., Goulet, J., Filali, A., and Munford, R.
,Banff, AB; Canada, 368 ,2010
Elias
Haddad
Rafick-Pierre
Sekaly
------------------------------------------------------
and
Daniel
Douek
HIV/Immunology
The Cross-Reactive Capacity of HIV-Specific CTLs Towards HIV Variant
Antigens Is Dependent on Their Cognate Peptides
MOTOZONO C., Takiguchi, M., and Ueno, T.
,Banff, AB; Canada, 312 ,2010
Division of Viral Immunology, Center for AIDS Research, Kumamoto University, 2-2-1
Honjo,
Kumamoto,
860-0811,
Japan
-----------------------------------------------------HIV/Immunology
Combined Blockade of the PD-1 and IL-10 Pathways Synergistically Enhance
HIV-Specific CD4 T Cell Functions
PORICHIS F., Kwon, D., Tighe, D., Pavlik, D., Zupkosky, J., McMullen, A., Kavanagh, D.,
Freeman, G., Walker, B., and Kaufmann, D.
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85 / 152
EUROPRISE SCIENCE UPDATE 10-17
,Banff, AB; Canada, 339 ,2010
1) PartnersAIDS Research Center, Massachusetts General, Boston, MA 02114; 2) Dana-Farber
Cancer Institute, Harvard Medical School, Boston, Massachusetts 02115, USA
-----------------------------------------------------HIV/Immunology
IL-16 DCs Loaded With Complement-Opsonised HIV Efficiently Induce
Expansion of Naive CD8+T Cells
POSCH W., Dierich, M., and Wilflingseder, D.
,Banff, AB; Canada, 355 ,2010
Dept.
of
Hygiene,
Innsbruck
Medical
------------------------------------------------------
University,
Innsbruck,
Austria
HIV/Immunology
FCGR Genetics in HIV Disease
POONIA B. and Pauza, D.
,Baltimore, MD; USA, 88.21 ,2010
IHV,
Baltimore,
------------------------------------------------------
MD,
United
States
HIV/Immunology
Changes in Host Microrna Expression in Monocyte-Derived Dendritic Cells
Following HIV-1 Infection
PICHULIK T., Danis, B., Khatamzas, E., Baker, J., Brain, O., McMichael, A., and Simmons, A.
,Banff, AB; Canada, 349 ,2010
Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, University of Oxford,
Headington,
Oxford
OX3
9DS,
UK
-----------------------------------------------------HIV/Immunology
Integrative Genomic Analysis of HIV-Specific CD8+ T Cells Reveal That BATF Is
a Key Regulator of T Cell Exhaustion
QUIGLEY M., Porichis, F., Pereyra, F., Nilsson, B., Eichbaum, Q., Julg, B., Jesneck, J.,
Brosnahan, K., Russell, K., Toth, I., Piechocka-Trocha, A., Shin, H., Kwon, D., Zupkosky, J.,
Freeman, G., Wherry, E., Walker, B., Ebert, B., Kaufmann, D., and Haining, W.
,Banff, AB; Canada, 354 ,2010
1) Department of Pediatric Oncology, Dana-Farber Cancer Institute, Harvard Medical School,
Boston, MA 02115; 2) Ragon Institute of MGH, MIT and Harvard, Charlestown MA 02129,
USA
------------------------------------------------------
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EUROPRISE SCIENCE UPDATE 10-17
HIV/Immunology
HIV-1 Neutralization in Primary Cells Is Less Efficient When Infection Is
Mediated by Cell-Cell Interaction
QING WEI, Edmonds, T., Haitao, Ding, Spurgin, J., Smith, K., Ochsenbauer, C., and Kaippes,
J.
,Banff, AB; Canada, 252 ,2010
University
of
Alabama
at
Birmingham,
Birmingham,
AL,
USA
-----------------------------------------------------HIV/Immunology
Differential NK Cell Subset Involvement in ADCC or Respond to MHC Class 1
Negative Target Cells
QINGQUAN LIU, Yongtao, Sun, Dedong, Huang, Song, Zhai, Yan, Zhuang, Suzannah, Rihn,
Walker, B., Altfeld, M., and Alter, G.
,Banff, AB; Canada, 247 ,2010
1) Department of Infectious Diseases, Tangdu Hospital, The Fourth Military Medical
University, Xi'an, China; 2) Ragon Institute of MGH, MIT and Harvard, Massachusetts
General
Hospital,
Harvard
Medical
School,
Boston,
Massachusetts
-----------------------------------------------------HIV/Immunology
Prevalence of Vaccine-Preventable Infections Among Hiv-Infected Children in
the Uk and Ireland Over 12 Years, 1996-2007
PAYNE H., Doerholt, K., Boyd, K., Judd, A., Sharland, M., Gibb, D., and Heath, P.
,Nice; France, 505 ,2010
1) Paediatric Infectious Disease, St Georges' Hospital; 2) MRC Clinical Trials Unit, London,
UK
-----------------------------------------------------HIV/Immunology
Interleukin (IL)-21, but Not IL-2, Induces Antiviral Activity and Costimulatory
Molecules in CD8 T Cells Without Promoting HIV Replication
PARMIGIANI A., Pallin, M., Lichtenheld, M., and Pahwa, S.
,Baltimore, MD; USA, 42.15 ,2010
University
of
Miami,
Miami,
FL,
------------------------------------------------------
United
States
HIV/Immunology
Maintaining CD28 Expression Prevents Replicative Senescence in Human CD 8
T Cells
PARISH S., Wu, J., and Effros, R.
,Baltimore, MD; USA, 50.23 ,2010
Pathology and Laboratory Medicine,
------------------------------------------------------
UCLA,
Los
Angeles,
CA,
United
--------------------------------------------------------------------------------------------------------------
87 / 152
States
EUROPRISE SCIENCE UPDATE 10-17
HIV/Immunology
Impact of GB Virus C (Hepatitis G Virus) in HIV-1 Pathogenesis
PERKINS M., Himelfarb, D., Edward, H., Brenchley, J., Jaye, A., Cotten, M., Stapleton, J.,
Roederer, M., Rowland-Jones, S., McMichael, A., Xu, X., and Douek, D.
,Banff, AB; Canada, 347 ,2010
1) Vaccine Research Center, NIAID, NIH, Bethesda, MD, USA; 2) MRC Human Immunology
Unit, WIMM, University of Oxford, Oxford, UK; 3) Laboratory of Molecular Microbiology,
NIAID, NIH, Bethesda, MD, USA; 4) MRC Gambia Unit, Fajara, The Gambia; 5) University
of
Iowa,
Iowa
City,
IA,
USA
-----------------------------------------------------HIV/Immunology
Host Determinants of HIV-1 Control in African Americans
PELAK K., Goldstein, D., Walley, N., Fellay, J., Dongliang, Ge, Shianna, K., Gumbs, C.,
Xiaojiang, Gao, Maia, J., Cronin, K., Hussain, S., Carrington, M., Michael, N., Weintrob, A.,
and IDCRP HIV working group
,Banff, AB; Canada, 335 ,2010
1) Center for Human Genome Variation, Duke Institute for Genome Sciences and Policy,
Duke University, Durham, NC 27708, USA; 2) Duke Institute for Genome Sciences and
Policy, Duke University, Durham, NC 27708, USA; 3) Cancer and Inflammation Program,
Laboratory of Experimental Immunology, SAIC-Frederick, Inc., NCI-Frederick, Frederick,
MD 21702, USA; 4) Department of Epidemiology, School of Public Health, University of
California, Los Angeles, CA 90095, USA; 5) Division of Retrovirology, Walter Reed Army
Institute of Research, Rockville, MD 20850, USA; 6) Infectious Disease Clinical Research
Program, Uniformed Services University of the Health Sciences, Bethesda, MD 20307, USA;
7)
NIAID
Center
for
HIV/AIDS
Vaccine
Immunology
(CHAVI)
-----------------------------------------------------HIV/Immunology
APOBEC3G Expression Is Induced in Highly HIV Susceptible CD4+CCR6+T
Cells by CCR6 Ligands
LAFFERTY M., Sun, L., DeMasi, L., Lu, W., and Garzino-Demo, A.
,Banff, AB; Canada, 208 ,2010
Institute of Human Virology, University of Maryland School Of Medicine, Baltimore MD
21201
-----------------------------------------------------HIV/Immunology
A Chinese Rhesus Macaque Model for Testing "Live" Microbicides
LAAENAUR L., Brichacek, B., Lee, P., Sanders-Beer, B., and Hamer, D.
,Banff, AB; Canada, 257 ,2010
1) Osel, Inc., Santa Clara, CA 95054, USA; 2) NCI, NIH, Bethesda, MD 20892, USA; 3)
BIOQUAL,
Inc.,
Rockville,
MD
20850,
USA
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HIV/Immunology
Phenotypical and Functional Studies of CD1d-Restricted NKT Cells and NK
Cells in Patients With Primary HIV-1 Infection Treated With Interleukin-2
KUYLENSTIERNA C., Snyder-Cappione, J., Gonzalez, V., Loo, C., Spotts, G., Hecht, F.,
Michaelsson, J., Moll, M., Nixon, D., and Sandberg, J.
,Banff, AB; Canada, 239 ,2010
Center for Infectious Medicine, Department of Medicine, Karolinska Institutet, Karolinska
University Hospital Huddinge, Stockholm, Sweden; Department of Medicine, San Francisco
General Hospital, University of California San Francisco, San Francisco, USA
-----------------------------------------------------HIV/Immunology
Low Levels of Varicella-Specific Antibodies in Treated Hiv-Infected Children
Results From Failure to Reactivate Anti-Vzv Memory Responses, Rather Than
Lower Initial Responses Or Accelerated Antibody Loss
L'HUILLIER A., Siegrist, C., Courvoisier, D., Ferry, T., Aebi, C., Cheseaux, J., Kind, C.,
Rudin, C., Nadal, D., Hirschel, B., Wyler, C., Posfay-Barbe, K., and Swiss Mother & Child
HIV Cohort Study (MoCHIV) Group
,Nice; France, 624 ,2010
1) Department of Pediatrics, Geneva Medical School and University Hospitals of Geneva; 2)
Department of Pathology and Immunology, University of Geneva; 3) Division of Clinical
Epidemiology, Geneva; 4) Department of Internal Medicine, Division of Infectious Diseases,
Geneva Medical School and University Hospitals of Geneva, Geneva; 5) Department of
Pediatrics and Institute for Infectious Diseases, University of Bern, Bern; 6) Department of
Pediatrics, University Hospital CHUV, Lausanne; 7) Ostschweizer Kinderspital, St. Gallen; 8)
University Children's Hospital, Basel; 9) Division of Infectious Diseases and Hospital
Epidemiology, University Children's Hospital of Zurich, Zurich, Switzerland
-----------------------------------------------------HIV/Immunology
Human NK Inhibitory Receptor KIR3DL1 Recognition of Conserved Regions of
HLA-B
LI FU and Burshtvn, D.
,Banff, AB; Canada, 205 ,2010
Department of Microbiology and Immunology, University of Alberta, Edmonton, AB, T6G
2S2,
Canada
-----------------------------------------------------HIV/Immunology
Innate Sensing of HIV-Infected Cells
LEPELLEY A., Louis, S., Sourisseau, M., Schilte, C., Mammano, F., Albert, M., and Schwartz,
O.
,Banff, AB; Canada, 304 ,2010
Virus
&
Immunity
Unit,
Institut
Pasteur,
Paris
75015,
France
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HIV/Immunology
Mathematical Models of Persistent Infections
KOCH?N BFAU - KOCH?N B. 1, Johnson, P., Blattman, J., Regoes, R., and Antia, R.
,Banff, AB; Canada, 237 ,2010
1)
Emory
U,
Atlanta;
2)
FHCRC,
Seattle;
3)
?TH,
------------------------------------------------------
Zurich
HIV/Immunology
Differences in the Frameshift-Regulating P1-Site in Treatment-Naive and
PIresistant HIV Isolates
KNOPS E., Théberge-Julien, G., Kaiser, R., Hoffman, D., Brakier-Gingras, L., and Verheyen, J.
,Sorrento; Italy, 6 ,2010
1) University of Cologne, Institute of Virology, Cologne, Germany; 2) University of Montreal,
Department of Biochemistry, Montreal, Canada; 3) University of Duisburg-Essen, Centre for
Medical
Biotechnology,
Essen,
Germany
-----------------------------------------------------HIV/Immunology
The Role of Adapter Protein-1 in MHC-I Trafficking in Antigen Presenting Cells
KULPA D., Del, Cid N., Raghavan, M., and Collins, K.
,Banff, AB; Canada, 256 ,2010
1) Department of Internal Medicine, Ann Arbor, Michigan, 48109, USA; 2) Department of
Microbiology and Immunology, University of Michigan, Ann Arbor, Michigan, 48109, USA
-----------------------------------------------------HIV/Immunology
Multiparametric Flow Analysis of HIV-Specific CD8 T-Cell Mediated Virus
Inhibition
KOPYCINSKI J., Cheeseman, H., Ashraf, A., Spentzou, A., Clark, L., Bergin, P., Gill, D.,
Gilmour, J., Cox, J., and Haves, P.
,Banff, AB; Canada, 235 ,2010
IAVI Human Immunology Laboratory, Imperial College London, Chelsea and Westminster
Hospital,
369
Fulham
Road,
London
SW10
9NH,
UK
-----------------------------------------------------HIV/Immunology
MHC Haplotype M3 Is Associated With Early Control of SHIVsbg Infection in
Mauritian Cynomolgus Macaques
MEE E., Berry, N., Ham, C., Aubertin, A., Hall, J., Stebbings, R., Page, M., Almond, N., and
Rose, N.
,Florence; Italy, P371 ,2010
1) National Institute for Biological Standards and Control, Health Protection Agency, South
Mimms,
UK;
2)
University
Louis
Pasteur,
Strasbourg,
France
-------------------------------------------------------------------------------------------------------------------------------------------------------------------
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HIV/Immunology
Characterization of A4ß7 Integrin Expression on Cervical T Lymphocytes
MCKINNON L., Izulla, P., Kimani, J., Nyanga, B., Cicala, C., Omu, Anzala A., Arthos, J., and
Kaul, R.
,Banff, AB; Canada, 304 ,2010
University of Toronto, University of Nairobi, National Institute of Health
-----------------------------------------------------HIV/Immunology
SIVmac251infection of Rhesus Macaques Destroys Secondary Lymphoid Tissue
Architecture and Depletes Naïve T Cell Populations
MING ZENG, Wietgrefe, S., Southern, P., Schacker, T., Reily, C., Silvestri, G., Lifson, J., and
Haase, A.
,Banff, AB; Canada, 449 ,2010
1) Department of Microbiology, Minneapolis, MN 55455, USA; 2) Department of Medicine,
Minneapolis, MN 55455, USA; 3) Department of Biostatistics, University of Minnesota,
Minneapolis, MN 55455, USA; 4) Department of Pathology, University of Pennsylvania
School of Medicine, Philadelphia, PA, 19104; 5) AIDS Vaccine Program, Science Applications
International Corporation-Frederick, Inc., National Cancer Institute, Frederick, MD 21702
-----------------------------------------------------HIV/Immunology
Early Selection for Escape Mutation in an SIV Nef Epitope Following Adoptive
Transfer of Virus-Specific CD8+ Tcell Clones During Acute Infection
MINANA J., Trivett, M., Bolton, D., Trubey, C., Estes, J., Yuan, Li, Smedley, J., Pung, R.,
Rosati, M., Jalah, R., Pavlakis, G., Felber, B., Piatak, M., Roederer, M., Lifson, J., Ott, D., and
Ohlen, C.
,Banff, AB; Canada, 367 ,2010
1) AIDS and Cancer Virus Program, Frederick, Maryland 21702, USA; 2) Laboratory Animal
Science Program, SAIC-Frederick Inc., Frederick, Maryland 21702, USA; 3) Human
Retrovirus Section, Frederick, Maryland 21702, USA; 4) Human Retrovirus Pathogenesis
Section, NCI-Frederick, Frederick, Maryland 21702, USA; 5) mmunoTechno!ogy Section,
Vaccine
Research
Center,
NIAID,
NIH,
Bethesda,
MD
20892
-----------------------------------------------------HIV/Immunology
Protective Effects of Monomeric and Dimeric Forms of the 2G12 Neutralizing
Antibody Against HIV-1 Infection in a Modified Humanized Mouse Model
LUO X., Lei, M., Feidi, R., West, A., Balazs, A., Yang, L., and Baltimore, D.
,Baltimore, MD; USA, 45.28 ,2010
Caltech,
Pasadena,
CA,
United
------------------------------------------------------
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States
EUROPRISE SCIENCE UPDATE 10-17
HIV/Immunology
Setting Up Multiple Barricades Along the HIV Infection Pathway-Learning From
Genetic Pathway Profile of HIV Resistant Sexworkers
MA LUO, Songok, M., Sainsbury, J., Kimani, J., Wachihi, C., Liang, B., Van, Domselaar G.,
Bielawny, T., Fowke, K., Ball, T., and Plummer, F.
,Banff, AB; Canada, 251 ,2010
1) Medical Microbiology, University of Manitoba, Canada; 2) National Microbiology
Laboratory, Winnipeg, Manitoba, Canada; 3) Medical Microbiology, University of Nairobi,
Nairobi,
Kenya
-----------------------------------------------------HIV/Immunology
Evaluation of Solid Matrix Transport Device (SampleTanker®) for Transport of
Plasma Between Clinical Sites for HIV-1 Resistance and Antibody Testing
LOVEDAY C., Lloyd, R., Macrae, E., Holodniy, M., Mathis, R., Burns, D., Cooper, J., and
Loveday, C.
,Sorrento; Italy, 55 ,2010
1) ICVC Charitable Trust, Clinical Virology, Buckinghamshire, United Kingdom; 2)
Technology Think Tank, LLC, Buford, USA; 3) Veterans Affairs Medical Centre, HIV/AIDS,
Palo
Alto,
USA
-----------------------------------------------------HIV/Immunology
HLA-B35-Cw4 Increases Both Vertical HIV Transmission and Progression
MARTINEZ-QUILES N., Martinez-Laso, J., Martin-Villa, J., Rey, D., Gomez-Prieto, P., PargaLozano, C., and rnaiz-Villena, A.
,Florence; Italy, P330 ,2010
1) University Complutense, Madrid, Spain; 2) Instituto de Salud Carlos III, Madrid, Spain; 3)
University Complutense, The Madrid Regional Blood Center, Madrid, Spain
-----------------------------------------------------HIV/Immunology
Recognition of Cryptic Epitopes Is a Ubiquitous Feature of AIDS Virus Infection
MANESS N., Walsh, A., Piaskowski, S., Wallace, L., Wilson, N., and Watkins, D.
,Banff, AB; Canada, 316 ,2010
Department of Pathology and Laboratory Medicine, University of Wisconsin-Madison
-----------------------------------------------------HIV/Immunology
Differences in HIV Entry and Trafficking in Primary Lymphocytes Versus
Epithelial Cell Line Models: Implications for the Assessment of HIV-1
Neutralizing Antibodies
MACEDO C., Brown, B., Wieczorek, L., Michae, N., and Polanis, V.
,Banff, AB; Canada, 301 ,2010
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EUROPRISE SCIENCE UPDATE 10-17
1) The US Military HIV Research Program, (MHRP); 2) Henry M. Jackson Foundation; 3)
Walter Reed Army Institute of Research, Rockville, MD, 20852, USA
-----------------------------------------------------HIV/Immunology
Estimating HIV Stoichiometries
MAGNUS C. and Regoes, R.
,Banff, AB; Canada, 302 ,2010
Institute
of
Integrative
Biology,
------------------------------------------------------
ETH
Zurich,
8092
Zurich,
Switzerland
HIV/Immunology
Cd8 T Cell Responses to a Novel, Highly Conserved HLA-A*0201(A2) Epitope in
HIV Gag
VALDES L., Costanzo, M., Ladell, K., Salkowitz, J., Yang, O., Price, D., and Kan-Mitchell, J.
,Banff, AB; Canada, 432 ,2010
1) University of Texas at EI Paso, EI Paso, TX 79968, USA; 2) Department of Medical
Biochemistry and Immunology, Cardiff University School of Medicine, Cardiff, Wales, UK;
3)
University
of
California
Los
Angeles,
Los
Angeles,
CA
-----------------------------------------------------HIV/Immunology
The Role of NK/DC Cross-Talk in HIV Pathogenesis
VALENTIN-TORRES A. and Bernstein, H.
,Baltimore, MD; USA, 94.5 ,2010
Case
Western
Reserve
University,
------------------------------------------------------
Cleveland,
OH,
United
States
HIV/Immunology
An Investigation into the Role of a CD4 Polymorphism in Susceptibility to HIV-1
Infection in an African Female Sex Worker Cohort
TUFF J., Ma, Luo, Kimani, J., Wachihi, C., Plummer, F., and Fowke, K.
,Banff, AB; Canada, 430 ,2010
National
Microbiology
Laboratory,
Winnipeg,
MB,
R3E
------------------------------------------------------
3R2,
Canada
HIV/Immunology
Loss of Polyclonal Memory B-Cells During Chronic HIV Infection Is Driven by
FOX03a-and TRAIL-Mediated Apoptosis and Is Rescued by IL-2
VAN GREVENYNGHE J., Noto, A., Da, Fonseca S., Peretz, Y., Dupuy, F., Procopio, F.,
Chomont, N., Saidl, E., Tremblay, C., Routy, J., Boulassel, M., Sekaly, R., and Haddad, E.
,Banff, AB; Canada, 463 ,2010
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EUROPRISE SCIENCE UPDATE 10-17
HIV/Immunology
Role of IL-7 and Type I IFN in Immune Activation of T Cells in HIV Infection
TCHEUNG L., Hurley, A., Wilhelm, C., Friesen, T., Roby, G., Rehm, C., Lane, C., and
Catalfamo, M.
,Banff, AB; Canada, 232 ,2010
CMRS/Laboratory of Immunoregulation, NIAID, NIH, Bethesda, MD, USA
-----------------------------------------------------HIV/Immunology
Antigen Processing Influences HIV-Specific Cytotoxic T Lymphocyte
Immunodominance
TENZER S., Wee, E., Burgevin, A., Stewart-Jones, G., Friis, L., Lamberth, K., Chang, C.,
Harndahl, M., Weimershaus, M., Gerstoft, J., Akkad, N., Fugger, L., Klenerman, P., Jones, E.,
McMichael, A., Buus, S., Schild, H., van, Endert P., and Iversen, A.
,Banff, AB; Canada, 219 ,2010
1) Inst. of Immunology, Univ. of Mainz, Mainz, Germany; 2) Weatherall Inst. of Molecular
Medicine, John Radcliffe Hospital, Oxford, UK; 3) Institut National de la Santé et de la
Recherche Médicale Unité 580, Univ. René Descartes, Paris, France; 4) Dept. Of Microbiology
and Immunology, Univ. of Copenhagen, Denmark; 5) Dept. of Infectious Diseases,
Rigshospitalet, The National Univ. Hospital, Copenhagen, Denmark; 6) Peter Medawar
Building for Pathogen Research, Nuffield Department of Clinical Medicine, Oxford
University, Oxford, UK; 7) Structural Biology Group, Wellcome Trust Centre for Human
Genetics,
Oxford,
UK
-----------------------------------------------------HIV/Immunology
Molecular Architecture of Trimeric SIV and HIV-1 Envelope Glycoproteins
SUBRAMANIAM S.
,Banff, AB; Canada, 031 ,2010
Center
for
Cancer
Research,
------------------------------------------------------
NCI,
NIH,
Bethesda,
MD
20892
HIV/Immunology
Extensive HLA-Driven Viral Diversity Following a Narrow-Source HIV-1
Outbreak in Rural China
TAO DONG, Yonghong, Zhang, Ke, Yi, X, Huiping, Yan, James, I., Yanchun, Peng, Blais, M.,
Gaudieri, S., Xinyue, Chen, Wenhui, Lun, Hao, Wu, Chun, Hui Zhao, Chang, C., Wen, Yan
Qu, Rostron, T., Ning, Li, Yu, Mao, Malla, S., Xiaoning, Xu, McMichael, A., John, M., and
Rowland-Jones, S.
,Banff, AB; Canada, 351 ,2010
1) MRC Human Immunology Unit, Weatherall Institute of Molecular Medicine, John
Radcliffe Hospital, Oxford, OX3 9DS, UK; 2) Beijing You An Hospital, Capital Medical
University, Beijing, PRC; 3) Ditan Infectious Diseases Hospital, Beijing, PRC; 4) Centre for
Clinical Immunology and Biomedical Statistics, Immunology & Infectious Diseases,
Murdoch University, WA, 6155, Australia; 5) School of Anatomy and Human Biology and
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EUROPRISE SCIENCE UPDATE 10-17
Centre for Forensic Science, University of Western Australia, Perth, 6009, Australia
-----------------------------------------------------HIV/Immunology
Receptors and Pathways Utilized by Dendritic Cells for Antigen Presentation of
Free and Complement Opsonized HIV
TJOMSLAND V., Che, K., Hinkula, J., Lifson, D., and Larsson, M.
,Banff, AB; Canada, 428 ,2010
1) Molecular Virology, Department of Molecular and Clinical Medicine, Linköping
University, 581 85 Linköping, Sweden; 2) SAIC/Fredrick, National Cancer Institute at
Fredrick,
Fredrick,
Maryland,
USA
-----------------------------------------------------HIV/Immunology
Antibody VRC01: To Be or Not To Be Like CD4
TONGQING ZHOU, Xueling, Wu, Young, Do Kwon, Ling, Xu, Yongping, Yang, Yang, Z.,
Nabel, G., Mascola, J., and Kwong, P.
,Banff, AB; Canada, 011 ,2010
Vaccine
Research
Center,
NIAID/NIH,
Bethesda,
MD,
USA
-----------------------------------------------------HIV/Immunology
A Multiparametric FACS Assay to Assess HIV-1 Tropism on T Cell Subsets
TILTON J., Harrison, J., Wilen, C., and Doms, R.
,Banff, AB; Canada, 426 ,2010
Department of Microbiology, University of Pennsylvania, Philadelphia, PA, USA
-----------------------------------------------------HIV/Immunology
Vaccinating Hiv-Positive Children in the West Midlands
TEOH L.
,Nice; France ,2010
Birmingham,
------------------------------------------------------
UK
HIV/Immunology
Diversity of the CD8+T Cell Repertoire Responding to an Immunodominant
Epitope Does Not Depend on the Context of Infection
VENTURI V., Rudd, B., Smithey, M., Sing, Sing Way, Davenport, M., and Nikolich-Zugich, J.
,Banff, AB; Canada, 439 ,2010
1) Computational Biology Unit, NSW, Australia; 2) Complex Systems in Biology Group,
Centre for Vascular Research, University of New South Wales, NSW, Australia; 3)
Department of Immunobiology and the Arizona Center on Aging, University of Arizona
College of Medicine, AZ, USA; 4) Department of Pediatrics, Center for Infectious Disease and
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EUROPRISE SCIENCE UPDATE 10-17
Microbiology Translational Research, University of Minnesota School of Medicine, MN, USA
-----------------------------------------------------HIV/Immunology
Co-Localization of Antigen Processing and Receptor Binding Sites in HIV
Gp120: A Mechanism to Explain the Difficulty in Eliciting Broadly Neutralizing
Antibodies
YU B., da, Fonseca D., O'Rourke, S., and Berman, P.
,Banff, AB; Canada, 164 ,2010
Department of Biomolecular Engineering, University of California Santa Cruz, Santa Cruz,
CA,
95064,
USA
-----------------------------------------------------HIV/Immunology
Cytotoxic T Lymphocytes, Virus Strategies and Sterilising Immunity
YATES A., van, Baalen M., and Antia, R.
,Banff, AB; Canada, 453 ,2010
1) Dept of Systems and Computational Biology, Albert Einstein College of Medicine, 1300
Morris ParkAvenue Bronx, NY 10461, USA; 2) Dept of Microbiology and Immunology,
Albert Einstein College of Medicine, 1300 Morris ParkAvenue Bronx, NY 10461, USA; 3)
Université Pierre et Marie Curie, Bât. A, 7ème Etage, Case 237, 7 Quai St.-Bernard, 75252
Paris, France; 4) Dept of Biology, Emory University, 1510 Clifton Road, Atlanta, GA 30322,
USA
-----------------------------------------------------HIV/Immunology
CD4+ T Cell Mediated B Cell Activation in Response to Inactivated HIV-1 Is
Highly Correlated With the Level of HIV-1 Viremia
ZERN E., Barnett, L., Sadagopal, L., and Kalams, S.
,Banff, AB; Canada, 450 ,2010
Vanderbilt
University
Medical
Center,
------------------------------------------------------
Nashville,
TN,
USA
HIV/Immunology
T Regulatory Cells in HIV-2 Infections Are Significantly Lower Than HIV-1 and
Positively Correlate With Immune Activation and Viral Loads
ZAIDI I., Jeffries, D., Rowland-Jones, S., Whittle, H., and Jaye, A.
,Banff, AB; Canada, 454 ,2010
1) Viral Diseases Program, MRC (UK) Laboratories, The Gambia; 2) Weatherall Institute of
Molecular Medicine, Medical Research Council Human Immunology Unit, John Radcliffe
Hospital,
Oxford,
United
Kingdom
------------------------------------------------------
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EUROPRISE SCIENCE UPDATE 10-17
HIV/Immunology
Gut-Homing Potential of and Th17 Profiles of HIV-Specific CD4+ and CD8+ TCells in HIV-Infected Subjects With Slow Disease Progression
WACLECHE V., Gosselin, A., Monteiro, P., Kared, H., Boulassel, M., Routy, J., and Ancuta,
P.
,Banff, AB; Canada, 102 ,2010
1) CHUM-Research Center, Saint Luc Hospital, Université de Montréal; 2) INSERM Unit 743,
Montréal, Quebec, Canada; 3) Montréal Chest Institute of the Royal Victoria Hospital, McGill
University,
Montreal,
Quebec,
Canada
-----------------------------------------------------HIV/Immunology
HIV Controller CD4+ T Cells Respond to Minimal Amounts of Gag Antigen Due
to High TCR Avidity
VINGERT B., Perez-Patrigeon, S., Jeannin, P., Lambotte, O., Boufassa, F., Kwok, W.,
Theodorou, I., Delfraissy, J., Thèze, J., and Chakrabarti, L.
,Banff, AB; Canada, 435 ,2010
1) Unité d'lmmunogénétique Cellulaire, Institut Pasteur, Paris, France; 2) AP-HP,
Department of Internal Medicine and Infectious Diseases, Bicêtre Hospital; 3) INSERM U822,
Bicêtre Hospital, Le Kremlin-Bicêtre, France; 4) Benaroya Research Institute at Virginia
Mason, Seattle, WA, USA; 5) INSERM U543, Pitié-Salpêtrière Hospital, Paris, France
-----------------------------------------------------HIV/Immunology
Early Genital Tract Compartmentalization During Acute SIV Infection
WHITNEY J., Hraber, P., Luedemann, C., Bhattacharya, T., Rao, S., Mascola, J., Korber, B.,
Nabel, G., and Letvin, N.
,Banff, AB; Canada, 440 ,2010
1) Division of Viral Pathogenesis, Department of Medicine, Beth Israel Deaconess Medical
Center, Harvard Medical School, Boston, Massachusetts, 02115; 2) Los Alamos National
Laboratory, Los Alamos, NM 87545; 3) Vaccine Research Center, National Institutes of
Allergy
and
Infectious
Diseases,
Bethesda,
MD
20892
-----------------------------------------------------HIV/Immunology
Synergistic Effect of Bacterial LPS and HIV Virions on Memory B Cell Death
WEI JIANG, Sieg, S., Hardin, C., and Lederman, M.
,Banff, AB; Canada, 220 ,2010
1) Center For AIDS Research, Department of Medicine, OH 44106; 2) Pathology Case
Western Reserve University and University Hospital of Cleveland, OH 44106
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EUROPRISE SCIENCE UPDATE 10-17
HIV/Immunology
Prevalent HLA Class I Allele Combinations Result in a Lack of HIV-1-Specific
CD8+ T Cell Responses and Higher Viral Set Point
STREECK H., Brumme, Z., Xiaojiang, Gao, Kwon, D., Addo, M., Rychert, J., Axten, K.,
Brumme, C., Pyo, A., Flanders, M., Boutwell, C., Allen, T., Yassine-Diab, B., Routy, J., Little,
S., Jessen, H., Kelleher, A., Hecht, F., Sekaly, R., Rosenberg, E., Harrigan, R., Bosch, R.,
Walker, B., Carrington, M., and Altfeld, M.
,Banff, AB; Canada, 420 ,2010
Ragon
Institute
of
MGH,
MIT
and
Harvard
-----------------------------------------------------HIV/Immunology
HIV-1 Control After Treatment Interruption Is Associated to Low Levels of HIV-1
DNA
SAEZ-CIRION A., vettand-Fenoe, V., Hocqueloux, L., Prazuck, T., Viard, J., Goujard, C.,
Sinet, M., Venet, A., Pancino, G., Rouzioux, C., and ANRS Visconti Group
,Banff, AB; Canada, 330 ,2010
1) Institut Pasteur, Unité de Régulation des Infections Rétrovirales, Paris, France; 2) AP-HP
Hôpital Necker and University Paris Descartes Paris, France; 3) CHR d'Orléans, Orléans,
France; 4) Hôpital Necker, Paris, France; 5) AP-HP Hôpital Bicêtre; 6) Inserm U802, Le
Kremlin-Bicêtre,
France
-----------------------------------------------------HIV/Immunology
Elite Controllers Recognize A Novel Subdominant Epitope in HIV Gag P24
SALKOWITZ J., Bansal, A., Li, J., Costanzo, M., Sidney, J., Sette, A., Yang, O., Goepfert, P.,
and Kan-Mitchell, J.
,Banff, AB; Canada, 353 ,2010
1) Dept. Biol Sci., Univ.Texas El Paso, El Paso, TX, 79968; 2) Dept Med., Univ Alabama
Birmingham, Birmingham, AL, 35294; 3) La Jolla Inst. Allergy Immunol., La Jolla, CA, 92037;
4) David Geffen School Med., Dept. Infect. Dis., UCLA, LosAngeles, CA, 90095
-----------------------------------------------------HIV/Immunology
Regulation of IRF-1 Expression and Responsiveness to IFN-Gamma in Kenyan
Women Resistant to HIV-1 Infection Involves NF-KappaB Binding and
Epigenetic Controls Via HDAC2 Recruitment
RUEY-CHYI S., Sivro, A., Kimani, J., Jaoko, W., Plummer, F., and Blake, Ball T.
,Banff, AB; Canada, 421 ,2010
1) Department of Medical Microbiology and Infectious Diseases; 2) Immunology, University
of Manitoba; 3) National Microbiology Laboratories, Winnipeg, Manitoba, R3E 0W3, Canada;
4) National HIV & Retrovirology Laboratories, Public Health Agency of Canada, Winnipeg,
Manitoba, R3E 0W3, Canada; 5) Department of Medical Microbiology University of Nairobi,
Nairobi,
Kenya
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EUROPRISE SCIENCE UPDATE 10-17
HIV/Immunology
Comprehensive Analysis of Frequency and Phenotvpe of T Regulatory Cells in
HIV Infection: CD39 Expression on FoxP3+T Regulatory Cells in HIV Infection
Correlates With Disease Progression
SCHULZE ZUR WIESCH J., Thomssen, A., Hartjen, P., Lehmann, C., Meyer-Olson, D.,
Colberg, K., Lohse, A., Rockstroh, J., Fätkenheuer, G., Hauber, J., and van, Lunzen J.
,Banff, AB; Canada, 404 ,2010
Medizinsche Klinik, Universitätsklinikum Hamburg Eppendorf, Germany, Martinistr. 52,
20246
Hamburg
-----------------------------------------------------HIV/Immunology
Dynamics of CTL Epitope Escape and Reversion in an African Subtype C
Cohort
SCHAEFER M., Claiborne, D., Prince, J., Mulenga, J., Jianming, Tang, Goepfert, P., Farmer,
P., Kaslow, R., Allen, S., and Hunter, E.
,Banff, AB; Canada, 401 ,2010
1) Emory University, Atlanta, GA, USA; 2) Zambia Blood Transfusion Service and ZEHRP,
Lusaka, Zambia; 3) University of Alabama at Birmingham, Birmingham, AL, USA
-----------------------------------------------------HIV/Immunology
Synthesis of Novel CADA Analog Prodrugs Designed As Down- Modulators of
the CD4 Receptor
SCARBROUGH E., Vermeire, K., Schols, D., and Bell, T.
,San Francisco, CA; USA, 158 ,2010
1) Department of Chemistry, University of Nevada, Reno, USA; 2) Rega Institute for Medical
Research, Department of Microbiology and Immunology, Katholieke Universiteit Leuven,
Leuven,
Belgium
-----------------------------------------------------HIV/Immunology
Memory Phenotypes of Polyfunctional HIV-Specific CD8+ T Cell Responses
RICHMOND M., McKinnon, L., Koesters, Kiazyk S., Wachihi, C., Kimani, M., Kimani, J.,
Plummer, F., and Ball, T.
,Banff, AB; Canada, 347 ,2010
1) Department of Medical Microbiology, University of Manitoba, Winnipeg, Canada; 2)
Department of Medical Microbiology, University of Nairobi, Nairobi, Kenya; 3) Department
of Medicine, University of Toronto, Toronto, Canada; 4) National Microbiology Laboratory,
Public Heath Agency of Canada, Winnipeg, Canada; 5) Department of Immunology,
University of Manitoba, Winnipeg, Canada; 6) National HIV & Retrovirology Laboratories,
Public
Health
Agency
of
Canada,
Winnipeg,
Canada
------------------------------------------------------
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EUROPRISE SCIENCE UPDATE 10-17
HIV/Immunology
Vaginal Langerhans Cells Resist Genomic Integration of HIV-1 but Transmit
Endocytosed Virions to Susceptible Target Cells
ROBINSON B., Ballweber, L., Kreger, A., Lentz, G., Fialkow, M., McElrath, M., and Hladik,
F.
,Banff, AB; Canada, 225 ,2010
University of Washington and Fred Hutchinson Cancer Research Center, Seattle, WA, USA
-----------------------------------------------------HIV/Immunology
Exploring HIV-1 Envelope Glycoprotein Trimer Stability
ROWCLIFFE E., Leaman, D., Agrawal, N., Kinkead, H., Du, S., Whalen, R., Burton, D., and
Zwick, M.
,Banff, AB; Canada, 453 ,2010
1) Dartment of Immunology and Microbial Science, La Jolla, CA 92037; 2) IAVI Neutralizing
Antibody Center, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla,
CA 92037; 3) Maxygen, 301 Galveston Drive, Redwood City, CA 94063; 4) Ragon Institute of
Massachusetts General Hospital, 149 13th street, Charlestown, MA 02129; 5) Massachusetts
Institute of Technology, 770 Massachusetts Avenue, Cambridge, MA 02138; 6) Harvard
University,
Massachusetts
Hall,
Cambridge,
MA
02139
-----------------------------------------------------HIV/Immunology
Induction of PD-1 Ligands on Primary Human Macrophages by HIV-1 Virions
RODRIGUEZ-GARCIA M., Porichis, F., de, Jong O., Levi, K., Diefenbach, T., Lifson, J.,
Kaufmann, D., and Kavanagh, D.
,Banff, AB; Canada, 348 ,2010
Ragon
Institute
of
MGH,
MIT
and
Harvard
-----------------------------------------------------HIV/Immunology
Patient Specific Transcriptional Profiling of Early Acute HIV-1 Infection
SKINNER J., Sharma, M., Baldwin, N., Lemoine, B., Blankenship, D., De, Vol E., Cohen, M.,
Soderberg, K., Denny, T., McMichael, A., Haynes, B., Banchereau, J., Chaussabel, D., and
CHAVI Clinical Site Team
,Banff, AB; Canada, 411 ,2010
1) Baylor Institute for Immunology Research-ANRS Center for Human Vaccines, INSERM
U899, 3434 Live Oak St., Dallas, Texas 75204; 2) Institute for Health Care Research and
Improvement, Baylor Health Care System, Dallas, Texas 75204; 3) University of North
Carolina, Chapel Hill, NC 27599; 4) Duke Institute for Genome Sciences and Policy, Duke
University, Durham, NC 27710; 5) Weatherall Institute of Molecular Medicine, John Radcliffe
Hospital, Headington , Oxford, United Kingdom; 6) Duke University School of Medicine,
Durham,
NC
27710
-------------------------------------------------------------------------------------------------------------------------------------------------------------------
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EUROPRISE SCIENCE UPDATE 10-17
HIV/Immunology
Nonpathogenic Natural SIV Infection
SILVESTRI G.
,Banff, AB; Canada, 009 ,2010
University
of
Pennsylvania
------------------------------------------------------
School
of
Medicine
HIV/Immunology
Identification and Characterization of Early Founder Populations in Rhesus
Macaques Vaginally Infected With SIVmac251
STONE M., Keele, B., Ma, Z., Bailes, E., Dutra, J., Hahn, B., Shaw, G., and Miller, C.
,Banff, AB; Canada, 418 ,2010
1) Center for Comparative Medicine; 2) California National Primate Research Center,
University of California, Davis, California 95616, USA; 3) Departments of Medicine,
Birmingham, Alabama 35294; 4) Microbiology, University of Alabama at Birmingham,
Birmingham, Alabama 35294; 5) Institute of Genetics, University of Nottingham, Nottingham
NG7
2UH,
United
Kingdom
-----------------------------------------------------HIV/Immunology
Rapid Degranulation of NK Cells Following Activation by HIV-Specific
Antibodies
STRATOV I., Chung, A., Rollman, E., Center, R., and Kent, S.
,Banff, AB; Canada, 419 ,2010
1) Department of Microbiology and Immunology, University of Melbourne, Melbourne,
Australia; 2) melbourne Sexual Health Centre, Carlton, Australia; 3) Infectious Diseases
Department, Alfred Hospital, Prahran, Australia; 4) Burnet Institute, Prahran, Australia
-----------------------------------------------------HIV/Immunology
Immunological and Viral Evolution on Failing Dual Boosted Protease Inhibitor
Regimen in HIV-1-Infected Salvage Patients
STEPHAN C., Bartha, V., Haberl, A., Bickel, M., Gute, P., Knecht, G., Doerr, H., Staszewski,
S., Brodt, H., and Stürmer, M.
,Sorrento; Italy, 16 ,2010
1) Klinikum der J. W. Goethe Universität Haus 68, Hivcenter, Frankfurt Main, Germany; 2)
Infektiologikum, Friedensstrasse, Frankfurt Main, Germany; 3) Infektiologikum,
Stresemannallee, Frankfurt Main, Germany; 4) Klinikum der J. W. Goethe Universität,
Medical
Virology
Institute,
Frankfurt
Main,
Germany
-----------------------------------------------------HIV/Immunology
Prediction of Neutralization Breadth by a HIV-1 Broadly Neutralizing Antibody
STAWISKI E., Wrin, T., Phung, P., and Haddad, M.
--------------------------------------------------------------------------------------------------------------
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EUROPRISE SCIENCE UPDATE 10-17
,Banff, AB; Canada, 416 ,2010
Chris Petropoulos Monogram Biosciences, South San Francisco, CA, 94080, USA
-----------------------------------------------------HIV/Immunology
A Systems Biology Approach for Immune Monitoring in HIV Resistant Sex
Workers From Nairobi, Kenya
STEIN D., Westmacott, G., Carpenter, M., Cheng, K., Plummer, F., and Blake, Ball T.
,Banff, AB; Canada, 417 ,2010
1) University of Manitoba; 2) Public Health Agency of Canada; 3) National HIV and
Retrovirology
Laboratories
-----------------------------------------------------HIV/Immunology
Mucosal Immune Responses to HIV Infection
SHACKLETT B.
,Banff, AB; Canada, 005 ,2010
Department of Medical Microbiology and Immunology, University of California, Davis, CA,
95616,
USA
-----------------------------------------------------HIV/Immunology
Analysis of HIV-1 Gag Epitopes of Two HLA Class I Alleles Associated With
Different Outcomes of HIV-1 Infection in the Pumwani Sex Worker Cohort
SEMENIUK C., Capina, R., Mendoza, M., Kimani, J., Wachihi, C., Kimani, M., Ball, T., Ma,
Luo, and Plummer, F.
,Banff, AB; Canada, 405 ,2010
1) National Microbiology Laboratory, Winnipeg, Manitoba, Canada; 2) Medical
Microbiology, University of Manitoba, Canada; 3) Medical Microbiology, University of
Nairobi,
Nairobi,
Kenya
-----------------------------------------------------HIV/Immunology
Influence of HLA-G Polymorphisms on Human Immunodeficiency Virus
Infection and Hepatitis C Virus Co-Infection in Brazilian Patients
SILVA G., Vianna, P., Veit, T., Mattevi, V., Lazzaretti, R., Sprinz, E., Kuhmmer, R., and Chies,
J.
,Florence; Italy, P306 ,2010
1) Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil; 2) Universidade Federal
de Ci êencias da Saúde de Porto Alegre, Porto Alegre, Brazil; 3) Hospital de Clínicas de Porto
Alegre,
Porto
Alegre,
Brazil
------------------------------------------------------
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EUROPRISE SCIENCE UPDATE 10-17
HIV/Immunology
The Presence of Neutralizing and Non-Neutralizing Anti-HIV Antibodies Inhibits
the Mobility of the Virus in Cervical Mucus
SHUKAIR S., Cianci, G., Dinh, M., Allen, S., Hammond, C., and Hope, T.
,Banff, AB; Canada, 410 ,2010
Dept. of Cell and Mol Biol, Northwestern University, Chicago, IL, 60611, USA
-----------------------------------------------------HIV/Immunology
Regulatory T Cells and Immune Activation in the Rectal Mucosa of HIV+
Subjects
SHAW J., Critchfield, J., Hunt, P., Youna, D., Garcia, J., Pollard, R., Deeks, S., and Shacklett,
B.
,Banff, AB; Canada, 407 ,2010
1) Department of Medical Microbiology and Immunology, University of California, Davis,
CA, 95616, USA; 2) Department of Medicine, University of California, San Francisco, CA,
94122,
USA
-----------------------------------------------------HIV/Immunology
Rapid Progression of Disease in HIV-2 Related to HLA-B15 Genotype
DE BREE G., Yindom, L., Carrington, M., Walton, R., Whittle, H., van, Tienen C., Vincent, T.,
Jave, A., de, Silva T., Cotton, M., Leligdowicz, A., Tao, Dong, and Rowland-Jones, S.
,Banff, AB; Canada, 138 ,2010
1) Medical Research Council, Human Immunology Unit, Oxford, United Kingdom; 2)
Medical Research Council (UK), The Gambia; 3) Cancer and Inflammation Programme,
Laboratory of Experimental Immunology, Frederick, USA; 4) Ragon Institute of MGH, MIT
and
Harvard,
Charleston,
USA
-----------------------------------------------------HIV/Immunology
Performance Evaluation of Two Multiplex Technologies for the Measurement of
Serum Cytokines in HIV-Infected Individuals
DABITAO D., Margolick, J., and Bream, J.
,Baltimore, MD; USA, 134.17 ,2010
W. Harry Feinstone Department of Molecular Microbiology and Immunology, Johns
Hopkins University, Bloomberg School of Public Health, Baltimore, MD, United States
-----------------------------------------------------HIV/Immunology
Spread of HIV Through T Cell Virological Synapses Enhances Multiplicity of
Infection
DEL PORTILLO A., Tripodi, J., LeBlanc, A., Najfeld, V., Levy, D., and Chen, B.
,Banff, AB; Canada, 128 ,2010
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103 / 152
EUROPRISE SCIENCE UPDATE 10-17
1) Division of Infectious Diseases, Department of Medicine, Mount Sinai School of Medicine,
New York, NY 10029; 2) Tumor Cytogenetics, Mount Sinai School of Medicine, New York,
NY 10029; 3) Basic Science and Craniofacial Biology, New York University College of
Dentistry,
New
York,
NY
10010
-----------------------------------------------------HIV/Immunology
Does Increased Expression of HLA-C Allow Better Control of HIV-1 Viral Load?
CORRAH T., Goonetilleke, N., Rostron, T., Tao, Dong, Deeks, S., Martin, J., McMichael, A.,
and Brackenridge, S.
,Banff, AB; Canada ,2010
1) Weatherall Institute of Molecular Medicine, University of Oxford, UK; 2) University of
California,
San
Francisco,
USA
-----------------------------------------------------HIV/Immunology
Exploring Antibody Recognition of the V3 Region on HIV-1
CLARK B., Auyeung, K., and Pantophlet, R.
,Banff, AB; Canada, 331 ,2010
Faculty of Health Sciences, Simon Fraser University, Burnaby, BC V5A1S6, Canada
-----------------------------------------------------HIV/Immunology
Multiple, Distinct Regulatory T Cell Populations Control Peripheral Blood and
Liver Immunity to Human Hepatitis C Virus Infections
CLAASSEN M., de, Knegt R., Janssen, H., and Boonstra, A.
,Banff, AB; Canada, 133 ,2010
Department of Gastroenterology and Hepatology, Erasmus MC; University Medical Center,
Rotterdam,
3015
CE,
the
Netherlands
-----------------------------------------------------HIV/Immunology
CTL Responses to HIV-1 During Acute and Chronic Infection
CULSHAW A., Mashishi, T., Spina, C., Richman, D., Rowland-Jones, S., and Tao, Dong
,Banff, AB; Canada, 133 ,2010
1) The MRC Human Immunology Unit, Weatherall Institute of Molecular Medicine, The
University of Oxford, The John Radcliffe Hospital, Oxford, OX3 9DS; 2) The University of
California-San Diego, VA San Diego Healthcare System, 3350 La Jolla Village Drive, San
Diego,
CA
92161
------------------------------------------------------
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EUROPRISE SCIENCE UPDATE 10-17
HIV/Immunology
Soluble IL-7Ra (CD127) Decreases IL-7 Activity and Is Increased in HIV
Infection
CRAWLEY A., Faucher, S., and Angel, J.
,Banff, AB; Canada, 139 ,2010
1) Ottawa Hospital Research Institute, Ottawa, Canada; 2) Department of Biochemistry,
Microbiology and Immunology, University of Ottawa, Ottawa, Canada; 3) National HIV
Immunology laboratory, National HIV and Retrovirology Labs, Centre for Infectious Disease
Prevention and Control Health Canada, Ottawa, Canada; 4) Division of Infectious Diseases,
Ottawa
Hospital-General
Campus,
Ottawa,
Canada
-----------------------------------------------------HIV/Immunology
Unravelling CD4 T Cell Dysfunction During Chronic Infection
CRAWFORD A. and Wherry, E.
,Baltimore, MD; USA, 39.17 ,2010
1) Wistar, Philadelphia, PA, United States; 2) U Penn, Philadelphia, PA, United States
-----------------------------------------------------HIV/Immunology
NK/DC Crosstalk and Regulation of Adaptive Immunity
ESTCOURT M., Andrews, D., Andoniou, C., and gli-Esposti, M.
,Banff, AB; Canada, 015 ,2010
Centre for Experimental Immunology, Lions Eye Institute and Immunology and Virology
Program, Centre for Ophthalmology and Visual Sciences, The University of Western
Australia,
Perth,
Western
Australia
-----------------------------------------------------HIV/Immunology
Damaged Intestinal Epithelial Integrity and Tissue Macrophage Dysfunction
Underlie Microbial Translocation in Simian Immunodeficiency Virus Infections
ESTES J., Harris, L., Klatt, N., Tabb, B., Pittaluga, S., Paiardini, M., Barclay, R., Smedley, J.,
Pung, R., Oliveira, K., Silvestri, G., Douek, D., Miller, C., Haase, A., Lifson, J., and Brenchley,
J.
,Banff, AB; Canada, 145 ,2010
1) AIDS and Cancer Virus Program, SAIC-Frederick, Inc., NCI-Frederick, Frederick, MD; 2)
Immunopathogenesis Unit, Lab of Molecular Microbiology, NIAID, NIH, Bethesda, MD; 3)
Lab of Pathology, NCI, NIH, Bethesda, MD; 4) Department of Pathology and Laboratory of
Medicine, University of Pennsylvania, Philadelphia, PA; 5) Centre for Regenerative
Medicine, University of Edinburgh, Edinburgh, Scotland; 6) Laboratory Animal Science
Program, SAIC-Frederick, Inc., NCI-Frederick, Frederick, MD; 7) AdvanDX, Inc, Woburn,
MA; 8) Human Immunology Section, Vaccine Research Center, NIAID, NIH, Bethesda, MD;
9) Center for Comparative Medicine, California National Primate Research Center,
University of California, Davis, CA; 10) Department of Microbiology, Medical School,
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105 / 152
EUROPRISE SCIENCE UPDATE 10-17
University
of
Minnesota,
------------------------------------------------------
Minneapolis,
MN
HIV/Immunology
Altered Sema4D Expression During HIV-1 Infection Is Associated With
Decreased HIV-Specific T Cell Responses
ERIKSSON E., Ho, E., Batista, M., Holditch, S., Milush, J., Long, B., Hunt, P., Deeks, S.,
Martin, J., and Nixon, D.
,Banff, AB; Canada, 263 ,2010
Division of Experimental Medicine, Department of Medicine, University of California San
Francisco,
San
Francisco,
CA
94110
-----------------------------------------------------HIV/Immunology
Significant Impairment in Innate Immune Cells Recruitment by Chronic
Untreated Antibodies to Mediate ADCC
DUGAST A., Barkume, C., Pechocka-Trocha, A., Toth, I., and Alter, G.
,Banff, AB; Canada, 142 ,2010
Ragon Institute, Partners AIDS Research Center, Massachusetts General Hospital, Harvard
Medical
School,
149,
13th
street,
Boston,
MA
02129
-----------------------------------------------------HIV/Immunology
Association of HLA-DRB1*0101 Exon 2 Mutations With HIV Progression
EGLITE E., Sochnev, A., and Viksna, L.
,Florence; Italy, P377 ,2010
1) Riga Stradins University (RSU), Riga, Latvia; 2) Laboratory for Clinical Immunology &
Immunogenetic,
Riga,
Latvia
-----------------------------------------------------HIV/Immunology
Neutralization of HIV-1 by Breast Milk in a Fc ? Receptor Expressing Cell Line
FOUDA G., Permar, S., Perez, G., and Montefiori, D.
,Banff, AB; Canada, 150 ,2010
Department of Surgery, Duke University Medical
------------------------------------------------------
Center, Durham,
NC,
27710
HIV/Immunology
Type I Interferon Increases the Sensitivity of Human Immunodeficiency Virus
(HIV)-Specific CD8+ T Lymphocytes to CD95/Fas-Mediated Apoptosis
FRAIETTA J., Mueller, Y., Do, D., Yang, G., Jacobson, J., and Katsikis, P.
,Baltimore, MD; USA, 42.22 ,2010
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106 / 152
EUROPRISE SCIENCE UPDATE 10-17
Microbiology and Immunology, Drexel University College of Medicine, Philadelphia , PA,
United
States
-----------------------------------------------------HIV/Immunology
Absent Correlation Between Cross-Reactive HIV-1 Specific Neutralizing Activity
in Serum and the Clinical Course of HIV-1 Infection
EULER Z., van, Gils M., Phung, P., Schweighardt, B., Wrin, T., and Schuitemaker, H.
,Banff, AB; Canada, 146 ,2010
1) Dept of Exp Immunology and Landsteiner Laboratory of the Academic Medical Center at
the University of Amsterdam, Amsterdam, The Netherlands; 2) Monogram Biosciences,
South
San
Francisco,
USA
-----------------------------------------------------HIV/Immunology
Immunodominant HIV-Specific CD8+ T-Cell Responses Are Common to Blood
and Rectal Mucosa, and Gag-Specific Mucosal Responses Dominate in HIV
Controllers
FERRE A., Lemongello, D., Morris, M., Garcia, J., Pollard, R., Hunt, P., Yee, H., Martin, J.,
Deeks, S., and Shacklett, B.
,Banff, AB; Canada, 147 ,2010
1) University of California, Davis, CA, 95616, USA; 2) University of California, San Francisco,
CA,
94110,
USA
-----------------------------------------------------HIV/Immunology
Recently Transmitted HIV and the Early Neutralizing Antibody Response
DERDEYN C., Alexander, M., Rong, Rong, Bing, Li, Lynch, R., Boeras, D., Murphy, M.,
Haaland, R., Ling, Yue, Mulenga, J., Karita, E., Allen, S., and Hunter, E.
,Banff, AB; Canada, 010 ,2010
1) Department of Pathology and Laboratory Medicine and the Emory Vaccine Center, Emory
University, Atlanta, GA, 30329, USA; 2) Zambia Emory HIV Research Project, Lusaka,
Zambia;
3)
Projet
San
Francisco,
Kigali,
Rwanda
-----------------------------------------------------HIV/Immunology
Role of PI3K and Autophagy in Virus-Stimulated IFN-a Production by Human
Plasmacytoid Dendritic Cells
DENG J., Singh, S., and Fitzgerald-Bocarsly, P.
,Baltimore, MD; USA, 136.46 ,2010
University of Medicine and Dentistry of New Jersey, Newark, NJ, United States
------------------------------------------------------
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EUROPRISE SCIENCE UPDATE 10-17
HIV/Immunology
Viral Regulation of a TLR/RLR-Independent Program of Host Cell Recognition
of HIV Infection
DOEHLE B., Chang, K., and Gale, M.
,Banff, AB; Canada, 153 ,2010
University of Washington School of Medicine, Department of Immunology, Seattle, WA
98195
-----------------------------------------------------HIV/Immunology
Investigation of the Sensitivity of Acute-Phase HIV-1 Isolates to Type I
Interferons
DIBBEN O., asa-Chapman, M., Lewis, J., McKnight, A., Williams, I., and Borrow, P.
,Banff, AB; Canada, 151 ,2010
The
Jenner
Institute,
University
of
Oxford,
RG20
7NN,
------------------------------------------------------
UK
HIV/Immunology
HIV-1 Infection Sensitizes CD4+ T Cells to Cell Death Induced by TNF-Alpha
BARNITZ R., Rao, S., and Lenardo, M.
,Banff, AB; Canada, 105 ,2010
1) Laboratory of Immunology, National Institute of Allergy and Infectious Diseases, National
Institutes of Health, Bethesda, MD 20892; 2) Immunology Graduate Group, University of
Pennsylvania,
Philadelphia,
PA
19104
-----------------------------------------------------HIV/Immunology
B Cells Diversify the HIV Env Genes and Promote Anti-Env Immunity
BALIN S., Platt, J., and Cascalho, M.
,Banff, AB; Canada, 123 ,2010
Departments of Surgery and Microbiology and Immunology. University of Michigan, Ann
Arbor,
M
I
48109-2200,
USA
-----------------------------------------------------HIV/Immunology
Concurrent Up-Regulation of Activation/Maturation Receptors and IFN-a by
Plasmacytoid Dendritic Cells in Response to HSV and HIV
AWOYOMI T., Singh, S., and Fitzgerald-Bocarsly, P.
,Baltimore, MD; USA, 130.8 ,2010
University of Medicine and Dentistry of New Jersey - Pathology and Laboratory Medicine,
Newark,
NJ,
United
States
------------------------------------------------------
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EUROPRISE SCIENCE UPDATE 10-17
HIV/Immunology
Induction and Maintenance of Systemic IL10 in Chronic LCMV Infection
BACA JONES C., Filippi, C., Ehrhardt, K., Sachithanantham, S., and von, Herrath M.
,Banff, AB; Canada, 104 ,2010
1) Developmental Immunology, La Jolla Institute for Allergy & Immunology, La Jolla, CA,
92037, USA; 2) Genomics Institute of the Novartis Research Foundation
-----------------------------------------------------HIV/Immunology
Identification of an IL-7 Responsive CD4+ Lymphoid Tissue Inducer Cell From
Adult Human Blood
BEKIARIS V., Greenberg ?FAU - Greenberg, Sedy, J., and Ware, C.
,Baltimore, MD; USA, 36.24 ,2010
La Jolla Institute for Allergy & Immunology, San Diego,
------------------------------------------------------
CA, United
States
HIV/Immunology
Higher Peripheral Treg Frequencies and T Cell Activation but Lower Absolute
Treg Numbers in HIV-1 Chronic Progressors Compared to Elite Controllers
ANOIN M., Fang, Wen, Kwon, D., Streeck, H., Pyo, A., Trocha, A., Toth, I., Law, K., Pereyra,
F., Alter, G., Altfeld, M., Kaufmann, D., Walker, B., and Addo, M.
,Banff, AB; Canada, 109 ,2010
1) Ragon Institute of MGH, Harvard and MIT, Boston, MA 02129, USA; 2) MGH Division of
Infectious
Diseases,
Boston,
MA,
02114,
USA
-----------------------------------------------------HIV/Immunology
HLA-B*5701 in HIV Infected Patients: Relevance for Abacavir Hypersensitivity
ATHANASSIADES T., Kitsiou, V., Kouniaki, D., Magafas, N., Chini, M., Lazanas, M., and
Papasteriades, C.
,Florence; Italy, P370 ,2010
1) Evangelismos Hospital, Athens, Greece; 2) Red Cross Hospital, Athens, Greece
-----------------------------------------------------HIV/Immunology
HLA Allelic Distribution in HIV-1 Monoinfected Patients and HIV-1/HCV
Coinfected Patients in Rio De Janeiro, Brazil
CASTILHO M., Fabricio-Silva, G., Domingues, E., Cardoso, J., Lima, D., Mello, R.,
Figueiredo, F., Ferreira, O., and Cristovao, Porto L.
,Florence; Italy, P376 ,2010
1) Institute of Biology Roberto Alcantara Gomes, UERJ, Rio de Janeiro, Brazil; 2) Faculty of
Medical
Sciences,
UERJ,
Rio
de
Janeiro,
Brazil
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EUROPRISE SCIENCE UPDATE 10-17
HIV/Immunology
The Antiviral Factor APOBEC3G Improves CTL Recognition of HIV-Infected T
Cells: Linking Intrinsic and Adaptive Immune Responses
CASARTELLI N., Guivel-Benhassine, F., Bouziat, R., Brandler, S., Schwartz, O., and Moris,
A.
,Banff, AB; Canada, 327 ,2010
1) Institut Pasteur, Unité Virus et Immunité, URA CNRS 3015; 2) Unité d'lmmunité Cellulaire
Antivirale, Paris, France; 3) UPMC, INSERM UMRS945, Hôpital Pitié-Salpêtrière, Paris,
France
-----------------------------------------------------HIV/Immunology
Bioinformatical Analvsis of Epitope Repertoire of HLA Class I Alleles
Associated With Different Outcomes of HIV-1 Infection
CAPINA R., Ma, Luo, Wachihi, C., Kimani, J., and Plummer, F.
,Banff, AB; Canada, 121 ,2010
1) National Microbiology Laboratory, Winnipeg, Manitoba, Canada; 2) Medical
Microbiology, University of Manitoba, Canada; 3) Medical Microbiology, University of
Nairobi,
Nairobi,
Kenya
-----------------------------------------------------HIV/Immunology
Natural Killer Cell Function and Disease Progression in Portuguese Patients
With HIV - an Immunogenetic Perspective
CARVALHO C., Lopes, D., Bettencourt, A., Leal, B., Maia, S., Vita, P., Almeida, F., Almeida,
I., Franca, M., Vasconcelos, C., Costa, P., and Silva, B.
,Florence; Italy, P375 ,2010
1) UMIB-Instituto de Ci encias Biomedicas de Abel Salazar, Porto, Portugal; 2) Centro
Hospitalar
do
Porto
Hospital
de
Santo
Antonio,
Porto,
Portugal
-----------------------------------------------------HIV/Immunology
Loss of TRAF1 From Ag-Specific T Cells During Persistent Viral Infection
Leads to Desensitization of the 4-1BB Signaling Pathway
CHAO WANG, Kim, Karamura, McPherson, A., Lin, G., Pellegrini, M., Lang, P., Calzascia,
T., Elford, A., Bernard, N., Jones, B., Ostrowski, M., Ohashi, P., and Watts, T.
,Banff, AB; Canada, 437 ,2010
University
of
Toronto,
Toronto,
ON,
Canada
------------------------------------------------------
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EUROPRISE SCIENCE UPDATE 10-17
HIV/Immunology
Contribution of Siglec-1 to HIV-1 Infection of Macrophages
CHASTAIN A., Zhongcheng, Zou, Moir, S., Ford, J., Trandem, K., Martinelli, E., Cicala, C.,
Arthos, J., Crocker, P., and Sun, P.
,Banff, AB; Canada, 157 ,2010
1) NIAID, National Institutes of Health, Rockville, MD 20852, USA; 2) University of Dundee,
Dundee
DD15EH,
UK
-----------------------------------------------------HIV/Immunology
Isolation of Cross-Clade HIV-Neutralizing Human Antibodies From Memory B
Cell Repertoires Using Short Term Culture and High-Throuehput Primarv
Neutralization Screens
CHAN-HUI P., Wrin, T., Simek, M., Phogat, S., Olsen, O., Hammond, P., Poignard, P.,
Walker, L., Mitcham, J., Fling, S., Team, P., Burton, D., and Moyle, M.
,Baltimore, MD; USA, 38.17 ,2010
1) Theraclone Sciences, Seattle, WA, United States; 2) Monogram Biosciences, South San
Francisco, CA, United States; 3) International AIDS Vaccine Initiative, New York, NY, United
States; 4) The Scripps Research Institute, La Jolla, CA, United States; 5) Ragon Institute of
MGH,
MIT
and
Harvard,
Boston,
MA,
United
States
-----------------------------------------------------HIV/Immunology
An Analysis of Genital Tract Derived HIV From Heterosexual Transmission
Pairs
BOERAS D., Hurlston, M., Godoshian, A., Derdeyn, C., Mulenga, J., Karita, E., Allen, S., and
Hunter, E.
,Banff, AB; Canada, 116 ,2010
1) Emory University, Atlanta, GA, USA; 2) Zambia Blood Transfusion Service and ZEHRP,
Lusaka,
Zambia;
3)
Projet
San
Francisco,
Kigali,
Rwanda
-----------------------------------------------------HIV/Immunology
HLA Class I Associations With Viral Variation Predicts a New HIV RT-Specific
T-Cell Epitope in a Single-Source HIV-1 Outbreak in Rural China
BLAIS M., Dong, T., Zhang, Y., Xu, K., Yan, H., John, M., and Rowland-Jones, S.
,Banff, AB; Canada, 113 ,2010
MRC Human Immunology Unit, Weatherall Institute of Molecular Medicine, Oxford, OX3
9DS,
UK
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EUROPRISE SCIENCE UPDATE 10-17
HIV/Immunology
IL-2 Induces Perforin Mediated Cytotoxicity in CD4 Cells Via STAT5 Signaling
BROWN D., Canfield, J., Lee, S., and Condon, S.
,Baltimore, MD; USA, 139.9 ,2010
School of Biological Sciences , University of Nebraska-Lincoln, Lincoln, NE, United States
-----------------------------------------------------HIV/Immunology
Adaptation of HIV-1 Envelope Glycoprotein to Humoral Immunity at a
Population Level
BUNNIK E., Euler, Z., Welkers, M., Grijsen, M., Prins, J., and Schuitemaker, H.
,Banff, AB; Canada, 119 ,2010
Department of Experimental Immunology, Academic Medical Center, University of
Amsterdam,
Amsterdam,
The
Netherlands
-----------------------------------------------------HIV/Immunology
Reduced Replication Capacity of Recombinant Viruses Encoding Acute/Early
HIV-1 Gag-Protease Sequences From Individuals Expressing Protective HLA
Class I Alleles
BROCKMAN M., Miura, T., Sela, J., Brumme, C., Markle, T., Rosato, P., Streeck, H., Block, B.,
Kadie, C., Jessen, H., Rychert, J., Rosenberg, E., Heckerman, D., Markowitz, M., Kelleher, A.,
Altfeld, M., Walker, B., Allen, T., and Brumme, Z.
,Banff, AB; Canada, 118 ,2010
1) Ragon Institute of MGH, MIT, and Harvard; 2) Simon Fraser University; 3) British
Columbia Centre for Excellence in HIV/AIDS; 4) Institute of Medical Science, University of
Tokyo; 5) Howard Hughes Medical Institute; 6) Microsoft Research; 7) Jessen Praxis, Berlin;
8) Aaron Diamond AIDS Research Center; 9) National Centre in HIV Epidemiology and
Clinical
Research,
University
of
New
South
Wales
-----------------------------------------------------HIV/Immunology
Temporal Analysis of SlVmac239 Infection and Evolution in 12 Cynomolgous
Macaques
BOWLES E., Parker, J., Uchtenhagen, H., Sahin, G., Sheik-Khalil, E., Achour, A., Fenvo, F.,
Soetz, A., and Stewart-Jones, G.
,Banff, AB; Canada, 167 ,2010
1) Weatherall Institute of Molecular Medicine. Oxford University, Oxford, UK; 2) Center for
Infectious Medicine, Department of Medicine, Karolinska University Hospital Huddinge,
Karolinska Institutet, Stockholm, Sweden; 3) Department of Laboratory Medicine, Lund
University,
Lund,
Sweden
------------------------------------------------------
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EUROPRISE SCIENCE UPDATE 10-17
HIV/Immunology
Altered NK Cell Differentiation of CD56bright/CD16-NK Cells With DownRegulation of CCR7 Is Associated With Increased Viral Load in HIV-1 Infection
HONG H., Eberhard, J., Bollmann, B., Keudel, P., Ballmaier, M., Zielinska-Skowronek, M.,
Schmidt, R., and Meyer-Olson, D.
,Banff, AB; Canada, 229 ,2010
1) Klinik für Immunologie und Rheumatologie, Medizinische Hochschule Hannover, 30625
Hannover, Germany; 2) Pädiatrische Hämatologie und Onkologie, Medizinische Hochschule
Hannover,
30625
Hannover,
Germany
-----------------------------------------------------HIV/Immunology
Evidence That GC1qR and DC-SIGN Associate on the Surface of Immature
Dendritic Cells
HOSSZU K., Vinayagasundaram, U., Vinayagasundaram, R., Santiago-Schwarz, F.,
Peerschke, E., and Ghebrehiwet, B.
,Baltimore, MD; USA, 136.24 ,2010
1) Genetics, Stony Brook University, Stony Brook , NY, United States; 2) Stony Brook
University, Dept. Medicine, Stony Brook , NY, United States; 3) SUNY Farmingdale,
Farmingdale, NY, United States; 4) Mount Sinai School of Medicine, New York, NY, United
States
-----------------------------------------------------HIV/Immunology
PD-1 Is Upregulated on Natural Killer Cells in Chronic HIV-1 Infection
HO E., Eriksson, E., Batista, M., Holditch, S., Milush, J., Long, B., Hunt, P., Deeks, S., Martin,
J., and Nixon, D.
,Banff, AB; Canada, 226 ,2010
Division of Experimental Medicine, Department of Internal Medicine, University of
California
San
Francisco,
San
Francisco,
CA,
94110,
USA
-----------------------------------------------------HIV/Immunology
Comprehensive Analysis of Escape Mutation From HIV-1-Specific Cytotoxic T
Cells Restricted by Asian Allele HLA-B*5401
HASHIMOTO M., Kitano, M., Oka, S., and Takiguchi, M.
,Banff, AB; Canada, 209 ,2010
Divisions of Viral Immunology, Centers forAIDS Research, Kumamoto University,
Kumamoto
860-0811,
Japan
------------------------------------------------------
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EUROPRISE SCIENCE UPDATE 10-17
HIV/Immunology
HIV-1 Up-Regulates Type 1 Long-Interspersed Nuclear Elements
Retrotransposition by Vif and Vpr
HAIHAN SONG, Yang, Xu, Jones, B., Mujib, S., Nixon, D., and Ostrowski, M.
,Banff, AB; Canada, 415 ,2010
1) Clinical Science Division, University of Toronto, Toronto ON, M5S 1A8, Canada; 2)
Department
of
Medicine,
UCSF,
San
Francisco
CA,
94143,
USA
-----------------------------------------------------HIV/Immunology
Viral Load in HIV+ Partner Associates With Exposed Uninfected Partners'
Capacity to Neutralize HIV-1 in Vitro
HASSELROT K., Bratt, G., Hirbod, T., Säberg, P., Ehnlund, M., Lopalco, L., Sandström, E.,
and Broliden, K.
,Banff, AB; Canada, 210 ,2010
Dept of Medicine, Unit of Infectious Diseases, Karolinska Institutet, Stockholm, Sweden
-----------------------------------------------------HIV/Immunology
Development of Neutralizing Antibodies Against Heterologous HIV Viruses Is
Common and Correlated With Viral Evolution to Escape Neutralizing
Antibodies
HECHT F., Phung, P., Wrin, T., Hartogensis, W., Bacchetti, P., Pilcher, C., Petropoulos, C.,
and Deeks, S.
,Banff, AB; Canada, 212 ,2010
University
of
California,
San
Francisco
-----------------------------------------------------HIV/Immunology
HLA-B*57 and -B*58 Fail to Control HIV Clade AE in Thailand
HEMPEL U., Buranapraditkun, S., Pitakpolrat, P., Phillips, L., Allgaier, R., Lorenzen, S.,
Hildebrand, W., Leitner, T., Matthews, P., Goulder, P., Walker, B., Ruxrungtham, K., and
Allen, T.
,Banff, AB; Canada, 213 ,2010
1) Ragon Institute of MGH, MIT and Harvard, Boston, MA, USA; 2) Vaccine and Cellular
Immunology Laboratory, Faculty of Medicine, Chulalongkorn University, Bangkok,
Thailand; 3) Dept. of Microbiology and Immunology, U. of Oklahoma, Oklahoma, USA; 4)
Theoretical Biology and Biophysics, Los Alamos National Laboratory, Los Alamos, New
Mexico,
USA;
5)
University
of
Oxford,
Oxford,
UK
------------------------------------------------------
--------------------------------------------------------------------------------------------------------------
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EUROPRISE SCIENCE UPDATE 10-17
HIV/Immunology
Effect of Antiretroviral Therapy Initiation on Mucosal T-Cells in HIV Infection
HAYES T., Critchfield, J., Knight, T., Yotter, T., Young, D., Pollard, R., Asmuth, D., and
Shacklett, B.
,Banff, AB; Canada, 211 ,2010
Department of Medical Microbiology and Immunology, University of California, Davis, CA,
95616,
USA
-----------------------------------------------------HIV/Immunology
Influence of HLA-Bw4 Alleles Protective for HIV on NK Cell Polyfunctional
Potential
KAMYA P., Boulet, S., Tremblay, C., and Bernard, N.
,Banff, AB; Canada, 226 ,2010
1) Immune Deficiency Treatment Centre, Montreal General Hospital and Research Institute
of the McGill University Health Center, Montreal, Quebec, Canada; 2) Centre de Recherche
du Centre Hospitalier de l'Université de Montréal, Montreal, Quebec, Canada; 3) Canadian
Cohort
of
HIV
Infected
Slow
Progressors
-----------------------------------------------------HIV/Immunology
Pathogenic SIVmac251 Infection Induces a Striking Acute-Phase Systemic
Cytokine Response Similar to That Observed in Acute HIV-1 Infection
KEATING S., Heitman, J., Stacey, A., Zahn, R., de la, Rosa M., Jinyan, Liu, Finstad
Persephone, Borrow S., Barouch, D., Letvin, N., Schmitz, J., and Norris, P.
,Banff, AB; Canada, 229 ,2010
Center for HIV/AIDS Vaccine Immunology Blood Systems Research Institute, University of
California,
San
Francisco,
CA,
94118,
USA
-----------------------------------------------------HIV/Immunology
Genetic Determinants of HIV-1 Infection and Progression to AIDS: Indian
Experience
KAUR G., Sharma, G., Vajpayee, M., and Mehra, N.
,Florence; Italy, P372 ,2010
All
India
Institute
of
Medical
Sciences,
------------------------------------------------------
New
Delhi,
--------------------------------------------------------------------------------------------------------------
115 / 152
India
EUROPRISE SCIENCE UPDATE 10-17
HIV/Immunology
Systemic Cytokine Levels Correlate With Disease Outcome in Chronic HIV
Infection
KEATING S., Golub, E., Heitman, J., Lebedeva, M., Jinbing, Zhang, Greenblatt, R., Desai, S.,
Landay, A., Gange, S., and Norris, P.
,Banff, AB; Canada, 322 ,2010
1) Blood Systems Research Institute; 2) University of California, San Francisco, CA; 3) Johns
Hopkins Bloomberg School of Public Health, Baltimore, MD; 4) Rush University Medical
Center,
Chicago,
IL
-----------------------------------------------------HIV/Immunology
Immunoregulatory Properties of HLA-G in HIV-1 Infection
JINGHE HUANG, Burke, P., Thai, Cung, Seiss, K., Beamon, J., Pereyra, F., Allen, R.,
Lichterfeld, M., and Yu, X.
,Banff, AB; Canada, 231 ,2010
1) Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA; 2) Boston
Biomedical Research Institute, Watertown, MA, USA; 3) Ragon Institute of MGH, MIT and
Harvard, Boston, MA, USA; 4) University of London, St. George Medical School, London,
UK; 5) Infectious Disease Division, Massachusetts General Hospital, Boston, MA, USA
-----------------------------------------------------HIV/Immunology
HLA B *08 FLK T Cell Clones From Chronic HIV Infection With the Same T Cell
Receptor Have Unique Polyfunctional Cytokine Profiles
GLANVILLE J., Ragoussis, loannis, Rowland-Jones, S., McMichael, A., and Tao, Dong
,Banff, AB; Canada, 211 ,2010
MRC Human Immunology Unit, Weatherall Institute of Molecular Medicine, University of
Oxford,
Oxford,
OX3
9DS,
UK
-----------------------------------------------------HIV/Immunology
CD4 Naïve Phenotype T Cells Are Recruited into the Proliferating T Cell Pool
Mainly As a Homeostatic Response to HIV Induced CD4 T Cell Depletion
FRIESEN T., Wilhelm, C., Proschan, M., Hurley, A., Tcheung, L., Adelsberger, J., Baseler, M.,
Maldarelli, F., Davey, R., Roby, G., Rehm, C., Lane, C., and Catalfamo, M.
,Banff, AB; Canada, 151 ,2010
1) CMRS/ Laboratory of Immunoregulation, NIAID, NIH, Bethesda, MD, USA; 2)
Biostatistics Research Branch, NIAID, NIH, Bethesda, MD, USA; 3) ScienceApplications
International
Corporation,
Frederick,
MD,
USA
------------------------------------------------------
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EUROPRISE SCIENCE UPDATE 10-17
HIV/Immunology
Analysis of T-Cell Subsets by the FluoroSpot Assay
GELIUS E., Axelsson, B., Zuber, B., Hallengärd, D., Mömer, A., Ernemar, T., Andersson, P.,
Fohlstedt, J., and Ahlborg, N.
,Banff, AB; Canada, 452 ,2010
1) Mabtech, Nacka Strand, Sweden; 2) Swedish Institute for Infectious Disease Control,
Stockholm,
Sweden
-----------------------------------------------------HIV/Immunology
HIV Disease Progression in Early Infection Varies by Infecting HIV-1 Subtype in
Sub Saharan Africa
GILMOUR J., Kamali, A., Karita, E., Lakhi, S., Sanders, E., Kaleebu, P., Anzala, O., Rida, W.,
Price, M., Amornkul, P., Cormier, E., and IAVI Early Infection Cohort Study Group
,Banff, AB; Canada, 158 ,2010
1) Medical Research Council/Uganda Virus Research Institute, Masaka and Entebbe; 2)
Rwanda Zambia HIV Research Group, Kigali, Lusaka and Copperbelt; 3) Kenya AIDS
Vaccine Initiative, Nairobi; 4) Center for Geographic Medicine-Coast, Kilifi; 5) Oxford
University, UK; 6) Desmond Tutu HIV Foundation, University of Cape Town, South Africa;
7) International AIDS Vaccine Initiative, New York, NY, US; 8) International AIDS Vaccine
Initiative, Nairobi, Kenya; 9) International AIDS Vaccine Initiative, Johannesburg, South
Africa; 10) International AIDS Vaccine Initiative, Amsterdam, The Netherlands; 11)
International AIDS Vaccine Initiative, New Delhi, India; 12) Contract Laboratory Services,
Johannesburg, South Africa; 13) Biostatistics Consultant, Arlington, VA, USA
-----------------------------------------------------HIV/Immunology
Yeast-Elicited Cross-Reactive Antibodies to HIV Env Glycans Recognize
Monomeric Gp120 but Bind Trimeric Env Poorly
GRAWAL-GAMSE C., Luallen, R., Yu, Geng, and Doms, R.
,Banff, AB; Canada, 104 ,2010
1) Department of Microbiology, University of Pennsylvania, Philadelphia, PA; 2) ProSci, Inc.,
Poway,
CA
-----------------------------------------------------HIV/Immunology
Differential MHC Class I Allele Expression in Distinct Lymphocyte Subsets
GREENE J., Wiseman, R., Lank, S., Burwitz, B., Lhost, J., and O'Connor, D.
,Banff, AB; Canada, 213 ,2010
1) Department of Pathology and Laboratory Medicine, University of Wisconsin-Madison,
Madison, WI, 53706, USA; 2) Wisconsin National Primate Research Center, University of
Wisconsin-Madison,
Madison,
Wisconsin,
53715,
USA
------------------------------------------------------
--------------------------------------------------------------------------------------------------------------
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EUROPRISE SCIENCE UPDATE 10-17
HIV/Immunology
HIV-1 Replication Activates CD4+T Cells With Specificities for Persistent
Herpes Viruses
HAAS A., Rehr, M., Graw, F., Rusert, P., Bossart, W., Kuster, H., Trkola, A., Gonthard, H.,
and Oxenius, A.
,Banff, AB; Canada, 217 ,2010
1) Institute of Microbiology, Zurich, Switzerland; 2) Institute of Integrative Biology, ETH
Zurich, Zurich, Switzerland; 3) Institute of Medical Virology, University of Zurich, Zurich,
Switzerland; 4) Division of Infectious Diseases and Hospital Epidemiology, University
Hospital
Zurich,
Zurich,
Switzerland
------------------------------------------------------
Pathology
Fungal Infections in Hiv Infected Patients
NILIMA K., Thanki, C., Frunza, S., Brad, G., Popoiu, C., Frunza, F., Popoiu, A., Pakai, R.,
Gafencu, M., Kundnani, L., and Shalini, B.
,Nice; France ,2010
1)
Timisoara,
Romania;
2)
Ahemdabad;
3)
Vadodara,
India
-----------------------------------------------------HIV/Pathology
Increased Cholesteryl Ester in HDL Along With Increased Triglyceride in HDL
and LDL of HIV Patients Suggests That a Defect in Reverse Cholesterol
Transport Contributes to HIV Dyslipedemia
GILLARD B., Raya, J., Coraza, I., Villanueva, J., Scott, L., Kamble, S., Sekhar, R.,
Balasubramanyam, A., and Pownall, H.
,San Francisco, CA; USA, P123 ,2010
Baylor
Coll
of
Med,
Houston,
TX
------------------------------------------------------
Recommendations & Policies
Review of the Revisions to the World Health Organization (WHO) Guidelines for
Antiretroviral Treatment
MOSS A.
,Galveston, TX; USA, S-79 ,2010
University
of
Houston
College
------------------------------------------------------
of
Pharmacy,
Houston,
--------------------------------------------------------------------------------------------------------------
118 / 152
Texas
EUROPRISE SCIENCE UPDATE 10-17
Vaccines, clinical
Screening for Help: CD4 T Cells in the Step Trial
PEUT V., DeRosa, S., Frahm, N., and McElrath, J.
,Banff, AB; Canada, 336 ,2010
Vaccine and Infectious Disease Institute, Fred Hutchinson Cancer Research Center; HIV
Vaccine
Trials
Network
-----------------------------------------------------HIV/Vaccines, clinical
HIV-1 Subtype Distribution in HIV-1 Positive Volunteers Prior and During the
Phase III Prime-Boost HIV-1 Vaccine Trial in Thailand (RV144)
TOVANABUTRA S., Kijak, G., Arroyo, M., Rerks-Ngarm, S., Nitayaphan, S., deSouza, M.,
Sanders-Buell, E., Bose, M., Assawadarachai, V., Rutvisuttinunt, W., Pitisuttithum, P., Chiu,
J., Paris, R., Robb, M., Birx, D., McCutchan, F., Michael, N., and Kim, J.
,Banff, AB; Canada, 429 ,2010
1) MHRP, Rockville, MD,, USA; 2) AFRIMS, Bangkok, Thailand; 3) MOPH, Thailand; 4)
Mahidol
University,
Bangkok,
Thailand;
5)
MOPH-TAVEG
Investigators
-----------------------------------------------------HIV/Vaccines, clinical
RV 144 Update: Vaccination With ALVAC and AIDSVAX to Prevent HIV-1
Infection in Thai Adults
RERKS-NGARM S., Pittisutthithum, P., Nitayaphan, S., Kaewkungwal, J., Chiu, J., Paris, R.,
Premsri, N., Namwat, C., de, Souza M., Adams, E., Benenson, M., Gurunathan, S., Tartaglia,
J., McNeil, J., Francis, D., Stablein, D., Birx, D., Chunsuttiwat, S., Khamboonruang, C.,
Thongcharoen, P., Robb, M., Michael, N., Kunasol, P., Kim, J., and MOPH-TAVEG,
collaborators
,Banff, AB; Canada, 360 ,2010
Department of Disease Control, Ministry of Public Health (MOPH), Thailand; Vaccine Trials
Centre, Faculty of Tropical Medicine, Mahidol University, Thailand; Thai Component,
Armed Forces Research Institute of Medical Sciences (AFRIMS), Thailand; Data Management
Unit, Faculty of Tropical Medicine, Mahidol University, Thailand; U.S. Army Medical
Component, AFRIMS, Thailand; Division of AIDS, National Institutes of Allergy and
Infectious Diseases (NIAID), National Institutes of Health (NIH), USA; sanofi pasteur,
Swiftwater, PA, USA; Global Solutions for Infectious Diseases (GSID), S. San Francisco, CA,
USA; EMMES Corporation, Rockville, MD, USA; Global AIDS Program, Centers for Disease
Control,
Atlanta,
GA,
USA
------------------------------------------------------
--------------------------------------------------------------------------------------------------------------
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EUROPRISE SCIENCE UPDATE 10-17
HIV/Vaccines, clinical
Serological Immunity to Adenovirus Serotype 5 Is Not Associated With Risk of
HIV Infection
CURLIN M., Cassis-Ghavami, F., Magaret, A., Spies, G., Duerr, A., Celum, C., Sanchez, J.,
Margolick, J., Detels, R., McElrath, M., and Corey, L.
,Banff, AB; Canada, 136 ,2010
1) University of Washington; 2) Fred Hutchinson Cancer Research Center; 3) Asociación
Civil Impacta Salud y Educación, Peru; 4) Johns Hopkins University; 5) University of
California
Los
Angeles;
6)
Multicenter
AIDS
Cohort
Study
-----------------------------------------------------HIV/Vaccines, clinical
Immunogenicity of the Thai Phase III (RV144) HIV Vaccine Regimen
DE SOUZA M., Trichavaroj, R., Schuetz, A., Chuenarom, W., Phuang-ngern, Y.,
Jongrakthaitae, S., Ratto-Kim, S., Nitayaphan, S., Dally, L., Rerks-Ngarm, S., Michael, N.,
Paris, R., Marovich, M., Currier, J., and Kim, J.
,Banff, AB; Canada, 159 ,2010
1) U.S. Military HIV Research Program (MHRP)/Armed Forces Research Institute of Medical
Sciences, Bangkok, Thailand; 2) MHRP, Rockville, MD, USA; 3) The Emmes Corporation,
Rockville, MD, USA; 4) Ministry of Public Health, Bangkok, Thailand
-----------------------------------------------------HIV/Vaccines, clinical
Increased HIV-Specific Immunity in HIV-Infected Individuals Vaccinated With a
DNA Prime, RAd5 Boost Regimen
CASAZZA J., Bowman, K., Ambrozak, D., Gordon, I., Roederer, M., Patterson, E., Stone, H.,
Enama, M., Nason, M., Ledgerwood, J., Graham, B., and Koup, R.
,Banff, AB; Canada, 122 ,2010
Vaccine
Research
Center,
NIAID,
NIH,
Bethesda,
MD
-----------------------------------------------------HIV/Vaccines, clinical
Population Epitope Maps of the Step and HVTN 054 HIV Vaccine Trials Reveal
Vaccine-Induced Epitope Hotspots
HERTZ T., Frahm, N., Horton, H., Friedrich, D., Corey, L., Self, S., Gilbert, P., Buchbinder, S.,
McElrath, M., and NIAID HIV Vaccine Trials Network (HVTN)
,Banff, AB; Canada, 214 ,2010
1) Fred Hutchinson Cancer Research Center and University of Washington, Seattle, WA; 2)
Seattle Biomedical Research Institute, Seattle, WA; 3) University of California San Francisco,
San
Francisco,
CA
------------------------------------------------------
--------------------------------------------------------------------------------------------------------------
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EUROPRISE SCIENCE UPDATE 10-17
HIV/Vaccines, clinical
Induction of Viral Inhibition in Clinical HIV Vaccine Trials of Diverse
Immunogens
HAYES P., Bergin, P., Spentzou, A., Cashin-Cox, M., Gill, D., Karita, E., Jaoko, W., Graham,
B., Pitisuttithum, P., Nitayaphan, S., Kim, J., Fast, P., Cox, J., de, Souza M., and Gilmour, J.
,Banff, AB; Canada, 155 ,2010
1) International AIDS Vaccine Initiative (IAVI) Human Immunology Laboratory, Imperial
College, London, UK; 2) Project San Francisco, Kigali, Rwanda; 3) Kenya AIDS Vaccine
Initiative, Nairobi, Kenya; 4) Dale and Betty Bumpers Vaccine Research Center, Bethesda,
USA; 5) Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand; 6)
Department of Retrovirology, Armed Forces Institute of Medical Sciences, Bangkok,
Thailand; 7) Department of Retrovirology, Military HIV Research Program, Rockville, MD,
USA;
8)
Research
and
Development,
IAVI,
New
York,
USA
-----------------------------------------------------HIV/Vaccines, clinical
Comparison of T Cell Responses Elicited Bv CD40L Adjuvanted ALVAC PrimeBoost and DNA Prime-ALVAC Boost HIV-1 Vaccine Regimen
JUN LIU, Bozorgz, A., Chang, M., Yue, F., and Ostrowksi, M.
,Banff, AB; Canada, 246 ,2010
1) Clinical Sciences Division; 2) Department of Immunology; 3) Li Ka Shing Knowledge
Institute,
St.
Michael's
Hospital,
University
of
Toronto
------------------------------------------------------
Vaccines, research
Systemic Innate Immune Responses to a DNA/MVA Candidate HIV Vaccine
NDERSEN-NISSEN E., Zak, D., Krishnamurty, A., Chang, J., Sato, A., Elizaga, M., Robinson,
H., Goepfert, P., Aderem, A., McElrath, M., and NIAID HIV Vaccine Trials Network(
,Banff, AB; Canada, 108 ,2010
1) Vaccine and Infectious Disease Institute, Fred Hutchinson Cancer Research Center
(FHCRC), Seattle, WA 98109; 2) Institute for Systems Biology, Seattle, WA; 3) Statistical
Center for HIV/AIDS Research and Prevention, FHCRC, Seattle, WA; 4) HIV Vaccine Trials
Network, FHCRC, Seattle, WA; 5) Geovax Labs Inc., Smyrna, GA; 6) Department of
Medicine, University of Alabama at Birmingham, Birmingham, AL 35924
------------------------------------------------------
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EUROPRISE SCIENCE UPDATE 10-17
HIV/Vaccines, research
Glucopyranosyl Lipid A (GLA), a Synthetic TLR4 Vaccine Adjuvant, Induces
Potent Th1-Promoting Immune Responses
MOUTAFTSI M., Bertholet, S., Vedvick, T., Guderian, J., Baldwin, S., Wndish, H., Coler, R.,
and Reed, S.
,Banff, AB; Canada, 313 ,2010
1) Infectious Disease Research Institute, Seattle, USA; 2) Immune Design Corp, Seattle, USA
-----------------------------------------------------HIV/Vaccines, research
HIV Subtype A and B Vaccines Based on Envelope Quasispecies
PISSANI F., Malherbe, D., Beckett, T., Stamatatos, L., Overbauqh, J., Robins, H., and
Haiqwood, N.
,Banff, AB; Canada, 337 ,2010
1) Departments of Molecular Microbiology & Immunology, OHSU; 2) Pathobiology &
Immunology, ONPRC, Portland, OR 97006; 3) Seattle Biomedical Research Institute; 4) Fred
Hutchinson
Cancer
Research
Center,
Seattle
WA,
USA
-----------------------------------------------------HIV/Vaccines, research
Transient but Recurrent CD4+ T Cell Activation, Hexon-Specific T Cell
Immunity and Neutralizing Antibody Responses After Ad5 Infection of Rhesus
Macaques
QURESHI H., Genescà, M., Fritts, L., Jun, Li, Casimiro, D., Shiver, J., Robertson, M., Bett, A.,
DiPasquale, J., Robert-Guroff, M., McChesney, M., and Miller, C.
,Banff, AB; Canada, 364 ,2010
1) Center for Comparative Medicine, Davis, CA.; 2) California National Primate Research
Center, University of California, Davis, CA.; 3) Merck Research Laboratories, West Point, PA;
4) National Cancer Institute, National Institutes of Health, Vaccine Branch, Bethesda, MD
-----------------------------------------------------HIV/Vaccines, research
Enhanced Expression of HIV Antigens and Improved Antigen Presentation
After Infection With Replication Competent Attenuated Vaccinia Virus in Vitro
QUAKKELAAR E., Redeker, A., Loof, N., Perdiguero, B., Heinen, P., Esteban, M., Kibler, K.,
Jacobs, B., Harari, A., Pantaleo, G., and Melief, C.
,Banff, AB; Canada, 342 ,2010
1) dept of IHB, LUMC, Leiden, the Netherlands; 2) CNB, CSIC, Madrid, Spain; 3) Arizona
State University, Tempe, AZ, USA; 4) div of Immunology and Allergy, CHUV, Lausanne,
Switzerland
------------------------------------------------------
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EUROPRISE SCIENCE UPDATE 10-17
HIV/Vaccines, research
A DNA Vaccine Encoding Conserved HIV CD4 Epitopes Induces Broad and
Polyfunctional Responses in BALB/c and HLA Class II-Transgenic Mice
PEREIRA RIBEIRO S., Santoro, Rosa D., Gonçalves, Fonseca S., Conti, Mairena E., Postól, E.,
Oliveira, S., Guilherme, L., Kalil, J., and Cunha-Neto, E.
,Banff, AB; Canada, 346 ,2010
1) Laboratory of Clinical Immunology and Allergy-LIM60, Division of Clinical Immunology
and Allergy, Department of Medicine; 2) Heart Institute (InCor), University of Sao Paulo
School of Medicine; 3) Institute for Investigation in Immunology-INCT, Sao Paulo, Brazil; 4)
Department of Biochemistry and Immunology, Federal University of Minas Gerais, Belo
Horizonte,
Brazil
-----------------------------------------------------HIV/Vaccines, research
Vaccine-Elicited Non-Neutralizing Envelope Antibodies in Sera and Mucosal
Secretions Contribute to Protection Against SHIV89.6Pin Rhesus Macaques
PENG XIAO, Jun, Zhao, Patterson, L., Brocca-Cofano, E., Venzon, D., Hidajat, R., Demberg,
T., and Robert-Guroff, M.
,Banff, AB; Canada, 444 ,2010
1) Vaccine Branch, Bethesda, MD 20892; 2) Biostatistics and Data Management Section, NIH,
NCI,
Bethesda,
MD
20892
-----------------------------------------------------HIV/Vaccines, research
GB Virus C Envelope Protein E2 Elicits Antibodies That React With a
Conserved Antigen on HIV-1 Particles and That Broadly Neutralize HIV-1
Infectivity
MOHR E., Jinhua, Xiang, McLinden, J., Kaufman, T., Qing, Chang, Klinzman, D., and
Stapleton, J.
,Banff, AB; Canada, 309 ,2010
University
of
Iowa
-----------------------------------------------------HIV/Vaccines, research
Prevention of Systemic Infection by a Multigenic Recombinant Protein Vaccine
After Heterologous R5 Clade C SHIV Challenge: Correlates of Protection
LAKHASHE S., Wang, W., Siddappa, N., Hu, S., Villinger, F., Else, J., Ruprecht, R., and
Rasmussen, R.
,Banff, AB; Canada, 366 ,2010
1) Cancer Immunology and AIDS, Dana-Farber Cancer Institute and Harvard University
Medical Center, Boston, MA, 02115; 2) University of Washington, Seattle, WA; 3) Yerkes
National
Primate
Research
Center,
Emory
University,
Atlanta,
GA
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Engineering the CD4+ T-Cell Response for Improved Immunity
LANDRY S., Kalaya, Steede N., Hossain, M., and Robinson, J.
,Banff, AB; Canada, 241 ,2010
Tulane
University
Health
------------------------------------------------------
Sciences
Center
HIV/Vaccines, research
Lentiviral Vector-Based Anti-HIV-1 Vaccination in Macaques Induces Strong TCell and Antibody Responses Post-Immunization, Significant Recall
Responses Post-SIVmac251 Challenge and Controls Viral Replication During
Setpoint and Chronic Phases
LEMIALE F., Cristillo, A., Shovlin, L., Morrow, M., Korokhov, N., Weiner, D., and Humeau,
L.
,Banff, AB; Canada, 243 ,2010
1) VIRxSYS Corporation, Gaithersburg, MD20877; 2) Advanced Biosciences Laboratories,
Kensington, MD 20895; 3) University of Pennsylvania School of Medicine, Philadelphia PA
19104
-----------------------------------------------------HIV/Vaccines, research
Future Directions in AIDS Vaccine Development
KOFF W.
,Banff, AB; Canada, 024 ,2010
Research & Development, International AIDS Vaccine Initiative, New York, NY 10038, USA
-----------------------------------------------------HIV/Vaccines, research
Electroporation of an HIV-1 DNA Vaccine Based on an Alphavirus Replicon
Vector Has a Dose-Sparing Effect
KNUDSEN M., Ljungberg, K., Hanke, T., and Liljeström, P.
,Banff, AB; Canada, 234 ,2010
1) Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, 171 77
Stockholm, Sweden; 2) MRC Human Immunology Unit, Weatherall Institute of Molecular
Medicine, University of Oxford, The John Radcliffe, Oxford OX3 9DS, United Kingdom
------------------------------------------------------
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HIV/Vaccines, research
Conserved Elements Vaccine for HIV-1 P24gag Is Immunogenic in Mice and
Macaques
KULKARNI V., Yan, J., Rolland, M., Le, Gall S., Mothe, B., Ganneru, B., Patel, V., Zhang, G.,
Rosati, M., Valentin, A., Pankhong, P., Elliott, S., Harris, A., Manocheewa, S., Sardesai, N.,
Weiner, D., Brander, C., Pavlakis, G., Felber, B., and Mullins, J.
,Banff, AB; Canada, 238 ,2010
1) NCI, Frederick, MD; 2) Univ. of Penn., Philadelphia, PA; 3) Univ. of Wash., Seattle, WA; 4)
Ragon Inst., Boston, MA; 5) IrsiCaixa-HIVACAT, Barcelona, SPAIN; 6) Inovio Biomedical
Corp.,
Blue
Bell,
PA
-----------------------------------------------------HIV/Vaccines, research
Enhanced Level and Quality of Memory T Cells Elicited by a Replicating AdHIVenv and -HIVtat Prime/Protein Boost Regimen Compared to Tat- or EnvOnly Regimens
KUATE S., Demberg, T., McKinnon, K., Srivastava, I., DiPasquale, J., Hidaiat, R., Patterson,
L., Barnett, S., and Robert-Guroff, M.
,Banff, AB; Canada, 237 ,2010
1) Vaccine Branch, NCI, Bethesda, MD; 2) Novartis Vaccines and Diagnostics, Cambridge,
MA
-----------------------------------------------------HIV/Vaccines, research
Vaccine Antigen Designs to Address HIV Variability
KORBER B.
,Banff, AB; Canada, 026 ,2010
T6, Theoretical Biology, Los Alamos National Laboratory, Los Alamos, NM, 87545, USA
-----------------------------------------------------HIV/Vaccines, research
RAd Prime/RLCMV Boost Vaccination Induces Long-Lasting HIV-1 Specific
Humoral and Cellular Immune Responses in Mice
LINGSHU WANG, Cheng, Cheng, Ko, S., Kong, W., Flatz, L., Schwartz, R., Gall, J., and
Nabel, G.
,Banff, AB; Canada, 438 ,2010
1) Vaccine Research Center, NIAID/NIH, 40 Convent Drive, Bethesda, MD 20892; 2) GenVec,
Inc,
65
West
Watkins
Mill
Road,
Gaithersburg,
MD
20878
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HIV/Vaccines, research
Cytotoxic Capacity of SIV-Specific-CD8+T Cells From SIV-Infected Rhesus
Macaques Measured Against Primary Autologous CD4+T Cells
MENDOZA D., Migueles, S., Rood, J., Franchini, G., Schneider, D., Trivett, M., Trubev, C.,
Coalter, V., Lifson, J., and Connors, M.
,Banff, AB; Canada, 306 ,2010
1) HIV-Specific Immunity Section, Laboratory of Immunoregulation, NIAID/NIH; 2)
Vaccine Branch, NCI/NIH Bethesda, MD 20892; 3) AIDS and Cancer Virus Program, SAICFrederick,
Inc.,
Frederick,
MD
21702
-----------------------------------------------------HIV/Vaccines, research
Vaccine Design: Lessons From Acute HIV-1 Infection
MCMICHAEL A., Goonetilleke, N., Liu, M., Borrow, P., Gray, C., Ferrari, G., Tomaras, G.,
Shaw, G., Hahn, B., Feng, Gao, Korber, B., Perelson, A., Letvin, N., Cohen, M., and Haynes,
B.
,Banff, AB; Canada, 007 ,2010
1) Oxford University; 2) National Institute for Communicable Diseases Johannesburg; 3)
Duke University; 4) University of Alabama at Birmingham; 5) Los Alamos National
Laboratory; 6) Harvard University; 7) University of North Carolina Chapel Hill
-----------------------------------------------------HIV/Vaccines, research
GB Virus C Envelope Protein E2 Elicits Polyvalent Antibodies That Cross-React
With HIV-1 Gp41 MPER (T-20) and Lipids
MCLINDEN J., Jinhua, Xiang, Mohr, E., Kaufman, T., Qing, Chang, and Stapleton, J.
,Banff, AB; Canada, 415 ,2010
-----------------------------------------------------HIV/Vaccines, research
Cross-Reactive Anti-HIV Neutralizing Antibody Responses During Acute / Early
HIV Infection
MIKELL I., Altfeld, M., Alter, G., and Stamatatos, L.
,Banff, AB; Canada, 361 ,2010
1) Seattle Biomedical Research Institute, Seattle, WA98109; 2) Department of Global Health,
University of Washington, Seattle, WA 98109; 3) Ragon Institute of Massachusetts General
Hospital, Massachusetts Institute of Technology and Harvard University, Boston, MA02114
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HIV/Vaccines, research
Adjuvant Effect on the Induction of Glycan-Specific Antibodies Against HIV
Env Using Single Yeast Glycoproteins
LUALLEN R., Hu, Fu, Bingfen, Liu, Doms, R., and Yu, Geng
,Banff, AB; Canada, 250 ,2010
1) ProSci Inc., Poway, CA; 2) Department of Microbiology, University of Pennsylvania,
Philadelphia,
PA
-----------------------------------------------------HIV/Vaccines, research
HIV Fragment Vaccine Induces Broader T Cell Response in Mice
LIU YE, Li, fusheng, Liu, yong, Hong, kunxue, Meng, xin, Chen, jianping, Sun, maosheng,
Self, S., and Shao, yiming
,Banff, AB; Canada, 248 ,2010
1) State Key Laboratory for Infectious Disease Prevention and Control, National Center for
AIDS/STD Control and Prevention, Chinese Center for Disease Control and Prevention,
Beijing, China; 2) Statistical Center for HIV/AIDS Research and Prevention, Fred Hutchinson
Cancer Research Center, 1100 Fairview Avenue N, Seattle, WA98109, USA; 3) Institute of
Medical Biology, Chinese Academy of Medical Sciences and Peking Union Medical College,
Kunming,
China
-----------------------------------------------------HIV/Vaccines, research
The Antiviral Efficacy of HIV-Specific CD8+ Tcells to a Conserved Epitope Is
Heavily Dependent on the Infecting HIV-1 Isolate
RANASINAHE S., Kramer, H., Wright, C., Kessler, B., de, Gleria K., Zhang, Y., Gillespie, G.,
Blais, M., Pichulik, T., Simmons, A., Rowland-Jones, S., McMichael, A., and Dona, T.
,Banff, AB; Canada, 344 ,2010
Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, U.K
-----------------------------------------------------HIV/Vaccines, research
HIV/SIV Vaccine Efficacy Dependent on the Dose of SIVmac251 Challenge
Exposure in Macaques
VACCARI M., Hryniewicz, A., Doster, M., Tsai, W., Venzon, D., Fenizia, C., Morgan, T.,
Poonam, P., Pavlakis, G., Felber, B., and Fmnchini, G.
,Banff, AB; Canada, 431 ,2010
1) Animal Models and Retroviral Vaccines Section; 2) Biostatistics and Data Management
Section, NCI, NIH, Bethesda, Maryland 20892; 3) Human Retrovirus Section, Frederick,
Maryland 21702-1201; 4) Human Retrovirus Pathogenesis Section, NCI-Frederick, NIH,
Frederick,
Maryland
21702-1201
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HIV/Vaccines, research
TSLP, a Promising New Mucosal Adjuvant for Intranasal Immunisation With
Gp140
VAN ROEY G., Arias, M., Tregoning, J., and Shattock, R.
,Banff, AB; Canada, 434 ,2010
Department of Cellular and Molecular Medicine, St George's University of London, London
SW17
ORE,
UK
-----------------------------------------------------HIV/Vaccines, research
Innate and Adaptive Immune Correlates of Vaccine-Induced Control of Mucosal
Transmission of SIV in Macaques
YONGJUN SUI, Qing, Zhu, Gagnon, S., Dzutsev, A., Terabe, M., Vaccari, M., Venzon, D.,
Klinman, D., Strober, W., Kelsall, B., Franchini, G., Belvakov, laor M., and Berzofsky, J.
,Banff, AB; Canada, 114 ,2010
1) Vaccine Branch, Bethesda, MD 20892; 2) Laboratory of Experimental Immunology,
National Cancer Institute, Bethesda, MD 20892; 3) Laboratory of Host Defenses, Bethesda,
MD 20892; 4) Laboratory of Molecular Immunology, National Institute of Allergy and
Infectious
Disease,
National
Institutes
of
Health,
Bethesda,
MD
20892
-----------------------------------------------------HIV/Vaccines, research
Deciphering HIV Epitope Production: Implications for Immunogen Design
ZHANG S., Lazaro, E., Zhang, M., and Le, Gall S.
,Banff, AB; Canada, 015 ,2010
Ragon Institute of MGH, MIT and Harvard, Harvard Medical School, Boston MA 02129,
USA
-----------------------------------------------------HIV/Vaccines, research
Biochemical, Biophysical Characterization and Immunogenicity of HIV
Envelopes Derived From Clade C Primary Early Isolates
ZAMBONELLI C., Dubey, A., Nandi, A., Matsuoka, K., Hartog, K., Wininger, M., Smith, L.,
Dey, A., Franti, M., Barnett, S., and Srivastava, I.
,Banff, AB; Canada, 448 ,2010
1) Protein Biochemistry, Cambridge, MA 02139; 2) Molecular Microbial Biology, Novartis
Vaccines and Diagnostics, 350 Massachusetts Avenue, Cambridge, MA 02139
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HIV/Vaccines, research
AS01, an Adjuvant System Potentiating Vaccines Against Complex Pathogens
VOSS G.
,Banff, AB; Canada, 025 ,2010
GlaxoSmithKline
Biologicals,
------------------------------------------------------
Rixensart,
Belgium
HIV/Vaccines, research
The Effect of Vaccine-Induced SIV-Specific Immune Response on Viral
Acquisition and Replication
WATKINS D.
,Banff, AB; Canada, 028 ,2010
1) Department of Pathology and Laboratory Medicine, University of Wisconsin-Madison,
Madison, Wisconsin; 2) Wisconsin National Primate Research Center, University of
Wisconsin-Madison,
Madison,
Wisconsin
-----------------------------------------------------HIV/Vaccines, research
Oral Vaccination With Lipid Vehicle-Entrapped Multivalent HIV Peptides
Enhances Specific Immune Responses
SAAD A., Sirskgj, D., Le, T., Anderson, D., Torres, J., Kumar, A., az-Mitoma, F., and Azizi, A.
,Banff, AB; Canada, 111 ,2010
1) Department of Pathology and Laboratory Medicine & Department of Microbiology and
Immunology, University of Ottawa, Ottawa, Canada; 2) Vaccine Research Center, Children's
Hospital of Eastern Ontario, Ottawa, Canada; 3) Variation Biotechnologies Inc, Ottawa,
Canada; 4) Davis School of Medicine, University of California, Davis, CA, USA
-----------------------------------------------------HIV/Vaccines, research
VSV Vectors Expressing Chimeric SIV Envelope Proteins Direct Antibody
Response Against Gp41
SCHELL J., Buonocore-Buzzelli, L., and Rose, J.
,Banff, AB; Canada, 402 ,2010
Department of Pathology, Yale University School of Medicine, New Haven, CT, USA
-----------------------------------------------------HIV/Vaccines, research
Macaques Vaccinated With SlVmac239?Nef Delay Acquisition and Control
Replication After Repeated Low Dose Heterologous SIV Challenge
REYNOLDS M., Weiler, A., Piaskouwski, S., Kolar, H., Weiker, M., Weisgrau, K.,
MakouVSky, R., McDermott, A., Boyle, R., Allison, D., Wilson, N., Koff, W., and Watkins, D.
,Banff, AB; Canada, 345 ,2010
1) AIDS Vaccine Research Laboratory, University of Wisconsin-Madison, Madison,
Wisconsin, 53711, USA; 2) lnternationalAIDS Vaccine Initiative, New York, New York 10038,
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EUROPRISE SCIENCE UPDATE 10-17
USA; 3) Department of Biostatistics, Section on Statistical Genetics, University of Alabama at
Birmingham, Birmingham, Alabama 35294, USA; 4) Department of Pathology and
Laboratory Medicine, University of Wisconsin-Madison, Wisconsin, 53711, USA
-----------------------------------------------------HIV/Vaccines, research
Strong Protection Against SIVsmE660 Mucosal Challenge Conferred by a
Novel, Heterologous, Prime-Boost Vaccine Regimen
ROSE N., Diller, K., Buonocore, L., Schell, J., Bahl, K., Hunter, M., Manc, P., Montefiori, D.,
Johnson, P., and Rose, J.
,Banff, AB; Canada, 350 ,2010
1) Department of Pathology, Yale University, New Haven, CT; 2) Tulane University Health
Sciences Center, New Orleans, LA; 3) Duke University Medical Center, Durham, NC; 4)
University
of
Pennsylvania
School
of
Medicine
-----------------------------------------------------HIV/Vaccines, research
HIV-Specific Antibodies Mediate Rapid Antibody-Dependent Cellular
Cytotoxicity Against Primary HIV-Infected CD4+ T Cells
SMALLS-MANTEY A., Klein, R., Doria-Rose, N., Laub, L., Rood, J., Migueles, S., and
Connors, M.
,Banff, AB; Canada, 412 ,2010
HIV-Specific Immunity Section, Laboratory of Immunoregulation, NIAID/NIH, Bethesda,
MD,
20892,
USA
-----------------------------------------------------HIV/Vaccines, research
HIV-1 Epidemic in India: Deciding the Decisive Lmmunogenetic Correlates for
Designing Vaccine Strategies
SHARMA G., Kaur, G., Singh, P., Vajpayee, M., Sharma, S., and Mehra, N.
,Banff, AB; Canada, 406 ,2010
1) Department of Transplant Immunology and Immunogenetics, All India Institute of
Medical Sciences, Ansari Nagar, New Delhi-110029, India; 2) Department of Microbiology,
All India Institute of Medical Sciences, Ansari Nagar, New Delhi-110029, India; 3)
Department of Medicine, All India Institute of Medical Sciences, Ansari Nagar, New Delhi110029,
India
-----------------------------------------------------HIV/Vaccines, research
Characterization of Neutralizing Quaternary Epitope Exposure on Soluble HIV-1
Env Constructs
DAVENPORT T., Robinson, J., and Stamatatos, L.
,Banff, AB; Canada, 137 ,2010
1) Pathobiology Program, Department of Global Health, University of Washington, Seattle,
Washington, 98195, USA; 2) Department of Pediatrics, Tulane University Medical Center,
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EUROPRISE SCIENCE UPDATE 10-17
New
Orleans,
Louisiana,
------------------------------------------------------
70012,
USA
HIV/Vaccines, research
HIV-1 Peptides Expressed by Recombinant Modified Vaccinia Virus Ankara
Activate Natural Killer Cells Capable of Controlling HIV Infection in Dendritic
Cells In Vitro
CUMMINGS J., Arnold, V., Yarbrough, K., Didier, C., Levy, Y., Barré-Sinoussi, F., and ScottAlgara, D.
,Banff, AB; Canada, 134 ,2010
ANRS HIV Vaccine Group. Unité de Régulation des Infections Rétrovirales, Institut Pasteur,
Paris,
75724,
France
-----------------------------------------------------HIV/Vaccines, research
Induction of Distinct Clonotypes by Overlapping HLA-A2-Restricted HIV GagEpitopes May Contribute to Their Subdominant Status
COSTANZO M., Li, Jinzhu, Salkowitz, J., Sidney, J., Sette, A., Ng, Hwee L., Yang, O.,
Ayyavoo, V., Price, D., Bansal, A., Goepfert, P., and Kan-Mitchell, J.
,Banff, AB; Canada, 131 ,2010
1) University of Texas at El Paso, El Paso, TX; 2) The La Jolla Institute for Allergy and
Immunology, La Jolla, CA; 3) University of California LosAngeles, LosAngeles, CA; 4)
University of Pittsburg, Pittsburg, PA; 5) Department of Medical Biochemistry and
Immunology, Cardiff University School of Medicine, Cardiff, Wales, UK; 6) University of
Alabama
at
Birmingham,
Birmingham,
AL
-----------------------------------------------------HIV/Vaccines, research
Targeting HIV Peptides to HIV Patient Dendritic Cells Via CD40 Elicits
Expansion of Multi-Epitope Polyfunctional CD4+ and CD8+T Cells
FLAMAR A., Yaming, Xue, Zurawski, S., Montes, M., Bryan, King, Sloan, L., Levy, Y.,
Banchereau, J., and Zurawski, G.
,Banff, AB; Canada, 148 ,2010
Baylor Institute for Immunology INSERM U899 - Center for Human Vaccines, Dallas Texas,
75204, USA; INSERM U841, Faculté de Médecine de Créteil, 94010, France; ANRS Vaccine
Programme,
France
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HIV/Vaccines, research
Live Attenuated SIV: Characterising the Role of Vaccine Persistence in
Protection
BERKHOUT B.
,Banff, AB; Canada, 112 ,2010
Laboratory of Experimental Virology, Department of Medical Microbiology, Academic
Medical
Center,
University
of
Amsterdam,
Amsterdam, The
Netherlands
-----------------------------------------------------HIV/Vaccines, research
Complement As an Endogenous Adjuvant for Dendritic Cell-Mediated Induction
of Retrovirus-Specific CTLs
BÁNKI Z., Posch, W., Ejaz, A., Oberhauser, V., Stoiber, H., Dittmer, U., Dierich, M.,
Hasenkrug, K., and Wilflingseder, D.
,Banff, AB; Canada, 449 ,2010
1) Department of Hygiene, Microbiology and Social Medicine, Innsbruck Medical University,
Innsbruck, Austria; 2) Institute of Virology, University of Duisburg-Essen, Essen, Germany;
3) Laboratory of Persistent Viral Diseases, Rocky Mountain Laboratories, Hamilton, MT,
USA
-----------------------------------------------------HIV/Vaccines, research
Enhanced Mucosal and Systemic Humoral Responses Following Intranasal
Immunization With HIV-1 Gp140 Combined With TLR-4 and Chitosan Adjuvants
ARIAS M., Van, Roey G., Tregoning, J., and Shattock, R.
,Banff, AB; Canada, 110 ,2010
Department of Cellular and Molecular Medicine, St George's University of London, London
SW17
0RE,
UK
-----------------------------------------------------HIV/Vaccines, research
Isolation of Cross-Clade HIV-Neutralizing Human Antibodies From Memory B
Cell Repertoires Using Short Term Culture and High-Throughput Primary
Neutralization Screens
CHAN-HUI P., Wrin, T., Simek, M., Phogat, S., Olsen, O., Hammond, P., Poignard, P.,
Walker, L., Mitcham, J., Fling, S., Team, P., Burton, D., and Moyle, M.
,Banff, AB; Canada, 127 ,2010
1) Theraclone Sciences Inc., Seattle, WA 98104; 2) Monogram Biosciences, South San
Francisco, CA 94080; 3) International AIDS Vaccine Initiative, New York, NY 10038; 4) The
Scripps
Research
Institute,
La
Jolla,
CA
92037
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HIV/Vaccines, research
A High Throughput Screen for Small Molecule Haptens Binding to an HIV-1
Neutralizing Antibody Yields Vaccine Leads
CAULFIELD M., Dudkin, V., Ottinger, E., Getty, K., Zuck, P., Kaufhold, R., Hepler, R.,
McGaughey, G., Citron, M., Hrin, R., Wang, Y., Miller, M., and Jovce, J.
,Banff, AB; Canada, 124 ,2010
1) Department of Vaccine Basic Research; Merck Research Labs, West Point, PA 19486; 2)
Department of Medicinal Chemistry; Merck Research Labs, West Point, PA 19486; 3)
Department of Automated Biotechnology; Merck Research Labs, West Point, PA 19486; 4)
Department of Chemistry Modeling and Informatics; Merck Research Labs, West Point, PA
19486; 5) Department of Antiviral Research; Merck Research Labs, West Point, PA 19486
-----------------------------------------------------HIV/Vaccines, research
Comparison of Intravenous and Low-Dose Rectal SIVmac251 Challenge Models
in the Setting of Adenovirus-Based Immunization
BOLTON D., Kaimei, Song, Kozlowski, P., Keele, B., Rao, S., and Roederer, M.
,Banff, AB; Canada, 117 ,2010
1) ImmunoTechnoloqy Section, Vaccine Research Center (VRC), NIAID, NIH, Bethesda, MD
20892; 2) Gene Therapy Program, LSU Health Sciences Center, New Orleans, LA 70012; 3)
AIDS and Cancer Virus Program, SAIC-Frederick / NCI-Frederick, Frederick, MD 21702; 4)
Laboratory
Animal
Medicine,
VRC
-----------------------------------------------------HIV/Vaccines, research
Recombinant Yellow Fever Vaccine Virus 17D Expressing SlVmac239 Gag
Induces SIV-Specific CD8+ T Cell Responses in Rhesus Macaques
BONALDO M., Martins, M., Rudersdorf, R., Mudd, P., Sacha, J., Piaskowski, S., Costa, Neves
P., Veloso de, Santana M., Vojnov, L., Capuano, S., Rakasz, E., Wilson, N., Fulkerson, J.,
Sadoff, J., Watkins, D., and Galler, R.
,Banff, AB; Canada, 303 ,2010
1) Laboratorio de Biologia Molecular de Flavivírus, Instituto Oswaldo Cruz - FIOCRUZ, Rio
de Janeiro, Brazil; 2) Department of Pathology and Laboratory Medicine, University of
Wisconsin-Madison, Madison, Wisconsin; 3) Wisconsin National Primate Research Center,
University of Wisconsin-Madison, Madison, Wisconsin; 4) Aeras Global TB Vaccine
Foundation, Rockville, MD; 5) Instituto de Tecnologia em Imunobiologicos, Fundação
Oswaldo
Cruz,
Rio
de
Janeiro,
Brazil
------------------------------------------------------
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HIV/Vaccines, research
HIV-1 Envelope-CD4 Receptor Complexes Elicit Broad T- and Bcell Immune
Responses As Well As Cross-Reactive Neutralizing Antibodies in Rhesus
Macaques
BOCRERS W., Davis, D., Mooij, P., Koopman, G., Verschoor, E., Martin, G., Martin, L., PeiJen, Lai R., Dey, A., Yide, Sun, Siddappa, N., Ruprecht, R., Montefiori, D., Burke, B.,
Srivastava, I., Heenev, J., and Barnett, S.
,Banff, AB; Canada, 162 ,2010
1) BPRC, Rijswijk, The Netherlands; 2) CEA, Gif sur Yvette, France; 3) University Cambridge,
Cambridge, UK; 4) Novartis, Cambridge, USA; 5) Dana-Farber Cancer Institute, Boston,
USA;
6)
Duke
University,
Durham,
USA
-----------------------------------------------------HIV/Vaccines, research
Ultra-Deep Sequencing During Acute HIV Infection Reveals the Earliest
Adaptive Changes to Host Selection Pressures
HENN M., Lennon, N., Jessen, H., Nusbaum, C., Altfeld, M., Birren, B., Walker, B., Allen, T.,
Boutwell, C., Malboeuf, C., Power, K., Casali, M., Charlebois, P., Berlin, A., Macalalad, A.,
Gladden, A., Levin, J., Ryan, E., Phillips, L., Erlich, R., Young, S., Green, L., Kemper, M.,
Axten, K., Berical, A., Streeck, H., Yaoyu, Wang, Zedlack, C., Brumme, Z., Brumme, C., Russ,
C., and Rosenberg, E.
,Banff, AB; Canada, 107 ,2010
1) Broad Institute, Cambridge, MA, USA; 2) Ragon Institute of MGH, MIT and Harvard,
Boston,
MA,
USA;
3)
HIV
Clinic
Praxis,
Jessen,
Berlin,
Germany
-----------------------------------------------------HIV/Vaccines, research
Characterization of HIV Epitope-Specific CD8+ T Cell Clonal Repertoires After
Vaccination
HILL B., Darrah, P., Ende, Z., Ambrozak, D., Brenchley, J., Venturi, V., Seder, R., and Douek,
D.
,Banff, AB; Canada, 216 ,2010
1) George Washington Univeristy, Washington, DC; 2) National Institutes of Allergy and
Infectious Diseases, Vaccine Research Center, National Institutes of Health, Bethesda MD
20892; 3) Immunopathogensis Unit, Laboratory of Molecular Biology, National Institutes of
Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892; 4) Center
for Vascular Research, University of New South Wales, Kensington NSW 2052, Austrailia
------------------------------------------------------
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HIV/Vaccines, research
Direct Comparison of Soluble Multimeric Forms of CD40L, CD27L, 4-1 BBL, and
BAFF to IL-12 and IL-15 As HIV DNA Vaccine Adjuvants
KANAGAVELU S., Termini, J., Liguo, Niu, Rivas, Y., Gupta, S., and Stone, G.
,Banff, AB; Canada, 227 ,2010
Department of Microbiology and Immunology, University of Miami, Miami, FL 33136, USA
-----------------------------------------------------HIV/Vaccines, research
Characterization of Simian Adenoviruses As the Base for a New Generation
OfAdenovirus Vaccine Vectors
KAHL C., Mcvey, D., Limbach, P., Balsley, N., Fultz, M., Glenn, A., Grier, R., Hiriyanna, S.,
Hoffman, C., McCullough, T., Moore, V., Semenova, E., Shilpa, Vinod Kumar, Cheng, Cheng,
Kong, W., Ko, S., Lingshu, Wang, Nabel, G., and Gall, J.
,Banff, AB; Canada, 153 ,2010
1) GenVec Inc, 65 W. Watkins Mill Road, Gaithersburg, MD; 2) Vaccine Research Center,
NIAID,
NIH,
Bethesda,
MD
-----------------------------------------------------HIV/Vaccines, research
Design of Improved CD4bs Mimetics for HIV-1 Immunization
KASSLER K. and Sticht, H.
,Banff, AB; Canada, 228 ,2010
Bioinformatics, Institute of Biochemistry, Friedrich- Alexander-Universität ErlangenNürnberg,
Fahrstraße
17,
91054
Erlangen,
Germany
-----------------------------------------------------HIV/Vaccines, research
Immunosafety Assessment of CD4 MAB-Based Bifunctional HIV Entry Inhibitor
(CD4-BFFI) Using In Vitro Immunoassays
KIRSCHENBAUM F., Bohini, S., Kropshofer, H., Cammack, N., Sankuratri, S., and
Changhua, Ji
,San Francisco, CA; USA, 71 ,2010
1) Roche Palo Alto, Palo Alto, USA; 2) Roche Basel, Basel, Switzerland
-----------------------------------------------------HIV/Vaccines, research
Improved Immunogenicity Conferred by Activated but Not Resting Apoptotic
Lymphocytes
JOHANSSON U., BrÅve, A., Sköld, A., Sushil, Kumar Pathak, Walther-Jallow, L., Wahren,
B., Hinkula, J., and Spetz, A.
,Banff, AB; Canada, 414 ,2010
1) Center for Infectious Medicine, Karolinska University Hospital Huddinge, Karolinska
Institutet, Stockholm, Sweden; 2) Department of Microbiology, Tumor and Cell Biology,
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EUROPRISE SCIENCE UPDATE 10-17
Karolinska Institutet, Stockholm, Sweden; 3) Department of Molecular and Clinical
Medicine,
Linkoping
University,
Linkoping,
Sweden
-----------------------------------------------------HIV/Vaccines, research
Comparison of Antibody Responses Induced by a Virus-Like Particle-Based
Vaccine Upon Intramuscular, Pulmonary, and Vaginal Delivery
HUNTER Z., Smyth, H., Durfee, P., and Chackerian, B.
,Baltimore, MD; USA, 48.14 ,2010
1) Biomedical Sciences Dept. of Molecular Genetics & Microbiology, University of New
Mexico, Albuquerque, NM, United States; 2) University of Texas, Austin, TX, United States
-----------------------------------------------------HIV/Vaccines, research
Novel VLPs Rapidly Induce High Titer Neutralizing Antibodies When Combined
With DNA Vaccines in Rabbits
JAWORSKI J., Kovarik, D., Malherbe, D., Brewer, Z., Doria-Rose, N., De, Berardinis P.,
Caivano, A., and Haigwood, N.
,Banff, AB; Canada, 207 ,2010
1) Oregon National Primate Research Center, OHSU, Beaverton, OR 97006; 2) MCB Program,
University of Washington, Seattle, WA 98195; 3) Seattle Biomedical Research Institute,
Seattle, WA 98109; 4) Institute for Protein Biochemistry, Naples, Italy
-----------------------------------------------------HIV/Vaccines, research
Comparative Analysis of Rare Adenovirus Serotypes and Their Effects on
Human Dendritic Cells
JOHNSON M., Petrovas, C., Santos, K., Prabhakar, R., Prout, T., Gall, J., Adams, W., Lore, K.,
Goulet, J., Haddad, E., Sekaly, R., and Koup, R.
,Banff, AB; Canada, 221 ,2010
Vaccine Research Center, NIAID, NIH, Bethesda, MD; GenVec Inc., Gaithersburg, MD;
Karolinska Institute, Stockholm, Sweden; University of Montreal, Montreal, Canada
-----------------------------------------------------HIV/Vaccines, research
Antibodies Elicited by a Heterologous Glycoprotein Mediate a Broad
Neutralization of HIV
JUNG S., Wend, H., Donhauser, N., Eißmann, K., Fleckenstein, B., and Reil, H.
,Banff, AB; Canada, 225 ,2010
University
of
Erlangen,
Department
of
Virology,
Erlangen,
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Germany
EUROPRISE SCIENCE UPDATE 10-17
HIV/Vaccines, research
Lessons Learned From Live Attenuated SIV
JOHNSON R.
,Banff, AB; Canada, 008 ,2010
1) Division of Immunology, New England Primate Research Center, Harvard Medical
School, Southborough, MA 01772; 2) Ragon Institute of Massachusetts General Hospital,
MIT, and Harvard, and Infectious Disease Unit, Massachusetts General Hospital, Boston,
MA
02115
-----------------------------------------------------HIV/Vaccines, research
Targeting the Vaginal Mucosa With Human Papilloma Virus Psudovirions
Delivering SIV DNA Vaccines
GORDON S., Kines, R., Kutsyna, G., Roberts, J., Fenizia, C., Hidajat, R., Cuburu, N., Buck, C.,
Bernardo, M., Robert, Guroff M., Graham, B., Lowy, D., Schiller, J., and Franchini, G.
,Banff, AB; Canada, 202 ,2010
1) Animal Models and Retroviral Vaccines Section, MD 20892; 2) Laboratory of Cellular
Oncology, Vaccine Branch, MD 20892; 3) Center for Cancer Research, National Cancer
Institute, MD 20892; 4) Vaccine Research Center, National Institute of Allergy and Infectious
Diseases, National Institute of Health Bethesda, MD 20892; 5) Science Applications
International Corporation (SAIC)-Frederick, Frederick, Maryland 21702, USA
-----------------------------------------------------HIV/Vaccines, research
NSG-Hu Mice Generate HIV Specific Human Immune Responses After Gp96
Vaccination
GONZALEZ L., Strbo, N., and Podack, E.
,Baltimore, MD; USA, 46.14 ,2010
Microbiology and Immunology, University of Miami Miller School of Medicine, Miami, FL,
United
States
-----------------------------------------------------HIV/Vaccines, research
Immune Activation of Human and Macaque Dendritic Cells and Macrophages
Upon Infection by HIV and Single Cycle SIV Viruses Encoding TRAF- Mediated
Activation Domains
GUNTA S., Termini, J., Liguo, Niu, Kanagavelu, S., Kornbluth, R., Evans, D., and Stone, G.
,Banff, AB; Canada, 205 ,2010
1) Department of Microbiology and Immunology, University of Miami, Miami, FL 33136; 2)
Department of Medicine, University of California, San Diego, La Jolla, CA 92103; 3) New
England Regional Primate Research Center, Harvard Medical School, Southborough, MA
01772
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EUROPRISE SCIENCE UPDATE 10-17
Virology
Molecular Epidemiology of the Transmission of HIV-1 Between Couples in the
Central Area of Portugal
MOTA V., Duque, V., Pereira-Vaz, J., Morais, C., Saraiva-da-Cunha, J., and Meliço-Silvestre,
A.
,Sorrento; Italy, 81 ,2010
1) Hospitais da Universidade de Coimbra, Lab Virologia, Coimbra, Portugal; 2) Hospitais da
Universidade
de
Coimbra,
Serviço
Infecciosas,
Coimbra,
Portugal
-----------------------------------------------------HIV/Virology
Study of the Mutations Associated to Integrase Inhibitor Resistance in Subtype
B and Non-B Human Immunodeficiency Virus Type 1
MONTAGNA C., Falasca, F., Russo, G., Bucci, M., Lichtner, M., Sanou, Sobze M., Graziano,
F., Maida, P., Vullo, V., Antonelli, G., and Turriziani, O.
,Sorrento; Italy, 73 ,2010
1) Sapienza University of Rome, Experimental Medicine Virology section, Rome, Italy; 2)
Sapienza University of Rome, Infectious and Tropical Diseases, Rome, Italy; 3) PIPAD, ONG,
Dschang,
Cameroon
-----------------------------------------------------HIV/Virology
Predictors of Immunological Failure Among Adult Patients Receiving
Antiretroviral Therapy (ART) at an HIV/AIDS Program in Uganda
MUHUMUZA S., Ssempiira, J., Semitala, F., Namusobya, J., and Kamya, M.
,Sorrento; Italy, 56 ,2010
Makerere
University,
Mulago-Mbarara
Joint
AIDS,
Kampala,
------------------------------------------------------
Uganda
HIV/Virology
Diversity of HIV-1 Subtype C Strains Isolated in Romania: a Phylogenetic
Analysis
PARASCHIV S., Foley, B., Florea, D., and Otelea, D.
,Sorrento; Italy, 93 ,2010
1) National Institute for Infectious Diseases M. Bals, Molecular Diagnostics Laboratory,
Bucharest, Romania; 2) HIV Databases, Los Alamos National Laboratory, LosAlamos, USA
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EUROPRISE SCIENCE UPDATE 10-17
HIV/Virology
Resistance Levels in Patients Failing Initial PI or NNRTI Combination Therapy
in Greece
PARASKEVIS D., Detsika, M., Magiorkinis, G., Zavitsanou, A., Magiorkinis, E., Lazanas, M.,
Chini, M., Paparizos, V., Kourkounti, A., Antoniadou, A., Poulakou, G., Sakka, V., Chrysos,
G., Sotiropoulos, A., Sabatakou, H., Daikos, G., Psychogiou, M., Gargalianos, P., Kordossis,
T., Skoutelis, A., Papastamopoulos, V., Georgiou, O., and Hatzakis, A.
,Sorrento; Italy, 80 ,2010
1) University of Athens Medical School, Hygiene Epidemiology and Medical Statistics,
Athens, Greece; 2) Red Cross General Hospital, Infectious Diseases Unit, Athens, Greece; 3)
University of Athens Medical School, "A. Syngros" General Hospital, Athens, Greece; 4)
University of Athens Medical School, Attikon General Hospital, Athens, Greece; 5) Tzaneion
General Hospital, Infectious Diseases Unit, Piraeus, Greece; 6) Hippokration General
Hospital, Infectious Diseases Unit, Athens, Greece; 7) University of Athens Medical School,
Propedeutic Medicine Laikon General Hospital, Athens, Greece; 8) University of Athens
Medical School, "G. Gennimatas" General Hospital, Athens, Greece; 9) University of Athens
Medical School, Pathophysiology Laikon General Hospital, Athens, Greece; 10)
Evangelismos
General
Hospital,
Infectious
Diseases
Unit,
Athens,
Greece
-----------------------------------------------------HIV/Virology
S/GSK1349572, a Next Generation Integrase Inhibitor (INI), Has Potential for a
High Genetic Barrier to Resistance Based on in Vitro Passage Study
KOBAYASHI M., Seki, T., Morimoto, C., Yoshinaga, T., Sato, A., Fujiwara, T., Johns, B., and
Underwood, M.
,Sorrento; Italy, 31 ,2010
1) SHIONOGI & CO. LTD., Discovery Research Laboratories, Osaka, Japan; 2) SHIONOGI &
CO. LTD., Pharmaceutical Development Division, Osaka, Japan; 3) GlaxoSmithKline Inc.,
Medicinal Chemistry, NC, USA; 4) GlaxoSmithKline Inc., Discovery Performance Unit, NC,
USA
-----------------------------------------------------HIV/Virology
The Role of HIV Recombination In Shaping the Current HIV Epidemic
MING ZHANG, Foley, B., Schultz, A., Macke, J., Bulla, I., Stanke, M., Morgenstern, B.,
Korber, B., and Leitner, T.
,Banff, AB; Canada, 160 ,2010
1) Los Alamos National Laboratory, Los Alamos, NM 87545, USA; 2) University of
Göttingen,
37077
Göttingen,
Germany
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HIV/Virology
Structure-Guided Approach for the Development of Molecular-Targeting
Agents for AIDS Therapy
MITSUYA H.
,Osaka; Japan, JS(JSCPT-JPS)-1-3 ,2010
Departments of Hematology, Rheumatology & Clinical Immunology, and Infectious
Diseases, Kumamoto University Graduate School of Medical and Pharmaceutical Sciences,
Kumamoto
860-8556,
Japan
-----------------------------------------------------HIV/Virology
Molecular Epidemiology of HIV-1 Subtypes Circulating in Russia Based on
Analysis of Pol Sequences in Plasma Samples Collected in 2007- 2009
MARLOWE N., Swanson, P., Fang, L., Holzmaye, V., Smith, P., Bruce, R., Thamm, S., and
Hackett, J.
,Sorrento; Italy, 77 ,2010
1) Celera, Research and Development, Alameda, USA; 2) Abbott Diagnostics, Emerging
Pathogens and Virus Discovery, Abbott Park, USA; 3) Abbott GmbH & Co, Abbott Molecular
Europe
Middle
East
Africa
and
India,
Vhiesbaden,
Germany
-----------------------------------------------------HIV/Virology
Pyrosequencing of HIV-1 Reverse Transcriptase to Reveal Minority Populations
of Resistant Virus Before Start of a NNRTI-Based Regimen
VANDEKERCKHOVE L., Vandenbroucke, I., Van, Eygen, V, Winters, B., Vogelaers, D.,
Stuyver, L., and Verhofstede, C.
,Sorrento; Italy, 37 ,2010
1) University Hospital Ghent, General Internal Medicine and Infectious Diseases, Ghent,
Belgium; 2) Virco, Virco, Mechelen, Belgium; 3) University Ghent, Aids Reference
Laboratory,
Ghent,
Belgium
-----------------------------------------------------HIV/Virology
HIV-Infected Patients With Positive MT-2 Cultures May Need More Frequent
Monitoring and/or HAART Initiation at Higher CD4 Counts
VAN 'T WOUT A., van, Sighem A., Welkers, M., Maurer, I., Mangas-Ruiz, M., HarskampHolwerda, A., Prins, J., Brinkman, K., de, Wolf F., Kootstra, N., and Schuitemaker, H.
,Sorrento; Italy, 21 ,2010
1) Academic Medical Center University of Amsterdam, Experimental Immunology,
Amsterdam, The Netherlands; 2) Stichting HIV Monitoring, Research, Amsterdam, The
Netherlands; 3) Academic Medical Center University of Amsterdam, Internal Medicine,
Amsterdam, The Netherlands; 4) Onze Lieve Vrouwe Gasthuis, Internal Medicine,
Amsterdam,
The
Netherlands
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HIV/Virology
Detection of Predicted CXCR4-Using HIV-1 Variants in Longitudinally Obtained
Paired Plasma and PBMC Samples Using 454-Sequencing
VAN 'T WOUT A., Bunnik, E., Swenson, L., Dong, W., Schuitemaker, H., and Harrigan, P.
,Sorrento; Italy, 39 ,2010
1) Academic Medical Center University of Amsterdam, Experimental Immunology,
Amsterdam, The Netherlands; 2) BC Centre for Excellence in HIV/AIDS, Research Labs,
Vancouver,
Canada
-----------------------------------------------------HIV/Virology
HIV-1 Integrase Mutation E157Q Has Low Impact on Integrase Inhibitor
Resistance: a Case Report
WIESMANN F., Braun, P., Van, Houtte M., Voigt, E., Ehret, R., Van, Wesenbeeck L., and
Knechten, H.
,Sorrento; Italy, 33 ,2010
1) PZB Aachen, Department of HIV Research, Aachen, Germany; 2) Virco BVBA, Clinical
Virology, Mechelen, Belgium; 3) Medical practice, Medical practice Cologne, Cologne,
Germany
-----------------------------------------------------HIV/Virology
HIV Drug Resistance in Children With Treatment Failure to First-Line Regimens
in Ho Chi Minh City, Vietnam
VO THI T., Colby, D., Khanh, T., Viet, T., Doanh, L., Tho, N., Thuy, H., An, B., and Giang, L.
,Sorrento; Italy, 63 ,2010
1) Hospital for Tropical Diseases, HAIVN Project, Ho Chi Minh, Vietnam; 2) Beth Israel
Deaconess Medical Center, HAIVN Project in Vietnam, Ho Chi Minh, Vietnam; 3) Pediatrics
Hospital Number 1, Infectious Diseases, Ho Chi Minh, Vietnam; 4) Pediatrics Hospital
Number 2, Infectious Diseases, Ho Chi Minh, Vietnam; 5) Harvard Medical School, HAIVN
Project in Vietnam, Ho Chi Minh, Vietnam; 6) Tam Binh Orphanage, Infectious Diseases, Ho
Chi Minh, Vietnam; 7) Provincial AIDS Committee, Care and Treatment Unit, Ho Chi Minh,
Vietnam
-----------------------------------------------------HIV/Virology
Determinants of Virological Response to Raltegravir (RAL)-Containing
Regimens and Prevalence of RAL-Resistance Associated Mutations at Failure
in ARCA
RUSCONI S., Vitiello, P., Adorni, F., Bruzzone, B., De, Luca A., Micheli, V., Meraviglia, P.,
Maserati, R., Di, Pietro M., Colao, G., Penco, G., Di, Biagio A., Punzi, G., Monno, L., and
Zazzi, M.
,Sorrento; Italy, 27 ,2010
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HIV/Virology
Evaluation of Drug Resistance Among HIV-1 B, C and F Subtypes Drug-Treated
Patients Followed in Central Italy
SANTORO M., Alteri, C., Ronga, L., Flandre, F., Mercurio, F., D'Arrigo, R., Gori, C.,
Palamara, G., Bertoli, A., Forbic, F., Salpini, R., Stazi, F., Boumis, E., Tozzi, V., ViscoComandini, U., Zaccarelli, M., Van, Houtte M., Pattery, T., Narciso, P., Antinori, A.,
Ceccherini-Silberstein, F., and Perno, C.
,Sorrento; Italy, 87 ,2010
1) University of Rome Tor Vergata, Experimental Medicine and Biochemical Sciences, Rome,
Italy; 2) Hôpital Pitié-Salpetrière, Paris, France; 3) INMI L Spallanzani, Antiviral Drug
Monitoring Unit, Rome, Italy; 4) IRCCS San Gallicano, Rome, Italy; 5) University Hospital
Tor Vergata, Molecular Virology, Rome, Italy; 6) INMI L Spallanzani, Infectious Diseases
Division,
Rome,
Italy;
7)
Virco
BVBA,
Mechelen,
Belgium
-----------------------------------------------------HIV/Virology
Characterisation of HIV-1 From Patients With Virological Failure to a Boosted
Protease Inhibitor Regimen
RATHCKE LILLEMARK M., Gerstoft, J., Obel, N., Kronborg, G., Pedersen, C., Bruun,
Jørgensen L., Vasehus, Madsen T., and Katzenstein, T.
,Sorrento; Italy, 14 ,2010
1) Statens Serum Institut, Department of Virology, Copenhagen, Denmark; 2) University
Hospital of Copenhagen, Department of Infectious Diseases, Copenhagen, Denmark; 3)
University Hospital of Copenhagen, Department of Infectious Diseases, Hvidovre, Denmark;
4) Odense University Hospital, Department of Infectious Diseases, Odense, Denmark
-----------------------------------------------------HIV/Virology
Raltegravir Genetic Resistance Patterns in HIV-2 Infected Patients Failing
Raltegravir-Containing Regimen
ROGUEBERT B., Matheron, S., Bénard, A., Leleu, J., Tubiana, R., Karmochkine, M., Chêne,
G., Damond, F., Brun-Vézinet, F., and Descamps, D.
,Sorrento; Italy, 99 ,2010
4) Pitié-Salpêtrière Hospital, Infectious Diseases, Paris, France; 5) HEGP Hospital, Infectious
Diseases, Paris, France; 6) French HIV-2 ANRS cohort CO5; 1) Bichat-Claude Bernard
Hospital, Virology, Paris, France; 2) Bichat-Claude Bernard Hospital, Infectious Diseases,
Paris,
France;
3)
INSERM
U593,
Statistics,
Bordeaux,
France
-----------------------------------------------------HIV/Virology
Severe Immune Suppression in Patients Exclusively Infected With HIV-1 R5
Variants Is Associated With a Higher Net Charge in Gp120 Variable Regions
SECLÉN E., González, M., Gonzalez-Lahoz, J., Soriano, V., and Poveda, E.
,Sorrento; Italy, 47 ,2010
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EUROPRISE SCIENCE UPDATE 10-17
Hospital
Carlos
III,
Department
------------------------------------------------------
of
Infectious
Diseases,
Madrid,
Spain
HIV/Virology
Consecutive Increase of HIV-1 Transmitted Drug Resistance Rate in Poland
STANCZAK G., Stanczak, J., Firlag-Burkacka, E., Wiercinska-Drapalo, A., Dyda, T., Zabek,
P., Cieply, J., and Horban, A.
,Sorrento; Italy, 72 ,2010
1) Hospital for Infectious Diseases, Molecular Diagnostics Laboratory, Warsaw, Poland; 2)
Hospital for Infectious Diseases, Outpatient Clinic, Warsaw, Poland; 3) Medical University of
Warsaw,
Infectious
Diseases
Department,
Warsaw,
Poland
-----------------------------------------------------HIV/Virology
HIV-1 Tropism and Drug Resistance Mutations in Subtype C-Infected Patients
From KwaZulu Natal
SINGH A., Sunpath, H., Page, T., Padayachi, N., Hiramen, K., Padayachi, N., Murphy, R.,
Coovadia, H., and Kuritzkes, D.
,Sorrento; Italy, 92 ,2010
1) University of Kwazulu Natal Nelson R Mandela School of Medicine Doris Duke Medical
Research Institute, HIV Pathogenesis Programme, Durban, South Africa; 2) McCord
Hospital, Durban, South Africa; 3) Massachusetts General Hospital, Boston, USA; 4)
University of Kwazulu Natal Nelson R Mandela School of Medicine Doris Duke Medical
Research Institute, Department of Paediatrics and Child Heath, Durban, South Africa; 5)
Harvard
Medical
School,
Division
of
AIDS,
Boston,
USA
-----------------------------------------------------HIV/Virology
Primary Resistance to Maraviroc in a Large Set of V3 Sequences From Recent
Seroconverters, Drug-Naïve, and Antiretroviral-Experienced HIV+ Patients
SECLÉN E., González, M., Zahonero, N., Lapaz, M., Corral, A., Rodríguez, C., del, Romero J.,
Aguilera, A., De, Mendoza C., Soriano, V., and Poveda, E.
,Sorrento; Italy, 19 ,2010
1) Hospital Carlos III, Department of Infectious Diseases, Madrid, Spain; 2) Centro Sanitario
Sandoval, Centro Sanitario Sandoval, Madrid, Spain; 3) Hospital CHUS-Conxo, Department
of
Microbiology,
Santiago
de
Compostela,
Spain
-----------------------------------------------------HIV/Virology
Polymorphisms in the Integrase Gene of Antiretroviral Therapy Naïve Patients
Infected With HIV-1 Non-B Subtypes: The SnoB Study
SIERRA S., Sichtig, N., Kaiser, R., Reuter, S., Bickel, M., Schülter, E., Altmann, A.,
Fätkenheuer, G., Dittmer, U., Pfister, H., and Esser, S.
,Sorrento; Italy, 36 ,2010
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EUROPRISE SCIENCE UPDATE 10-17
1) University of Cologne, Institute of Virology, Cologne, Germany; 2) University of
Duesseldorf, Department of Gastroenterology Hepatology and Infectiology, Duesseldorf,
Germany; 3) University of Frankfurt, Department of Internal Medicine II, Frankfurt,
Germany; 4) Max Planck Institute for Informatics, The Computational Biology and Applied
Algorithmics Department, Saarbruecken, Germany; 5) University of Cologne, Department of
Internal Medicine I, Cologne, Germany; 6) University of Duisburg Essen, Institute of
Virology, Essen, Germany; 7) University of Duisburg Essen, Department of Dermatology,
Essen,
Germany
-----------------------------------------------------HIV/Virology
Transmission of Drug Resistance, X4 Variants and Non-B Subtypes in a Large
Cohort of HIV Recent Seroconverters in Spain
DE MENDOZA C., Rodriguez, C., Aguilera, A., Gutierrez, F., Leiva, P., Eiros, J., Garcia, F.,
Caballero, E., Lapaz, M., and Soriano, V.
,Sorrento; Italy, 69 ,2010
1) Spanish HIV Seroconverter Study Group; 2) Hospital Carlos III, Infectious Diseases,
Madrid, Spain; 3) Centro Sanitario Sandoval, Infectious Diseases, Madrid, Spain; 4) Hospital
CONXO-CHUS, Microbiology, Santiago, Spain; 5) Hospital de Elche, Infectious Diseases,
Elche, Spain; 6) Hospital de Central de Asturias, Microbiology, Oviedo, Spain; 7) Hospital
Clinico, Microbiology, Valladolid, Spain; 8) Hospital Clinico, Microbiology, Granada, Spain;
9)
Hospital
Vall
de
Hebrón,
Microbiology,
Barcelona,
Spain
-----------------------------------------------------HIV/Virology
Phylogenetic Analysis of HIV-1 B and Non-B Subtypes in Newly Diagnosed
Individuals in Ireland
DE GASCUN C., Regan, C., O'Halloran, J., Farrell, G., Coughlan, S., Powderly, W., Bergin,
C., and Hall, W.
,Sorrento; Italy, 91 ,2010
1) University College Dublin, National Virus Reference Laboratory, Dublin, Ireland; 2) Mater
Misericordiae Hospital, Infectious Diseases, Dublin, Ireland; 3) St James' Hospital,
Genitourinary Medicine and Infectious Diseases, Dublin, Ireland; 4) University College
Dublin,
School
of
Medicine
and
Medical
Science,
Dublin,
Ireland
-----------------------------------------------------HIV/Virology
Declining Prevalence of HIV 1 Transmitted Drug Resistance in Ireland 20042008
DE GASCUN C., Regan, C., Coughlan, S., Bergin, C., Powderly, W., and Hall, W.
,Sorrento; Italy, 71 ,2010
1) University College Dublin, National Virus Reference Laboratory, Dublin, Ireland; 2) St
James' Hospital, Genitourinary Medicine and Infectious Diseases, Dublin, Ireland; 3)
University College Dublin, School of Medicine and Medical Science, Dublin, Ireland
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HIV/Virology
Dynamic Escape of Pre-Existing Raltegravir-Resistant HIV-1 From Raltegravir
Pressure
CODOÑER F., Pou, C., Thielen, A., García, F., Delgado, R., Dalmau, D., varez-Tejado, M.,
Clotet, B., RuíZ, L., and Paredes, R.
,Sorrento; Italy, 51 ,2010
1) IrsiCaixa Retrovirology Lab., H. Univ. Germans Trias i Pujol, Badalona, Spain; 2) Max
Planck Institute für Informatik, MPI, Saarbücken, Germany; 3) Servicio de Microbiologia,
Hospital San Cecilio, Granada, Spain; 4) Servicio de Microbiologia, Hospital 12 de Octubre,
Madrid, Spain; 5) Servei de Malalties Infeccioses, Mútua de Terrassa, Terrassa, Spain; 6)
Applied Science, Roche Diagnostics SL, Sant Cugat del Vallès, Spain; 7) IrsiCaixa
Retrovirology Lab & Lluita contra la SIDA Fndn, Internal Medicine Department H. Univ.
Germans
Trias
i
Pujol,
Badalona,
Spain
-----------------------------------------------------HIV/Virology
Resistance Mutations and HIV-1 Genetic Diversity Among Newly Diagnosed
Patients in Two Different Geographical Areas of Spain
CUEVAS M., Delgado, E., Thomson, M., Fernández-García, A., González-Galeano, M.,
Sánchez-Martínez, M., Pinilla, M., García, V., Sánchez-García, A., and Pérez-Alvarez, L.
,Sorrento; Italy, 84 ,2010
1) Instituto de Salud Carlos III, HIV Biology and Variability Unit, Madrid, Spain; 2) Study
group of HIV-1 newly diagnosed patients in Galicia and the Basque Country
-----------------------------------------------------HIV/Virology
Trends, Along a Decade, of Antiretroviral Resistance in a Newly Diagnosed
HIV-1 Cohort of From Galicia, Spain, Including Diverse Genetic Forms
DELGADO E., Cuevas, M., Fernández-García, A., Thomson, M., es, Ga, Ocampo, A.,
Sánchez-Martínez, M., Ojea de, Castro R., Sánchez-García, A., López-Alvarez, M., García, V.,
Mariño, A., Pinilla, M., Rodríguez, R., and Pérez-Alvarez, L.
,Sorrento; Italy, 85 ,2010
1) Instituto de Salud Carlos III, Biology and Variability of HIV, Majadahonda Madrid, Spain;
2) Hospital Xeral Cies, Infectious Diseases, Vigo Pontevedra, Spain; 3) Complejo Hospitalario
de Pontevedra, Infectious Diseases, Pontevedra, Spain; 4) Hospital Xeral Calde, Infectious
Diseases, Lugo, Spain; 5) Hospital Arquitecto Marcide, Infectious Diseases, Ferrol A Coruña,
Spain; 6) Complejo Hospitalario de Ourense, Infectious Diseases, Ourense, Spain
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Sudden Viral Load Increase As an Indicator of HIV-1 Superinfection in HAARTNaive HIV-Infected Patients
DOYLE T., Ambrose, J., Garcia, A., Strang, A., Foster, G., Cambiano, V., Phillips, A., and
Geretti, A.
,Sorrento; Italy, 89 ,2010
1) UCL medical school, Infection and Immunity, London, United Kingdom; 2) UCL medical
school,
Infection
&
Population
Health,
London,
United
Kingdom
-----------------------------------------------------HIV/Virology
Emergence of Resistance to the New Drug Classes in an Italian National
Database: 2007-2009
DI GIAMBENEDETTO S., Fanti, I., Prosperi, M., Bruzzone, B., Baldanti, F., Penco, G., Meini,
G., Di, Biagio A., Paolini, E., Micheli, V., Meraviglia, P., Chiodera, A., Corsi, P., Gonnelli, A.,
Zazzi, M., and De, Luca A.
,Sorrento; Italy, 70 ,2010
1) Institute of Clinical Infectious Diseases, Catholic University, Rome, Italy; 2) Unit of
Infectious Diseases, Siena University Hospital, Italy; 3) Microbiology and Virology
Laboratory, San Martino Hospital, Genoa, Italy; 4) Unit of Virology, IRCCS San Matteo
Hospital, Pavia, Italy; 5) Clinic of Infectious Diseases, Galliera Hospitals, Genoa, Italy; 6)
Department of Molecular Biology, University of Siena, Italy; 7) Unit of Immunohematology
and Transfusional Medicine, Cremona Hospital, Cremona, Italy; 8) Microbiology Laboratory,
L. Sacco Hospital, Milan, Italy; 9) Second Department of Infectious disease, L. Sacco Hospital,
Milan, Italy; 10) Dept. of Infectious Diseases, H. Macerata, Macerata, Italy; 11) Division of
Infectious Diseases, Careggi University Hospital, Italy; 12) ARCA database
-----------------------------------------------------HIV/Virology
Faster HIV-1 Disease Progression Among Brazilian Recently Infected Individual
Harboring CXCR4 Using Strains
DIAZ R., Sucupira, M., Sanabani, S., Tomiyama, H., Sauer, M., Sabino, E., Janini, L., and
Kallas, E.
,Sorrento; Italy, 65 ,2010
1) Federal University of Sao Paulo, Retrovirology Laboratory, Sao Paulo, Brazil; 2) USP,
Immunology, Sao Paulo, Brazil; 3) USP, Blood Centers, Sao Paulo, Brazil
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HIV/Virology
Evaluation of Hiv-1 Genetic Diversity in Infected Mothers From Two Regions of
Portugal Enrolled in A Study of Mother-To-Child Transmission
BANDEIRA V., Castela, J., Areias, M., Alexandrino, A., and Pádua, E.
,Nice; France ,2010
1)
Lisboa;
2)
Porto,
------------------------------------------------------
Portugal
HIV/Virology
ARV Resistance in HIV-1 From Drug-Naive and Treated Patients in Bulgaria
BESHKOV D., Alexiev, I., Georgieva, V., Karamacheva, L., and Elenkov, I.
,Sorrento; Italy, 78 ,2010
1) Nat. Center of Infectious and Parasitic Diseases, National HIV Confirmatory Lab, Sofia,
Bulgaria; 2) Hospital of Infectious Diseases, Department of Immunodeficiency, Sofia,
Bulgaria
-----------------------------------------------------HIV/Virology
Rega 8: An Improved Genotypic Interpretation System That Significantly
Predicts HIV-Therapy Response for B and Non-B Subtypes
BEHEYDT G., Vercauteren, J., Libin, P., Imbrechts, S., Camacho, R., Clotet, B., De, Luca A.,
Grossman, Z., Kaiser, R., Sonnerborg, A., Torti, C., Van, Wijngaerden E., Zazzi, M., Geretti,
A., Vandamme, A., and Prosperi, M.
,Sorrento; Italy, 50 ,2010
-----------------------------------------------------HIV/Virology
Prevalence of HIV-1 Subtypes and Drug Resistance Mutations in ResRIS, the
National Drug Resistance Database of the Spanish AIDS Research Network
ANTA L., Aguilera, A., Blanco, J., Garcia, F., Iribarren, J., Pérez-Elías, M., Sánchez-Hellín, V.,
Leal, M., Llibre, J., Soriano, V., and De, Mendoza C.
,Sorrento; Italy, 96 ,2010
1) Hospital Carlos III, Infectious Diseases, Madrid, Spain; 2) Hospital Conxo-CHUS,
Microbiology, Santiago de Compostela, Spain; 3) Hospital Clinic, Infectious Diseases,
Barcelona, Spain; 4) Hospital Clinico San Cecilio, Microbiology, Granada, Spain; 5) Hospital
de Donostia, Infectious Diseases, San Sebastián, Spain; 6) Hospital Ramón y Cajal, Infectious
Diseases, Madrid, Spain; 7) Hospital General, Infectious Diseases, Elche, Spain; 8) Hospital
Virgen del Rocio, Infectious Diseases, Sevilla, Spain; 9) Hospital Germans Trias i Pujol,
Infectious Diseases, Badalona, Spain; 10) Resistance Platform of the Spanish AIDS Research
Network
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HIV/Virology
Identification of a New HIV-1 Circulating Recombinant Form (CRF44-DB) in
Spain
ANTA L., Blanco, J., Aguilera, A., García, F., Iribarren, J., Gutiérrez, C., Gutiérrez, F., Leal,
M., Llibre, J., Soriano, V., and De, Mendoza C.
,Sorrento; Italy, 97 ,2010
1) Hospital Carlos III, Infectious Diseases, Madrid, Spain; 2) Hospital Clinic, Infectious
Diseases, Barcelona, Spain; 3) Hospital Conxo-CHUS, Microbiology, Santiago de
Compostela, Spain; 4) Hospital Clinico San Cecilio, Microbiology, Granada, Spain; 5)
Hospital de Donostia, Infectious Diseases, San Sebastián, Spain; 6) Hospital Ramón y Cajal,
Infectious Diseases, Madrid, Spain; 7) Hospital General, Infectious Diseases, Elche, Spain; 8)
Hospital Virgen del Rocio, Infectious Diseases, Sevilla, Spain; 9) Hospital Germans Trias i
Pujol, Infectious Diseases, Badalona, Spain; 10) Spanish AIDS Research Network
-----------------------------------------------------HIV/Virology
HIV-1 Diversity Among Different Risk Groups in Bulgaria
ALEXIEV I., Beshkov, D., Georgieva, V., and Elenkov, I.
,Sorrento; Italy, 94 ,2010
1) Nat. Center of Infectious and Parasitic Diseases, National HIV Confirmatory Laboratory,
Sofia, Bulgaria; 2) Hospital of Infectious Diseases, Department of Immunodeficiency, Sofia,
Bulgaria
-----------------------------------------------------HIV/Virology
Transmitted Drug Resistance in HIV-1 CRF06_Cpx Infected Patients in Estonia
in 2008
AVI R., Huik, K., Pauskar, M., Krispin, T., Karki, T., Ustina, V., and Lutsar, I.
,Sorrento; Italy, 74 ,2010
1) University of Tartu, Institute of Microbiology, Tartu, Estonia; 2) West-Tallinn Central
Hospital,
HIV
Reference
Laboratory,
Tallinn,
Estonia
-----------------------------------------------------HIV/Virology
Mutations at the C-Terminal Domain of RT in HIV-1+ Patients Failing Nevirapine
or Efavirenz Do Not Display Strong Impact on Etravirine Susceptibility
ARREDONDO M., Zahonero, N., Corral, A., Garrido, C., Poveda, E., González-Lahoz, J.,
Soriano, V., and De, Mendoza C.
,Sorrento; Italy, 18 ,2010
Hospital
Carlos
III,
Infectious
Diseases
Department,
Madrid,
Spain
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Impact of Baseline HIV-1 Integrase Polymorphisms With Virological Outcome in
Patients Starting a Raltegravir-Containing Regimen
ARMENIA D., Fabeni, L., Malet, I., D'Arrigo, R., Reigadas, S., Micheli, V., Cento, V., Trotta,
M., Lo, Caputo S., Santoro, M., Svicher, V., Flandre, P., Bruzzone, B., Di, Perri G., Capetti, A.,
Narciso, P., Masquelier, B., Rizzardini, G., Calvez, V., Gomes da, Silva H., Antinori, A.,
Marcelin, A., Perno, C., and Ceccherini-Silberstein, F.
,Sorrento; Italy, 28 ,2010
1) University of Rome "Tor Vergata", Department of Experimental Medicine and Biochemical
Science, Rome, Italy; 2) Pitié-Salpetrière Hospital, Department of Virology and Biological
Immunology, Paris, France; 3) IMMI "L. Spallanzani", Antiviral Drugs Monitoring Unit &
Infectious Disease Divisions, Rome, Italy; 4) Bordeaux University Hospital, Department of
Virology, Bordeaux, France; 5) L. Sacco Hospital, Infectious Disease Division, Milan, Italy; 6)
SM Annunziata Hospital, Infectious Disease Division, Florence, Italy; 7) San Martino
Hospital, Microbiology and Virology Laboratory, Genoa, Italy; 8) University of Turin,
"Amedeo di Savoia Hospital", Department of Infectious Diseases Turin, Italy; 9) Lisbon New
University, Faculty of Medical Sciences, Department of Cellular and Molecular Biology,
Lisbon,
Portugal
-----------------------------------------------------HIV/Virology
Drug Resistance Mutations in HIV-1+ Non-B Subtypes in Spain - More Frequent
and No Preferential Selection of K65R in Clade C Than in Other Subtypes
ARREDONDO M., Sánchez, C., Garrido, C., Anta, L., Fernández, J., Rivas, P., Soriano, V.,
and De, Mendoza C.
,Sorrento; Italy, 95 ,2010
Hospital
Carlos
III,
Infectious
Diseases
Department,
Madrid,
Spain
-----------------------------------------------------HIV/Virology
Decreasing Prevalence and 5-Year Incidence of Major NRTI-, NNRTI- and PIMutations in ART- Experienced HIV-Patients in Stockholm, Sweden
BONTELL I., Johansson, B., Bratt, G., Albert, J., and Sonnerborg, A.
,Sorrento; Italy, 83 ,2010
1) Karolinska Institutet, Department of Medicine, Huddinge, Sweden; 2) Karolinska
Institutet, Department of Laboratory Medicine, Huddinge, Sweden; 3) Stockholm South
General Hospital, Department of Dermato-Veneorology, Stockholm, Sweden; 4) Swedish
Institute for Infectious Disease Control, Department of Virology, Stockholm, Sweden
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HIV/Virology
The Influence of PCR Amplification Variation on the Ability of PopulationBased PCR to Detect Non-R5 HIV
HARRIGAN R., Zhong, X., Lewis, M., Dong, W., Knapp, D., Swenson, L., McGovern, R., and
Heera, J.
,Sorrento; Italy, 38 ,2010
1) BC Centre for Excellence in HIV/AIDS, Research Laboratories, Vancouver, Canada; 2)
Pfizer,
Sandwich,
United
Kingdom;
3)
Pfizer,
New
York,
USA
-----------------------------------------------------HIV/Virology
Integrase Inhibitor Resistance-Associated Mutations Have No Impact on
Performance of the Abbott ReaITime HIV-1 Assay
HACKETT J., Luk, K., and Swanson, P.
,Sorrento; Italy, 43 ,2010
Abbott
Diagnostics,
Virus
------------------------------------------------------
Discovery,
Abbott
Park,
USA
HIV/Virology
HIV Drug Resistance Patterns of Maternal HAART Cohorts to Prevent HIV
Postnatal Mother-to-Child Transmission in Rwanda
KARASI J., Peltier, C., Servais, J., Ndayisaba, G., Makombe, N., Courteille, O., Omes-Karasi,
C., Devaux, C., Schmit, J., and Arendt, V.
,Sorrento; Italy, 53 ,2010
1) Centre de Recherche Public-Santé, Retrovirology Laboratory, Luxembourg, Luxembourg;
2) Lux Development, AMATA Study, Kigali, Rwanda; 3) centre de Recherche Public-Santé,
retrovirology Laboratory, Luxembourg, Luxembourg; 4) National Reference Laboratory,
Immuno-Virology,
Kigali,
Rwanda
-----------------------------------------------------HIV/Virology
Development of Resistance to the Natural HIV-1 Entry Virus Inhibitory Peptide
(VIRIP)
GONZALEZ E., Pau, Mena M., rmand-Ugon, M., Ballana, E., Clotet, B., and Esté, J.
,San Francisco, CA; USA, 65 ,2010
IrsiCaixa,
Badalona,
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Spain
EUROPRISE SCIENCE UPDATE 10-17
HIV/Virology
Residual Activity of Raltegravir Despite Multiple N155H Pathway Resistance
Mutations
FUN A., Van, Baelen K., van, Lelyveld S., Schipper, P., Stuyver, L., Wensing, A., and Nijhuis,
M.
,Sorrento; Italy, 34 ,2010
1) University Medical Center, Dept. of Virology, Utrecht, The Netherlands; 2) Virco BVBA,
Mechelen, Belgium; 3) University Medical Center, Dept. of Internal Medicine, Utrecht, The
Netherlands
-----------------------------------------------------HIV/Virology
Differences in Susceptibility to Darunavir and Etravirine Reported by Two
Genotypic Interpretation Systems
GARCIA F., Alvarez, M., Guillot, V., parra, M., Bernal, S., Lozano, F., Hernández-Quero, J.,
and Palomares, J.
,Sorrento; Italy, 58 ,2010
1) H. Clinico San Cecilio, Microbiology, Granada, Spain; 2) H. U Virgen de Valme,
Microbiology, Sevilla, Spain; 3) H. U Virgen de Valme, Infectious Diseases, Sevilla, Spain; 4)
H.
Clinico
San
Cecilio,
Infectious
Diseases,
Granada,
Spain
-----------------------------------------------------HIV/Virology
Resistance Patterns in HIV+ Patients Failing Raltegravir Outside Clinical Trials
- the Spanish Integrase Resistance (SINRES) Group
GARRIDO PAVON C., Garcia, F., Zahonero, N., Sanchez-Hellin, V., Imaz, A., GarciaBujalance, S., Viciana, I., Galindo, M., Soriano, V., De, Mendoza C., and Sinres Study Group(
,Sorrento; Italy, 35 ,2010
1) Hospital Carlos III, Infectious Diseases, Madrid, Spain; 2) Hospital San Cecilio, Granada,
Spain; 3) Hospital General Universitario, Elche, Spain; 4) Hospital Vall d'Hebrón, Barcelona,
Spain; 5) Hospital La Paz, Madrid, Spain; 6) Hospital Virgen de la Victoria, Málaga, Spain; 7)
Hospital
Clínico,
Valencia,
Spain;
8)
Spain
-----------------------------------------------------HIV/Virology
Resistance Mutations in the Viral Protease Alter the in Vitro Resistance Profiles
of Bevirimat
FUN A., van, Maarseveen N., Maas, R., Schipper, P., and Nijhuis, M.
,Sorrento; Italy, 3 ,2010
University Medical Center, Dept. of Virology, Utrecht,
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The
Netherlands
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Temporal Changes in HIV Drug Resistant Prevalences Across the World.
Review
FRENTZ D., Boucher, C., and van, de, V
,Sorrento; Italy, 68 ,2010
Erasmus
Medical
Center,
Virology,
------------------------------------------------------
Rotterdam,
The
Netherlands
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