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Chapter 17: Adaptive (specific) Immunity Adaptive Immunity
Chapter 17: Adaptive (specific) Immunity Adaptive Immunity

... • Subsequently, they circulate/reside in blood & various lymphoid tissues ...
BRUCELLOSIS AND THE INNATE IMMUNE SYSTEM (Part 3)
BRUCELLOSIS AND THE INNATE IMMUNE SYSTEM (Part 3)

... Cellular components – All cells of the immune system have their origin in the bone marrow. The myeloid progenitor (stem) cell in the bone marrow gives rise to erythrocytes, platelets, neutrophils, monocytes/macrophages and dendritic cells whereas the lymphoid progenitor (stem) cell gives rise to the ...
VIEW
VIEW

... The ability of T lymphocytes to mount an immune response against a diverse array of pathogens is primarily conveyed by the aminoacid sequence of the hypervariable complementary determining region 3 (CDR3) regions of the T cell receptor (TCR). The genes that encode the two primary types of TCRs, αβ a ...
The Immune system
The Immune system

... Antigen – presenting cells (APC) Dendritic Cells (DC) • DCs are the interface between innate and adaptive immunity • DCs are immature as they circulate waiting to encounter pathogens. At this point, they are highly phagocytic, but not good stimulators of adaptive T cell responses • Once they are ac ...
antigen processing and presentation
antigen processing and presentation

... respectively. CD4 cells recognize antigen plus class II MHC molecules while CD8 cells recognize antigen plus class I MHC molecules. In addition, intercellular adhesion molecules and co-stimulatory molecules are involved in T-cell activation. The humoral immunity can be dependent or independent on T ...
ANTIGEN PROCESSING AND PRESENTATION
ANTIGEN PROCESSING AND PRESENTATION

... antigens, respectively. CD4 cells recognize antigen plus class II MHC molecules while CD8 cells recognize antigen plus class I MHC molecules. In addition, intercellular adhesion molecules and co-stimulatory molecules are involved in T-cell activation. The humoral immunity can be dependent or indepen ...
Antigens and Antibodies
Antigens and Antibodies

Master Answers for the Autoimmune Disease Small group Master
Master Answers for the Autoimmune Disease Small group Master

... macrophages that in turn release pro-inflammatory cytokines that can destroy cartilage. It is not known why and how the complexes home preferentially to joints- it may be that they bind to citrullinated proteins in cartilage. A clinician can intervene at many steps in the process. First-get the pati ...
Lesson 1 - The Immune System
Lesson 1 - The Immune System

... • Memory cells are T cells and B cells that remember specific pathogens. • A vaccination is a substance prepared from killed or weakened pathogens that is introduced into the body to produce immunity. ...
Non-specific (innate) immune system Specific (adaptive) immune
Non-specific (innate) immune system Specific (adaptive) immune

... immune system Includes chemical and physical barriers (the first line of defence) and responses such as inflammation (the second line of defence). Its effects are rapid, shortlived and non-specific. Found in all ...
Molecular Medicine and Gene Therapy
Molecular Medicine and Gene Therapy

... – Gene transfer of cytokines or other immune mediators to augment host immune response – The genetic modification of neoplastic cells to promote immunogenecity – The treatment of localized cancers with genes encloding viral or bacterial enzymes that convert prodrug into toxic metabolits – Transfer o ...
Selling a Product or Service - PC-REF
Selling a Product or Service - PC-REF

... immune system, to fight disease • T-cells identified as the major “soldiers” capable of eliminating cancer (Killer T-cells) “Terminators” • Cancer cells display unique markers or flags (antigen) that can be recognized by Dendritic Cells (DC) “Detectives” • DC to activate T-cells = killer cells to re ...
Stereotyped and specific gene expression programs in human innate immune responses to bacteria.
Stereotyped and specific gene expression programs in human innate immune responses to bacteria.

... humans as hosts for both commensal and pathogenic microorganisms. Innate responses are a crucial element in the body’s defense against the daily threats posed by potential pathogens breaching epithelial barriers; many and perhaps most human cells respond to molecular signs of microbial invasion by i ...
guide2109.ppt [Compatibility Mode]
guide2109.ppt [Compatibility Mode]

... can quickly reach the site of an invasion where they can react directly with antigens - molecules that the body recognizes as foreign substances. When activated, the complement proteins can trigger inflammation attract eater cells such as macrophages to the area coat intruders so that eater cells ar ...
Teaching Slides
Teaching Slides

... Image at: http://imagebank.hematology.org/AssetDetail.aspx?AssetID=4105&AssetType=Asset ...
Primary Immunodeficiencies
Primary Immunodeficiencies

... SCID - low numbers/absence of T cells and sometimes of B cells; lack of B cell functions due to T cell function impairment T-PIDs - normal numbers of T, B, NK cells; T cells are non-functional; B cell function may be affected B-PIDs - B cells non-functional or absent; T and NK cells are normal DNA r ...
When They Say There`s No Hope: Nutritional Approaches to
When They Say There`s No Hope: Nutritional Approaches to

... According to alternative medicine experts, however, a solid, longterm nutritional foundation, coupled with lifestyle modification, can alleviate or even reverse autoimmune dysfunction and help combat fully developed autoimmune diseases. ...
Presentation
Presentation

... – P-selectin: made by platelets and activated (inflammed) endothelium – E-selectin: made by activated (inflammed) endothelium • E- and P-selectin ligands expressed on neutrophils, monocytes, activated T lymphocytes ...
Slide 1
Slide 1

... • The cells of innate immunity interact with one another and with other host cells during the initiation and effector stages of innate and adaptive immune responses ...
Slide 1
Slide 1

... • The cells of innate immunity interact with one another and with other host cells during the initiation and effector stages of innate and adaptive immune responses ...
CELLULAR IMMUNE RESPONSE
CELLULAR IMMUNE RESPONSE

... HUMORAL IMMUNE RESPONSE • Antibody response to T (cell) dependent antigens – Ig receptors on B cell recognize Ag but cross-linking inadequate to activate cell – Therefore need second signal from T helper cell; thus – 1) Ag binds to Ig receptor on B cell as above – 2) Some bound Ag internalized, pro ...
The importance of nutrition in immunity
The importance of nutrition in immunity

... the site of infection. Further, so-called dendritic cells have phagocytotic activity, but their role is not to destroy pathogens. Rather, they function as antigen-presenting cells, displaying elements of ingested antigens on their surface. They are involved in innate immune responses - by producing ...
Bacterial Interactions with Host
Bacterial Interactions with Host

... infectious agents may suppress the host’s immune responses. HIV infects the CD4+ T-helper lymphocytes which lead to the collapse of the immune system. – tuberculosis was more common during the measles outbreak ...
13. Caner Gene Therapy
13. Caner Gene Therapy

... 13. Cancer Gene Therapy 13.1 Introduction  Gene therapy is the insertion of genes into an individual’s cells and tissues to treat a disease, and hereditary diseases in which a defective mutant allele is replaced with a functional one. ...
The Immune System and Effects of the Active Ingredients in Re:Sist
The Immune System and Effects of the Active Ingredients in Re:Sist

... • Non-specific immune stimulation on a general level • Stimulates “early warning system” of epithelial tissues in the gut • Allows immune system to determine appropriate type of response • Increases macrophage activity which indicates a more balanced immune response versus antibody activity • Immune ...
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Immunomics

Immunomics is the study of immune system regulation and response to pathogens using genome-wide approaches. With the rise of genomic and proteomic technologies, scientists have been able to visualize biological networks and infer interrelationships between genes and/or proteins; recently, these technologies have been used to help better understand how the immune system functions and how it is regulated. Two thirds of the genome is active in one or more immune cell types and less than 1% of genes are uniquely expressed in a given type of cell. Therefore, it is critical that the expression patterns of these immune cell types be deciphered in the context of a network, and not as an individual, so that their roles be correctly characterized and related to one another. Defects of the immune system such as autoimmune diseases, immunodeficiency, and malignancies can benefit from genomic insights on pathological processes. For example, analyzing the systematic variation of gene expression can relate these patterns with specific diseases and gene networks important for immune functions.Traditionally, scientists studying the immune system have had to search for antigens on an individual basis and identify the protein sequence of these antigens (“epitopes”) that would stimulate an immune response. This procedure required that antigens be isolated from whole cells, digested into smaller fragments, and tested against T- and B-cells to observe T- and B- cell responses. These classical approaches could only visualize this system as a static condition and required a large amount of time and labor.Immunomics has made this approach easier by its ability to look at the immune system as a whole and characterize it as a dynamic model. It has revealed that some of the immune system’s most distinguishing features are the continuous motility, turnover, and plasticity of its constituent cells. In addition, current genomic technologies, like microarrays, can capture immune system gene expression over time and can trace interactions of microorganisms with cells of the innate immune system. New, proteomic approaches, including T-cell and B-cells-epitope mapping, can also accelerate the pace at which scientists discover antibody-antigen relationships.
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