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Charles T. Spencer Ph.D. Affiliation: University of Texas at El Paso Biological Sciences "Infectious and Immunological Diseases","Neurological Disorders and Mental Health","Obesity and Metabolic Syndromes","Women's Health and Reproductive Biology" Title: Dr. Rank: Assistant Professor Address: 500 W University Ave Bioscience Research Building 5.148 El Paso, TX 79968 Contact: Email: [email protected] Telephone: 915 747-8776 Narrative NKT cells are a subset of white blood cells that regulate immune response to bacterial, viral and parasitic infections. They also prevent unwanted immune responses that cause autoimmune diseases such as type I diabetes and multiple sclerosis. Therefore, the objective of the experiments described here is to gain insight into the mechanism(s) by which NKT cells regulate immune responses to infections such as Francisella spp. including Francisella tularensis, F. holarctica, and F. novicida, a relative of F. tularensis which causes tularemic-like disease in mice, Mycobacterium tublerculosis the eitiological agent of tuberculosis, and Listeria monocytogenes (Lm), a common intestinal pathogen that causes food poisoning. All of these bacteria survive in cells of the immune system and are thereby protected from much of the immune response. In order to eliminate this infection, small molecules of the immune system called cytokines must be released into the system to activate the cells where these bacteria survive. NKT cells are capable of releasing numerous cytokines as well as causing or preventing the release of cytokines from other cells. Over-production of cytokines is detrimential to the host so fine control over cytokines is necessary for health. NKT cells appear to be central to this level of control. Awards and Honors 2012 AAI - Travel Award for presentation at Immunology 2012 2013 ASCB Minority Affairs Committee - Professional Development Symposium 2015 2016 ASCB - Faculty Research and Educational Development program 2015 AAI - Travel Award for presentation at Immunology 2015 2016 ASCB - Faculty Research and Educational Development Travel award 2016 AAI - Travel Award for presentation at Immunology 2016 Original Articles 1. Nune KC, Somani MC, Spencer CT & Misra RDK. Materials Technology. Cellular response of Staphylococcus aureus to nanostructured metallic biomedical devices: surface binding and mechanism of disruption of colonization. 2016; 1-10. Publications 1. Duarte TT, Spencer CT. Personalized Proteomics: The Future of Precision Medicine. PubMed Proteomes. 2016; 4(4). 2. Xia M, Hesser DC, De P, Sakala IG, Spencer CT, Kirkwood JS, Abate G, Chatterjee D, PubMed Dobos KM, Hoft DF. A Subset of Protective ?9d2 T Cells Is Activated by Novel Mycobacterial Glycolipid Components. Infect Immun. 2016 Sep; 84(9):2449-62. 3. Abate G, Spencer CT, Hamzabegovic F, Blazevic A, Xia M, Hoft DF. Mycobacterium- PubMed Specific ?9d2 T Cells Mediate Both Pathogen-Inhibitory and CD40 Ligand-Dependent Antigen Presentation Effects Important for Tuberculosis Immunity. Infect Immun. 2015 Dec 07; 84(2):580-9. 4. Spencer CT, Bezbradica JS, Ramos MG, Arico CD, Conant SB, Gilchuk P, Gray JJ, PubMed Zheng M, Niu X, Hildebrand W, Link AJ, Joyce S. Viral infection causes a shift in the self peptide repertoire presented by human MHC class I molecules. Proteomics Clin Appl. 2015 Dec; 9(11-12):1035-52. 5. Gilchuk P, Spencer CT, Conant SB, Hill T, Gray JJ, Niu X, Zheng M, Erickson JJ, Boyd PubMed KL, McAfee KJ, Oseroff C, Hadrup SR, Bennink JR, Hildebrand W, Edwards KM, Crowe JE, Williams JV, Buus S, Sette A, Schumacher TN, Link AJ, Joyce S. Discovering naturally processed antigenic determinants that confer protective T cell immunity. J Clin Invest. 2013 May; 123(5):1976-87. 6. Spencer CT, Dragovic SM, Conant SB, Gray JJ, Zheng M, Samir P, Niu X, Moutaftsi M, PubMed Van Kaer L, Sette A, Link AJ, Joyce S. Sculpting MHC class II-restricted self and nonself peptidome by the class I Ag-processing machinery and its impact on Th-cell responses. Eur J Immunol. 2013 May; 43(5):1162-72. 7. Spencer CT, Abate G, Sakala IG, Xia M, Truscott SM, Eickhoff CS, Linn R, Blazevic A, Metkar SS, Peng G, Froelich CJ, Hoft DF. Granzyme A produced by ?(9)d(2) T cells induces human macrophages to inhibit growth of an intracellular pathogen. PLoS Pathog. 2013 Jan; 9(1):e1003119. 8. Gordy LE, Bezbradica JS, Flyak AI, Spencer CT, Dunkle A, Sun J, Stanic AK, Boothby PubMed MR, He YW, Zhao Z, Van Kaer L, Joyce S. IL-15 regulates homeostasis and terminal maturation of NKT cells. J Immunol. 2011 Dec 15; 187(12):6335-45. PubMed 9. Hoft DF, Babusis E, Worku S, Spencer CT, Lottenbach K, Truscott SM, Abate G, Sakala PubMed IG, Edwards KM, Creech CB, Gerber MA, Bernstein DI, Newman F, Graham I, Anderson EL, Belshe RB. Live and inactivated influenza vaccines induce similar humoral responses, but only live vaccines induce diverse T-cell responses in young children. J Infect Dis. 2011 Sep 15; 204(6):845-53. 10. Spencer CT, Gilchuk P, Dragovic SM, Joyce S. Minor histocompatibility antigens: PubMed presentation principles, recognition logic and the potential for a healing hand. Curr Opin Organ Transplant. 2010 Aug; 15(4):512-25. 11. Lee K, Gudapati P, Dragovic S, Spencer C, Joyce S, Killeen N, Magnuson MA, Boothby PubMed M. Mammalian target of rapamycin protein complex 2 regulates differentiation of Th1 and Th2 cell subsets via distinct signaling pathways. Immunity. 2010 Jun 25; 32(6):743-53. 12. Spencer CT, Abate G, Blazevic A, Hoft DF. Only a subset of phosphoantigen- PubMed responsive gamma9delta2 T cells mediate protective tuberculosis immunity. J Immunol. 2008 Oct 01; 181(7):4471-84. THANK YOU FOR USING THE RTRN RESEARCH COLLABORATION AND PROFESSIONAL NETWORKING SERVICE. RTRN Data Coordinating Center Mississippi e-Center @ Jackson State University 1230 Raymond Road, Box 1800, Jackson, Mississippi 39204 Phone: 601-979-0332, Fax: 601-979-0338, e-mail: [email protected]