This proposal is intended to address the educational activity of this Cooperative Center for TranslationResearch on Human Immunology and Biodefense, entitled; 'Cellular Immunity to Category A-C Viruses inHumans'. In order to accomplish the goal of training new investigators in human immunology it will benecessary to train graduate/post-graduate students, technical professionals and junior faculty in the nextgeneration of functional assays of real time cellular immune responses. We expect this training will be usedfor a broad range of basic viral immunology and translational research projects.The specific educational goals are to develop hands-on 1 to 2-week tutorials in T cell researchmethodologies. The overall initial aim is to recruit highly motivated and experienced graduate and postgraduateresearchers in need of advanced training in new technologies to be applied to their research inhuman and viral immunology. By targeting young investigators we expect broad application of newapproaches to be applied early in the research on Category A-C agents which will lead to more rapidadvancements in understanding the pathogenesis and early detection in patients with these infectiousdiseases. Examples include new FACS techniques, hereafter referred to as tetramer-binding analyses,using soluble multimers of the major histocompatibility complex (MHC) and peptide to directly stain antigenspecificT cells. The proposed educational training will focus on hands-on experimentation and will educatenew laboratories and lead to more rapid insights into the roles of virus-specific T cells in emerging viralthreats. In addition, we believe these tutorial educational approaches will facilitate the development ofstandardized approaches to measuring CMI allowing comparisons to be made across laboratories.Ultimately this will improve both the ability to assess this critical arm of the immune response following viralinfection or vaccination, as well as enable standardization of assays to allow for future comparison of resultsacross study populations.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program--Cooperative Agreements (U19)
Project #
3U19AI057319-05S1
Application #
7698563
Study Section
Special Emphasis Panel (ZAI1-PTM-I (M4))
Project Start
2008-04-15
Project End
2009-03-31
Budget Start
2008-04-15
Budget End
2009-03-31
Support Year
5
Fiscal Year
2008
Total Cost
$207,951
Indirect Cost
Name
University of Massachusetts Medical School Worcester
Department
Type
DUNS #
603847393
City
Worcester
State
MA
Country
United States
Zip Code
01655
Mathew, Anuja (2017) Humanized mouse models to study human cell-mediated and humoral responses to dengue virus. Curr Opin Virol 25:76-80
Ramirez, Alejandro; Co, Mary; Mathew, Anuja (2016) CpG Improves Influenza Vaccine Efficacy in Young Adult but Not Aged Mice. PLoS One 11:e0150425
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Woda, Marcia; Mathew, Anuja (2015) Fluorescently labeled dengue viruses as probes to identify antigen-specific memory B cells by multiparametric flow cytometry. J Immunol Methods 416:167-77
Becerra-Artiles, Aniuska; Dominguez-Amorocho, Omar; Stern, Lawrence J et al. (2015) A Simple Proteomics-Based Approach to Identification of Immunodominant Antigens from a Complex Pathogen: Application to the CD4 T Cell Response against Human Herpesvirus 6B. PLoS One 10:e0142871
Jaiswal, Smita; Smith, Kenneth; Ramirez, Alejandro et al. (2015) Dengue virus infection induces broadly cross-reactive human IgM antibodies that recognize intact virions in humanized BLT-NSG mice. Exp Biol Med (Maywood) 240:67-78
Canetta, Sarah E; Bao, Yuanyuan; Co, Mary Dawn T et al. (2014) Serological documentation of maternal influenza exposure and bipolar disorder in adult offspring. Am J Psychiatry 171:557-63
Yin, Liusong; Stern, Lawrence J (2014) Measurement of Peptide Binding to MHC Class II Molecules by Fluorescence Polarization. Curr Protoc Immunol 106:5.10.1-12

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