This program project contains four projects, each focusing different aspects of T cell recognition relevant to autoimmunity. The project includes 7 investigators with experience in T cell immunity. Project I is an attempt to identify the antigen or antigens that trigger autoreactive T cells in Insulin Dependent Diabetes Mellitus. It attempts this in the NOD strain of mice and in humans with IDDM. It includes cellular and biochemical approaches, as well as approaches using molecular biology. Project II is an attempt to understand the biochemical and cellular basis of autoimmune myocarditis. Using primarily the model of myocarditid triggered by immunization with heart myosin, the purpose will be to identify the antigenic epitopes and how they are presented to T cells, Project III examines a model of transgenic mice that express the influenza virus hemagglutinin in their beta cells of the islets of Langerhans and which become diabetic. The cellular basis of injury and the biochemistry of recognition will be examined. Project IV examines the basic response of T cells in secondary lymphoid organs from mice expressing a transgene for a known T cell receptor to a peptide from ovalbumin. This is an ideal model to give new insights into the conditions that induce immunity or tolerance.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program Projects (P01)
Project #
1P01AI031238-01
Application #
3092116
Study Section
Special Emphasis Panel (SRC (85))
Project Start
1991-09-01
Project End
1995-07-31
Budget Start
1991-09-01
Budget End
1992-07-31
Support Year
1
Fiscal Year
1991
Total Cost
Indirect Cost
Name
Washington University
Department
Type
Schools of Medicine
DUNS #
062761671
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Hickman-Brecks, Cynthia L; Racz, Jennifer L; Meyer, Debra M et al. (2011) Th17 cells can provide B cell help in autoantibody induced arthritis. J Autoimmun 36:65-75
Hsu, Fong-Fu; Turk, John (2010) Electrospray ionization multiple-stage linear ion-trap mass spectrometry for structural elucidation of triacylglycerols: assignment of fatty acyl groups on the glycerol backbone and location of double bonds. J Am Soc Mass Spectrom 21:657-69
Ise, Wataru; Kohyama, Masako; Nutsch, Katherine M et al. (2010) CTLA-4 suppresses the pathogenicity of self antigen-specific T cells by cell-intrinsic and cell-extrinsic mechanisms. Nat Immunol 11:129-35
Hsu, Fong-Fu; Lakshmi, Vijaya M; Zenser, Terry V (2009) Characterization of new metabolites from in vivo biotransformation of 2-amino-3-methylimidazo[4,5-f]quinoline in mouse by mass spectrometry. J Mass Spectrom 44:1359-68
Studelska, Daniel R; Mandik-Nayak, Laura; Zhou, Xiaodong et al. (2009) High affinity glycosaminoglycan and autoantigen interaction explains joint specificity in a mouse model of rheumatoid arthritis. J Biol Chem 284:2354-62
Oya, Yoshihiro; Watanabe, Norihiko; Owada, Takayoshi et al. (2008) Development of autoimmune hepatitis-like disease and production of autoantibodies to nuclear antigens in mice lacking B and T lymphocyte attenuator. Arthritis Rheum 58:2498-510
Wilker, Peter R; Kohyama, Masako; Sandau, Michelle M et al. (2008) Transcription factor Mef2c is required for B cell proliferation and survival after antigen receptor stimulation. Nat Immunol 9:603-12
Wilker, Peter R; Sedy, John R; Grigura, Vadim et al. (2007) Evidence for carbohydrate recognition and homotypic and heterotypic binding by the TIM family. Int Immunol 19:763-73
Berenson, Lisa S; Gavrieli, Maya; Farrar, J David et al. (2006) Distinct characteristics of murine STAT4 activation in response to IL-12 and IFN-alpha. J Immunol 177:5195-203
Berenson, Lisa S; Yang, Jianfei; Sleckman, Barry P et al. (2006) Selective requirement of p38alpha MAPK in cytokine-dependent, but not antigen receptor-dependent, Th1 responses. J Immunol 176:4616-21

Showing the most recent 10 out of 38 publications