The hypothesis underlying the proposed project is that a beta granule associated protein (betaGAP) is the principal antigen for a panel of islet-reactive, diabetogenic T cell clones derived from the NOD mouse. Our primary objective, and the first aim, of the project continuation is to purify this protein antigen to homogeneity in order to obtain a sequence and definitive identification. Under the second aim, we plan to investigate whether antibodies with reactivity to beta granules are directed to the same antigens as T cells.
The third aim i s to analyze T cell receptor (TCR) sequences from the T cell clones to determine whether any distinct patterns of TCR gene usage can be detected. The significance of the proposed work lies in the fact that while a growing number of candidate antigens is being investigated for relevance to diabetes, no one antigen has been identified as the principal target of the autoreactive T cells that mediate disease. Our panel of well- characterized, diabetogenic T cell clones provides one of the best systems available to investigate this question. The value of these T cells as tools to probe disease-relevant beta cell antigens is indicated by two important features: (1) their ability to rapidly induce diabetes in two-week old mice, and (2) all of the diabetogenic clones tested react to a beta granule membrane associated protein, suggesting an immunodominant antigen.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK044132-06
Application #
2414815
Study Section
Immunological Sciences Study Section (IMS)
Program Officer
Akolkar, Beena
Project Start
1992-05-01
Project End
1999-04-30
Budget Start
1997-05-01
Budget End
1999-04-30
Support Year
6
Fiscal Year
1997
Total Cost
Indirect Cost
Name
University of Colorado Denver
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
065391526
City
Aurora
State
CO
Country
United States
Zip Code
80045
Bergman, B; McManaman, J L; Haskins, K (2000) Biochemical characterization of a beta cell membrane fraction antigenic for autoreactive T cell clones. J Autoimmun 14:343-51
Piganelli, J D; Martin, T; Haskins, K (1998) Splenic macrophages from the NOD mouse are defective in the ability to present antigen. Diabetes 47:1212-8
Dallas-Pedretti, A; McDuffie, M; Haskins, K (1995) A diabetes-associated T-cell autoantigen maps to a telomeric locus on mouse chromosome 6. Proc Natl Acad Sci U S A 92:1386-90
Bergman, B; Haskins, K (1994) Islet-specific T-cell clones from the NOD mouse respond to beta-granule antigen. Diabetes 43:197-203