The objectives of this project are to determine the structure and function of the T-cell immune recptor for insulin and to ascertain how its modulation affects antigen specific T-cell activation. These objectives will be accomplished by using established T-cell clones and newly generated T-cell hybridomas reactive with bovine insulin to prepare antibodies that specifically recognize the T-cell immune receptor. These anti-receptor reagents will then be used to invessigate and modulate the biochemical and physiological events which accompany antigen-specific activation of T cells and culminate in final T-cell effector function. The biochemical and functional characterization of the T-cell receptor and the intracellular events it modulates will be critical to our understanding of the factors controlling the antigen-specific response of this immunoregulatory cell. Aberrant regulation of the immune system has been implicated in the etiology of Type I diabetes mellitus and such therapeutic problems as insulin """"""""allergy"""""""" and the development of insulin antibodies. Delineation of the mechanism and consequences of immune T-cell recognition of insulin will allow strategies for specific immunotherapy in diabetes.

Project Start
1984-07-01
Project End
1987-06-30
Budget Start
1985-07-01
Budget End
1986-06-30
Support Year
2
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Type
Schools of Medicine
DUNS #
791277940
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Shapiro, D N; Varani, J; Ginsburg, I (1989) Activation of a murine T-cell hybridoma by cationized bacteria. Immunology 67:478-83
Shapiro, D N; Adams, B S; Niederhuber, J E (1985) Antigen-specific T cell activation results in an increase in cytoplasmic free calcium. J Immunol 135:2256-61
Long, M W; Shapiro, D N (1985) Immune regulation of in vitro murine megakaryocyte development. Role of T lymphocytes and Ia antigen expression. J Exp Med 162:2053-67