The syngeneic or autologous mixed lymphocyte reaction (SMLR) has been defined as a T cell proliferative response to in vitro stimulation with syngeneic or autologous non-T cells, bearing Ia antigens. Although the SMLR has been well characterized, the nature and functional significance of the responding T cells in vivo has not been resolved. To address these issues we have developed a series of T cell clones which recognize self-Ia in the absence of foreign antigens. These cells serve as helper T cells in the proliferation of antigen reactive T cells and alloreactive cytotoxic T cells and trigger the proliferation and differentiation of resting B cells, but in preliminary experiments do not appear to contain antigen reactive T cells. Based on these observations we wish to : 1) determine if autoreactive T cells which respond in the SMLR are antigen responsive T cells; 2) identify a T cell marker specific for autoreactive but not alloreactive T cells and to prepare monoclonal antibodies for the characterization of the T cell receptor which recognizes self-Ia; 3) analyze the immunoregulatory role of autoreactive T cells in vitro and determine the effects of in vivo depletion of SMLR reactive T cells on the immune response; and 4) analyze the basis of the response of normal Lyl+2-/L3T4+ T cells to autoreactive T cells. Experiments have been designed to determine if low affinity T cell receptor interactions with Ia are essential in the triggering of T cells and to analyze the relationship of autoreactive T cell clones to cloned antigen-specific T cell lines. These experiments will utilize a series of well characterized autoreactive T cell clones for preparation of T cell hybridomas and monoclonal antibodies to the T cell receptor for Ia with the ultimate goal of characterizing the T cell receptor for self-Ia and its relationship to the antigen-specific T cell receptor. Our recent observation that normal Lyl+2-/L3T4+ T cells respond specifically to autoreactive T cells suggests that there may be an autoregulatory network and preliminary experiments to investigate the specificity and basis of recognition of this T-T interaction are outlined. These experiments should shed light on the role of autoreactive T cells on regulation of the immune response and may provide insights as to how these cells participate in autoimmunity and neoplasia.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI022132-02
Application #
3132866
Study Section
Immunological Sciences Study Section (IMS)
Project Start
1985-12-01
Project End
1989-11-30
Budget Start
1986-12-01
Budget End
1987-11-30
Support Year
2
Fiscal Year
1987
Total Cost
Indirect Cost
Name
University of Kentucky
Department
Type
Schools of Medicine
DUNS #
832127323
City
Lexington
State
KY
Country
United States
Zip Code
40506
Bryson, J S; Jennings, C D; Caywood, B E et al. (1991) Strain specificity in the induction of syngeneic graft-versus-host disease in mice. Transplantation 51:911-3
Bryson, J S; Jones, L A; Caywood, B E et al. (1990) In vivo regulation of the murine syngeneic mixed lymphocyte reaction. Cell Immunol 129:138-50
Bryson, J S; Jennings, C D; Caywood, B E et al. (1989) Induction of a syngeneic graft-versus-host disease-like syndrome in DBA/2 mice. Transplantation 48:1042-7