During the past four years, H-2 linked control of the autoimmune response of mice to murine thyroglobulin (MTg) was worked out in detail. During the next grant period, we plan to examine the role of non-H-2 genes, especially those concerned with immunoglobulin synthesis, define the idiotype population engaged in this autoimmune response, identify the idiotypes that are related to the pathogenic manifestations, correlate the production of the major pathogenic idiotypes with particular populations of anti-idiotypes and regulatory T-cells, and develop methods for arresting production of the harmful idiotypes. Ultimately the studies of murine thyroiditis will be correlated with findings in human cases of chronic lymphocytic thyroiditis.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis, Diabetes, Digestive and Kidney Diseases (NIADDK)
Type
Research Project (R01)
Project #
5R01AM031632-03
Application #
3152310
Study Section
Immunological Sciences Study Section (IMS)
Project Start
1983-09-01
Project End
1987-06-30
Budget Start
1985-09-01
Budget End
1987-06-30
Support Year
3
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Type
Schools of Public Health
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Kuppers, R C; Suiter, T; Gleichmann, E et al. (1988) The induction of organ-specific antibodies during the graft-vs.-host reaction. Eur J Immunol 18:161-6
Rose, N R (1988) Autoimmune endocrinopathies. In Vivo 2:35-40
Kong, Y M; Simon, L L; Creemers, P et al. (1986) In vitro T cell proliferation and cytotoxicity in murine autoimmune thyroiditis. Mt Sinai J Med 53:46-52
Rose, N R; Burek, C L (1986) Genetic predisposition to thyroid autoimmune disease: introduction. Mt Sinai J Med 53:3-5
Rose, N R; Burek, C L (1985) The genetics of thyroiditis as a prototype of human autoimmune disease. Ann Allergy 54:261-71