The aims of this project are to obtain information from experimental islet transplantation models in rodents which can be applied to the transplantation of islet tissue in humans to reverse insulin dependent diabetes. Three aspects of islet transplantation are to be studied. (1) An investigation of the mechanisms of tolerance which develop in animals carrying cultured allografts and the nature of the antigens that induce this tolerance. This study holds enormous potential for general clinical transplantation in that it may be possible to reduce or eliminate immunosuppression in transplant recipients. (2) A study to investigate the possibility that cell mediated autoimmune attack of islet tissue is restricted by the major histocompatibility complex of the recipient, that is cultured isografts transplanted to spontaneous diabetic animals may be susceptible to autoimmune attack whereas allografts are not. The relationship between the time after onset of disease and the susceptibility of the graft to autoimmune attack will also be investigated. This part of the project has major clinical significance in determining the desirability of matching graft and recipient tissue at the MHC and selecting the optimal time after the onset of disease to transplant islet tissue. (3) To determine the feasibility of using cryopreservation to store fetal proislet tissue. This would allow the development of a bank of donor tissue and would provide the degree of flexibility required if we are to attempt to manipulate the immune system of the recipient prior to transplantation.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis, Diabetes, Digestive and Kidney Diseases (NIADDK)
Type
Research Project (R01)
Project #
5R01AM033470-02
Application #
3152818
Study Section
Surgery, Anesthesiology and Trauma Study Section (SAT)
Project Start
1984-04-01
Project End
1989-03-31
Budget Start
1985-04-01
Budget End
1986-03-31
Support Year
2
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of Colorado Denver
Department
Type
Schools of Medicine
DUNS #
065391526
City
Aurora
State
CO
Country
United States
Zip Code
80045
Gill, R G; Lafferty, K J (1989) Regulation of lymphokine release involving a novel form of T-T collaboration. Transplant Proc 21:2700-2
Gill, R G; Rosenberg, A S; Lafferty, K J et al. (1989) Characterization of primary T cell subsets mediating rejection of pancreatic islet grafts. J Immunol 143:2176-8
Pontesilli, O; Carotenuto, P; Hayward, A R et al. (1989) A cytotoxic monoclonal islet cell surface antibody from the NOD mouse. J Clin Lab Immunol 28:161-8
Haug, C E; Babcock, S K; Lafferty, K J et al. (1988) Islet graft function. Comparison of portal versus systemic venous insulin delivery. Transplantation 45:992-4
Gill, R G; Wang, Y; Lafferty, K J (1988) Spontaneous tolerance induction in adult animals transplanted with allogeneic islets. Transplant Proc 20:61-3
Hao, L; Wang, Y; Gill, R G et al. (1988) CD4 T cells and allograft rejection. Transplant Proc 20:56-60
Hao, L; Wang, Y; Gill, R G et al. (1987) Role of the L3T4+ T cell in allograft rejection. J Immunol 139:4022-6
Wang, Y; Hao, L; Gill, R G et al. (1987) Autoimmune diabetes in NOD mouse is L3T4 T-lymphocyte dependent. Diabetes 36:535-8
Pontesilli, O; Carotenuto, P; Gazda, L S et al. (1987) Circulating lymphocyte populations and autoantibodies in non-obese diabetic (NOD) mice: a longitudinal study. Clin Exp Immunol 70:84-93
Gill, R G; Babcock, S K; Lafferty, K J (1987) A quantitative analysis of antigen-triggered lymphokine production by activated T cells. J Immunol 138:1130-6

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