Pancreatic islet-specific T-cell clones from nonobese diabetic mice.

Kathryn Haskins(University of Colorado Health), Mary Portas(University of Colorado Health), Barbara Bergman(University of Colorado Health), K. J. Lafferty(University of Colorado Health), Brenda Bradley(University of Colorado Health)
Proceedings of the National Academy of Sciences
October 1, 1989
Cited by 242Open Access
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Abstract

We have produced a panel of islet-specific T-cell clones from nonobese diabetic (NOD) mice. These clones proliferate and make interleukin 2 in an antigen-specific manner in response to NOD antigen-presenting cells and islet cells. Most of the clones respond to islet-cell antigen from different mouse strains but only in the presence of antigen-presenting cells bearing the class II major histocompatibility complex of the NOD mouse. In vivo, the clones mediate the destruction of islet, but not pituitary, grafts. Furthermore, pancreatic sections from a disease transfer experiment with one of the clones showed a pronounced cellular infiltration and degranulation of islets in nondiabetic (CBA x NOD)F1 recipients.


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