Diabetes, Vol 38, Issue 12 1647-1651, Copyright © 1989 by American Diabetes Association
Prevention of diabetes in NOD mice by injection of autoreactive T-lymphocytes
EP Reich, D Scaringe, J Yagi, RS Sherwin and CA Janeway
Section of Immunobiology, Howard Hughes Medical Institute, New Haven, Connecticut.
The nonobese diabetic (NOD) mouse develops a high incidence of autoimmune
diabetes and is believed to be a good model for insulin-dependent diabetes
mellitus (IDDM) in humans. We isolated T-lymphocyte lines from islets of
newly diabetic NOD mice, some of which are autoreactive to NOD spleen
cells. Because autoreactive T-lymphocytes have been implicated in immune
suppression, we injected NOD mice with an autoreactive T-lymphocyte line.
The injected mice had a marked decrease in incidence of IDDM compared with
control mice. Moreover, their islets showed no insulitis at 1 yr of age. We
conclude that autoreactive T-lymphocytes can prevent the development of
IDDM in NOD mice. This result suggests that 1) islets contain both effector
cells capable of damaging pancreatic beta-cells and cells able to regulate
this autoimmune response, and 2) development of IDDM depends on the balance
between these opposing forces.