Prevention of Type I Diabetes in NOD Mice by Adjuvant Immunotherapy

  1. Bhagirath Singh
  1. Department of Immunology and the Muttart Diabetes Research and Training Centre, University of Alberta Edmonton, Alberta, Canada
  1. Address correspondence and reprint requests to Dr. Bhagirath Singh, Department of Immunology, 8-60 Medical Sciences Building, University of Alberta, Edmonton, Alberta T6G 2H7, Canada.

Abstract

The nonobese diabetic (NOD) mouse is an excellent model of insulin-dependent (type I) human diabetes mellitus. We report that a single injection of complete Freund's adjuvant (CFA) given at an early age (5 wk) prevented the appearance of diabetes and greatly increased the life span of NOD mice without additional therapy. No treated mouse developed hyperglycemia by the age of 12 mo (n = 13), whereas all untreated mice died of diabetes before 8 mo of age (n = 38). All CFA-treated mice were alive and healthy at 12 mo of age. Some CFA-treated NOD mice that were monitored for long-term survival are still alive with no sign of disease at 18 mo of age (n = 5). Administration of CFA resulted in decreased in vitro splenic lymphocyte proliferative responses to alloantigen and mitogen. Cell-mixing experiments indicated that antigen-nonspecific inhibitory cells were elicited in the spleen and increased in the bone marrow. These regulatory cells were Thy-1 ; and nonadherent to nylon wool, as has been described for natural suppressor (NS) cells. These data lend support to a relationship between the boosting of endogenous NS activity and the establishment of tolerance to self in the context of autoimmunity. Our results suggest that early nonspecific immunotherapy of genetically predisposed individuals could prevent the development of autoimmune diabetes.

  • Received August 1, 1989.
  • Revision received January 4, 1990.
  • Accepted January 4, 1990.
| Table of Contents