Autoimmune diabetes onset results from qualitative rather than quantitative age-dependent changes in pathogenic T-cells

Diabetes. 2005 May;54(5):1415-22. doi: 10.2337/diabetes.54.5.1415.

Abstract

Diabetogenic T-cells can be detected in pre-diabetic nonobese diabetic (NOD) mice after transfer in NOD-SCID recipients. Here we demonstrate that 6-week-old pre-diabetic NOD mice, >2 months before disease onset, already harbor pathogenic T-cells in equal numbers to overtly diabetic animals. The delay in diabetes appearance is explained by the presence of regulatory CD4+ CD25+ T-cells that control diabetogenic effectors and that are, in our hands, transforming growth factor (TGF)-beta-dependent. Our present results suggest, however, that diabetes onset is only partly explained by a decline in this regulatory T-cell activity. Another major factor appears to be the progressive resistance of diabetogenic cells to TGF-beta-dependent mediated inhibition. We propose that progression to overt disease correlates with the pathogenic T-cell's escape from TGF-beta-dependent T-cell-mediated regulation.

MeSH terms

  • Adoptive Transfer
  • Aging / immunology*
  • Animals
  • CD4-Positive T-Lymphocytes / immunology
  • Cytokines / blood
  • Diabetes Mellitus, Type 1 / immunology*
  • Lymphocyte Activation
  • Mice
  • Mice, Inbred NOD
  • Mice, SCID
  • Receptors, Interleukin-2 / blood
  • Spleen / immunology
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / pathology

Substances

  • Cytokines
  • Receptors, Interleukin-2