Modulating protective and pathogenic CD4+ subsets via CD137 in type 1 diabetes

Junichiro Irie, Yuehong Wu, Kritika Kachapati, Robert S. Mittler, William M. Ridgway

Research output: Contribution to journalArticlepeer-review

46 Citations (Scopus)


CD137 (TNFRSF9) is an activation-inducible T-cell costimulatory molecule and a member of the tumor necrosis factor (TNF) receptor superfamily. Cd137 is also a candidate gene (in the Idd9.3 interval) for autoimmune diabetes in NOD mice. Here, we demonstrate that anti-CD137 treatment protects NOD mice from diabetes. Anti-CD137-treated mice are not protected from insulitis and still harbor pathogenic T-cells, as demonstrated by transfer studies. Transfer of CD4+, but not CD8+, cells from anti-CD137-treated pre-diabetic NOD mice into NOD-scid mice delayed diabetes onset. Anti-CD137 treatment significantly increased the number of CD4+CD25+ cells, which demonstrated intracellular Foxp3 expression and in vitro suppressive activity. The CD4+CD25+ cell subset from anti-CD137-treated mice transferred complete protection from diabetes, whereas the CD4+CD25- cell subset offered no significant protection. Anti-CD137 treatment of NODscid recipients of diabetic spleen cells, however, hastened the onset of disease, showing that the effect of anti-CD137 treatment depends on the balance of pathogenic and protective cells. These results support a critical role for CD137 acting in the early phase of autoimmune diabetes to enhance regulatory cell production. Disease-associated CD137 alleles are likely ineffectual at stimulating a regulatory T-cell population sufficient to prevent disease.

Original languageEnglish
Pages (from-to)186-196
Number of pages11
Issue number1
Publication statusPublished - 2007 Jan
Externally publishedYes

ASJC Scopus subject areas

  • Internal Medicine
  • Endocrinology, Diabetes and Metabolism


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