ICOS Mediates the Development of Insulin-Dependent Diabetes Mellitus in Nonobese Diabetic Mice
Author(s) -
Daniel Hawiger,
Elise Tran,
Wei Du,
Carmen J. Booth,
Wen Li,
Chen Dong,
Richard A. Flavell
Publication year - 2008
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.180.5.3140
Subject(s) - insulitis , nod mice , nod , diabetes mellitus , endocrinology , insulin , regulator , medicine , cytokine , autoimmune disease , t cell , type 1 diabetes , immunology , autoimmunity , immune system , disease , biology , biochemistry , gene
Initiation of diabetes in NOD mice can be mediated by the costimulatory signals received by T cells. The ICOS is found on Ag-experienced T cells where it acts as a potent regulator of T cell responses. To determine the function of ICOS in diabetes, we followed the course of autoimmune disease and examined T cells in ICOS-deficient NOD mice. The presence of ICOS was indispensable for the development of insulitis and hyperglycemia in NOD mice. In T cells, the deletion of ICOS resulted in a decreased production of the Th1 cytokine IFN-gamma, whereas the numbers of regulatory T cells remained unchanged. We conclude that ICOS is critically important for the induction of the autoimmune process that leads to diabetes.
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