Stimulation of CD25+CD4+ regulatory T cells through GITR breaks immunological self-tolerance

J Shimizu, S Yamazaki, T Takahashi, Y Ishida… - Nature …, 2002 - nature.com
J Shimizu, S Yamazaki, T Takahashi, Y Ishida, S Sakaguchi
Nature immunology, 2002nature.com
Abstract CD25+ CD4+ regulatory T cells in normal animals are engaged in the maintenance
of immunological self-tolerance. We show here that glucocorticoid-induced tumor necrosis
factor receptor family–related gene (GITR, also known as TNFRSF18)—a member of the
tumor necrosis factor–nerve growth factor (TNF-NGF) receptor gene superfamily—is
predominantly expressed on CD25+ CD4+ T cells and on CD25+ CD4+ CD8− thymocytes in
normal naïve mice. We found that stimulation of GITR abrogated CD25+ CD4+ T cell …
Abstract
CD25+CD4+ regulatory T cells in normal animals are engaged in the maintenance of immunological self-tolerance. We show here that glucocorticoid-induced tumor necrosis factor receptor family–related gene (GITR, also known as TNFRSF18)—a member of the tumor necrosis factor–nerve growth factor (TNF-NGF) receptor gene superfamily—is predominantly expressed on CD25+CD4+ T cells and on CD25+CD4+CD8 thymocytes in normal naïve mice. We found that stimulation of GITR abrogated CD25+CD4+ T cell–mediated suppression. In addition, removal of GITR-expressing T cells or administration of a monoclonal antibody to GITR produced organ-specific autoimmune disease in otherwise normal mice. Thus, GITR plays a key role in dominant immunological self-tolerance maintained by CD25+CD4+ regulatory T cells and could be a suitable molecular target for preventing or treating autoimmune disease.
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