Engagement of glucocorticoid-induced TNFR family-related receptor on effector T cells by its ligand mediates resistance to suppression by CD4+ CD25+ T cells

GL Stephens, RS McHugh, MJ Whitters… - The Journal of …, 2004 - journals.aai.org
GL Stephens, RS McHugh, MJ Whitters, DA Young, D Luxenberg, BM Carreno, M Collins…
The Journal of Immunology, 2004journals.aai.org
Abstract Nonactivated CD4+ CD25+ regulatory T cells constitutively express glucocorticoid-
induced TNFR family-related receptor (GITR), a TNFR family member whose engagement
was presumed to abrogate regulatory T cell-mediated suppression. Using GITR−/− mice, we
report that GITR engagement on CD25−, not CD25+ T cells abrogates T cell-mediated
suppression. Mouse APCs constitutively express GITR ligand (GITR-L), which is down-
regulated following TLR signaling in vivo. Although GITR−/− CD25− T cells were capable of …
Abstract
Nonactivated CD4+ CD25+ regulatory T cells constitutively express glucocorticoid-induced TNFR family-related receptor (GITR), a TNFR family member whose engagement was presumed to abrogate regulatory T cell-mediated suppression. Using GITR−/− mice, we report that GITR engagement on CD25−, not CD25+ T cells abrogates T cell-mediated suppression. Mouse APCs constitutively express GITR ligand (GITR-L), which is down-regulated following TLR signaling in vivo. Although GITR−/− CD25− T cells were capable of mounting proliferative responses, they were incapable of proliferation in the presence of physiological numbers of CD25+ T cells. Thus, GITR-L provides an important signal for CD25− T cells, rendering them resistant to CD25+-mediated regulation at the initiation of the immune response. The down-regulation of GITR-L by inflammatory stimuli may enhance the susceptibility of effector T cells to suppressor activity during the course of an infectious insult.
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