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Publication : GITR triggering induces expansion of both effector and regulatory CD4+ T cells in vivo.

First Author  van Olffen RW Year  2009
Journal  J Immunol Volume  182
Issue  12 Pages  7490-500
PubMed ID  19494272 Mgi Jnum  J:149300
Mgi Id  MGI:3848277 Doi  10.4049/jimmunol.0802751
Citation  van Olffen RW, et al. (2009) GITR triggering induces expansion of both effector and regulatory CD4+ T cells in vivo. J Immunol 182(12):7490-500
abstractText  Glucocorticoid-induced TNF receptor family-related protein (GITR) is expressed on activated and regulatory T cells, but its role on these functionally opposing cell types is not fully understood. Here we describe that transgenic expression of GITR's unique ligand (GITRL) induces a prominent increase of both effector and regulatory CD4(+) T cells, but not CD8(+) T cells. Regulatory T cells from GITRL transgenic mice are phenotypically activated and retain their suppressive capacity. The accumulation of effector and regulatory T cells is not due to enhanced differentiation of naive T cells, but is a direct result of increased proliferation. Functional consequences of increased numbers of both regulatory and effector T cells were tested in an autoimmune model and show that GITR stimulation is protective, as it significantly delays disease induction. These data indicate that GITR regulates the balance between regulatory and effector CD4(+) T cells by enhancing proliferation of both populations in parallel.
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