T cell-produced transforming growth factor-β1 controls T cell tolerance and regulates Th1- and Th17-cell differentiation

被引:616
作者
Li, Ming O.
Wan, Yisong Y.
Flavell, Richard A.
机构
[1] Yale Univ, Sch Med, Immunobiol Sect, New Haven, CT 06520 USA
[2] Howard Hughes Med Inst, New Haven, CT 06520 USA
关键词
D O I
10.1016/j.immuni.2007.03.014
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
TGF-beta 1 is a regulatory cytokine with a pleiotropic role in immune responses. TGF-beta 1 is widely expressed in leukocytes and stromal cells. However, the functions of TGF-beta 1 expressed by specific lineages of cells remain unknown in vivo. Here, we show that mice with a T cell-specific deletion of the Tgfb1 gene developed lethal immunopathology in multiple organs, and this development was associated with enhanced T cell proliferation, activation, and CD4(+) T cell differentiation into T helper 1 (Th1) and Th2 cells. TGF-beta 1 produced by Foxp3-expressing regulatory T cells was required to inhibit Th1-cell differentiation and inflammatory-bowel disease in a transfer model. In addition, T cell-produced TGF-beta 1 promoted Th17-cell differentiation and was indispensable for the induction of experimental autoimmune encephalomyelitis. These findings reveal essential roles for T cell-produced TGF-beta 1 in controlling differentiation of T helper cells and controlling inflammatory diseases.
引用
收藏
页码:579 / 591
页数:13
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