生物
T细胞
实验性自身免疫性脑脊髓炎
细胞生物学
转化生长因子
免疫系统
细胞因子
间质细胞
细胞
T辅助细胞
FOXP3型
免疫学
细胞分化
细胞生长
癌症研究
基因
遗传学
作者
Ming O. Li,Yisong Y. Wan,Richard A. Flavell
出处
期刊:Immunity
[Elsevier]
日期:2007-05-01
卷期号:26 (5): 579-591
被引量:696
标识
DOI:10.1016/j.immuni.2007.03.014
摘要
Summary TGF-β1 is a regulatory cytokine with a pleiotropic role in immune responses. TGF-β1 is widely expressed in leukocytes and stromal cells. However, the functions of TGF-β1 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-β1 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-β1 promoted Th17-cell differentiation and was indispensable for the induction of experimental autoimmune encephalomyelitis. These findings reveal essential roles for T cell-produced TGF-β1 in controlling differentiation of T helper cells and controlling inflammatory diseases.
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