TGF-β1 maintains suppressor function and Foxp3 expression in CD4+CD25+ regulatory T cells

被引:815
作者
Marie, JC
Letterio, JJ
Gavin, M
Rudensky, AY [1 ]
机构
[1] Univ Washington, Dept Immunol, Seattle, WA 98195 USA
[2] Univ Washington, Howard Hughes Med Inst, Seattle, WA 98195 USA
[3] NCI, Lab Cell Regulat & Carcinogensis, Bethesda, MD 20892 USA
关键词
D O I
10.1084/jem.20042276
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Transforming growth factor (TGF)-beta 1 is a major pluripotential cytokine with a pronounced immunosuppressive effect and its deficiency results in lethal autoimmunity in mice. However, mechanisms of its immunosuppressive action are not completely understood. Here, we report that TGF-beta 1 supports the maintenance of Foxp3 expression, regulatory function, and homeostasis in peripheral CD4(+)CD25(+) regulatory T ( T reg) cells, but is not required for their thymic development. We found that in 8-10-d-old TGF-beta 1-deficient mice, peripheral, but not thymic, T reg cells are significantly reduced in numbers. Moreover, our experiments suggest that a defect in TGF-beta-mediated signaling in T reg cells is associated with a decrease in Foxp3 expression and suppressor activity. Thus, our results establish an essential link between TGF-beta 1 signaling in peripheral T reg cells and T reg cell maintenance in vivo.
引用
收藏
页码:1061 / 1067
页数:7
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