Foxp3 Programs the Development and Function of CD4+CD25+ Regulatory T Cells (Reprinted from vol 4, pg 330-336, 2003)

被引:6049
作者
Fontenot, Jason D. [1 ]
Gavin, Marc A. [1 ]
Rudensky, Alexander Y. [1 ]
机构
[1] Univ Washington, Howard Hughes Med Inst, Dept Immunol, Box 357370, Seattle, WA 98195 USA
基金
美国国家卫生研究院;
关键词
POSITIVE SELECTION; MOUSE; AUTOIMMUNITY; ENTEROPATHY; HOMEOSTASIS; SCURFIN; DISEASE; PROTEIN; MICE;
D O I
10.1038/ni904
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CD4(+)CD25(+) regulatory T cells are essential for the active suppression of autoimmunity. Here we report that the forkhead transcription factor Foxp3 is specifically expressed in CD4+CD25+ regulatoryT cells and is required for their development.The lethal autoimmune syndrome observed in Foxp3-mutant scurfy mice and Foxp3-null mice results from a CD4+CD25+ regulatory T cell deficiency and not from a cell-intrinsic defect of (CD4+CD25)-T cells. CD4+CD25+ regulatory T cells rescue disease development and preferentially expand when transferred into neonatal Foxp3deficient mice. Furthermore, ectopic expression of Foxp3 confers suppressor function on peripheral (CD4+CD25)-T cells. Thus, Foxp3 is a critical regulator of CD4+CD25+ regulatoryT cell development and function.
引用
收藏
页码:986 / 992
页数:7
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