Regulatory T cells prevent catastrophic autoimmunity throughout the lifespan of mice

被引:1416
作者
Kim, Jeong M.
Rasmussen, Jeffrey P.
Rudensky, Alexander Y. [1 ]
机构
[1] Univ Washington, Dept Immunol, Seattle, WA 98195 USA
[2] Univ Washington, Howard Hughes Med Inst, Seattle, WA 98195 USA
关键词
D O I
10.1038/ni1428
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Mice lacking the transcription factor Foxp3 (Foxp3(-)) lack regulatory T (T-reg) cells and develop fatal autoimmune pathology. In Foxp3(-) mice, many activated effector T cells express self-reactive T cell receptors that are expressed in T-reg cells in wild-type mice. Thus, in wild-type mice, most self-reactive thymocytes escaping negative selection are diverted into the T-reg lineage, and whether T-reg cells are critical in self-tolerance in wild-type mice remains unknown. Here, acute in vivo ablation of T-reg cells demonstrated a vital function for T-reg cells in neonatal and adult mice. We suggest that self-reactive T cells are continuously suppressed by T-reg cells and that when suppression is relieved, self-reactive T cells become activated and facilitate accelerated maturation of dendritic cells.
引用
收藏
页码:191 / 197
页数:7
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