Antigen-dependent proliferation of CD4+ CD25+ regulatory T cells in vivo

被引:488
作者
Walker, LSK [1 ]
Chodos, A [1 ]
Eggena, M [1 ]
Dooms, H [1 ]
Abbas, AK [1 ]
机构
[1] Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94143 USA
基金
英国惠康基金;
关键词
CD4(+) T lymphocytes; peripheral tolerance; autoantigen; regulatory T cells; autoimmunity;
D O I
10.1084/jem.20030315
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The failure of CD25(+) regulatory T cells (T-regs) to proliferate after T cell receptor (TCR) stimulation in vitro has lead to their classification as naturally anergic. Here we use T-reg, expressing a transgenic TCR to show that despite anergy in vitro, T-regs proliferate in response to immunization in vivo. T-regs also proliferate and accumulate locally in response to transgenically expressed tissue antigen whereas their CD25(-) counterparts are depleted at such sites. Collectively, these data suggest that the anergic state that characterizes CD25(+) T-regs in vitro may not accurately reflect their responsiveness in vivo. These observations support a model in which T-reg population dynamics are shaped by the local antigenic environment.
引用
收藏
页码:249 / 258
页数:10
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