Toll-like receptors on regulatory T cells: expanding immune regulation

被引:162
作者
Sutmuller, Roger P. M.
Morgan, Mary E.
Netea, Mihai G.
Grauer, Oliver
Adema, Gosse J. [1 ]
机构
[1] Radboud Univ, Nijmegen Med Ctr, Tumor Immunol Lab, NL-6500 HB Nijmegen, Netherlands
[2] Radboud Univ, Nijmegen Med Ctr, Dept Internal Med, NL-6500 HB Nijmegen, Netherlands
[3] Univ Regensburg, Dept Neurol, D-93053 Regensburg, Germany
关键词
D O I
10.1016/j.it.2006.06.005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Regulatory T (Treg) cells maintain peripheral tolerance and limit effector responses to prevent excessive immune-mediated tissue damage. However, recent research reveals that Treg cells also dampen the induction of immune responses and, thus, must be controlled to enable the effective protection against infections and cancer. Until now, this control of Treg-cell function has been believed to be by communication through cytokines or by stimulation through co-stimulatory molecules on antigen-presenting cells. However, new evidence has demonstrated that Treg cells can also sense pathogens directly through Toll-like receptors (TLRs) and, consequently, modify their behaviour. This review examines the ramifications of TLR engagement on Treg cells and conventional T cells, and discusses the potential role of TLRs on Treg cells and the consequences for disease therapy.
引用
收藏
页码:387 / 393
页数:7
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