The dynamic co-evolution of memory and regulatory CD4+ T cells in the periphery

被引:169
作者
Akbar, Arne N. [1 ]
Vukmanovic-Stejic, Milica
Taams, Leonie S.
Macallan, Derek C.
机构
[1] UCL, Dept Immunol & Mol Pathol, Div Infect & Immun, Windeyer Inst Med Sci, London W1T 4JF, England
[2] Kings Coll London, Dept Immunobiol, Guys Hosp, London SE1 9RT, England
[3] St Georges Univ London, Ctr Infect, Div Cellular & Mol Med, London SW17 0RE, England
基金
英国生物技术与生命科学研究理事会;
关键词
D O I
10.1038/nri2037
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Whereas memory T cells are required to maintain immunity, regulatory T cells have to keep the immune system in check to prevent excessive inflammation and/or autoimmunity. Both cell types must be present during the lifetime of the organism. However, it is not clear whether both subsets are regulated in tandem or independently of each other, especially because thymic involution severely restricts the production of T-cell populations during ageing. In this Opinion article, we discuss recent evidence in both mice and humans that supports the hypothesis that some CD4(+)CD25(+)FOXP3(+) regulatory T cells can differentiate from rapidly proliferating memory T cells in the periphery.
引用
收藏
页码:231 / 237
页数:7
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