Regulatory T cell memory

被引:258
作者
Rosenblum, Michael D. [1 ]
Way, Sing Sing [2 ,3 ]
Abbas, Abul K. [4 ]
机构
[1] Univ Calif San Francisco, Dept Dermatol, San Francisco, CA 94143 USA
[2] Cincinnati Childrens Hosp, Div Infect Dis, Cincinnati, OH 45229 USA
[3] Cincinnati Childrens Hosp, Perinatal Inst, Cincinnati, OH 45229 USA
[4] Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94143 USA
关键词
TRANSCRIPTION FACTOR; CUTTING EDGE; LEISHMANIA-MAJOR; EFFECTOR; CD4(+); CD8(+); GENERATION; EXPRESSION; DIFFERENTIATION; SPECIFICITY;
D O I
10.1038/nri.2015.1
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Memory for antigen is a defining feature of adaptive immunity. Antigen-specific lymphocyte populations show an increase in number and function after antigen encounter and more rapidly re-expand upon subsequent antigen exposure. Studies of immune memory have primarily focused on effector B cells and T cells with microbial specificity, using prime-challenge models of infection. However, recent work has also identified persistently expanded populations of antigen-specific regulatory T cells that protect against aberrant immune responses. In this Review, we consider the parallels between memory effector T cells and memory regulatory T cells, along with the functional implications of regulatory memory in autoimmunity, antimicrobial host defence and maternal-fetal tolerance. In addition, we discuss emerging evidence for regulatory T cell memory in humans and key unanswered questions in this rapidly evolving field.
引用
收藏
页码:90 / 101
页数:12
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