FOXP3+ regulatory T cells in the human immune system

被引:1916
作者
Sakaguchi, Shimon [1 ,2 ]
Miyara, Makoto [3 ,4 ]
Costantino, Cristina M. [5 ]
Hafler, David A. [6 ,7 ]
机构
[1] Kyoto Univ, Dept Expt Pathol, Inst Frontier Med Sci, Kyoto 6068507, Japan
[2] Osaka Univ, WPI Immunol Frontier Res Ctr, Suita, Osaka 5650871, Japan
[3] Hop La Pitie Salpetriere, AP HP, INSERM,UMR S945, Dept Internal Med 2,Lab Immunochim, F-75013 Paris, France
[4] Hop La Pitie Salpetriere, AP HP, INSERM,UMR S945, Lab Immunol Cellulaire & Tissulaire, F-75013 Paris, France
[5] Mt Sinai Sch Med, Dept Pharmacol & Syst Therapeut, New York, NY 10029 USA
[6] Harvard Univ, Sch Med, Boston, MA 02115 USA
[7] Yale Univ, Dept Neurol & Immunobiol, Sch Med, New Haven, CT 06520 USA
基金
日本学术振兴会;
关键词
IN-VITRO; CUTTING EDGE; SELF-TOLERANCE; GRANZYME-B; CONSTITUTIVELY EXPRESS; MEDIATED SUPPRESSION; EX-VIVO; ACTIVATION; EFFECTOR; NAIVE;
D O I
10.1038/nri2785
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Forkhead box P3 (FOXP3)(+) regulatory T (T-Reg) cells are potent mediators of dominant self tolerance in the periphery. But confusion as to the identity, stability and suppressive function of human T-Reg cells has, to date, impeded the general therapeutic use of these cells. Recent studies have suggested that human T-Reg cells are functionally and phenotypically diverse. Here we discuss recent findings regarding human T-Reg cells, including the ontogeny and development of T-Reg cell subsets that have naive or memory phenotypes, the unique mechanisms of suppression mediated by T-Reg cell subsets and factors that regulate T-Reg cell lineage commitment. We discuss future studies that are needed for the successful therapeutic use of human T-Reg cells.
引用
收藏
页码:490 / 500
页数:11
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