共 123 条
FOXP3+ regulatory T cells in the human immune system
被引:1916
作者:

Sakaguchi, Shimon
论文数: 0 引用数: 0
h-index: 0
机构:
Kyoto Univ, Dept Expt Pathol, Inst Frontier Med Sci, Kyoto 6068507, Japan
Osaka Univ, WPI Immunol Frontier Res Ctr, Suita, Osaka 5650871, Japan Kyoto Univ, Dept Expt Pathol, Inst Frontier Med Sci, Kyoto 6068507, Japan

Miyara, Makoto
论文数: 0 引用数: 0
h-index: 0
机构:
Hop La Pitie Salpetriere, AP HP, INSERM,UMR S945, Dept Internal Med 2,Lab Immunochim, F-75013 Paris, France
Hop La Pitie Salpetriere, AP HP, INSERM,UMR S945, Lab Immunol Cellulaire & Tissulaire, F-75013 Paris, France Kyoto Univ, Dept Expt Pathol, Inst Frontier Med Sci, Kyoto 6068507, Japan

Costantino, Cristina M.
论文数: 0 引用数: 0
h-index: 0
机构:
Mt Sinai Sch Med, Dept Pharmacol & Syst Therapeut, New York, NY 10029 USA Kyoto Univ, Dept Expt Pathol, Inst Frontier Med Sci, Kyoto 6068507, Japan

Hafler, David A.
论文数: 0 引用数: 0
h-index: 0
机构:
Harvard Univ, Sch Med, Boston, MA 02115 USA
Yale Univ, Dept Neurol & Immunobiol, Sch Med, New Haven, CT 06520 USA Kyoto Univ, Dept Expt Pathol, Inst Frontier Med Sci, Kyoto 6068507, Japan
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
相关论文
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Univ Antwerp, Fac Med, Dept Immunol Allergol Rheumatol, B-2610 Antwerp, Belgium
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Roncarolo, Maria-Grazia
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