Naturally arising Foxp3-expressing CD25+CD4+ regulatory T cells in self-tolerance and autoimmune disease

被引:106
作者
Sakaguchi, S. [1 ]
Setoguchi, R. [1 ]
Yagi, H. [1 ]
Nomura, T. [1 ]
机构
[1] Kyoto Univ, Dept Expt Pathol, Inst Frontier Med Sci, Sakyo Ku, Kyoto 6068507, Japan
来源
CURRENT CONCEPTS IN AUTOIMMUNITY AND CHRONIC INFLAMATION | 2006年 / 305卷
关键词
D O I
10.1007/3-540-29714-6_3
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Naturally arising CD25(+)CD4(+) regulatory T cells, which express the transcription factor Foxp3, play key roles in the maintenance of immunologic self-tolerance and negative control of a variety of physiological and pathological immune responses. The majority of them are produced by the normal thymus as a functionally mature T cell subpopulation specialized for suppressive function. Their generation is in part genetically and developmentally controlled. Genetically determined or environmentally induced abnormality in CD25(+)CD4(+) regulatory T cell development, maintenance, and function can be a cause of autoimmune disease in humans.
引用
收藏
页码:51 / 66
页数:16
相关论文
共 56 条
[1]   Homeostasis of peripheral CD4+ T cells:: IL-2Rα and IL-2 shape a population of regulatory cells that controls CD4+ T cell numbers [J].
Almeida, ARM ;
Legrand, N ;
Papiernik, M ;
Freitas, AA .
JOURNAL OF IMMUNOLOGY, 2002, 169 (09) :4850-4860
[2]   Autoimmune disease as a consequence of developmental abnormality of a T cell subpopulation [J].
Asano, M ;
Toda, M ;
Sakaguchi, N ;
Sakaguchi, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 184 (02) :387-396
[3]  
Bachmann MF, 1999, J IMMUNOL, V163, P1128
[4]   Suppressor T cells in human diseases [J].
Baecher-Allan, C ;
Hafler, DA .
JOURNAL OF EXPERIMENTAL MEDICINE, 2004, 200 (03) :273-276
[5]   Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse [J].
Brunkow, ME ;
Jeffery, EW ;
Hjerrild, KA ;
Paeper, B ;
Clark, LB ;
Yasayko, SA ;
Wilkinson, JE ;
Galas, D ;
Ziegler, SF ;
Ramsdell, F .
NATURE GENETICS, 2001, 27 (01) :68-73
[6]   Autoreactive T cells in healthy individuals [J].
Danke, NA ;
Koelle, DM ;
Yee, C ;
Beheray, S ;
Kwok, WW .
JOURNAL OF IMMUNOLOGY, 2004, 172 (10) :5967-5972
[7]   QTL influencing autoimmune diabetes and encephalomyelitis map to a 0.15-cM region containing I/2 [J].
Encinas, JA ;
Wicker, LS ;
Peterson, LB ;
Mukasa, A ;
Teuscher, C ;
Sobel, R ;
Weiner, HL ;
Seidman, CE ;
Seidman, JG ;
Kuchroo, VK .
NATURE GENETICS, 1999, 21 (02) :158-160
[8]   Continuous activation of autoreactive CD4+ CD25+ regulatory T cells in the steady state [J].
Fisson, S ;
Darrasse-Jèze, G ;
Litvinova, E ;
Septier, F ;
Klatzmann, D ;
Liblau, R ;
Salomon, BL .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 198 (05) :737-746
[9]   Foxp3 Programs the Development and Function of CD4+CD25+ Regulatory T Cells (Reprinted from vol 4, pg 330-336, 2003) [J].
Fontenot, Jason D. ;
Gavin, Marc A. ;
Rudensky, Alexander Y. .
JOURNAL OF IMMUNOLOGY, 2017, 198 (03) :986-992
[10]   EVIDENCE THAT THE T-CELL REPERTOIRE OF NORMAL RATS CONTAINS CELLS WITH THE POTENTIAL TO CAUSE DIABETES - CHARACTERIZATION OF THE CD4+ T-CELL SUBSET THAT INHIBITS THIS AUTOIMMUNE POTENTIAL [J].
FOWELL, D ;
MASON, D .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 177 (03) :627-636