The role of the transcription factor Foxp3 in the development of regulatory T cells

被引:135
作者
Kim, Jeong M.
Rudensky, Alexander
机构
[1] Univ Washington, Sch Med, Howard Hughes Med Inst, Seattle, WA 98195 USA
[2] Univ Washington, Sch Med, Dept Immunol, Seattle, WA 98195 USA
关键词
D O I
10.1111/j.0105-2896.2006.00426.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Early studies of mice subjected to neonatal thymectomy and analyses of adoptive T-cell transfer into lymphopenic hosts led to the identification of a specialized subset of regulatory CD4(+) T cells capable of suppressing various manifestations of autoimmunity. Recently, a combination of genetic, molecular, and traditional cellular approaches provided novel powerful means to investigate the biology of these cells. Here, we review earlier and current work from our laboratory, establishing a dedicated function for the transcription factor Foxp3 in the process of regulatory T-cell lineage commitment and a role for TCR- and cytokine-mediated signals in regulation of Foxp3 expression.
引用
收藏
页码:86 / 98
页数:13
相关论文
共 76 条
[41]   Discovering the origins of immunological competence [J].
Miller, JFAP .
ANNUAL REVIEW OF IMMUNOLOGY, 1999, 17 :1-17
[42]   THYMUS AND REPRODUCTION - SEX-LINKED DYSGENESIA OF GONAD AFTER NEONATAL THYMECTOMY IN MICE [J].
NISHIZUK.Y ;
SAKAKURA, T .
SCIENCE, 1969, 166 (3906) :753-&
[43]   Acquisition of anergic and suppressive activities in transforming growth factor-β-costimulated CD4+CD25- T cells [J].
Park, HB ;
Paik, DJ ;
Jang, E ;
Hong, S ;
Youn, J .
INTERNATIONAL IMMUNOLOGY, 2004, 16 (08) :1203-1213
[44]   AN X-LINKED SYNDROME OF DIARRHEA, POLYENDOCRINOPATHY, AND FATAL INFECTION IN INFANCY [J].
POWELL, BR ;
BUIST, NRM ;
STENZEL, P .
JOURNAL OF PEDIATRICS, 1982, 100 (05) :731-737
[45]   OX-22HIGH CD4+ T-CELLS INDUCE WASTING DISEASE WITH MULTIPLE ORGAN PATHOLOGY - PREVENTION BY THE OX-22LOW SUBSET [J].
POWRIE, F ;
MASON, D .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 172 (06) :1701-1708
[46]  
REISER H, 1994, IMMUNOLOGY, V81, P532
[47]   DEPENDENCE OF MUTATION FREQUENCY ON RADIATION DOSE RATE IN FEMALE MICE [J].
RUSSELL, WL ;
RUSSELL, LB ;
CUPP, MB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1959, 45 (01) :18-23
[48]  
SAD S, 1994, J IMMUNOL, V153, P3514
[49]   STUDY ON CELLULAR EVENTS IN POST-THYMECTOMY AUTOIMMUNE OOPHORITIS IN MICE .2. REQUIREMENT OF LYT-1 CELLS IN NORMAL FEMALE MICE FOR THE PREVENTION OF OOPHORITIS [J].
SAKAGUCHI, S ;
TAKAHASHI, T ;
NISHIZUKA, Y .
JOURNAL OF EXPERIMENTAL MEDICINE, 1982, 156 (06) :1577-1586
[50]   ORGAN-SPECIFIC AUTOIMMUNE-DISEASES INDUCED IN MICE BY ELIMINATION OF T-CELL SUBSET .1. EVIDENCE FOR THE ACTIVE PARTICIPATION OF T-CELLS IN NATURAL SELF-TOLERANCE - DEFICIT OF A T-CELL SUBSET AS A POSSIBLE CAUSE OF AUTOIMMUNE-DISEASE [J].
SAKAGUCHI, S ;
FUKUMA, K ;
KURIBAYASHI, K ;
MASUDA, T .
JOURNAL OF EXPERIMENTAL MEDICINE, 1985, 161 (01) :72-87