Immunologic tolerance maintained by CD25+ CD4+ regulatory T cells:: their common role in controlling autoimmunity, tumor immunity, and transplantation tolerance

被引:1246
作者
Sakaguchi, S
Sakaguchi, N
Shimizu, J
Yamazaki, S
Sakihama, T
Itoh, M
Kuniyasu, Y
Nomura, T
Toda, M
Takahashi, T
机构
[1] Kyoto Univ, Inst Frontier Med Sci, Dept Expt Pathol, Sakyo Ku, Kyoto 6068507, Japan
[2] Tokyo Metropolitan Inst Gerontol, Dept Immunopathol, Tokyo, Japan
[3] Univ Tsukuba, Sch Med, Dept Dermatol, Tsukuba, Ibaraki 305, Japan
[4] Jikei Med Univ, Dept Med, Tokyo, Japan
[5] Mie Univ, Sch Med, Dept Immunol, Tsu, Mie 514, Japan
关键词
D O I
10.1034/j.1600-065X.2001.1820102.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
There is accumulating evidence that T-cell-mediated dominant control of self-reactive T-cells contributed, to the maintenance of immunologic self-tolerance and its alteration can cause autoimmune disease. Efforts to delineate such a regulatory T-cell population have revealed that CD25(+) cells in the CD4(+) population in normal naive animals bear the ability to prevent autoimmune disease in vivo and, upon antigenic stimulation, suppress the activation/proliferation of other T cells in vitro, The CD25(+) CD4(+) regulatory T cells, which are naturally anergic and suppressive, appear to be produced by the normal thymus as a functionally distinct subpopulation of T cells. They play critical roles not only in preventing autoimmunity but also in controlling tumor immunity and transplantation tolerance.
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页码:18 / 32
页数:15
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