白细胞介素2受体
自身免疫
免疫学
生物
移植
免疫耐受
免疫
人口
克隆缺失
免疫系统
T细胞
抗原
细胞生物学
T细胞受体
医学
内科学
环境卫生
作者
Shimon Sakaguchi,Noriko Sakaguchi,Jun Shimizu,Sayuri Yamazaki,Toshiko Sakihama,Misako Itoh,Yuhshi Kuniyasu,Takashi Nomura,Masaaki Toda,Takeshi Takahashi
标识
DOI:10.1034/j.1600-065x.2001.1820102.x
摘要
Summary: There is accumulating evidence that T‐cell‐mediated dominant control of self‐reactive T‐cells contributes 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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