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天然产生的调节性CD4 + T细胞对自身免疫的控制。

Control of autoimmunity by naturally arising regulatory CD4+ T cells.

作者信息

Hori Shohei, Takahashi Takeshi, Sakaguchi Shimon

机构信息

Laboratory of Immunopathology, Research Center for Allergy and Immunology, The Institute for Physical and Chemical Research (RIKEN), Yokohama 230-0045, Japan.

出版信息

Adv Immunol. 2003;81:331-71. doi: 10.1016/s0065-2776(03)81008-8.

Abstract

Naturally acquired immunological self-tolerance is not entirely accounted for by clonal deletion, anergy, and ignorance. It is now well established that the T cell-repertoire of healthy individuals harbors self-reactive lymphocytes with a potential to cause autoimmune disease and these lymphocytes are under dominant control by a unique subpopulation of CD4+ T cells now called regulatory T cells. Efforts to delineate these Treg cells naturally present in normal individuals have revealed that they are enriched in the CD25+ CD4+ population. The identification of the CD25 molecule as a useful marker for naturally arising CD4+ regulatory T cells has made it possible to investigate many key aspects of their immunobiology, including their antigen specificities and the cellular/molecular pathways involved in their development and their mechanisms of action. Furthermore, reduction or dysfunction of the CD25+ CD4+ regulatory T cell population can be responsible for certain autoimmune diseases in humans.

摘要

天然获得的免疫自我耐受不能完全用克隆清除、失能和忽视来解释。现在已经明确,健康个体的T细胞库中存在具有引发自身免疫疾病潜力的自身反应性淋巴细胞,并且这些淋巴细胞受到现在称为调节性T细胞的独特CD4 + T细胞亚群的主导控制。对正常个体中天然存在的这些调节性T细胞进行描述的研究表明,它们在CD25 + CD4 +群体中富集。将CD25分子鉴定为天然产生的CD4 +调节性T细胞的有用标志物,使得研究其免疫生物学的许多关键方面成为可能,包括它们的抗原特异性以及参与其发育的细胞/分子途径和作用机制。此外,CD25 + CD4 +调节性T细胞群体的减少或功能障碍可能导致人类的某些自身免疫疾病。

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