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FOXP3 对 CD4+CD25+调节性 T 细胞的影响。

Influence of FOXP3 on CD4+CD25+ regulatory T cells.

机构信息

Benaroya Research Institute, Immunology Program, Seattle, WA 98101, USA.

出版信息

Expert Rev Clin Immunol. 2006 Jul;2(4):639-47. doi: 10.1586/1744666X.2.4.639.

Abstract

FOXP3, a member of the forkhead family of transcriptional regulatory proteins, is expressed predominantly in CD4(+)CD25(+) regulatory T cells. These cells are vital for maintaining peripheral tolerance. A lack of FOXP3 results in severe lymphoproliferative disease and autoimmunity in both mouse and humans, which is the result of an absence of CD4(+)CD25(+)FOXP3(+) regulatory cells. This review discusses the role that this protein plays in the commitment and function of regulatory T cells and its characteristics of FOXP3. We then discuss how, in humans, the induction of FOXP3 in nonregulatory CD4(+) T cells can result in the generation of regulatory T cells in the periphery. A finding that has implications on both how autoimmunity is regulated in vivo as well an impact on the development of therapeutic interventions for the treatment of autoimmunity.

摘要

叉头框蛋白 P3(FOXP3)是转录调节蛋白叉头框家族的一个成员,主要表达于 CD4(+)CD25(+)调节性 T 细胞。这些细胞对于维持外周耐受至关重要。FOXP3 的缺失会导致人和小鼠出现严重的淋巴增殖性疾病和自身免疫,这是由于缺乏 CD4(+)CD25(+)FOXP3(+)调节性细胞所致。本综述讨论了该蛋白在调节性 T 细胞的分化和功能中所起的作用及其 FOXP3 的特点。然后我们讨论了在人类中,非调节性 CD4(+)T 细胞中 FOXP3 的诱导如何导致外周调节性 T 细胞的产生。这一发现不仅影响了体内自身免疫的调控,而且对治疗自身免疫的治疗干预措施的发展也有影响。

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