Fontenot Jason D, Rudensky Alexander Y
Department of Immunology, University of Washington School of Medicine, Seattle, Washington 98195, USA.
Nat Immunol. 2005 Apr;6(4):331-7. doi: 10.1038/ni1179.
The random generation of antigen receptors in developing lymphocytes results in a considerable risk of autoimmunity. Regulatory T cells (T(reg) cells) act in a dominant, trans-acting way to actively suppress immune activation and maintain immune tolerance. Here, we discuss the principal advances in our understanding of the molecular mechanisms of T(reg) cell development and function with particular emphasis on the forkhead transcription factor Foxp3. Accumulating evidence suggests that T(reg) cells represent a dedicated T cell lineage and that Foxp3 functions as the T(reg) cell lineage specification factor. The aggressive early-onset lymphoproliferative syndrome resulting from Foxp3 deficiency identifies T(reg) cells as vital mediators of immunological tolerance to self and Foxp3 as the mediator of the genetic mechanism of dominant tolerance.
发育中的淋巴细胞中抗原受体的随机产生会导致自身免疫的巨大风险。调节性T细胞(T(reg)细胞)以显性、反式作用的方式发挥作用,积极抑制免疫激活并维持免疫耐受。在此,我们讨论在理解T(reg)细胞发育和功能的分子机制方面取得的主要进展,特别强调叉头转录因子Foxp3。越来越多的证据表明,T(reg)细胞代表一种特定的T细胞谱系,且Foxp3作为T(reg)细胞谱系特异性因子发挥作用。Foxp3缺陷导致的侵袭性早发性淋巴细胞增殖综合征将T(reg)细胞确定为对自身免疫耐受的重要介质,并将Foxp3确定为显性耐受遗传机制的介质。