Benaroya Research Institute, Immunology Program, Seattle, WA 98101, USA.
Expert Rev Clin Immunol. 2006 Jul;2(4):639-47. doi: 10.1586/1744666X.2.4.639.
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.
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。