Xu Jin-Ge, Chen Ling-Song
Department of Hematology, General Hospital of Xuzhou Mining Group, Xuzhou, Jiangsu Province, China.
Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2011 Dec;19(6):1528-31.
It is now established that CD4(+)CD25(+)regulatory T (Treg) cells expressing transcription factor FOXP3, a regulatory subpopulation of T cells, is indispensable for the maintenance of immunological self-tolerance and immune homeostasis. FOXP3 expression in Treg cells is specific and it is the key control factor for the development, activation and function of Treg cells. At present, CD4(+)FOXP3(+)T lymphocytes are often used to define Treg cells for scientific research. But recent studies show that human CD4(+)FOXP3(+)T cells are phenotypically and functionally heterogeneous, including suppressive and non suppressive T cells. The different functions of these cell subsets can be distinguished by phenotypic differences. This review discusses the recent research progress about phenotypic characteristics and functional heterogeneity of CD4(+)FOXP3(+)T cell subsets.
现已证实,表达转录因子FOXP3的CD4(+)CD25(+)调节性T(Treg)细胞,作为T细胞的一个调节亚群,对于维持免疫自身耐受性和免疫稳态不可或缺。Treg细胞中FOXP3的表达具有特异性,它是Treg细胞发育、激活和功能的关键控制因子。目前,CD4(+)FOXP3(+)T淋巴细胞常被用于科研中定义Treg细胞。但最近的研究表明,人类CD4(+)FOXP3(+)T细胞在表型和功能上具有异质性,包括抑制性和非抑制性T细胞。这些细胞亚群的不同功能可通过表型差异来区分。本综述讨论了关于CD4(+)FOXP3(+)T细胞亚群表型特征和功能异质性的最新研究进展。