Luckheeram Rishi Vishal, Zhou Rui, Verma Asha Devi, Xia Bing
Department of Gastroenterology, Zhongnan Hospital, Wuhan University School of Medicine, Wuhan 430071, China.
Clin Dev Immunol. 2012;2012:925135. doi: 10.1155/2012/925135. Epub 2012 Mar 14.
CD4⁺T cells are crucial in achieving a regulated effective immune response to pathogens. Naive CD4⁺T cells are activated after interaction with antigen-MHC complex and differentiate into specific subtypes depending mainly on the cytokine milieu of the microenvironment. Besides the classical T-helper 1 and T-helper 2, other subsets have been identified, including T-helper 17, regulatory T cell, follicular helper T cell, and T-helper 9, each with a characteristic cytokine profile. For a particular phenotype to be differentiated, a set of cytokine signaling pathways coupled with activation of lineage-specific transcription factors and epigenetic modifications at appropriate genes are required. The effector functions of these cells are mediated by the cytokines secreted by the differentiated cells. This paper will focus on the cytokine-signaling and the network of transcription factors responsible for the differentiation of naive CD4⁺T cells.
CD4⁺T细胞在实现对病原体的调节性有效免疫反应中至关重要。初始CD4⁺T细胞在与抗原-MHC复合物相互作用后被激活,并主要根据微环境的细胞因子环境分化为特定亚型。除了经典的辅助性T细胞1型和辅助性T细胞2型,还鉴定出了其他亚群,包括辅助性T细胞17、调节性T细胞、滤泡辅助性T细胞和辅助性T细胞9,每个亚群都有独特的细胞因子谱。为了分化出特定的表型,需要一组细胞因子信号通路,以及谱系特异性转录因子的激活和适当基因处的表观遗传修饰。这些细胞的效应功能由分化细胞分泌的细胞因子介导。本文将重点关注负责初始CD4⁺T细胞分化的细胞因子信号传导和转录因子网络。