Agnello Davide, Lankford Carla S R, Bream Jay, Morinobu Akio, Gadina Massimo, O'Shea John J, Frucht David M
Molecular Immunology and Inflammation Branch, National Institute of Arthritis, Musculoskeletal and Skin Diseases, National Institutes of Health, Building 10, Room 9N262, 10 Center Drive, MSC 1820, Bethesda, Maryland 20802-1820, USA.
J Clin Immunol. 2003 May;23(3):147-61. doi: 10.1023/a:1023381027062.
The differentiation of naive CD4+ T cells into subsets of T helper cells is a pivotal process with major implications for host defense and the pathogenesis of immune-mediated diseases. Though the basic paradigm was discovered more than 15 years ago, new discoveries continue to be made that offer fresh insights into the regulation of this process. T helper (TH)1 cells produce interferon (IFN)-gamma, promoting cell-mediated immunity and control of intracellular pathogens. We now know that TH1 differentiation is regulated by transcription factors such as T-bet, Stat1, and Stat4, as well as cytokines such as IL-12, IL-23, IL-27, type I IFNs, and IFN-gamma. In contrast, TH2 cells produce IL-4, which promotes allergic responses and is important in host defense against helminths. The transcription factors Stat6, GATA-3, c-Maf, NFATs, and the cytokine IL-4 promote TH2 differentiation. These key regulators of TH differentiation are the subject of this review.
初始CD4+ T细胞分化为辅助性T细胞亚群是一个关键过程,对宿主防御和免疫介导疾病的发病机制具有重要影响。尽管基本模式在15年多以前就已被发现,但仍不断有新发现为这一过程的调控提供新见解。辅助性T(TH)1细胞产生干扰素(IFN)-γ,促进细胞介导的免疫并控制细胞内病原体。我们现在知道,TH1分化受转录因子如T-bet、Stat1和Stat4以及细胞因子如IL-12、IL-23、IL-27、I型IFN和IFN-γ的调控。相比之下,TH2细胞产生IL-4,促进过敏反应,在宿主抵御蠕虫方面很重要。转录因子Stat6、GATA-3、c-Maf、NFAT以及细胞因子IL-4促进TH2分化。这些TH分化的关键调节因子是本综述的主题。