Department of Surgery, University of British Columbia, and Immunity and Infection Research Centre, Vancouver Coastal Health Research Institute, Vancouver, Canada.
Clin Exp Immunol. 2010 Feb;159(2):109-19. doi: 10.1111/j.1365-2249.2009.04037.x. Epub 2009 Nov 11.
T helper (Th) cell have a central role in modulating immune responses. While Th1 and Th2 cells have long been known to regulate cellular and humoral immunity, Th17 cells have been identified only recently as a Th lineage that regulates inflammation via production of distinct cytokines such as interleukin (IL)-17. There is growing evidence that Th17 cells are pathological in many human diseases, leading to intense interest in defining their origins, functions and developing strategies to block their pathological effects. The cytokines that regulate Th17 differentiation have been the focus of much debate, due primarily to inconsistent findings from studies in humans. Evidence from human disease suggests that their in vivo development is driven by specialized antigen-presenting cells. Knowledge of how Th17 cells interact with other immune cells is limited, but recent data suggest that Th17 cells may not be subject to strict cellular regulation by T regulatory cells. Notably, Th17 cells and T regulatory cells appear to share common developmental pathways and both cell types retain significant plasticity. Herein, we will discuss the molecular and cellular regulation of Th17 cells with an emphasis on studies in humans.
辅助性 T 细胞(Th)在调节免疫反应中起着核心作用。虽然 Th1 和 Th2 细胞早已被认为调节细胞和体液免疫,但 Th17 细胞最近才被确定为一种通过产生独特的细胞因子(如白细胞介素-17,IL-17)来调节炎症的 Th 细胞谱系。越来越多的证据表明,Th17 细胞在许多人类疾病中是病理性的,这导致人们强烈关注定义其起源、功能以及开发阻断其病理性作用的策略。调节 Th17 分化的细胞因子一直是争论的焦点,主要是因为人类研究中的结果不一致。来自人类疾病的证据表明,它们在体内的发育是由专门的抗原呈递细胞驱动的。关于 Th17 细胞如何与其他免疫细胞相互作用的知识有限,但最近的数据表明,Th17 细胞可能不受 T 调节细胞的严格细胞调节。值得注意的是,Th17 细胞和 T 调节细胞似乎共享共同的发育途径,并且这两种细胞类型都保持着显著的可塑性。本文将重点讨论人类研究中 Th17 细胞的分子和细胞调节。