Departments of Neurology and Immunobiology, Yale School of Medicine, New Haven, Connecticut 06520.
Cold Spring Harb Perspect Med. 2018 Dec 3;8(12):a029041. doi: 10.1101/cshperspect.a029041.
Multiple sclerosis (MS) is a genetically mediated autoimmune disease of the central nervous system. Allelic variants lead to lower thresholds of T-cell activation resulting in activation of autoreactive T cells. Environmental factors, including, among others, diet, vitamin D, and smoking, in combination with genetic predispositions, play a substantial role in disease development and activation of autoreactive T cells. FoxP3 regulatory T cells (Tregs) have emerged as central in the control of autoreactive T cells. A consistent finding in patients with MS is defects in Treg cell function with reduced suppression of effector T cells and production of proinflammatory cytokines. Emerging data suggests that functional Tregs become effector-like T cells with loss of function associated with T-bet expression and interferon γ (IFN-γ) secretion.
多发性硬化症(MS)是一种中枢神经系统的遗传介导自身免疫性疾病。等位基因变体导致 T 细胞激活的阈值降低,从而导致自身反应性 T 细胞的激活。环境因素,包括饮食、维生素 D 和吸烟等,与遗传易感性一起,在疾病发展和自身反应性 T 细胞的激活中起着重要作用。FoxP3 调节性 T 细胞(Tregs)已成为控制自身反应性 T 细胞的核心。MS 患者的一个一致发现是 Treg 细胞功能缺陷,效应 T 细胞的抑制作用降低,促炎细胞因子的产生减少。新出现的数据表明,功能性 Tregs 变成具有功能丧失的效应样 T 细胞,与 T 细胞表达和干扰素 γ(IFN-γ)分泌相关的功能丧失。