Laboratory of Immunology, National Eye Institute, National Institute of Health, Bethesda, Maryland 20892-1857, USA.
J Interferon Cytokine Res. 2011 Oct;31(10):733-44. doi: 10.1089/jir.2011.0042. Epub 2011 Jul 25.
Autoimmune uveitis is a complex group of sight-threatening diseases that arise without a known infectious trigger. The disorder is often associated with immunological responses to retinal proteins. Experimental models of autoimmune uveitis targeting retinal proteins have led to a better understanding of the basic immunological mechanisms involved in the pathogenesis of uveitis and have provided a template for the development of novel therapies. The disease in humans is believed to be T cell-dependent, as clinical uveitis is ameliorated by T cell-targeting therapies. The roles of T helper 1 (Th1) and Th17 cells have been major topics of interest in the past decade. Studies in uveitis patients and experiments in animal models have revealed that Th1 and Th17 cells can both be pathogenic effectors, although, paradoxically, some cytokines produced by these subsets can also be protective, depending on when and where they are produced. The major proinflammatory as well as regulatory cytokines in uveitis, the therapeutic approaches, and benefits of targeting these cytokines will be discussed in this review.
自身免疫性葡萄膜炎是一组复杂的致盲性眼病,其发生没有明确的感染诱因。该疾病通常与视网膜蛋白的免疫反应有关。针对视网膜蛋白的自身免疫性葡萄膜炎实验模型,使人们对葡萄膜炎发病机制中涉及的基本免疫学机制有了更好的理解,并为新疗法的开发提供了模板。人们认为人类的这种疾病依赖于 T 细胞,因为 T 细胞靶向疗法可以改善临床葡萄膜炎。在过去十年中,Th1 和 Th17 细胞的作用一直是研究的重点。葡萄膜炎患者的研究和动物模型的实验表明,Th1 和 Th17 细胞都可以作为致病性效应物,尽管矛盾的是,这些亚群产生的一些细胞因子也可以具有保护作用,具体取决于它们何时以及在何处产生。本文将讨论葡萄膜炎中的主要促炎和调节性细胞因子、治疗方法以及针对这些细胞因子的治疗益处。