Laboratory of Immunology, National Eye Institute, NIH, Bethesda, Maryland 20892, USA.
J Clin Invest. 2010 Sep;120(9):3073-83. doi: 10.1172/JCI42440. Epub 2010 Sep 1.
Autoimmune and inflammatory uveitis are a group of potentially blinding intraocular inflammatory diseases that arise without a known infectious trigger and are often associated with immunological responses to unique retinal proteins. In the United States, about 10% of the cases of severe visual handicap are attributed to this group of disorders. As I discuss here, experimental models of ocular autoimmunity targeting retinal proteins have brought about a better understanding of the basic immunological mechanisms involved in the pathogenesis of uveitis and are serving as templates for the development of novel therapies.
自身免疫性和炎症性葡萄膜炎是一组潜在致盲性眼内炎症性疾病,其发生没有明确的感染诱因,通常与针对独特视网膜蛋白的免疫反应有关。在美国,约有 10%的严重视力障碍病例归因于这组疾病。正如我在这里讨论的那样,针对视网膜蛋白的眼部自身免疫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。