The Immunopharmacology Research Group, Medical School, University of Tampere, Tampere, Finland.
Basic Clin Pharmacol Toxicol. 2010 Jan;106(1):13-21. doi: 10.1111/j.1742-7843.2009.00452.x. Epub 2009 Jul 22.
Rheumatoid arthritis (RA) is a chronic, autoimmune reaction-driven systemic inflammatory disease that affects joints and several other organs. Although anti-TNF therapy and combination therapy with traditional anti-rheumatic drugs have improved the treatment of RA, still quite a significant proportion of patients do not reach adequate anti-rheumatic response. The understanding of the pathogenesis of RA has developed markedly during the last two decades, and this has brought up new targets for anti-rheumatic therapy. B cells have been found to have a pivotal role in the development of arthritis both in experimental models and in humans. Rituximab, an anti-CD20 antibody that depletes B cells, has been introduced in the treatment of RA, and it has proven to be safe and efficacious in RA. This review gives an overview on the mechanism of action of rituximab in RA and summarizes the published clinical data of rituximab in the treatment of RA.
类风湿关节炎(RA)是一种慢性、自身免疫反应驱动的系统性炎症性疾病,影响关节和其他几个器官。虽然抗 TNF 治疗和传统抗风湿药物的联合治疗改善了 RA 的治疗效果,但仍有相当大比例的患者无法达到足够的抗风湿反应。在过去的二十年中,RA 的发病机制的理解有了显著的发展,这为抗风湿治疗带来了新的靶点。在实验模型和人类中,B 细胞被发现对关节炎的发展起着关键作用。利妥昔单抗,一种抗 CD20 抗体,可以耗竭 B 细胞,已被引入 RA 的治疗中,并已被证明在 RA 中是安全有效的。这篇综述概述了利妥昔单抗在 RA 中的作用机制,并总结了利妥昔单抗治疗 RA 的已发表临床数据。