Kazkaz Hanadi, Isenberg David
Centre for Rheumatology, The Middlesex Hospital, Arthur Stanley House, 40-50 Tottenham Street, London W1T 4NJ, UK.
Curr Opin Pharmacol. 2004 Aug;4(4):398-402. doi: 10.1016/j.coph.2004.03.006.
B cells play an important role in the pathogenesis of many autoimmune diseases. Selective targeting of these cells has been recently achieved using a chimeric monoclonal antibody against the pan B cell surface marker CD20 (rituximab). This antibody was originally developed for the treatment of non-Hodgkin's lymphoma. It was found to be effective, well tolerated and had a very good safety profile. Recent studies have demonstrated the efficacy of rituximab in several refractory autoimmune disorders including rheumatoid arthritis, systemic lupus erythematosus, immune thrombocytopenic purpura, chronic cold agglutinin disease, IgM-mediated neuropathies and mixed cryoglobulinemia.
B细胞在许多自身免疫性疾病的发病机制中起重要作用。最近,通过使用针对泛B细胞表面标志物CD20的嵌合单克隆抗体(利妥昔单抗)实现了对这些细胞的选择性靶向。这种抗体最初是为治疗非霍奇金淋巴瘤而开发的。人们发现它有效、耐受性良好且安全性极佳。最近的研究表明,利妥昔单抗在几种难治性自身免疫性疾病中有效,包括类风湿性关节炎、系统性红斑狼疮、免疫性血小板减少性紫癜、慢性冷凝集素病、IgM介导的神经病变和混合性冷球蛋白血症。