美罗华
单克隆抗体
CD20
免疫学
内化
细胞毒性T细胞
抗体
医学
效应器
单克隆
淋巴瘤
类风湿性关节炎
癌症研究
生物
内科学
受体
生物化学
体外
作者
Stephen A. Beers,H. T. Claude Chan,Ruth R. French,Mark S. Cragg,Martin J. Glennie
标识
DOI:10.1053/j.seminhematol.2010.01.001
摘要
The last decade has seen the monoclonal antibody (mAb), rituximab, transform clinical management of many non-Hodgkin lymphomas and more recently provide new opportunities for controlling autoimmune conditions, such as rheumatoid arthritis. Although not yet fully determined, the explanation for this success appears to lie with the inherent properties of its target, CD20, which allow rituximab to recruit potent cytotoxic effectors with unusual efficiency. In this review we detail the properties of CD20 that make it such an effective therapeutic target and describe how different mAbs change the membrane distribution and internalization of CD20 and have distinct modes of cytotoxic activity.
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