奥图穆马
CD20
美罗华
单克隆抗体
抗体依赖性细胞介导的细胞毒性
慢性淋巴细胞白血病
表位
抗体
癌症研究
抗原
医学
分子生物学
化学
免疫学
出处
期刊:Hematology Meeting Reports (formerly Haematologica Reports)
日期:2009-06-23
卷期号:2 (5)
摘要
Ofatumumab, the first fully human anti-CD20 monoclonal antibody, targets a novel epitope of the CD20 molecule on B-cells and releases only very slowly from the target compared with rituximab. The antibody is generated via transgenic mouse and hybridoma technology. Compared with rituximab, ofatumumab has similar ADCC, but stronger CDC, even to lymphoma cells with a low CD20 antigen density and a high number of CD55 and CD59 complement inhibitory molecules present in the cell membrane. In addition, ofatumumab kills fresh B-CLL cells resistant to rituximab. In the cynomolgus monkey model, the ofatumumab-depletion of B-cells from peripheral blood and lymph nodes lasted longer than the depletion induced by rituximab. Given the above, ofatumumab has the potential to treat B-cell malignancies with low CD20 expression, such as B-CLL and rituximab-refractory follicular lymphoma.
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