阿仑单抗介导的血液恶性肿瘤细胞毒性机制

Thomas S. Lin
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引用次数: 0

摘要

单克隆抗体为实体和血液系统恶性肿瘤提供了一种集中的治疗方法。Alemtuzumab是一种靶向CD52抗原的正常和恶性淋巴细胞的嵌合单克隆抗体,被批准用于治疗复发性慢性淋巴细胞白血病患者。其杀伤细胞的主要机制包括补体依赖性细胞毒性、抗体依赖性细胞毒性和细胞凋亡。对这些细胞毒性途径的相对重要性进行持续的研究对于提高对阿仑单抗和其他单克隆抗体在体内发挥其有益抗肿瘤活性的作用机制的理解是必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mechanisms of Alemtuzumab-Mediated Cytotoxicity in Hematologic Malignancies

Monoclonal antibodies offer a focused therapeutic approach for solid and hematologic malignancies. Alemtuzumab is a chimeric monoclonal antibody that targets the CD52 antigen on normal and malignant lymphoid cells and is approved for the treatment of patients with relapsed chronic lymphocytic leukemia. Its main mechanistic cell-killing effects include complement-dependent cytoxicity, antibody-dependent cell-mediated cytotoxicity, and apoptosis. Ongoing investigation into the relative importance of these cytotoxic pathways is necessary for improved understanding of the mechanisms of action by which alemtuzumab and other monoclonal antibodies exert their beneficial antitumor activity in vivo.

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