Villamor Neus, Montserrat Emili, Colomer Dolors
Unitat d'Hematopatologia, Hospital Clínic, Barcelona, Spain.
Semin Oncol. 2003 Aug;30(4):424-33. doi: 10.1016/s0093-7754(03)00261-6.
Monoclonal antibodies (MoAbs) are increasingly used in the treatment of patients with hematological malignancies and autoimmune diseases. The most commonly employed humanized and chimeric MoAbs are rituximab, alemtuzumab (Campath-1H, Ilex Pharmaceuticals, San Antonio, TX), and gemtuzumab-ozogamicin (Mylotarg, Wyeth-Ayerst Laboratories, St Davids, PA). The mechanism of action of these antibodies, and host and cellular factors influencing the response, are not completely known. Induction of apoptosis, antibody-dependent cell cytotoxicity (ADCC), and complement-mediated cell death (CDC) is the proposed mechanism of action of these antibodies. We review the current understanding of the mechanism of action of and resistance to these MoAbs.
单克隆抗体(MoAbs)越来越多地用于治疗血液系统恶性肿瘤和自身免疫性疾病患者。最常用的人源化和嵌合单克隆抗体是利妥昔单抗、阿仑单抗(Campath-1H,Ilex制药公司,得克萨斯州圣安东尼奥)和吉妥单抗-奥佐米星(Mylotarg,惠氏-艾尔斯特实验室,宾夕法尼亚州圣大卫斯)。这些抗体的作用机制以及影响反应的宿主和细胞因素尚不完全清楚。诱导凋亡、抗体依赖性细胞毒性(ADCC)和补体介导的细胞死亡(CDC)是这些抗体的作用机制。我们综述了目前对这些单克隆抗体的作用机制和耐药性的认识。