双特异性抗体
多发性骨髓瘤
细胞毒性T细胞
抗体
淋巴瘤
主要组织相容性复合体
免疫系统
抗原
免疫疗法
抗原呈递
CD3型
白血病
CD8型
医学
癌症研究
免疫学
T细胞
生物
单克隆抗体
体外
生物化学
作者
Joshua Kassner,Basma Abdellatif,Samuel Yamshon,Jorge Monge,Justin D. Kaner
标识
DOI:10.1016/j.trecan.2024.06.001
摘要
Over the past 30 years the incorporation of monoclonal antibody (mAb) treatments into the management of hematologic malignancies has led to significant improvements in patient outcomes. The key limitation of mAb treatments is the necessity for target antigen presentation on major histocompatibility complex (MHC) and costimulatory molecules to elicit a cytotoxic immune response. With the advent of bispecific antibodies (BsAbs), these limitations can be overcome through direct stimulation of cytotoxic T cells, thus limiting tumor cell evasion. BsAbs are rapidly being incorporated into treatment regimens for hematologic malignancies, and there are now seven FDA-approved treatments in this class, six of which have been approved in the past year. In this review we describe the function, complications, and clinical trial data available for CD3 BsAbs in the treatment of lymphoma, myeloma, and leukemia.
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