电穿孔
CD3型
双特异性抗体
抗原
抗体
多发性骨髓瘤
遗传增强
癌症研究
T细胞
细胞因子释放综合征
免疫毒素
免疫学
医学
嵌合抗原受体
生物
基因
单克隆抗体
免疫系统
CD8型
生物化学
作者
Fengping Peng,Yuan Wang,Jiliang Zhao,Hui Liu,Zhaoyun Liu,Kai Ding,Hongkai Zhang,Rong Fu
摘要
Summary The delivery of bispecific antibodies (BsAbs) targeting B‐cell maturation antigen (BCMA) and CD3 using the gene therapy approach is a promising alternative for BsAb administration in patients with multiple myeloma (MM). In the present study, we evaluated the efficacy of this approach using a xenograft model. Tumour growth was significantly delayed in mice treated with single electroporation‐enhanced intramuscular injection of plasmid DNA encoding BCMA/CD3 BsAb in contrast to the vehicle control‐treated group. Limited toxicity was observed following treatment. This study demonstrates that the gene therapy‐based approach for the delivery of BCMA/CD3 BsAb is effective and safe for the treatment of MM.
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