Department of Biological Sciences, National University of Singapore, Singapore, Singapore.
Department of Haematology-Oncology, National University Cancer Institute Singapore, National University Health System, Singapore, Singapore.
PLoS One. 2022 Jun 16;17(6):e0267475. doi: 10.1371/journal.pone.0267475. eCollection 2022.
Vγ9Vδ2 T cells are immune effector cells capable of killing multiple myeloma (MM) cells and have been tested in clinical trials to treat MM patients. To enhance the MM cell killing function of Vγ9Vδ2 T cells, we introduced a BCMA-specific CAR into ex vivo expanded Vγ9Vδ2 T cells through electroporation of the CAR-encoding mRNA. The modified Vγ9Vδ2 T cells displayed a high cytolytic activity against BCMA-expressing MM cell lines in vitro, while sparing BCMA-negative cells, including normal B cells and monocytes. Subsequently, we intravenously injected KMS-11 human MM cells to generate a xenograft mouse model. The treatment of the tumor-bearing mice with Zometa and anti-BCMA CAR- Vγ9Vδ2 T cells resulted in a significant reduction of tumor burden in the femur region, as well as the overall tumor burden. In association with the decrease in tumor burden, the survival of the MM cell-inoculated mice was markedly prolonged. Considering the potential of Vγ9Vδ2 T cells to be used as off-the-shelf products, the modification of these cells with a BCMA-specific CAR could be an attractive option for cancer immunotherapy against bone marrow cancer MM.
γ9δ2 T 细胞是一种能够杀伤多发性骨髓瘤(MM)细胞的免疫效应细胞,已在临床试验中用于治疗 MM 患者。为了增强 γ9δ2 T 细胞对 MM 细胞的杀伤功能,我们通过电穿孔将编码 CAR 的 mRNA 导入体外扩增的 γ9δ2 T 细胞中,从而引入了一种 BCMA 特异性 CAR。修饰后的 γ9δ2 T 细胞在体外对表达 BCMA 的 MM 细胞系表现出高细胞溶解活性,同时对包括正常 B 细胞和单核细胞在内的 BCMA 阴性细胞具有细胞选择性。随后,我们静脉注射 KMS-11 人 MM 细胞,以生成异种移植小鼠模型。用唑来膦酸和抗 BCMA CAR-γ9δ2 T 细胞治疗荷瘤小鼠,导致股骨区域和总体肿瘤负担的显著减少。与肿瘤负担的减少相关联的是,接种 MM 细胞的小鼠的存活时间显著延长。考虑到 γ9δ2 T 细胞作为现成产品的应用潜力,用 BCMA 特异性 CAR 修饰这些细胞可能是针对骨髓癌 MM 的癌症免疫治疗的一个有吸引力的选择。