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表达 BCMA 特异性嵌合抗原受体的 Vγ9Vδ2 T 细胞抑制多发性骨髓瘤异种移植瘤生长

英文原题:Vγ9Vδ2 T cells expressing a BCMA-Specific chimeric antigen receptor inhibit multiple myeloma xenograft growth.

查看英文原题

Vγ9Vδ2 T cells expressing a BCMA-Specific chimeric antigen receptor inhibit multiple myeloma xenograft growth.

PubMed 2022/06/16(内容时间) PLoS One Q2 · IF 2.8(JCR 2025)

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中文摘要

Vγ9Vδ2 T细胞是能够杀伤多发性骨髓瘤(MM)细胞的免疫效应细胞,并已在临床试验中用于治疗MM患者。为了增强Vγ9Vδ2 T细胞对MM细胞的杀伤功能,我们通过电穿孔导入编码CAR的mRNA,将BCMA特异性CAR引入体外扩增的Vγ9Vδ2 T细胞中。修饰后的Vγ9Vδ2 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,同时不损伤BCMA阴性细胞,包括正常B细胞和单核细胞。随后,我们静脉注射KMS-11人MM细胞以建立异种移植小鼠模型。用Zometa和抗BCMA CAR-Vγ9Vδ2 T细胞治疗荷瘤小鼠,显著减少了股骨区域的肿瘤负荷以及整体肿瘤负荷。与肿瘤负荷降低相关,接种MM细胞的小鼠生存期显著延长。考虑到Vγ9Vδ2 T细胞作为现货型产品的潜力,用BCMA特异性CAR修饰这些细胞可能成为针对骨髓瘤MM的癌症免疫治疗的一个有吸引力的选择。

展开英文摘要原文

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.

论文信息

作者
Zhang X、Ng YY、Du Z、Li Z、Chen C、Xiao L、Chng WJ、Wang S
单位
Department of Biological Sciences, National University of Singapore, Singapore, Singapore.Singapore
文献类型
非美国政府资助研究
期刊
PloS one2022
原文标识
PubMed 35709135 · DOI 10.1371/journal.pone.0267475