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

被引:10
|
作者
Zhang, Xi [1 ]
Ng, Yu Yang [1 ]
Du, Zhicheng [1 ]
Li, Zhendong [1 ]
Chen, Can [1 ]
Xiao, Lin [1 ]
Chng, Wee Joo [2 ,3 ,4 ]
Wang, Shu [1 ]
机构
[1] Natl Univ Singapore, Dept Biol Sci, Singapore, Singapore
[2] Natl Univ Hlth Syst, Natl Univ Canc Inst Singapore, Dept Haematol Oncol, Singapore, Singapore
[3] Natl Univ Singapore, Canc Sci Inst Singapore, Singapore, Singapore
[4] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Med, Singapore, Singapore
来源
PLOS ONE | 2022年 / 17卷 / 06期
基金
英国医学研究理事会;
关键词
MATURATION ANTIGEN; ZOLEDRONIC ACID; THERAPY; EXPANSION;
D O I
10.1371/journal.pone.0267475
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
V gamma 9V delta 2 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 V gamma 9V delta 2 T cells, we introduced a BCMA-specific CAR into ex vivo expanded V gamma 9V delta 2 T cells through electroporation of the CAR-encoding mRNA. The modified V gamma 9V delta 2 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- V gamma 9V delta 2 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 V gamma 9V delta 2 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.
引用
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页数:12
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