Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0267475
Title: Vγ9Vδ2 T cells expressing a BCMA-Specific chimeric antigen receptor inhibit multiple myeloma xenograft growth
Authors: Zhang, X 
Ng, YY 
Du, Z 
Li, Z 
Chen, C
Xiao, L 
Chng, WJ 
Wang, S 
Keywords: Animals
B-Cell Maturation Antigen
Heterografts
Humans
Immunotherapy, Adoptive
Mice
Multiple Myeloma
Receptors, Chimeric Antigen
T-Lymphocytes
Issue Date: 1-Jan-2022
Publisher: Public Library of Science (PLoS)
Citation: Zhang, X, Ng, YY, Du, Z, Li, Z, Chen, C, Xiao, L, Chng, WJ, Wang, S (2022-01-01). Vγ9Vδ2 T cells expressing a BCMA-Specific chimeric antigen receptor inhibit multiple myeloma xenograft growth. PloS one 17 (6) : e0267475-. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0267475
Abstract: 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.
Source Title: PloS one
URI: https://scholarbank.nus.edu.sg/handle/10635/228995
ISSN: 19326203
DOI: 10.1371/journal.pone.0267475
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