bioRxiv · 10.1101/2025.01.23.634500
Avoidance of fratricide and improved efficacy of CD33-MSLN CAR-iNK cells in treating acute myeloid leukemia
Abstract
Acute myeloid leukemia (AML) patients are often older, which brings challenges of endurance and persistent efficacy of autologous CAR-T cell therapies. Allogenic CAR-NK cell therapies may offer reduced toxicities and enhanced anti-leukemic potential against AML. In this study, we designed a novel CD33-mesothelin loop CAR (Loop CAR) and evaluated its anti-tumor efficacy in human umbilical cord blood-derived NK (UCB-NK) cells and human pluripotent stem cell-derived NK (hPSC-iNK) cells. The Loop CAR exhibited superior cytotoxicity against dual-antigen-positive tumor cell lines and primary AML cells. To further avoid fratricide caused by endogenous CD33 expression in NK cells, we established a hPSC-derived cell line via knockout of CD33 gene (CD33KO) and engineered Loop CAR. Rather than enforced expression of exogenous CD16, we generated abundant mature CD33KO-Loop CAR-iNK cells highly expressing endogenous CD16 via an organoid induction approach. This innovative strategy effectively mitigated NK cell fratricide and significantly enhanced CD33 and mesothelin-mediated specific cytotoxicity. Moreover, the CD33KO-Loop CAR-iNK cells demonstrated superior tumor-killing activity in AML xenograft mice and significantly prolonged survival. hPSC-derived CD33KO-Loop CAR-iNK cells possess unique advantages and translational potential for treating AML.
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Wang, Y., Zheng, X., Wang, Z., Xiao, Z., Lin, Y., Zhang, F., Liu, Y., Liu, P., Weng, Q., Zhang, L., Xia, C., Huang, D., Liu, L., Zhu, Y., Zhang, Q., Qi, H., Chen, Y., Shen, Y., Zhang, C., Xu, J., Zhao, Y., Wu, J., Wang, T., Zhang, M., Li, M., Qian, W., Liang, A., Du, X., Yang, W., Zhu, X., Hu, F., Wang, J.. 2025-01-26. Avoidance of fratricide and improved efficacy of CD33-MSLN CAR-iNK cells in treating acute myeloid leukemia. https://doi.org/10.1101/2025.01.23.634500
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