Off-the-shelf cell therapy with induced pluripotent stem cell-derived natural killer cells

被引:0
作者
Michelle L. Saetersmoen
Quirin Hammer
Bahram Valamehr
Dan S. Kaufman
Karl-Johan Malmberg
机构
[1] University of Oslo,The KG Jebsen Center for Cancer Immunotherapy
[2] Karolinska Institute,Department of Medicine, Huddinge
[3] Fate Therapeutics Inc.,Department of Medicine
[4] University of California San Diego,Institute for Cancer research
[5] Oslo University Hospital,undefined
来源
Seminars in Immunopathology | 2019年 / 41卷
关键词
Induced pluripotent stem cells; Natural killer cells; Off-the-shelf; Cell therapy; Chimeric antigen receptor; Cancer immunotherapy;
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摘要
Cell therapy is emerging as a very promising therapeutic modality against cancer, spearheaded by the clinical success of chimeric antigen receptor (CAR) modified T cells for B cell malignancies. Currently, FDA-approved CAR-T cell products are based on engineering of autologous T cells harvested from the patient, typically using a central manufacturing facility for gene editing before the product can be delivered to the clinic and infused to the patients. For a broader implementation of advanced cell therapy and to reduce costs, it would be advantageous to use allogeneic “universal” cell therapy products that can be stored in cell banks and provided upon request, in a manner analogous to biopharmaceutical drug products. In this review, we outline a roadmap for development of off-the-shelf cell therapy based on natural killer (NK) cells derived from induced pluripotent stem cells (iPSCs). We discuss strategies to engineer iPSC-derived NK (iPSC-NK) cells for enhanced functional potential, persistence, and homing.
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页码:59 / 68
页数:9
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