| Literature DB >> 30361801 |
Michelle L Saetersmoen1, Quirin Hammer2, Bahram Valamehr3, Dan S Kaufman4, Karl-Johan Malmberg5,6,7.
Abstract
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.Entities:
Keywords: Cancer immunotherapy; Cell therapy; Chimeric antigen receptor; Induced pluripotent stem cells; Natural killer cells; Off-the-shelf
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Year: 2018 PMID: 30361801 DOI: 10.1007/s00281-018-0721-x
Source DB: PubMed Journal: Semin Immunopathol ISSN: 1863-2297 Impact factor: 9.623