生物
诱导多能干细胞
免疫疗法
白细胞介素21
白细胞介素12
NK-92
癌症研究
细胞生物学
淋巴因子激活杀伤细胞
细胞毒性T细胞
免疫学
癌症免疫疗法
免疫系统
胚胎干细胞
体外
T细胞
生物化学
基因
作者
Hiroyuki Matsubara,Akira Niwa,Tatsutoshi Nakahata,Megumu K. Saito
标识
DOI:10.1016/j.bbrc.2019.03.085
摘要
Natural killer (NK) cells are innate lymphocytes and show cytotoxicity against tumor cells without prior antigen specific stimulation. Because of their innate properties, NK cells are being considered for immunotherapies against various malignancies or leukemia. Human pluripotent stem cells (hPSCs) are capable of inducing enough NK cells for allogeneic transplantation. However, current induction protocols require feeder cells or human or bovine serum for the differentiation and expansion of NK cells, which incurs potential risk for contamination and may cause lot dependency in the cells. To address these issues, here we established a differentiation protocol for developing functional NK cells from hPSCs under a completely chemically-defined condition. The resultant PSC-derived NK cells show comparable phenotypes to those produced under serum-containing condition, exerting strong killing potential against a leukemia cell line in vitro and resistance to tumor growth in vivo. Our protocol can be a useful tool for applying PSC-derived NK cells to future cellular cancer immunotherapies.
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