诱导多能干细胞
免疫疗法
细胞毒性T细胞
生物
过继性细胞移植
癌症免疫疗法
细胞疗法
干细胞
免疫学
癌症研究
T细胞
胚胎干细胞
细胞生物学
免疫系统
基因
遗传学
体外
作者
Frank Cichocki,Sjoukje J. C. van der Stegen,Jeffrey S. Miller
出处
期刊:Blood
[American Society of Hematology]
日期:2022-11-03
卷期号:141 (8): 846-855
被引量:35
标识
DOI:10.1182/blood.2022016205
摘要
The development of methods to derive induced pluripotent stem cells (iPSCs) has propelled stem cell research, and has the potential to revolutionize many areas of medicine, including cancer immunotherapy. These cells can be propagated limitlessly and can differentiate into nearly any specialized cell type. The ability to perform precise multigene engineering at the iPSC stage, generate master cell lines after clonal selection, and faithfully promote differentiation along natural killer (NK) cells and T-cell lineages is now leading to new opportunities for the administration of off-the-shelf cytotoxic lymphocytes with direct antigen targeting to treat patients with relapsed/refractory cancer. In this review, we highlight the recent progress in iPSC editing and guided differentiation in the development of NK- and T-cell products for immunotherapy. We also discuss some of the potential barriers that remain in unleashing the full potential of iPSC-derived cytotoxic effector cells in the adoptive transfer setting, and how some of these limitations may be overcome through gene editing.
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