诱导多能干细胞
T细胞受体
免疫疗法
细胞疗法
干细胞
免疫系统
过继性细胞移植
癌症研究
癌症免疫疗法
T细胞
抗原
白血病
医学
生物
细胞生物学
免疫学
胚胎干细胞
生物化学
基因
作者
Hiroshi Kawamoto,Kyoko Masuda,Seiji Nagano
标识
DOI:10.1007/978-981-99-9781-7_14
摘要
In the field of cancer immunotherapy, the effectiveness of a method in which patient-derived T cells are genetically modified ex vivo and administered to patients has been demonstrated. However, problems remain with this method, such as (1) time-consuming, (2) costly, and (3) difficult to guarantee the quality. To overcome these barriers, strategies to regenerate T cells using iPSC technology are being pursued by several groups in the last decade. The authors have been developing a method by which specific TCR genes are introduced into iPSCs and T cells are generated from those iPSCs (TCR-iPSC method). At present, our group is preparing this approach for clinical trial, where iPSCs provided from the iPSC project are transduced with WT1 antigen-specific TCR that had been already clinically tested, and killer T cells are generated from such TCR-iPSCs, to be administered to acute myeloid leukemia patients. While the adoptive T cell therapies have been mainly directed to be used in cancer immunotherapy, it is possible to apply these approaches to viral infections. Strategies by other groups to regenerate various types of T cells from iPSCs will also be introduced.
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