嵌合抗原受体
抗原
食品药品监督管理局
医学
CD19
T细胞
癌症研究
生物
免疫系统
免疫学
生物信息学
细胞疗法
细胞
药理学
遗传学
作者
Young-Ho Lee,Chan Hyuk Kim
标识
DOI:10.1007/s12272-019-01136-x
摘要
Engineering T cells with a chimeric antigen receptor (CAR) that reprograms their antigen selectivity and signaling has recently emerged as one of the most promising therapeutic approaches for treating cancers. For example, two CD19-specific CAR T cell (CAR-T) therapies have shown remarkable responses in patients with relapsed/refractory B-cell cancers, and were approved by the US Food and Drug Administration in 2017. This initial clinical success has spurred an explosion of interests in this novel therapy from both academia and industry, and results from basic and clinical research have enabled the rapid evolution of the CAR-T field. In this review, we describe the basic structure of the CAR and discuss how each of its domains affect the efficacy and safety of CAR-T therapies. In addition, we discuss some of the novel concepts and other considerations that are essential for ensuring the future success of CAR-T therapy.
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