嵌合抗原受体
抗原
基因工程
T细胞受体
自身免疫
生物
T细胞
免疫学
计算生物学
癌症研究
免疫系统
遗传学
基因
作者
Michel Sadelain,Isabelle Rivière,Stanley R. Riddell
出处
期刊:Nature
[Springer Nature]
日期:2017-05-23
卷期号:545 (7655): 423-431
被引量:839
摘要
Genetically engineered T cells are powerful new medicines, offering hope for curative responses in patients with cancer. Chimaeric antigen receptors (CARs) are a class of synthetic receptors that reprogram lymphocyte specificity and function. CARs targeting CD19 have demonstrated remarkable potency in B cell malignancies. Engineered T cells are applicable in principle to many cancers, pending further progress to identify suitable target antigens, overcome immunosuppressive tumour microenvironments, reduce toxicities, and prevent antigen escape. Advances in the selection of optimal T cells, genetic engineering, and cell manufacturing are poised to broaden T-cell-based therapies and foster new applications in infectious diseases and autoimmunity.
科研通智能强力驱动
Strongly Powered by AbleSci AI