转导(生物物理学)
生物
转基因
转染
病毒载体
嵌合抗原受体
细胞生物学
质粒
HEK 293细胞
遗传增强
基因
分子生物学
遗传学
T细胞
重组DNA
生物物理学
免疫系统
作者
Norihiro Watanabe,Mary Kathryn McKenna
标识
DOI:10.1016/bs.mcb.2021.06.014
摘要
The generation of chimeric antigen receptor (CAR) T cells requires the transfer of the CAR gene into primary T cells. Among various gene transfer strategies, gammaretroviral vectors have been widely used to generate CAR T cells for both preclinical and clinical settings. Here we describe the detailed method of generating CAR T cells utilizing gammaretroviral vectors. This approach consists of two parallel parts: (1) production of the gammaretroviral particles and (2) gammaretroviral transduction of activated T cells. The gammaretroviral particles are produced by co-transfecting the gammaretroviral vector with packaging plasmids into 293T cells. The manufactured viral particles then efficiently infect activated T cells where the CAR transgene is integrated into host genomic DNA, resulting in stable expression of the CAR molecule on the surface of T cells.
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