转基因
嵌合抗原受体
转染
病毒载体
质粒
HEK 293细胞
载体(分子生物学)
细胞生物学
生物
T细胞
病毒学
DNA
分子生物学
基因
重组DNA
遗传学
免疫系统
作者
Feiyan Mo,Maksim Mamonkin
标识
DOI:10.1007/978-1-0716-0146-4_8
摘要
Manufacturing chimeric antigen receptor (CAR)-modified T cells requires incorporation of the CAR transgene, for which viral vectors are most often used. Here, we describe the generation of CAR T cells using primary human T cells and a non-self-inactivating gammaretroviral vector encoding a CAR transgene. The gammaretroviral vector is produced by 293T cells transiently transfected with DNA plasmids encoding necessary components of the viral vector. The resulting viral particles efficiently infect activated T cells and integrate the CAR transgene into the genome of dividing cells for stable expression.
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