转导(生物物理学)
嵌合抗原受体
抗原
生物
T细胞
转基因
细胞生物学
病毒载体
分子生物学
免疫系统
免疫学
遗传学
基因
生物化学
重组DNA
作者
Pauline Loos,Lauralie Short,Gillian Savage,Laura Evgin
出处
期刊:Methods in molecular biology
日期:2023-12-10
卷期号:: 41-53
标识
DOI:10.1007/978-1-0716-3593-3_4
摘要
The development of chimeric antigen receptor (CAR) T cells has been a revolutionary technology for the treatment of relapsed and refractory leukemias and lymphomas. The synthetic CAR molecule redirects T cell function toward tumor surface-expressed antigens through a single-chain variable fragment (scFv) fused to CD3z and intracellular costimulatory domains. Here, we describe a protocol for the generation of CAR T cells using primary mouse T cells and a gammaretroviral vector encoding a CAR transgene. This protocol outlines several transduction and expansion methods based on the use of two transduction enhancers, RetroNectin® and Vectofusin®-1, and cell culture systems such as conventional plates or G-Rex® devices.
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