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使用γ-逆转录病毒载体生成嵌合抗原受体(CAR)T细胞。

Generation of CAR T-cells using γ-retroviral vector.

作者信息

Watanabe Norihiro, McKenna Mary Kathryn

机构信息

Center for Cell and Gene Therapy, Baylor College of Medicine, Houston, TX, United States.

Center for Cell and Gene Therapy, Baylor College of Medicine, Houston, TX, United States.

出版信息

Methods Cell Biol. 2022;167:171-183. doi: 10.1016/bs.mcb.2021.06.014. Epub 2021 Jul 30.

Abstract

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.

摘要

嵌合抗原受体(CAR)T细胞的产生需要将CAR基因转移到原代T细胞中。在各种基因转移策略中,γ逆转录病毒载体已被广泛用于在临床前和临床环境中产生CAR T细胞。在这里,我们描述了利用γ逆转录病毒载体产生CAR T细胞的详细方法。该方法包括两个并行部分:(1)γ逆转录病毒颗粒的生产和(2)活化T细胞的γ逆转录病毒转导。γ逆转录病毒颗粒是通过将γ逆转录病毒载体与包装质粒共转染到293T细胞中产生的。然后,制造的病毒颗粒有效地感染活化的T细胞,其中CAR转基因整合到宿主基因组DNA中,导致CAR分子在T细胞表面稳定表达。

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Generation of CAR T-cells using γ-retroviral vector.使用γ-逆转录病毒载体生成嵌合抗原受体(CAR)T细胞。
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