慢病毒
CD8型
嵌合抗原受体
细胞毒性T细胞
T细胞
转基因
转导(生物物理学)
基因
分子生物学
细胞生物学
生物
病毒学
抗原
免疫学
遗传学
人类免疫缺陷病毒(HIV)
免疫系统
体外
生物化学
病毒性疾病
作者
Vivian Fung,Isaac Rosado-Sánchez,Megan K. Levings
出处
期刊:Methods in molecular biology
日期:2021-01-01
卷期号:: 227-254
被引量:5
标识
DOI:10.1007/978-1-0716-1311-5_19
摘要
Lentivirus-mediated gene transfer is an efficient method to introduce a variety of transgenes to human T cells. Here we describe a protocol to transduce human CD4+, CD8+, or CD4+ regulatory T cells. To illustrate the method, we use transduction with lentivirus encoding an HLA-A2-specific chimeric antigen receptor (CAR) and a transduction marker as an example. Methods to isolate, transduce, purify, and expand CD4+ and CD8+ T cells as well as regulatory T cells are provided. We also describe how to carry out cytotoxicity or suppression assays to assess the function of the resulting CAR T cell or CAR regulatory T cells, respectively.
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