Protocol for production of tonic CAR T cells with dasatinib.

IF 1.3 Q4 BIOCHEMICAL RESEARCH METHODS
Léa Rosselle, Thibault Leray, Sandy Joaquina, Benjamin Caulier, Emmet McCormack, Pascal Gelebart, Sébastien Wälchli, Else Marit Inderberg
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引用次数: 0

Abstract

Chimeric antigen receptors (CARs) are synthetic molecules composed of an extracellular antigen-binding domain and an intracellular signaling domain, leading to tonic signaling and manufacturing challenges. We present a protocol for the expansion of tonic CARs by using a Food and Drug Administration (FDA)-approved kinase inhibitor, dasatinib. We report steps for T cell transduction with retrovirus, expansion and verification of CAR quality using flow cytometry, and killing assay. At only 30 nM, dasatinib improves tonic CAR T cell proliferation and quality after expansion. For complete details on the use and execution of this protocol, please refer to Caulier et al.1.

用达沙替尼生产补强型CAR - T细胞的方案。
嵌合抗原受体(CARs)是由细胞外抗原结合域和细胞内信号域组成的合成分子,导致滋补信号和制造挑战。我们提出了一种方案,通过使用食品和药物管理局(FDA)批准的激酶抑制剂达沙替尼来扩大补性car。我们报告了用逆转录病毒进行T细胞转导的步骤,利用流式细胞术扩增和验证CAR质量,以及杀死试验。仅在30 nM时,达沙替尼可改善扩增后CAR - T细胞的增殖和质量。有关本协议使用和执行的完整细节,请参见Caulier等人1。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
STAR Protocols
STAR Protocols Biochemistry, Genetics and Molecular Biology-General Biochemistry, Genetics and Molecular Biology
CiteScore
2.00
自引率
0.00%
发文量
789
审稿时长
10 weeks
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