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使用达沙替尼生产滋补性嵌合抗原受体T细胞的方案。

Protocol for production of tonic CAR T cells with dasatinib.

作者信息

Rosselle Léa, Leray Thibault, Joaquina Sandy, Caulier Benjamin, McCormack Emmet, Gelebart Pascal, Wälchli Sébastien, Inderberg Else Marit

机构信息

Translational Research Unit, Section for Cellular Therapy, Department of Oncology, Oslo University Hospital, Oslo, Norway.

Translational Research Unit, Section for Cellular Therapy, Department of Oncology, Oslo University Hospital, Oslo, Norway; Medical Faculty, University of Oslo, Oslo, Norway.

出版信息

STAR Protoc. 2025 Mar 21;6(1):103529. doi: 10.1016/j.xpro.2024.103529. Epub 2024 Dec 30.

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..

摘要

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,会导致持续性信号传导和生产挑战。我们提出了一种使用美国食品药品监督管理局(FDA)批准的激酶抑制剂达沙替尼来扩增持续性CARs的方案。我们报告了用逆转录病毒进行T细胞转导、使用流式细胞术进行CAR质量的扩增和验证以及杀伤试验的步骤。仅在30 nM时,达沙替尼就能改善持续性CAR T细胞扩增后的增殖和质量。有关此方案的使用和执行的完整详细信息,请参阅Caulier等人的文章。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5c5/11750262/46cc1223adc2/fx1.jpg

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