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用于评估嵌合抗原受体T细胞疗法的生物发光急性髓系白血病人源化小鼠模型的开发方案。

Protocol for the development of a bioluminescent AML-PDX mouse model for the evaluation of CAR T cell therapy.

作者信息

Safont Mireia Mayoral, Leitch Calum, Popa Mihaela, Gjerstad May Eriksen, Caulier Benjamin, Inderberg Else Marit, Wälchli Sébastien, Gelebart Pascal, McCormack Emmet

机构信息

Precision Oncology Research Group, University of Bergen, Bergen, Norway; Department of Clinical Science, University of Bergen, Bergen, Norway; Kinn Therapeutics, Bergen, Norway.

Precision Oncology Research Group, University of Bergen, Bergen, Norway; Department of Clinical Science, University of Bergen, Bergen, Norway; Centre for Cancer Biomarkers (CCBIO), University of Bergen, Bergen, Norway.

出版信息

STAR Protoc. 2024 Dec 20;5(4):103522. doi: 10.1016/j.xpro.2024.103522. Epub 2024 Dec 12.

Abstract

Patient-derived xenograft (PDX) models of acute myeloid leukemia (AML-PDX) offer advantages over cell line models by capturing the complexity and heterogeneity of patient-derived samples. Here, we present a protocol for developing a bioluminescent AML-PDX model in mice to evaluate chimeric antigen receptor (CAR) T cell therapy. We describe steps for transducing, engrafting, expanding, and enriching AML-PDX cells. We then detail procedures for in vitro and in vivo validation of the AML-PDX model for the evaluation of CAR T cell immunotherapy. For complete details on the use and execution of this protocol, please refer to Caulier et al..

摘要

急性髓系白血病患者来源的异种移植(AML-PDX)模型通过捕捉患者来源样本的复杂性和异质性,比细胞系模型具有优势。在此,我们展示了一种在小鼠中建立生物发光AML-PDX模型以评估嵌合抗原受体(CAR)T细胞疗法的方案。我们描述了转导、植入、扩增和富集AML-PDX细胞的步骤。然后,我们详细介绍了用于评估CAR T细胞免疫疗法的AML-PDX模型的体外和体内验证程序。有关本方案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/95c5/11699402/f00d4e737e15/fx1.jpg

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