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用于CAR T细胞临床前评估的同基因小鼠模型

Syngeneic Mouse Models for Pre-Clinical Evaluation of CAR T Cells.

作者信息

Ahmed Eman N, Cutmore Lauren C, Marshall John F

机构信息

Centre for Tumour Biology, Barts Cancer Institute, Queen Mary University of London, London EC1M 6BQ, UK.

College of Medicine, Alfaisal University, Riyadh 11533, Saudi Arabia.

出版信息

Cancers (Basel). 2024 Sep 18;16(18):3186. doi: 10.3390/cancers16183186.

Abstract

Chimeric antigen receptor (CAR) T cells have revolutionized the treatment of hematological malignancies. Unfortunately, this improvement has yet to be translated into the solid tumor field. Current immunodeficient models used in pre-clinical testing often overestimate the efficacy of CAR T cell therapy as they fail to recapitulate the immunosuppressive tumor microenvironment characteristic of solid tumors. As CAR T cell monotherapy is unlikely to be curative for many solid tumors, combination therapies must be investigated, for example, stromal remodeling agents and immunomodulators. The evaluation of these combination therapies requires a fully immunocompetent mouse model in order to recapitulate the interaction between the host's immune system and the CAR T cells. This review will discuss the need for improved immunocompetent murine models for the pre-clinical evaluation of CAR T cells, the current use of such models and future directions.

摘要

嵌合抗原受体(CAR)T细胞彻底改变了血液系统恶性肿瘤的治疗方式。遗憾的是,这一进展尚未转化到实体瘤领域。目前临床前测试中使用的免疫缺陷模型往往高估了CAR T细胞疗法的疗效,因为它们无法重现实体瘤特有的免疫抑制肿瘤微环境。由于CAR T细胞单一疗法对许多实体瘤不太可能治愈,因此必须研究联合疗法,例如基质重塑剂和免疫调节剂。评估这些联合疗法需要一个具有完全免疫活性的小鼠模型,以便重现宿主免疫系统与CAR T细胞之间的相互作用。本综述将讨论在临床前评估CAR T细胞时对改进的具有免疫活性的小鼠模型的需求、此类模型的当前应用情况以及未来方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb6c/11430534/418affbc2f57/cancers-16-03186-g001.jpg

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