Ahmed Eman N, Cutmore Lauren C, Marshall John F
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.
Cancers (Basel). 2024 Sep 18;16(18):3186. doi: 10.3390/cancers16183186.
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.
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。