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嵌合抗原受体T细胞疗法中的代谢挑战与干预措施

Metabolic challenges and interventions in CAR T cell therapy.

作者信息

Peng Jhan-Jie, Wang Limei, Li Zhiyu, Ku Cheng-Lung, Ho Ping-Chih

机构信息

Department of Fundamental Oncology, University of Lausanne, Lausanne, Switzerland.

Ludwig Institute for Cancer Research, University of Lausanne, Epalinges, Switzerland.

出版信息

Sci Immunol. 2023 Apr 14;8(82):eabq3016. doi: 10.1126/sciimmunol.abq3016.

Abstract

Chimeric antigen receptor (CAR) T cells have achieved true clinical success in treating hematological malignancy patients, laying the foundation of CAR T cells as a new pillar of cancer therapy. Although these promising effects have generated strong interest in expanding the treatment of CAR T cells to solid tumors, reproducible demonstration of clinical efficacy in the setting of solid tumors has remained challenging to date. Here, we review how metabolic stress and signaling in the tumor microenvironment, including intrinsic determinants of response to CAR T cell therapy and extrinsic obstacles, restrict the efficacy of CAR T cell therapy in cancer treatment. In addition, we discuss the use of novel approaches to target and rewire metabolic programming for CAR T cell manufacturing. Last, we summarize strategies that aim to improve the metabolic adaptability of CAR T cells to enhance their potency in mounting antitumor responses and survival within the tumor microenvironment.

摘要

嵌合抗原受体(CAR)T细胞在治疗血液系统恶性肿瘤患者方面已取得了真正的临床成功,为CAR T细胞作为癌症治疗的新支柱奠定了基础。尽管这些令人鼓舞的效果引发了人们对将CAR T细胞治疗扩展至实体瘤的浓厚兴趣,但迄今为止,在实体瘤环境中可重复证明临床疗效仍然具有挑战性。在此,我们综述肿瘤微环境中的代谢应激和信号传导,包括对CAR T细胞治疗反应的内在决定因素和外在障碍,如何限制CAR T细胞疗法在癌症治疗中的疗效。此外,我们讨论了使用新方法来靶向和重塑CAR T细胞制造过程中的代谢程序。最后,我们总结了旨在提高CAR T细胞代谢适应性以增强其在肿瘤微环境中产生抗肿瘤反应和存活能力的策略。

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