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免疫代谢:免疫治疗耐药的新维度。

Immunometabolism: a new dimension in immunotherapy resistance.

机构信息

Department of Oncology, The Second Xiangya Hospital, Central South University, Changsha, 410011, China.

NHC Key Laboratory of Carcinogenesis and Key Laboratory of Carcinogenesis and Cancer Invasion of the Chinese Ministry of Education, Cancer Research Institute, Central South University, Changsha, 410078, China.

出版信息

Front Med. 2023 Aug;17(4):585-616. doi: 10.1007/s11684-023-1012-z. Epub 2023 Sep 19.

Abstract

Immune checkpoint inhibitors (ICIs) have demonstrated unparalleled clinical responses and revolutionized the paradigm of tumor treatment, while substantial patients remain unresponsive or develop resistance to ICIs as a single agent, which is traceable to cellular metabolic dysfunction. Although dysregulated metabolism has long been adjudged as a hallmark of tumor, it is now increasingly accepted that metabolic reprogramming is not exclusive to tumor cells but is also characteristic of immunocytes. Correspondingly, people used to pay more attention to the effect of tumor cell metabolism on immunocytes, but in practice immunocytes interact intimately with their own metabolic function in a way that has never been realized before during their activation and differentiation, which opens up a whole new frontier called immunometabolism. The metabolic intervention for tumor-infiltrating immunocytes could offer fresh opportunities to break the resistance and ameliorate existing ICI immunotherapy, whose crux might be to ascertain synergistic combinations of metabolic intervention with ICIs to reap synergic benefits and facilitate an adjusted anti-tumor immune response. Herein, we elaborate potential mechanisms underlying immunotherapy resistance from a novel dimension of metabolic reprogramming in diverse tumor-infiltrating immunocytes, and related metabolic intervention in the hope of offering a reference for targeting metabolic vulnerabilities to circumvent immunotherapeutic resistance.

摘要

免疫检查点抑制剂(ICIs)在肿瘤治疗领域取得了前所未有的临床疗效,并改变了治疗模式,但仍有相当一部分患者对 ICI 单药治疗无反应或产生耐药性,这可归因于细胞代谢功能障碍。尽管代谢失调长期以来一直被认为是肿瘤的一个标志,但现在越来越多的人接受这样一种观点,即代谢重编程不仅是肿瘤细胞的特征,也是免疫细胞的特征。相应地,人们过去更多地关注肿瘤细胞代谢对免疫细胞的影响,但实际上,免疫细胞在激活和分化过程中与自身代谢功能密切相互作用,这种相互作用以前从未被认识到,这开辟了一个名为免疫代谢的全新领域。对肿瘤浸润免疫细胞的代谢干预可能为打破耐药性和改善现有的 ICI 免疫治疗提供新的机会,其关键可能是确定代谢干预与 ICI 的协同组合,以获得协同效益,并促进调整后的抗肿瘤免疫反应。在此,我们从不同肿瘤浸润免疫细胞的代谢重编程的新角度阐述了免疫治疗耐药的潜在机制,以及相关的代谢干预,以期为靶向代谢脆弱性以规避免疫治疗耐药性提供参考。

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