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肠道微生物群在肿瘤、免疫和免疫治疗中的作用。

The role of the gut microbiota in tumor, immunity, and immunotherapy.

机构信息

Department of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, China.

出版信息

Front Immunol. 2024 Jun 5;15:1410928. doi: 10.3389/fimmu.2024.1410928. eCollection 2024.


DOI:10.3389/fimmu.2024.1410928
PMID:38903520
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11188355/
Abstract

In recent years, with the deepening understanding of the gut microbiota, it has been recognized to play a significant role in the development and progression of diseases. Particularly in gastrointestinal tumors, the gut microbiota influences tumor growth by dysbiosis, release of bacterial toxins, and modulation of host signaling pathways and immune status. Immune checkpoint inhibitors (ICIs) have greatly improved cancer treatment efficacy by enhancing immune cell responses. Current clinical and preclinical studies have demonstrated that the gut microbiota and its metabolites can enhance the effectiveness of immunotherapy. Furthermore, certain gut microbiota can serve as biomarkers for predicting immunotherapy responses. Interventions targeting the gut microbiota for the treatment of gastrointestinal diseases, especially colorectal cancer (CRC), include fecal microbiota transplantation, probiotics, prebiotics, engineered bacteria, and dietary interventions. These approaches not only improve the efficacy of ICIs but also hold promise for enhancing immunotherapy outcomes. In this review, we primarily discuss the role of the gut microbiota and its metabolites in tumors, host immunity, and immunotherapy.

摘要

近年来,随着人们对肠道微生物群的深入了解,人们认识到其在疾病的发生和发展中起着重要作用。特别是在胃肠道肿瘤中,肠道微生物群通过失调、释放细菌毒素以及调节宿主信号通路和免疫状态来影响肿瘤的生长。免疫检查点抑制剂(ICIs)通过增强免疫细胞的反应,极大地提高了癌症治疗的疗效。目前的临床和临床前研究表明,肠道微生物群及其代谢物可以增强免疫治疗的效果。此外,某些肠道微生物群可以作为预测免疫治疗反应的生物标志物。针对肠道微生物群治疗胃肠道疾病(特别是结直肠癌(CRC))的干预措施包括粪便微生物群移植、益生菌、益生元、工程菌和饮食干预。这些方法不仅提高了 ICI 的疗效,而且为增强免疫治疗效果提供了希望。在这篇综述中,我们主要讨论了肠道微生物群及其代谢物在肿瘤、宿主免疫和免疫治疗中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d10/11188355/bd6953879ad0/fimmu-15-1410928-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d10/11188355/66abbd128f95/fimmu-15-1410928-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d10/11188355/fa32bb601215/fimmu-15-1410928-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d10/11188355/bd6953879ad0/fimmu-15-1410928-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d10/11188355/66abbd128f95/fimmu-15-1410928-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d10/11188355/fa32bb601215/fimmu-15-1410928-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d10/11188355/bd6953879ad0/fimmu-15-1410928-g003.jpg

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[7]
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[9]
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[10]
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本文引用的文献

[1]
Pretreatment with an antibiotics cocktail enhances the protective effect of probiotics by regulating SCFA metabolism and Th1/Th2/Th17 cell immune responses.

BMC Microbiol. 2024-3-18

[2]
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JCI Insight. 2024-1-23

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Nat Med. 2023-8

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