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以肠道微生物群为靶点进行疾病的免疫治疗。

Targeting gut microbiota for immunotherapy of diseases.

作者信息

Yu Ya-Jie, Liu Xiao-Dong, Liao Cai, Yu Rui, Wang Xin, Li Ming, Wang Yun

机构信息

Department of Clinical Pharmacology, School of Pharmacy, China Medical University, No.77 Puhe Road, Shenyang North New Area, Shenyang, 110122, Liaoning, China.

Department of Pharmacy, Shengjing Hospital of China Medical University, Shenyang, Liaoning, China.

出版信息

Arch Toxicol. 2024 Aug;98(8):2429-2439. doi: 10.1007/s00204-024-03770-x. Epub 2024 May 9.

DOI:10.1007/s00204-024-03770-x
PMID:38722348
Abstract

With advances in next-generation sequencing technology, there is growing evidence that the gut microbiome plays a key role in the host's innate and adaptive immune system. Gut microbes and their metabolites directly or indirectly regulate host immune cells. Crucially, dysregulation of the gut microbiota is often associated with many immune system diseases. In turn, microbes modulate disease immunotherapy. Data from preclinical to clinical studies suggest that the gut microbiota may influence the effectiveness of tumor immunotherapy, particularly immune checkpoint inhibitors (ICIs). In addition, the most critical issue now is a COVID-19 vaccine that generates strong and durable immunity. A growing number of clinical studies confirm the potential of gut microbes to enhance the efficacy of COVID-19 vaccines. However, it is still unclear how gut bacteria interact with immune cells and what treatments are based on gut microbes. Here, we outline recent advances in the effects and mechanisms of the gut microbiota and its metabolites (tryptophan metabolites, bile acids, short-chain fatty acids, and inosine) on different immune cells (dendritic cells, CD4T cells, and macrophages). It also highlights innovative intervention strategies and clinical trials of microbiota-based checkpoint blocking therapies for tumor immunity, and ongoing efforts to maintain the long-term immunogenicity of COVID-19 vaccines. Finally, the challenges to be overcome in this area are discussed. These provide an important basis for further research and clinical translation of gut microbiota.

摘要

随着下一代测序技术的进步,越来越多的证据表明肠道微生物群在宿主的固有免疫和适应性免疫系统中发挥着关键作用。肠道微生物及其代谢产物直接或间接调节宿主免疫细胞。至关重要的是,肠道微生物群的失调通常与许多免疫系统疾病有关。反过来,微生物也会调节疾病的免疫治疗。从临床前到临床研究的数据表明,肠道微生物群可能会影响肿瘤免疫治疗的效果,尤其是免疫检查点抑制剂(ICI)。此外,目前最关键的问题是研发出一种能产生强大而持久免疫力的新冠疫苗。越来越多的临床研究证实了肠道微生物增强新冠疫苗疗效的潜力。然而,肠道细菌如何与免疫细胞相互作用以及基于肠道微生物的治疗方法仍不清楚。在此,我们概述了肠道微生物群及其代谢产物(色氨酸代谢产物、胆汁酸、短链脂肪酸和肌苷)对不同免疫细胞(树突状细胞、CD4 T细胞和巨噬细胞)的作用及机制的最新进展。还强调了基于微生物群的肿瘤免疫检查点阻断疗法的创新干预策略和临床试验,以及为维持新冠疫苗长期免疫原性所做的持续努力。最后,讨论了该领域有待克服的挑战。这些为肠道微生物群的进一步研究和临床转化提供了重要依据。

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引用本文的文献

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Front Immunol. 2025 Aug 1;16:1638352. doi: 10.3389/fimmu.2025.1638352. eCollection 2025.
2
A two-step, two-sample Mendelian randomization analysis investigating the interplay between gut microbiota, immune cells, and melanoma skin cancer.一项两步、两样本孟德尔随机化分析,研究肠道微生物群、免疫细胞与黑色素瘤皮肤癌之间的相互作用。
Medicine (Baltimore). 2024 Nov 8;103(45):e40432. doi: 10.1097/MD.0000000000040432.

本文引用的文献

1
Dietary L-Tryptophan consumption determines the number of colonic regulatory T cells and susceptibility to colitis via GPR15.膳食 L-色氨酸的摄入通过 GPR15 决定结肠调节性 T 细胞的数量和结肠炎易感性。
Nat Commun. 2023 Nov 14;14(1):7363. doi: 10.1038/s41467-023-43211-4.
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Short-chain fatty acids stimulate dendrite elongation in dendritic cells by inhibiting histone deacetylase.短链脂肪酸通过抑制组蛋白去乙酰化酶来刺激树突状细胞的树突伸长。
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Regulatory T cells in the face of the intestinal microbiota.
肠道微生物群面前的调节性 T 细胞。
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Macrophages in intestinal homeostasis and inflammatory bowel disease.肠道稳态和炎症性肠病中的巨噬细胞。
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Endoplasmic reticulum stress in the intestinal epithelium initiates purine metabolite synthesis and promotes Th17 cell differentiation in the gut.肠上皮细胞中的内质网应激会引发嘌呤代谢物的合成,并促进肠道中 Th17 细胞的分化。
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Current Knowledge of Th22 Cell and IL-22 Functions in Infectious Diseases.Th22细胞与白细胞介素-22在传染病中的功能的当前认知
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Crosstalk between Gut Microbiota and Host Immunity: Impact on Inflammation and Immunotherapy.肠道微生物群与宿主免疫之间的相互作用:对炎症和免疫治疗的影响
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The gut microbiota and metabolome are associated with diminished COVID-19 vaccine-induced antibody responses in immunosuppressed inflammatory bowel disease patients.肠道微生物组和代谢组与免疫抑制性炎症性肠病患者 COVID-19 疫苗诱导的抗体反应减弱有关。
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