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口腔-肠道微生物群综合疗法:预防细菌易位以管理全身性疾病的新视角。

Integrated oral-gut microbiota therapy: a novel perspective on preventing bacterial translocation for systemic disease management.

作者信息

Zhu Jie, Jiang Ziyi, Yu Fangli, Gao Linglin, Wang Xiaomei, Wang Qiang

机构信息

Institute of Infection, Immunology and Tumor Microenvironment, Wuchang Hospital Affiliated to Wuhan University of Science and Technology, Medical College, Wuhan University of Science and Technology, Wuhan, China.

Department of Gynecology, Maternal and Child Health Hospital of Hubei Province Graduate Joint Training Base, School of Medicine, Wuhan University of Science and Technology, Wuhan, China.

出版信息

Front Cell Infect Microbiol. 2025 Jul 28;15:1641816. doi: 10.3389/fcimb.2025.1641816. eCollection 2025.

Abstract

Oral dysbiosis increases the risk of oral diseases and systemic diseases, with many related conditions overlapping with systemic diseases triggered by gut dysbiosis. Studies have shown that the oral cavity serves as an endogenous reservoir for gut microbial strains, influencing the homeostasis of both oral and gut microbiota through interactions involving bacterial translocation, microbial metabolites, immune cells, and inflammatory factors. In specific disease contexts, certain microbial communities [e.g., , ], metabolites (e.g., short-chain fatty acids, gingipains), ligands (e.g., lipopolysaccharides, peptidoglycans), or host responses may vary. However, substantial evidence has firmly established the central role of microbiota in oral-gut crosstalk. These findings position the oral-gut axis as a potential causal mechanism linking systemic diseases. Compared with healthy non-cancer subjects, cancer patients exhibit significant differences in oral microbial abundance and diversity. For instance, is associated with an increased risk of colorectal cancer(CRC), while and may serve as potential biomarkers for hepatocellular carcinoma. Notably, oral pathogens or their metabolites can translocate along the oral-gut axis or due to certain oral activities (e.g., toothbrushing, tooth extraction), contributing to the initiation and progression of inflammation and tumorigenesis. For example, can accumulate in the liver, where its fimbrial protein FimA binds to Toll-like receptor 2 (TLR2), complement receptor 3 (CR3), and CXC-chemokine receptor 4 (CXCR4), triggering various immune responses that promote the development of non-alcoholic fatty liver disease(NAFLD). This review systematically summarizes recent advances in understanding the role of the oral microbiota and the oral-gut axis in systemic diseases, along with their underlying pathological mechanisms. It particularly highlights the translational value of integrating oral and gut microbiota research, offering novel insights for the prevention and precision treatment of systemic disorders. The unique and heterogeneous microbiota within the oral microbiota and the oral-gut axis may serve as novel diagnostic biomarkers or therapeutic targets for diseases associated with oral and gut dysbiosis.

摘要

口腔生态失调会增加患口腔疾病和全身性疾病的风险,许多相关情况与肠道生态失调引发的全身性疾病相互重叠。研究表明,口腔是肠道微生物菌株的内源性储存库,通过涉及细菌易位、微生物代谢产物、免疫细胞和炎症因子的相互作用,影响口腔和肠道微生物群的稳态。在特定疾病背景下,某些微生物群落[例如, , ]、代谢产物(例如短链脂肪酸、牙龈蛋白酶)、配体(例如脂多糖、肽聚糖)或宿主反应可能会有所不同。然而,大量证据已确凿地证实了微生物群在口腔-肠道串扰中的核心作用。这些发现将口腔-肠道轴定位为连接全身性疾病的潜在因果机制。与健康的非癌症受试者相比,癌症患者的口腔微生物丰度和多样性存在显著差异。例如, 与结直肠癌(CRC)风险增加有关,而 和 可能作为肝细胞癌的潜在生物标志物。值得注意的是,口腔病原体或其代谢产物可沿口腔-肠道轴转移,或由于某些口腔活动(例如刷牙、拔牙)而转移,从而导致炎症和肿瘤发生的起始和进展。例如, 可在肝脏中积聚,其菌毛蛋白FimA与Toll样受体2(TLR2)、补体受体3(CR3)和CXC趋化因子受体4(CXCR4)结合,触发各种免疫反应,促进非酒精性脂肪性肝病(NAFLD)的发展。本综述系统地总结了在理解口腔微生物群和口腔-肠道轴在全身性疾病中的作用及其潜在病理机制方面的最新进展。它特别强调了整合口腔和肠道微生物群研究的转化价值,为全身性疾病的预防和精准治疗提供了新的见解。口腔微生物群和口腔-肠道轴内独特且异质的微生物群可能作为与口腔和肠道生态失调相关疾病的新型诊断生物标志物或治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce3f/12336206/d5e5f324d08b/fcimb-15-1641816-g001.jpg

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