Open Access
CC BY 4.0 · Semin Liver Dis
DOI: 10.1055/a-2679-3641
Review Article

Microbial Modulation of the Gut–Liver Axis in Autoimmune Liver Diseases

Shihui Wei
1   State Key Laboratory for the Diagnosis and Treatment of Infectious Diseases, National Clinical Research Center for Infectious Diseases, National Medical Center for Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou City, China
,
Juan Lu
1   State Key Laboratory for the Diagnosis and Treatment of Infectious Diseases, National Clinical Research Center for Infectious Diseases, National Medical Center for Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou City, China
› Author Affiliations

Funding This research receives grants from the Fundamental Research Funds for the Central Universities (grant number: 2025ZFJH03); the Central Guidance Fund for Local Science and Technology Development (grant number: 2024ZY01054).


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Abstract

Autoimmune liver diseases (AILDs), including autoimmune hepatitis, primary biliary cholangitis, and primary sclerosing cholangitis, are chronic inflammatory conditions influenced by complex interactions among genetic, environmental, and immunological factors. Recent studies have highlighted the critical role of the gut microbiota in regulating immune responses beyond the gastrointestinal tract via the gut–liver axis. This review examines the interactions between intestinal microecology and AILDs, with a focus on mechanisms such as bacterial translocation, disruption of the intestinal barrier, and modulation of microbial metabolites. Dysbiosis, involving alterations in both bacterial and fungal communities, has been associated with immune dysregulation and hepatic inflammation. Evidence indicates that short-chain fatty acids, bile acids, and microbial products such as lipopolysaccharides influence hepatic immune tolerance and inflammatory signaling pathways. Several diagnostic and therapeutic approaches, including probiotics, fecal microbiota transplantation, and bile acid regulation, have shown potential to slow or alter disease progression. However, the clinical translation of these findings remains limited due to interindividual variability and the complex nature of the gut–liver axis. Continued research is needed to develop precision medicine strategies that can harness intestinal microecology for improved management of AILDs.

Data Availability

Data will be made available on request.


Ethics Approval and Consent to Participate

Not applicable.


Consent for Publication

Not applicable.


Authors' Contribution

S.W.: writing—original draft, visualization, methodology, data curation, conceptualization. J.L.: conceptualization, supervision, writing—review and editing.




Publication History

Article published online:
27 August 2025

© 2025. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/)

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