Role of microbiome in autoimmune liver diseases

Author:

Schneider Kai Markus1ORCID,Kummen Martin234ORCID,Trivedi Palak J.5678ORCID,Hov Johannes R.23910ORCID

Affiliation:

1. Department of Medicine III, University Hospital RWTH Aachen, Aachen, Germany

2. Norwegian PSC Research Center, Department of Transplantation Medicine, Oslo University Hospital Oslo, Norway

3. Institute of Clinical Medicine, University of Oslo, Oslo, Norway

4. Department of Oncology, Oslo University Hospital, Oslo, Norway

5. National Institute for Health and Care Research Birmingham Biomedical Research Centre, Centre for Liver and Gastroenterology Research, University of Birmingham, UK

6. Liver Unit, University Hospitals Birmingham Queen Elizabeth, Birmingham, UK

7. Institute of Immunology and Immunotherapy, University of Birmingham, UK

8. Institute of Applied Health Research, University of Birmingham, UK

9. Research Institute of Internal Medicine, Oslo University Hospital, Rikshospitalet, Oslo, Norway

10. Section of Gastroenterology, Department of Transplantation Medicine, Oslo University Hospital, Rikshospitalet, Oslo, Norway

Abstract

The microbiome plays a crucial role in integrating environmental influences into host physiology, potentially linking it to autoimmune liver diseases, such as autoimmune hepatitis, primary biliary cholangitis, and primary sclerosing cholangitis. All autoimmune liver diseases are associated with reduced diversity of the gut microbiome and altered abundance of certain bacteria. However, the relationship between the microbiome and liver diseases is bidirectional and varies over the course of the disease. This makes it challenging to dissect whether such changes in the microbiome are initiating or driving factors in autoimmune liver diseases, secondary consequences of disease and/or pharmacological intervention, or alterations that modify the clinical course that patients experience. Potential mechanisms include the presence of pathobionts, disease-modifying microbial metabolites, and more nonspecific reduced gut barrier function, and it is highly likely that the effect of these change during the progression of the disease. Recurrent disease after liver transplantation is a major clinical challenge and a common denominator in these conditions, which could also represent a window to disease mechanisms of the gut-liver axis. Herein, we propose future research priorities, which should involve clinical trials, extensive molecular phenotyping at high resolution, and experimental studies in model systems. Overall, autoimmune liver diseases are characterized by an altered microbiome, and interventions targeting these changes hold promise for improving clinical care based on the emerging field of microbiota medicine.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Hepatology

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