The Role of the Gut-Liver Axis in Metabolic Dysfunction-Associated Fatty Liver Disease

Front Immunol. 2021 Apr 16:12:660179. doi: 10.3389/fimmu.2021.660179. eCollection 2021.

Abstract

The complex interplay between the gut microbiota, the intestinal barrier, the immune system and the liver is strongly influenced by environmental and genetic factors that can disrupt the homeostasis leading to disease. Among the modulable factors, diet has been identified as a key regulator of microbiota composition in patients with metabolic syndrome and related diseases, including the metabolic dysfunction-associated fatty liver disease (MAFLD). The altered microbiota disrupts the intestinal barrier at different levels inducing functional and structural changes at the mucus lining, the intercellular junctions on the epithelial layer, or at the recently characterized vascular barrier. Barrier disruption leads to an increased gut permeability to bacteria and derived products which challenge the immune system and promote inflammation. All these alterations contribute to the pathogenesis of MAFLD, and thus, therapeutic approaches targeting the gut-liver-axis are increasingly being explored. In addition, the specific changes induced in the intestinal flora may allow to characterize distinctive microbial signatures for non-invasive diagnosis, severity stratification and disease monitoring.

Keywords: gut abnormalities; intestinal immunity; intestinal microbiota; metabolic liver disease; steatosis.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • CCR5 Receptor Antagonists / therapeutic use
  • Dysbiosis / immunology
  • Dysbiosis / microbiology
  • Gastrointestinal Microbiome / immunology*
  • Humans
  • Imidazoles / therapeutic use
  • Intestinal Mucosa / immunology*
  • Intestinal Mucosa / metabolism
  • Intestinal Mucosa / microbiology
  • Liver / immunology*
  • Liver / metabolism
  • Liver / pathology
  • Metabolic Syndrome / drug therapy
  • Metabolic Syndrome / immunology*
  • Metabolic Syndrome / metabolism
  • Non-alcoholic Fatty Liver Disease / drug therapy
  • Non-alcoholic Fatty Liver Disease / immunology*
  • Non-alcoholic Fatty Liver Disease / metabolism
  • Sulfoxides / therapeutic use

Substances

  • CCR5 Receptor Antagonists
  • Imidazoles
  • Sulfoxides
  • cenicriviroc