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Non-alcoholic fatty liver disease: the interplay between metabolism, microbes and immunity

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NATURE METABOLISM
卷 3, 期 12, 页码 1596-1607

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NATURE PORTFOLIO
DOI: 10.1038/s42255-021-00501-9

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资金

  1. excellence initiative VASCage (Centre for Promoting Vascular Health in the Ageing Community), an RAMP
  2. D K-Centre award (COMET programme (Competence Centers for Excellent Technologies)) - Austrian Ministry for Transport, Innovation and Technology
  3. Austrian Ministry for Digital and Economic Affairs
  4. federal state Tyrol
  5. federal state Salzburg
  6. federal state Vienna
  7. CRC TRR179
  8. German Center for Infection Research, Munich site
  9. Austrian Science Fund (FWF) [P33070]
  10. Austrian Science Fund (FWF) [P33070] Funding Source: Austrian Science Fund (FWF)

向作者/读者索取更多资源

Non-alcoholic fatty liver disease (NAFLD) is a global pandemic that particularly affects patients with obesity and type 2 diabetes. The complex interplay between metabolic dysregulation, altered gut microbiome and dysregulated innate and adaptive immunity contributes to the pathology and progression of NAFLD.
Non-alcoholic fatty liver disease (NAFLD) has emerged pandemically across the globe and particularly affects patients with obesity and type 2 diabetes. NAFLD is a complex systemic disease that is characterised by hepatic lipid accumulation, lipotoxicity, insulin resistance, gut dysbiosis and inflammation. In this review, we discuss how metabolic dysregulation, the gut microbiome, innate and adaptive immunity and their interplay contribute to NAFLD pathology. Lipotoxicity has been shown to instigate liver injury, inflammation and insulin resistance. Synchronous metabolic dysfunction, obesity and related nutritional perturbation may alter the gut microbiome, in turn fuelling hepatic and systemic inflammation by direct activation of innate and adaptive immune responses. We review evidence suggesting that, collectively, these unresolved exogenous and endogenous cues drive liver injury, culminating in liver fibrosis and advanced sequelae of this disorder such as liver cirrhosis and hepatocellular carcinoma. Understanding NAFLD as a complex interplay between metabolism, gut microbiota and the immune response will challenge the clinical perception of NAFLD and open new therapeutic avenues. Tilg et al. explore how metabolic dysfunction, altered gut microbiome and dysregulated innate and adaptive immunity contribute to NAFLD and how the interplay between these factors mediates disease progression.

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