The bidirectional immune crosstalk in metabolic dysfunction-associated steatotic liver disease.

Cell Metab

Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH 45220, USA; Division of Immunobiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA; Immunology Graduate Program, University of Cincinnati College of Medicine, Cincinnati, OH 45220, USA; Medical Scientist Training Program, University of Cincinnati College of Medicine, Cincinnati, OH 45220, USA; Center for Inflammation and Tolerance, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA. Electronic address:

Published: November 2023

AI Article Synopsis

  • Metabolic dysfunction-associated steatotic liver disease (MASLD) significantly increases the risk of severe liver diseases, yet effective treatments are lacking.
  • The disease involves complex immune responses where both innate and adaptive immune systems play a role, but their interactions and cooperative effects on MASLD are not fully understood.
  • This review discusses various immune cell types and their bidirectional communication processes that affect MASLD, suggesting that understanding these interactions could lead to new therapeutic strategies.

Article Abstract

Metabolic dysfunction-associated steatotic liver disease (MASLD) is an unabated risk factor for end-stage liver diseases with no available therapies. Dysregulated immune responses are critical culprits of MASLD pathogenesis. Independent contributions from either the innate or adaptive arms of the immune system or their unidirectional interplay are commonly studied in MASLD. However, the bidirectional communication between innate and adaptive immune systems and its impact on MASLD remain insufficiently understood. Given that both innate and adaptive immune cells are indispensable for the development and progression of inflammation in MASLD, elucidating pathogenic contributions stemming from the bidirectional interplay between these two arms holds potential for development of novel therapeutics for MASLD. Here, we review the immune cell types and bidirectional pathways that influence the pathogenesis of MASLD and highlight potential pharmacologic approaches to combat MASLD based on current knowledge of this bidirectional crosstalk.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10680147PMC
http://dx.doi.org/10.1016/j.cmet.2023.10.009DOI Listing

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