Metabolic Dysfunction-Associated Steatohepatitis: Is There Evidence for Fractured CD4+ T-Cell Tolerance in the Immunopathogenesis
5 affiliations
- 1Department of Pediatrics, Indiana University School of Medicine, Indianapolis, Indiana
- 2Riley Children's Health, Indianapolis, Indiana
- 3Nutrition and Molecular Metabolism Center, Indiana University School of Medicine, Indianapolis, Indiana
- 4Department of Anatomy, Cell Biology, and Physiology, Indiana University School of Medicine, Indianapolis, Indiana
- 5Department of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, Indiana
Abstract
Metabolic dysfunction–associated liver disease is defined by hepatic steatosis with concomitant metabolic risk factors and is the leading cause of chronic liver disease. In approximately one-third of individuals, the disease progresses to metabolic dysfunction–associated steatohepatitis, a more severe form encompassing steatosis with inflammation and hepatocellular injury predisposing to liver failure, cirrhosis, and hepatocellular carcinoma. The mechanism(s) responsible for this aberrant inflammation are unknown. In this review, we explore the breakdown of the hepatic tolerogenic environment in metabolic dysfunction–associated steatohepatitis with discussion on fractured CD4+ T cell tolerance as an integral driver of the progression of metabolic dysfunction–associated liver disease to metabolic dysfunction–associated steatohepatitis.
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BibTeX
@article{russi2026metabolic,
title = {{Metabolic Dysfunction-Associated Steatohepatitis: Is There Evidence for Fractured CD4+ T-Cell Tolerance in the Immunopathogenesis}},
author = {Abigail E. Russi and Brian J. DeBosch},
journal = {Cellular and Molecular Gastroenterology and Hepatology},
year = {2026},
month = sep,
doi = {10.1016/j.jcmgh.2026.101899},
url = {https://doi.org/10.1016/j.jcmgh.2026.101899},
note = {CC BY-NC-ND 4.0},
}
RIS
TY - JOUR
TI - Metabolic Dysfunction-Associated Steatohepatitis: Is There Evidence for Fractured CD4+ T-Cell Tolerance in the Immunopathogenesis
AU - Abigail E. Russi
AU - Brian J. DeBosch
PY - 2026
DA - 2026/09/19
JO - Cellular and Molecular Gastroenterology and Hepatology
DO - 10.1016/j.jcmgh.2026.101899
UR - https://doi.org/10.1016/j.jcmgh.2026.101899
AB - Metabolic dysfunction–associated liver disease is defined by hepatic steatosis with concomitant metabolic risk factors and is the leading cause of chronic liver disease. In approximately one-third of individuals, the disease progresses to metabolic dysfunction–associated steatohepatitis, a more severe form encompassing steatosis with inflammation and hepatocellular injury predisposing to liver failure, cirrhosis, and hepatocellular carcinoma. The mechanism(s) responsible for this aberrant inflammation are unknown. In this review, we explore the breakdown of the hepatic tolerogenic environment in metabolic dysfunction–associated steatohepatitis with discussion on fractured CD4+ T cell tolerance as an integral driver of the progression of metabolic dysfunction–associated liver disease to metabolic dysfunction–associated steatohepatitis.
SN - 2352-345X
ER -