Ammonia in the crosshairs: microbial targets for metabolic dysfunction–associated steatohepatitis prevention

Metabolic dysfunction-associated steatohepatitis (MASH) is increasingly linked to disruptions of the gut/liver axis, yet the microbial mechanisms driving disease progression remain incompletely defined. Here, Qu et al. have identified ileal microbial ammonia production by Clostridium perfringens as a mechanistic driver of epithelial barrier dysfunction and hepatic CD8+ T cell remodeling in MASH. In nonhuman primate and mouse models of MASH, the authors demonstrated that the glycine-based tripeptide DT-109 restored gut barrier integrity and attenuated FosB-mediated CCL5 expression in CD8+ T cells via inhibition of bacterial nitrite reductase A-mediated microbial ammonia production. These findings position microbial nitrogen metabolism as a tractable therapeutic target and highlight metabolite-focused microbiome interventions as a potential MASH intervention.

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Publication Details

Journal
Journal of Clinical Investigation
Published
2026-06-30
DOI
https://doi.org/10.1172/jci207921
Primary Topic
Liver Disease Diagnosis and Treatment
Type
article
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article

Ammonia in the crosshairs: microbial targets for metabolic dysfunction–associated steatohepatitis prevention

Vanessa Leone, Arion KENNEDY
Journal of Clinical Investigation
Liver Disease Diagnosis and Treatment
article

Ammonia in the crosshairs: microbial targets for metabolic dysfunction–associated steatohepatitis prevention

Vanessa Leone, Arion KENNEDY
article en

Abstract

Metabolic dysfunction-associated steatohepatitis (MASH) is increasingly linked to disruptions of the gut/liver axis, yet the microbial mechanisms driving disease progression remain incompletely defined. Here, Qu et al. have identified ileal microbial ammonia production by Clostridium perfringens as a mechanistic driver of epithelial barrier dysfunction and hepatic CD8+ T cell remodeling in MASH. In nonhuman primate and mouse models of MASH, the authors demonstrated that the glycine-based tripeptide DT-109 restored gut barrier integrity and attenuated FosB-mediated CCL5 expression in CD8+ T cells via inhibition of bacterial nitrite reductase A-mediated microbial ammonia production. These findings position microbial nitrogen metabolism as a tractable therapeutic target and highlight metabolite-focused microbiome interventions as a potential MASH intervention.

Journal of Clinical InvestigationVol. 136(13)
University of Wisconsin–Madison (US), North Carolina State University (US)
Good health and well-being
Openalex Percentile: Top 8%
Liver Disease Diagnosis and Treatment
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Ammonia in the crosshairs: microbial targets for metabolic dysfunction–associated steatohepatitis prevention — Vanessa Leone, Arion KENNEDY · Journal of Clinical Investigation (2026) | TGRS Research Map | TGRS