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Observational Study
. 2025 Jul 1;82(1):127-139.
doi: 10.1097/HEP.0000000000001046. Epub 2024 Sep 25.

Viral antibody response predicts morbidity and mortality in alcohol-associated hepatitis

Collaborators, Affiliations
Observational Study

Viral antibody response predicts morbidity and mortality in alcohol-associated hepatitis

Cynthia L Hsu et al. Hepatology. .

Abstract

Background and aims: Alcohol-associated hepatitis (AH) is associated with very high mortality despite abstinence from alcohol; up to 40% of patients die within 6 months of diagnosis. Patients with AH are especially prone to infections, which can lead to multiorgan dysfunction and poorer prognosis.

Approach and results: We performed comprehensive serological profiling of the viral and bacterial infection history of 36 healthy controls, 48 patients with alcohol use disorder, and 224 patients with AH from 2 multicenter observational studies. We used systematic viral and bacterial epitope scanning by VirScan, a phage-display immunoprecipitation and sequencing technology that detects the peptides recognized by antibodies in patient sera, to comprehensively analyze antiviral and antibacterial antibodies and identify serologic biomarkers to predict patient outcomes. We found significant differences in the serological profiles of the 3 populations. The number of serum antibody epitopes in patients with alcohol use disorder during abstinence was increased compared with during active alcohol use. A decreased number and diversity of viral and bacterial antibody targets were detected in the sera of patients with AH, particularly those with a higher Child-Pugh score. In patients with AH, a decrease in the serum antiviral, but not antibacterial, antibody repertoire was associated with decompensation and mortality. Ninety-day mortality in AH could be predicted using a serum viral epitope signature.

Conclusions: Abstinence from alcohol is associated with a significant increase in serum viral and bacterial antibody response. Decreased serum antiviral antibody repertoire is predictive of decompensation of liver disease and mortality in patients with AH.

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Conflict of interest statement

Conflicts of Interest:

Elizabeth C. Verna received grants from Salix. Juan G. Abraldes consults for 89Bio. AstraZeneca, Boehringer Ingelheim, Boston Pharmaceuticals, and Novo Nordisk. He received grants from Advanz, Cook, and Gilead. Robert S. Brown Jr. consults and received grants from AbbVie, Intercept, and Mirum. He consults for eGenesis, Gilead, and Mallinckrodt. He received grants from Durect. Victor Vargas advises Ipsen. He received grants from Intercept. Debbie L. Shawcross consults and received grants from EnteroBiotix and Norgine. She consults for Apollo Therapeutics, MRM Health, and Satellite Bio. Philippe Mathurin is on the speakers’ bureau for AbbVie and Gilead. Ramon Bataller consults for Boehringer Ingelheim, GlaxoSmithKline, and Novo Nordisk. He is on the speakers’ bureau for AbbVie and Gilead. Bernd Schnabl consults and received grants from Intercept. He consults for Ambys Medicines, Ferring Research Institute, Gelesis, HOST Therabiomics, Mabwell, Patara, Surrozen, and Takeda. He received grants from Axial Biotherapeutics, BiomX, CymaBay, NGM Bio, Prodigy Biotech, and Synlogic Operating Company. He owns stock in Nterica Bio. The remaining authors have no conflicts to report.

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