IgY antibodies against cytolysin reduce ethanol-induced liver disease in mice

Author:

Cabré Noemí1ORCID,Hartmann Phillipp123ORCID,Llorente Cristina1ORCID,Kouno Tetsuya1ORCID,Wang Yanhan14ORCID,Zeng Suling14ORCID,Kim Hyun Young5ORCID,Zhang Xinlian6ORCID,Kisseleva Tatiana5ORCID,Iyer Subramanian7ORCID,Kudumala Sirisha7ORCID,Schnabl Bernd14ORCID

Affiliation:

1. Department of Medicine, University of California San Diego, La Jolla, California, USA

2. Department of Pediatrics, University of California, San Diego, La Jolla, California, USA

3. Division of Gastroenterology, Hepatology & Nutrition, Rady Children’s Hospital San Diego, San Diego, California, USA

4. Department of Medicine, VA San Diego Healthcare System, San Diego, California, USA

5. Department of Surgery, University of California, San Diego, La Jolla, California, USA

6. Division of Biostatistics and Bioinformatics, Herbert Wertheim School of Public Health and Human Longevity Science, University of California, San Diego, La Jolla, California, USA

7. Prodigy Biotech Inc., West Chester, Pennsylvania, USA

Abstract

Background and Aims: Patients with severe alcohol-associated hepatitis have high morbidity and mortality. Novel therapeutic approaches are urgently needed. The aims of our study were to confirm the predictive value of cytolysin-positive Enterococcus faecalis (E. faecalis) for mortality in patients with alcohol-associated hepatitis and to assess the protective effect of specific chicken immunoglobulin Y (IgY) antibodies against cytolysin in vitro and in a microbiota-humanized mouse model of ethanol-induced liver disease. Approach and Results: We investigated a multicenter cohort of 26 subjects with alcohol-associated hepatitis and confirmed our previous findings that the presence of fecal cytolysin-positive E. faecalis predicted 180-day mortality in those patients. After combining this smaller cohort with our previously published multicenter cohort, the presence of fecal cytolysin has a better diagnostic area under the curve, better other accuracy measures, and a higher odds ratio to predict death in patients with alcohol-associated hepatitis than other commonly used liver disease models. In a precision medicine approach, we generated IgY antibodies against cytolysin from hyperimmunized chickens. Neutralizing IgY antibodies against cytolysin reduced cytolysin-induced cell death in primary mouse hepatocytes. The oral administration of IgY antibodies against cytolysin decreased ethanol-induced liver disease in gnotobiotic mice colonized with stool from cytolysin-positive patients with alcohol-associated hepatitis. Conclusions: E. faecalis cytolysin is an important mortality predictor in alcohol-associated hepatitis patients, and its targeted neutralization through specific antibodies improves ethanol-induced liver disease in microbiota-humanized mice.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Hepatology

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