溶细胞素
医学
抗体
粪肠球菌
免疫学
酒精性肝炎
肝病
中和
微生物学
酒精性肝病
生物
内科学
肝硬化
毒力
生物化学
遗传学
基因
细菌
金黄色葡萄球菌
作者
Noemí Cabré,Phillipp Hartmann,Cristina Llorente,Tetsuya Kouno,Yanhan Wang,Su-Ling Zeng,Hyun Young Kim,Xinlian Zhang,Tatiana Kisseleva,S. Iyer,Sirisha Kudumala,Bernd Schnabl
出处
期刊:Hepatology
[Wiley]
日期:2023-02-23
卷期号:78 (1): 295-306
被引量:5
标识
DOI:10.1097/hep.0000000000000324
摘要
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.
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