AI Article Synopsis

  • Chronic liver injury can lead to cirrhosis and end-stage liver disease (ESLD), which are major causes of death globally.
  • The study focused on the immune and inflammatory characteristics of ESLD from four noncancer causes: HBV-ALF, ALF, AILD, and AH, using data from liver tissue and blood samples.
  • Findings indicated that, apart from HBV-induced ESLD, there were no significant differences in the immune and inflammatory environments among patients with other noncancerous ESLD, and IL-15 was identified as a potential prognostic marker for these patients.

Article Abstract

Chronic liver injury eventually progresses to cirrhosis and end-stage liver disease (ESLD), which are the leading causes of death in patients with liver disease worldwide. ESLD has a variety of etiologies and a complex pathogenesis. This study analyzed the characteristics of ESLD by studying the immune microenvironment and inflammatory microenvironment of ESLD caused by 4 noncancer diseases, including HBV-ALF, ALF, AILD, and AH. We collected transcriptome data from noncancer ESLD patients, collected liver tissue samples and blood samples from ESLD liver transplant patients, and analyzed the immune and inflammatory microenvironments in the liver and blood. The results showed that with the exception of HBV-induced ESLD, there were no significant differences in immune microenvironment scores among patients with ESLD caused by other noncancer diseases. Moreover, there were no significant differences in the inflammatory microenvironment in the liver and blood of patients with ESLD caused by the 4 noncancer diseases. Furthermore, we found that the cytokine, IL-15, could predict the prognosis of ESLD patients.

Download full-text PDF

Source
http://dx.doi.org/10.1089/jir.2022.0172DOI Listing

Publication Analysis

Top Keywords

inflammatory microenvironment
12
liver disease
12
esld caused
12
caused noncancer
12
noncancer diseases
12
esld
10
immune inflammatory
8
liver
8
end-stage liver
8
immune microenvironment
8

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!