Increased hepatocyte fas expression and apoptosis in HIV and hepatitis C virus coinfection

J Infect Dis. 2005 Nov 1;192(9):1566-76. doi: 10.1086/491736. Epub 2005 Sep 29.

Abstract

Background: Chronic hepatitis C disease (CHC) follows an accelerated course in human immunodeficiency virus (HIV) coinfection. The reasons for this are unclear. Fas-mediated hepatocyte apoptosis is involved in the pathogenesis of hepatitis C virus (HCV) infection. We sought to compare the expression of Fas on hepatocytes and irreversible apoptosis of hepatocytes among patients with CHC with and without HCV/HIV coinfection.

Methods: Fas-immunostained hepatocytes were semiquantified, and apoptotic hepatocytes were detected by staining caspase-cleaved cytokeratin 18 filaments and counted across the entire section of liver-biopsy specimens from HCV-infected patients with and without HCV/HIV coinfection.

Results: One hundred thirty-four HCV/HIV-coinfected and 100 HCV-infected patients were included. HCV/HIV coinfection was associated with both diffuse distribution of Fas-stained hepatocytes (adjusted odds ratio [AOR], 7.4 [95% confidence interval {CI}, 3.8-14.4]) and with apoptotic hepatocyte counts greater than the median (AOR, 2.5 [95% CI, 1.5-4.5]). In HCV/HIV-coinfected patients, CD4+ cell nadir<200 cells/mL was associated with both Fas expression (AOR, 2.9 [95% CI, 1.3-6.8]) and hepatocyte apoptosis (AOR, 2.3 [95% CI, 1.1-4.9]).

Conclusion: HCV/HIV-coinfected patients show higher levels of hepatocytes expressing Fas and undergoing irreversible apoptosis than do HCV-infected patients. However, low CD4+ cell nadirs in coinfected patients are associated with hepatocyte Fas expression and apoptosis.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Apoptosis*
  • Biopsy
  • CD4 Lymphocyte Count
  • Cell Count
  • Cross-Sectional Studies
  • Female
  • Fibrosis / pathology
  • HIV Infections / complications*
  • HIV Infections / immunology
  • HIV Infections / metabolism*
  • Hepatitis C, Chronic / complications*
  • Hepatitis C, Chronic / metabolism*
  • Hepatitis C, Chronic / pathology
  • Hepatocytes / cytology
  • Hepatocytes / metabolism*
  • Humans
  • Immunohistochemistry
  • Liver / cytology
  • Liver / metabolism*
  • Liver / physiology*
  • Male
  • Middle Aged
  • fas Receptor / metabolism*

Substances

  • fas Receptor