Impact of Hepatitis C Virus/Schistosoma mansoni Coinfection on the Circulating Levels of HCV-NS4 Protein and Extracellular-Matrix Deposition in Patients with Different Hepatic Fibrosis Stages

Am J Trop Med Hyg. 2016 Nov 2;95(5):1044-1050. doi: 10.4269/ajtmh.16-0129. Epub 2016 Aug 15.

Abstract

Hepatitis C virus (HCV)/Schistosoma mansoni coinfection is common in Egypt and other developing countries. This study aimed to investigate the influence of HCV/S. mansoni coinfection on the concentration of HCV-nonstructural protein-4 (NS4) in addition to collagen III and matrix metalloproteinase-1 (MMP-1) in different hepatic fibrosis stages. We found that coinfected patients (N = 186) showed significantly (P < 0.05, Mann-Whitney U test) higher concentrations of HCV-NS4, collagen III, and collagen III/MMP-1 ratio (CMR) than those with HCV monoinfection (N = 104) in different fibrosis stages. Conversely, coinfected patients showed significantly lower concentrations of MMP-1 when compared with HCV monoinfection. The elevated levels of CMR in case of HCV monoinfection yielded an estimated odds ratio of 1.8 and 2.6 for developing significant fibrosis (F2-F4) and cirrhosis (F4), respectively. HCV/S. mansoni coinfection increased the risk for developing F2-F4 and F4 several fold yielding an estimated odds ratio of 11.1 and 5.2, respectively. This means that coinfected patients have a 6-fold and 2-fold increased risk of developing F2-F4 and F4, respectively, over HCV-monoinfected patients. Thus, elevated levels of HCV-NS4 and CMR in HCV/S. mansoni coinfection suggest increased susceptibility of coinfected patients, compared with those with HCV monoinfection, for accelerating hepatic fibrosis progression.

MeSH terms

  • Adult
  • Alanine Transaminase / blood
  • Alkaline Phosphatase / blood
  • Animals
  • Aspartate Aminotransferases / blood
  • Cohort Studies
  • Coinfection / parasitology*
  • Coinfection / virology*
  • Collagen Type III / genetics
  • Collagen Type III / metabolism
  • Disease Progression
  • Egypt
  • Extracellular Matrix Proteins / genetics
  • Extracellular Matrix Proteins / metabolism*
  • Female
  • Hepacivirus / isolation & purification
  • Humans
  • Liver Cirrhosis / parasitology*
  • Liver Cirrhosis / virology*
  • Logistic Models
  • Male
  • Matrix Metalloproteinase 1 / genetics
  • Matrix Metalloproteinase 1 / metabolism
  • Middle Aged
  • Risk Factors
  • Schistosoma mansoni / isolation & purification
  • Viral Nonstructural Proteins / blood*

Substances

  • Collagen Type III
  • Extracellular Matrix Proteins
  • NS4 protein, hepatitis C virus
  • Viral Nonstructural Proteins
  • Aspartate Aminotransferases
  • Alanine Transaminase
  • Alkaline Phosphatase
  • MMP1 protein, human
  • Matrix Metalloproteinase 1