Soluble CD14 levels are increased and inversely correlated with the levels of hepatitis B surface antigen in chronic hepatitis B patients

J Med Virol. 2003 Oct;71(2):188-94. doi: 10.1002/jmv.10469.

Abstract

Because it was observed recently that yeast-derived recombinant HBsAg interacts in a lipopolysaccharide binding protein-dependent manner with CD14 expressed on human monocytes, we investigated whether HBsAg influences the serum levels of sCD14, lipopolysaccharide binding protein and C-reactive protein in hepatitis B patients. Samples from acute and chronic hepatitis B and chronic hepatitis C patients were tested. All analytes were measured using commercial assays. HBsAg was quantified using an NIBSC titrated standard. sCD14 levels were higher in chronic hepatitis B and C patients than in healthy controls (P = 0.0006 and P < 0.0001, respectively). In chronic hepatitis B patients an inverse correlation was found between sCD14 and HBsAg (P = 0.0309). Lipopolysaccharide binding protein and C-reactive protein levels were higher in acute hepatitis B patients than in control subjects (P = 0.0217 and P = 0.0034, respectively). In chronic hepatitis B and C, sCD14 and C-reactive protein levels were higher in cirrhotic than in non-cirrhotic patients (P = 0.0072 and P = 0.0223, respectively).

MeSH terms

  • Acute-Phase Proteins*
  • Adolescent
  • Adult
  • Aged
  • C-Reactive Protein / metabolism
  • Carrier Proteins / blood
  • Hepatitis B / blood
  • Hepatitis B / immunology
  • Hepatitis B / virology
  • Hepatitis B Surface Antigens / blood*
  • Hepatitis B, Chronic / blood
  • Hepatitis B, Chronic / immunology*
  • Hepatitis B, Chronic / virology*
  • Hepatitis C, Chronic / blood
  • Hepatitis C, Chronic / immunology
  • Hepatitis C, Chronic / virology
  • Humans
  • Lipopolysaccharide Receptors / blood*
  • Lipopolysaccharides / metabolism
  • Liver Cirrhosis / blood
  • Liver Cirrhosis / immunology
  • Liver Cirrhosis / virology
  • Membrane Glycoproteins*
  • Middle Aged

Substances

  • Acute-Phase Proteins
  • Carrier Proteins
  • Hepatitis B Surface Antigens
  • Lipopolysaccharide Receptors
  • Lipopolysaccharides
  • Membrane Glycoproteins
  • lipopolysaccharide-binding protein
  • C-Reactive Protein