Modifications of plasma platelet-activating factor (PAF)-acetylhydrolase/PAF system activity in patients with chronic hepatitis C virus infection

J Viral Hepat. 2007 Jan;14(1):22-8. doi: 10.1111/j.1365-2893.2006.00766.x.

Abstract

Hepatitis C virus (HCV) chronically infects about 200 million individuals worldwide and leads to severe liver and lymphatic diseases. HCV circulates in the serum, associated with apoB-containing lipoproteins. Platelet-activating factor (PAF), a pro-inflammatory mediator, is mainly modulated by plasma PAF-acetylhydrolase (pPAF-AH), associated with ApoB100-containing low-density lipoproteins (LDL). The aim of the study was to evaluate the potential effects of chronic HCV infection on the PAF/pPAF-AH system. HCV-RNA was detected in plasma, peripheral blood mononuclear cells (PBMC) and liver samples. Plasma PAF levels, pPAF-AH activity, ApoB100 serum titres and pPAF-AH mRNA levels in cultured macrophages were determined. Plasma PAF levels were significantly higher and pPAF-AH activity was significantly lower in HCV patients than in controls. No significant modifications of pPAF-AH mRNA in macrophages or in ApoB100 values were observed in HCV patients compared with controls. Patients who cleared HCV after antiviral treatment showed a complete restoration of pPAF-AH activity and significant decrease of PAF levels during the follow-up. No data exist about the PAF/pPAF-AH system behaviour during HCV infection. This study shows that in HCV patients modifications of pPAF-AH activity/PAF levels take place and that HCV clearance restored pPAF-AH activity. This suggests that circulating viral particles play a role in PAF/pPAF-AH system modifications and such an alteration could be involved in HCV-related damage.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 1-Alkyl-2-acetylglycerophosphocholine Esterase / blood*
  • 1-Alkyl-2-acetylglycerophosphocholine Esterase / genetics
  • Antiviral Agents / therapeutic use
  • Apolipoprotein B-100 / blood
  • Female
  • Hepacivirus / growth & development*
  • Hepatitis C, Chronic / blood*
  • Hepatitis C, Chronic / drug therapy
  • Hepatitis C, Chronic / virology
  • Humans
  • Macrophages / metabolism
  • Male
  • Middle Aged
  • Platelet Activating Factor / metabolism*
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / blood
  • Reverse Transcriptase Polymerase Chain Reaction
  • Viremia / blood
  • Viremia / drug therapy
  • Viremia / virology

Substances

  • Antiviral Agents
  • Apolipoprotein B-100
  • Platelet Activating Factor
  • RNA, Messenger
  • 1-Alkyl-2-acetylglycerophosphocholine Esterase