Heptitis B and C virus infection in HBsAg-negative alcoholics without i.v. drug abuse or previous blood transfusions

  • Fritz von Weizsäcker
  • , Eiki Maeda
  • , Nancy Brown
  • , Thierry Poynard
  • , Eithan Galun
  • , Siegfried Labeit
  • , Jean Claude Caput
  • , Terukatsu Arima
  • , Hubert Blum
  • , Jack R. Wands*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

The presence of low level hepatitis B virus (HBV) and hepatitis C virus (HCV) infections was assessed in serum from 67 hepatitis B surface antigen (HBsAg) negative alcoholics from France without previous blood transfusions and/or i.v. drug abuse. It was found that 19 67 (28%) of this alcoholic population had past exposure to HBV as shown by the presence of antibodies to the surface (anti-HBs), core (anti-HBc) and e (anti-HBe) antigens. Two patients (3%) had low level circulating encapsidated HBV as determined by the highly sensitive capture PCR technique. Previous exposure to HCV was assessed by three serological tests: the first generation ELISA (C-100-3), a second generation recombinant immunoblot assay (RIBA II) and a radioimmunoassay based on highly conserved HCV core peptide sequences; 7 67 (10.5%) were found to be reactive in at least two serological tests. Among 64 serum samples available for RNA PCR testing, 6 were found to be HCV RNA positive (9.4%). Taken together, 8 67 (13%) of this alcoholic population were positive for HCV by RNA PCR and/or at least two serological tests. We conclude, that even in the absence of known risk factors and HBsAg negativity, patients with alcoholic liver disease have a significantly higher prevalence of markers of past or ongoing HBV or HCV infection than healthy individuals.

Original languageEnglish
Pages (from-to)80-87
Number of pages8
JournalInternational Hepatology Communications
Volume4
Issue number2
DOIs
StatePublished - Aug 1995
Externally publishedYes

Bibliographical note

Funding Information:
This work was supported by grants AA-02666, CA-3571 1 and AA-08169 from the National Institutes of Health. F.v.W. was supported by a fellowship from the Deutsche Forschungsgemeinschaft. J.R.W. is the recipient of a Research Scientist Award AA-00048.

Keywords

  • Alcoholic liver disease
  • Latent HBV infection
  • Latent HCV infection
  • Synthetic oligopeptide

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