Analysis of hepatitis C virus-inoculated chimpanzees reveals unexpected clinical profiles

J Virol. 1998 Apr;72(4):2589-99. doi: 10.1128/JVI.72.4.2589-2599.1998.

Abstract

The clinical course of hepatitis C virus (HCV) infections in a chimpanzee cohort was examined to better characterize the outcome of this valuable animal model. Results of a cross-sectional study revealed that a low percentage (39%) of HCV-inoculated chimpanzees were viremic based on reverse transcription (RT-PCR) analysis. A correlation was observed between viremia and the presence of anti-HCV antibodies. The pattern of antibodies was dissimilar among viremic chimpanzees and chimpanzees that cleared the virus. Viremic chimpanzees had a higher prevalence of antibody reactivity to NS3, NS4, and NS5. Since an unexpectedly low percentage of chimpanzees were persistently infected with HCV, a longitudinal analysis of the virological profile of a small panel of HCV-infected chimpanzees was performed to determine the kinetics of viral clearance and loss of antibody. This study also revealed that a low percentage (33%) of HCV-inoculated chimpanzees were persistently viremic. Analysis of serial bleeds from six HCV-infected animals revealed four different clinical profiles. Viral clearance with either gradual or rapid loss of anti-HCV antibody was observed in four animals within 5 months postinoculation. A chronic-carrier profile characterized by persistent HCV RNA and anti-HCV antibody was observed in two animals. One of these chimpanzees was RT-PCR positive, antibody negative for 5 years and thus represented a silent carrier. If extrapolated to the human population, these data would imply that a significant percentage of unrecognized HCV infections may occur and that silent carriers may represent potentially infectious blood donors.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Alanine Transaminase / metabolism
  • Animals
  • Capsid / immunology
  • Cohort Studies
  • Cross-Sectional Studies
  • Cysteine Endopeptidases / immunology
  • Disease Models, Animal
  • Hepacivirus / genetics
  • Hepacivirus / immunology
  • Hepacivirus / physiology*
  • Hepatitis C / immunology*
  • Hepatitis C / physiopathology
  • Hepatitis C / virology*
  • Hepatitis C Antibodies / blood
  • Humans
  • Longitudinal Studies
  • Pan troglodytes
  • RNA, Viral
  • Viral Nonstructural Proteins / immunology
  • Virus Latency

Substances

  • Hepatitis C Antibodies
  • NS3 protein, hepatitis C virus
  • NS4 protein, hepatitis C virus
  • RNA, Viral
  • Viral Nonstructural Proteins
  • Alanine Transaminase
  • NS-5 protein, hepatitis C virus
  • Cysteine Endopeptidases
  • NS2-3 protease