Chemoimmunotherapy of chronic hepatitis B virus infection in the woodchuck model overcomes immunologic tolerance and restores T-cell responses to pre-S and S regions of the viral envelope protein

J Virol. 2007 Oct;81(19):10614-24. doi: 10.1128/JVI.00691-07. Epub 2007 Jul 25.

Abstract

Treatment of chronic hepatitis B virus (HBV) infection could combine potent antiviral drugs and therapeutic vaccines to overcome immunological tolerance and induce the recovery phenotype to protect against disease progression. Conventional vaccination of woodchucks chronically infected with the woodchuck hepatitis virus (WHV) elicited differential T-cell response profiles depending on whether or not carriers were treated with the potent antiviral drug clevudine (CLV), which significantly reduces viral and antigen loads. The differential T-cell responses defined both CLV-dependent and CLV-independent epitopes of the pre-S and S regions of the WHV envelope protein. Only combined treatment involving CLV and conventional vaccine therapeutically restored the T-cell response profile of chronic WHV carrier woodchucks to that seen in prophylactic vaccination and in recovery from acute WHV infection. The results have implications for mechanisms of immunological tolerance operating in chronic HBV infection and suggest that such combined chemoimmunotherapy may be useful for treatment of humans with chronic HBV infection.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Antiviral Agents / therapeutic use*
  • Arabinofuranosyluracil / analogs & derivatives*
  • Arabinofuranosyluracil / therapeutic use
  • Carrier State
  • Combined Modality Therapy
  • Disease Models, Animal*
  • Epitopes / chemistry
  • Epitopes / immunology
  • Female
  • Hepatitis B Antibodies / immunology
  • Hepatitis B Surface Antigens / chemistry
  • Hepatitis B Surface Antigens / immunology
  • Hepatitis B Vaccines / therapeutic use*
  • Hepatitis B Virus, Woodchuck*
  • Hepatitis B, Chronic / drug therapy*
  • Hepatitis B, Chronic / therapy
  • Immune Tolerance*
  • Immunotherapy
  • Marmota / immunology*
  • Marmota / virology
  • T-Lymphocytes / immunology
  • Vaccination
  • Viral Envelope Proteins / chemistry
  • Viral Envelope Proteins / immunology

Substances

  • Antiviral Agents
  • Epitopes
  • Hepatitis B Antibodies
  • Hepatitis B Surface Antigens
  • Hepatitis B Vaccines
  • Viral Envelope Proteins
  • Arabinofuranosyluracil
  • clevudine