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Intrinsic Viral Factors Are the Dominant Determinants of the Hepatitis C Virus Response to Interferon Alpha Treatment in Chimeric Mice.
Chen, Ran; Kobewka, Michelle; Addison, William; Lachance, Gerald; Tyrrell, D Lorne.
Affiliation
  • Chen R; Department of Medical Microbiology and Immunology, Edmonton, Alberta, Canada.
  • Kobewka M; Li Ka Shing Institute of Virology, Katz Centre for Health Research, Edmonton, Alberta, Canada.
  • Addison W; Department of Medical Microbiology and Immunology, Edmonton, Alberta, Canada.
  • Lachance G; Li Ka Shing Institute of Virology, Katz Centre for Health Research, Edmonton, Alberta, Canada.
  • Tyrrell DL; Department of Medical Microbiology and Immunology, Edmonton, Alberta, Canada.
PLoS One ; 11(1): e0147007, 2016.
Article in En | MEDLINE | ID: mdl-26765841
BACKGROUND: Hepatitis C virus infection is a global health problem. New direct-acting antiviral agents have been recently approved. However, due to their high cost and some genotypes remaining difficult to treat, interferon-based therapy with pegylated interferon and ribavirin likely may remain a component of hepatitis C virus treatment for some patients. Unfortunately, pegylated interferon / ribavirin treatment achieved favorable outcomes in less than 50% of patients. Factors determining the outcome to pegylated interferon/ribavirin include both host and viral factors. It has been a major challenge to separate the host and viral factors in most in vivo systems. AIMS & METHODS: We used two hepatitis C virus strains from patients with different interferon-sensitivities and three hepatocyte donors, each with distinct interleukin 28B and interferon lambda 4 single nucleotide polymorphisms to investigate the contributions of viral and host factors to the response of hepatitis C virus to interferon treatment in chimeric mice. RESULTS AND CONCLUSIONS: We found that viral factors were the dominant factors in determining the interferon treatment outcomes in chimeric mice. Host factors, such as pre-treatment liver interferon-stimulated gene expression and single nucleotide polymorphisms near interleukin 28B and interferon lambda 4 coding regions, were less important determinants of the response to interferon in the chimeric mice than they were in patients. Our results also suggest that a complete immune system as seen in patients may be required for host factors such as single nucleotide polymorphisms near interleukin 28B/interferon lambda 4 and pre-treatment liver interferon-stimulated gene upregulation to have an effect on the interferon response.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Antiviral Agents / Interferon-alpha / Hepatitis C / Hepacivirus / Host-Pathogen Interactions Type of study: Prognostic_studies Limits: Animals / Humans Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2016 Document type: Article Affiliation country: Canadá Country of publication: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Antiviral Agents / Interferon-alpha / Hepatitis C / Hepacivirus / Host-Pathogen Interactions Type of study: Prognostic_studies Limits: Animals / Humans Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2016 Document type: Article Affiliation country: Canadá Country of publication: Estados Unidos