Altered effector functions of NK cells in chronic hepatitis C are associated with IFNL3 polymorphism

J Leukoc Biol. 2015 Aug;98(2):283-94. doi: 10.1189/jlb.4A1014-520R. Epub 2015 Jun 1.

Abstract

Interferon α-mediated effector functions of NK cells may contribute to the control of HCV replication and the pathogenesis of liver disease. The single-nucleotide polymorphism rs12979860 near IFNL3 (previously known as IL28B) is important in response to IFN-α treatment and in spontaneous resolution of acute hepatitis C. The role of the IFNL3 polymorphism in NK cell function is unclear. Thus, we investigated the role of IFNL3 polymorphism in type I IFN-dependent regulation of NK cell functions in patients with cHC and healthy control subjects. We demonstrated a marked polarization of NK cells toward cytotoxicity in response to IFN-α stimulation in patients with hepatitis C. That TRAIL up-regulation was present, particularly in patients with the IFNL3-TT allele, was supported by a shift in the pSTAT-1:pSTAT-4 ratios toward pSTAT-1. In patients bearing the IFNL3-TT allele, NK cell effector function correlated with liver disease activity. In contrast, higher cytokine production of NK cells was observed in healthy individuals with the IFNL3-CC genotype, which may support spontaneous HCV clearance in acute infection. Overall, these findings show that the role of NK cells may differ in chronic infection vs. early antiviral defense and that the IFNL3 genotype differentially influences NK cell function.

Keywords: HCV; IFN-α; IFN-γ; STATs; TRAIL; cytotoxicity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Alleles
  • Antiviral Agents / therapeutic use
  • Case-Control Studies
  • Female
  • Gene Expression Regulation
  • Genotype
  • Hepatitis C / immunology
  • Hepatitis C, Chronic / drug therapy
  • Hepatitis C, Chronic / genetics*
  • Hepatitis C, Chronic / immunology
  • Hepatitis C, Chronic / pathology
  • Humans
  • Interferon-alpha / therapeutic use
  • Interferons
  • Interleukins / genetics*
  • Interleukins / immunology
  • Killer Cells, Natural / immunology*
  • Killer Cells, Natural / pathology
  • Killer Cells, Natural / virology
  • Liver / immunology
  • Liver / pathology
  • Liver / virology
  • Male
  • Middle Aged
  • Polymorphism, Single Nucleotide*
  • STAT1 Transcription Factor / genetics
  • STAT1 Transcription Factor / immunology
  • STAT4 Transcription Factor / genetics
  • STAT4 Transcription Factor / immunology
  • Signal Transduction
  • TNF-Related Apoptosis-Inducing Ligand / genetics
  • TNF-Related Apoptosis-Inducing Ligand / immunology
  • Viral Load / immunology

Substances

  • Antiviral Agents
  • interferon-lambda, human
  • Interferon-alpha
  • Interleukins
  • STAT1 Transcription Factor
  • STAT1 protein, human
  • STAT4 Transcription Factor
  • STAT4 protein, human
  • TNF-Related Apoptosis-Inducing Ligand
  • TNFSF10 protein, human
  • Interferons