IFN-α production by human mononuclear cells infected with varicella-zoster virus through TLR9-dependent and -independent pathways

Cell Mol Immunol. 2011 Mar;8(2):181-8. doi: 10.1038/cmi.2010.84. Epub 2011 Feb 14.

Abstract

Understanding the defense mechanisms of the host of an organism is important for infection control. In previous studies, we demonstrated that interferon-α (IFN-α), but not IL-12, was produced by human peripheral blood mononuclear cells infected with varicella-zoster virus (VZV). Here, we investigated what kind of cell(s) and which signal molecule(s) are involved in IFN-α production. Using cell isolation and ELISA, we found that plasmacytoid dendritic cells (pDCs) were responsible for IFN-α production during VZV infection. We also found that Toll-like receptor 9 (TLR9) was involved in VZV-induced IFN-α production because inhibitory CpG oligodeoxynucleotide inhibited IFN-α production. UV-inactivated VZV-induced IFN-α production was lower than that of active VZV, indicating another TLR9-independent pathway. Further studies demonstrated that double-stranded RNA-dependent protein kinase, but not DNA-dependent protein kinase was involved in VZV-induced IFN-α production. Together, these results suggest that pDCs play an important role in IFN-α production during VZV infection through TLR9-dependent and -independent pathways.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptive Immunity
  • Adult
  • DNA-Activated Protein Kinase / metabolism
  • Dendritic Cells / immunology
  • Herpes Zoster / enzymology
  • Herpes Zoster / immunology
  • Herpes Zoster / virology
  • Herpesvirus 3, Human / immunology*
  • Humans
  • Immunity, Innate
  • Interferon-alpha / biosynthesis*
  • Leukocytes, Mononuclear / enzymology
  • Leukocytes, Mononuclear / immunology*
  • Leukocytes, Mononuclear / virology*
  • Mitogen-Activated Protein Kinases / metabolism
  • NF-kappa B / metabolism
  • Signal Transduction / immunology*
  • Toll-Like Receptor 9 / immunology*
  • eIF-2 Kinase / metabolism

Substances

  • Interferon-alpha
  • NF-kappa B
  • TLR9 protein, human
  • Toll-Like Receptor 9
  • DNA-Activated Protein Kinase
  • eIF-2 Kinase
  • Mitogen-Activated Protein Kinases