The activation of B cells enhances DC-SIGN expression and promotes susceptibility of B cells to HPAI H5N1 infection

Biochem Biophys Res Commun. 2017 Sep 2;490(4):1301-1306. doi: 10.1016/j.bbrc.2017.07.017. Epub 2017 Jul 5.

Abstract

The interplay between highly pathogenic avian influenza (HPAI) H5N1 virus and immune cells has been extensively studied for years, as host immune components are thought to play significant roles in promoting the systemic spread of the virus and responsible for cytokine storm. Previous studies suggested that the interaction of B cells and monocytes could promote HPAI H5N1 infection by enhancing avian influenza virus receptor expression. In this study, we further investigate the relationship between the HPAI H5N1 virus, activated B cells, and DC-SIGN expression. DC-SIGN has been described as an important factor for mediating various types of viral infection. Here, we first demonstrate that HPAI H5N1 infection could induce an activation of B cells, which was associated with DC-SIGN expression. Using CD40L and recombinant IL-4 for B cell stimulation, we determined that DC-SIGN expressed on activated B cells was able to enhance its susceptibility to HPAI H5N1 infection. Our findings uncover the interplay between this H5N1 virus and B cells and provide important information in understanding how the virus overcomes our immune system, contributing to its unusual immunopathogenesis.

Keywords: Activation; B cells; DC-SIGN; H5N1; Pathogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • B-Lymphocytes / immunology
  • B-Lymphocytes / virology*
  • B7-2 Antigen / genetics
  • B7-2 Antigen / immunology
  • Birds / virology
  • CD40 Ligand / pharmacology
  • Cell Adhesion Molecules / genetics
  • Cell Adhesion Molecules / immunology*
  • Disease Susceptibility
  • Gene Expression Regulation
  • Host-Pathogen Interactions*
  • Humans
  • Influenza A Virus, H5N1 Subtype / isolation & purification
  • Influenza A Virus, H5N1 Subtype / physiology*
  • Interleukin-4 / pharmacology
  • Lectins, C-Type / genetics
  • Lectins, C-Type / immunology*
  • Lymphocyte Activation / drug effects
  • Primary Cell Culture
  • Receptors, Cell Surface / genetics
  • Receptors, Cell Surface / immunology*
  • Recombinant Proteins / pharmacology
  • Signal Transduction

Substances

  • B7-2 Antigen
  • CD86 protein, human
  • Cell Adhesion Molecules
  • DC-specific ICAM-3 grabbing nonintegrin
  • IL4 protein, human
  • Lectins, C-Type
  • Receptors, Cell Surface
  • Recombinant Proteins
  • CD40 Ligand
  • Interleukin-4