High doses of recombinant mannan-binding lectin inhibit the binding of influenza A(H1N1)pdm09 virus with cells expressing DC-SIGN

APMIS. 2017 Jul;125(7):655-664. doi: 10.1111/apm.12695. Epub 2017 May 11.

Abstract

The pandemic influenza A (H1N1)pdm09 virus continues to be a threat to human health. Low doses of mannan-binding lectin (MBL) (<1 μg/mL) were shown not to protect against influenza A(H1N1)pdm09 infection. However, the effect of high doses of MBL has not been investigated. Dendritic cell-specific intercellular adhesion molecule-3 grabbing non-integrin (DC-SIGN) has been proposed as an alternative receptor for influenza A(H1N1)pdm09 virus. In this study, we examined the expression of DC-SIGN on DCs as well as on acute monocytic leukemia cell line, THP-1. High doses of recombinant or human MBL inhibited binding of influenza A(H1N1)pdm09 to both these cell types in the presence of complement derived from bovine serum. Further, anti-DC-SIGN monoclonal antibody inhibited binding of influenza A(H1N1)pdm09 to both DC-SIGN-expressing DCs and THP-1 cells. This study demonstrates that high doses of MBL can inhibit binding of influenza A(H1N1)pdm09 virus to DC-SIGN-expressing cells in the presence of complement. Our results suggest that DC-SIGN may be an alternative receptor for influenza A(H1N1)pdm09 virus.

Keywords: Influenza A (H1N1)pdm09 virus; dendritic cell-specific intercellular adhesion molecule-3 grabbing non-integrin; mannan-binding lectin.

MeSH terms

  • Animals
  • Cell Adhesion Molecules / metabolism*
  • Cells, Cultured
  • Complement System Proteins / metabolism
  • Dendritic Cells / chemistry
  • Dendritic Cells / virology*
  • Humans
  • Influenza A Virus, H1N1 Subtype / drug effects
  • Influenza A Virus, H1N1 Subtype / immunology
  • Influenza A Virus, H1N1 Subtype / physiology*
  • Lectins, C-Type / metabolism*
  • Mannose-Binding Lectin / genetics
  • Mannose-Binding Lectin / metabolism*
  • Monocytes / chemistry
  • Monocytes / virology*
  • Receptors, Cell Surface / metabolism*
  • Receptors, Virus / metabolism
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism*
  • Virus Attachment / drug effects*

Substances

  • Cell Adhesion Molecules
  • DC-specific ICAM-3 grabbing nonintegrin
  • Lectins, C-Type
  • MBL2 protein, human
  • Mannose-Binding Lectin
  • Receptors, Cell Surface
  • Receptors, Virus
  • Recombinant Proteins
  • Complement System Proteins