Haemagglutinin-neuraminidase from HPIV3 mediates human NK regulation of T cell proliferation via NKp44 and NKp46

J Gen Virol. 2018 Jun;99(6):763-767. doi: 10.1099/jgv.0.001070. Epub 2018 Apr 23.

Abstract

HPIV3 is a respiratory virus causing airway diseases, including pneumonia, croup, and bronchiolitis, during infancy and childhood. Currently there is no effective vaccine or anti-viral therapy for this virus. Studies have suggested that poor T cell proliferation following HPIV3 infection is responsible for impaired immunological memory associated with this virus. We have previously demonstrated that NK cells mediate regulation of T cell proliferation during HPIV3 infection. Here we add to these studies by demonstrating that the regulation of T cell proliferation during HPIV3 infection is mediated via NK receptors NKp44 and NKp46 and involves the surface glycoprotein haemagglutinin-neuraminidase but not the fusion protein of the virus. These studies extend our knowledge of the regulatory repertoire of NK cells and provide mechanistic insights which may explain reoccurring failures of vaccines against this virus.

Keywords: HPIV3; IL-2; T cell proliferation; hemaggluttinin-neuriminidase; human NK cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Proliferation
  • Cells, Cultured
  • Gene Expression Regulation
  • HN Protein / chemistry*
  • HN Protein / genetics
  • Humans
  • Killer Cells, Natural / immunology*
  • Lipopolysaccharide Receptors / metabolism
  • Natural Cytotoxicity Triggering Receptor 1 / genetics
  • Natural Cytotoxicity Triggering Receptor 1 / metabolism*
  • Natural Cytotoxicity Triggering Receptor 2 / genetics
  • Natural Cytotoxicity Triggering Receptor 2 / metabolism*
  • Parainfluenza Virus 3, Human / chemistry*
  • Parainfluenza Virus 3, Human / genetics
  • Receptors, Natural Killer Cell / genetics
  • Receptors, Natural Killer Cell / metabolism
  • T-Lymphocytes / cytology*
  • T-Lymphocytes / immunology

Substances

  • HN Protein
  • Lipopolysaccharide Receptors
  • NCR1 protein, human
  • NCR2 protein, human
  • Natural Cytotoxicity Triggering Receptor 1
  • Natural Cytotoxicity Triggering Receptor 2
  • Receptors, Natural Killer Cell