The combination of type I IFN, TNF-α, and cell surface receptor engagement with dendritic cells enables NK cells to overcome immune evasion by dengue virus

J Immunol. 2014 Nov 15;193(10):5065-75. doi: 10.4049/jimmunol.1302240. Epub 2014 Oct 15.

Abstract

Clinical studies have suggested the importance of the NK cell response against dengue virus (DenV), an arboviral infection that afflicts >50 million individuals each year. However, a comprehensive understanding of the NK cell response against dengue-infected cells is lacking. To characterize cell-contact mechanisms and soluble factors that contribute to the antidengue response, primary human NK cells were cocultured with autologous DenV-infected monocyte-derived dendritic cells (DC). NK cells responded by cytokine production and the lysis of target cells. Notably, in the absence of significant monokine production by DenV-infected DC, it was the combination of type I IFNs and TNF-α produced by DenV-infected DC that was important for stimulating the IFN-γ and cytotoxic responses of NK cells. Cell-bound factors enhanced NK cell IFN-γ production. In particular, reduced HLA class I expression was observed on DenV-infected DC, and IFN-γ production was enhanced in licensed/educated NK cell subsets. NK-DC cell contact was also identified as a requirement for a cytotoxic response, and there was evidence for both perforin/granzyme as well as Fas/Fas ligand-dependent pathways of killing by NK cells. In summary, our results have uncovered a previously unappreciated role for the combined effect of type I IFNs, TNF-α, and cell surface receptor-ligand interactions in triggering the antidengue response of primary human NK cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Communication / immunology
  • Coculture Techniques
  • Cytotoxicity, Immunologic
  • Dendritic Cells / immunology*
  • Dendritic Cells / virology
  • Dengue Virus / immunology*
  • Fas Ligand Protein / genetics
  • Fas Ligand Protein / immunology
  • Gene Expression Regulation
  • Granzymes / genetics
  • Granzymes / immunology
  • Histocompatibility Antigens Class I / genetics
  • Histocompatibility Antigens Class I / immunology*
  • Humans
  • Immune Evasion
  • Interferon Type I / genetics
  • Interferon Type I / immunology*
  • Killer Cells, Natural / immunology*
  • Killer Cells, Natural / virology
  • Perforin / genetics
  • Perforin / immunology
  • Signal Transduction
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / immunology*
  • fas Receptor / genetics
  • fas Receptor / immunology

Substances

  • FAS protein, human
  • Fas Ligand Protein
  • Histocompatibility Antigens Class I
  • Interferon Type I
  • Tumor Necrosis Factor-alpha
  • fas Receptor
  • Perforin
  • Granzymes