Viral infection switches non-plasmacytoid dendritic cells into high interferon producers

Nature. 2003 Jul 17;424(6946):324-8. doi: 10.1038/nature01783. Epub 2003 Jun 22.

Abstract

Type I interferons (IFN-I) are important cytokines linking innate and adaptive immunity. Plasmacytoid dendritic cells make high levels of IFN-I in response to viral infection and are thought to be the major source of the cytokines in vivo. Here, we show that conventional non-plasmacytoid dendritic cells taken from mice infected with a dendritic-cell-tropic strain of lymphocytic choriomeningitis virus make similarly high levels of IFN-I on subsequent culture. Similarly, non-plasmacytoid dendritic cells secrete high levels of IFN-I in response to double-stranded RNA (dsRNA), a major viral signature, when the latter is introduced into the cytoplasm to mimic direct viral infection. This response is partially dependent on the cytosolic dsRNA-binding enzyme protein kinase R and does not require signalling through toll-like receptor (TLR) 3, a surface receptor for dsRNA. Furthermore, we show that sequestration of dsRNA by viral NS1 (refs 6, 7) explains the inability of conventional dendritic cells to produce IFN-I on infection with influenza. Our results suggest that multiple dendritic cell types, not just plasmacytoid cells, can act as specialized interferon-producing cells in certain viral infections, and reveal the existence of a TLR-independent pathway for dendritic cell activation that can be the target of viral interference.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3 Cells
  • Animals
  • CpG Islands / genetics
  • Dendritic Cells / immunology*
  • Dendritic Cells / metabolism*
  • Interferon Type I / biosynthesis*
  • Interferon Type I / genetics
  • Interferon Type I / immunology
  • Interferon-alpha / biosynthesis
  • Interferon-alpha / immunology
  • Lymphocytic Choriomeningitis / immunology*
  • Lymphocytic choriomeningitis virus / immunology
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / metabolism
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • RNA, Double-Stranded / immunology
  • RNA, Double-Stranded / metabolism
  • Receptors, Cell Surface / genetics
  • Receptors, Cell Surface / metabolism
  • Signal Transduction
  • Toll-Like Receptor 3
  • Toll-Like Receptors
  • eIF-2 Kinase / metabolism

Substances

  • Interferon Type I
  • Interferon-alpha
  • Membrane Glycoproteins
  • RNA, Double-Stranded
  • Receptors, Cell Surface
  • Toll-Like Receptor 3
  • Toll-Like Receptors
  • eIF-2 Kinase