Critical roles for both STAT1-dependent and STAT1-independent pathways in the control of primary dengue virus infection in mice

J Immunol. 2005 Sep 15;175(6):3946-54. doi: 10.4049/jimmunol.175.6.3946.

Abstract

Dengue virus (DEN), a flavivirus, causes dengue fever and dengue hemorrhagic fever/dengue shock syndrome, the most common mosquito-borne viral illnesses in humans worldwide. In this study, using STAT1(-/-) mice bearing two different mutant stat1 alleles in the 129/Sv/Ev background, we demonstrate that IFNR-dependent control of primary DEN infection involves both STAT1-dependent and STAT1-independent mechanisms. The STAT1 pathway is necessary for clearing the initial viral load, whereas the STAT1-independent pathway controls later viral burden and prevents DEN disease in mice. The STAT1-independent responses in mice with primary DEN infection included the early activation of B and NK cells as well as the up-regulation of MHC class I molecules on macrophages and dendritic cells. Infection of bone marrow-derived dendritic cell cultures with either DEN or Sindbis virus, another positive-strand RNA virus, confirmed the early vs late natures of the STAT1-dependent and STAT1-independent pathways. Collectively, these data begin to define the nature of the STAT1-dependent vs the STAT1-independent pathway in vivo.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • B-Lymphocytes / virology
  • Dendritic Cells / immunology
  • Dendritic Cells / virology
  • Dengue / immunology*
  • Dengue Virus
  • Histocompatibility Antigens Class I
  • Killer Cells, Natural / virology
  • Macrophages / immunology
  • Mice
  • Mice, Knockout
  • Receptors, Interferon / physiology
  • STAT1 Transcription Factor / deficiency
  • STAT1 Transcription Factor / metabolism*
  • STAT1 Transcription Factor / physiology
  • Signal Transduction / immunology*
  • Viral Load

Substances

  • Histocompatibility Antigens Class I
  • Receptors, Interferon
  • STAT1 Transcription Factor
  • Stat1 protein, mouse