Subcapsular sinus macrophages limit dissemination of West Nile virus particles after inoculation but are not essential for the development of West Nile virus-specific T cell responses

Virology. 2014 Feb:450-451:278-89. doi: 10.1016/j.virol.2013.12.021. Epub 2014 Jan 10.

Abstract

Macrophages encounter flaviviruses early after injection by arthropod vectors. Using in vivo imaging of mice inoculated with firefly luciferase-expressing single-cycle flavivirus particles (FLUC-SCFV), we examined the initial dissemination of virus particles in the presence or absence of lymph node (LN)-resident macrophages. Higher luciferase activity, indicating higher SCFV gene expression, was detected in the footpad of macrophage-depleted mice after 24h post infection (hpi). Moreover, FLUC-SCFV particles disseminated to the spleen within 14 hpi in macrophage-depleted, but not control mice. Although macrophages presented SCFV to naïve T cells in vitro, depletion of subcapsular sinus (SCS) macrophages did not alter the magnitude or effector function of the WNV-specific CD8(+) T cell response. Together, these results indicate that SCS macrophages play a role in limiting the dissemination of SCFV early in infection but are not required for the generation of a polyfunctional WNV-specific CD8(+) T cell response in the draining LN.

Keywords: CD8(+) T cell; RepliVAX; Single-cycle flavivirus; West Nile virus; subcapsular sinus macrophages.

Publication types

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

MeSH terms

  • Animals
  • CD8-Positive T-Lymphocytes / immunology*
  • Chemokine CCL2 / immunology
  • Interleukin-6 / immunology
  • Lymph Nodes / immunology
  • Lymph Nodes / virology
  • Macrophages / immunology
  • Macrophages / virology*
  • Mice
  • Mice, Inbred C57BL
  • Species Specificity
  • Spleen / immunology
  • Spleen / virology
  • West Nile Fever / immunology*
  • West Nile Fever / virology
  • West Nile virus / genetics
  • West Nile virus / physiology*

Substances

  • Chemokine CCL2
  • Interleukin-6