Effects of cidofovir treatment on cytokine induction in murine models of cowpox and vaccinia virus infection

Antiviral Res. 2006 Nov;72(2):125-33. doi: 10.1016/j.antiviral.2006.05.005. Epub 2006 May 30.

Abstract

Cytokine profiles during cowpox and vaccinia (WR strain) virus infections were characterized in intranasal (i.n.) and intraperitoneal (i.p.) models in BALB/c mice. The time-course of induction and effects of cidofovir treatment on interferon (IFN)-gamma, IFN-gamma inducible protein (IP)-10, interleukin (IL)-6, and monocyte chemoattractant protein (MCP)-1 were determined. The four mouse infection models have distinct patterns of cytokine induction. Cowpox virus i.p. and vaccinia virus i.n. infections showed increased induction throughout the time studied. Cowpox virus i.n. infection resulted in delayed induction of IFN-gamma and IP-10. Cytokine levels were fairly constant during vaccinia virus i.p. infections. Cidofovir treatment (100mg/kg/day i.p. for 2 days) significantly suppressed certain cytokine (IFN- gamma, IL-6, IL-10, IL-11, IP-10, LIF, MCP-1, MCP-3, MCP-5, MIP-1 gamma, and TIMP-1) levels to near normal relative to uninfected animals, as well as prevented mortality and reduced virus titers significantly. Characterization of cytokine responses has implications for understanding the immune responses and pathogeneses of viral infections in these mouse models.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Antiviral Agents / pharmacology
  • Antiviral Agents / therapeutic use*
  • Cidofovir
  • Cowpox / drug therapy
  • Cowpox / immunology*
  • Cytokines / biosynthesis*
  • Cytosine / analogs & derivatives*
  • Cytosine / pharmacology
  • Cytosine / therapeutic use
  • Disease Models, Animal
  • Female
  • Lung / virology
  • Mice
  • Mice, Inbred BALB C
  • Organophosphonates / pharmacology
  • Organophosphonates / therapeutic use*
  • Vaccinia / drug therapy
  • Vaccinia / immunology*
  • Vaccinia virus / drug effects*

Substances

  • Antiviral Agents
  • Cytokines
  • Organophosphonates
  • Cytosine
  • Cidofovir