Oseltamivir treatment of mice before or after mild influenza infection reduced cellular and cytokine inflammation in the lung

Influenza Other Respir Viruses. 2011 Sep;5(5):343-50. doi: 10.1111/j.1750-2659.2011.00235.x. Epub 2011 Mar 31.

Abstract

Background: Lung inflammation is a critical determinant of influenza infection outcomes but is seldom evaluated in animal studies of oseltamivir (OS), which have focused on viral titre and survival.

Objectives: To study the effects of pre- and post-infection dosing with OS on viral replication and inflammation in a mouse model of non-lethal influenza infection.

Methods: BALB/c mice were infected with a laboratory-adapted H3N1 strain of influenza. In pre-dosing studies, OS was gavaged twice daily (1 and 10 mg/kg/day) from 4 hours prior to infection and continuing for 5 days (d) post-infection (p.i). In the second post-infection dosing study, dosing at 10 mg/kg/day began at 24-48 hours p.i. Mice were dissected at d3, d5 and d7 p.i. (pre-dosing study) and d5 p.i. (post-dosing study). Lung viral titres were determined by plaque assay. Bronchoalveolar lavage fluid (BALF) was collected and used for the quantitation of inflammatory cells and mediators.

Results: Pre-infection dosing of OS reduced total cells, neutrophils and macrophages in BALF. With pre- or post-infection dosing, the pro-inflammatory mediators TNF-α, IL-1β, IL-6 and granulocyte-macrophage colony-stimulating factor, the neutrophil chemokines keratinocyte-derived chemokine and MIP-1α and the macrophage chemokine MCP-1 were reduced in BALF. Pre-dosing with 1 mg/kg OS did not reduce viral titres, while 10 mg/kg slightly reduced viral titres at d3 and d5 p.i.

Conclusions: Oseltamivir reduced the inflammatory response to influenza when given pre- or post-infection. This anti-inflammatory effect may contribute to the clinical benefit of OS.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antiviral Agents / therapeutic use*
  • Cytokines / immunology*
  • Disease Models, Animal
  • Humans
  • Influenza A virus / drug effects
  • Influenza A virus / physiology
  • Influenza, Human / drug therapy*
  • Influenza, Human / immunology
  • Influenza, Human / virology
  • Lung / drug effects
  • Lung / immunology*
  • Lung / virology
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Oseltamivir / therapeutic use*
  • Treatment Outcome

Substances

  • Antiviral Agents
  • Cytokines
  • Oseltamivir