Impacts of allergic airway inflammation on lung pathology in a mouse model of influenza A virus infection

PLoS One. 2017 Feb 28;12(2):e0173008. doi: 10.1371/journal.pone.0173008. eCollection 2017.

Abstract

Influenza A virus is the respiratory pathogen responsible for influenza. Infection by the 2009 pandemic influenza A (H1N1) virus caused severe lower airway inflammation and pneumonia. Asthma is a chronic inflammatory disorder of the airways that affects the entire brachial tree, and was one of the commonest underlying medical conditions among patients hospitalized with the 2009 pandemic influenza virus infection. Although respiratory virus infections are the major causes of asthma exacerbation, the mechanism by which influenza exacerbates asthma is poorly understood. Animal models of disease comorbidity are crucial to understanding host-pathogen interactions and elucidating complex pathologies. Existing murine models of influenza virus infection in asthmatics show that asthmatic mice are highly resistant to influenza virus infection, which contradicts clinical observations in humans. Here, we developed a murine model of influenza virus/asthma comorbidity using NC/Nga mice, which are highly sensitive to allergic reactions such as atopic dermatitis and allergic airway inflammation. This model was then used to examine the impact of allergic airway inflammation on lung pathology in the 2009 pandemic influenza virus infected mice. The results showed that induction of acute allergic airway inflammation in pre-existing influenza virus infection had additive effects on exacerbation of lung pathology, which mirrors findings in human epidemiological studies. In contrast, pre-existing allergic airway inflammation protected from subsequent influenza virus infection, which was compatible with those of previous murine models of influenza virus infection in asthmatic mice. These variable outcomes of this murine model indicate that the temporal relation between allergic airway inflammation and influenza virus infection might play a critical role in asthma and influenza comorbidity. Thus, this murine model will further our understanding of how influenza virus infection affects an asthmatic host and may aid the development of strategies to improve treatments and outcomes for asthmatics harboring influenza virus infection.

MeSH terms

  • Animals
  • Bronchoalveolar Lavage Fluid
  • Chemokines / metabolism
  • Cytokines / metabolism
  • Disease Models, Animal
  • Female
  • Hypersensitivity / immunology*
  • Immunohistochemistry
  • Inflammation / immunology*
  • Influenza A virus / immunology*
  • Influenza A virus / pathogenicity*
  • Mice
  • Mice, Inbred BALB C
  • Orthomyxoviridae Infections / immunology*

Substances

  • Chemokines
  • Cytokines

Grants and funding

The work described in this report was supported by grants from the Japanese Ministry of Health, Labor, and Welfare, and Research Program on Emerging and Re-emerging Infectious Diseases from Japan Agency for Medical Research and Development. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.