Projects per year
Abstract
In this study we assessed the effects of antigen exposure in mice pre‐sensitized with allergen following viral infection on changes in lung function, cellular responses and tight junction ex-pression. Female BALB/c mice were sensitized to ovalbumin and infected with influenza A before receiving a second ovalbumin sensitization and challenge with saline, ovalbumin (OVA) or house dust mite (HDM). Fifteen days post‐infection, bronchoalveolar inflammation, serum antibodies, responsiveness to methacholine and barrier integrity were assessed. There was no effect of infection alone on bronchoalveolar lavage cellular inflammation 15 days post‐infection; however, OVA or HDM challenge resulted in increased bronchoalveolar inflammation dominated by eosino-phils/neutrophils or neutrophils, respectively. Previously infected mice had higher serum OVA-specific IgE compared with uninfected mice. Mice previously infected, sensitized and challenged with OVA were most responsive to methacholine with respect to airway resistance, while HDM challenge caused significant increases in both tissue damping and tissue elastance regardless of previous infection status. Previous influenza infection was associated with decreased claudin‐1 expression in all groups and decreased occludin expression in OVA or HDM‐challenged mice. This study demonstrates the importance of the respiratory epithelium in pre‐sensitized individuals, where in-fluenza‐infection‐induced barrier disruption resulted in increased systemic OVA sensitization and downstream effects on lung function.
Original language | English |
---|---|
Article number | 8790 |
Journal | International Journal of Molecular Sciences |
Volume | 22 |
Issue number | 16 |
DOIs | |
Publication status | Published - 2 Aug 2021 |
Fingerprint
Dive into the research topics of 'Previous influenza infection exacerbates allergen specific response and impairs airway barrier integrity in pre‐sensitized mice'. Together they form a unique fingerprint.Projects
- 1 Finished
-
Does Abnormal Epithelial Function Facilitate Aero Allergen Sensitization
Stick, S. (Investigator 01), Kicic, A. (Investigator 02), Larcombe, A. (Investigator 03), Zosky, G. (Investigator 04), Rigby, P. (Investigator 05) & Knight, D. (Investigator 06)
NHMRC National Health and Medical Research Council
1/01/12 → 31/12/14
Project: Research