4.7 Article

Previous Influenza Infection Exacerbates Allergen Specific Response and Impairs Airway Barrier Integrity in Pre-Sensitized Mice

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出版社

MDPI
DOI: 10.3390/ijms22168790

关键词

house dust mite; lung function; BALB; c mice; influenza; tight junctions; epithelial barrier integrity

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  1. National Health and Medical Research Council (NHRMC) [1026494]

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This study found that challenge with ovalbumin or house dust mite in mice resulted in bronchoalveolar inflammation, with previously infected mice showing higher levels of OVA-specific IgE in serum. Mice previously infected, sensitized, and challenged with OVA were most responsive to methacholine, while HDM challenge caused significant increases in tissue damping and tissue elastance. Influenza infection was associated with decreased claudin-1 expression and occludin expression in OVA or HDM-challenged mice, demonstrating the importance of respiratory epithelium in pre-sensitized individuals.
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 expression. 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 eosinophils/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 influenza-infection-induced barrier disruption resulted in increased systemic OVA sensitization and downstream effects on lung function.

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