Toll-like receptor 7 gene deficiency and early-life Pneumovirus infection interact to predispose toward the development of asthma-like pathology in mice
Date
2013
Authors
Kaiko, G.
Loh, Z.
Spann, K.
Lynch, J.
Lalwani, A.
Zheng, Z.
Davidson, S.
Uematsu, S.
Akira, S.
Hayball, J.
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Journal article
Citation
Journal of Allergy and Clinical Immunology, 2013; 131(5):1331-1349
Statement of Responsibility
Gerard E. Kaiko, Zhixuan Loah, Kirsten Spann, Jason P. Lynch, Amit Lalwani, Zhenglong Zheng, Sophia Davidson, Satoshi Uematsu, Shizuo Akira, John Hayball, Kerrilyn R. Diener, Katherine J. Baines, Jodie L. Simpson, Paul S. Foster and Simon Phipps
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Abstract
BACKGROUND: Respiratory tract viruses are a major environmental risk factor for both the inception and exacerbations of asthma. Genetic defects in Toll-like receptor (TLR) 7–mediated signaling, impaired type I interferon responses, or both have been reported in asthmatic patients, although their contribution to the onset and exacerbation of asthma remains poorly understood. OBJECTIVE: We sought to determine whether Pneumovirus infection in the absence of TLR7 predisposes to bronchiolitis and the inception of asthma. METHODS: Wild-type and TLR7-deficient (TLR72/2) mice were inoculated with the rodent-specific pathogen pneumonia virus of mice at 1 (primary), 7 (secondary), and 13 (tertiary) weeks of age, and pathologic features of bronchiolitis or asthma were assessed. In some experiments infected mice were exposed to low-dose cockroach antigen. RESULTS: TLR7 deficiency increased viral load in the airway epithelium, which became sloughed and necrotic, and promoted an IFN-a/blow, IL-12p70low, IL-1bhigh, IL-25high, and IL-33high cytokine microenvironment that was associated with the recruitment of type 2 innate lymphoid cells/nuocytes and increased TH2-type cytokine production. Viral challenge of TLR72/2 mice induced all of the cardinal pathophysiologic features of asthma, including tissue eosinophilia, mast cell hyperplasia, IgE production, airway smooth muscle alterations, and airways hyperreactivity in a memory CD41 T cell–dependent manner. Importantly, infections with pneumonia virus of mice promoted allergic sensitization to inhaled cockroach antigen in the absence but not the presence of TLR7. CONCLUSION: TLR7 gene defects and Pneumovirus infection interact to establish an aberrant adaptive response that might underlie virus-induced asthma exacerbations in later life.
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© 2013 American Academy of Allergy, Asthma & Immunology