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    Upper Airway Cell Transcriptomics Identify a Major New Immunological Phenotype with Strong Clinical Correlates in Young Children with Acute Wheezing.

    Access Status
    Fulltext not available
    Authors
    Khoo, S.
    Read, J.
    Franks, K.
    Zhang, Guicheng
    Bizzintino, J.
    Coleman, L.
    McCrae, C.
    Öberg, L.
    Troy, N.
    Prastanti, F.
    Everard, J.
    Oo, S.
    Borland, M.
    Maciewicz, R.
    Le Souëf, P.
    Laing, I.
    Bosco, A.
    Date
    2019
    Type
    Journal Article
    
    Metadata
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    Citation
    Khoo, S. and Read, J. and Franks, K. and Zhang, G. and Bizzintino, J. and Coleman, L. and McCrae, C. et al. 2019. Upper Airway Cell Transcriptomics Identify a Major New Immunological Phenotype with Strong Clinical Correlates in Young Children with Acute Wheezing.. J Immunol.
    Source Title
    J Immunol
    DOI
    10.4049/jimmunol.1800178
    ISSN
    1550-6606
    School
    School of Public Health
    URI
    http://hdl.handle.net/20.500.11937/74236
    Collection
    • Curtin Research Publications
    Abstract

    Asthma exacerbations are triggered by rhinovirus infections. We employed a systems biology approach to delineate upper-airway gene network patterns underlying asthma exacerbation phenotypes in children. Cluster analysis unveiled distinct IRF7hi versus IRF7lo molecular phenotypes, the former exhibiting robust upregulation of Th1/type I IFN responses and the latter an alternative signature marked by upregulation of cytokine and growth factor signaling and downregulation of IFN-?. The two phenotypes also produced distinct clinical phenotypes. For IRF7lo children, symptom duration prior to hospital presentation was more than twice as long from initial symptoms (p = 0.011) and nearly three times as long for cough (p < 0.001), the odds ratio of admission to hospital was increased more than 4-fold (p = 0.018), and time to recurrence was shorter (p = 0.015). In summary, our findings demonstrate that asthma exacerbations in children can be divided into IRF7hi versus IRF7lo phenotypes with associated differences in clinical phenotypes.

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