| Literature DB >> 30745463 |
Siew-Kim Khoo1,2, James Read2, Kimberley Franks1,2, Guicheng Zhang1,3,4, Joelene Bizzintino1,2, Laura Coleman1,2, Christopher McCrae5, Lisa Öberg5, Niamh M Troy2, Franciska Prastanti1,2, Janet Everard1,2, Stephen Oo6, Meredith L Borland6,7,8, Rose A Maciewicz5, Peter N Le Souëf2,6, Ingrid A Laing1,2, Anthony Bosco9.
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-γ. 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.Entities:
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Year: 2019 PMID: 30745463 DOI: 10.4049/jimmunol.1800178
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422