The effect of inhaled IFN-β on worsening of asthma symptoms caused by viral infections. A randomized trial.

Ratko Djukanović (Collaborator), Tim Harrison (Collaborator), Sebastian Johnston (Collaborator), Flic Gabbay, Peter Wark (Collaborator), Neil C Thomson (Collaborator), Robert Niven (Collaborator), Dave Singh, Helen Reddel (Collaborator), Donna E Davies (Collaborator), Richard Marsden, Christine Boxall (Collaborator), Vincent Plagnol, Stephen T Holgate (Collaborator), Christopher Brightling (Collaborator), Phillip Bardin (Collaborator), Liam Heaney (Collaborator), Lorcan McGarvey (Collaborator), Ian Sabroe (Collaborator), Bernard Higgins (Collaborator)Mark Arya (Collaborator), Christopher Strang (Collaborator), Najib Rahman (Collaborator), Babatunde Oyesile (Collaborator), Hawys Thomas (Collaborator), Essam Hakim (Collaborator), Phillip Monk (Collaborator), Jody Brookes (Collaborator), Sarah Dudley (Collaborator), Rona Beegan (Collaborator), Joanna Samways (Collaborator), INTERCIA Study Group

    Research output: Contribution to journalArticlepeer-review

    Abstract

    RATIONALE: Ex vivo, bronchial epithelial cells from people with asthma are more susceptible to rhinovirus infection caused by deficient induction of the antiviral protein, IFN-β. Exogenous IFN-β restores antiviral activity. OBJECTIVES: To compare the efficacy and safety of inhaled IFN-β with placebo administered to people with asthma after onset of cold symptoms to prevent or attenuate asthma symptoms caused by respiratory viruses. METHODS: A total of 147 people with asthma on inhaled corticosteroids (British Thoracic Society Steps 2-5), with a history of virus-associated exacerbations, were randomized to 14-day treatment with inhaled IFN-β (n = 72) or placebo (n = 75) within 24 hours of developing cold symptoms and were assessed clinically, with relevant samples collected to assess virus infection and antiviral responses. MEASUREMENTS AND MAIN RESULTS: A total of 91% of randomized patients developed a defined cold. In this modified intention-to-treat population, asthma symptoms did not get clinically significantly worse (mean change in six-item Asthma Control Questionnaire
    Original languageEnglish
    Pages (from-to)145-154
    Number of pages9
    JournalAmerican Journal of Respiratory and Critical Care Medicine
    Volume190
    Issue number2
    DOIs
    Publication statusPublished - 15 Jul 2014

    Keywords

    • innate immunity
    • respiratory virus
    • treatment

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