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


Autoria(s): Djukanović, Ratko; Harrison, Tim; Johnston, Sebastian L; Gabbay, Flic; Wark, Peter; Thomson, Neil C; Niven, Robert; Singh, Dave; Reddel, Helen K; Davies, Donna E; Marsden, Richard; Boxall, Christine; Dudley, Sarah; Plagnol, Vincent; Holgate, Stephen T; Monk, Phillip; INTERCIA Study Group; McGarvey, Lorcan
Data(s)

15/07/2014

Resumo

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-b. Exogenous IFN-b restores antiviral activity.<br/><br/>Objectives: To compare the efficacy and safety of inhaled IFN-b with placebo administered to people with asthma after onset of cold symptoms to prevent or attenuate asthma symptoms caused by respiratory viruses.<br/><br/>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-b (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.<br/><br/>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<br/>(mean change in six-item Asthma Control Questionnaire ,0.5) and IFN-b treatment had no significant effect on this primary endpoint, although it enhanced morning peak expiratory flow recovery (P = 0.033), reduced the need for additional treatment, and boosted innate immunity as assessed by blood and sputum biomarkers. In an exploratory analysis of the subset ofmore difficult-to-treat, Step 4-5 peoplewith asthma (n = 27 IFN-b; n = 31 placebo), Asthma Control Questionnaire-6 increased significantly on placebo; this was prevented by IFN-b (P = 0.004).<br/><br/>Conclusions: Although the trial did not meet its primary endpoint, it suggests that inhaled IFN-b is a potential treatment for virus-induced deteriorations of asthma in difficult-to-treat people with asthma and supports the needforfurther, adequately powered, trialsin this population. Clinical trial registered with www.clinicaltrials.gov (NCT 01126177).

Identificador

http://pure.qub.ac.uk/portal/en/publications/the-effect-of-inhaled-ifn-on-worsening-of-asthma-symptoms-caused-by-viral-infections-a-randomized-trial(b4510628-d359-4e23-9f7b-f8379a0eccda).html

http://dx.doi.org/10.1164/rccm.201312-2235OC

Idioma(s)

eng

Direitos

info:eu-repo/semantics/restrictedAccess

Fonte

Djukanović , R , Harrison , T , Johnston , S L , Gabbay , F , Wark , P , Thomson , N C , Niven , R , Singh , D , Reddel , H K , Davies , D E , Marsden , R , Boxall , C , Dudley , S , Plagnol , V , Holgate , S T , Monk , P , INTERCIA Study Group & McGarvey , L 2014 , ' The effect of inhaled IFN-β on worsening of asthma symptoms caused by viral infections. a randomized trial ' American Journal of Respiratory and Critical Care Medicine , vol 190 , no. 2 , pp. 145-154 . DOI: 10.1164/rccm.201312-2235OC

Palavras-Chave #Administration, Inhalation #Adolescent #Adrenal Cortex Hormones #Adult #Aged #Anti-Asthmatic Agents #Antiviral Agents #Asthma #Disease Progression #Double-Blind Method #Drug Administration Schedule #Drug Therapy, Combination #Female #Humans #Intention to Treat Analysis #Interferon-beta #Male #Middle Aged #Questionnaires #Respiratory Tract Infections #Severity of Illness Index #Treatment Outcome #Virus Diseases #Young Adult
Tipo

article