The Journal of Allergy and Clinical Immunology
Volume 119, Issue 2 , Pages 322-327, February 2007

The effects of inhaled budesonide and formoterol in combination and alone when given directly after allergen challenge

From the Firestone Institute for Respiratory Health and the Department of Medicine, St Joseph's Hospital and McMaster University Medical Center, McMaster University

Received 14 August 2006; accepted 10 October 2006. published online 12 December 2006.

Hamilton, Ontario, Canada

Background

The use of combination inhaled budesonide and formoterol as maintenance and reliever therapy significantly improves the risk and the time to exacerbations in asthma.

Objectives

To explore the mechanisms underlying the effect of the reliever dose on exacerbations by examining the effect of combination therapy on the allergen challenge model when given after allergen exposure.

Methods

In a randomized, double-blind crossover study, single doses of budesonide/formoterol (400/12 μg), formoterol (12 μg), budesonide (400 μg), or placebo were administered during the acute bronchoconstriction response (early airway response) immediately after allergen inhalation in 15 patients with mild asthma. Allergen-induced late airway response (LAR), sputum inflammatory markers, airway hyperresponsiveness, and exhaled nitric oxide were measured.

Results

All active treatments significantly attenuated the LAR, with budesonide/formoterol significantly better than its monocomponents (maximum FEV1 fall: placebo, [mean ± SEM] 21.2% ± 3.1%; budesonide/formoterol, 4.2% ± 1.4%; formoterol, 7.5% ± 1.7%; budesonide, 10.4% ± 1.6%). Allergen-induced change in methacholine PC20 was significantly attenuated by budesonide/formoterol, but not by its monocomponents. Sputum cell counts and exhaled nitric oxide increased significantly after all allergen challenges, with no significant attenuation by any of the treatments. Therapy with combination and formoterol alone, but not budesonide, significantly reduced the early airway response.

Conclusion

A single dose of budesonide/formoterol was superior to its monocomponents in attenuating the allergen-induced LAR and airway hyperresponsiveness. These effects may represent the contribution of the reliever dose to the budesonide/formoterol maintenance and reliever regimen.

Clinical implications

The protective effect against allergic airway responses with a single reliever dose of budesonide/formoterol is predominantly related to greater functional antagonism of airway smooth muscles.

Key words: Budesonide/formoterol, allergic asthma, reliever combination therapy use

Abbreviations used: AHR, Airway hyperresponsiveness, DD, Doubling dose, EAR, Early airway response, ECP, Eosinophil cationic protein, eNO, Exhaled nitric oxide, ICS, Inhaled corticosteroid, LABA, Long-acting β2-agonist, LAR, Late airway response, MCC, Metachromatic cell, TCC, Total cell count

 

 Supported in part by AstraZeneca, Lund, Sweden.Disclosure of potential conflict of interest: G. Gauvreau has consultant arrangements with Topigen Pharma Inc, Tanox, Novartis Pharma UK Ltd, MedImmune Inc, and Altana Inc and has received grant support from Pfizer, Altana, GlaxoSmithKline, Topigen, and MedImmune. P. M. O'Byrne has consultant arrangements with Altana, AstraZeneca, GlaxoSmithKline, Topigen, and Biolipox and has received grant support from Altana, AstraZeneca, GlaxoSmithKline, Topigen, Biolipox, MedImmune, Pfizer, IVAX, and Boehringer Ingleheim. The rest of the authors have declared that they have no conflict of interest.Some of the data from this paper were presented in abstract form at the American Thoracic Society Meeting, May 2006, San Diego, Calif.

PII: S0091-6749(06)02134-8

doi:10.1016/j.jaci.2006.10.018

The Journal of Allergy and Clinical Immunology
Volume 119, Issue 2 , Pages 322-327, February 2007