Comparison of incremental and bolus dose inhaled allergen challenge in asthmatic patients

Citation
Da. Taylor et al., Comparison of incremental and bolus dose inhaled allergen challenge in asthmatic patients, CLIN EXP AL, 30(1), 2000, pp. 56-63
Citations number
28
Categorie Soggetti
Clinical Immunolgy & Infectious Disease",Immunology
Journal title
CLINICAL AND EXPERIMENTAL ALLERGY
ISSN journal
09547894 → ACNP
Volume
30
Issue
1
Year of publication
2000
Pages
56 - 63
Database
ISI
SICI code
0954-7894(200001)30:1<56:COIABD>2.0.ZU;2-Q
Abstract
Background Attenuation of airway responses to inhaled allergen is increasin gly used to evaluate anti-asthma drugs. Many studies use different allergen challenge methods and the presence of the late asthmatic response can be i dentified by a screening challenge with inhalation of incremental doses of allergen. Once defined, subsequent challenges are often administered as a c onstant dose based on the dose from the screening challenge. Previously, co nstant dose challenges have been employed but never validated. Objective A comparative study of two methods of delivering inhaled allergen by evaluating the responses of an incremental dose allergen challenge and the same cumulative dose administered as a bolus over a single inhalation. Methods Thirty-five male patients with mild allergic asthma underwent incre mental dose challenge followed 3-6 weeks later by a bolus dose challenge. B ronchoconstrictor responses were expressed as the maximum percentage fall i n FEV1 from baseline during the early (0-2 h) and late (4-10 h) asthmatic r esponses and area under the percentage change in FEV1-time curve (AUC). Results There were no significant differences between the challenges. The m ean +/- SEM fall in FEV, following incremental and bolus dose challenge was 33.1 +/- 1.8% and 29.9 +/- 2.2% during the early response, and 36.9 +/- 2. 4% and 34.0 +/- 3.1% during the late response, respectively. The mean +/- S EM AUC following incremental and bolus dose challenge was 35 +/- 3 and 33 /- 3 Delta%FEV1/h for the AUC(0-2 h), 147 +/- 12 and 139 +/- 16 Delta%FEV1/ h for the AUC(4-10 h), and 204 +/- 14 and 190 +/- 19 Delta%FEV1/h for the A UC(0-10 h) , respectively. Conclusion Bolus dose allergen challenge is a safe method to administer inh aled allergen in clinical trials with a valid response when compared with i ncremental dose allergen challenge.