Effect of IVL745, a VLA-4 antagonist, on allergen-induced bronchoconstriction in patients with asthma
| Autor: | Virginia Norris, Hasan Arshad, Stephen T. Holgate, Barry Miller, Shashank Rohatagi, Duyen Tran, Malcolm Boyce, Lee Choong, Sylvaine Millet, Zoe Corden, Stephane Kirkesseli, Brian P. O'Connor |
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| Rok vydání: | 2005 |
| Předmět: |
Adult
Male medicine.medical_specialty Allergy Bronchoconstriction Immunology Integrin alpha4beta1 Placebo Gastroenterology Bronchial Provocation Tests Double-Blind Method Internal medicine Benzene Derivatives medicine Humans Immunology and Allergy Asthma Cross-Over Studies business.industry Phenylurea Compounds Area under the curve Drug Tolerance Allergens Middle Aged medicine.disease Crossover study respiratory tract diseases Exhaled nitric oxide Sputum Female Methacholine Propionates Safety medicine.symptom business medicine.drug |
| Zdroj: | Journal of Allergy and Clinical Immunology. 116:761-767 |
| ISSN: | 0091-6749 |
| Popis: | Background Very late antigen (VLA-4) antagonists have been proposed as potential therapies for diseases in which cell recruitment and accumulation are causative. Asthma, which is characterized by airway inflammation involving the accumulation of eosinophils and mononuclear cells, is one such disease. Objective We sought to assess the effect of IVL745, a VLA-4 antagonist, on the early and late asthmatic response (LAR) and on markers of airway inflammation after allergen inhalation. Methods The study was of a placebo-controlled, double-blind, randomized, 2-way crossover design. Sixteen subjects with mild-to-moderate asthma controlled with short-acting β 2 -agonists only and with a LAR to inhaled allergen participated in the study. At one treatment period they took 20 mg of IVL745 and one treatment period placebo. Both treatments were taken twice daily for 7 days, with a single dose on day 8. Treatments were separated by a washout period of at least 2 weeks. On day 7 of each treatment period, sputum was induced and collected, and exhaled nitric oxide (NO) was measured. On day 8, an inhaled bolus allergen challenge was performed, and blood was taken for pharmacokinetics. On day 9, exhaled NO was measured, and a methacholine challenge was done. On day 10, sputum was induced and collected. Adverse events, peak expiratory flow (PEF), use of short-acting β 2 -agonists, and asthma symptoms were recorded daily throughout the study. Results There was no statistically significant difference between IVL745 and placebo in the effect on the LAR after allergen challenge, as measured by the area under the curve of the percentage change in FEV 1 from the prechallenge baseline (mean [SEM], −81.99 [18.80] after IVL745 and −72.58 [21.29] after placebo; 95% CI of difference, −36 to 16.8; P = .46) or by the maximum percentage change from the prechallenge baseline (mean [SEM], −23.44 [4.73] after IVL745 and −21.30 [5.17] after placebo; 95% CI of difference, −11 to 6.29; P = .60). There was a statistically significant decrease in the percentage of eosinophils in sputum on day 7 of treatment with IVL745 (mean [SEM], 7.32 [1.46]) compared with placebo (mean [SEM], 15.00 [1.92]; 95% CI of difference, −13 to −1.2; P = .02). There was no statistically significant difference between IVL745 and placebo with respect to the early asthmatic response, methacholine hyperresponsiveness, exhaled NO, postallergen sputum, symptoms, inhaled β 2 -agonist use, or PEF. Conclusion In patients with mild-to-moderate atopic asthma, IVL745 did not affect the early and late response to inhaled allergen or markers of airway inflammation, except for a modest reduction in sputum eosinophils. |
| Databáze: | OpenAIRE |
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