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Effect of salmeterol on allergen‐induced airway inflammation in mild allergic asthma
Author(s) -
Boulet L.P.,
Chakir J.,
Milot J.,
Boutet M.,
Laviolette M.
Publication year - 2001
Publication title -
clinical and experimental allergy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.462
H-Index - 154
eISSN - 1365-2222
pISSN - 0954-7894
DOI - 10.1046/j.1365-2222.2001.01014.x
Subject(s) - medicine , methacholine , allergen , inhalation , bronchoalveolar lavage , asthma , placebo , salmeterol , gastroenterology , immunology , allergy , anesthesia , provocation test , lung , respiratory disease , pathology , alternative medicine
A previous study suggested that the long‐acting β 2 ‐adrenergic agonist salmeterol (SM) had inhibitory effects on bronchial mucosal inflammation 6 hours after allergen exposure. To further evaluate the influence of SM on allergen‐induced airway inflammation. We studied, in a randomized, double‐blind, cross‐over trial, 16 mild asthmatic patients who had a dual asthmatic response to allergen inhalation. Subjects received 50 µg of SM or placebo (P), twice daily for 1 week each, separated by a 2‐week wash‐out period. At the end of each treatment period, after withholding SM for 24 h, they had a methacholine inhalation test (medication was resumed after the test), followed 24 h later by an AC with the concentration of allergen that had induced a LAR at baseline. Airway inflammation was assessed 24 h after the AC by bronchoalveolar lavage (BAL) ( n  = 16) and bronchial biopsies ( n  = 13). As expected, SM improved baseline FEV 1 and PC 20 ( P  ≤ 0.009) and decreased the allergen‐induced early bronchoconstrictive response. There were no significant differences in BAL cell counts after the two treatments. On bronchial biopsies, numbers (median, mm 2 ) of submucosal CD45 (P: 43 ± 23; SM: 161 ± 43, P  = 0.031), CD45 R o (P: 37 ± 19; SM: 126 ± 41, P  = 0.047) and AA1 positive cells (P: 38 ± 6, SM: 65 ± 17, P  = 0.006) were significantly higher after SM than P treatment. The numbers of CD4 (P: 11 ± 10; SM: 32 ± 7, P  = 0.085), HLA‐DR (P: 65 ± 30; SM: 116 ± 36, P  = 0.079) and EG2 positive cells (P: 25 ± 15; SM: 38 ± 26, P  = 0.09) tended to increase with SM treatment. In summary, compared to placebo, 1 week of regular use of SM is associated with an increase in bronchial inflammatory cells 24 h after AC. This is in keeping with the recommendation that salmeterol should only be used with an anti‐inflammatory agent, particularly in the context of significant allergen exposure.

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