Inhaled beclomethasone dipropionate reverts tolerance to the protective effect of salmeterol on allergen challenge

Citation
D. Giannini et al., Inhaled beclomethasone dipropionate reverts tolerance to the protective effect of salmeterol on allergen challenge, CHEST, 115(3), 1999, pp. 629-634
Citations number
26
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Journal title
CHEST
ISSN journal
00123692 → ACNP
Volume
115
Issue
3
Year of publication
1999
Pages
629 - 634
Database
ISI
SICI code
0012-3692(199903)115:3<629:IBDRTT>2.0.ZU;2-E
Abstract
Study objective: One week of regular treatment with salmeterol can induce t olerance to the protective effect of a beta(2)-agonist on early airway resp onse to allergen (EAR). The objective was to assess whether inhaled cortico steroids revert tolerance to salmeterol. Study design: The study had a rand omized, double-blind, placebo-controlled design. Patients and methods: Twelve subjects with mild allergic asthma and positiv e result of specific bronchial provocation test (sBPT) to allergen underwen t three sBPTs, separated by 1 week. sBPT was done in all subjects after a s ingle dose (T-1) and after 1 week of regular treatment with inhaled salmete rol (50 mu g bid) (T-2) in order to induce tolerance. Subjects were then ra ndomized to receive either the same dose of salmeterol + beclomethasone dip ropionate (BDP, 500 mu g bid) (group 1, n = 6) or placebo + BDP (group 2, n = 6) for 1 week before sBPT (T-3). Results: After a single dose of salmeterol (T-1), all subjects were protect ed against EAR, whereas after 1 week of regular treatment, the protective e ffect of salmeterol was totally or partially lost (T-2). Maximum FEV1 perce nt fall (Max Delta FEV1%) after allergen inhalation was significantly highe r at T-2 than at T-1. All subjects except one of group 1 were protected aga inst EAR after salmeterol + BDP (T-3), and Max Delta FEV1% at T-3 (median, 12%; range, 4 to 6%) was significantly lower than T-2 (median, 22%; range, 12 to 43%; p < 0.05 by Wilcoxon test). Subjects of group 2 did not show any significant protection against EAR after placebo + BDP treatment (T-3) Max Delta FEV1% at T-2 (median, 31%; range, 9 to 40%) and T-3 (median, 31%; ra nge, 3 to 42%; not significant). Conclusions: In conclusion, the addition of inhaled BDP partially restored the bronchoprotective effect of salmeterol on allergen challenge that was l ost after 1 week of regular treatment with salmeterol alone. This ability o f BDP in reverting tolerance cannot be ascribed to a direct effect of corti costeroids per se on allergen challenge in this group of asthmatics.