Allergen challenge increases capsaicin-evoked cough responses in patients with allergic asthma.


Journal

The Journal of allergy and clinical immunology
ISSN: 1097-6825
Titre abrégé: J Allergy Clin Immunol
Pays: United States
ID NLM: 1275002

Informations de publication

Date de publication:
09 2019
Historique:
received: 22 06 2018
revised: 24 10 2018
accepted: 30 11 2018
pubmed: 21 1 2019
medline: 30 5 2020
entrez: 21 1 2019
Statut: ppublish

Résumé

Cough is a common and troublesome symptom in asthmatic patients, but little is known about the neuronal pathways that trigger cough. The mechanisms by which airway inflammation, airway hyperresponsiveness, and variable airflow obstruction cause cough are unclear. We sought to investigate the effects of allergen exposure on cough reflex sensitivity. We performed a 9-visit, randomized, single-blind, placebo-controlled, 2-way crossover study comparing cough responses to inhaled capsaicin in patients with mild atopic asthma after allergen challenge compared with diluent control. Full-dose capsaicin challenge was performed at screening to determine the capsaicin dose inducing a half-maximal response, which was subsequently administered at 30 minutes and 24 hours after inhaled allergen/diluent challenge. Spontaneous coughing was measured for 24 hours after allergen/diluent. Methacholine challenge and sputum induction were performed before and after allergen/diluent challenge. Twelve steroid-naive subjects completed the study (6 female subjects; mean age, 34.8 years). Allergen inhalation caused both an early (mean ± SD, 38.2% ± 13.0%) and late (mean ± SD, 23.7% ± 13.2%) decrease in FEV Allergen-induced bronchoconstriction and airway eosinophilia result in increased cough reflex sensitivity to capsaicin associated with an increase in 24-hour spontaneous coughing.

Sections du résumé

BACKGROUND
Cough is a common and troublesome symptom in asthmatic patients, but little is known about the neuronal pathways that trigger cough. The mechanisms by which airway inflammation, airway hyperresponsiveness, and variable airflow obstruction cause cough are unclear.
OBJECTIVE
We sought to investigate the effects of allergen exposure on cough reflex sensitivity.
METHODS
We performed a 9-visit, randomized, single-blind, placebo-controlled, 2-way crossover study comparing cough responses to inhaled capsaicin in patients with mild atopic asthma after allergen challenge compared with diluent control. Full-dose capsaicin challenge was performed at screening to determine the capsaicin dose inducing a half-maximal response, which was subsequently administered at 30 minutes and 24 hours after inhaled allergen/diluent challenge. Spontaneous coughing was measured for 24 hours after allergen/diluent. Methacholine challenge and sputum induction were performed before and after allergen/diluent challenge.
RESULTS
Twelve steroid-naive subjects completed the study (6 female subjects; mean age, 34.8 years). Allergen inhalation caused both an early (mean ± SD, 38.2% ± 13.0%) and late (mean ± SD, 23.7% ± 13.2%) decrease in FEV
CONCLUSION
Allergen-induced bronchoconstriction and airway eosinophilia result in increased cough reflex sensitivity to capsaicin associated with an increase in 24-hour spontaneous coughing.

Identifiants

pubmed: 30660644
pii: S0091-6749(19)30035-1
doi: 10.1016/j.jaci.2018.11.050
pii:
doi:

Substances chimiques

Allergens 0
Capsaicin S07O44R1ZM

Banques de données

ISRCTN
['ISRCTN79930571']

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

788-795.e1

Subventions

Organisme : Wellcome Trust
ID : 207504/B/17/Z
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/K015141/1
Pays : United Kingdom

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2019 American Academy of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.

Auteurs

Imran Satia (I)

Department of Medicine, Division of Respirology, McMaster University, Hamilton, Ontario, Canada; Division of Infection, Immunity and Respiratory Medicine, University of Manchester, and the Manchester Academic Health Science Centre, Manchester, United Kingdom.

Richard Watson (R)

Department of Medicine, Division of Respirology, McMaster University, Hamilton, Ontario, Canada.

Tara Scime (T)

Department of Medicine, Division of Respirology, McMaster University, Hamilton, Ontario, Canada.

Rachel J Dockry (RJ)

Division of Infection, Immunity and Respiratory Medicine, University of Manchester, and the Manchester Academic Health Science Centre, Manchester, United Kingdom; NHS Foundation Trust, University of Manchester, Manchester, United Kingdom.

Shilpi Sen (S)

Division of Infection, Immunity and Respiratory Medicine, University of Manchester, and the Manchester Academic Health Science Centre, Manchester, United Kingdom; NHS Foundation Trust, University of Manchester, Manchester, United Kingdom.

James W Ford (JW)

Division of Infection, Immunity and Respiratory Medicine, University of Manchester, and the Manchester Academic Health Science Centre, Manchester, United Kingdom; NHS Foundation Trust, University of Manchester, Manchester, United Kingdom.

Patrick D Mitchell (PD)

Department of Medicine, University of Calgary, Calgary, Alberta, Canada.

Stephen J Fowler (SJ)

Division of Infection, Immunity and Respiratory Medicine, University of Manchester, and the Manchester Academic Health Science Centre, Manchester, United Kingdom; NHS Foundation Trust, University of Manchester, Manchester, United Kingdom.

Gail M Gauvreau (GM)

Department of Medicine, Division of Respirology, McMaster University, Hamilton, Ontario, Canada.

Paul M O'Byrne (PM)

Department of Medicine, Division of Respirology, McMaster University, Hamilton, Ontario, Canada; Division of Infection, Immunity and Respiratory Medicine, University of Manchester, and the Manchester Academic Health Science Centre, Manchester, United Kingdom.

Jaclyn A Smith (JA)

Division of Infection, Immunity and Respiratory Medicine, University of Manchester, and the Manchester Academic Health Science Centre, Manchester, United Kingdom; NHS Foundation Trust, University of Manchester, Manchester, United Kingdom. Electronic address: jacky.smith@manchester.ac.uk.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH