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Airway responses and inflammation in subjects with asthma after four days of repeated high-single-dose allergen challenge

BACKGROUND: Both standard and low-dose allergen provocations are an established tool in asthma research to improve our understanding of the pathophysiological mechanism of allergic asthma. However, clinical symptoms are less likely to be induced. Therefore, we designed a protocol for repetitive high...

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Autores principales: Schulze, Johannes, Voss, Sandra, Zissler, Ulrich, Rose, Markus A, Zielen, Stefan, Schubert, Ralf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3445853/
https://www.ncbi.nlm.nih.gov/pubmed/22989372
http://dx.doi.org/10.1186/1465-9921-13-78
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author Schulze, Johannes
Voss, Sandra
Zissler, Ulrich
Rose, Markus A
Zielen, Stefan
Schubert, Ralf
author_facet Schulze, Johannes
Voss, Sandra
Zissler, Ulrich
Rose, Markus A
Zielen, Stefan
Schubert, Ralf
author_sort Schulze, Johannes
collection PubMed
description BACKGROUND: Both standard and low-dose allergen provocations are an established tool in asthma research to improve our understanding of the pathophysiological mechanism of allergic asthma. However, clinical symptoms are less likely to be induced. Therefore, we designed a protocol for repetitive high-dose bronchial allergen challenges to generate clinical symptoms and airway inflammation. METHODS: A total of 27 patients aged 18 to 40 years with positive skin-prick tests and mild asthma underwent repetitive high-dose allergen challenges with household dust mites for four consecutive days. Pulmonary function and exhaled NO were measured at every visit. Induced sputum was analysed before and after the allergen challenges for cell counts, ECP, IL-5, INF-γ, IL-8, and the transcription factor Foxp3. RESULTS: We found a significant decrease in pulmonary function, an increased use of salbutamol and the development of a late asthmatic response and bronchial hyperresponsiveness, as well as a significant induction of eNO, eosinophils, and Th-2 cytokines. Repeated provocation was feasible in the majority of patients. Two subjects had severe adverse events requiring prednisolone to cope with nocturnal asthma symptoms. CONCLUSIONS: Repeated high-dose bronchial allergen challenges resulted in severe asthma symptoms and marked Th-2-mediated allergic airway inflammation. The high-dose challenge model is suitable only in an attenuated form in diseased volunteers for proof-of-concept studies and in clinical settings to reduce the risk of severe asthma exacerbations. TRIAL REGISTRATION: ClinicalTrials.govNCT00677209
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spelling pubmed-34458532012-09-20 Airway responses and inflammation in subjects with asthma after four days of repeated high-single-dose allergen challenge Schulze, Johannes Voss, Sandra Zissler, Ulrich Rose, Markus A Zielen, Stefan Schubert, Ralf Respir Res Research BACKGROUND: Both standard and low-dose allergen provocations are an established tool in asthma research to improve our understanding of the pathophysiological mechanism of allergic asthma. However, clinical symptoms are less likely to be induced. Therefore, we designed a protocol for repetitive high-dose bronchial allergen challenges to generate clinical symptoms and airway inflammation. METHODS: A total of 27 patients aged 18 to 40 years with positive skin-prick tests and mild asthma underwent repetitive high-dose allergen challenges with household dust mites for four consecutive days. Pulmonary function and exhaled NO were measured at every visit. Induced sputum was analysed before and after the allergen challenges for cell counts, ECP, IL-5, INF-γ, IL-8, and the transcription factor Foxp3. RESULTS: We found a significant decrease in pulmonary function, an increased use of salbutamol and the development of a late asthmatic response and bronchial hyperresponsiveness, as well as a significant induction of eNO, eosinophils, and Th-2 cytokines. Repeated provocation was feasible in the majority of patients. Two subjects had severe adverse events requiring prednisolone to cope with nocturnal asthma symptoms. CONCLUSIONS: Repeated high-dose bronchial allergen challenges resulted in severe asthma symptoms and marked Th-2-mediated allergic airway inflammation. The high-dose challenge model is suitable only in an attenuated form in diseased volunteers for proof-of-concept studies and in clinical settings to reduce the risk of severe asthma exacerbations. TRIAL REGISTRATION: ClinicalTrials.govNCT00677209 BioMed Central 2012 2012-09-19 /pmc/articles/PMC3445853/ /pubmed/22989372 http://dx.doi.org/10.1186/1465-9921-13-78 Text en Copyright ©2012 Schulze et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Schulze, Johannes
Voss, Sandra
Zissler, Ulrich
Rose, Markus A
Zielen, Stefan
Schubert, Ralf
Airway responses and inflammation in subjects with asthma after four days of repeated high-single-dose allergen challenge
title Airway responses and inflammation in subjects with asthma after four days of repeated high-single-dose allergen challenge
title_full Airway responses and inflammation in subjects with asthma after four days of repeated high-single-dose allergen challenge
title_fullStr Airway responses and inflammation in subjects with asthma after four days of repeated high-single-dose allergen challenge
title_full_unstemmed Airway responses and inflammation in subjects with asthma after four days of repeated high-single-dose allergen challenge
title_short Airway responses and inflammation in subjects with asthma after four days of repeated high-single-dose allergen challenge
title_sort airway responses and inflammation in subjects with asthma after four days of repeated high-single-dose allergen challenge
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3445853/
https://www.ncbi.nlm.nih.gov/pubmed/22989372
http://dx.doi.org/10.1186/1465-9921-13-78
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