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The Impact of Muscarinic Receptor Antagonists on Airway Inflammation: A Systematic Review

Long-acting muscarinic receptor antagonists (LAMAs) are the cornerstone for the treatment of chronic obstructive pulmonary disease (COPD); furthermore, tiotropium is approved as add-on therapy in severe asthmatic patients. Accumulating evidence suggests that LAMAs may modulate airway contractility a...

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Autores principales: Calzetta, Luigino, Coppola, Angelo, Ritondo, Beatrice Ludovica, Matino, Matteo, Chetta, Alfredo, Rogliani, Paola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7886086/
https://www.ncbi.nlm.nih.gov/pubmed/33603353
http://dx.doi.org/10.2147/COPD.S285867
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author Calzetta, Luigino
Coppola, Angelo
Ritondo, Beatrice Ludovica
Matino, Matteo
Chetta, Alfredo
Rogliani, Paola
author_facet Calzetta, Luigino
Coppola, Angelo
Ritondo, Beatrice Ludovica
Matino, Matteo
Chetta, Alfredo
Rogliani, Paola
author_sort Calzetta, Luigino
collection PubMed
description Long-acting muscarinic receptor antagonists (LAMAs) are the cornerstone for the treatment of chronic obstructive pulmonary disease (COPD); furthermore, tiotropium is approved as add-on therapy in severe asthmatic patients. Accumulating evidence suggests that LAMAs may modulate airway contractility and airway hyperresponsiveness not only by blocking muscarinic acetylcholine receptors (mAchRs) expressed on airway smooth muscle but also via anti-inflammatory mechanisms by blocking mAchRs expressed on inflammatory cells, submucosal glands, and epithelial cells. The aim of this systematic review, performed according to the PRISMA-P guidelines, was to provide a synthesis of the literature on the anti-inflammatory impact of muscarinic receptor antagonists in the airways. Most of the current evidence originates from studies on tiotropium, that demonstrated a reduction in synthesis and release of cytokines and chemokines, as well as the number of total and differential inflammatory cells, induced by different pro-inflammatory stimuli. Conversely, few data are currently available for aclidinium and glycopyrronium, whereas no studies on the potential anti-inflammatory effect of umeclidinium have been reported. Overall, a large body of evidence supports the beneficial impact of tiotropium against airway inflammation. Further well-designed randomized controlled trials are needed to better elucidate the anti-inflammatory mechanisms leading to the protective effect of LAMAs against exacerbations via identifying suitable biomarkers.
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spelling pubmed-78860862021-02-17 The Impact of Muscarinic Receptor Antagonists on Airway Inflammation: A Systematic Review Calzetta, Luigino Coppola, Angelo Ritondo, Beatrice Ludovica Matino, Matteo Chetta, Alfredo Rogliani, Paola Int J Chron Obstruct Pulmon Dis Review Long-acting muscarinic receptor antagonists (LAMAs) are the cornerstone for the treatment of chronic obstructive pulmonary disease (COPD); furthermore, tiotropium is approved as add-on therapy in severe asthmatic patients. Accumulating evidence suggests that LAMAs may modulate airway contractility and airway hyperresponsiveness not only by blocking muscarinic acetylcholine receptors (mAchRs) expressed on airway smooth muscle but also via anti-inflammatory mechanisms by blocking mAchRs expressed on inflammatory cells, submucosal glands, and epithelial cells. The aim of this systematic review, performed according to the PRISMA-P guidelines, was to provide a synthesis of the literature on the anti-inflammatory impact of muscarinic receptor antagonists in the airways. Most of the current evidence originates from studies on tiotropium, that demonstrated a reduction in synthesis and release of cytokines and chemokines, as well as the number of total and differential inflammatory cells, induced by different pro-inflammatory stimuli. Conversely, few data are currently available for aclidinium and glycopyrronium, whereas no studies on the potential anti-inflammatory effect of umeclidinium have been reported. Overall, a large body of evidence supports the beneficial impact of tiotropium against airway inflammation. Further well-designed randomized controlled trials are needed to better elucidate the anti-inflammatory mechanisms leading to the protective effect of LAMAs against exacerbations via identifying suitable biomarkers. Dove 2021-02-12 /pmc/articles/PMC7886086/ /pubmed/33603353 http://dx.doi.org/10.2147/COPD.S285867 Text en © 2021 Calzetta et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Review
Calzetta, Luigino
Coppola, Angelo
Ritondo, Beatrice Ludovica
Matino, Matteo
Chetta, Alfredo
Rogliani, Paola
The Impact of Muscarinic Receptor Antagonists on Airway Inflammation: A Systematic Review
title The Impact of Muscarinic Receptor Antagonists on Airway Inflammation: A Systematic Review
title_full The Impact of Muscarinic Receptor Antagonists on Airway Inflammation: A Systematic Review
title_fullStr The Impact of Muscarinic Receptor Antagonists on Airway Inflammation: A Systematic Review
title_full_unstemmed The Impact of Muscarinic Receptor Antagonists on Airway Inflammation: A Systematic Review
title_short The Impact of Muscarinic Receptor Antagonists on Airway Inflammation: A Systematic Review
title_sort impact of muscarinic receptor antagonists on airway inflammation: a systematic review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7886086/
https://www.ncbi.nlm.nih.gov/pubmed/33603353
http://dx.doi.org/10.2147/COPD.S285867
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