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 hyper-responsiveness 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.

Calzetta, L., Coppola, A., Ritondo, B., Matino, M., Chetta, A., Rogliani, P. (2021). The impact of muscarinic receptor antagonists on airway inflammation: a systematic review. INTERNATIONAL JOURNAL OF COPD, 16, 257-279 [10.2147/COPD.S285867].

The impact of muscarinic receptor antagonists on airway inflammation: a systematic review

Rogliani, P
2021-01-01

Abstract

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 hyper-responsiveness 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.
2021
Pubblicato
Rilevanza internazionale
Review
Esperti anonimi
Settore MED/10 - MALATTIE DELL'APPARATO RESPIRATORIO
Settore MEDS-07/A - Malattie dell'apparato respiratorio
English
Con Impact Factor ISI
muscarinic receptor antagonist
LAMA
tiotropium
inflammation
systematic review
Calzetta, L., Coppola, A., Ritondo, B., Matino, M., Chetta, A., Rogliani, P. (2021). The impact of muscarinic receptor antagonists on airway inflammation: a systematic review. INTERNATIONAL JOURNAL OF COPD, 16, 257-279 [10.2147/COPD.S285867].
Calzetta, L; Coppola, A; Ritondo, B; Matino, M; Chetta, A; Rogliani, P
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/285494
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