Rethinking bronchiectasis as an inflammatory disease
- PMID: 38971168
- DOI: 10.1016/S2213-2600(24)00176-0
Rethinking bronchiectasis as an inflammatory disease
Abstract
Bronchiectasis is understood to be the result of a complex interaction between infection, impaired mucociliary clearance, inflammation, and lung damage. Current therapeutic approaches to bronchiectasis are heavily focused on management of infection along with enhancing mucus clearance. Long-term antibiotics have had limited success in clinical trials, suggesting a need to re-evaluate the concept of bronchiectasis as an infective disorder. We invoke the example of asthma, for which treatment paradigms shifted away from targeting smooth muscle constriction, towards permanently suppressing airway inflammation, reducing risk and ultimately inducing remission with precision anti-inflammatory treatments. In this Review, we argue that bronchiectasis is primarily a chronic inflammatory disease, requiring early identification of at-risk individuals, and we introduce a novel concept of disease activity with important implications for clinical practice and future research. A new generation of novel anti-inflammatory treatments are under development and repurposing of anti-inflammatory agents from other diseases could revolutionise patient care.
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Conflict of interest statement
Declaration of interests MS reports having received grant support (institutional) from GSK, Trudell Pharma, and the Tel Aviv League for Pulmonary Diseases; consulting fees (personal) from Astra Zeneca, Boehringer Ingelheim, Dexcel Pharma, GSK, Kamada, Synchrony Medical, Truemed, Vertex, and Zambon; travel grants (institutional) from Boehringer Ingelheim, Astra Zeneca, and Kamada; payment or honoraria from Astra Zeneca, Boehringer Ingelheim, Kamada, GSK, and Sanofi; participation on a data safety and monitoring board or advisory board for Bonus Biotherapeutics, Boehringer Ingelheim, Vertex, and Astra Zeneca; and is management board member for the Israeli Pulmonology Society, Israeli Society for Tuberculosis and Mycobacterial Diseases, and the associate editor for the American Journal of Respiratory and Critical Care Medicine. SHC reports consulting fees from CSL Behring, Boehringer Ingelheim, and Pneumagen, and payment for lectures from Astrazeneca and Chiesi; participation on DSMB for Inovio Pharmaceuticals and Imam Abdulrahman Bin Faisal University (Dammam, Saudi Arabia). JDC reports grants or contracts from Grifols; consulting fees from Antabio, AstraZeneca, Boehringer Ingelheim, Chiesi, Glaxosmithkline, Grifols, Insmed, Janssen, Novartis, Pfizer, and Zambon; and leadership or fiduciary roles as Chair of European Respiratory Society Bronchiectasis Guideline Task Force, Chief Editor of European Respiratory Journal, and Chair of the European Multicentre Bronchiectasis Audit and Research Collaboration Clinical Research Collaboration. All other authors declare no competing interests.
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