Clinical, molecular and microbial characterisation of the eosinophilic endotype of bronchiectasis: data from the EMBARC-BRIDGE study

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Authors: Jennifer Pollock, Jeffrey T. J. Huang, Morven Shuttleworth, Merete Long, Hollian Richardson, Daniela Alferes de Lima, Elena Kuzmanova, Clare Clarke, Michal Shteinberg, Stefano Aliberti, Charles Haworth, S H Chotirmall
+10 more E Polverino, Pieter Goeminne, Michael Loebinger, Natalie Lorent, Felix C Ringshausen, Oriol Sibila, Eva Rodriguez-Suarez, Christopher McCrae, Amelia Shoemark, James Chalmers
Cited by: 5
References: 38

Abstract

Objectives Eosinophilic bronchiectasis is defined by a blood eosinophil count (BEC) ≥300 cells/µL, but blood eosinophils imperfectly reflect airway eosinophilic inflammation. Here, we investigated the relationship between eosinophilic airway inflammation, blood eosinophils and clinical severity in bronchiectasis and explored the phenotype associated with eosinophilic bronchiectasis. Methods Sputum from 180 patients with stable CT-confirmed bronchiectasis was utilised to investigate airway levels of eosinophil proteins (eosinophil peroxidase (EPX), eosinophil derived-neurotoxin (EDN), eosinophil cationic protein (ECP), major basic protein (MBP) and Galectin-10 (Gal-10)) using a novel stable isotope dilution liquid chromatography-tandem mass spectrometry (LC-MS/MS) assay. To profile eosinophilic bronchiectasis, a nested analysis of patients with BEC 0.35 kUA/L, 24.5% vs 3.8%) in eosinophilic bronchiectasis. Sputum inflammatory biomarkers and clinical parameters did not differ between groups. Conclusions LC-MS/MS can detect eosinophilic inflammation within bronchiectasis sputum. Weak associations between elevated airway eosinophil proteins, bronchiectasis severity and P. aeruginosa infection were observed. Direct measurement of eosinophilic airway inflammation provides additional information in addition to BECs. Eosinophilic bronchiectasis associated with P. aeruginosa infection and Aspergillus sensitisation.

Fields of Study & Subjects

Cystic Fibrosis Research Advances Neonatal Respiratory Health Research Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis

Publication details

Journal / source
Thorax
Publisher
BMJ
Volume
81
Issue
7
Pages
642–653
Publication date
13 February 2026
Language
EN