Airway IL-1β is related to disease severity and mucociliary function in bronchiectasis

Eur Respir J. 2024 Aug 15;64(2):2301966. doi: 10.1183/13993003.01966-2023. Print 2024 Aug.

Abstract

Rationale: The inflammasome is a key regulatory complex of the inflammatory response leading to interleukin-1β (IL-1β) release and activation. IL-1β amplifies inflammatory responses and induces mucus secretion and hyperconcentration in other diseases. The role of IL-1β in bronchiectasis has not been investigated.

Objectives: To characterise the role of airway IL-1β in bronchiectasis, including the association with mucus properties, ciliary function, airway inflammation, microbiome and disease severity.

Methods: Stable bronchiectasis patients were enrolled in an international cohort study (n=269). IL-1β was measured in sputum supernatant. A validation cohort also had sputum rheology and hydration measured (n=53). For analysis, patients were stratified according to the median value of IL-1β in the population (high versus low) to compare disease severity, airway infection, microbiome (16S rRNA sequencing), inflammation and caspase-1 activity. Primary human nasal epithelial cells grown in air-liquid interface culture were used to study the effect of IL-1β on cilia function.

Results: Patients with high sputum IL-1β had more severe disease, increased caspase-1 activity and an increased T-helper type 1, T-helper type 2 and neutrophil inflammatory response compared with patients with low IL-1β. The active-dominant form of IL-1β was associated with increased disease severity. High IL-1β was related to higher relative abundance of Proteobacteria in the microbiome and increased mucus solid content and viscoelastic properties. Chronic IL-1β treatment reduced the functionality of cilia and tight junctions of epithelial cells in vitro.

Conclusions: A subset of stable bronchiectasis patients show increased airway IL-1β, suggesting pulmonary inflammasome activation is linked with more severe disease, airway infection, mucus dehydration and epithelial dysfunction.

MeSH terms

  • Adult
  • Aged
  • Bronchiectasis* / metabolism
  • Bronchiectasis* / microbiology
  • Bronchiectasis* / physiopathology
  • Caspase 1 / metabolism
  • Cilia / metabolism
  • Cohort Studies
  • Female
  • Humans
  • Inflammasomes / metabolism
  • Inflammation
  • Interleukin-1beta* / metabolism
  • Male
  • Microbiota
  • Middle Aged
  • Mucociliary Clearance*
  • Mucus / metabolism
  • RNA, Ribosomal, 16S / genetics
  • Severity of Illness Index*
  • Sputum* / metabolism

Substances

  • Interleukin-1beta
  • Inflammasomes
  • IL1B protein, human
  • Caspase 1
  • RNA, Ribosomal, 16S