# Diminished airway host innate response in people with cystic fibrosis who experience frequent pulmonary exacerbations

**Authors:** Claire J. Houston, Aya Alkhatib, Gísli G. Einarsson, Michael M. Tunney, Clifford C. Taggart, Damian G. Downey

PMC · DOI: 10.1183/13993003.01228-2023 · The European Respiratory Journal · 2024-02-22

## TL;DR

People with cystic fibrosis who have frequent lung flare-ups show a weaker natural immune defense in their airways, which may explain why they get sick more often.

## Contribution

This study identifies a diminished innate host protein defense in frequent exacerbators with cystic fibrosis.

## Key findings

- Sputum from frequent exacerbators showed lower levels of innate defense proteins like SLPI, lipocalin-1, and cystatin SA.
- Frequent exacerbators had higher inflammatory markers (IL-1β and IL-8) and bacterial load in sputum.
- Sputum from frequent exacerbators could cleave SLPI in a neutrophil elastase-dependent manner.

## Abstract

Pulmonary exacerbations are clinically impactful events that accelerate cystic fibrosis (CF) lung disease progression. The pathophysiological mechanisms underlying an increased frequency of pulmonary exacerbations have not been explored.

To compare host immune response during intravenous antibiotic treatment of pulmonary exacerbations in people with CF who have a history of frequent versus infrequent exacerbations.

Adults with CF were recruited at onset of antibiotic treatment of a pulmonary exacerbation and were categorised as infrequent or frequent exacerbators based on their pulmonary exacerbation frequency in the previous 12 months. Clinical parameters, sputum bacterial load and sputum inflammatory markers were measured on day 0, day 5 and at the end of treatment. Shotgun proteomic analysis was performed on sputum using liquid chromatography-mass spectrometry.

Many sputum proteins were differentially enriched between infrequent and frequent exacerbators (day 0 n=23 and day 5 n=31). The majority of these proteins had a higher abundance in infrequent exacerbators and were secreted innate host defence proteins with antimicrobial, antiprotease and immunomodulatory functions. Several differentially enriched proteins were validated using ELISA and Western blot including secretory leukocyte protease inhibitor (SLPI), lipocalin-1 and cystatin SA. Sputum from frequent exacerbators demonstrated potent ability to cleave exogenous recombinant SLPI in a neutrophil elastase dependent manner. Frequent exacerbators had increased sputum inflammatory markers (interleukin (IL)-1β and IL-8) and total bacterial load compared to infrequent exacerbators.

A diminished innate host protein defence may play a role in the pathophysiological mechanisms of frequent CF pulmonary exacerbations. Frequent exacerbators may benefit from therapies targeting this dysregulated host immune response.

Characterisation of the sputum proteome of people with CF who experience infrequent and frequent exacerbations reveals that a diminished innate host protein defence may play a role in the pathophysiological mechanisms of CF frequent exacerbations
https://bit.ly/3v7DWvr

## Linked entities

- **Proteins:** SLPI (secretory leukocyte peptidase inhibitor), IL8L1 (interleukin 8-like 1)
- **Diseases:** cystic fibrosis (MONDO:0009061)

## Full-text entities

- **Genes:** ELANE (elastase, neutrophil expressed) [NCBI Gene 1991] {aka ELA2, GE, HLE, HNE, NE, PMN-E}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, SLPI (secretory leukocyte peptidase inhibitor) [NCBI Gene 6590] {aka ALK1, ALP, BLPI, HUSI, HUSI-1, HUSI-I}, CST2 (cystatin SA) [NCBI Gene 1470], LCN1 (lipocalin 1) [NCBI Gene 3933] {aka PMFA, TLC, TP, VEGP}
- **Diseases:** cystic fibrosis (MESH:D003550), cystic fibrosis (CF) lung disease (MESH:C563237), inflammatory (MESH:D007249), Pulmonary (MESH:D008171)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10882324/full.md

## References

59 references — full list in the complete paper: https://tomesphere.com/paper/PMC10882324/full.md

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Source: https://tomesphere.com/paper/PMC10882324