4.7 Article

Inhaled Corticosteroids Selectively Alter the Microbiome and Host Transcriptome in the Small Airways of Patients with Chronic Obstructive Pulmonary Disease

期刊

BIOMEDICINES
卷 10, 期 5, 页码 -

出版社

MDPI
DOI: 10.3390/biomedicines10051110

关键词

COPD; inhaled corticosteroids; 16S rRNA gene sequencing; mRNA-sequencing; transcriptomics; bronchoscopy; fluticasone; budesonide; microbiome; inflammation

资金

  1. Canadian Institute of Health Research
  2. British Columbia Lung Association
  3. Natural Sciences and Engineering Research Council (NSERC) Canada
  4. MITACS Accelerate Fellowship
  5. MITACS Accelerate Program
  6. MITACS
  7. Providence Airway Centre
  8. St. Paul's Foundation
  9. Michael Smith Foundation for Health Research
  10. Tier 2 Canada Research Chair in Translational Airway Biology
  11. Michael Smith Foundation for Health Research-Health Professional-Investigator Award
  12. Tier 1 Canada Research Chair in COPD
  13. AstraZeneca(R)

向作者/读者索取更多资源

Changes in the microbiome following inhaled corticosteroid/long-acting beta 2-agonist combination therapy in COPD patients are related to alterations in the host transcriptome in the small airways. This may explain why some COPD patients treated with inhaled corticosteroids may be at an increased risk for airway infections.
Background: Patients with chronic obstructive pulmonary disease (COPD) are commonly treated with inhaled corticosteroid/long-acting beta 2-agonist combination therapy. While previous studies have investigated the host-microbiome interactions in COPD, the effects of specific steroid formulations on this complex cross-talk remain obscure. Methods: We collected and evaluated data from the Study to Investigate the Differential Effects of Inhaled Symbicort and Advair on Lung Microbiota (DISARM), a randomized controlled trial. Bronchoscopy was performed on COPD patients before and after treatment with salmeterol/fluticasone, formoterol/budesonide or formoterol-only. Bronchial brush samples were processed for microbial 16S rRNA gene sequencing and host mRNA sequencing. Longitudinal changes in the microbiome at a community, phylum and genus level were correlated with changes in host gene expression using a Spearman's rank correlation test. Findings: In COPD patients treated with salmeterol/fluticasone, the expression levels of 676 host genes were significantly correlated to changes in the alpha diversity of the small airways. At a genus level, the expression levels of 122 host genes were significantly related to changes in the relative abundance of Haemophilus. Gene enrichment analyses revealed the enrichment of pathways and biological processes related to innate and adaptive immunity and inflammation. None of these changes were evident in patients treated with formoterol/budesonide or formoterol alone. Interpretation: Changes in the microbiome following salmeterol/fluticasone treatment are related to alterations in the host transcriptome in the small airways of patients with COPD. These data may provide insights into why some COPD patients treated with inhaled corticosteroids may be at an increased risk for airway infection, including pneumonia. Funding: The Canadian Institute of Health Research, the British Columbia Lung Association, and an investigator-initiated grant from AstraZeneca.

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