HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Airway bacteria drive a progressive COPD-like phenotype in mice with polymeric immunoglobulin receptor deficiency.

Abstract
Mechanisms driving persistent airway inflammation in chronic obstructive pulmonary disease (COPD) are incompletely understood. As secretory immunoglobulin A (SIgA) deficiency in small airways has been reported in COPD patients, we hypothesized that immunobarrier dysfunction resulting from reduced SIgA contributes to chronic airway inflammation and disease progression. Here we show that polymeric immunoglobulin receptor-deficient (pIgR(-/-)) mice, which lack SIgA, spontaneously develop COPD-like pathology as they age. Progressive airway wall remodelling and emphysema in pIgR(-/-) mice are associated with an altered lung microbiome, bacterial invasion of the airway epithelium, NF-κB activation, leukocyte infiltration and increased expression of matrix metalloproteinase-12 and neutrophil elastase. Re-derivation of pIgR(-/-) mice in germ-free conditions or treatment with the anti-inflammatory phosphodiesterase-4 inhibitor roflumilast prevents COPD-like lung inflammation and remodelling. These findings show that pIgR/SIgA deficiency in the airways leads to persistent activation of innate immune responses to resident lung microbiota, driving progressive small airway remodelling and emphysema.
AuthorsBradley W Richmond, Robert M Brucker, Wei Han, Rui-Hong Du, Yongqin Zhang, Dong-Sheng Cheng, Linda Gleaves, Rasul Abdolrasulnia, Dina Polosukhina, Peter E Clark, Seth R Bordenstein, Timothy S Blackwell, Vasiliy V Polosukhin
JournalNature communications (Nat Commun) Vol. 7 Pg. 11240 (Apr 05 2016) ISSN: 2041-1723 [Electronic] England
PMID27046438 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S.)
Chemical References
  • Aminopyridines
  • Benzamides
  • Cyclopropanes
  • Immunoglobulin A, Secretory
  • NF-kappa B
  • Phosphodiesterase 4 Inhibitors
  • Receptors, Polymeric Immunoglobulin
  • Roflumilast
  • Cyclic Nucleotide Phosphodiesterases, Type 4
  • Leukocyte Elastase
  • Matrix Metalloproteinase 12
  • matrix metallopeptidase 12, mouse
Topics
  • Aging (immunology, pathology)
  • Airway Remodeling (immunology)
  • Aminopyridines (pharmacology)
  • Animals
  • Benzamides (pharmacology)
  • Cyclic Nucleotide Phosphodiesterases, Type 4 (genetics, immunology)
  • Cyclopropanes (pharmacology)
  • Disease Models, Animal
  • Gene Expression Regulation
  • Host-Pathogen Interactions
  • Humans
  • Immunity, Innate
  • Immunoglobulin A, Secretory (genetics)
  • Leukocyte Elastase (genetics, immunology)
  • Lung (drug effects, immunology, microbiology, pathology)
  • Matrix Metalloproteinase 12 (genetics, immunology)
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Microbiota (immunology)
  • NF-kappa B (genetics, immunology)
  • Phosphodiesterase 4 Inhibitors (pharmacology)
  • Pulmonary Disease, Chronic Obstructive (drug therapy, genetics, immunology, microbiology)
  • Pulmonary Emphysema (drug therapy, genetics, immunology, microbiology)
  • Receptors, Polymeric Immunoglobulin (deficiency, genetics, immunology)
  • Respiratory Mucosa (drug effects, immunology, microbiology, pathology)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: