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The complex relationship between inflammation and lung function in severe asthma.

Abstract
Asthma is a common respiratory disease affecting ∼300 million people worldwide. Airway inflammation is thought to contribute to asthma pathogenesis, but the direct relationship between inflammation and airway hyperresponsiveness (AHR) remains unclear. This study investigates the role of inflammation in a steroid-insensitive, severe allergic airway disease model and in severe asthmatics stratified by inflammatory profile. First, we used the T-helper (T(H))-17 cells adoptive transfer mouse model of asthma to induce pulmonary inflammation, which was lessened by tumor necrosis factor (TNF)-α neutralization or neutrophil depletion. Although decreased airspace inflammation following TNFα neutralization and neutrophil depletion rescued lung compliance, neither intervention improved AHR to methacholine, and tissue inflammation remained elevated when compared with control. Further, sputum samples were collected and analyzed from 41 severe asthmatics. In severe asthmatics with elevated levels of sputum neutrophils, but low levels of eosinophils, increased inflammatory markers did not correlate with worsened lung function. This subset of asthmatics also had significantly higher levels of T(H)17-related cytokines in their sputum compared with severe asthmatics with other inflammatory phenotypes. Overall, this work suggests that lung compliance may be linked with cellular inflammation in the airspace, whereas T-cell-driven AHR may be associated with tissue inflammation and other pulmonary factors.
AuthorsM L Manni, J B Trudeau, E V Scheller, S Mandalapu, M M Elloso, J K Kolls, S E Wenzel, J F Alcorn
JournalMucosal immunology (Mucosal Immunol) Vol. 7 Issue 5 Pg. 1186-98 (Sep 2014) ISSN: 1935-3456 [Electronic] United States
PMID24549277 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Chemical References
  • Bronchoconstrictor Agents
  • Cytokines
  • Methacholine Chloride
Topics
  • Adolescent
  • Adult
  • Age of Onset
  • Aged
  • Aged, 80 and over
  • Animals
  • Asthma (complications, immunology, physiopathology)
  • Bronchial Hyperreactivity (immunology)
  • Bronchoconstrictor Agents (pharmacology)
  • Child
  • Cytokines (immunology)
  • Female
  • Humans
  • Inflammation (complications)
  • Lung (drug effects, pathology, physiology)
  • Male
  • Methacholine Chloride (pharmacology)
  • Mice
  • Mice, Transgenic
  • Middle Aged
  • Severity of Illness Index
  • Sputum (immunology)

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