Hypothesis & Theory ARTICLE

Front. Immunol., 15 March 2011 | http://dx.doi.org/10.3389/fimmu.2011.00007

Acute exacerbations in COPD and their control with oral immunization with non-typeable Haemophilus influenzae

  • 1 School of Biomedical Sciences and Pharmacy, Faculty of Health, University of Newcastle, NSW, Australia
  • 2 Department of Immunology, Hunter Area Pathology Service, John Hunter Hospital, Newcastle, NSW, Australia

Chronic obstructive pulmonary disease (COPD) a term based on the demonstration of irreversible airways obstruction, introduced to unify a range of chronic progressive diseases of the airways consequent upon inhalation of toxins. While disease is initiated and progressed by inhaled toxins, an additional pathway of damage has emerged, with particular relevance to acute exacerbations. Exacerbations of disease due to an increase in the level of intrabronchial inflammation have taken on a new significance as their role in determining both acute and chronic outcomes is better understood. This “second pathway” of disease is a consequence of bacterial colonization of damaged airways. Although bacteria have been linked to acute episodes in COPD over 50 years, only recently has quality data on antibiotic usage and the detection of “exacerbation isolates” of non-typeable Haemophilus influenzae (NTHi) provided strong argument in support of a pathogenic role. Yet a poor correlation between detection of colonizing bacteria and clinical status remained a concern in attempts to explain a role for bacteria in a classical infection model. This presentation discusses a hypothesis that acute exacerbations reflect a T cell-dependent hypersensitivity response to colonizing bacteria, with IL-17 dependent accumulation of neutrophils within the bronchus, as the main outcome measure. Critical protection against exacerbations following oral administration of NTHi, an immunotherapy that drives a TH17 T cell response from Peyer’s patches, reduces the load of intrabronchial bacteria while preventing access of inhaled bacteria into small airways. Immunotherapy augments a physiological “loop” based on aspiration of bronchus content into the gut. A second “hypersensitivity” mechanism may cause bronchospasm – in both COPD and treatment-resistant asthma – due to specific IgE antibody directed against colonizing bacteria, as oral NTHi abrogates wheeze in subjects with recurrent “wheezy bronchitis.”

Keywords: COPD, chronic obstructive pulmonary disease, emphysema, respiratory, airways

Citation: Clancy RL, and Dunkley M (2011) Acute exacerbations in COPD and their control with oral immunization with non-typeable Haemophilus influenzae. Front. Immun. 2:7. doi:10.3389/fimmu.2011.00007

Received: 23 December 2010; Accepted: 21 February 2011;
Published online: 15 March 2011.

Edited by:

Allan Cripps, Griffith University, Australia

Reviewed by:

Ruth Foxwell, Unversity of Canberra, Australia
Carlos Alberto Guzman, Helmholtz Centre for Infection Research, Germany

Copyright: © 2011 Clancy and Dunkley. This is an open-access article subject to an exclusive license agreement between the authors and Frontiers Media SA, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are credited.

*Correspondence: Robert L. Clancy, Department of Immunology and Microbiology, Level 4, David Maddison Clinical Sciences Building, University of Newcastle, Newcastle, NSW 2308, Australia e-mail: robert.clancy@ newcastle.edu.au