Cystic fibrosis: inflammatory response to infection with Burkholderia cepacia and Pseudomonas aeruginosa

Eur Respir J. 1999 Aug;14(2):435-8. doi: 10.1034/j.1399-3003.1999.14b32.x.


Pulmonary colonization by Burkholderia cepacia in cystic fibrosis (CF) may be associated with enhanced deterioration of pulmonary function. This may be due to a more florid host inflammatory response than in colonization by Pseudomonas aeruginosa, leading to greater lung injury. Circulating markers of inflammation were determined during infective exacerbations and periods of clinical stability in an 18 month prospective study in adults with CF colonized by P. aeruginosa (n=41). B. cepacia (n=13) and in adults who intermittently grew B. cepacia (n=6). There were no differences between the levels of the inflammation markers measured in the three groups (P. aeruginosa, B. cepacia, B. cepacia intermittent) at any of the assessment points. When clinically stable, levels of inflammatory markers in all groups were elevated compared to a matched non-CF population, indicating, continuous inflammation and the potential for lung damage between infective exacerbations. This study does not support the hypothesis that pulmonary colonization with Burkholderia cepacia is associated with a heightened inflammatory response compared with Pseudomonas aeruginosa colonization.

Publication types

  • Comparative Study

MeSH terms

  • Adult
  • Burkholderia Infections / immunology*
  • Burkholderia cepacia / immunology*
  • Cystic Fibrosis / diagnosis
  • Cystic Fibrosis / immunology*
  • Follow-Up Studies
  • Humans
  • Inflammation Mediators / blood*
  • Lung / immunology
  • Pneumonia, Bacterial / diagnosis
  • Pneumonia, Bacterial / immunology*
  • Prospective Studies
  • Pseudomonas Infections / diagnosis
  • Pseudomonas Infections / immunology*
  • Pseudomonas aeruginosa / immunology*


  • Inflammation Mediators