Journal
PEDIATRIC PULMONOLOGY
Volume 49, Issue 11, Pages 1065-1075Publisher
WILEY
DOI: 10.1002/ppul.22982
Keywords
cystic fibrosis; upper airways; nasal lavage; Pseudomonas aeruginosa; cytokines
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BackgroundThe upper (UAW) and lower (LAW) airways of patients with cystic fibrosis (CF) have the same ion-channel defects, but little is known about similarities and differences in host immunological responses at the two levels. AimIdentification and comparison of both levels' pathogen colonization and resulting immunological host responses. MethodsThe UAW and LAW of 40 CF patients were non-invasively assessed by nasal lavage and induced sputum. Pathogen colonization, cytology, and the concentrations of inflammatory mediators (TNF-, MPO, matrix metalloprotease (MMP)-9, tissue inhibitor of metalloprotease (TIMP)-1, regulated upon activation, normal T-cell expressed and presumably secreted (RANTES), and interleukin (IL)-1, -5, -6, -8, and -10) were measured. ResultsInflammatory responses were more pronounced in the LAW than the UAW. Pseudomonas aeruginosa LAW colonization is accompanied by a significantly enhanced neutrophil (PMN)-dominated response (P=0.041) and IL-8 concentration (P=0.01) not observed in P. aeruginosa UAW colonization. In contrast, sinonasal P. aeruginosa colonization resulted in elevated RANTES (P=0.039) and reduced MMP-9 (P=0.023) and TIMP-1 (P=0.035) concentrations. Interestingly, LAW P. aeruginosa colonization was associated with reduced sinonasal concentrations of MMP-9 (P=0.01) and TIMP-1 (P=0.02), a finding independent of UAW colonization for MMP-9. ConclusionCF UAW and LAW show distinct inflammatory profiles and differentiated responses upon P. aeruginosa colonization. Assessment of UAW colonization and MMP-9 are predictive of chronic pulmonary colonization with P. aeruginosa. Thus, this linkage between CF UAW and LAW can provide new clinical and scientific implications. Pediatr Pulmonol. 2014; 49:1065-1075. (c) 2014 Wiley Periodicals, Inc.
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