Abstract

Pseudomonas aeruginosa sinusitis may be the focus for intermittent lung colonization in patients with cystic fibrosis (CF). The sinusitis may induce elevated IgA levels in nasal secretion and saliva against P. aeruginosa.
Original languageEnglish
JournalJournal of Cystic Fibrosis
Volume12
Issue number1
Pages (from-to)81-7
Number of pages7
ISSN1569-1993
DOIs
Publication statusPublished - 2013

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