2022
DOI: 10.3889/oamjms.2022.10835
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The Levels of the Human-β-Defensin-2 and LL-37 in the Sputum of Children with Cystic Fibrosis: A Case–control Study and Literature Review

Abstract: BACKGROUND: Cystic fibrosis (CF) is a genetic disorder with an autosomal-recessive type of inheritance. Based on their host-defending and pro-inflammatory functions, antimicrobial peptides (AMPs) likely have one of the central roles in the pathogenesis of lung disease in CF. AIM: The purpose of the study was to measure the concentration of AMPs in the sputum of children with CF and evaluate any correlation with a bacterial profile of the lungs. METHODS: Lung colonization was evaluated using a culture-dependent… Show more

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“…Levels of hBD-2 and hCAP-18/LL37 in CF sputum have been demonstrated to be higher than in control specimens [282], confirming previous results regarding the lack of correlation of increased AMPs levels and P. aeruginosa infection when AMPs were studied in BALF [283]. Together with the results obtained by Xiao et al [217], overall, these data indicate that sputum is an easily accessible and representative sample of airway secretions for the measurement of AMP levels.…”
Section: Cystic Fibrosis (Table 2)supporting
confidence: 86%
“…Levels of hBD-2 and hCAP-18/LL37 in CF sputum have been demonstrated to be higher than in control specimens [282], confirming previous results regarding the lack of correlation of increased AMPs levels and P. aeruginosa infection when AMPs were studied in BALF [283]. Together with the results obtained by Xiao et al [217], overall, these data indicate that sputum is an easily accessible and representative sample of airway secretions for the measurement of AMP levels.…”
Section: Cystic Fibrosis (Table 2)supporting
confidence: 86%