[HTML][HTML] Cholesteryl esters are elevated in the lipid fraction of bronchoalveolar lavage fluid collected from pediatric cystic fibrosis patients

DC Ma, AJ Yoon, KF Faull, R Desharnais… - PLoS …, 2015 - journals.plos.org
DC Ma, AJ Yoon, KF Faull, R Desharnais, ET Zemanick, E Porter
PLoS One, 2015journals.plos.org
Background Host-derived lipids including cholesteryl esters (CEs) such as cholesteryl
linoleate have emerged as important antibacterial effectors of innate immunity in the airways
and cholesteryl linoleate has been found elevated in the context of inflammation. Cystic
fibrosis (CF) patients suffer from chronic infection and severe inflammation in the airways.
Here, we identified and quantified CEs in bronchoalveolar lavage fluid (BALF) from CF
patients and non-CF disease controls, and tested whether CE concentrations are linked to …
Background
Host-derived lipids including cholesteryl esters (CEs) such as cholesteryl linoleate have emerged as important antibacterial effectors of innate immunity in the airways and cholesteryl linoleate has been found elevated in the context of inflammation. Cystic fibrosis (CF) patients suffer from chronic infection and severe inflammation in the airways. Here, we identified and quantified CEs in bronchoalveolar lavage fluid (BALF) from CF patients and non-CF disease controls, and tested whether CE concentrations are linked to the disease.
Materials and Methods
CEs in BALF from 6 pediatric subjects with CF and 7 pediatric subjects with non-CF chronic lung disease were quantified by mass spectral analysis using liquid chromatography coupled with tandem mass spectrometry and multiple reaction monitoring. BALFs were also examined for total lipid, total protein, albumin, and, as a marker for inflammation, human neutrophil peptide (HNP) 1–3 concentrations. Statistical analysis was conducted after log 10 transformation of the data.
Results
Total lipid/protein ratio was reduced in CF BALF (p = 0.018) but the concentrations of CEs, including cholesteryl linoleate, were elevated in the total lipid fraction in CF BALF compared to non-CF disease controls (p < 0.050). In addition, the concentrations of CEs and HNP1-3 correlated with one another (p < 0.050).
Conclusions
The data suggests that the lipid composition of BALF is altered in CF with less total lipid relative to protein but with increased CE concentrations in the lipid fraction, likely contributed by inflammation. Future longitudinal studies may reveal the suitability of CEs as a novel biomarker for CF disease activity which may provide new information on the lipid mediated pathophysiology of the disease.
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