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DOI 10.1371/journal.pone.0162672

Медицинская библиотека · PloS one · 2016

Sputum Leucine-Rich Alpha-2 Glycoprotein as a Marker of Airway Inflammation in Asthma.

Honda Hiromi, Fujimoto Minoru, Miyamoto Shintaro, Ishikawa Nobuhisa, Serada Satoshi, Hattori Noboru, Nomura Shintaro, Kohno Nobuoki, Yokoyama Akihito, Naka Tetsuji

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Аннотация

BACKGROUND

Asthma is a chronic inflammatory disease of airways, but an ideal biomarker that accurately reflects ongoing airway inflammation has not yet been established. The aim of this study was to examine the potential of sputum leucine-rich alpha-2 glycoprotein (LRG) as a new biomarker for airway inflammation in asthma.

METHODS

We obtained induced sputum samples from patients with asthma (N = 64) and healthy volunteers (N = 22) and measured LRG concentration by sandwich enzyme-linked immunosorbent assay (ELISA). Ovalbumin (OVA)-induced asthma model mice were used to investigate the mechanism of LRG production during airway inflammation. The LRG concentrations in the bronchoalveolar lavage fluid (BALF) obtained from mice were determined by ELISA and mouse lung sections were stained with anti-LRG antibody and periodic acid-Schiff (PAS) reagent.

RESULTS

Sputum LRG concentrations were significantly higher in patients with asthma than in healthy volunteers (p = 0.00686). Consistent with patients' data, BALF LRG levels in asthma model mice were significantly higher than in control mice (p = 0.00013). Immunohistochemistry of lung sections from asthma model mice revealed that LRG was intensely expressed in a subpopulation of bronchial epithelial cells, which corresponded with PAS-positive mucus producing cells.

CONCLUSION

These findings suggest that sputum LRG is a promising biomarker of local inflammation in asthma.

Для цитирования: Honda Hiromi, Fujimoto Minoru, Miyamoto Shintaro, Ishikawa Nobuhisa, Serada Satoshi, Hattori Noboru, Nomura Shintaro, Kohno Nobuoki, Yokoyama Akihito, Naka Tetsuji. Sputum Leucine-Rich Alpha-2 Glycoprotein as a Marker of Airway Inflammation in Asthma.. PloS one. 2016. DOI: 10.1371/journal.pone.0162672.

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