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DOI 10.1016/j.jaci.2016.10.034

Медицинская библиотека · The Journal of allergy and clinical immunology · 2016

Identification of IL-17F/frequent exacerbator endotype in asthma.

Ricciardolo Fabio L M, Sorbello Valentina, Folino Anna, Gallo Fabio, Massaglia Gian Mario, Favatà Gabriella, Conticello Salvatore, Vallese Davide, Gani Federica, Malerba Mario, Folkerts Gert, Rolla Giovanni, Profita Mirella, Mauad Thais, Di Stefano Antonino, Ciprandi Giorgio

СтатьяНаблюдательное исследованиеПеревод пока не подготовлен

Аннотация

BACKGROUND

Severe asthma might be associated with overexpression of Th17 cytokines, which induce neutrophil recruitment via neutrophil-mobilizing cytokines in airways.

OBJECTIVE

To study IL-17-related cytokines in nasal/bronchial biopsies from controls and mild asthmatics (MAs) to severe asthmatics (SAs) in relation to exacerbation rate.

METHODS

Inflammatory cells and IL-17A+, IL-17F+, IL-21+, IL-22+, and IL-23+ cells were examined by immunohistochemistry in cryostat sections of bronchial/nasal biopsies obtained from 33 SAs (21 frequent exacerbators [FEs]), 31 MAs (3 FEs), and 14 controls. IL-17F protein was also measured by ELISA in bronchial/nasal lysates and by immunohistochemistry in bronchial tissue obtained from subjects who died because of fatal asthma. Immunofluorescence/confocal microscopy was used for IL-17F colocalization.

RESULTS

Higher number (P < .05) of neutrophils, IL-17A+, IL-17F+, and IL-21+ cells in bronchial biopsies and higher numbers (P < .01) of IL-17F+ and IL-21+ cells in nasal biopsies were observed in SAs compared with MAs. Bronchial IL-17F+ cells correlated with bronchial neutrophils (r = 0.54), exacerbation rate (r = 0.41), and FEV1 (r = -0.46). Nasal IL-17F+ cells correlated with bronchial IL-17F (r = 0.35), exacerbation rate (r = 0.47), and FEV1 (r = -0.61). FEs showed increased number of bronchial neutrophils/eosinophils/CD4+/CD8+ cells and bronchial/nasal IL-17F+ cells. Receiver operating characteristic curve analysis evidenced predictive cutoff values of bronchial neutrophils and nasal/bronchial IL-17F for discriminating between asthmatics and controls, between MAs and SAs and between FEs and non-FEs. IL-17F protein increased in bronchial/nasal lysates of SAs and FEs and in bronchial tissue of fatal asthma. IL-17F colocalized in CD4+/CD8+ cells.

CONCLUSIONS

IL-17-related cytokines expression was amplified in bronchial/nasal mucosa of neutrophilic asthma prone to exacerbation, suggesting a pathogenic role of IL-17F in FEs.

Для цитирования: Ricciardolo Fabio L M, Sorbello Valentina, Folino Anna, Gallo Fabio, Massaglia Gian Mario, Favatà Gabriella, Conticello Salvatore, Vallese Davide, Gani Federica, Malerba Mario, Folkerts Gert, Rolla Giovanni, Profita Mirella, Mauad Thais, Di Stefano Antonino, Ciprandi Giorgio. Identification of IL-17F/frequent exacerbator endotype in asthma.. The Journal of allergy and clinical immunology. 2016. DOI: 10.1016/j.jaci.2016.10.034.

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