Literature DB >> 29545279

Elastase activity on sputum neutrophils correlates with severity of lung disease in cystic fibrosis.

A Susanne Dittrich1,2,3,4, Iris Kühbandner1,2,3, Stefanie Gehrig1,2,4,5, Verena Rickert-Zacharias1,2,4,5, Matthew Twigg6, Sabine Wege2,3, Clifford C Taggart6, Felix Herth2,3, Carsten Schultz2,4,5, Marcus A Mall7,2,4,8,9.   

Abstract

Neutrophil elastase (NE) is a key risk factor for severity of cystic fibrosis (CF) lung disease. Recent studies identified increased NE activity on the surface of airway neutrophils from CF-like mice and patients with CF. However, the role of surface-bound NE in CF lung disease remains unknown. We determined the relationship between surface-bound NE activity and severity of lung disease in CF.Surface-bound NE activity was measured on sputum neutrophils from 35 CF patients and eight healthy controls using novel lipidated Förster resonance energy transfer reporters and correlated with free NE activity, neutrophil counts, interleukin-8, myeloperoxidase and antiproteases in sputum supernatant, and with lung function parameters.Surface-bound NE activity was increased in CF compared to healthy controls (p<0.01) and correlated with free NE activity (p<0.05) and other inflammation markers (p<0.001). Surface-bound and free NE activity correlated with forced expiratory volume in 1 s % predicted (p<0.01 and p<0.05), but only surface-bound NE activity correlated with plethysmographic functional residual capacity % pred (p<0.01) in patients with CF.We demonstrate that surface-bound NE activity on airway neutrophils correlates with severity of lung disease in patients with CF. Our results suggest that surface-bound NE activity may play an important role in the pathogenesis and serve as novel biomarker in CF lung disease.
Copyright ©ERS 2018.

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Year:  2018        PMID: 29545279     DOI: 10.1183/13993003.01910-2017

Source DB:  PubMed          Journal:  Eur Respir J        ISSN: 0903-1936            Impact factor:   16.671


  22 in total

1.  Systemic levels of anti-PAD4 autoantibodies correlate with airway obstruction in cystic fibrosis.

Authors:  Ruchi Yadav; Dae-Goon Yoo; J Michelle Kahlenberg; S Louis Bridges; Oluwadamilola Oni; Hanwen Huang; Arlene Stecenko; Balázs Rada
Journal:  J Cyst Fibros       Date:  2019-01-10       Impact factor: 5.482

2.  Elastase Exocytosis by Airway Neutrophils Is Associated with Early Lung Damage in Children with Cystic Fibrosis.

Authors:  Camilla Margaroli; Luke W Garratt; Hamed Horati; A Susanne Dittrich; Timothy Rosenow; Samuel T Montgomery; Dario L Frey; Milton R Brown; Carsten Schultz; Lokesh Guglani; Anthony Kicic; Limin Peng; Bob J Scholte; Marcus A Mall; Hettie M Janssens; Stephen M Stick; Rabindra Tirouvanziam
Journal:  Am J Respir Crit Care Med       Date:  2019-04-01       Impact factor: 21.405

Review 3.  Targeting Proteases in Cystic Fibrosis Lung Disease. Paradigms, Progress, and Potential.

Authors:  Michael C McKelvey; Sinéad Weldon; Daniel F McAuley; Marcus A Mall; Clifford C Taggart
Journal:  Am J Respir Crit Care Med       Date:  2020-01-15       Impact factor: 21.405

4.  SPLUNC1 degradation by the cystic fibrosis mucosal environment drives airway surface liquid dehydration.

Authors:  Megan J Webster; Boris Reidel; Chong D Tan; Arunava Ghosh; Neil E Alexis; Scott H Donaldson; Mehmet Kesimer; Carla M P Ribeiro; Robert Tarran
Journal:  Eur Respir J       Date:  2018-10-04       Impact factor: 16.671

5.  Chronic bacterial pulmonary infections in advanced cystic fibrosis differently affect the level of sputum neutrophil elastase, IL-8 and IL-6.

Authors:  Grzegorz Majka; Henryk Mazurek; Magdalena Strus; Marta Ciszek-Lenda; Rafał Szatanek; Agnieszka Pac; Edyta Golińska; Janusz Marcinkiewicz
Journal:  Clin Exp Immunol       Date:  2021-06-16       Impact factor: 5.732

6.  The Detection of Bile Acids in the Lungs of Paediatric Cystic Fibrosis Patients Is Associated with Altered Inflammatory Patterns.

Authors:  Jose A Caparrós-Martín; Stephanie Flynn; F Jerry Reen; David F Woods; Patricia Agudelo-Romero; Sarath C Ranganathan; Stephen M Stick; Fergal O'Gara
Journal:  Diagnostics (Basel)       Date:  2020-05-06

Review 7.  Proteases, Mucus, and Mucosal Immunity in Chronic Lung Disease.

Authors:  Michael C McKelvey; Ryan Brown; Sinéad Ryan; Marcus A Mall; Sinéad Weldon; Clifford C Taggart
Journal:  Int J Mol Sci       Date:  2021-05-09       Impact factor: 5.923

8.  Noscapine Acts as a Protease Inhibitor of In Vitro Elastase-Induced Collagen Deposition in Equine Endometrium.

Authors:  Ana Amaral; Carina Fernandes; Anna Szóstek-Mioduchowska; Maria Rosa Rebordão; Dariusz Jan Skarzynski; Graça Ferreira-Dias
Journal:  Int J Mol Sci       Date:  2021-05-19       Impact factor: 5.923

9.  Sputum and Plasma Neutrophil Elastase in Stable Adult Patients With Cystic Fibrosis in Relation to Chronic Pseudomonas Aeruginosa Colonization.

Authors:  Atqah AbdulWahab; Mona Allangawi; Merlin Thomas; Ilham Bettahi; Siveen K Sivaraman; Jayakumar Jerobin; Prem Chandra; Manjunath Ramanjaneya; Abdul-Badi Abou-Samra
Journal:  Cureus       Date:  2021-06-26

Review 10.  Immunomodulation in Cystic Fibrosis: Why and How?

Authors:  Vincent D Giacalone; Brian S Dobosh; Amit Gaggar; Rabindra Tirouvanziam; Camilla Margaroli
Journal:  Int J Mol Sci       Date:  2020-05-08       Impact factor: 5.923

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