ERJ
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Permissions
Right arrowRequest Permissions
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by De Rose, V.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by De Rose, V.
Eur Respir J 2002; 19:333-340
Copyright ©ERS Journals Ltd 2002


Mechanisms and markers of airway inflammation in cystic fibrosis

V. De Rose

Dept of Clinical and Biological Sciences, Respiratory Disease Division, University of Turin, Turin, Italy

CORRESPONDENCE: V. De Rose, Clinica di Malattie dell'Apparato Respiratorio, Dipartimento di Scienze Cliniche e Biologiche, Università di Torino, Osp. S.Luigi Gonzaga, Regione Gonzole 10, 10043, Orbassano, Torino, Italy. Fax: 39 119038639. E-mail: virginia.derose@unito.it

Keywords: airway inflammation, cystic fibrosis, inflammatory markers

Received: March 22, 2001
Accepted May 8, 2001

Abstract

Airway inflammation is now recognized as a major factor in the pathogenesis of lung disease in cystic fibrosis (CF). Its most characteristic feature is a marked and persistent influx into the airways of neutrophils, which damage the lung by releasing noxious mediators, such as reactive oxygen species and proteolytic enzymes.

Recent studies suggest that inflammation occurs very early and may even happen in the absence of infection. Furthermore, links between CF transmembrane conductance regulator dysfunction and both infection and inflammation are postulated; dysregulation of cytokine production and abnormal epithelial host defences have been regarded as causes of sustained inflammation.

Bronchoalveolar lavage and the evaluation of neutrophils and inflammatory mediators provide the most accurate picture of airway inflammation. Routine bronchoscopy with bronchoalveolar lavage, however, is unpleasant for the patient and usually is of no immediate benefit to the management of individual cases.

Therefore, surrogate markers collected by noninvasive procedures would be of great assistance in the follow-up of cystic fibrosis patients. Several markers have been evaluated in the sputum, serum and urine of cystic fibrosis patients and related to the degree of airway inflammation. Long-term studies are needed to confirm their potential clinical utility and specificity, and to determine which can be used clinically to monitor disease outcome and efficacy of treatment.




This article has been cited by other articles:


Home page
Am. J. Physiol. Lung Cell. Mol. Physiol.Home page
S. Below, A. Konkel, C. Zeeck, C. Muller, C. Kohler, S. Engelmann, and J.-P. Hildebrandt
Virulence factors of Staphylococcus aureus induce Erk-MAP kinase activation and c-Fos expression in S9 and 16HBE14o- human airway epithelial cells
Am J Physiol Lung Cell Mol Physiol, March 1, 2009; 296(3): L470 - L479.
[Abstract] [Full Text] [PDF]


Home page
J Med MicrobiolHome page
E. Caraher, J. Collins, G. Herbert, P. G. Murphy, C. G. Gallagher, M. J. Crowe, M. Callaghan, and S. McClean
Evaluation of in vitro virulence characteristics of the genus Pandoraea in lung epithelial cells
J. Med. Microbiol., January 1, 2008; 57(1): 15 - 20.
[Abstract] [Full Text] [PDF]


Home page
Eur Respir JHome page
C. Bergeron, M. K. Tulic, and Q. Hamid
Tools used to measure airway remodelling in research
Eur. Respir. J., March 1, 2007; 29(3): 596 - 604.
[Abstract] [Full Text] [PDF]


Home page
JEMHome page
X. Xu, D. Zhang, H. Zhang, P. J. Wolters, N. P. Killeen, B. M. Sullivan, R. M. Locksley, C. A. Lowell, and G. H. Caughey
Neutrophil histamine contributes to inflammation in mycoplasma pneumonia
J. Exp. Med., December 25, 2006; 203(13): 2907 - 2917.
[Abstract] [Full Text] [PDF]


Home page
J. Pharmacol. Exp. Ther.Home page
S. Attucci, A. Gauthier, B. Korkmaz, P. Delepine, M. F.-D. Martino, F. Saudubray, P. Diot, and F. Gauthier
EPI-hNE4, a Proteolysis-Resistant Inhibitor of Human Neutrophil Elastase and Potential Anti-Inflammatory Drug for Treating Cystic Fibrosis
J. Pharmacol. Exp. Ther., August 1, 2006; 318(2): 803 - 809.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Respir. Crit. Care Med.Home page
D. L. Chen, T. W. Ferkol, M. A. Mintun, J. E. Pittman, D. B. Rosenbluth, and D. P. Schuster
Quantifying Pulmonary Inflammation in Cystic Fibrosis with Positron Emission Tomography
Am. J. Respir. Crit. Care Med., June 15, 2006; 173(12): 1363 - 1369.
[Abstract] [Full Text] [PDF]


Home page
ChestHome page
C. Bergeron and L.-P. Boulet
Structural changes in airway diseases: characteristics, mechanisms, consequences, and pharmacologic modulation.
Chest, April 1, 2006; 129(4): 1068 - 1087.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Lung Cell. Mol. Physiol.Home page
O. Tabary, H. Corvol, E. Boncoeur, K. Chadelat, C. Fitting, J. M. Cavaillon, A. Clement, and J. Jacquot
Adherence of airway neutrophils and inflammatory response are increased in CF airway epithelial cell-neutrophil interactions
Am J Physiol Lung Cell Mol Physiol, March 1, 2006; 290(3): L588 - L596.
[Abstract] [Full Text] [PDF]


Home page
NEJMHome page
M. R. Elkins, M. Robinson, B. R. Rose, C. Harbour, C. P. Moriarty, G. B. Marks, E. G. Belousova, W. Xuan, P. T.P. Bye, and the National Hypertonic Saline in Cystic Fibrosis
A Controlled Trial of Long-Term Inhaled Hypertonic Saline in Patients with Cystic Fibrosis
N. Engl. J. Med., January 19, 2006; 354(3): 229 - 240.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Respir. Crit. Care Med.Home page
A. J. Sloane, R. A. Lindner, S. S. Prasad, L. T. Sebastian, S. K. Pedersen, M. Robinson, P. T. Bye, D. W. Nielson, and J. L. Harry
Proteomic Analysis of Sputum from Adults and Children with Cystic Fibrosis and from Control Subjects
Am. J. Respir. Crit. Care Med., December 1, 2005; 172(11): 1416 - 1426.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Respir. Crit. Care Med.Home page
A. J. Kettle, T. Chan, I. Osberg, R. Senthilmohan, A. L. P. Chapman, T. J. Mocatta, and J. S. Wagener
Myeloperoxidase and Protein Oxidation in the Airways of Young Children with Cystic Fibrosis
Am. J. Respir. Crit. Care Med., December 15, 2004; 170(12): 1317 - 1323.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Respir. Crit. Care Med.Home page
K. Paul, E. Rietschel, M. Ballmann, M. Griese, D. Worlitzsch, J. Shute, C. Chen, T. Schink, G. Doring, S. van Koningsbruggen, et al.
Effect of Treatment with Dornase Alpha on Airway Inflammation in Patients with Cystic Fibrosis
Am. J. Respir. Crit. Care Med., March 15, 2004; 169(6): 719 - 725.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Respir. Crit. Care Med.Home page
M. Gilljam, Y. Moltyaner, G. P. Downey, R. Devlin, P. Durie, A. M. Cantin, J. Zielenski, and D. E. Tullis
Airway Inflammation and Infection in Congenital Bilateral Absence of the Vas Deferens
Am. J. Respir. Crit. Care Med., January 15, 2004; 169(2): 174 - 179.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2002 by the European Respiratory Society.