Clara cell 16 protein in COPD sputum: A marker of small airways damage?

被引:46
作者
Braido, Fulvio [1 ]
Riccio, Anna M. [1 ]
Guerra, Laura [1 ]
Gamalero, Cinzia [1 ]
Zolezzi, Alberto [1 ]
Tarantini, Francesco [1 ]
De Giovanni, Barbara [1 ]
Folli, Chiara [1 ]
Descalzi, Desideria [1 ]
Canonica, Giorgio Walter [1 ]
机构
[1] Univ Genoa, Dept Internal Med, I-16312 Genoa, Italy
关键词
Clara cell protein; COPD; airways inflammation; sputum;
D O I
10.1016/j.rmed.2007.05.023
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Rationale: The development of chronic obstructive pulmonary disease (COPD) in smokers and their susceptibility to infections is not fully understood. Recent evidences suggest that Clara cells play a part in host defense, immunomodulatory response and airways remodelling through the production of specific factors such as Clara cell 16 (CC-16). This protein has never been related to patients' lung function tests, blood gases parameters and diseases severity. Objectives: To evaluate a possible correlation between CC-16 expression in sputum, measured by a new methodological approach, and the degree of severity in patients with moderate and severe COPD. We also analyzed possible correlations between CC-16 and cytological sputum population, arterial blood gases and lung function. Main Findings: We analyzed 20 patients, mean age 72.95, classified on the basis of the global initiative for chronic obstructive lung disease guidelines (GOLD 2006). The samples were processed for cytological analysis and CC-16 levels were assessed by Western blot. We found lower levels of CC-16 in severe COPD compared to moderate ones (p < 0.027). No statistically significant differences were found between CC-16 expression and sputum cellularity (except for macrophages), arterial blood gases, and spirometric parameters. Multiple linear regression analysis of CC-16 versus functional and cytological parameters showed no significance. Conclusions: We found a significantly different expression of CC-16 in COPD patients, according to their stage of severity, as defined by the GOLD 2006 guidelines. Considering CC-16 properties in innate immunity, a possible Link between protein expression, innate immune system, and COPD infectious exacerbations may be hypothesized but further investigation are needed. (C) 2007 Published by Elsevier Ltd.
引用
收藏
页码:2119 / 2124
页数:6
相关论文
共 26 条
[2]   Clava cell specific protein (CC16) expression after acute lung inflammation induced by intratracheal lipopolysaccharide administration [J].
Arsalane, K ;
Broeckaert, F ;
Knoops, B ;
Wiedig, M ;
Toubeau, G ;
Bernard, A .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2000, 161 (05) :1624-1630
[3]   SURFACTANT PHOSPHOLIPIDS - SYNTHESIS AND STORAGE [J].
BATENBURG, JJ .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 262 (04) :L367-L385
[4]  
BERNARD A, 1992, EUR RESPIR J, V5, P1231
[5]  
BERNARD A, 1998, BIOMARKERS MED WORKP, V273, P283
[6]   Lung hyperpermeability, CLARA-CELL secretory protein (CC16), and susceptibility to ozone of five inbred strains of mice [J].
Broeckaert, F ;
Clippe, A ;
Wattiez, R ;
Falmagne, P ;
Bernard, A .
INHALATION TOXICOLOGY, 2003, 15 (12) :1209-1230
[7]  
Broeckaert F, 2000, ANN NY ACAD SCI, V923, P68
[8]   Desloratadine and levocetirizine improve nasal symptoms, airflow, and allergic inflammation in patients with perennial allergic rhinitis: A pilot study [J].
Ciprandi, G ;
Cirillo, I ;
Vizzaccaro, A ;
Civardi, E ;
Barberi, S ;
Allen, M ;
Marseglia, GL .
INTERNATIONAL IMMUNOPHARMACOLOGY, 2005, 5 (13-14) :1800-1808
[9]   Cytokines and therapy in COPD - A promising combination? [J].
de Boer, WI .
CHEST, 2002, 121 (05) :209S-218S
[10]   Severity of airflow limitation is associated with severity of airway inflammation in smokers [J].
Di Stefano, A ;
Capelli, A ;
Lusuardi, M ;
Balbo, P ;
Vecchio, C ;
Maestrelli, P ;
Mapp, CE ;
Fabbri, LM ;
Donner, CF ;
Saetta, M .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1998, 158 (04) :1277-1285