Markers of eosinophilic and neutrophilic inflammation in bronchoalveolar lavage of asthmatic and atopic children

被引:32
|
作者
Snijders, D.
Agostini, S. [2 ]
Bertuola, F.
Panizzolo, C.
Baraldo, S. [2 ]
Turato, G. [2 ]
Faggian, D. [3 ]
Plebani, M. [3 ]
Saetta, M. [2 ]
Barbato, A. [1 ]
机构
[1] Univ Padua, Dept Pediat, Pediat Pulmonol Unit, I-35128 Padua, Italy
[2] Univ Padua, Dept Cardiac Thorac Vasc Sci, I-35128 Padua, Italy
[3] Univ Padua, Inst Lab Med, I-35128 Padua, Italy
关键词
asthma; atopy; BAL mediators; eosinophils; neutrophils; AIRWAY INFLAMMATION; CHILDHOOD ASTHMA; INDUCED SPUTUM; CATIONIC PROTEIN; INFANTILE WHEEZE; ACTIVATION; HYPERRESPONSIVENESS; ASSOCIATION; PHENOTYPES; PROFILES;
D O I
10.1111/j.1398-9995.2009.02282.x
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
P>Background: Recent studies performing fiberoptic bronchoscopy in children have improved our understanding of asthma pathophysiology. Eosinophilic, but also neutrophilic, inflammation has been described in asthma, but the relationship with atopy was incompletely investigated. The aim of this study is to examine inflammatory cells and mediators in children with asthma compared to the appropriate controls, i.e. atopic children without asthma and children with no atopy or asthma. Moreover, asthmatic children were analysed separately based on the presence of atopy and stratified by age. Methods: We recruited 191 children undergoing fiberoptic bronchoscopy for appropriate indications: 91 asthmatics (aged 1.4-17 years), 44 atopics without asthma (1.6-17.8 years) and 56 nonasthmatic nonatopic controls (1.4-14 years). In bronchoalveolar lavage, total and differential cell counts and inflammatory mediators, including ECP, eotaxin, IL-8 and TNF alpha, were analysed. Results: Eosinophils and ECP levels were increased in asthmatic children when compared to controls (P = 0.002 and P = 0.01, respectively), but also atopic children without asthma had increased ECP levels compared to controls (P = 0.0001). Among asthmatic children, eosinophils and ECP levels were not different between atopic and nonatopic individuals. Neither neutrophils nor the related mediators (IL-8 and TNF alpha) differed significantly in the three groups. This pattern of inflammation was observed in both preschool and school-aged asthmatic children. Conclusions: This study suggests that markers of eosinophilic, but not neutrophilic inflammation, are increased in asthmatic children and also in atopic children without asthma. Of interest, in asthmatic children, the activation of the eosinophilic response is not solely because of the presence of atopy.
引用
收藏
页码:978 / 985
页数:8
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