Epithelial stress and structural remodelling in childhood asthma

被引:150
作者
Fedorov, IA
Wilson, SJ
Davies, DE
Holgate, ST [1 ]
机构
[1] Southampton Gen Hosp, Sch Med, Div Infect Inflammat & Repair, Southampton SO16 6YD, Hants, England
[2] City Clin Hosp 1, Chelyabinsk, Russia
关键词
D O I
10.1136/thx.2004.030262
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: In adult asthma the bronchial epithelium shows high expression of the epidermal growth factor receptor ( EGFR) and the cyclin dependent kinase inhibitor, p21(waf), linked to ongoing stress and injury. Methods: To determine if these are early markers of disease, sections of bronchial specimens obtained post mortem or by bronchoscopy from non-asthmatic (n = 7), moderate ( n = 7), or severe ( n = 9) asthmatic children aged 5-15 years were examined immunohistochemically. All severe and one moderately asthmatic children were receiving inhaled corticosteroids. Results: The lamina reticularis of the asthmatic biopsy sections was found to be thicker (p = 0.01) than normal with increased deposition of collagen III (p = 0.007); submucosal eosinophil numbers did not differ between groups. As in adults, there was an asthma-related increase in epithelial EGFR (p < 0.002) but there was no evidence of proliferation, with Ki67 being reduced (p = 0.001) and p21(waf) increased (p < 0.004). The thickness of the lamina reticularis was significantly correlated with epithelial EGFR (rho = 0.77, p < 0.001). Conclusions: These data provide evidence that, in asthmatic children, the epithelium is stressed or injured without significant eosinophilic inflammation. This change in the epithelial phenotype is associated with collagen deposition in the lamina reticularis, suggesting that the epithelial mesenchymal trophic unit is active early in, and may contribute to, the pathogenesis of asthma.
引用
收藏
页码:389 / 394
页数:6
相关论文
共 46 条
[1]  
Bousquet J, 2000, CLIN EXP ALLERGY, V30, P2
[2]   MYOFIBROBLASTS AND SUBEPITHELIAL FIBROSIS IN BRONCHIAL-ASTHMA [J].
BREWSTER, CEP ;
HOWARTH, PH ;
DJUKANOVIC, R ;
WILSON, J ;
HOLGATE, ST ;
ROCHE, WR .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1990, 3 (05) :507-511
[3]   Asthmatic bronchial epithelium is more susceptible to oxidant-induced apoptosis [J].
Bucchieri, F ;
Puddicombe, SM ;
Lordan, JL ;
Richter, A ;
Buchanan, D ;
Wilson, SJ ;
Ward, J ;
Zummo, G ;
Howarth, PH ;
Djukanovic, R ;
Holgate, ST ;
Davies, DE .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2002, 27 (02) :179-185
[4]   Brush biopsy and mucosal biopsy [J].
Bush, A ;
Pohunek, P .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2000, 162 (02) :S18-S22
[5]  
Busse William W., 2000, Journal of Allergy and Clinical Immunology, V106, P1033
[6]   THE STRUCTURE OF LARGE AND SMALL AIRWAYS IN NONFATAL AND FATAL ASTHMA [J].
CARROLL, N ;
ELLIOT, J ;
MORTON, A ;
JAMES, A .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1993, 147 (02) :405-410
[7]  
*CHILDH ASTHM MAN, 2000, NEW ENGLAND J MED, V0343
[8]   Ultrastructural examination of bronchial biopsy specimens from children with moderate asthma [J].
Çokugras, H ;
Akçakaya, N ;
Seçkin, I ;
Camcioglu, Y ;
Sarimurat, N ;
Aksoy, F .
THORAX, 2001, 56 (01) :25-29
[9]   Epidermal growth factor in the lungs of infants developing chronic lung disease [J].
Currie, AE ;
Vyas, JR ;
MacDonald, J ;
Field, D ;
Kotecha, S .
EUROPEAN RESPIRATORY JOURNAL, 2001, 18 (05) :796-800
[10]   Airway remodeling in asthma: New insights [J].
Davies, DE ;
Wicks, J ;
Powell, RM ;
Puddicombe, SM ;
Holgate, ST .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2003, 111 (02) :215-225