Local genetic and environmental factors in asthma disease pathogenesis: chronicity and persistence mechanisms

被引:95
作者
Holgate, S. T.
Davies, D. E.
Powell, R. M.
Howarth, P. H.
Haitchi, H. M.
Holloway, Jim
机构
[1] Southampton Gen Hosp, Div Infect Inflammat & Repair, Southampton SO16 6YD, Hants, England
[2] Southampton Gen Hosp, IIR Div, Southampton SO16 6YD, Hants, England
[3] Southampton Gen Hosp, Div Human Genet, Sch Med, Southampton SO16 6YD, Hants, England
基金
英国医学研究理事会;
关键词
asthma; environment; genetics; inflammation; remodelling; risk factors;
D O I
10.1183/09031936.00087506
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
While asthma is an inflammatory disorder of the airways usually associated with atopy, an important additional component is involvement of the epithelium and underlying mesenchyme acting as atrophic unit (EMTU). In addition to allergens, a wide range of environmental factors interact with the EMTU, such as virus infections, environmental tobacco smoke and pollutants, to initiate tissue damage and aberrant repair responses that are translated into remodelling of the airways. While candidate gene association studies have revealed polymorphic variants that influence asthmatic inflammation, positional cloning of previously unknown genes is identifying a high proportion of novel genes in the EMTU. Dipeptidyl peptidase (DPP) 10 and disintegrin and metalloproteinase (ADAM)33 are newly identified genes strongly associated with asthma that are preferentially expressed in the airway epithelium and underlying mesenchyme, respectively. Also of increasing importance is the recognition that genes associated with asthma and atopy have important interactions with the environment through epigenetic mechanisms that influence their expression. This type of research will not only identify biomarkers of different types of asthma across the full range of phenotypic expression, but will also identify novel therapeutic targets that could influence the natural history of the heterogenes lung disease.
引用
收藏
页码:793 / 803
页数:11
相关论文
共 103 条
[61]   Epithelial cell modulation of airway fibrosis in asthma [J].
Olman, MA .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2003, 28 (02) :125-128
[62]  
Otsu Akiko, 2002, Allergology International, V51, P213, DOI 10.1046/j.1440-1592.2002.00268.x
[63]   Early thickening of the reticular basement membrane in children with difficult asthma [J].
Payne, DNR ;
Rogers, AV ;
Ädelroth, E ;
Bandi, V ;
Guntupalli, KK ;
Bush, A ;
Jeffery, PK .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2003, 167 (01) :78-82
[64]   Is allergen exposure the major primary cause of asthma? [J].
Pearce, N ;
Douwes, J ;
Beasley, R .
THORAX, 2000, 55 (05) :424-431
[65]   How much asthma is really attributable to atopy? [J].
Pearce, N ;
Pekkanen, J ;
Beasley, R .
THORAX, 1999, 54 (03) :268-272
[66]   Mice are not a good model of human airway disease [J].
Persson, CGA .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2002, 166 (01) :6-7
[67]   Familial resemblance of asthma severity in the EGEA* study [J].
Pin, I ;
Siroux, V ;
Cans, C ;
Kauffmann, F ;
Maccario, J ;
Pison, C ;
Dizier, MH .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2002, 165 (02) :185-189
[68]  
POHUNEK P, 1998, EUR RESP J S2K, V11, pS160
[69]   The splicing and fate of ADAM33 transcripts in primary human airways fibroblasts [J].
Powell, RM ;
Wicks, J ;
Holloway, JW ;
Holgate, ST ;
Davies, DE .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2004, 31 (01) :13-21
[70]   Defective production of soluble HLA-G molecules by peripheral blood monocytes in patients with asthma [J].
Rizzo, R ;
Mapp, CE ;
Melchiorri, L ;
Maestrelli, P ;
Visentin, A ;
Ferretti, S ;
Bononi, I ;
Miotto, D ;
Baricordi, OR .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2005, 115 (03) :508-513