IFNγ and CXCR-1 gene polymorphisms in idiopathic bronchiectasis

被引:19
作者
Boyton, R. J.
Reynolds, C.
Wahid, F. N.
Jones, M. G.
Ozerovitch, L.
Ahmad, T.
Chaudhry, A.
Jewell, D. P.
Kon, O. M.
Smith, J.
Rose, M.
Newman-Taylor, A. J.
Cole, P.
Wilson, R.
Altmann, D. M.
机构
[1] Univ London Imperial Coll Sci Technol & Med, Lung Immunol Grp, MRC, Fac Med,Infect & Immun & Natl Heart & Lund Inst, London SW7 2AZ, England
[2] Royal Brompton & Natl Heart Hosp, Host Def Unit, Dept Resp Med, London SW3 6NP, England
[3] Univ London Imperial Coll Sci Technol & Med, Hammersmith Hosp, Dept Infect Dis & Immun, Human Dis Immunogenet Grp, London W12 0NN, England
[4] Univ London Imperial Coll Sci Technol & Med, Dept Occupat & Environm Med, NHLI, London SW3 6NP, England
[5] Univ Oxford, Gastroenterol Unit, Gibson Labs, Oxford OX2 6QX, England
[6] Univ Cambridge, Dept Med, Addenbrookes Hosp, Cambridge CB2 1QQ, England
[7] St Marys Hosp, Chest & Allergy Dept, London W2 1NY, England
[8] Univ London Imperial Coll Sci Technol & Med, Harefield Hosp, Heart Sci Ctr, Harefield UB9 6JH, Middx, England
来源
TISSUE ANTIGENS | 2006年 / 68卷 / 04期
基金
英国医学研究理事会;
关键词
bronchiectasis; CXC receptor 1; human genetics; interferon-gamma; ulcerative colitis;
D O I
10.1111/j.1399-0039.2006.00670.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
Idiopathic bronchiectasis is a disease of chronic, bacterial lung infection, unresolving inflammation and progressive lung damage. Bronchiectasis can be associated with autoimmune diseases including ulcerative colitis. Defects of both innate and adaptive immunity have been proposed. The airway inflammation is characterized by interleukin-8 (IL-8) expression and infliltration by neutrophils and T cells. Here we investigated two candidate gene polymorphisms that may contribute to disease susceptibility: a CXCR-1 (+2607 G/C) gene polymorphism that is implicated in IL-8 binding and neutrophil trafficking as well as the interferon-gamma (IFN gamma) (+874 T/A) polymorphism which is linked to levels of IFN gamma production. These polymorphisms were distributed similarly in the idiopathic bronchiectasis group and controls, suggesting that these two candidate gene polymorphisms are not associated with disease susceptibility.
引用
收藏
页码:325 / 330
页数:6
相关论文
共 36 条
[1]
Bronchial inflammation and colonization in patients with clinically stable bronchiectasis [J].
Angrill, J ;
Agustí, C ;
De Celis, R ;
Filella, X ;
Rañó, A ;
Elena, M ;
De la Bellacasa, JP ;
Xaubet, A ;
Torres, A .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2001, 164 (09) :1628-1632
[2]
End-organ dysfunction in cystic fibrosis - Association with angiotensin I converting enzyme and cytokine gene polymorphisms [J].
Arkwright, PD ;
Pravica, V ;
Geraghty, PJ ;
Super, M ;
Webb, AK ;
Schwarz, M ;
Hutchinson, IV .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2003, 167 (03) :384-389
[3]
CA repeat allele polymorphism in the first intron of the human interferon-γ gene is associated with lung allograft fibrosis [J].
Awad, M ;
Pravica, V ;
Perrey, C ;
El Gamel, A ;
Yonan, N ;
Sinnott, PJ ;
Hutchinson, IV .
HUMAN IMMUNOLOGY, 1999, 60 (04) :343-346
[4]
Animal models of mucosal inflammation and their relation to human inflammatory bowel disease [J].
Blumberg, RS ;
Saubermann, LJ ;
Strober, W .
CURRENT OPINION IN IMMUNOLOGY, 1999, 11 (06) :648-656
[5]
HLA-C and killer cell immunoglobulin-like receptor genes in idiopathic bronchiectasis [J].
Boyton, RJ ;
Smith, J ;
Ward, R ;
Jones, M ;
Ozerovitch, L ;
Wilson, R ;
Rose, M ;
Trowsdale, J ;
Altmann, DM .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2006, 173 (03) :327-333
[6]
Pulmonary defences to acute respiratory infection [J].
Boyton, RJ ;
Openshaw, PJ .
BRITISH MEDICAL BULLETIN, 2002, 61 :1-12
[7]
*BRIT THOR SOC NEB, 1997, THORAX S2, V52, pS4
[8]
BUTLAND RJA, 1981, Q J MED, V50, P63
[9]
CAMUS P, 1993, MEDICINE, V72, P151
[10]
Bronchiectasis in systemic diseases [J].
Cohen, M ;
Sahn, SA .
CHEST, 1999, 116 (04) :1063-1074