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嗜酸性粒细胞趋化因子-2基因多态性与血浆嗜酸性粒细胞趋化因子-2浓度的关联

Association of eotaxin-2 gene polymorphisms with plasma eotaxin-2 concentration.

作者信息

Min Ji-Won, Lee June-Hyuk, Park Choon-Sik, Chang Hun Soo, Rhim Tai Youn, Park Sung-Woo, Jang An-Soo, Shin Hyoung-Doo

机构信息

Division of Allergy and Respiratory Medicine, Department of Internal Medicine, Soonchunhyang University Bucheon Hospital, 1174, Jung Dong, Wonmi Ku, Bucheon, Gyeonggi Do, 420-021, Korea.

Department of Genetic Epidemiology, SNP Genetics, Inc., 11th Floor, MaeHun B/D, 13 Chongro 4 Ga, Chongro-Gu, Seoul, Korea, 110-834.

出版信息

J Hum Genet. 2005;50(3):118-123. doi: 10.1007/s10038-005-0230-3. Epub 2005 Mar 3.

DOI:10.1007/s10038-005-0230-3
PMID:15744457
Abstract

Chemokine (C-C motif) ligand 24 (CCL24, eotaxin-2) is a CC chemokine that recruits and activates cells bearing the CC chemokine receptor 3, which play a major role in asthma. Previously, we observed a significant association between a single nucleotide polymorphism (SNP) in eotaxin-2 (CCL24+1272A--> G) and a lower risk of asthma. Consequently, this study has followed up on those genetic effects by evaluating the association between the SNP and plasma eotaxin-2 concentration in 172 asthmatics and 135 normal controls. Asthmatics had significantly higher plasma eotaxin-2 levels than did normal controls (P=0.02). The SNP (CCL24+1272A--> G) and two haplotypes (ht2 and ht6) were strongly associated with plasma eotaxin-2 levels in asthmatics (CCL24+1272A--> G: P=0.006, ht2: P=0.006, and ht6: P=0.002). The CCL24+1272A--> G allele and the ht2 and ht6 haplotypes showed a gene-dose effect on the plasma eotaxin-2 levels in asthmatics (P=0.005-0.032). In conclusion, the susceptibility of patients with asthma to high eotaxin-2 production may be due to genetic effects of the CCL24+1272A--> G polymorphism, ht2 and ht6 haplotypes.

摘要

趋化因子(C-C基序)配体24(CCL24,嗜酸性粒细胞趋化因子-2)是一种CC趋化因子,可募集并激活携带CC趋化因子受体3的细胞,该受体在哮喘中起主要作用。此前,我们观察到嗜酸性粒细胞趋化因子-2中的单核苷酸多态性(SNP)(CCL24 +1272A→G)与较低的哮喘风险之间存在显著关联。因此,本研究通过评估172例哮喘患者和135例正常对照中该SNP与血浆嗜酸性粒细胞趋化因子-2浓度之间的关联,对这些遗传效应进行了随访。哮喘患者的血浆嗜酸性粒细胞趋化因子-2水平显著高于正常对照(P = 0.02)。SNP(CCL24 +1272A→G)和两种单倍型(ht2和ht6)与哮喘患者的血浆嗜酸性粒细胞趋化因子-2水平密切相关(CCL24 +1272A→G:P = 0.006,ht2:P = 0.006,ht6:P = 0.002)。CCL24 +1272A→G等位基因以及ht2和ht6单倍型对哮喘患者的血浆嗜酸性粒细胞趋化因子-2水平显示出基因剂量效应(P = 0.005 - 0.032)。总之,哮喘患者对高嗜酸性粒细胞趋化因子-2产生的易感性可能归因于CCL24 +1272A→G多态性、ht2和ht6单倍型的遗传效应。

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Concerted expression of eotaxin-1, eotaxin-2, and eotaxin-3 in human bronchial epithelial cells.嗜酸性粒细胞趋化因子-1、嗜酸性粒细胞趋化因子-2和嗜酸性粒细胞趋化因子-3在人支气管上皮细胞中的协同表达。
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Genome wide association identifies PPFIA1 as a candidate gene for acute lung injury risk following major trauma.全基因组关联分析鉴定 PPFIA1 为重大创伤后急性肺损伤风险的候选基因。
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The chemokine network. II. On how polymorphisms and alternative splicing increase the number of molecular species and configure intricate patterns of disease susceptibility.趋化因子网络。II. 多态性和可变剪接如何增加分子种类数量并构建复杂的疾病易感性模式。
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IL-13 and IL-4 cause eotaxin release in human airway smooth muscle cells: a role for ERK.白细胞介素-13和白细胞介素-4可促使人类气道平滑肌细胞释放嗜酸性粒细胞趋化因子:细胞外信号调节激酶的作用
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Effects of an interleukin-5 blocking monoclonal antibody on eosinophils, airway hyper-responsiveness, and the late asthmatic response.白细胞介素-5阻断单克隆抗体对嗜酸性粒细胞、气道高反应性和哮喘迟发反应的影响。
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Regulation of human eotaxin generation by Th1-/Th2-derived cytokines.Th1/Th2衍生细胞因子对人嗜酸性粒细胞趋化因子生成的调节。
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