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激活杀伤细胞免疫球蛋白样受体基因与强直性脊柱炎易感性增加有关。

Activating killer immunoglobulin-like receptors genes are associated with increased susceptibility to ankylosing spondylitis.

作者信息

Díaz-Peña R, Vidal-Castiñeira J R, Mulero J, Sánchez A, Queiro R, López-Larrea C

机构信息

Department of Immunology, Hospital Universitario Central de Asturias, Oviedo, Spain; Faculty of Health Sciences, Universidad Autónoma de Chile, Talca, Chile.

出版信息

Clin Exp Immunol. 2015 May;180(2):201-6. doi: 10.1111/cei.12568.

DOI:10.1111/cei.12568
PMID:25491925
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4408154/
Abstract

The aim of this study was to analyse the association of specific killer cell immunoglobulin-like receptors (KIR) genes and haplotypes with susceptibility to ankylosing spondylitis (AS) and its different clinical manifestations in a Spanish population. The presence or absence of all KIR genes was studied for their association with AS. A total of 176 patients with AS and 435 healthy control subjects were selected for this study based on clinical criteria. The commercial KIR-sequence-specific oligonucleotides (SSO) typing kit was used to investigate KIR typing. Frequencies of KIR2DS1 and KIR3DS1 genes were increased significantly in patients compared with healthy controls [52·8 versus 38·2%, PBonf < 0·01, odds ratio (OR) = 1·81 (1·28-2·59); 51·7 versus 37·5%, PBonf < 0·01, OR = 1·79 (1·25-2·54)]. Moreover, the frequency of activating genotypes in the AS patient group was significantly higher than in the healthy control group (P < 0·05). KIR2DS1 and KIR3DS1, in addition to human leucocyte antigen (HLA)-B27, may play an important role in the pathogenesis of AS. However, we show that the contribution of the KIR genes to AS susceptibility extends beyond the association with individual KIRs, with an imbalance between activating and inhibitory KIR genes seeming to influence the susceptibility to AS.

摘要

本研究旨在分析特定杀伤细胞免疫球蛋白样受体(KIR)基因及单倍型与西班牙人群强直性脊柱炎(AS)易感性及其不同临床表现之间的关联。研究了所有KIR基因的有无与AS的相关性。根据临床标准,本研究共选取了176例AS患者和435例健康对照者。使用商业化的KIR序列特异性寡核苷酸(SSO)分型试剂盒进行KIR分型检测。与健康对照相比,患者中KIR2DS1和KIR3DS1基因的频率显著增加[52.8%对38.2%,经Bonferroni校正P<0.01,优势比(OR)=1.81(1.28 - 2.59);51.7%对37.5%,经Bonferroni校正P<0.01,OR = 1.79(1.25 - 2.54)]。此外,AS患者组中激活基因型的频率显著高于健康对照组(P<0.05)。KIR2DS1和KIR3DS1,除了人类白细胞抗原(HLA)-B27外,可能在AS的发病机制中起重要作用。然而,我们发现KIR基因对AS易感性的影响不仅限于与单个KIR的关联,激活型和抑制型KIR基因之间的失衡似乎也影响AS的易感性。

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