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Colloquium paper: genome-wide patterns of population structure and admixture among Hispanic/Latino populations.学术研讨会论文:西班牙裔/拉丁裔人群的全基因组人口结构和混合模式。
Proc Natl Acad Sci U S A. 2010 May 11;107 Suppl 2(Suppl 2):8954-61. doi: 10.1073/pnas.0914618107. Epub 2010 May 5.
2
Autoantibody profiles in systemic sclerosis: predictive value for clinical evaluation and prognosis.系统性硬化症中的自身抗体谱:对临床评估和预后的预测价值。
J Dermatol. 2010 Jan;37(1):42-53. doi: 10.1111/j.1346-8138.2009.00762.x.
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The genetics of scleroderma (systemic sclerosis).硬皮病(系统性硬化症)的遗传学。
Curr Opin Rheumatol. 2010 Mar;22(2):133-8. doi: 10.1097/BOR.0b013e3283367c17.
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Association of HLA class II genes with systemic sclerosis in Spanish patients.HLA Ⅱ类基因与西班牙系统性硬皮病患者的相关性研究。
J Rheumatol. 2009 Dec;36(12):2733-6. doi: 10.3899/jrheum.090377. Epub 2009 Nov 2.
5
Major histocompatibility complex (MHC) class II alleles, haplotypes and epitopes which confer susceptibility or protection in systemic sclerosis: analyses in 1300 Caucasian, African-American and Hispanic cases and 1000 controls.主要组织相容性复合体 (MHC) Ⅱ类等位基因、单倍型和表位在系统性硬化症中易感性或保护作用的分析:在 1300 例白种人、非裔美国人和西班牙裔病例和 1000 例对照中进行的分析。
Ann Rheum Dis. 2010 May;69(5):822-7. doi: 10.1136/ard.2009.111906. Epub 2009 Jul 12.
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Targeting the antigen-binding site of HLA-restricting alleles in treatment of autoimmune disease.靶向HLA限制性等位基因的抗原结合位点治疗自身免疫性疾病。
Crit Rev Immunol. 2007;27(3):271-88. doi: 10.1615/critrevimmunol.v27.i3.60.
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Improving the sensitivity of the American College of Rheumatology classification criteria for systemic sclerosis.提高美国风湿病学会系统性硬化症分类标准的敏感性。
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9
Sequence-specific primed PCR (PCR-SSP) typing of HLA Class I and Class II alleles.人类白细胞抗原(HLA)I类和II类等位基因的序列特异性引物聚合酶链反应(PCR-SSP)分型
Methods Mol Med. 2007;134:51-60. doi: 10.1007/978-1-59745-223-6_4.
10
Polymorphism of immunoglobulin enhancer element HS1,2A: allele *2 associates with systemic sclerosis. Comparison with HLA-DR and DQ allele frequency.免疫球蛋白增强子元件HS1,2A的多态性:*2等位基因与系统性硬化症相关。与HLA - DR和DQ等位基因频率的比较。
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意大利和西班牙系统性硬化症 II 类人类白细胞抗原分析。

Analysis of Class II human leucocyte antigens in Italian and Spanish systemic sclerosis.

机构信息

Referral Center for Systemic Autoimmune Diseases, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico and University of Milan, Via Pace 9, 20122 Milan, Italy.

出版信息

Rheumatology (Oxford). 2012 Jan;51(1):52-9. doi: 10.1093/rheumatology/ker335. Epub 2011 Nov 15.

DOI:10.1093/rheumatology/ker335
PMID:22087014
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3276293/
Abstract

OBJECTIVE

To determine the role of Class II HLAs in SSc patients from Italy and Spain and in SSc patients of Caucasian ancestry.

METHODS

Nine hundred and forty-four SSc patients (Italy 392 patients; Spain 452 patients) and 1320 ethnically matched healthy controls (Italy 398 patients; Spain 922 patients) were genotyped up to the fourth digit by PCR with sequence-specific oligonucleotides for HLA-DRB1, DQA1 and DQB1 loci. Patients included 390 ACA-positive and 254 anti-topo I-positive subjects. Associations between SSc or SSc-specific antibodies and HLA alleles or HLA haplotypes were sought via the chi-square test after 10 000-fold permutation testing. A meta-analysis including this study cohort and other Caucasoids samples was also conducted.

RESULTS

In both the cohorts, the strongest association was observed between the HLA-DRB11104 allele and SSc or anti-topo I antibodies. The HLA-DRB11104 -DQA10501 -DQB10301 haplotype was overrepresented in Italian [odds ratio (OR) = 2.069, 95% asymptotic CIs (CI(95)) 1.486, 2.881; P < 0.001] and in Spanish patients (OR = 6.707, CI(95) 3.974, 11.319; P < 0.001) as well as in anti-topo-positive patients: Italy (OR = 2.642, CI(95) 1.78, 3.924; P < 0.001) and Spain (OR = 20.625, CI(95) 11.536, 36.876; P < 0.001). In both the populations we also identified an additional risk allele (HLA-DQB103) and a protective allele (HLA-DQB10501) in anti-topo-positive patients. The meta-analysis showed different statistically significant associations, the most interesting being the differential association between HLA-DRB1*01 alleles and ACAs (OR = 1.724, CI(95) 1.482, 2.005; P < 0.001) or topo I antibodies (OR = 0.5, CI(95) 0.384, 0.651; P < 0.001).

CONCLUSIONS

We describe multiple robust associations between SSc and HLA Class II antigens in Caucasoids that may help to understand the genetic architecture of SSc.

摘要

目的

确定意大利和西班牙的 SSc 患者以及白种人 SSc 患者中 II 类 HLA 的作用。

方法

944 名 SSc 患者(意大利 392 名患者;西班牙 452 名患者)和 1320 名匹配的健康对照者(意大利 398 名患者;西班牙 922 名患者)通过 PCR 与序列特异性寡核苷酸进行基因分型,达到第四位数字,用于 HLA-DRB1、DQA1 和 DQB1 基因座。患者包括 390 名 ACA 阳性和 254 名抗拓扑异构酶 I 阳性患者。通过 10000 次随机置换检验后,通过卡方检验寻找 SSc 或 SSc 特异性抗体与 HLA 等位基因或 HLA 单倍型之间的关联。还进行了一项荟萃分析,包括该研究队列和其他白种人群样本。

结果

在两个队列中,与 HLA-DRB11104 等位基因与 SSc 或抗拓扑异构酶 I 抗体之间的关联最强。HLA-DRB11104-DQA10501-DQB10301 单倍型在意大利(比值比(OR)=2.069,95%渐近置信区间(CI(95))1.486,2.881;P<0.001)和西班牙患者中过度表达(OR=6.707,CI(95)3.974,11.319;P<0.001)以及抗拓扑异构酶 I 阳性患者中:意大利(OR=2.642,CI(95)1.78,3.924;P<0.001)和西班牙(OR=20.625,CI(95)11.536,36.876;P<0.001)。在两个群体中,我们还在抗拓扑异构酶 I 阳性患者中鉴定出了一个额外的风险等位基因(HLA-DQB103)和一个保护性等位基因(HLA-DQB10501)。荟萃分析显示出不同的统计学显著关联,最有趣的是 HLA-DRB1*01 等位基因与 ACA(OR=1.724,CI(95)1.482,2.005;P<0.001)或拓扑异构酶 I 抗体(OR=0.5,CI(95)0.384,0.651;P<0.001)之间的差异关联。

结论

我们描述了白种人 SSc 与 HLA II 类抗原之间的多种稳健关联,这可能有助于理解 SSc 的遗传结构。