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The polygenic nature of inhibitors in hemophilia A: results from the Hemophilia Inhibitor Genetics Study (HIGS) Combined Cohort.血友病 A 抑制剂的多基因性质:来自血友病抑制剂遗传学研究 (HIGS) 联合队列的结果。
Blood. 2013 Feb 21;121(8):1446-54. doi: 10.1182/blood-2012-06-434803. Epub 2012 Dec 6.
2
A major determinant of the immunogenicity of factor VIII in a murine model is independent of its procoagulant function.在一个小鼠模型中,VIII 因子的免疫原性的一个主要决定因素与其促凝血功能无关。
Blood. 2012 Sep 20;120(12):2512-20. doi: 10.1182/blood-2012-02-412361. Epub 2012 Jul 31.
3
F8 gene mutation type and inhibitor development in patients with severe hemophilia A: systematic review and meta-analysis.F8 基因突变类型和严重血友病 A 患者抑制剂的开发:系统评价和荟萃分析。
Blood. 2012 Mar 22;119(12):2922-34. doi: 10.1182/blood-2011-09-379453. Epub 2012 Jan 26.
4
Surgery and inhibitor development in hemophilia A: a systematic review.血友病 A 的手术治疗和抑制剂研发:系统综述。
J Thromb Haemost. 2011 Oct;9(10):1948-58. doi: 10.1111/j.1538-7836.2011.04467.x.
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The therapeutic potential of carbon monoxide.一氧化碳的治疗潜力。
Nat Rev Drug Discov. 2010 Sep;9(9):728-43. doi: 10.1038/nrd3228.
6
Blood-induced joint disease: the pathophysiology of hemophilic arthropathy.血液相关性关节病:血友病性关节病的病理生理学。
J Thromb Haemost. 2010 Sep;8(9):1895-902. doi: 10.1111/j.1538-7836.2010.03962.x.
7
Role of heme oxygenase-1 in human endothelial cells: lesson from the promoter allelic variants.血红素加氧酶-1 在人内皮细胞中的作用:启动子等位基因变异的启示。
Arterioscler Thromb Vasc Biol. 2010 Aug;30(8):1634-41. doi: 10.1161/ATVBAHA.110.207316. Epub 2010 May 27.
8
The multifactorial etiology of inhibitor development in hemophilia: genetics and environment.血友病抑制剂产生的多因素病因:遗传与环境。
Semin Thromb Hemost. 2009 Nov;35(8):723-34. doi: 10.1055/s-0029-1245105. Epub 2010 Feb 18.
9
Mechanisms of cell protection by heme oxygenase-1.血红素加氧酶-1 的细胞保护机制。
Annu Rev Pharmacol Toxicol. 2010;50:323-54. doi: 10.1146/annurev.pharmtox.010909.105600.
10
Induction of heme oxygenase-1 in factor VIII-deficient mice reduces the immune response to therapeutic factor VIII.VIII 因子缺乏症小鼠中诱导血红素加氧酶-1 的表达可降低对治疗性 VIII 因子的免疫应答。
Blood. 2010 Apr 1;115(13):2682-5. doi: 10.1182/blood-2009-04-216408. Epub 2009 Nov 4.

在严重的血友病 A 中,针对治疗性因子 VIII 的抑制性抗体的产生与 HMOX1 启动子中的微卫星多态性有关。

Development of inhibitory antibodies to therapeutic factor VIII in severe hemophilia A is associated with microsatellite polymorphisms in the HMOX1 promoter.

出版信息

Haematologica. 2013 Oct;98(10):1650-5. doi: 10.3324/haematol.2013.084665. Epub 2013 May 28.

DOI:10.3324/haematol.2013.084665
PMID:23716558
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3789472/
Abstract

Induction of heme oxygenase-1, a stress-inducible enzyme with anti-inflammatory activity, reduces the immunogenicity of therapeutic factor VIII in experimental hemophilia A. In humans, heme oxygenase-1 expression is modulated by polymorphisms in the promoter of the heme oxygenase-1-encoding gene (HMOX1). We investigated the relationship between polymorphisms in the HMOX1 promoter and factor VIII inhibitor development in severe hemophilia A. We performed a case-control study on 99 inhibitor-positive patients and 263 patients who did not develop inhibitors within the first 150 cumulative days of exposure to therapeutic factor VIII. Direct sequencing and DNA fragment analysis were used to study (GT)n polymorphism and single nucleotide polymorphisms located at -1135 and -413 in the promoter of HMOX1. We assessed associations between the individual allele frequencies or genotypes, and inhibitor development. Our results demonstrate that inhibitor-positive patients had a higher frequency of alleles with large (GT)n repeats (L: n≥30), which are associated with lesser heme oxygenase-1 expression (odds ratio 2.31; 95% confidence interval 1.46-3.66; P<0.001]. Six genotypes (L/L, L/M, L/S, M/M, M/S and S/S) of (GT)n repeats were identified (S: n<21; M: 21≤n<30). The genotype group including L alleles (L/L, L/M and L/S) was statistically more frequent among inhibitor-positive than inhibitor-negative patients, as compared to the other genotypes (33.3% versus 17.1%) (odds ratio 2.21, 95% confidence interval 1.30-3.76; P<0.01). To our knowledge, this is the first association identified between HMOX1 promoter polymorphism and development of anti-drug antibodies. Our study paves the way towards modulation of the endogenous anti-inflammatory machinery of hemophilia patients to reduce the risk of inhibitor development.

摘要

诱导血红素加氧酶-1(一种具有抗炎活性的应激诱导酶)可降低实验性血友病 A 中治疗性因子 VIII 的免疫原性。在人类中,血红素加氧酶-1 的表达受血红素加氧酶-1 编码基因(HMOX1)启动子中的多态性调节。我们研究了 HMOX1 启动子多态性与重度血友病 A 中因子 VIII 抑制剂发展之间的关系。我们对 99 例抑制剂阳性患者和 263 例在接受治疗性因子 VIII 治疗的前 150 个累积天内未产生抑制剂的患者进行了病例对照研究。直接测序和 DNA 片段分析用于研究 HMOX1 启动子中的(GT)n 多态性和位于-1135 和-413 处的单核苷酸多态性。我们评估了个体等位基因频率或基因型与抑制剂发展之间的关系。我们的结果表明,抑制剂阳性患者具有较大(GT)n 重复(L:n≥30)的等位基因频率较高,这与血红素加氧酶-1 表达减少有关(比值比 2.31;95%置信区间 1.46-3.66;P<0.001)。确定了(GT)n 重复的 6 种基因型(L/L、L/M、L/S、M/M、M/S 和 S/S)(S:n<21;M:21≤n<30)。与其他基因型相比,包含 L 等位基因(L/L、L/M 和 L/S)的基因型组在抑制剂阳性患者中比抑制剂阴性患者更常见(33.3%比 17.1%)(比值比 2.21,95%置信区间 1.30-3.76;P<0.01)。据我们所知,这是首次发现 HMOX1 启动子多态性与抗药物抗体的发展之间存在关联。我们的研究为调节血友病患者的内源性抗炎机制以降低抑制剂发展的风险铺平了道路。