首页> 外文期刊>Transfusion: The Journal of the American Association of Blood Banks >Anti-'Mi(a)' immunization is associated with HLA-DRB1*0901.
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Anti-'Mi(a)' immunization is associated with HLA-DRB1*0901.

机译:抗“ Mi(a)”免疫与HLA-DRB1 * 0901相关。

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摘要

BACKGROUND: Anti-"Mi(a)" is one of the most important irregular red blood cell antibodies found in Taiwan. The aim of this study was to investigate whether specific HLA-DRB1 alleles are associated with anti-"Mi(a)" production. STUDY DESIGN AND METHODS: A case-control retrospective study was performed on 68 patients showing presence of anti-"Mi(a)" and 219 unrelated control subjects from the Mackay Memorial Hospital. HLA-DRB1 genotyping was carried out using sequence-based typing method. Fisher's exact test using 2 x 2 contingency tables was used to analyze significance of the association between DRB1 polymorphisms and presence of anti-"Mi(a)" in patients. RESULTS: HLA-DRB1*0901 allele frequency in the anti-"Mi(a)" group (30%) was significantly higher than in the control group (16%) with an odds ratio of 2.27 (95% confidence interval, 1.44-3.55; p = 0.0005; p(c) = 0.016). CONCLUSION: HLA-DRB1*0901 is significantly more prevalent in the anti-"Mi(a)" patients group than in the control group. It is suggested that cells from DR9 individuals might present processed "Mi(a)" antigen-allospecific peptides more effectively than cells from individuals carrying other DR phenotypes. Finally, it was predicted that two epitopes, derived from the MiIII glycophorin amino acid sequence, were likely to bind preferentially with the DR9 molecule. Further work will be necessary to determine if these epitopes are responsible for anti-"Mi(a)" alloimmunization.
机译:背景:抗“ Mi(a)”是台湾发现的最重要的不规则红细胞抗体之一。这项研究的目的是调查特定的HLA-DRB1等位基因是否与抗“ Mi(a)”产生有关。研究设计和方法:病例对照回顾性研究对麦凯纪念医院的68例显示存在抗“ Mi(a)”的患者和219名无关受试者进行了对照。使用基于序列的分型方法进行HLA-DRB1基因分型。使用2 x 2列联表的Fisher精确检验来分析DRB1多态性与患者存在的抗“ Mi(a)”之间关联的显着性。结果:抗“ Mi(a)”组的HLA-DRB1 * 0901等位基因频率(30%)显着高于对照组(16%),优势比为2.27(95%置信区间为1.44) 3.55; p = 0.0005; p(c)= 0.016)。结论:抗“ Mi(a)”患者组中HLA-DRB1 * 0901的患病率明显高于对照组。建议来自DR9个体的细胞可能比来自携带其他DR表型的个体的细胞更有效地呈递经过加工的“ Mi(a)”抗原allospecific肽。最后,据预测,源自MiIII糖蛋白氨基酸序列的两个表位可能优先与DR9分子结合。确定这些表位是否负责抗“ Mi(a)”同种免疫反应将是必要的。

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