首页> 外文期刊>Vox Sanguinis: International Journal of Blood Transfusion and Immunohaematology >A novel simple assay system for the detection of human platelet antigen 15 (HPA‐15) alloantibodies based on three techniques: an HPA‐15 expressing cell line, a monoclonal antibody‐specific antigen‐capture method and mixed‐passive haemagglutination
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A novel simple assay system for the detection of human platelet antigen 15 (HPA‐15) alloantibodies based on three techniques: an HPA‐15 expressing cell line, a monoclonal antibody‐specific antigen‐capture method and mixed‐passive haemagglutination

机译:基于三种技术检测人血小板抗原15(HPA-15)的新型简单测定系统:HPA-15表达细胞系,单克隆抗体特异性抗原捕获方法和混合被动血凝凝集方法

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Background and objectives To detect HPA‐15 alloantibodies, we previously developed a human platelet antigen 15 (HPA‐15)‐expressing cell line‐based modified rapid monoclonal antibody immobilization of platelet antigen (CL‐MR‐MAIPA) assay. In this study, the protocol was modified for easier performance by introducing the mixed‐passive haemagglutination (MPHA) principle. Material and methods In total, 20 samples that tested negative for HPA alloantibodies and eight that tested positive for HPA‐15 alloantibodies (two and six positive for HPA‐15a and HPA‐15b antibodies, respectively) by CL‐MR‐MAIPA assay were used in this study. HPA‐15 cell lines were incubated with serum/plasma and then solubilized. The lysate was transferred to a round‐bottom well, which was coated with anti‐human CD109 monoclonal antibodies. After incubation and repeated washings, sheep red blood cells, coated with anti‐human IgG, were added to the wells. Haemagglutination was assessed the next day. Results The proposed cell line‐based immune complex capture‐dependent mixed‐passive haemagglutination (CL‐IC‐MPHA) assay consisted of four steps, but required only 2?h to perform, except for overnight incubation for haemagglutination. Two HPA‐15a alloantibody samples were reactive only for HPA‐15a cells, and six HPA‐15b alloantibody samples were reactive only for HPA‐15b cells with the CL‐IC‐MPHA assay. The 20 samples that tested negative for HPA alloantibodies did not react with HPA‐15a or HPA‐15b cells. These data indicated that the CL‐IC‐MPHA assay was highly specific and sensitive. Unfortunately, the CL‐IC‐MPHA assay's analytic sensitivity was twofold to eightfold lower than that of the CL‐MR‐MAIPA assay. Conclusion A novel, easy‐to‐perform protocol was successfully developed to detect HPA‐15 alloantibodies with high specificity and sensitivity.
机译:检测HPA-15 AlloAlibodies的背景和目的,我们以前开发了一种人血小板抗原15(HPA-15) - 扩张的细胞系改性的血小板抗原(CL-MR-MAIPA)测定的改性的快速单克隆抗体固定化。在本研究中,通过引入混合被动血凝(MPHA)原理来修改方案以更容易的性能。使用总共20种样品的材料和方法,用于通过CL-MR-MAIPA测定测试HPA AlloAlibodies和HPA-15 AlloAlibodies(两和六种HPA-15A和HPA-15B抗体的阳性)的八个样品在这个研究中。将HPA-15细胞系与血清/血浆一起温育,然后溶解。将裂解物转移至圆底孔,其涂有抗人CD109单克隆抗体。孵育并反复洗涤后,涂覆有抗人IgG的绵羊红细胞加入到孔中。血凝凝血在第二天评估。结果提出的基于细胞系的免疫复合捕获依赖性混合 - 无源血凝(Cl-IC-MPHA)测定由四个步骤组成,但仅需要2μm,除了过夜孵化进行血凝孵化。两个HPA-15A Alloantibody样品仅针对HPA-15A细胞反应,并且六个HPA-15B Alloantibody样品仅针对HPA-15B细胞反应,具有CL-IC-MPHA测定。测试HPA Alloantibodies阴性的20个样品与HPA-15A或HPA-15B细胞没有反应。这些数据表明Cl-IC-MPHA测定是高度特异性和敏感的。不幸的是,CL-IC-MPHA测定的分析敏感性低于CL-MR-MAIPA测定的八倍。结论成功开发了一种新颖的,易于执行的方案,以检测具有高特异性和灵敏度的HPA-15 AlloAlibodies。

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