Evaluation of sequence-specific priming and real-time polymerase chain reaction assays for detecting HLA-B*51 alleles confirmed by sequence-based typing.

Tissue antigens Pub Date : 2012-10-01 Epub Date: 2012-08-02 DOI:10.1111/j.1399-0039.2012.01942.x
Y Park, Y S Kim, S I Kim, H Kim, H S Kim
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引用次数: 2

Abstract

The human leukocyte antigen (HLA)-B*51 genotype is one of the well-known genetic factors associated with the development of Behcet's disease. We evaluated three sequence-specific priming (SSP) assays and one real-time PCR assay for detecting HLA-B*51 alleles using 93 whole blood samples, which were genotyped by high-resolution sequence-based typing (SBT). All HLA-B*51 alleles determined by SBT were detected by the four evaluated assays, and the results for all HLA-B alleles other than HLA-B*51 were negative on all assays. Thus, all HLA-B51 tests showed 100% sensitivity and 100% specificity for detecting HLA-B*51 alleles. The three SSP assays and the real-time PCR test for HLA-B*51 genotyping are simple, but reliable for detecting HLA-B*51 alleles in clinical laboratories.

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序列特异性引物和实时聚合酶链反应检测经序列分型确认的HLA-B*51等位基因
人类白细胞抗原(HLA)-B*51基因型是众所周知的与白塞病发展相关的遗传因素之一。我们使用93份全血样本,对3种序列特异性引物(SSP)和1种实时PCR检测HLA-B*51等位基因的方法进行了评估,并通过高分辨率序列分型(SBT)对这些样本进行了基因分型。4种评价方法均检测到SBT检测到的所有HLA-B*51等位基因,除HLA-B*51等位基因外,其余等位基因均为阴性。因此,所有HLA-B51试验检测HLA-B*51等位基因的敏感性为100%,特异性为100%。三种SSP法和实时PCR法检测HLA-B*51基因分型方法简单,但在临床实验室检测HLA-B*51等位基因时可靠。
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来源期刊
Tissue antigens
Tissue antigens 医学-病理学
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