Evaluation of Two Commercial HLA-B27 Real-Time PCR Kits

被引:5
|
作者
Cho, Eun Hae [1 ]
Lee, Sang Gon [1 ]
Seok, Jeong Ho [1 ]
Park, Bo Ya Na [1 ]
Lee, Eun Hee [1 ]
机构
[1] Greencross Reference Lab, Yongin 449913, South Korea
来源
KOREAN JOURNAL OF LABORATORY MEDICINE | 2009年 / 29卷 / 06期
关键词
Real Time PCR; HLA-B27; PCR-SSP; ANKYLOSING-SPONDYLITIS; SUBTYPES; PROBES; ASSAY;
D O I
10.3343/kjlm.2009.29.6.589
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: The standard PCR with sequence-specific primers (SSP) is a widely used method of HLA-B27 typing in clinical practice. The aim of our study was to evaluate 2 Korean HLA-B27 kits with different real-time PCR chemistries. Methods: To validate the accuracy of real-time PCR kits, we selected 28 HLA-B27-positive samples and 33 HLA-B27-negative samples with a wide range of different HLA-B specificities typed by standard PCR-SSP. The 2 real-time PCR kits used were the AccuPower(R) HLA-B27 real-time PCR kit (Bioneer, Korea) with TaqMan probes and the Real-Q(TM) HLA-B*27 detection kit (BioSewoom, Korea) with SYBR Green I dye for melting curve analysis. Results: All 61 samples typed by PCR-SSP demonstrated a perfect concordance with the 2 real-time PCR assays. It was possible to clearly discriminate between HLA-B27-positive and -negative samples in both real-time assays. Conclusions: In summary, both real-time PCR assays for HLA-B27 were fast, reliable, well-adapted for routine laboratory testing, and attractive alternatives to the conventional PCR-SSP method. (Korean J Lab Med 2009;29:589-93)
引用
收藏
页码:589 / 593
页数:5
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