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用于人类白细胞抗原抗体检测的Lifecodes LSA I类和II类单抗原试剂盒结果的实验室间比较。

Interlaboratory Comparison of the Results of Lifecodes LSA Class I and Class II Single Antigen Kits for Human Leukocyte Antigen Antibody Detection.

作者信息

Oh Eun-Jee, Park Hyewon, Park Kyoung Un, Kang Eun-Suk, Kim Hyon-Suk, Song Eun Young

机构信息

Department of Laboratory Medicine, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.

Department of Laboratory Medicine, Seoul National University College of Medicine, Seoul, Korea.

出版信息

Ann Lab Med. 2015 May;35(3):321-8. doi: 10.3343/alm.2015.35.3.321. Epub 2015 Apr 1.

Abstract

BACKGROUND

Although single antigen bead assays (SAB) are approved qualitative tests, the median fluorescence intensity (MFI) values obtained from SAB are frequently used in combination with quantitative significances for diagnostic purposes. To gauge the reproducibility of SAB results, we assessed the interlaboratory variability of MFI values using identical kits with reagents from the same lot and the manufacturer's protocol.

METHODS

Six serum samples containing HLA-specific antibodies were analyzed at five laboratories by using Lifecodes LSA Class I and Class II SAB kits (Immucor, USA) from the same lot, according to the manufacturer's protocol. We analyzed the concordance of qualitative results according to distinct MFI cutoffs (1,000, 3,000, 5,000, and 10,000), and the correlation of quantitative MFI values obtained by the participating laboratories. The CV for MFI values were analyzed and grouped by mean MFI values from the five laboratories (<1,000; 1,000-2,999; 3,000-4,999; 5,000-9,999; and ≥10,000).

RESULTS

The categorical results obtained from the five laboratories exhibited concordance rates of 96.0% and 97.2% for detection of HLA class I and class II antibodies, respectively. The Pearson correlation coefficients for MFI values of class I and class II antibodies were between 0.947-0.991 and 0.992-0.997, respectively. The median CVs for the MFI values among five laboratories in the lower MFI range (<1,000) were significantly higher than those for the other MFI ranges (all P<0.01).

CONCLUSIONS

Analysis of SAB performed in five laboratories using identical protocols and reagents from the same lot resulted in high levels of concordance and strong correlation of results.

摘要

背景

尽管单抗原珠试验(SAB)是经批准的定性检测方法,但从SAB获得的中位荧光强度(MFI)值经常与定量意义结合用于诊断目的。为了评估SAB结果的可重复性,我们使用相同试剂盒及来自同一批次的试剂并按照制造商方案评估了MFI值的实验室间变异性。

方法

按照制造商方案,五个实验室使用来自同一批次的美国Immucor公司的Lifecodes LSA I类和II类SAB试剂盒,对六份含有HLA特异性抗体的血清样本进行分析。我们根据不同的MFI临界值(1000、3000、5000和10000)分析定性结果的一致性,以及参与实验室获得的定量MFI值的相关性。根据五个实验室的平均MFI值(<1000;1000 - 2999;3000 - 4999;5000 - 9999;及≥10000)对MFI值的变异系数(CV)进行分析和分组。

结果

五个实验室获得的分类结果显示,检测HLA I类和II类抗体的一致率分别为96.0%和97.2%。I类和II类抗体MFI值的Pearson相关系数分别在0.947 - 0.991和0.992 - 0.997之间。在较低MFI范围(<1000)内,五个实验室MFI值的中位CV显著高于其他MFI范围(所有P<0.01)。

结论

五个实验室使用相同方案和同一批次试剂进行的SAB分析结果具有高度一致性和强相关性。

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