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一种三重单分子免疫测定法的开发,可同时测定人血清样本中的表皮生长因子受体(EGFR)配体双调蛋白、β细胞素和转化生长因子α。

Development of a three-plex single molecule immunoassay enabling measurement of the EGFR ligands amphiregulin, betacellulin and transforming growth factor α simultaneously in human serum samples.

作者信息

Olsen Dorte Aalund, Kjaer Ina Mathilde, Brandslund Ivan

机构信息

Department of Clinical Immunology and Biochemistry, Lillebaelt Hospital, Vejle, Denmark; Institute of Regional Health Research, University of Southern Denmark, Odense, Denmark.

Department of Clinical Immunology and Biochemistry, Lillebaelt Hospital, Vejle, Denmark; Institute of Regional Health Research, University of Southern Denmark, Odense, Denmark.

出版信息

J Immunol Methods. 2018 Aug;459:63-69. doi: 10.1016/j.jim.2018.05.002. Epub 2018 May 24.

DOI:10.1016/j.jim.2018.05.002
PMID:29803775
Abstract

BACKGROUND

Prior to large studies in breast cancer patients and healthy individuals we established a sensitive three-plex immunoassay to measure the EGFR ligands amphiregulin (AR), betacellulin (BTC) and transforming growth factor α (TGF-α) simultaneously in human serum samples.

METHOD

The three-plex immunoassay was developed using single molecule array (Simoa) technology and requires only 20 μL of serum.

RESULTS

AR, BTC and TGF-α were first established as three single-plex assays. Multiplexing the three single-plex assays showed no significant cross reactivity between the reagents. The concentrations of the ligands in serum samples showed correlations r ≥ 0.84 between the single-plex and three-plex methods. The three-plex assay demonstrated limit of detection levels at 0.16 ng/L for AR, 0.23 ng/L for BTC and 0.22 ng/L for TGF-α. Total coefficients of variations were 8.5%-31% for AR, 11%-21.8% for BTC and 12.4%-16.2% for TGF-α. Spiking experiments showed a mean recovery of 97% for AR, 86% for BTC and 81% for TGF-α. The concentrations of the EGFR ligands did not change significantly after series of freeze thaw cycles or incubation at 22 °C for up to 24 h.

CONCLUSION

This robust three-plex assay with up to 40-fold increase in sensitivity relative to conventional ELISA is the first published method that has the required sensitivity to measure AR, BTC and TGF-α simultaneously in human blood samples.

摘要

背景

在对乳腺癌患者和健康个体进行大规模研究之前,我们建立了一种灵敏的三联免疫测定法,用于同时检测人血清样本中的表皮生长因子受体(EGFR)配体双调蛋白(AR)、β细胞素(BTC)和转化生长因子α(TGF-α)。

方法

采用单分子阵列(Simoa)技术开发了这种三联免疫测定法,仅需20μL血清。

结果

AR、BTC和TGF-α最初是作为三种单联测定法建立的。将这三种单联测定法进行多重检测时,试剂之间未显示出明显的交叉反应。血清样本中配体的浓度在单联法和三联法之间显示出r≥0.84的相关性。三联测定法显示AR的检测限为0.16 ng/L,BTC为0.23 ng/L,TGF-α为0.22 ng/L。AR的总变异系数为8.5%-31%,BTC为11%-21.8%,TGF-α为12.4%-16.2%。加标实验显示AR的平均回收率为97%,BTC为86%,TGF-α为81%。在一系列冻融循环或在22°C下孵育长达24小时后,EGFR配体的浓度没有显著变化。

结论

这种强大的三联测定法相对于传统酶联免疫吸附测定(ELISA)的灵敏度提高了40倍,是首次发表的能够在人血样本中同时检测AR、BTC和TGF-α并具有所需灵敏度的方法。

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