MicroRNA In Vitro Diagnostics Using Immunoassay Analyzers

被引:32
作者
Kappel, Andreas [1 ]
Backes, Christina [2 ]
Huang, Yiwei [1 ]
Zafari, Sachli [2 ]
Leidinger, Petra [3 ]
Meder, Benjamin [4 ]
Schwarz, Herbert [6 ]
Gumbrecht, Walter [1 ]
Meese, Eckart [3 ]
Staehler, Cord F. [5 ]
Keller, Andreas [2 ]
机构
[1] Siemens AG, Corp Technol, Erlangen, Germany
[2] Univ Saarland, Fac Med, Clin Bioinformat, D-66123 Saarbrucken, Germany
[3] Univ Saarland, Dept Human Genet, D-66123 Saarbrucken, Germany
[4] Univ Heidelberg Hosp, Internal Med 3, Heidelberg, Germany
[5] Siemens Healthcare, Strategy, Erlangen, Germany
[6] Siemens Healthcare Diagnost Prod GmbH, Marburg, Germany
关键词
LUNG-CANCER; WHOLE-BLOOD; MULTIPLE-SCLEROSIS; MIRNA PROFILES; DISEASE; EXPRESSION; ANTIBODY; ASSAY;
D O I
10.1373/clinchem.2014.232165
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
100118 [医学信息学]; 100208 [临床检验诊断学];
摘要
BACKGROUND: The implementation of new biomarkers into clinical practice is one of the most important areas in medical research. Besides their clinical impact, novel in vitro diagnostic markers promise to have a substantial effect on healthcare costs. Although numerous publications report the discovery of biomarkers, only a fraction of those markers are routinely used. One key challenge is a measurement system that is compatible with clinical workflows. METHODS: We designed a new immunoassay for microRNA (miRNA) quantification. The assay combines streptavidin-linked microparticles, a biotinylated catcher oligonucleotide complementary to a single miRNA species, and finally, a monoclonal antibody to DNA/RNA heterohybrids labeled with acridinium ester. Importantly, our assay runs on standard immunoassay analyzers. After a technical validation of the assay, we evaluated the clinical performance on 4 Alzheimer disease miRNAs. RESULTS: Our assay has an analytical specificity of 99.4% and is at the same time sensitive (concentrations in the range of 1 pmol/L miRNA can be reliably profiled). Because the novel approach did not require amplification steps, we obtained high reproducibility for up to 40 biological replicates. Importantly, our assay prototype exhibited a time to result of <3 h. With human blood samples, the assay was able to measure 4 miRNAs that can detect Alzheimer disease with a diagnostic accuracy of 82% and showed a Pearson correlation >0.994 with the gold standard qRT-PCR. CONCLUSIONS: Our miRNA immunoassay allowed the measurement of miRNA signatures with sufficient analytical sensitivity and high specificity on commonly available laboratory equipment. (C) 2014 American Association for Clinical Chemistry
引用
收藏
页码:600 / 607
页数:8
相关论文
共 26 条
[1]
[Anonymous], 2012, WORLDWIDE MARKET IN
[2]
[Anonymous], 2009, RECOMMENDATION 4 95, P15
[3]
CHARACTERIZATION OF MONOCLONAL-ANTIBODY TO DNA.RNA AND ITS APPLICATION TO IMMUNODETECTION OF HYBRIDS [J].
BOGUSLAWSKI, SJ ;
SMITH, DE ;
MICHALAK, MA ;
MICKELSON, KE ;
YEHLE, CO ;
PATTERSON, WL ;
CARRICO, RJ .
JOURNAL OF IMMUNOLOGICAL METHODS, 1986, 89 (01) :123-130
[4]
Real-time quantification of microRNAs by stem-loop RT-PCR [J].
Chen, CF ;
Ridzon, DA ;
Broomer, AJ ;
Zhou, ZH ;
Lee, DH ;
Nguyen, JT ;
Barbisin, M ;
Xu, NL ;
Mahuvakar, VR ;
Andersen, MR ;
Lao, KQ ;
Livak, KJ ;
Guegler, KJ .
NUCLEIC ACIDS RESEARCH, 2005, 33 (20) :e179.1-e179.9
[5]
The ADVIA Centaur® infectious disease assays:: a technical review [J].
Dwyer, R .
JOURNAL OF CLINICAL VIROLOGY, 2004, 30 :S1-S5
[6]
Most mammalian mRNAs are conserved targets of microRNAs [J].
Friedman, Robin C. ;
Farh, Kyle Kai-How ;
Burge, Christopher B. ;
Bartel, David P. .
GENOME RESEARCH, 2009, 19 (01) :92-105
[7]
German Medical Association and Paul Ehrlich Institute, 2007, GUIDELINES COLLECTIO
[8]
Whole blood-derived miRNA profiles as potential new tools for ovarian cancer screening [J].
Haeusler, S. F. M. ;
Keller, A. ;
Chandran, P. A. ;
Ziegler, K. ;
Zipp, K. ;
Heuer, S. ;
Krockenberger, M. ;
Engel, J. B. ;
Hoenig, A. ;
Scheffler, M. ;
Dietl, J. ;
Wischhusen, J. .
BRITISH JOURNAL OF CANCER, 2010, 103 (05) :693-700
[9]
Comprehensive analysis of microRNA profiles in multiple sclerosis including next-generation sequencing [J].
Keller, Andreas ;
Leidinger, Petra ;
Steinmeyer, Florian ;
Staehler, Cord ;
Franke, Andre ;
Hemmrich-Stanisak, Georg ;
Kappel, Andreas ;
Wright, Ian ;
Doerr, Jan ;
Paul, Friedemann ;
Diem, Ricarda ;
Tocariu-Krick, Beatrice ;
Meder, Benjamin ;
Backes, Christina ;
Meese, Eckart ;
Ruprecht, Klemens .
MULTIPLE SCLEROSIS JOURNAL, 2014, 20 (03) :295-303
[10]
Keller A, 2011, NAT METHODS, V8, P841, DOI [10.1038/NMETH.1682, 10.1038/nmeth.1682]