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Cited 5 time in webofscience Cited 5 time in scopus
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Diagnostic Performance and Comparative Evaluation of the Architect, Liaison, and Platelia Epstein-Barr Virus Antibody Assaysopen access

Authors
Park, YounheePark, Borae G.Ha, JihyeKim, Hyon-Suk
Issue Date
Sep-2018
Publisher
KOREAN SOC LABORATORY MEDICINE
Keywords
Epstein-Barr virus; Assay; Diagnostic performance; DNA; Antibody; Immunoglobulin
Citation
ANNALS OF LABORATORY MEDICINE, v.38, no.5, pp 458 - 465
Pages
8
Indexed
SCIE
SCOPUS
KCI
Journal Title
ANNALS OF LABORATORY MEDICINE
Volume
38
Number
5
Start Page
458
End Page
465
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2020.sw.kumedicine/29005
DOI
10.3343/alm.2018.38.5.458
ISSN
2234-3806
2234-3814
Abstract
Background: Epstein-Barr Virus (EBV) is one of the most prevalent causes of viral infection in humans. EBV infection stage (acute, past, or absent infection) is typically determined using a combination of assays that detect EBV-specific markers, such as IgG and IgM antibodies against the EBV viral capsid antigen (VCA) and IgG antibodies against the EBV nuclear antigen (EBNA). We compared the diagnostic performance and agreement of results between three commercial EBV antibody assays using an EBV performance panel (SeraCare Life Science, Milford, MA, USA) as a reference. Methods: EBV antibody tests of EBV VCA IgM, VCA IgG, and EBNA IgG antibodies were performed by the Architect (Abbott Diagnostics, Wiesbaden, Germany), Liaison (DiaSorin, Saluggia, Italy), and Platelia (Bio-Rad, Marnes-la-Coquette, France) assays. Agreement between the three assays was evaluated using 279 clinical samples, and EBV DNA and antibody test results were compared. Results: The three EBV antibody assays showed good diagnostic performance with good and excellent agreement with the performance panel (kappa coefficient, >0.6). The overall VCA IgM positivity rate was higher in EBV DNA-positive samples than in EBV DNA-negative samples for all three EBV antibody assays (P=0.02). The three EBV antibody assays exhibited good agreement in results for the clinical samples. Conclusions: The diagnostic performance of the three EBV antibody assays was acceptable, and they showed comparable agreement in results for the clinical samples.
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