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Antibody tests in detecting SARS-CoV-2 infection: A meta-analysis

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Autore
Kontou P.I., Braliou G.G., Dimou N.L., Nikolopoulos G., Bagos P.G.
Data
2020
Language
en
DOI
10.3390/diagnostics10050319
Soggetto
immunoglobulin G
immunoglobulin M
virus antigen
Article
chemiluminescence immunoassay
coronavirus disease 2019
diagnostic test accuracy study
enzyme immunoassay
enzyme linked immunosorbent assay
gold standard
human
immunoassay
immunofluorescence test
intermethod comparison
lateral flow immunoassay
meta analysis
nonhuman
pandemic
sensitivity and specificity
serodiagnosis
seroprevalence
Severe acute respiratory syndrome coronavirus 2
systematic review
MDPI AG
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Abstract
The emergence of Coronavirus disease 2019 (COVID-19) caused by SARS-CoV-2 made imperative the need for diagnostic tests that can identify the infection. Although Nucleic Acid Test (NAT) is considered to be the gold standard, serological tests based on antibodies could be very helpful. However, individual studies are usually inconclusive, thus, a comparison of different tests is needed. We performed a systematic review and meta-analysis in PubMed, medRxiv and bioRxiv. We used the bivariate method for meta-analysis of diagnostic tests pooling sensitivities and specificities. We evaluated IgM and IgG tests based on Enzyme-linked immunosorbent assay (ELISA), Chemiluminescence Enzyme Immunoassays (CLIA), Fluorescence Immunoassays (FIA), and the Lateral Flow Immunoassays (LFIA). We identified 38 studies containing data from 7848 individuals. Tests using the S antigen are more sensitive than N antigen-based tests. IgG tests perform better compared to IgM ones and show better sensitivity when the samples were taken longer after the onset of symptoms. Moreover, a combined IgG/IgM test seems to be a better choice in terms of sensitivity than measuring either antibody alone. All methods yield high specificity with some of them (ELISA and LFIA) reaching levels around 99%. ELISA- and CLIA-based methods perform better in terms of sensitivity (90%-94%) followed by LFIA and FIA with sensitivities ranging from 80% to 89%. ELISA tests could be a safer choice at this stage of the pandemic. LFIA tests are more attractive for large seroprevalence studies but show lower sensitivity, and this should be taken into account when designing and performing seroprevalence studies. © 2020 by the authors. Licensee MDPI, Basel, Switzerland.
URI
http://hdl.handle.net/11615/75103
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