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Diagnostic performance of four lateral flow immunoassays for Covid-19 antibodies in Peruvian population

Datos Bibliográficos

ID19592007
AutoresRodrigo Calderon-Flores (0000-0002-3457-8594, Universidad Peruana Cayetano Heredia), Guillermo Caceres-Cardenas (0000-0003-1447-5608, Universidad Peruana Cayetano Heredia), Karla Alí (Universidad Peruana Cayetano Heredia), Margaretha De Vos (0000-0003-3059-2986, FIND), Devy Emperador (0000-0002-8228-1824, FIND), Tatiana Cáceres (0000-0003-0516-5202, Universidad Peruana Cayetano Heredia), Anika Eca (0000-0003-4578-688X, Universidad Peruana Cayetano Heredia), Luz Villa-Castillo (0000-0002-2589-7171, Universidad Peruana Cayetano Heredia), Audrey Albertini (FIND), Jilian A Sacks (0000-0003-4815-4693, FIND), César Ugarte‐Gil (0000-0002-2833-9087, Universidad Peruana Cayetano Heredia, autor de correspondencia)
EditoresMiguel Ángel García-Bereguiain (0000-0003-0025-3609)
Año2023
Volumen3
Número6
Páginase0001555
Fecha de publicación2023-06-02
Peer ReviewedSí
Open AccessSí
TipoARTICLE
RevistaPLOS Global Public Health (JOURNAL)
Identificadores de la revistaISSN: 2767-3375 • E-ISSN: 2767-3375
EditorialPublic Library of Science (PLoS) (PUBLISHER)
DOI10.1371/journal.pgph.0001555
PMID37267241
OpenAlexW4379197715
IdiomaEN
Referencias citadas27

Serological assays have been used in seroprevalence studies to inform the dynamics of COVID-19. Lateral flow immunoassay (LFIA) tests are a very practical technology to use for this objective; however, one of their challenges may be variable diagnostic performance. Given the numerous available LFIA tests, evaluation of their accuracy is critical before real-world implementation. We performed a retrospective diagnostic evaluation study to independently determine the diagnostic accuracy of 4 different antibody-detection LFIA tests: Now Check (Bionote), CareStart (Access bio), Covid-19 BSS (Biosynex) and OnSite (CTK Biotech). The sample panel was comprised of specimens collected and stored in biobanks; specifically, specimens that were RT-PCR positive for SARS-CoV-2 collected at various times throughout the COVID-19 disease course and those that were collected before the pandemic, during 2018 or earlier, from individuals with upper respiratory symptoms but were negative for tuberculosis. Clinical performance (sensitivity and specificity) was analyzed overall, and subset across individual antibody isotypes, and days from symptoms onset. A very high specificity (98% - 100%) was found for all four tests. Overall sensitivity was variable, ranging from 29% [95% CI: 21%-39%] to 64% [95% CI: 54%-73%]. When considering detection of IgM only, the highest sensitivity was 42% [95% CI: 32%-52%], compared to 57% [95% CI: 47%-66%] for IgG only. When the analysis was restricted to at least 15 days since symptom onset, across any isotype, the sensitivity reached 90% for all four brands. All four LFIA tests proved effective for identifying COVID-19 antibodies when two conditions were met: 1) at least 15 days have elapsed since symptom onset and 2) a sample is considered positive when either IgM or IgG is present. With these considerations, the use of this assays could help in seroprevalence studies or further exploration of its potential uses

Antibody · Disease · Population · Serology · Seroprevalence · COVID-19 Clinical Research Studies · Medicine · SARS-CoV-2 and COVID-19 Research · SARS-CoV-2 detection and testing · Immunology · Internal Medicine · Virology

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  • Evaluación en condiciones de campo de una prueba serológica rápida para detección de anticuerpos IgM e IgG contra Sars-CoV-2

    Open Access•Margot Vidal-Anzardo, Gilmer Solis-Sánchez et al.•Revista Peruana de Medicina…•2020

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