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Dried blood spot specimens for SARS-CoV-2 antibody testing: A multi-site, multi-assay comparison

The true severity of infection due to COVID-19 is under-represented because it is based on only those who are tested. Although nucleic acid amplifications tests (NAAT) are the gold standard for COVID-19 diagnostic testing, serological assays provide better population-level SARS-CoV-2 prevalence esti...

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Detalles Bibliográficos
Autores principales: Cholette, François, Mesa, Christine, Harris, Angela, Ellis, Hannah, Cachero, Karla, Lacap, Philip, Galipeau, Yannick, Langlois, Marc-André, Gingras, Anne-Claude, Yansouni, Cedric P., Papenburg, Jesse, Cheng, Matthew P., Chakraborty, Pranesh, Stein, Derek R., Van Caeseele, Paul, Bartlett, Sofia, Krajden, Mel, Goldfarb, David, McGeer, Allison, Osiowy, Carla, Hankins, Catherine, Mazer, Bruce, Drebot, Michael, Kim, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8651133/
https://www.ncbi.nlm.nih.gov/pubmed/34874948
http://dx.doi.org/10.1371/journal.pone.0261003
Descripción
Sumario:The true severity of infection due to COVID-19 is under-represented because it is based on only those who are tested. Although nucleic acid amplifications tests (NAAT) are the gold standard for COVID-19 diagnostic testing, serological assays provide better population-level SARS-CoV-2 prevalence estimates. Implementing large sero-surveys present several logistical challenges within Canada due its unique geography including rural and remote communities. Dried blood spot (DBS) sampling is a practical solution but comparative performance data on SARS-CoV-2 serological tests using DBS is currently lacking. Here we present test performance data from a well-characterized SARS-CoV-2 DBS panel sent to laboratories across Canada representing 10 commercial and 2 in-house developed tests for SARS-CoV-2 antibodies. Three commercial assays identified all positive and negative DBS correctly corresponding to a sensitivity, specificity, positive predictive value, and negative predictive value of 100% (95% CI = 72.2, 100). Two in-house assays also performed equally well. In contrast, several commercial assays could not achieve a sensitivity greater than 40% or a negative predictive value greater than 60%. Our findings represent the foundation for future validation studies on DBS specimens that will play a central role in strengthening Canada’s public health policy in response to COVID-19.