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

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dc.contributor.author
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
COVID-19 Immunity Task Force (CITF) working group
dc.date.accessioned
2024-11-18T20:31:27Z
dc.date.available
2024-11-18T20:31:27Z
dc.date.issued
2021-12-07
dc.description.abstract - en
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.
dc.description.sponsorship
Marc-André Langlois (M.-A.L.) holds a Canada Research Chair in Molecular Virology and Intrinsic Immunity. This study was supported in part by a COVID-19 Rapid Response grant to M.-A.L. by the Canadian Institute of Health Research (CIHR; OV1-170355) and by a grant supplement by the COVID-19 Immunity Task Force (CITF).
dc.identifier.doi
https://doi.org/10.1371/journal.pone.0261003
dc.identifier.issn
1932-6203
dc.identifier.pubmedID
34874948
dc.identifier.uri
https://open-science.canada.ca/handle/123456789/3165
dc.language.iso
en
dc.publisher - en
PLOS
dc.rights - en
Creative Commons Attribution 4.0 International (CC BY 4.0)
dc.rights - fr
Creative Commons Attribution 4.0 International (CC BY 4.0)
dc.rights.uri - en
https://creativecommons.org/licenses/by/4.0/
dc.rights.uri - fr
https://creativecommons.org/licenses/by/4.0/deed.fr
dc.subject - en
Health
Coronavirus diseases
dc.subject - fr
Santé
Maladie à coronavirus
dc.subject.en - en
Health
Coronavirus diseases
dc.subject.fr - fr
Santé
Maladie à coronavirus
dc.title - en
Dried blood spot specimens for SARS-CoV-2 antibody testing: A multi-site, multi-assay comparison
dc.type - en
Article
dc.type - fr
Article
local.acceptedmanuscript.articlenum
e0261003
local.article.journalissue
12
local.article.journaltitle - en
PLoS ONE
local.article.journalvolume
16
local.pagination
1-19
local.peerreview - en
Yes
local.peerreview - fr
Oui
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