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

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DOI

https://doi.org/10.1371/journal.pone.0261003

Language of the publication
English
Date
2021-12-07
Type
Article
Author(s)
  • 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
Publisher
PLOS

Abstract

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.

Subject

  • Health,
  • Coronavirus diseases

Rights

Pagination

1-19

Peer review

Yes

Identifiers

PubMed ID
34874948
ISSN
1932-6203

Article

Journal title
PLoS ONE
Journal volume
16
Journal issue
12
Article number
e0261003

Sponsors

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).

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Communicable diseases

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