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Evaluation of serological assays for SARS-CoV-2 antibody testing from dried blood spots collected from cohorts with prior SARS-CoV-2 infection.
Catlett, Beth; Starr, Mitchell; Machalek, Dorothy A; Danwilai, Thidarat; Palmer, Michael; Kelly, Andrew; Kaldor, John; Dore, Gregory J; Darley, David; Matthews, Gail; Cunningham, Philip H.
Affiliation
  • Catlett B; NSW State Reference Laboratory for HIV, St Vincent's Centre for Applied Medical Research, Darlinghurst, Sydney, New South Wales, Australia.
  • Starr M; The Kirby Institute, UNSW Sydney, Sydney, New South Wales, Australia.
  • Machalek DA; St Vincent's Hospital, Sydney, New South Wales, Australia.
  • Danwilai T; NSW State Reference Laboratory for HIV, St Vincent's Centre for Applied Medical Research, Darlinghurst, Sydney, New South Wales, Australia.
  • Palmer M; St Vincent's Hospital, Sydney, New South Wales, Australia.
  • Kelly A; The Kirby Institute, UNSW Sydney, Sydney, New South Wales, Australia.
  • Kaldor J; Centre for Women's Infectious Diseases, The Royal Women's Hospital, Melbourne, Australia.
  • Dore GJ; NSW State Reference Laboratory for HIV, St Vincent's Centre for Applied Medical Research, Darlinghurst, Sydney, New South Wales, Australia.
  • Darley D; St Vincent's Hospital, Sydney, New South Wales, Australia.
  • Matthews G; NSW State Reference Laboratory for HIV, St Vincent's Centre for Applied Medical Research, Darlinghurst, Sydney, New South Wales, Australia.
  • Cunningham PH; St Vincent's Hospital, Sydney, New South Wales, Australia.
J Clin Virol Plus ; 2(3): 100093, 2022 Aug.
Article in En | MEDLINE | ID: mdl-35765384
Background: Dried blood spot (DBS) specimens are a useful serosurveillance tool particularly in hard-to-reach populations but their application for detecting SARS-CoV-2 infection is poorly characterised. Objectives: To compare detection of naturally acquired SARS-CoV-2 antibodies in paired DBS and serum specimens using commercially available serological immunoassays. Study Design: Specimens were collected through St Vincent's Hospital observational post COVID-19 cohort study (ADAPT). Laboratory spotted DBS from venepuncture were initially tested on seven assays, a DBS validation completed on three with clinically collected fingerstick DBSs tested on one. Results: Sensitivity for Euroimmun nucleocapsid (NCP) IgG ELISA from laboratory spotted DBS (n=145), Euroimmun spike, IgG ELISA from laboratory spotted DBS (n=161), and Binding Site total antibody ELISA from clinically collected fingerstick DBS (n=391) was 100% (95% CI: 95.8-100%), 100% (95% CI: 95.8-100%) and 92.9% (95% CI: 89.5-95.5%), respectively. Specificity was 66.2% (95% CI: 53.6-77.0%), 96% (95% CI: 88.7-99.1%) and 98.8% (95% CI: 93.3-99.9%), respectively. All three assays' results displayed a strong positive correlation between DBS compared to paired serum. Conclusions: The Binding Site™ spike total antibody and Euroimmun™ spike IgG ELISAs provided good analytical performance, demonstrating that DBS specimens could facilitate specimen collection in the epidemiological surveillance of SARS-CoV-2 infection. This is highly applicable in populations and settings where venepuncture is problematic (including community based regional/remote settings, nursing homes, prisons, and schools).
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Full text: 1 Database: MEDLINE Type of study: Observational_studies Language: En Year: 2022 Type: Article

Full text: 1 Database: MEDLINE Type of study: Observational_studies Language: En Year: 2022 Type: Article