Development of a high-throughput SARS-CoV-2 antibody testing pathway using dried blood spot specimens
BACKGROUND: Serological assays for Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) have roles in seroepidemiology, convalescent plasma-testing, antibody durability and vaccine studies. Currently, SARS-CoV-2 serology is performed using serum/plasma collected by venepuncture. Dried blood spot (DBS) testing offers significant advantages as it is minimally invasive, avoids venepuncture with specimens being mailed to the laboratory.
METHODS: A pathway utilizing a newborn screening laboratory infrastructure was developed using an enzyme-linked immunosorbent assay to detect IgG antibodies against the receptor-binding domain of the SARS-CoV-2 spike protein in DBS specimens. Paired plasma and DBS specimens from SARS-CoV-2 antibody-positive and -negative subjects and polymerase chain reaction positive subjects were tested. DBS specimen stability, effect of blood volume and punch location were also evaluated.
RESULTS: DBS specimens from antibody-negative (n = 85) and -positive (n = 35) subjects and polymerase chain reaction positive subjects (n = 11) had a mean (SD; range) optical density (OD) of 0.14 (0.046; 0.03-0.27), 0.98 (0.41; 0.31-1.64) and 1.12 (0.37; 0.49-1.54), respectively. An action value OD >0.28 correctly assigned all cases. The weighted Deming regression for comparison of the DBS and the plasma assay yielded: y = 0.004041 + 1.005x, r = 0.991, Sy/x 0.171, n = 82. Extraction efficiency of antibodies from DBS specimens was >99%. DBS specimens were stable for at least 28 days at ambient room temperature and humidity.
CONCLUSIONS: SARS-CoV-2 IgG receptor-binding domain antibodies can be reliably detected in DBS specimens. DBS serological testing offers lower costs than either point of care or serum/plasma assays that require patient travel, phlebotomy and hospital/clinic resources; the development of a DBS assay may be particularly important for resource poor settings.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2021 |
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Erschienen: |
2021 |
Enthalten in: |
Zur Gesamtaufnahme - volume:58 |
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Enthalten in: |
Annals of clinical biochemistry - 58(2021), 2 vom: 01. März, Seite 123-131 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Moat, Stuart J [VerfasserIn] |
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Links: |
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Anmerkungen: |
Date Completed 22.03.2021 Date Revised 11.02.2024 published: Print-Electronic Citation Status MEDLINE |
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doi: |
10.1177/0004563220981106 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM318361132 |
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100 | 1 | |a Moat, Stuart J |e verfasserin |4 aut | |
245 | 1 | 0 | |a Development of a high-throughput SARS-CoV-2 antibody testing pathway using dried blood spot specimens |
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500 | |a published: Print-Electronic | ||
500 | |a Citation Status MEDLINE | ||
520 | |a BACKGROUND: Serological assays for Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) have roles in seroepidemiology, convalescent plasma-testing, antibody durability and vaccine studies. Currently, SARS-CoV-2 serology is performed using serum/plasma collected by venepuncture. Dried blood spot (DBS) testing offers significant advantages as it is minimally invasive, avoids venepuncture with specimens being mailed to the laboratory | ||
520 | |a METHODS: A pathway utilizing a newborn screening laboratory infrastructure was developed using an enzyme-linked immunosorbent assay to detect IgG antibodies against the receptor-binding domain of the SARS-CoV-2 spike protein in DBS specimens. Paired plasma and DBS specimens from SARS-CoV-2 antibody-positive and -negative subjects and polymerase chain reaction positive subjects were tested. DBS specimen stability, effect of blood volume and punch location were also evaluated | ||
520 | |a RESULTS: DBS specimens from antibody-negative (n = 85) and -positive (n = 35) subjects and polymerase chain reaction positive subjects (n = 11) had a mean (SD; range) optical density (OD) of 0.14 (0.046; 0.03-0.27), 0.98 (0.41; 0.31-1.64) and 1.12 (0.37; 0.49-1.54), respectively. An action value OD >0.28 correctly assigned all cases. The weighted Deming regression for comparison of the DBS and the plasma assay yielded: y = 0.004041 + 1.005x, r = 0.991, Sy/x 0.171, n = 82. Extraction efficiency of antibodies from DBS specimens was >99%. DBS specimens were stable for at least 28 days at ambient room temperature and humidity | ||
520 | |a CONCLUSIONS: SARS-CoV-2 IgG receptor-binding domain antibodies can be reliably detected in DBS specimens. DBS serological testing offers lower costs than either point of care or serum/plasma assays that require patient travel, phlebotomy and hospital/clinic resources; the development of a DBS assay may be particularly important for resource poor settings | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Research Support, Non-U.S. Gov't | |
650 | 4 | |a COVID-19 | |
650 | 4 | |a Dried blood spots | |
650 | 4 | |a SARS-CoV-2 | |
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650 | 7 | |a Immunoglobulin G |2 NLM | |
650 | 7 | |a Spike Glycoprotein, Coronavirus |2 NLM | |
650 | 7 | |a spike protein, SARS-CoV-2 |2 NLM | |
700 | 1 | |a Zelek, Wioleta M |e verfasserin |4 aut | |
700 | 1 | |a Carne, Emily |e verfasserin |4 aut | |
700 | 1 | |a Ponsford, Mark J |e verfasserin |4 aut | |
700 | 1 | |a Bramhall, Kathryn |e verfasserin |4 aut | |
700 | 1 | |a Jones, Sara |e verfasserin |4 aut | |
700 | 1 | |a El-Shanawany, Tariq |e verfasserin |4 aut | |
700 | 1 | |a Wise, Matt P |e verfasserin |4 aut | |
700 | 1 | |a Thomas, Annette |e verfasserin |4 aut | |
700 | 1 | |a George, Chloe |e verfasserin |4 aut | |
700 | 1 | |a Fegan, Christopher |e verfasserin |4 aut | |
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700 | 1 | |a Webb, Russell |e verfasserin |4 aut | |
700 | 1 | |a Weeks, Ian |e verfasserin |4 aut | |
700 | 1 | |a Morgan, B Paul |e verfasserin |4 aut | |
700 | 1 | |a Jolles, Stephen |e verfasserin |4 aut | |
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