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

Erscheinungsjahr:

2021

Erschienen:

2021

Enthalten in:

Zur Gesamtaufnahme - volume:58

Enthalten in:

Annals of clinical biochemistry - 58(2021), 2 vom: 01. März, Seite 123-131

Sprache:

Englisch

Beteiligte Personen:

Moat, Stuart J [VerfasserIn]
Zelek, Wioleta M [VerfasserIn]
Carne, Emily [VerfasserIn]
Ponsford, Mark J [VerfasserIn]
Bramhall, Kathryn [VerfasserIn]
Jones, Sara [VerfasserIn]
El-Shanawany, Tariq [VerfasserIn]
Wise, Matt P [VerfasserIn]
Thomas, Annette [VerfasserIn]
George, Chloe [VerfasserIn]
Fegan, Christopher [VerfasserIn]
Steven, Rachael [VerfasserIn]
Webb, Russell [VerfasserIn]
Weeks, Ian [VerfasserIn]
Morgan, B Paul [VerfasserIn]
Jolles, Stephen [VerfasserIn]

Links:

Volltext

Themen:

Antibodies
Antibodies, Viral
COVID-19
Dried blood spots
Enzyme-linked immunosorbent assay
Immunoglobulin G
Journal Article
Research Support, Non-U.S. Gov't
SARS-CoV-2
Spike Glycoprotein, Coronavirus
Spike protein, SARS-CoV-2

Anmerkungen:

Date Completed 22.03.2021

Date Revised 11.02.2024

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1177/0004563220981106

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM318361132