Diagnostic performance of two serological assays for the detection of SARS-CoV-2 specific antibodies: surveillance after vaccination

https://doi.org/10.1016/j.diagmicrobio.2022.115650Get rights and content

Abstract

Massive vaccination programs are being carried out to limit the SARS-CoV-2 pandemic that started in December 2019. Serological tests are of major importance as an indicator of circulation of the virus and to assess how vaccine-induced immunity progresses.

An Enzyme-Linked Immunosorbent Assay (ELISA) and a Lateral Flow Assay (LFA) have been developed based on the SARS-CoV-2 recombinant Receptor Binding Domain (RBD) and the combination of Spike and Nucleoprotein, respectively. The validation with 1272 serum samples by comparison with INgezim COVID 19 DR showed good diagnostic performance (sensitivity: 93.2%-97.2%; specificity: 98.3%-99.3%) for detection of previous contact with SARS-CoV-2. Moreover, according to our results, these assays can help in the serosurveillance during and after vaccination, by detecting the humoral immune response as soon as 15 days postvaccination and identifying low-respondents. Hence, these tests could play a key role in the progression to a COVID-19 free world, helping to adjust future vaccination protocols.

Keywords

SARS-CoV-2
COVID-19
Vaccination
Serology
RBD
Spike protein

Abbreviations

EDC
1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride
NHS
N-Hydroxysuccinimide
PBS
phosphate buffered saline pH 7.4

Cited by (0)

The present work was carried out at Eurofins Ingenasa.

These authors contributed equally.

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