| Literature DB >> 33534090 |
Lisa Müller1, Philipp Niklas Ostermann1, Andreas Walker1, Tobias Wienemann2, Alexander Mertens3, Ortwin Adams1, Marcel Andree1, Sandra Hauka1, Nadine Lübke1, Verena Keitel3, Ingo Drexler1, Veronica Di Cristanziano4, Derik Franz Hermsen5, Rolf Kaiser4, Friedrich Boege5, Florian Klein4, Heiner Schaal1, Jörg Timm6, Tina Senff7.
Abstract
Evaluation and power of seroprevalence studies depend on the performed serological assays. The aim of this study was to assess four commercial serological tests from EUROIMMUN, DiaSorin, Abbott, and Roche as well as an in-house immunofluorescence and neutralization test for their capability to identify SARS-CoV-2 seropositive individuals in a high-prevalence setting. Therefore, 42 social and working contacts of a German super-spreader were tested. Consistent with a high-prevalence setting, 26 of 42 were SARS-CoV-2 seropositive by neutralization test (NT), and immunofluorescence test (IFT) confirmed 23 of these 26 positive test results (NT 61.9% and IFT 54.8% seroprevalence). Four commercial assays detected anti-SARS-CoV-2 antibodies in 33.3-40.5% individuals. Besides an overall discrepancy between the NT and the commercial assays regarding their sensitivity, this study revealed that commercial SARS-CoV-2 spike-based assays are better to predict the neutralization titer than nucleoprotein-based assays are.Entities:
Keywords: COVID-19; Immunofluorescence test; Neutralizing antibodies; SARS-CoV-2; Serology; Seroprevalence
Year: 2021 PMID: 33534090 PMCID: PMC7856849 DOI: 10.1007/s10096-021-04169-7
Source DB: PubMed Journal: Eur J Clin Microbiol Infect Dis ISSN: 0934-9723 Impact factor: 3.267