Author:
Burgold-Voigt Sindy,Müller Elke,Zopf David,Monecke Stefan,Braun Sascha D.,Frankenfeld Katrin,Kiehntopf Michael,Weis Sebastian,Schumacher Thomas,Pletz Mathias W.,Ehricht Ralf,Hotz Thomas,Enders Petra,Koch Renate,Mai Steffen,Ullrich Matthias,Richert Cora,Eibner Cornelius,Meinung Bettina,Stötzer Kay,Köhler Julia,Kiehntopf Michael,Cipowicz Hans,Pinkwart Christine,Proquitté Hans,Bauer Michael,Dickmann Petra,Licht Annika,Scholz Juliane,Wetzker Wibke,Hartung Anita,Weiß Daniel,Thieme Lara,Hanf Gabi,Schnizer Clara,Müller Jasmin,Kosenkow Jennifer,Röstel Franziska,Guerra Joel,Makarewicz Oliwia,Kolanos Steffi,Ankert Juliane,Hagel Stefan,Bahrs Christina,Andreas Nico,Marquardt Raphaela,Kamradt Thomas,Baumgart Sabine,Deinhardt-Emmer Stefanie,Kuhn Sebastian,Löffler Bettina,Baier Michael,Glöckner Stefan,Scherag André,Pletz Mathias W.,
Abstract
AbstractStrategies to contain the current SARS-CoV-2 pandemic rely, beside vaccinations, also on molecular and serological testing. For any kind of assay development, screening for the optimal antigen is essential. Here we describe the verification of a new protein microarray with different commercially available preparations significant antigens of SARS-CoV-2 that can be used for the evaluation of the performance of these antigens in serological assays and for antibody screening in serum samples. Antigens of other pathogens that are addressed by widely used vaccinations were also included. To evaluate the accuracy of 21 different antigens or antigen preparations on the microarray, receiver operating characteristics (ROC) curve analysis using ELISA results as reference were performed. Except for a single concentration, a diagnostic sensitivity of 1 was determined for all antigen preparations. A diagnostic specificity, as well as an area under the curve (AUC) of 1 was obtained for 16 of 21 antigen preparations. For the remaining five, the diagnostic specificity ranged from 0.942 to 0.981 and AUC from 0.974 to 0.999. The optimized assay was subsequently also applied to determine the immune status of previously tested individuals and/or to detect the immunization status after COVID-19 vaccination. Microarray evaluation of the antibody profiles of COVID-19 convalescent and post vaccination sera showed that the IgG response differed between these groups, and that the choice of the test antigen is crucial for the assay performance. Furthermore, the results showed that the immune response is highly individualized, depended on several factors (e.g., age or sex), and was not directly related to the severity of disease. The new protein microarray provides an ideal method for the parallel screening of many different antigens of vaccine-preventable diseases in a single sample and for reliable and meaningful diagnostic tests, as well as for the development of safe and specific vaccines.
Funder
Freistaat Thüringen
European Social Fund
German Federal Ministry of Education and Research
Thuringian Ministry for Economic Affairs, Science and Digital Society
Leibniz-Institut für Photonische Technologien e.V.
Publisher
Springer Science and Business Media LLC