<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kroidl I</submitter><funding>University Hospital, LMU Munich</funding><funding>Universitätsklinik München</funding><funding>Euroimmun and Roche provided kits and machines for analyses at discounted rates for the study</funding><funding>Bavarian State Ministry of Science and the Arts</funding><funding>European-wide Consortium ORCHESTRA</funding><funding>German Ministry for Education and Research</funding><pagination>200</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10474769</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>20(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Measuring specific anti-SARS-CoV-2 antibodies has become one of the main epidemiological tools to survey the ongoing SARS-CoV-2 pandemic, but also vaccination response. The WHO made available a set of well-characterized samples derived from recovered individuals to allow normalization between different quantitative anti-Spike assays to defined Binding Antibody Units (BAU).&lt;h4>Methods&lt;/h4>To assess sero-responses longitudinally, a cohort of ninety-nine SARS-CoV-2 RT-PCR positive subjects was followed up together with forty-five vaccinees without previous infection but with two vaccinations. Sero-responses were evaluated using a total of six different assays: four measuring anti-Spike proteins (converted to BAU), one measuring anti-Nucleocapsid proteins and one SARS-CoV-2 </pubmed_abstract><journal>Virology journal</journal><pubmed_title>Studying temporal titre evolution of commercial SARS-CoV-2 assays reveals significant shortcomings of using BAU standardization for comparison.</pubmed_title><pmcid>PMC10474769</pmcid><funding_grant_id>01KI20271</funding_grant_id><funding_grant_id>101016167</funding_grant_id><pubmed_authors>Weigl N</pubmed_authors><pubmed_authors>Keßler A</pubmed_authors><pubmed_authors>Leidl R</pubmed_authors><pubmed_authors>Gasser M</pubmed_authors><pubmed_authors>Schandelmaier P</pubmed_authors><pubmed_authors>Puchinger K</pubmed_authors><pubmed_authors>Thiel V</pubmed_authors><pubmed_authors>Mayrhofer R</pubmed_authors><pubmed_authors>Durner J</pubmed_authors><pubmed_authors>Golschan E</pubmed_authors><pubmed_authors>Bohnlein 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L</pubmed_authors><pubmed_authors>Sintu-Sempta L</pubmed_authors><pubmed_authors>Saathoff E</pubmed_authors><pubmed_authors>KoCo19/ORCHESTRA Study Group</pubmed_authors><pubmed_authors>Anderson J</pubmed_authors><pubmed_authors>Putz P</pubmed_authors><pubmed_authors>Olbrich L</pubmed_authors><pubmed_authors>Forster F</pubmed_authors><pubmed_authors>Hannes M</pubmed_authors><pubmed_authors>Bemirayev O</pubmed_authors><pubmed_authors>Vollmayr V</pubmed_authors><pubmed_authors>Fuchs C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Studying temporal titre evolution of commercial SARS-CoV-2 assays reveals significant shortcomings of using BAU standardization for comparison.</name><description>&lt;h4>Background&lt;/h4>Measuring specific anti-SARS-CoV-2 antibodies has become one of the main epidemiological tools to survey the ongoing SARS-CoV-2 pandemic, but also vaccination response. The WHO made available a set of well-characterized samples derived from recovered individuals to allow normalization between different quantitative anti-Spike assays to defined Binding Antibody Units (BAU).&lt;h4>Methods&lt;/h4>To assess sero-responses longitudinally, a cohort of ninety-nine SARS-CoV-2 RT-PCR positive subjects was followed up together with forty-five vaccinees without previous infection but with two vaccinations. Sero-responses were evaluated using a total of six different assays: four measuring anti-Spike proteins (converted to BAU), one measuring anti-Nucleocapsid proteins and one SARS-CoV-2 </description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Sep</publication><modification>2025-04-18T18:48:44.405Z</modification><creation>2024-11-08T22:53:52.194Z</creation></dates><accession>S-EPMC10474769</accession><cross_references><pubmed>37658454</pubmed><doi>10.1186/s12985-023-02167-z</doi></cross_references></HashMap>