<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Midorikawa R</submitter><funding>Fujirebio</funding><funding>Astellas Pharma Inc.</funding><funding>National Hospital Organization</funding><funding>Mitsubishi Tanabe Pharma Corporation</funding><funding>Takeda Pharmaceutical Company Limited</funding><pagination>965</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9144302</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(5)</volume><pubmed_abstract>Serological detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) nucleocapsid (N), spike (S), and neutralizing antibodies (Abs) is commonly undertaken to evaluate the efficacy of vaccination. However, the relative efficiency of different SARS-CoV-2 Ab detection systems has not been extensively investigated. Here, we evaluated serological test systems in vaccinated Japanese. SARS-CoV-2 N, S, and neutralizing Abs in sera of 375 healthy subjects a mean 253 days after vaccination were assessed. The sensitivity of Elecsys Anti-SARS-CoV-2 S (Roche S) and Anti-SARS-CoV-2 S IgG (Fujirebio S) was 100% and 98.9%, respectively, with a specificity of 100% for both. The sensitivity of Anti-SARS-CoV-2 neutralizing Ab (MBL Neu) was 2.7%, and the specificity was 100%. Fujirebio S correlated with Roche S (rho = 0.9182, &lt;i>p&lt;/i> = 3.97 × 10&lt;sup>-152&lt;/sup>). Fujirebio S (rho = 0.1295, &lt;i>p&lt;/i> = 0.0121) and Roche S (rho = 0.1232, &lt;i>p&lt;/i> = 0.0170) correlated weakly with MBL Neu. However, Roche S did correlate with MBL Neu in patients with COVID-19 (rho = 0.8299, &lt;i>p&lt;/i> = 1.01 × 10&lt;sup>-12&lt;/sup>) and in healthy subjects more recently after vaccination (mean of 90 days, rho = 0.5306, &lt;i>p&lt;/i> = 0.0003). Thus, the Fujirebio S and Roche S results were very similar, but neither correlated with neutralizing antibody titers by MBL Neu at a later time after vaccination.</pubmed_abstract><journal>Viruses</journal><pubmed_title>Detection of SARS-CoV-2 Nucleocapsid, Spike, and Neutralizing Antibodies in Vaccinated Japanese.</pubmed_title><pmcid>PMC9144302</pmcid><funding_grant_id>NA</funding_grant_id><pubmed_authors>Midorikawa R</pubmed_authors><pubmed_authors>Nagai H</pubmed_authors><pubmed_authors>Nakama M</pubmed_authors><pubmed_authors>Oka S</pubmed_authors><pubmed_authors>Furukawa H</pubmed_authors><pubmed_authors>Tohma S</pubmed_authors><pubmed_authors>Higuchi T</pubmed_authors><pubmed_authors>Nagai N</pubmed_authors></additional><is_claimable>false</is_claimable><name>Detection of SARS-CoV-2 Nucleocapsid, Spike, and Neutralizing Antibodies in Vaccinated Japanese.</name><description>Serological detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) nucleocapsid (N), spike (S), and neutralizing antibodies (Abs) is commonly undertaken to evaluate the efficacy of vaccination. However, the relative efficiency of different SARS-CoV-2 Ab detection systems has not been extensively investigated. Here, we evaluated serological test systems in vaccinated Japanese. SARS-CoV-2 N, S, and neutralizing Abs in sera of 375 healthy subjects a mean 253 days after vaccination were assessed. The sensitivity of Elecsys Anti-SARS-CoV-2 S (Roche S) and Anti-SARS-CoV-2 S IgG (Fujirebio S) was 100% and 98.9%, respectively, with a specificity of 100% for both. The sensitivity of Anti-SARS-CoV-2 neutralizing Ab (MBL Neu) was 2.7%, and the specificity was 100%. Fujirebio S correlated with Roche S (rho = 0.9182, &lt;i>p&lt;/i> = 3.97 × 10&lt;sup>-152&lt;/sup>). Fujirebio S (rho = 0.1295, &lt;i>p&lt;/i> = 0.0121) and Roche S (rho = 0.1232, &lt;i>p&lt;/i> = 0.0170) correlated weakly with MBL Neu. However, Roche S did correlate with MBL Neu in patients with COVID-19 (rho = 0.8299, &lt;i>p&lt;/i> = 1.01 × 10&lt;sup>-12&lt;/sup>) and in healthy subjects more recently after vaccination (mean of 90 days, rho = 0.5306, &lt;i>p&lt;/i> = 0.0003). Thus, the Fujirebio S and Roche S results were very similar, but neither correlated with neutralizing antibody titers by MBL Neu at a later time after vaccination.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 May</publication><modification>2025-04-18T22:59:09.29Z</modification><creation>2025-02-19T03:25:15.775Z</creation></dates><accession>S-EPMC9144302</accession><cross_references><pubmed>35632710</pubmed><doi>10.3390/v14050965</doi></cross_references></HashMap>