<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Younes N</submitter><funding>Qatar National Research Fund</funding><pagination>1318</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9415525</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10(8)</volume><pubmed_abstract>&lt;b>Background:&lt;/b> Limited commercial LFA assays are available to provide a reliable quantitative measurement of the total binding antibody units (BAU/mL) against the receptor-binding domain of the SARS-CoV-2 spike protein (S-RBD). &lt;b>Aim:&lt;/b> This study aimed to evaluate the performance of the fluorescence LFA FinecareTM 2019-nCoV S-RBD test along with its reader (Model No.: FS-113) against the following reference methods: (i) the FDA-approved GenScript surrogate virus-neutralizing assay (sVNT); and (ii) three highly performing automated immunoassays: BioMérieux VIDAS&lt;sup>®&lt;/sup>3, Ortho VITROS&lt;sup>®&lt;/sup>, and Mindray CL-900i&lt;sup>®&lt;/sup>. &lt;b>Methods:&lt;/b> Plasma from 488 vaccinees was tested by all aforementioned assays. Fingerstick whole-blood samples from 156 vaccinees were also tested by FinecareTM. &lt;b>Results and conclusions:&lt;/b> FinecareTM showed 100% specificity, as none of the pre-pandemic samples tested positive. Equivalent FinecareTM results were observed among the samples taken from fingerstick or plasma (Pearson correlation &lt;i>r&lt;/i> = 0.9, &lt;i>p&lt;/i> &amp;lt; 0.0001), suggesting that fingerstick samples are sufficient to quantitate the S-RBD BAU/mL. A moderate correlation was observed between FinecareTM and sVNT (&lt;i>r =&lt;/i> 0.5, &lt;i>p&lt;/i> &amp;lt; 0.0001), indicating that FinecareTM can be used for rapid prediction of the neutralizing antibody (nAb) post-vaccination. FinecareTM BAU results showed strong correlation with VIDAS&lt;sup>®&lt;/sup>3 (&lt;i>r =&lt;/i> 0.6, &lt;i>p&lt;/i> &amp;lt; 0.0001) and moderate correlation with VITROS&lt;sup>®&lt;/sup> (&lt;i>r&lt;/i> = 0.5, &lt;i>p&lt;/i> &amp;lt; 0.0001) and CL-900i&lt;sup>®&lt;/sup> (&lt;i>r&lt;/i> = 0.4, &lt;i>p&lt;/i> &amp;lt; 0.0001), suggesting that FinecareTM can be used as a surrogate for the advanced automated assays to measure S-RBD BAU/mL.</pubmed_abstract><journal>Vaccines</journal><pubmed_title>Validation of a Novel Fluorescent Lateral Flow Assay for Rapid Qualitative and Quantitative Assessment of Total Anti-SARS-CoV-2 S-RBD Binding Antibody Units (BAU) from Plasma or Fingerstick Whole-Blood of COVID-19 Vaccinees.</pubmed_title><pmcid>PMC9415525</pmcid><funding_grant_id>UREP28-173-3- 057</funding_grant_id><pubmed_authors>Paul J</pubmed_authors><pubmed_authors>Abou-Saleh H</pubmed_authors><pubmed_authors>AlHamaydeh FM</pubmed_authors><pubmed_authors>Ismail A</pubmed_authors><pubmed_authors>Al-Sadeq DW</pubmed_authors><pubmed_authors>Younes N</pubmed_authors><pubmed_authors>Abo-Halawa BY</pubmed_authors><pubmed_authors>Nasrallah GK</pubmed_authors><pubmed_authors>Zedan HT</pubmed_authors><pubmed_authors>Daas HI</pubmed_authors><pubmed_authors>Thomas S</pubmed_authors><pubmed_authors>Aboalmaaly S</pubmed_authors><pubmed_authors>Ataelmannan S</pubmed_authors><pubmed_authors>Al Farsi A</pubmed_authors><pubmed_authors>Abu-Raddad LJ</pubmed_authors><pubmed_authors>Al-Buainain R</pubmed_authors><pubmed_authors>Majdalawieh AF</pubmed_authors><pubmed_authors>Elsharafi AE</pubmed_authors><pubmed_authors>Yassine HM</pubmed_authors><pubmed_authors>Shurrab FM</pubmed_authors><pubmed_authors>Al Saadi AS</pubmed_authors></additional><is_claimable>false</is_claimable><name>Validation of a Novel Fluorescent Lateral Flow Assay for Rapid Qualitative and Quantitative Assessment of Total Anti-SARS-CoV-2 S-RBD Binding Antibody Units (BAU) from Plasma or Fingerstick Whole-Blood of COVID-19 Vaccinees.</name><description>&lt;b>Background:&lt;/b> Limited commercial LFA assays are available to provide a reliable quantitative measurement of the total binding antibody units (BAU/mL) against the receptor-binding domain of the SARS-CoV-2 spike protein (S-RBD). &lt;b>Aim:&lt;/b> This study aimed to evaluate the performance of the fluorescence LFA FinecareTM 2019-nCoV S-RBD test along with its reader (Model No.: FS-113) against the following reference methods: (i) the FDA-approved GenScript surrogate virus-neutralizing assay (sVNT); and (ii) three highly performing automated immunoassays: BioMérieux VIDAS&lt;sup>®&lt;/sup>3, Ortho VITROS&lt;sup>®&lt;/sup>, and Mindray CL-900i&lt;sup>®&lt;/sup>. &lt;b>Methods:&lt;/b> Plasma from 488 vaccinees was tested by all aforementioned assays. Fingerstick whole-blood samples from 156 vaccinees were also tested by FinecareTM. &lt;b>Results and conclusions:&lt;/b> FinecareTM showed 100% specificity, as none of the pre-pandemic samples tested positive. Equivalent FinecareTM results were observed among the samples taken from fingerstick or plasma (Pearson correlation &lt;i>r&lt;/i> = 0.9, &lt;i>p&lt;/i> &amp;lt; 0.0001), suggesting that fingerstick samples are sufficient to quantitate the S-RBD BAU/mL. A moderate correlation was observed between FinecareTM and sVNT (&lt;i>r =&lt;/i> 0.5, &lt;i>p&lt;/i> &amp;lt; 0.0001), indicating that FinecareTM can be used for rapid prediction of the neutralizing antibody (nAb) post-vaccination. FinecareTM BAU results showed strong correlation with VIDAS&lt;sup>®&lt;/sup>3 (&lt;i>r =&lt;/i> 0.6, &lt;i>p&lt;/i> &amp;lt; 0.0001) and moderate correlation with VITROS&lt;sup>®&lt;/sup> (&lt;i>r&lt;/i> = 0.5, &lt;i>p&lt;/i> &amp;lt; 0.0001) and CL-900i&lt;sup>®&lt;/sup> (&lt;i>r&lt;/i> = 0.4, &lt;i>p&lt;/i> &amp;lt; 0.0001), suggesting that FinecareTM can be used as a surrogate for the advanced automated assays to measure S-RBD BAU/mL.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Aug</publication><modification>2024-11-15T17:11:46.3Z</modification><creation>2024-11-15T17:11:46.3Z</creation></dates><accession>S-EPMC9415525</accession><cross_references><pubmed>36016206</pubmed><doi>10.3390/vaccines10081318</doi></cross_references></HashMap>