<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Svetlova J</submitter><funding>Russian Science Foundation</funding><pagination>13220</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9655829</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>23(21)</volume><pubmed_abstract>Mutations in surface proteins enable emerging variants of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) to escape a substantial fraction of neutralizing antibodies and may thus weaken vaccine-driven immunity. To compare available vaccines and justify revaccination, rapid evaluation of antibody (Ab) responses to currently circulating SARS-CoV-2 variants of interest (VOI) and concern (VOC) is needed. Here, we developed a multiplex protein microarray-based system for rapid profiling of anti-SARS-CoV-2 Ab levels in human sera. The microarray system was validated using sera samples from SARS-CoV-2-free donors and those diagnosed with COVID-19 based on PCR and enzyme immunoassays. Microarray-based profiling of vaccinated donors revealed a substantial difference in anti-VOC Ab leve</pubmed_abstract><journal>International journal of molecular sciences</journal><pubmed_title>Microarray Profiling of Vaccination-Induced Antibody Responses to SARS-CoV-2 Variants of Interest and Concern.</pubmed_title><pmcid>PMC9655829</pmcid><funding_grant_id>22-25-00420</funding_grant_id><pubmed_authors>Kharlampieva D</pubmed_authors><pubmed_authors>Gustin D</pubmed_authors><pubmed_authors>Shirokov D</pubmed_authors><pubmed_authors>Svetlova J</pubmed_authors><pubmed_authors>Varizhuk A</pubmed_authors><pubmed_authors>Lazarev V</pubmed_authors><pubmed_authors>Shokina V</pubmed_authors><pubmed_authors>Vedekhina T</pubmed_authors><pubmed_authors>Manuvera V</pubmed_authors><pubmed_authors>Matyushkina D</pubmed_authors><pubmed_authors>Aldarov K</pubmed_authors><pubmed_authors>Bespyatykh J</pubmed_authors><pubmed_authors>Prusakov K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Microarray Profiling of Vaccination-Induced Antibody Responses to SARS-CoV-2 Variants of Interest and Concern.</name><description>Mutations in surface proteins enable emerging variants of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) to escape a substantial fraction of neutralizing antibodies and may thus weaken vaccine-driven immunity. To compare available vaccines and justify revaccination, rapid evaluation of antibody (Ab) responses to currently circulating SARS-CoV-2 variants of interest (VOI) and concern (VOC) is needed. Here, we developed a multiplex protein microarray-based system for rapid profiling of anti-SARS-CoV-2 Ab levels in human sera. The microarray system was validated using sera samples from SARS-CoV-2-free donors and those diagnosed with COVID-19 based on PCR and enzyme immunoassays. Microarray-based profiling of vaccinated donors revealed a substantial difference in anti-VOC Ab leve</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Oct</publication><modification>2025-04-25T23:22:47.639Z</modification><creation>2025-04-06T09:23:08.035Z</creation></dates><accession>S-EPMC9655829</accession><cross_references><pubmed>36362010</pubmed><doi>10.3390/ijms232113220</doi></cross_references></HashMap>