<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11(4)</volume><submitter>Ding Y</submitter><pubmed_abstract>Waves of breakthrough infections by SARS-CoV-2 Omicron subvariants currently pose a global challenge to the control of the COVID-19 pandemic. We previously reported a pVAX1-based DNA vaccine candidate, pAD1002, that encodes a receptor-binding domain (RBD) chimera of SARS-CoV-1 and Omicron BA.1. In mouse and rabbit models, pAD1002 plasmid induced cross-neutralizing Abs against heterologous sarbecoviruses, including SARS-CoV-1 and SARS-CoV-2 wildtype, Delta and Omicron variants. However, these antisera failed to block the recent emerging Omicron subvariants BF.7 and BQ.1. To solve this problem, we replaced the BA.1 RBD-encoding DNA sequence in pAD1002 with that of BA.4/5. The resulting construct, namely pAD1016, elicited SARS-CoV-1 and SARS-CoV-2 RBD-specific IFN-γ&lt;sup>+&lt;/sup> cellular respo</pubmed_abstract><journal>Vaccines</journal><pagination>778</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10144402</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A COVID-19 DNA Vaccine Candidate Elicits Broadly Neutralizing Antibodies against Multiple SARS-CoV-2 Variants including the Currently Circulating Omicron BA.5, BF.7, BQ.1 and XBB.</pubmed_title><pmcid>PMC10144402</pmcid><pubmed_authors>Fan F</pubmed_authors><pubmed_authors>Gao XM</pubmed_authors><pubmed_authors>Ding Y</pubmed_authors><pubmed_authors>Wang B</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Zhao G</pubmed_authors><pubmed_authors>Xu X</pubmed_authors><pubmed_authors>Zhao H</pubmed_authors><pubmed_authors>Wang L</pubmed_authors></additional><is_claimable>false</is_claimable><name>A COVID-19 DNA Vaccine Candidate Elicits Broadly Neutralizing Antibodies against Multiple SARS-CoV-2 Variants including the Currently Circulating Omicron BA.5, BF.7, BQ.1 and XBB.</name><description>Waves of breakthrough infections by SARS-CoV-2 Omicron subvariants currently pose a global challenge to the control of the COVID-19 pandemic. We previously reported a pVAX1-based DNA vaccine candidate, pAD1002, that encodes a receptor-binding domain (RBD) chimera of SARS-CoV-1 and Omicron BA.1. In mouse and rabbit models, pAD1002 plasmid induced cross-neutralizing Abs against heterologous sarbecoviruses, including SARS-CoV-1 and SARS-CoV-2 wildtype, Delta and Omicron variants. However, these antisera failed to block the recent emerging Omicron subvariants BF.7 and BQ.1. To solve this problem, we replaced the BA.1 RBD-encoding DNA sequence in pAD1002 with that of BA.4/5. The resulting construct, namely pAD1016, elicited SARS-CoV-1 and SARS-CoV-2 RBD-specific IFN-γ&lt;sup>+&lt;/sup> cellular respo</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Mar</publication><modification>2025-04-04T19:18:37.49Z</modification><creation>2024-11-09T14:47:28.609Z</creation></dates><accession>S-EPMC10144402</accession><cross_references><pubmed>37112691</pubmed><doi>10.3390/vaccines11040778</doi></cross_references></HashMap>