<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(32)</volume><submitter>Cui L</submitter><pubmed_abstract>Currently available vaccines against COVID-19 showed high efficacy against the original strain of SARS-CoV-2 but progressively lower efficacy against new variants. In response to emerging SARS-CoV-2 strains, we propose chimeric DNA vaccines encoding the spike antigen, including a combination of selected key mutations from different variants of concern. We developed two DNA vaccines, pVAX-S1-TM-D614G and pVAX-S1-TM-INDUK (INDUK), encoding the SARS-CoV-2 S1 spike subunit in fusion with the transmembrane region that allows protein trimerization as predicted by &lt;i>in silico&lt;/i> analysis. pVAX-S1-TM-D614G included the dominant D614G substitution, while the chimeric vaccine INDUK contained additional selected mutations from the Delta (E484Q and L452R) and Alpha (N501Y and A570D) variants. Consid</pubmed_abstract><journal>ACS omega</journal><pagination>34624-34635</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11325517</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Enhancing Immune Responses against SARS-CoV-2 Variants in Aged Mice with INDUK: A Chimeric DNA Vaccine Encoding the Spike S1-TM Subunits.</pubmed_title><pmcid>PMC11325517</pmcid><pubmed_authors>Renzi S</pubmed_authors><pubmed_authors>Pozzi D</pubmed_authors><pubmed_authors>Pesce L</pubmed_authors><pubmed_authors>Marchini C</pubmed_authors><pubmed_authors>Cui L</pubmed_authors><pubmed_authors>Quagliarini E</pubmed_authors><pubmed_authors>Cardarelli F</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Bartozzi B</pubmed_authors><pubmed_authors>Xiao S</pubmed_authors><pubmed_authors>Orlando F</pubmed_authors><pubmed_authors>Amici A</pubmed_authors><pubmed_authors>Provinciali M</pubmed_authors><pubmed_authors>Giacconi R</pubmed_authors><pubmed_authors>Galeazzi R</pubmed_authors><pubmed_authors>Malavolta M</pubmed_authors><pubmed_authors>Caracciolo G</pubmed_authors><pubmed_authors>Giorgini G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Enhancing Immune Responses against SARS-CoV-2 Variants in Aged Mice with INDUK: A Chimeric DNA Vaccine Encoding the Spike S1-TM Subunits.</name><description>Currently available vaccines against COVID-19 showed high efficacy against the original strain of SARS-CoV-2 but progressively lower efficacy against new variants. In response to emerging SARS-CoV-2 strains, we propose chimeric DNA vaccines encoding the spike antigen, including a combination of selected key mutations from different variants of concern. We developed two DNA vaccines, pVAX-S1-TM-D614G and pVAX-S1-TM-INDUK (INDUK), encoding the SARS-CoV-2 S1 spike subunit in fusion with the transmembrane region that allows protein trimerization as predicted by &lt;i>in silico&lt;/i> analysis. pVAX-S1-TM-D614G included the dominant D614G substitution, while the chimeric vaccine INDUK contained additional selected mutations from the Delta (E484Q and L452R) and Alpha (N501Y and A570D) variants. Consid</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Aug</publication><modification>2026-06-03T00:39:57.447Z</modification><creation>2025-04-19T13:51:55.688Z</creation></dates><accession>S-EPMC11325517</accession><cross_references><pubmed>39157118</pubmed><doi>10.1021/acsomega.4c03285</doi></cross_references></HashMap>