<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>27(10)</volume><submitter>Martinez EJ</submitter><funding>DOD</funding><pubmed_abstract>The rapid emergence of SARS-CoV-2 variants of concern (VoC) and the threat of future zoonotic sarbecovirus spillover emphasizes the need for broadly protective next-generation vaccines and therapeutics. We utilized SARS-CoV-2 spike ferritin nanoparticle (SpFN), and SARS-CoV-2 receptor binding domain ferritin nanoparticle (RFN) immunogens, in an equine model to elicit hyperimmune sera and evaluated its sarbecovirus neutralization and protection capacity. Immunized animals rapidly elicited sera with the potent neutralization of SARS-CoV-2 VoC, and SARS-CoV-1 pseudoviruses, and potent binding against receptor binding domains from sarbecovirus clades 1b, 1a, 2, 3, and 4. Purified equine polyclonal IgG provided protection against Omicron XBB.1.5 virus in the K18-hACE2 transgenic mouse model. Th</pubmed_abstract><journal>iScience</journal><pagination>110624</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11440237</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>SARS-CoV-2 ferritin nanoparticle vaccines produce hyperimmune equine sera with broad sarbecovirus activity.</pubmed_title><pmcid>PMC11440237</pmcid><pubmed_authors>Peterson CE</pubmed_authors><pubmed_authors>Collins ND</pubmed_authors><pubmed_authors>Duso D</pubmed_authors><pubmed_authors>Sankhala RS</pubmed_authors><pubmed_authors>Reagan M</pubmed_authors><pubmed_authors>Gambacurta J</pubmed_authors><pubmed_authors>Lanzer K</pubmed_authors><pubmed_authors>Vasan S</pubmed_authors><pubmed_authors>Choe M</pubmed_authors><pubmed_authors>Thomas PV</pubmed_authors><pubmed_authors>Gromowski GD</pubmed_authors><pubmed_authors>Kimner J</pubmed_authors><pubmed_authors>Kuklis C</pubmed_authors><pubmed_authors>King J</pubmed_authors><pubmed_authors>Dussupt V</pubmed_authors><pubmed_authors>Corbett C</pubmed_authors><pubmed_authors>Kummer L</pubmed_authors><pubmed_authors>Joyce MG</pubmed_authors><pubmed_authors>Mayer SV</pubmed_authors><pubmed_authors>Hart T</pubmed_authors><pubmed_authors>Mendez-Rivera L</pubmed_authors><pubmed_authors>Rees PA</pubmed_authors><pubmed_authors>Chang WC</pubmed_authors><pubmed_authors>Soman S</pubmed_authors><pubmed_authors>Hvizdos J</pubmed_authors><pubmed_authors>Jensen JL</pubmed_authors><pubmed_authors>Kaundinya J</pubmed_authors><pubmed_authors>Fernandes A</pubmed_authors><pubmed_authors>Modjarrad K</pubmed_authors><pubmed_authors>Chen WH</pubmed_authors><pubmed_authors>Cookenham T</pubmed_authors><pubmed_authors>Krebs SJ</pubmed_authors><pubmed_authors>Hajduczki A</pubmed_authors><pubmed_authors>Michael NL</pubmed_authors><pubmed_authors>Martinez EJ</pubmed_authors><pubmed_authors>Murzello K</pubmed_authors></additional><is_claimable>false</is_claimable><name>SARS-CoV-2 ferritin nanoparticle vaccines produce hyperimmune equine sera with broad sarbecovirus activity.</name><description>The rapid emergence of SARS-CoV-2 variants of concern (VoC) and the threat of future zoonotic sarbecovirus spillover emphasizes the need for broadly protective next-generation vaccines and therapeutics. We utilized SARS-CoV-2 spike ferritin nanoparticle (SpFN), and SARS-CoV-2 receptor binding domain ferritin nanoparticle (RFN) immunogens, in an equine model to elicit hyperimmune sera and evaluated its sarbecovirus neutralization and protection capacity. Immunized animals rapidly elicited sera with the potent neutralization of SARS-CoV-2 VoC, and SARS-CoV-1 pseudoviruses, and potent binding against receptor binding domains from sarbecovirus clades 1b, 1a, 2, 3, and 4. Purified equine polyclonal IgG provided protection against Omicron XBB.1.5 virus in the K18-hACE2 transgenic mouse model. Th</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Oct</publication><modification>2026-07-15T04:15:14.546Z</modification><creation>2025-04-04T08:17:33.27Z</creation></dates><accession>S-EPMC11440237</accession><cross_references><pubmed>39351195</pubmed><doi>10.1016/j.isci.2024.110624</doi></cross_references></HashMap>