<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Pino M</submitter><funding>National Institute of Allergy and Infectious Diseases</funding><funding>Office of Public Affairs</funding><funding>Childhood Infections and Vaccines Children Healthcare of Atlanta 712 Woodruff Health Sciences Center</funding><funding>NIAID NIH HHS</funding><funding>Baylor University</funding><funding>Yerkes National Primate Research Center, Emory University</funding><funding>National Institutes of Health</funding><funding>Scientific Advisory Board of MaxHealth 724 Biotechnology LLC</funding><funding>NIH HHS</funding><pagination>eabh3634</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9119307</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>6(61)</volume><pubmed_abstract>Ongoing SARS-CoV-2 vaccine development is focused on identifying stable, cost-effective, and accessible candidates for global use, specifically in low and middle-income countries. Here, we report the efficacy of a rapidly scalable, novel yeast expressed SARS-CoV-2 specific receptor-binding domain (RBD) based vaccine in rhesus macaques. We formulated the RBD immunogen in alum, a licensed and an emerging alum adsorbed TLR-7/8 targeted, 3M-052-alum adjuvants. The RBD+3M-052-alum adjuvanted vaccine promoted better RBD binding and effector antibodies, higher CoV-2 neutralizing antibodies, improved Th1 biased CD4+T cell reactions, and increased CD8+ T cell responses when compared to the alum-alone adjuvanted vaccine. RBD+3M-052-alum induced a significant reduction of SARS-CoV-2 virus in respirat</pubmed_abstract><journal>Science immunology</journal><pubmed_title>A yeast expressed RBD-based SARS-CoV-2 vaccine formulated with 3M-052-alum adjuvant promotes protective efficacy in non-human primates.</pubmed_title><pmcid>PMC9119307</pmcid><funding_grant_id>75N9301900065</funding_grant_id><funding_grant_id>22206</funding_grant_id><funding_grant_id>3U19AI057266-17S1</funding_grant_id><funding_grant_id>U19 AI057266</funding_grant_id><funding_grant_id>TLR-7/8 723</funding_grant_id><funding_grant_id>US 2019/0142935</funding_grant_id><funding_grant_id>P51 OD011132</funding_grant_id><funding_grant_id>U19 AI090023</funding_grant_id><funding_grant_id>HHSN272201800004C</funding_grant_id><funding_grant_id>2020 COVID-19 CURE A</funding_grant_id><funding_grant_id>P30 A050509</funding_grant_id><funding_grant_id>ORIP/OD P51OD011132</funding_grant_id><funding_grant_id>3U19AI057266-715</funding_grant_id><funding_grant_id>HIPC COVID-19 S</funding_grant_id><funding_grant_id>COVID-19 RBD</funding_grant_id><funding_grant_id>P51-OD011132</funding_grant_id><funding_grant_id>U19AI090023</funding_grant_id><pubmed_authors>Pacheco-Sanchez G</pubmed_authors><pubmed_authors>Gumber S</pubmed_authors><pubmed_authors>Jean SM</pubmed_authors><pubmed_authors>Sette A</pubmed_authors><pubmed_authors>Paiardini M</pubmed_authors><pubmed_authors>Pollara J</pubmed_authors><pubmed_authors>Mielke D</pubmed_authors><pubmed_authors>Lee J</pubmed_authors><pubmed_authors>Gao H</pubmed_authors><pubmed_authors>Wood JS</pubmed_authors><pubmed_authors>Suthar MS</pubmed_authors><pubmed_authors>Abid T</pubmed_authors><pubmed_authors>Liu Z</pubmed_authors><pubmed_authors>Dutta D</pubmed_authors><pubmed_authors>Edara VV</pubmed_authors><pubmed_authors>Wang S</pubmed_authors><pubmed_authors>Strych U</pubmed_authors><pubmed_authors>Shenvi N</pubmed_authors><pubmed_authors>Sekaly RP</pubmed_authors><pubmed_authors>Hotez PJ</pubmed_authors><pubmed_authors>Montefiori DC</pubmed_authors><pubmed_authors>Stammen RL</pubmed_authors><pubmed_authors>Wei J</pubmed_authors><pubmed_authors>Shen X</pubmed_authors><pubmed_authors>Smith JC</pubmed_authors><pubmed_authors>Connor-Stroud F</pubmed_authors><pubmed_authors>Kasturi SP</pubmed_authors><pubmed_authors>Vanderford TH</pubmed_authors><pubmed_authors>Pollet J</pubmed_authors><pubmed_authors>Zhan B</pubmed_authors><pubmed_authors>Latif MB</pubmed_authors><pubmed_authors>Tomai MA</pubmed_authors><pubmed_authors>Pereira Ribeiro S</pubmed_authors><pubmed_authors>Ferrari G</pubmed_authors><pubmed_authors>Bottazzi ME</pubmed_authors><pubmed_authors>Floyd K</pubmed_authors><pubmed_authors>Weiskopf D</pubmed_authors><pubmed_authors>Kozlowski PA</pubmed_authors><pubmed_authors>Kirejczyk S</pubmed_authors><pubmed_authors>LaBranche CC</pubmed_authors><pubmed_authors>Fox CB</pubmed_authors><pubmed_authors>Chen WH</pubmed_authors><pubmed_authors>Easley K</pubmed_authors><pubmed_authors>Pino M</pubmed_authors><pubmed_authors>Eisel N</pubmed_authors><pubmed_authors>Cohen J</pubmed_authors><pubmed_authors>Tomaras GD</pubmed_authors></additional><is_claimable>false</is_claimable><name>A yeast expressed RBD-based SARS-CoV-2 vaccine formulated with 3M-052-alum adjuvant promotes protective efficacy in non-human primates.</name><description>Ongoing SARS-CoV-2 vaccine development is focused on identifying stable, cost-effective, and accessible candidates for global use, specifically in low and middle-income countries. Here, we report the efficacy of a rapidly scalable, novel yeast expressed SARS-CoV-2 specific receptor-binding domain (RBD) based vaccine in rhesus macaques. We formulated the RBD immunogen in alum, a licensed and an emerging alum adsorbed TLR-7/8 targeted, 3M-052-alum adjuvants. The RBD+3M-052-alum adjuvanted vaccine promoted better RBD binding and effector antibodies, higher CoV-2 neutralizing antibodies, improved Th1 biased CD4+T cell reactions, and increased CD8+ T cell responses when compared to the alum-alone adjuvanted vaccine. RBD+3M-052-alum induced a significant reduction of SARS-CoV-2 virus in respirat</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Jul</publication><modification>2026-05-09T15:04:56.79Z</modification><creation>2025-04-04T08:38:53.627Z</creation></dates><accession>S-EPMC9119307</accession><cross_references><pubmed>34266981</pubmed><doi>10.1126/sciimmunol.abh3634</doi></cross_references></HashMap>