<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chen R</submitter><funding>Fundamental Research Funds for the Central Universities</funding><funding>Guangzhou Basic and Applied Basic Research Program</funding><funding>Special Research and Development Program of Guangzhou</funding><funding>Important Key Program of Natural Science Foundation of China</funding><funding>Pearl River S and T Nova Program of Guangzhou</funding><funding>Special 2019-nCoV Program of NSFC</funding><funding>National Natural Science Foundation of China</funding><funding>High-level Biosafety Laboratory Construction Program of the Science and Technology Projects of Guangdong Province of China</funding><funding>Emergency Key Program of Guangzhou Laboratory</funding><funding>Exchange Program of NSFC</funding><funding>Shenzhen Science and Technology Program</funding><pagination>e2105378</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9008796</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(11)</volume><pubmed_abstract>The SARS-CoV-2 Delta (B.1.617.2) strain is a variant of concern (VOC) that has become the dominant strain worldwide in 2021. Its transmission capacity is approximately twice that of the original strain, with a shorter incubation period and higher viral load during infection. Importantly, the breakthrough infections of the Delta variant have continued to emerge in the first-generation vaccine recipients. There is thus an urgent need to develop a novel vaccine with SARS-CoV-2 variants as the major target. Here, receptor binding domain (RBD)-conjugated nanoparticle vaccines targeting the Delta variant, as well as the early and Beta/Gamma strains, are developed. Under both a single-dose and a prime-boost strategy, these RBD-conjugated nanoparticle vaccines induce the abundant neutralizing anti</pubmed_abstract><journal>Advanced science (Weinheim, Baden-Wurttemberg, Germany)</journal><pubmed_title>Development of Receptor Binding Domain (RBD)-Conjugated Nanoparticle Vaccines with Broad Neutralization against SARS-CoV-2 Delta and Other Variants.</pubmed_title><pmcid>PMC9008796</pmcid><funding_grant_id>201806010118</funding_grant_id><funding_grant_id>2021B1212030012</funding_grant_id><funding_grant_id>32100743</funding_grant_id><funding_grant_id>82150710553</funding_grant_id><funding_grant_id>82041002</funding_grant_id><funding_grant_id>JCYJ20200109142601702</funding_grant_id><funding_grant_id>202102021094</funding_grant_id><funding_grant_id>EKPG21-24</funding_grant_id><funding_grant_id>92169201</funding_grant_id><funding_grant_id>81971918</funding_grant_id><funding_grant_id>202102021058</funding_grant_id><funding_grant_id>202008070010</funding_grant_id><funding_grant_id>2021qntd43</funding_grant_id><funding_grant_id>JSGG20200225150431472</funding_grant_id><funding_grant_id>81730060</funding_grant_id><funding_grant_id>82171825</funding_grant_id><pubmed_authors>Peng Y</pubmed_authors><pubmed_authors>Zhang H</pubmed_authors><pubmed_authors>Deng J</pubmed_authors><pubmed_authors>Wu B</pubmed_authors><pubmed_authors>Deng K</pubmed_authors><pubmed_authors>Wang G</pubmed_authors><pubmed_authors>Lin Y</pubmed_authors><pubmed_authors>Zou F</pubmed_authors><pubmed_authors>Liang C</pubmed_authors><pubmed_authors>Wu S</pubmed_authors><pubmed_authors>Liang L</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Chen R</pubmed_authors><pubmed_authors>Deng X</pubmed_authors><pubmed_authors>Yuan Y</pubmed_authors><pubmed_authors>Zhou M</pubmed_authors><pubmed_authors>Xi Z</pubmed_authors><pubmed_authors>Li C</pubmed_authors><pubmed_authors>Pan T</pubmed_authors><pubmed_authors>Li R</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Bu X</pubmed_authors><pubmed_authors>Zhang Z</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>He X</pubmed_authors><pubmed_authors>Yan H</pubmed_authors><pubmed_authors>Ke C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Development of Receptor Binding Domain (RBD)-Conjugated Nanoparticle Vaccines with Broad Neutralization against SARS-CoV-2 Delta and Other Variants.</name><description>The SARS-CoV-2 Delta (B.1.617.2) strain is a variant of concern (VOC) that has become the dominant strain worldwide in 2021. Its transmission capacity is approximately twice that of the original strain, with a shorter incubation period and higher viral load during infection. Importantly, the breakthrough infections of the Delta variant have continued to emerge in the first-generation vaccine recipients. There is thus an urgent need to develop a novel vaccine with SARS-CoV-2 variants as the major target. Here, receptor binding domain (RBD)-conjugated nanoparticle vaccines targeting the Delta variant, as well as the early and Beta/Gamma strains, are developed. Under both a single-dose and a prime-boost strategy, these RBD-conjugated nanoparticle vaccines induce the abundant neutralizing anti</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Apr</publication><modification>2025-04-05T00:40:03.296Z</modification><creation>2024-11-15T17:04:57.924Z</creation></dates><accession>S-EPMC9008796</accession><cross_references><pubmed>35142444</pubmed><doi>10.1002/advs.202105378</doi></cross_references></HashMap>