<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Meng X</submitter><funding>Pathogen Ecology, Immune Characteristics and New Vaccine Research of Giant Pandas</funding><funding>the Jilin Province Youth Talent Support Project</funding><pagination>2406280</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11443554</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(1)</volume><pubmed_abstract>Rabies, caused by the Rabies virus (RABV), is a highly fatal zoonotic disease. Existing rabies vaccines have demonstrated good immune efficacy, but the complexity of immunization procedures and high cost has impeded the elimination of RABV, particularly in the post-COVID-19 era. There is a pressing need for safer and more effective rabies vaccines that streamline vaccination protocols and reduce expense. To meet this need, we have developed a potential rabies vaccine candidate called ALVAC-RABV-VLP, utilizing CRISPR/Cas9 gene editing technology. This vaccine employs a canarypox virus vector (ALVAC) to generate RABV virus-like particles (VLPs). In mice, a single dose of ALVAC-RABV-VLP effectively activated dendritic cells (DCs), follicular helper T cells (Tfh), and the germinal centre (GC)/</pubmed_abstract><journal>Emerging microbes &amp; infections</journal><pubmed_title>A single dose of an ALVAC vector-based RABV virus-like particle candidate vaccine induces a potent immune response in mice, cats and dogs.</pubmed_title><pmcid>PMC11443554</pmcid><funding_grant_id>2019-93-1</funding_grant_id><pubmed_authors>Xia X</pubmed_authors><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Cong H</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Meng X</pubmed_authors><pubmed_authors>Zhao Y</pubmed_authors><pubmed_authors>Li N</pubmed_authors><pubmed_authors>Feng N</pubmed_authors><pubmed_authors>Wang S</pubmed_authors><pubmed_authors>Wang T</pubmed_authors><pubmed_authors>Gao Y</pubmed_authors><pubmed_authors>Wang W</pubmed_authors><pubmed_authors>Yan F</pubmed_authors></additional><is_claimable>false</is_claimable><name>A single dose of an ALVAC vector-based RABV virus-like particle candidate vaccine induces a potent immune response in mice, cats and dogs.</name><description>Rabies, caused by the Rabies virus (RABV), is a highly fatal zoonotic disease. Existing rabies vaccines have demonstrated good immune efficacy, but the complexity of immunization procedures and high cost has impeded the elimination of RABV, particularly in the post-COVID-19 era. There is a pressing need for safer and more effective rabies vaccines that streamline vaccination protocols and reduce expense. To meet this need, we have developed a potential rabies vaccine candidate called ALVAC-RABV-VLP, utilizing CRISPR/Cas9 gene editing technology. This vaccine employs a canarypox virus vector (ALVAC) to generate RABV virus-like particles (VLPs). In mice, a single dose of ALVAC-RABV-VLP effectively activated dendritic cells (DCs), follicular helper T cells (Tfh), and the germinal centre (GC)/</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Dec</publication><modification>2026-06-06T22:14:39.771Z</modification><creation>2025-04-06T22:37:46.859Z</creation></dates><accession>S-EPMC11443554</accession><cross_references><pubmed>39295522</pubmed><doi>10.1080/22221751.2024.2406280</doi></cross_references></HashMap>