<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(51)</volume><submitter>Fan N</submitter><pubmed_abstract>It is urgent to develop more effective mRNA vaccines against the emerging severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants owing to the immune escape. Here, we constructed a novel mRNA delivery system [IC8/Mn lipid nanoparticles (IC8/Mn LNPs)]with high immunogenicity, via introducing a stimulator of interferon genes (STING) agonist [manganese (Mn)] based on a newly synthesized ionizable lipid (IC8). It was found that Mn can not only promote maturation of antigen-presenting cells via activating STING pathway but also improve mRNA expression by facilitating lysosomal escape for the first time. Subsequently, IC8/Mn LNPs loaded with mRNA encoding the Spike protein of SARS-CoV-2 Delta or Omicron variant (IC8/Mn@D or IC8/Mn@O) were prepared. Both mRNA vaccines induced substantial specific immunoglobulin G responses against Delta or Omicron. IC8/Mn@D displayed strong pseudovirus neutralization ability, T helper 1-biased immune responses, and good safety. It can be concluded that IC8/Mn LNPs have great potential for developing Mn-coordinated mRNA vaccines with robust immunogenicity and good safety.</pubmed_abstract><journal>Science advances</journal><pagination>eabq3500</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9788765</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Manganese-coordinated mRNA vaccines with enhanced mRNA expression and immunogenicity induce robust immune responses against SARS-CoV-2 variants.</pubmed_title><pmcid>PMC9788765</pmcid><pubmed_authors>Chen K</pubmed_authors><pubmed_authors>Zhao C</pubmed_authors><pubmed_authors>Gu Y</pubmed_authors><pubmed_authors>Huang H</pubmed_authors><pubmed_authors>Fan N</pubmed_authors><pubmed_authors>Xiao W</pubmed_authors><pubmed_authors>Zheng Q</pubmed_authors><pubmed_authors>Wei Y</pubmed_authors><pubmed_authors>Qin S</pubmed_authors><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Li S</pubmed_authors><pubmed_authors>Zhang Z</pubmed_authors><pubmed_authors>He Z</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>He X</pubmed_authors><pubmed_authors>Jiang X</pubmed_authors><pubmed_authors>Zhu R</pubmed_authors><pubmed_authors>Song X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Manganese-coordinated mRNA vaccines with enhanced mRNA expression and immunogenicity induce robust immune responses against SARS-CoV-2 variants.</name><description>It is urgent to develop more effective mRNA vaccines against the emerging severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants owing to the immune escape. Here, we constructed a novel mRNA delivery system [IC8/Mn lipid nanoparticles (IC8/Mn LNPs)]with high immunogenicity, via introducing a stimulator of interferon genes (STING) agonist [manganese (Mn)] based on a newly synthesized ionizable lipid (IC8). It was found that Mn can not only promote maturation of antigen-presenting cells via activating STING pathway but also improve mRNA expression by facilitating lysosomal escape for the first time. Subsequently, IC8/Mn LNPs loaded with mRNA encoding the Spike protein of SARS-CoV-2 Delta or Omicron variant (IC8/Mn@D or IC8/Mn@O) were prepared. Both mRNA vaccines induced substantial specific immunoglobulin G responses against Delta or Omicron. IC8/Mn@D displayed strong pseudovirus neutralization ability, T helper 1-biased immune responses, and good safety. It can be concluded that IC8/Mn LNPs have great potential for developing Mn-coordinated mRNA vaccines with robust immunogenicity and good safety.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2026-06-04T08:01:26.297Z</modification><creation>2025-04-04T21:09:49.542Z</creation></dates><accession>S-EPMC9788765</accession><cross_references><pubmed>36563159</pubmed><doi>10.1126/sciadv.abq3500</doi></cross_references></HashMap>