<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lee A</submitter><funding>NIDDK NIH HHS</funding><funding>NIAID NIH HHS</funding><funding>U.S. Department of Health &amp;amp; Human Services | National Institutes of Health</funding><pagination>549</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8795432</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(1)</volume><pubmed_abstract>Adjuvants hold great potential in enhancing vaccine efficacy, making the understanding and improving of adjuvants critical goals in vaccinology. The TLR7/8 agonist, 3M-052, induces long-lived humoral immunity in non-human primates and is currently being evaluated in human clinical trials. However, the innate mechanisms of 3M-052 have not been fully characterized. Here, we perform flow cytometry, single cell RNA-seq and ATAC-seq to profile the kinetics, transcriptomics and epigenomics of innate immune cells in murine draining lymph nodes following 3M-052-Alum/Ovalbumin immunization. We find that 3M-052-Alum/OVA induces a robust antiviral and interferon gene program, similar to the yellow fever vaccine, which is known to confer long-lasting protection. Activation of myeloid cells in dLNs persists through day 28 and single cell analysis reveals putative TF-gene regulatory programs in distinct myeloid cells and heterogeneity of monocytes. This study provides a comprehensive characterization of the transcriptomics and epigenomics of innate populations in the dLNs after vaccination.</pubmed_abstract><journal>Nature communications</journal><pubmed_title>A molecular atlas of innate immunity to adjuvanted and live attenuated vaccines, in mice.</pubmed_title><pmcid>PMC8795432</pmcid><funding_grant_id>U19 AI057266</funding_grant_id><funding_grant_id>R01 AI048638; R37 DK057665; U19 AI057266; U19 AI090023</funding_grant_id><funding_grant_id>R37 DK057665</funding_grant_id><funding_grant_id>U19 AI057229</funding_grant_id><funding_grant_id>U19 AI109662</funding_grant_id><funding_grant_id>U19 AI090023</funding_grant_id><funding_grant_id>R01 AI048638</funding_grant_id><funding_grant_id>R01 AI125197</funding_grant_id><pubmed_authors>Lee A</pubmed_authors><pubmed_authors>Wimmers F</pubmed_authors><pubmed_authors>Arunachalam PS</pubmed_authors><pubmed_authors>Tomai M</pubmed_authors><pubmed_authors>Fox CB</pubmed_authors><pubmed_authors>Luo W</pubmed_authors><pubmed_authors>Scott MKD</pubmed_authors><pubmed_authors>Khatri P</pubmed_authors><pubmed_authors>Pulendran B</pubmed_authors></additional><is_claimable>false</is_claimable><name>A molecular atlas of innate immunity to adjuvanted and live attenuated vaccines, in mice.</name><description>Adjuvants hold great potential in enhancing vaccine efficacy, making the understanding and improving of adjuvants critical goals in vaccinology. The TLR7/8 agonist, 3M-052, induces long-lived humoral immunity in non-human primates and is currently being evaluated in human clinical trials. However, the innate mechanisms of 3M-052 have not been fully characterized. Here, we perform flow cytometry, single cell RNA-seq and ATAC-seq to profile the kinetics, transcriptomics and epigenomics of innate immune cells in murine draining lymph nodes following 3M-052-Alum/Ovalbumin immunization. We find that 3M-052-Alum/OVA induces a robust antiviral and interferon gene program, similar to the yellow fever vaccine, which is known to confer long-lasting protection. Activation of myeloid cells in dLNs persists through day 28 and single cell analysis reveals putative TF-gene regulatory programs in distinct myeloid cells and heterogeneity of monocytes. This study provides a comprehensive characterization of the transcriptomics and epigenomics of innate populations in the dLNs after vaccination.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jan</publication><modification>2024-11-14T03:50:34.242Z</modification><creation>2024-11-14T03:50:34.242Z</creation></dates><accession>S-EPMC8795432</accession><cross_references><pubmed>35087093</pubmed><doi>10.1038/s41467-022-28197-9</doi></cross_references></HashMap>