<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sanchez J</submitter><funding>Horizon 2020 Framework Programme</funding><funding>NIAID NIH HHS</funding><funding>Seventh Framework Programme</funding><pagination>586124</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7683801</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Our previous work has demonstrated the benefits of transcutaneous immunization in targeting Langerhans cells and preferentially inducing CD8 T-cell responses.&lt;h4>Methods&lt;/h4>In this randomized phase Ib clinical trial including 20 HIV uninfected volunteers, we compared the safety and immunogenicity of the MVA recombinant vaccine expressing HIV-B antigen (MVA-B) by transcutaneous and intramuscular routes. We hypothesized that the quality of innate and adaptive immunity differs according to the route of immunization and explored the quality of the vector vaccine-induced immune responses. We also investigated the early blood transcriptome and serum cytokine levels to identify innate events correlated with the strength and quality of adaptive immunity.&lt;h4>Results&lt;/h4>We demon</pubmed_abstract><journal>Frontiers in immunology</journal><pubmed_title>Immune Profiles Identification by Vaccinomics After MVA Immunization in Randomized Clinical Study.</pubmed_title><pmcid>PMC7683801</pmcid><funding_grant_id>P01 AI131568</funding_grant_id><pubmed_authors>Bonduelle O</pubmed_authors><pubmed_authors>Esteban M</pubmed_authors><pubmed_authors>Gomez CE</pubmed_authors><pubmed_authors>Perez S</pubmed_authors><pubmed_authors>Combadiere B</pubmed_authors><pubmed_authors>Soria A</pubmed_authors><pubmed_authors>Vogt A</pubmed_authors><pubmed_authors>Sanchez J</pubmed_authors><pubmed_authors>Llano A</pubmed_authors><pubmed_authors>Mothe B</pubmed_authors><pubmed_authors>Lama JR</pubmed_authors><pubmed_authors>Fernandez-Maldonado M</pubmed_authors><pubmed_authors>Garcia F</pubmed_authors><pubmed_authors>Goncalves E</pubmed_authors><pubmed_authors>Gonzales P</pubmed_authors><pubmed_authors>Fernandez MA</pubmed_authors><pubmed_authors>de Bernard S</pubmed_authors><pubmed_authors>Pedruzzi E</pubmed_authors><pubmed_authors>Brander C</pubmed_authors><pubmed_authors>Cedeno S</pubmed_authors><pubmed_authors>Nourikyan J</pubmed_authors><pubmed_authors>Ganoza C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Immune Profiles Identification by Vaccinomics After MVA Immunization in Randomized Clinical Study.</name><description>&lt;h4>Background&lt;/h4>Our previous work has demonstrated the benefits of transcutaneous immunization in targeting Langerhans cells and preferentially inducing CD8 T-cell responses.&lt;h4>Methods&lt;/h4>In this randomized phase Ib clinical trial including 20 HIV uninfected volunteers, we compared the safety and immunogenicity of the MVA recombinant vaccine expressing HIV-B antigen (MVA-B) by transcutaneous and intramuscular routes. We hypothesized that the quality of innate and adaptive immunity differs according to the route of immunization and explored the quality of the vector vaccine-induced immune responses. We also investigated the early blood transcriptome and serum cytokine levels to identify innate events correlated with the strength and quality of adaptive immunity.&lt;h4>Results&lt;/h4>We demon</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020</publication><modification>2026-04-08T02:59:46.276Z</modification><creation>2021-02-20T00:56:29Z</creation></dates><accession>S-EPMC7683801</accession><cross_references><pubmed>33244316</pubmed><doi>10.3389/fimmu.2020.586124</doi></cross_references></HashMap>