Immune Profiles Identification by Vaccinomics After MVA Immunization in Randomized Clinical Study

Bibliographic Details
Title: Immune Profiles Identification by Vaccinomics After MVA Immunization in Randomized Clinical Study
Authors: Jorge Sanchez, Elena Gonçalves, Anuska Llano, Pedro Gonzáles, María Fernández-Maldonado, Annika Vogt, Angele Soria, Susana Perez, Samandhy Cedeño, Marco Antonio Fernández, Julien Nourikyan, Simon de Bernard, Carmela Ganoza, Eric Pedruzzi, Olivia Bonduelle, Beatriz Mothe, Carmen E. Gòmez, Mariano Esteban, Felipe Garcia, Javier R. Lama, Christian Brander, Behazine Combadiere
Source: Frontiers in Immunology, Vol 11 (2020)
Publisher Information: Frontiers Media S.A., 2020.
Publication Year: 2020
Collection: LCC:Immunologic diseases. Allergy
Subject Terms: immunogenicity, cutaneous vaccination, intramuscular route, vaccinia virus vector, transcriptome, Immunologic diseases. Allergy, RC581-607
More Details: BackgroundOur previous work has demonstrated the benefits of transcutaneous immunization in targeting Langerhans cells and preferentially inducing CD8 T-cell responses.MethodsIn 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.ResultsWe demonstrate that MVA-B vaccine is safe by both routes, but that the quality and intensity of both innate and adaptive immunity differ significantly. Transcutaneous vaccination promoted CD8 responses in the absence of antibodies and slightly affected gene expression, involving mainly genes associated with metabolic pathways. Intramuscular vaccination, on the other hand, drove robust changes in the expression of genes involved in IL-6 and interferon signalling pathways, mainly those associated with humoral responses, and also some levels of CD8 response.ConclusionThus, vaccine delivery route perturbs early innate responses that shape the quality of adaptive immunity.Clinical Trial Registrationhttp://ClinicalTrials.gov, identifier PER-073-13.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1664-3224
Relation: https://www.frontiersin.org/articles/10.3389/fimmu.2020.586124/full; https://doaj.org/toc/1664-3224
DOI: 10.3389/fimmu.2020.586124
Access URL: https://doaj.org/article/7de6587d92de4cdd98f362c26b6bf00a
Accession Number: edsdoj.7de6587d92de4cdd98f362c26b6bf00a
Database: Directory of Open Access Journals
More Details
ISSN:16643224
DOI:10.3389/fimmu.2020.586124
Published in:Frontiers in Immunology
Language:English