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dc.contributor.authorTeran-Navarro, Héctor
dc.contributor.authorSalcines-Cuevas, David
dc.contributor.authorCalderón-González, Ricardo
dc.contributor.authorTobes, Raquel
dc.contributor.authorCalvo-Montes, Jorge
dc.contributor.authorPérez-Del Molino Bernal, Inmaculada Concepción
dc.contributor.authorYañez-Diaz, Sonsoles
dc.contributor.authorFresno, Manuel
dc.contributor.authorÁlvarez-Domínguez, Carmen
dc.date2021
dc.date.accessioned2021-11-29T10:06:37Z
dc.date.available2021-11-29T10:06:37Z
dc.identifier.issn1664-3224
dc.identifier.urihttps://reunir.unir.net/handle/123456789/12162
dc.description.abstractCross-reactive vaccines recognize common molecular patterns in pathogens and are able to confer broad spectrum protection against different infections. Antigens common to pathogenic bacteria that induce broad immune responses, such as the glyceraldehyde-3-phosphate dehydrogenase (GAPDH) of the genera Listeria, Mycobacterium, or Streptococcus, whose sequences present more than 95% homology at the N-terminal GAPDH(1-22) peptide, are putative candidates for universal vaccines. Here, we explore vaccine formulations based on dendritic cells (DC) loaded with two molecular forms of Listeria monocytogenes GAPDH (LM-GAPDH), such as mRNA carriers or recombinant proteins, and compare them with the same molecular forms of three other antigens used in experimental vaccines, listeriolysin O of Listeria monocytogeness, Ag85A of Mycobacterium marinum, and pneumolysin of Streptococcus pneumoniae. DC loaded with LM-GAPDH recombinant proteins proved to be the safest and most immunogenic vaccine vectors, followed by mRNA encoding LM-GAPDH conjugated to lipid carriers. In addition, macrophages lacked sufficient safety as vaccines for all LM-GAPDH molecular forms. The ability of DC loaded with LM-GAPDH recombinant proteins to induce non-specific DC activation explains their adjuvant potency and their capacity to trigger strong CD4(+) and CD8(+) T cell responses explains their high immunogenicity. Moreover, their capacity to confer protection in vaccinated mice against challenges with L. monocytogenes, M. marinum, or S. pneumoniae validated their efficiency as cross-reactive vaccines. Cross-protection appears to involve the induction of high percentages of GAPDH(1-22) specific CD4(+) and CD8(+) T cells stained for intracellular IFN-gamma, and significant levels of peptide-specific antibodies in vaccinated mice. We concluded that DC vaccines loaded with L. monocytogenes GAPDH recombinant proteins are cross-reactive vaccines that seem to be valuable tools in adult vaccination against Listeria, Mycobacterium, and Streptococcus taxonomic groups.es_ES
dc.language.isoenges_ES
dc.publisherFrontiers in immunologyes_ES
dc.relation.ispartofseries;vol. 12
dc.relation.urihttps://www.frontiersin.org/articles/10.3389/fimmu.2021.632304/fulles_ES
dc.rightsopenAccesses_ES
dc.subjectglyceraldehyde-3-phosphate-dehydrogenasees_ES
dc.subjectlisteriosises_ES
dc.subjectpneumoniaes_ES
dc.subjecttuberculosises_ES
dc.subjectcross-reactive vaccineses_ES
dc.subjectinnate immunityes_ES
dc.subjectWOS(2)es_ES
dc.subjectScopuses_ES
dc.titleA Comparison Between Recombinant Listeria GAPDH Proteins and GAPDH Encoding mRNA Conjugated to Lipids as Cross-Reactive Vaccines for Listeria, Mycobacterium, and Streptococcuses_ES
dc.typearticlees_ES
reunir.tag~ARIes_ES
dc.identifier.doihttps://doi.org/10.3389/fimmu.2021.632304


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