Publication:
The Bacterial Mucosal Immunotherapy MV130 Protects Against SARS-CoV-2 Infection and Improves COVID-19 Vaccines Immunogenicity.

dc.contributor.authorDel Fresno, Carlos
dc.contributor.authorGarcía-Arriaza, Juan
dc.contributor.authorMartínez-Cano, Sarai
dc.contributor.authorHeras-Murillo, Ignacio
dc.contributor.authorJarit-Cabanillas, Aitor
dc.contributor.authorAmores-Iniesta, Joaquin
dc.contributor.authorBrandi, Paola
dc.contributor.authorDunphy, Gillian
dc.contributor.authorSuay-Corredera, Carmen
dc.contributor.authorPricolo, Maria Rosaria
dc.contributor.authorVicente, Natalia
dc.contributor.authorLópez-Perrote, Andrés
dc.contributor.authorCabezudo, Sofía
dc.contributor.authorGonzález-Corpas, Ana
dc.contributor.authorLlorca, Oscar
dc.contributor.authorAlegre-Cebollada, Jorge
dc.contributor.authorGaraigorta, Urtzi
dc.contributor.authorGastaminza, Pablo
dc.contributor.authorEsteban, Mariano
dc.contributor.authorSancho, David
dc.contributor.funderAsociación Española Contra el Cáncer
dc.contributor.funderFundación La Caixa
dc.contributor.funderUnión Europea. Comisión Europea. Horizonte Europa
dc.contributor.funderEuropean Molecular Biology Organization
dc.contributor.funderMarie Curie
dc.contributor.funderUnión Europea. Fondo Europeo de Desarrollo Regional (FEDER/ERDF)
dc.contributor.funderInstituto de Salud Carlos III
dc.contributor.funderFundación Banco Santander
dc.contributor.funderAgencia Estatal de Investigación (España)
dc.contributor.funderComunidad de Madrid (España)
dc.contributor.funderFundación ProCNIC
dc.date.accessioned2022-10-25T14:12:29Z
dc.date.available2022-10-25T14:12:29Z
dc.date.issued2021-11
dc.description.abstractCOVID-19-specific vaccines are efficient prophylactic weapons against SARS-CoV-2 virus. However, boosting innate responses may represent an innovative way to immediately fight future emerging viral infections or boost vaccines. MV130 is a mucosal immunotherapy, based on a mixture of whole heat-inactivated bacteria, that has shown clinical efficacy against recurrent viral respiratory infections. Herein, we show that the prophylactic intranasal administration of this immunotherapy confers heterologous protection against SARS-CoV-2 infection in susceptible K18-hACE2 mice. Furthermore, in C57BL/6 mice, prophylactic administration of MV130 improves the immunogenicity of two different COVID-19 vaccine formulations targeting the SARS-CoV-2 spike (S) protein, inoculated either intramuscularly or intranasally. Independently of the vaccine candidate and vaccination route used, intranasal prophylaxis with MV130 boosted S-specific responses, including CD8+-T cell activation and the production of S-specific mucosal IgA antibodies. Therefore, the bacterial mucosal immunotherapy MV130 protects against SARS-CoV-2 infection and improves COVID-19 vaccines immunogenicity.es_ES
dc.description.peerreviewedes_ES
dc.description.sponsorshipCF was supported by AECC Foundation (INVES192DELF) and is currently funded by the Miguel Servet program (ID: CP20/00106) (ISCIII). IH-M receives the support of a fellowship from la Caixa Foundation (ID 100010434, fellowship code: LCF/BQ/IN17/ 11620074) and from the European Union’s Horizon 2020 research and innovation program under the Marie SkłodowskaCurie grant agreement no. 713673. AJ-C is a postgraduate fellow of the City Council of Madrid at the Residencia de Estudiantes (2020–2021). GD is supported by an European Molecular Biology Organization (EMBO) Long-term fellowship (ALTF 379-2019). This project has received funding from the European Union's Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie grant agreement No. Project number 892965. OL and JA-C acknowledge Comunidad de Madrid (Tec4Bio-CM, S2018/NMT-4443, FEDER). Work in OL laboratory was funded by CNIO with the support of the projects Y2018/BIO4747 and P2018/NMT4443 from Comunidad de Madrid and co-funded by the European Social Fund and the European Regional Development Fund. The CNIO is supported by the Instituto de Salud Carlos III (ISCIII). Work at CNB and CISA is funded by the Spanish Health Ministry, Instituto de Salud Carlos III (ISCIII), Fondo COVID-19 grant COV20/00151, and Fondo Supera COVID-19 (Crue Universidades-Banco Santander) (to JG-A). Work in the DS laboratory is funded by the CNIC; by the European Research Council (ERC-2016-Consolidator Grant 725091); by Agencia Estatal de Investigación (PID2019- 108157RB); by Comunidad de Madrid (B2017/BMD-3733 Immunothercan-CM); by Fondo Solidario Juntos (Banco Santander); by a research agreement with Inmunotek S.L.; and by Fundació La Marató de TV3 (201723). The CNIC is supported by the Instituto de Salud Carlos III (ISCIII), the MICINN, and the Pro CNIC Foundation.es_ES
dc.format.page748103es_ES
dc.format.volume12es_ES
dc.identifier.citationFront Immunol . 2021 Nov 18;12:748103es_ES
dc.identifier.doi10.3389/fimmu.2021.748103es_ES
dc.identifier.e-issn1664-3224es_ES
dc.identifier.journalFrontiers in immunologyes_ES
dc.identifier.pubmedID34867974es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/15094
dc.language.isoenges_ES
dc.publisherFrontiers Media
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/ES/CP20/00106es_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/ES/100010434es_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/ES/11620074es_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/ES/Tec4Bio-CMes_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/ES/S2018/NMT-4443es_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/ES/Y2018/BIO4747es_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/ES/P2018/NMT4443es_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/ES/COV20/00151es_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/ES/PID2019-108157RBes_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/ES/B2017/BMD-3733es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/H2020/713673es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/H2020/ALTF 379-2019es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/H2020/892965es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/H2020/RC-2016-ConsolidatorGrant725091es_ES
dc.relation.publisherversiondoi: 10.3389/fimmu.2021.748103es_ES
dc.repisalud.institucionCNICes_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.meshAdministration, Mucosales_ES
dc.subject.meshAnimalses_ES
dc.subject.meshAntibodies, Virales_ES
dc.subject.meshBacteriaes_ES
dc.subject.meshCD8-Positive T-Lymphocyteses_ES
dc.subject.meshCOVID-19es_ES
dc.subject.meshCOVID-19 Vaccineses_ES
dc.subject.meshImmunity, Heterologouses_ES
dc.subject.meshImmunity, Innatees_ES
dc.subject.meshImmunogenicity, Vaccinees_ES
dc.subject.meshImmunoglobulin Aes_ES
dc.subject.meshImmunologic Factorses_ES
dc.subject.meshMicees_ES
dc.subject.meshSARS-CoV-2es_ES
dc.subject.meshVaccinationes_ES
dc.titleThe Bacterial Mucosal Immunotherapy MV130 Protects Against SARS-CoV-2 Infection and Improves COVID-19 Vaccines Immunogenicity.es_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
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