Preclinical immune efficacy against SARS-CoV-2 beta B.1.351 variant by MVA-based vaccine candidates

17 Pág.

Saved in:
Bibliographic Details
Main Authors: Pérez Ramírez, Patricia, Albericio, Guillermo, Astorgano, David, Flores, Sara, Sánchez-Corzo, Cristina, Sánchez-Cordón, P. J., Luczkowiak, Joanna, Delgado, Rafael, Casasnovas, José María, Esteban, Mariano, García-Arriaza, Juan
Other Authors: Ministerio de Sanidad (España)
Format: artículo biblioteca
Language:English
Published: Frontiers Media 2023-12-12
Subjects:COVID-19, MVA-based vaccine, S protein, SARS-CoV-2, Efficacy, Immunogenicity, Mice, Variants of concern,
Online Access:http://hdl.handle.net/10261/349371
http://dx.doi.org/10.13039/501100003339
http://dx.doi.org/10.13039/501100004837
http://dx.doi.org/10.13039/501100004587
http://dx.doi.org/10.13039/501100000780
http://dx.doi.org/10.13039/501100011033
https://api.elsevier.com/content/abstract/scopus_id/85180695762
Tags: Add Tag
No Tags, Be the first to tag this record!
id dig-inia-es-10261-349371
record_format koha
institution INIA ES
collection DSpace
country España
countrycode ES
component Bibliográfico
access En linea
databasecode dig-inia-es
tag biblioteca
region Europa del Sur
libraryname Biblioteca del INIA España
language English
topic COVID-19
MVA-based vaccine
S protein
SARS-CoV-2
Efficacy
Immunogenicity
Mice
Variants of concern
COVID-19
MVA-based vaccine
S protein
SARS-CoV-2
Efficacy
Immunogenicity
Mice
Variants of concern
spellingShingle COVID-19
MVA-based vaccine
S protein
SARS-CoV-2
Efficacy
Immunogenicity
Mice
Variants of concern
COVID-19
MVA-based vaccine
S protein
SARS-CoV-2
Efficacy
Immunogenicity
Mice
Variants of concern
Pérez Ramírez, Patricia
Albericio, Guillermo
Astorgano, David
Flores, Sara
Sánchez-Corzo, Cristina
Sánchez-Cordón, P. J.
Luczkowiak, Joanna
Delgado, Rafael
Casasnovas, José María
Esteban, Mariano
García-Arriaza, Juan
Preclinical immune efficacy against SARS-CoV-2 beta B.1.351 variant by MVA-based vaccine candidates
description 17 Pág.
author2 Ministerio de Sanidad (España)
author_facet Ministerio de Sanidad (España)
Pérez Ramírez, Patricia
Albericio, Guillermo
Astorgano, David
Flores, Sara
Sánchez-Corzo, Cristina
Sánchez-Cordón, P. J.
Luczkowiak, Joanna
Delgado, Rafael
Casasnovas, José María
Esteban, Mariano
García-Arriaza, Juan
format artículo
topic_facet COVID-19
MVA-based vaccine
S protein
SARS-CoV-2
Efficacy
Immunogenicity
Mice
Variants of concern
author Pérez Ramírez, Patricia
Albericio, Guillermo
Astorgano, David
Flores, Sara
Sánchez-Corzo, Cristina
Sánchez-Cordón, P. J.
Luczkowiak, Joanna
Delgado, Rafael
Casasnovas, José María
Esteban, Mariano
García-Arriaza, Juan
author_sort Pérez Ramírez, Patricia
title Preclinical immune efficacy against SARS-CoV-2 beta B.1.351 variant by MVA-based vaccine candidates
title_short Preclinical immune efficacy against SARS-CoV-2 beta B.1.351 variant by MVA-based vaccine candidates
title_full Preclinical immune efficacy against SARS-CoV-2 beta B.1.351 variant by MVA-based vaccine candidates
title_fullStr Preclinical immune efficacy against SARS-CoV-2 beta B.1.351 variant by MVA-based vaccine candidates
title_full_unstemmed Preclinical immune efficacy against SARS-CoV-2 beta B.1.351 variant by MVA-based vaccine candidates
title_sort preclinical immune efficacy against sars-cov-2 beta b.1.351 variant by mva-based vaccine candidates
publisher Frontiers Media
publishDate 2023-12-12
url http://hdl.handle.net/10261/349371
http://dx.doi.org/10.13039/501100003339
http://dx.doi.org/10.13039/501100004837
http://dx.doi.org/10.13039/501100004587
http://dx.doi.org/10.13039/501100000780
http://dx.doi.org/10.13039/501100011033
https://api.elsevier.com/content/abstract/scopus_id/85180695762
work_keys_str_mv AT perezramirezpatricia preclinicalimmuneefficacyagainstsarscov2betab1351variantbymvabasedvaccinecandidates
AT albericioguillermo preclinicalimmuneefficacyagainstsarscov2betab1351variantbymvabasedvaccinecandidates
AT astorganodavid preclinicalimmuneefficacyagainstsarscov2betab1351variantbymvabasedvaccinecandidates
AT floressara preclinicalimmuneefficacyagainstsarscov2betab1351variantbymvabasedvaccinecandidates
AT sanchezcorzocristina preclinicalimmuneefficacyagainstsarscov2betab1351variantbymvabasedvaccinecandidates
AT sanchezcordonpj preclinicalimmuneefficacyagainstsarscov2betab1351variantbymvabasedvaccinecandidates
AT luczkowiakjoanna preclinicalimmuneefficacyagainstsarscov2betab1351variantbymvabasedvaccinecandidates
AT delgadorafael preclinicalimmuneefficacyagainstsarscov2betab1351variantbymvabasedvaccinecandidates
AT casasnovasjosemaria preclinicalimmuneefficacyagainstsarscov2betab1351variantbymvabasedvaccinecandidates
AT estebanmariano preclinicalimmuneefficacyagainstsarscov2betab1351variantbymvabasedvaccinecandidates
AT garciaarriazajuan preclinicalimmuneefficacyagainstsarscov2betab1351variantbymvabasedvaccinecandidates
_version_ 1802819898729037824
spelling dig-inia-es-10261-3493712024-05-21T07:02:07Z Preclinical immune efficacy against SARS-CoV-2 beta B.1.351 variant by MVA-based vaccine candidates Pérez Ramírez, Patricia Albericio, Guillermo Astorgano, David Flores, Sara Sánchez-Corzo, Cristina Sánchez-Cordón, P. J. Luczkowiak, Joanna Delgado, Rafael Casasnovas, José María Esteban, Mariano García-Arriaza, Juan Ministerio de Sanidad (España) Instituto de Salud Carlos III Conferencia de Rectores de las Universidades Españolas Consejo Superior de Investigaciones Científicas (España) Fundación la Caixa Ministerio de Ciencia e Innovación (España) Agencia Estatal de Investigación (España) European Commission Albericio, Guillermo [0000-0003-0190-4848] Astorgano, David [0000-0002-2969-1840] Sánchez-Cordón, P. J. [0000-0002-7202-6475] Luczkowiak, Joanna [0000-0001-6950-9372] Delgado, Rafael [0000-0002-6912-4736] Esteban, Mariano [0000-0003-0846-2827] García-Arriaza, Juan [0000-0002-5167-5724] COVID-19 MVA-based vaccine S protein SARS-CoV-2 Efficacy Immunogenicity Mice Variants of concern 17 Pág. The constant appearance of new severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants of concern (VoCs) has jeopardized the protective capacity of approved vaccines against coronavirus disease-19 (COVID-19). For this reason, the generation of new vaccine candidates adapted to the emerging VoCs is of special importance. Here, we developed an optimized COVID-19 vaccine candidate using the modified vaccinia virus Ankara (MVA) vector to express a full-length prefusion-stabilized SARS-CoV-2 spike (S) protein, containing 3 proline (3P) substitutions in the S protein derived from the beta (B.1.351) variant, termed MVA-S(3Pbeta). Preclinical evaluation of MVA-S(3Pbeta) in head-to-head comparison to the previously generated MVA-S(3P) vaccine candidate, expressing a full-length prefusion-stabilized Wuhan S protein (with also 3P substitutions), demonstrated that two intramuscular doses of both vaccine candidates fully protected transgenic K18-hACE2 mice from a lethal challenge with SARS-CoV-2 beta variant, reducing mRNA and infectious viral loads in the lungs and in bronchoalveolar lavages, decreasing lung histopathological lesions and levels of proinflammatory cytokines in the lungs. Vaccination also elicited high titers of anti-S Th1-biased IgGs and neutralizing antibodies against ancestral SARS-CoV-2 Wuhan strain and VoCs alpha, beta, gamma, delta, and omicron. In addition, similar systemic and local SARS-CoV-2 S-specific CD4+ and CD8+ T-cell immune responses were elicited by both vaccine candidates after a single intranasal immunization in C57BL/6 mice. These preclinical data support clinical evaluation of MVA-S(3Pbeta) and MVA-S(3P), to explore whether they can diversify and potentially increase recognition and protection of SARS-CoV-2 VoCs. The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This research was supported by Fondo COVID-19 grant COV20/00151 (Spanish Health Ministry, Instituto de Salud Carlos III (ISCIII)), Fondo Supera COVID-19 grant (Crue Universidades-Banco Santander), and Spanish Research Council (CSIC) grant 202120E079 (to JG-A); CSIC grant 2020E84, la Caixa Banking Foundation grant CF01-00008, Ferrovial, and MAPFRE donations (to ME); and Spanish Ministry of Science and Innovation (MCIN)/Spanish Research Agency (AEI)/10.13039/501100011033 grant (PID2020-114481RB-I00; to JG-A and ME). This research work was also funded by the European Commission-Next Generation EU, through CSIC’s Global Health Platform (PTI Salud Global) (to JG-A and ME). JG-A and ME acknowledges financial support from the Spanish State Research Agency, AEI/10.13039/501100011033, through the “Severo Ochoa” Programme for Centres of Excellence in R&D (SEV-2013-0347, SEV-2017-0712). JC acknowledges MCIN and CSIC support (project number 202020E079). RD received grants from ISCIII (FIS PI2100989), the European Commission Horizon 2020 Framework Programme (Project VIRUSCAN FETPROACT-2016: 731868 and Project EPIC-CROWN-2: 101046084), and Fundacioín Caixa-Health Research HR18-00469 (Project StopEbola). Peer reviewed 2024-03-06T07:18:37Z 2024-03-06T07:18:37Z 2023-12-12 artículo http://purl.org/coar/resource_type/c_6501 Frontiers in Immunology 14: e1264323 (2023) http://hdl.handle.net/10261/349371 10.3389/fimmu.2023.1264323 1664-3224 http://dx.doi.org/10.13039/501100003339 http://dx.doi.org/10.13039/501100004837 http://dx.doi.org/10.13039/501100004587 http://dx.doi.org/10.13039/501100000780 http://dx.doi.org/10.13039/501100011033 38155964 2-s2.0-85180695762 https://api.elsevier.com/content/abstract/scopus_id/85180695762 en #PLACEHOLDER_PARENT_METADATA_VALUE# #PLACEHOLDER_PARENT_METADATA_VALUE# info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2020-114481RB-I00/ES/DESARROLLO, FUNCION INMUNE Y EFICACIA DE CANDIDATOS VACUNALES FRENTE AL SARS-COV-2%2FCOVID-19 BASADOS EN EL VECTOR POXVIRUS MVA/ info:eu-repo/grantAgreement/EC/H2020/731868 Frontiers in immunology Publisher's version https://doi.org/10.3389/fimmu.2023.1264323 Sí open application/pdf Frontiers Media