The mRNA-1273 vaccine induces cross-variant antibody responses to SARS-CoV-2 with distinct profiles in individuals with or without pre-existing immunity

mRNA-based vaccines effectively induce protective neutralizing antibodies against SARS-CoV-2, the etiological agent of COVID-19. Yet, the kinetics and compositional patterns of vaccine-induced antibody responses to the original strain and emerging variants of concern remain largely unknown. Here we...

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Autores: Tejedor Vaquero, Sonia, 1988-, Campos Mata, Leire de, 1991-, Ramada Rodilla, José María, 1961-, Díaz, Pilar, Navarro-Barriuso, Juan, Ribas-Llauradó, Clara, Rodrigo Melero, Natalia, Carolis, Carlo, Cerutti, Andrea, 1965-, Gimeno Martínez, Ramón, Magri, Giuliana, 1978-
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2021
País:España
Institución:Universitat Pompeu Fabra
Repositorio:Repositorio Digital de la UPF
OAI Identifier:oai:repositori.upf.edu:10230/52261
Acceso en línea:http://hdl.handle.net/10230/52261
http://dx.doi.org/10.3389/fimmu.2021.737083
Access Level:acceso abierto
Palabra clave:COVID-19 (Malaltia)
Vacunació
Immunitat
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spelling The mRNA-1273 vaccine induces cross-variant antibody responses to SARS-CoV-2 with distinct profiles in individuals with or without pre-existing immunityTejedor Vaquero, Sonia, 1988-Campos Mata, Leire de, 1991-Ramada Rodilla, José María, 1961-Díaz, PilarNavarro-Barriuso, JuanRibas-Llauradó, ClaraRodrigo Melero, NataliaCarolis, CarloCerutti, Andrea, 1965-Gimeno Martínez, RamónMagri, Giuliana, 1978-COVID-19 (Malaltia)VacunacióImmunitatmRNA-based vaccines effectively induce protective neutralizing antibodies against SARS-CoV-2, the etiological agent of COVID-19. Yet, the kinetics and compositional patterns of vaccine-induced antibody responses to the original strain and emerging variants of concern remain largely unknown. Here we characterized serum antibody classes and subclasses targeting the spike receptor-binding domain of SARS-CoV-2 wild type and α, β, γ and δ variants in a longitudinal cohort of SARS-CoV-2 naïve and COVID-19 recovered individuals receiving the mRNA-1273 vaccine. We found that mRNA-1273 vaccine recipients developed a SARS-CoV-2-specific antibody response with a subclass profile comparable to that induced by natural infection. Importantly, these antibody responses targeted both wild type SARS-CoV-2 as well as its α, β, γ and δ variants. Following primary vaccination, individuals with pre-existing immunity showed higher induction of all antibodies but IgG3 compared to SARS-CoV-2-naïve subjects. Unlike naïve individuals, COVID-19 recovered subjects did not mount a recall antibody response upon the second vaccine dose. In these individuals, secondary immunization resulted in a slight reduction of IgG1 against the receptor-binding domain of β and γ variants. Despite the lack of recall humoral response, vaccinees with pre-existing immunity still showed higher titers of IgG1 and IgA to all variants analyzed compared to fully vaccinated naïve individuals. Our findings indicate that mRNA-1273 vaccine triggered cross-variant antibody responses with distinct profiles in vaccinees with or without pre-existing immunity and suggest that individuals with prior history of SARS-CoV-2 infection may not benefit from the second mRNA vaccine dose with the current standard regimen.This study was supported by the COVID-19 call grant from Generalitat de Catalunya, Department of Health (to GM), grant Miguel Servet research program (to GM) and by National Health Institute Carlos III (ISCIII) through the project COV20_00508 grant (Co-funded by European Regional Development Fund/European Social Fund “a way to make Europe) (to RG)Frontiers Media202220222021info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfapplication/pdfhttp://hdl.handle.net/10230/52261http://dx.doi.org/10.3389/fimmu.2021.737083reponame:Repositorio Digital de la UPFinstname:Universitat Pompeu FabraInglésFrontiers in Immunology. 2021;12:737083.© 2021 Sonia Tejedor Vaquero et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these termshttps://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccessoai:repositori.upf.edu:10230/522612026-06-12T07:21:37Z
dc.title.none.fl_str_mv The mRNA-1273 vaccine induces cross-variant antibody responses to SARS-CoV-2 with distinct profiles in individuals with or without pre-existing immunity
title The mRNA-1273 vaccine induces cross-variant antibody responses to SARS-CoV-2 with distinct profiles in individuals with or without pre-existing immunity
spellingShingle The mRNA-1273 vaccine induces cross-variant antibody responses to SARS-CoV-2 with distinct profiles in individuals with or without pre-existing immunity
Tejedor Vaquero, Sonia, 1988-
COVID-19 (Malaltia)
Vacunació
Immunitat
title_short The mRNA-1273 vaccine induces cross-variant antibody responses to SARS-CoV-2 with distinct profiles in individuals with or without pre-existing immunity
title_full The mRNA-1273 vaccine induces cross-variant antibody responses to SARS-CoV-2 with distinct profiles in individuals with or without pre-existing immunity
title_fullStr The mRNA-1273 vaccine induces cross-variant antibody responses to SARS-CoV-2 with distinct profiles in individuals with or without pre-existing immunity
title_full_unstemmed The mRNA-1273 vaccine induces cross-variant antibody responses to SARS-CoV-2 with distinct profiles in individuals with or without pre-existing immunity
title_sort The mRNA-1273 vaccine induces cross-variant antibody responses to SARS-CoV-2 with distinct profiles in individuals with or without pre-existing immunity
dc.creator.none.fl_str_mv Tejedor Vaquero, Sonia, 1988-
Campos Mata, Leire de, 1991-
Ramada Rodilla, José María, 1961-
Díaz, Pilar
Navarro-Barriuso, Juan
Ribas-Llauradó, Clara
Rodrigo Melero, Natalia
Carolis, Carlo
Cerutti, Andrea, 1965-
Gimeno Martínez, Ramón
Magri, Giuliana, 1978-
author Tejedor Vaquero, Sonia, 1988-
author_facet Tejedor Vaquero, Sonia, 1988-
Campos Mata, Leire de, 1991-
Ramada Rodilla, José María, 1961-
Díaz, Pilar
Navarro-Barriuso, Juan
Ribas-Llauradó, Clara
Rodrigo Melero, Natalia
Carolis, Carlo
Cerutti, Andrea, 1965-
Gimeno Martínez, Ramón
Magri, Giuliana, 1978-
author_role author
author2 Campos Mata, Leire de, 1991-
Ramada Rodilla, José María, 1961-
Díaz, Pilar
Navarro-Barriuso, Juan
Ribas-Llauradó, Clara
Rodrigo Melero, Natalia
Carolis, Carlo
Cerutti, Andrea, 1965-
Gimeno Martínez, Ramón
Magri, Giuliana, 1978-
author2_role author
author
author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv COVID-19 (Malaltia)
Vacunació
Immunitat
topic COVID-19 (Malaltia)
Vacunació
Immunitat
description mRNA-based vaccines effectively induce protective neutralizing antibodies against SARS-CoV-2, the etiological agent of COVID-19. Yet, the kinetics and compositional patterns of vaccine-induced antibody responses to the original strain and emerging variants of concern remain largely unknown. Here we characterized serum antibody classes and subclasses targeting the spike receptor-binding domain of SARS-CoV-2 wild type and α, β, γ and δ variants in a longitudinal cohort of SARS-CoV-2 naïve and COVID-19 recovered individuals receiving the mRNA-1273 vaccine. We found that mRNA-1273 vaccine recipients developed a SARS-CoV-2-specific antibody response with a subclass profile comparable to that induced by natural infection. Importantly, these antibody responses targeted both wild type SARS-CoV-2 as well as its α, β, γ and δ variants. Following primary vaccination, individuals with pre-existing immunity showed higher induction of all antibodies but IgG3 compared to SARS-CoV-2-naïve subjects. Unlike naïve individuals, COVID-19 recovered subjects did not mount a recall antibody response upon the second vaccine dose. In these individuals, secondary immunization resulted in a slight reduction of IgG1 against the receptor-binding domain of β and γ variants. Despite the lack of recall humoral response, vaccinees with pre-existing immunity still showed higher titers of IgG1 and IgA to all variants analyzed compared to fully vaccinated naïve individuals. Our findings indicate that mRNA-1273 vaccine triggered cross-variant antibody responses with distinct profiles in vaccinees with or without pre-existing immunity and suggest that individuals with prior history of SARS-CoV-2 infection may not benefit from the second mRNA vaccine dose with the current standard regimen.
publishDate 2021
dc.date.none.fl_str_mv 2021
2022
2022
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/10230/52261
http://dx.doi.org/10.3389/fimmu.2021.737083
url http://hdl.handle.net/10230/52261
http://dx.doi.org/10.3389/fimmu.2021.737083
dc.language.none.fl_str_mv Inglés
language_invalid_str_mv Inglés
dc.relation.none.fl_str_mv Frontiers in Immunology. 2021;12:737083.
dc.rights.none.fl_str_mv https://creativecommons.org/licenses/by/4.0/
info:eu-repo/semantics/openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by/4.0/
eu_rights_str_mv openAccess
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dc.publisher.none.fl_str_mv Frontiers Media
publisher.none.fl_str_mv Frontiers Media
dc.source.none.fl_str_mv reponame:Repositorio Digital de la UPF
instname:Universitat Pompeu Fabra
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