mRNA-1273 boost after BNT162b2 vaccination generates comparable SARS-CoV-2-specific functional responses in naïve and COVID-19-recovered individuals

IntroductionCOVID-19 vaccines based on mRNA have represented a revolution in the biomedical research field. The initial two-dose vaccination schedule generates potent humoral and cellular responses, with a massive protective effect against severe COVID-19 and death. Months after this vaccination, le...

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Main Authors: Roberto Lozano-Rodríguez, José Avendaño-Ortíz, Verónica Terrón, Karla Montalbán-Hernández, José Casalvilla-Dueñas, Marta Bergón-Gutiérrez, Pablo Mata-Martínez, Alejandro Martín-Quirós, Miguel Ángel García-Garrido, Álvaro del Balzo-Castillo, María Peinado, Laura Gómez, Irene Llorente-Fernández, Gema Martín-Miguel, Carmen Herrero-Benito, Lissette López-Morejón, Carmen Vela-Olmo, Carolina Cubillos-Zapata, Eduardo López-Collazo, Carlos del Fresno
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-04-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2023.1136029/full
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author Roberto Lozano-Rodríguez
Roberto Lozano-Rodríguez
José Avendaño-Ortíz
José Avendaño-Ortíz
Verónica Terrón
Verónica Terrón
Karla Montalbán-Hernández
Karla Montalbán-Hernández
José Casalvilla-Dueñas
José Casalvilla-Dueñas
Marta Bergón-Gutiérrez
Marta Bergón-Gutiérrez
Pablo Mata-Martínez
Pablo Mata-Martínez
Alejandro Martín-Quirós
Miguel Ángel García-Garrido
Álvaro del Balzo-Castillo
Álvaro del Balzo-Castillo
María Peinado
Laura Gómez
Irene Llorente-Fernández
Gema Martín-Miguel
Carmen Herrero-Benito
Lissette López-Morejón
Carmen Vela-Olmo
Carolina Cubillos-Zapata
Carolina Cubillos-Zapata
Carolina Cubillos-Zapata
Eduardo López-Collazo
Eduardo López-Collazo
Eduardo López-Collazo
Carlos del Fresno
Carlos del Fresno
author_facet Roberto Lozano-Rodríguez
Roberto Lozano-Rodríguez
José Avendaño-Ortíz
José Avendaño-Ortíz
Verónica Terrón
Verónica Terrón
Karla Montalbán-Hernández
Karla Montalbán-Hernández
José Casalvilla-Dueñas
José Casalvilla-Dueñas
Marta Bergón-Gutiérrez
Marta Bergón-Gutiérrez
Pablo Mata-Martínez
Pablo Mata-Martínez
Alejandro Martín-Quirós
Miguel Ángel García-Garrido
Álvaro del Balzo-Castillo
Álvaro del Balzo-Castillo
María Peinado
Laura Gómez
Irene Llorente-Fernández
Gema Martín-Miguel
Carmen Herrero-Benito
Lissette López-Morejón
Carmen Vela-Olmo
Carolina Cubillos-Zapata
Carolina Cubillos-Zapata
Carolina Cubillos-Zapata
Eduardo López-Collazo
Eduardo López-Collazo
Eduardo López-Collazo
Carlos del Fresno
Carlos del Fresno
author_sort Roberto Lozano-Rodríguez
collection DOAJ
description IntroductionCOVID-19 vaccines based on mRNA have represented a revolution in the biomedical research field. The initial two-dose vaccination schedule generates potent humoral and cellular responses, with a massive protective effect against severe COVID-19 and death. Months after this vaccination, levels of antibodies against SARS-CoV-2 waned, and this promoted the recommendation of a third vaccination dose.MethodsWe have performed an integral and longitudinal study of the immunological responses triggered by the booster mRNA-1273 vaccination, in a cohort of health workers previously vaccinated with two doses of the BNT162b2 vaccine at University Hospital La Paz located in Madrid, Spain. Circulating humoral responses and SARS-CoV-2-specific cellular reactions, after ex vivo restimulation of both T and B cells (cytokines production, proliferation, class switching), have been analyzed. Importantly, all along these studies, the analyses have been performed comparing naïve and subjects recovered from COVID-19, addressing the influence of a previous infection by SARS-CoV-2. Furthermore, as the injection of the third vaccination dose was contemporary to the rise of the Omicron BA.1 variant of concern, T- and B-cell-mediated cellular responses have been comparatively analyzed in response to this variant.ResultsAll these analyses indicated that differential responses to vaccination due to a previous SARS-CoV-2 infection were balanced following the boost. The increase in circulating humoral responses due to this booster dropped after 6 months, whereas T-cell-mediated responses were more stable along the time. Finally, all the analyzed immunological features were dampened in response to the Omicron variant of concern, particularly late after the booster vaccination.ConclusionThis work represents a follow-up longitudinal study for almost 1.5 years, analyzing in an integral manner the immunological responses triggered by the prime-boost mRNA-based vaccination schedule against COVID-19.
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spelling doaj.art-7381bc1db10a43eebad5271b062269782023-04-21T04:36:17ZengFrontiers Media S.A.Frontiers in Immunology1664-32242023-04-011410.3389/fimmu.2023.11360291136029mRNA-1273 boost after BNT162b2 vaccination generates comparable SARS-CoV-2-specific functional responses in naïve and COVID-19-recovered individualsRoberto Lozano-Rodríguez0Roberto Lozano-Rodríguez1José Avendaño-Ortíz2José Avendaño-Ortíz3Verónica Terrón4Verónica Terrón5Karla Montalbán-Hernández6Karla Montalbán-Hernández7José Casalvilla-Dueñas8José Casalvilla-Dueñas9Marta Bergón-Gutiérrez10Marta Bergón-Gutiérrez11Pablo Mata-Martínez12Pablo Mata-Martínez13Alejandro Martín-Quirós14Miguel Ángel García-Garrido15Álvaro del Balzo-Castillo16Álvaro del Balzo-Castillo17María Peinado18Laura Gómez19Irene Llorente-Fernández20Gema Martín-Miguel21Carmen Herrero-Benito22Lissette López-Morejón23Carmen Vela-Olmo24Carolina Cubillos-Zapata25Carolina Cubillos-Zapata26Carolina Cubillos-Zapata27Eduardo López-Collazo28Eduardo López-Collazo29Eduardo López-Collazo30Carlos del Fresno31Carlos del Fresno32The Innate Immune Response Group, Hospital la Paz Institute for Health Research (IdiPAZ), La Paz University Hospital, Madrid, SpainTumor Immunology Laboratory, Hospital la Paz Institute for Health Research (IdiPAZ), La Paz University Hospital, Madrid, SpainThe Innate Immune Response Group, Hospital la Paz Institute for Health Research (IdiPAZ), La Paz University Hospital, Madrid, SpainTumor Immunology Laboratory, Hospital la Paz Institute for Health Research (IdiPAZ), La Paz University Hospital, Madrid, SpainThe Innate Immune Response Group, Hospital la Paz Institute for Health Research (IdiPAZ), La Paz University Hospital, Madrid, SpainTumor Immunology Laboratory, Hospital la Paz Institute for Health Research (IdiPAZ), La Paz University Hospital, Madrid, SpainThe Innate Immune Response Group, Hospital la Paz Institute for Health Research (IdiPAZ), La Paz University Hospital, Madrid, SpainTumor Immunology Laboratory, Hospital la Paz Institute for Health Research (IdiPAZ), La Paz University Hospital, Madrid, SpainThe Innate Immune Response Group, Hospital la Paz Institute for Health Research (IdiPAZ), La Paz University Hospital, Madrid, SpainTumor Immunology Laboratory, Hospital la Paz Institute for Health Research (IdiPAZ), La Paz University Hospital, Madrid, SpainThe Innate Immune Response Group, Hospital la Paz Institute for Health Research (IdiPAZ), La Paz University Hospital, Madrid, SpainImmunomodulation Laboratory, Hospital la Paz Institute for Health Research (IdiPAZ), La Paz University Hospital, Madrid, SpainThe Innate Immune Response Group, Hospital la Paz Institute for Health Research (IdiPAZ), La Paz University Hospital, Madrid, SpainImmunomodulation Laboratory, Hospital la Paz Institute for Health Research (IdiPAZ), La Paz University Hospital, Madrid, SpainEmergency Department and Emergent Pathology Research Group, Hospital la Paz Institute for Health Research (IdiPAZ), La Paz University Hospital, Madrid, SpainEmergency Department and Emergent Pathology Research Group, Hospital la Paz Institute for Health Research (IdiPAZ), La Paz University Hospital, Madrid, SpainThe Innate Immune Response Group, Hospital la Paz Institute for Health Research (IdiPAZ), La Paz University Hospital, Madrid, SpainEmergency Department and Emergent Pathology Research Group, Hospital la Paz Institute for Health Research (IdiPAZ), La Paz University Hospital, Madrid, SpainEmergency Department and Emergent Pathology Research Group, Hospital la Paz Institute for Health Research (IdiPAZ), La Paz University Hospital, Madrid, SpainEmergency Department and Emergent Pathology Research Group, Hospital la Paz Institute for Health Research (IdiPAZ), La Paz University Hospital, Madrid, SpainIntensive Care Unit, Infanta Cristina University Hospital, Parla, Madrid, SpainPediatric Intensive Care Unit, 12 de Octubre University Hospital, Madrid, SpainEmergency Department and Emergent Pathology Research Group, Hospital la Paz Institute for Health Research (IdiPAZ), La Paz University Hospital, Madrid, SpainEurofins-Ingenasa, Madrid, SpainEurofins-Ingenasa, Madrid, SpainThe Innate Immune Response Group, Hospital la Paz Institute for Health Research (IdiPAZ), La Paz University Hospital, Madrid, SpainTumor Immunology Laboratory, Hospital la Paz Institute for Health Research (IdiPAZ), La Paz University Hospital, Madrid, SpainCentro de Investigación Biomédica en Red (CIBER) of Respiratory Diseases (CIBERES), Madrid, SpainThe Innate Immune Response Group, Hospital la Paz Institute for Health Research (IdiPAZ), La Paz University Hospital, Madrid, SpainTumor Immunology Laboratory, Hospital la Paz Institute for Health Research (IdiPAZ), La Paz University Hospital, Madrid, SpainCentro de Investigación Biomédica en Red (CIBER) of Respiratory Diseases (CIBERES), Madrid, SpainThe Innate Immune Response Group, Hospital la Paz Institute for Health Research (IdiPAZ), La Paz University Hospital, Madrid, SpainImmunomodulation Laboratory, Hospital la Paz Institute for Health Research (IdiPAZ), La Paz University Hospital, Madrid, SpainIntroductionCOVID-19 vaccines based on mRNA have represented a revolution in the biomedical research field. The initial two-dose vaccination schedule generates potent humoral and cellular responses, with a massive protective effect against severe COVID-19 and death. Months after this vaccination, levels of antibodies against SARS-CoV-2 waned, and this promoted the recommendation of a third vaccination dose.MethodsWe have performed an integral and longitudinal study of the immunological responses triggered by the booster mRNA-1273 vaccination, in a cohort of health workers previously vaccinated with two doses of the BNT162b2 vaccine at University Hospital La Paz located in Madrid, Spain. Circulating humoral responses and SARS-CoV-2-specific cellular reactions, after ex vivo restimulation of both T and B cells (cytokines production, proliferation, class switching), have been analyzed. Importantly, all along these studies, the analyses have been performed comparing naïve and subjects recovered from COVID-19, addressing the influence of a previous infection by SARS-CoV-2. Furthermore, as the injection of the third vaccination dose was contemporary to the rise of the Omicron BA.1 variant of concern, T- and B-cell-mediated cellular responses have been comparatively analyzed in response to this variant.ResultsAll these analyses indicated that differential responses to vaccination due to a previous SARS-CoV-2 infection were balanced following the boost. The increase in circulating humoral responses due to this booster dropped after 6 months, whereas T-cell-mediated responses were more stable along the time. Finally, all the analyzed immunological features were dampened in response to the Omicron variant of concern, particularly late after the booster vaccination.ConclusionThis work represents a follow-up longitudinal study for almost 1.5 years, analyzing in an integral manner the immunological responses triggered by the prime-boost mRNA-based vaccination schedule against COVID-19.https://www.frontiersin.org/articles/10.3389/fimmu.2023.1136029/fullmRNA vaccineCOVID-19 boosterSARS-CoV-2-specificnaïverecovered from COVID-19
spellingShingle Roberto Lozano-Rodríguez
Roberto Lozano-Rodríguez
José Avendaño-Ortíz
José Avendaño-Ortíz
Verónica Terrón
Verónica Terrón
Karla Montalbán-Hernández
Karla Montalbán-Hernández
José Casalvilla-Dueñas
José Casalvilla-Dueñas
Marta Bergón-Gutiérrez
Marta Bergón-Gutiérrez
Pablo Mata-Martínez
Pablo Mata-Martínez
Alejandro Martín-Quirós
Miguel Ángel García-Garrido
Álvaro del Balzo-Castillo
Álvaro del Balzo-Castillo
María Peinado
Laura Gómez
Irene Llorente-Fernández
Gema Martín-Miguel
Carmen Herrero-Benito
Lissette López-Morejón
Carmen Vela-Olmo
Carolina Cubillos-Zapata
Carolina Cubillos-Zapata
Carolina Cubillos-Zapata
Eduardo López-Collazo
Eduardo López-Collazo
Eduardo López-Collazo
Carlos del Fresno
Carlos del Fresno
mRNA-1273 boost after BNT162b2 vaccination generates comparable SARS-CoV-2-specific functional responses in naïve and COVID-19-recovered individuals
Frontiers in Immunology
mRNA vaccine
COVID-19 booster
SARS-CoV-2-specific
naïve
recovered from COVID-19
title mRNA-1273 boost after BNT162b2 vaccination generates comparable SARS-CoV-2-specific functional responses in naïve and COVID-19-recovered individuals
title_full mRNA-1273 boost after BNT162b2 vaccination generates comparable SARS-CoV-2-specific functional responses in naïve and COVID-19-recovered individuals
title_fullStr mRNA-1273 boost after BNT162b2 vaccination generates comparable SARS-CoV-2-specific functional responses in naïve and COVID-19-recovered individuals
title_full_unstemmed mRNA-1273 boost after BNT162b2 vaccination generates comparable SARS-CoV-2-specific functional responses in naïve and COVID-19-recovered individuals
title_short mRNA-1273 boost after BNT162b2 vaccination generates comparable SARS-CoV-2-specific functional responses in naïve and COVID-19-recovered individuals
title_sort mrna 1273 boost after bnt162b2 vaccination generates comparable sars cov 2 specific functional responses in naive and covid 19 recovered individuals
topic mRNA vaccine
COVID-19 booster
SARS-CoV-2-specific
naïve
recovered from COVID-19
url https://www.frontiersin.org/articles/10.3389/fimmu.2023.1136029/full
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