Cargando…

Age-related immune response heterogeneity to SARS-CoV-2 vaccine BNT162b2

Although two-dose mRNA vaccination provides excellent protection against SARS-CoV-2, there is little information about vaccine efficacy against variants of concern (VOC) in individuals above eighty years of age(1). Here we analysed immune responses following vaccination with the BNT162b2 mRNA vaccin...

Descripción completa

Detalles Bibliográficos
Autores principales: Collier, Dami A., Ferreira, Isabella A. T. M., Kotagiri, Prasanti, Datir, Rawlings P., Lim, Eleanor Y., Touizer, Emma, Meng, Bo, Abdullahi, Adam, Elmer, Anne, Kingston, Nathalie, Graves, Barbara, Le Gresley, Emma, Caputo, Daniela, Bergamaschi, Laura, Smith, Kenneth G. C., Bradley, John R., Ceron-Gutierrez, Lourdes, Cortes-Acevedo, Paulina, Barcenas-Morales, Gabriela, Linterman, Michelle A., McCoy, Laura E., Davis, Chris, Thomson, Emma, Lyons, Paul A., McKinney, Eoin, Doffinger, Rainer, Wills, Mark, Gupta, Ravindra K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8373615/
https://www.ncbi.nlm.nih.gov/pubmed/34192737
http://dx.doi.org/10.1038/s41586-021-03739-1
_version_ 1783739970886828032
author Collier, Dami A.
Ferreira, Isabella A. T. M.
Kotagiri, Prasanti
Datir, Rawlings P.
Lim, Eleanor Y.
Touizer, Emma
Meng, Bo
Abdullahi, Adam
Elmer, Anne
Kingston, Nathalie
Graves, Barbara
Le Gresley, Emma
Caputo, Daniela
Bergamaschi, Laura
Smith, Kenneth G. C.
Bradley, John R.
Ceron-Gutierrez, Lourdes
Cortes-Acevedo, Paulina
Barcenas-Morales, Gabriela
Linterman, Michelle A.
McCoy, Laura E.
Davis, Chris
Thomson, Emma
Lyons, Paul A.
McKinney, Eoin
Doffinger, Rainer
Wills, Mark
Gupta, Ravindra K.
author_facet Collier, Dami A.
Ferreira, Isabella A. T. M.
Kotagiri, Prasanti
Datir, Rawlings P.
Lim, Eleanor Y.
Touizer, Emma
Meng, Bo
Abdullahi, Adam
Elmer, Anne
Kingston, Nathalie
Graves, Barbara
Le Gresley, Emma
Caputo, Daniela
Bergamaschi, Laura
Smith, Kenneth G. C.
Bradley, John R.
Ceron-Gutierrez, Lourdes
Cortes-Acevedo, Paulina
Barcenas-Morales, Gabriela
Linterman, Michelle A.
McCoy, Laura E.
Davis, Chris
Thomson, Emma
Lyons, Paul A.
McKinney, Eoin
Doffinger, Rainer
Wills, Mark
Gupta, Ravindra K.
author_sort Collier, Dami A.
collection PubMed
description Although two-dose mRNA vaccination provides excellent protection against SARS-CoV-2, there is little information about vaccine efficacy against variants of concern (VOC) in individuals above eighty years of age(1). Here we analysed immune responses following vaccination with the BNT162b2 mRNA vaccine(2) in elderly participants and younger healthcare workers. Serum neutralization and levels of binding IgG or IgA after the first vaccine dose were lower in older individuals, with a marked drop in participants over eighty years old. Sera from participants above eighty showed lower neutralization potency against the B.1.1.7 (Alpha), B.1.351 (Beta) and P.1. (Gamma) VOC than against the wild-type virus and were more likely to lack any neutralization against VOC following the first dose. However, following the second dose, neutralization against VOC was detectable regardless of age. The frequency of SARS-CoV-2 spike-specific memory B cells was higher in elderly responders (whose serum showed neutralization activity) than in non-responders after the first dose. Elderly participants showed a clear reduction in somatic hypermutation of class-switched cells. The production of interferon-γ and interleukin-2 by SARS-CoV-2 spike-specific T cells was lower in older participants, and both cytokines were secreted primarily by CD4 T cells. We conclude that the elderly are a high-risk population and that specific measures to boost vaccine responses in this population are warranted, particularly where variants of concern are circulating.
format Online
Article
Text
id pubmed-8373615
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-83736152021-09-02 Age-related immune response heterogeneity to SARS-CoV-2 vaccine BNT162b2 Collier, Dami A. Ferreira, Isabella A. T. M. Kotagiri, Prasanti Datir, Rawlings P. Lim, Eleanor Y. Touizer, Emma Meng, Bo Abdullahi, Adam Elmer, Anne Kingston, Nathalie Graves, Barbara Le Gresley, Emma Caputo, Daniela Bergamaschi, Laura Smith, Kenneth G. C. Bradley, John R. Ceron-Gutierrez, Lourdes Cortes-Acevedo, Paulina Barcenas-Morales, Gabriela Linterman, Michelle A. McCoy, Laura E. Davis, Chris Thomson, Emma Lyons, Paul A. McKinney, Eoin Doffinger, Rainer Wills, Mark Gupta, Ravindra K. Nature Article Although two-dose mRNA vaccination provides excellent protection against SARS-CoV-2, there is little information about vaccine efficacy against variants of concern (VOC) in individuals above eighty years of age(1). Here we analysed immune responses following vaccination with the BNT162b2 mRNA vaccine(2) in elderly participants and younger healthcare workers. Serum neutralization and levels of binding IgG or IgA after the first vaccine dose were lower in older individuals, with a marked drop in participants over eighty years old. Sera from participants above eighty showed lower neutralization potency against the B.1.1.7 (Alpha), B.1.351 (Beta) and P.1. (Gamma) VOC than against the wild-type virus and were more likely to lack any neutralization against VOC following the first dose. However, following the second dose, neutralization against VOC was detectable regardless of age. The frequency of SARS-CoV-2 spike-specific memory B cells was higher in elderly responders (whose serum showed neutralization activity) than in non-responders after the first dose. Elderly participants showed a clear reduction in somatic hypermutation of class-switched cells. The production of interferon-γ and interleukin-2 by SARS-CoV-2 spike-specific T cells was lower in older participants, and both cytokines were secreted primarily by CD4 T cells. We conclude that the elderly are a high-risk population and that specific measures to boost vaccine responses in this population are warranted, particularly where variants of concern are circulating. Nature Publishing Group UK 2021-06-30 2021 /pmc/articles/PMC8373615/ /pubmed/34192737 http://dx.doi.org/10.1038/s41586-021-03739-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Collier, Dami A.
Ferreira, Isabella A. T. M.
Kotagiri, Prasanti
Datir, Rawlings P.
Lim, Eleanor Y.
Touizer, Emma
Meng, Bo
Abdullahi, Adam
Elmer, Anne
Kingston, Nathalie
Graves, Barbara
Le Gresley, Emma
Caputo, Daniela
Bergamaschi, Laura
Smith, Kenneth G. C.
Bradley, John R.
Ceron-Gutierrez, Lourdes
Cortes-Acevedo, Paulina
Barcenas-Morales, Gabriela
Linterman, Michelle A.
McCoy, Laura E.
Davis, Chris
Thomson, Emma
Lyons, Paul A.
McKinney, Eoin
Doffinger, Rainer
Wills, Mark
Gupta, Ravindra K.
Age-related immune response heterogeneity to SARS-CoV-2 vaccine BNT162b2
title Age-related immune response heterogeneity to SARS-CoV-2 vaccine BNT162b2
title_full Age-related immune response heterogeneity to SARS-CoV-2 vaccine BNT162b2
title_fullStr Age-related immune response heterogeneity to SARS-CoV-2 vaccine BNT162b2
title_full_unstemmed Age-related immune response heterogeneity to SARS-CoV-2 vaccine BNT162b2
title_short Age-related immune response heterogeneity to SARS-CoV-2 vaccine BNT162b2
title_sort age-related immune response heterogeneity to sars-cov-2 vaccine bnt162b2
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8373615/
https://www.ncbi.nlm.nih.gov/pubmed/34192737
http://dx.doi.org/10.1038/s41586-021-03739-1
work_keys_str_mv AT collierdamia agerelatedimmuneresponseheterogeneitytosarscov2vaccinebnt162b2
AT ferreiraisabellaatm agerelatedimmuneresponseheterogeneitytosarscov2vaccinebnt162b2
AT kotagiriprasanti agerelatedimmuneresponseheterogeneitytosarscov2vaccinebnt162b2
AT datirrawlingsp agerelatedimmuneresponseheterogeneitytosarscov2vaccinebnt162b2
AT limeleanory agerelatedimmuneresponseheterogeneitytosarscov2vaccinebnt162b2
AT touizeremma agerelatedimmuneresponseheterogeneitytosarscov2vaccinebnt162b2
AT mengbo agerelatedimmuneresponseheterogeneitytosarscov2vaccinebnt162b2
AT abdullahiadam agerelatedimmuneresponseheterogeneitytosarscov2vaccinebnt162b2
AT agerelatedimmuneresponseheterogeneitytosarscov2vaccinebnt162b2
AT elmeranne agerelatedimmuneresponseheterogeneitytosarscov2vaccinebnt162b2
AT kingstonnathalie agerelatedimmuneresponseheterogeneitytosarscov2vaccinebnt162b2
AT gravesbarbara agerelatedimmuneresponseheterogeneitytosarscov2vaccinebnt162b2
AT legresleyemma agerelatedimmuneresponseheterogeneitytosarscov2vaccinebnt162b2
AT caputodaniela agerelatedimmuneresponseheterogeneitytosarscov2vaccinebnt162b2
AT bergamaschilaura agerelatedimmuneresponseheterogeneitytosarscov2vaccinebnt162b2
AT smithkennethgc agerelatedimmuneresponseheterogeneitytosarscov2vaccinebnt162b2
AT bradleyjohnr agerelatedimmuneresponseheterogeneitytosarscov2vaccinebnt162b2
AT cerongutierrezlourdes agerelatedimmuneresponseheterogeneitytosarscov2vaccinebnt162b2
AT cortesacevedopaulina agerelatedimmuneresponseheterogeneitytosarscov2vaccinebnt162b2
AT barcenasmoralesgabriela agerelatedimmuneresponseheterogeneitytosarscov2vaccinebnt162b2
AT lintermanmichellea agerelatedimmuneresponseheterogeneitytosarscov2vaccinebnt162b2
AT mccoylaurae agerelatedimmuneresponseheterogeneitytosarscov2vaccinebnt162b2
AT davischris agerelatedimmuneresponseheterogeneitytosarscov2vaccinebnt162b2
AT thomsonemma agerelatedimmuneresponseheterogeneitytosarscov2vaccinebnt162b2
AT lyonspaula agerelatedimmuneresponseheterogeneitytosarscov2vaccinebnt162b2
AT mckinneyeoin agerelatedimmuneresponseheterogeneitytosarscov2vaccinebnt162b2
AT doffingerrainer agerelatedimmuneresponseheterogeneitytosarscov2vaccinebnt162b2
AT willsmark agerelatedimmuneresponseheterogeneitytosarscov2vaccinebnt162b2
AT guptaravindrak agerelatedimmuneresponseheterogeneitytosarscov2vaccinebnt162b2