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Duration of SARS-CoV-2 Immune Responses Up to Six Months Following Homologous or Heterologous Primary Immunization with ChAdOx1 nCoV-19 and BNT162b2 mRNA Vaccines

Heterologous primary immunization against SARS-CoV-2 is part of applied recommendations. However, little is known about duration of immune responses after heterologous vaccine regimens. To evaluate duration of immune responses after primary vaccination with homologous adeno-vectored ChAdOx1 nCoV-19...

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Autores principales: Marking, Ulrika, Havervall, Sebastian, Greilert-Norin, Nina, Ng, Henry, Blom, Kim, Nilsson, Peter, Phillipson, Mia, Hober, Sophia, Nilsson, Charlotta, Mangsbo, Sara, Christ, Wanda, Klingström, Jonas, Gordon, Max, Åberg, Mikael, Thålin, Charlotte
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8953845/
https://www.ncbi.nlm.nih.gov/pubmed/35334989
http://dx.doi.org/10.3390/vaccines10030359
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author Marking, Ulrika
Havervall, Sebastian
Greilert-Norin, Nina
Ng, Henry
Blom, Kim
Nilsson, Peter
Phillipson, Mia
Hober, Sophia
Nilsson, Charlotta
Mangsbo, Sara
Christ, Wanda
Klingström, Jonas
Gordon, Max
Åberg, Mikael
Thålin, Charlotte
author_facet Marking, Ulrika
Havervall, Sebastian
Greilert-Norin, Nina
Ng, Henry
Blom, Kim
Nilsson, Peter
Phillipson, Mia
Hober, Sophia
Nilsson, Charlotta
Mangsbo, Sara
Christ, Wanda
Klingström, Jonas
Gordon, Max
Åberg, Mikael
Thålin, Charlotte
author_sort Marking, Ulrika
collection PubMed
description Heterologous primary immunization against SARS-CoV-2 is part of applied recommendations. However, little is known about duration of immune responses after heterologous vaccine regimens. To evaluate duration of immune responses after primary vaccination with homologous adeno-vectored ChAdOx1 nCoV-19 vaccine (ChAd) or heterologous ChAd/BNT162b2 mRNA vaccine (BNT), anti-spike-IgG and SARS-CoV-2 VOC-neutralizing antibody responses were measured in 354 healthcare workers (HCW) at 2 weeks, 3 months, 5 months and 6 months after the second vaccine dose. T-cell responses were investigated using a whole blood interferon gamma (IFN-γ) release assay 2 weeks and 3 months post second vaccine dose. Two hundred and ten HCW immunized with homologous BNT were enrolled for comparison of antibody responses. In study participants naïve to SARS-CoV-2 prior to vaccination, heterologous ChAd/BNT resulted in 6-fold higher peak anti-spike IgG antibody titers compared to homologous ChAd vaccination. The half-life of antibody titers was 3.1 months (95% CI 2.8–3.6) following homologous ChAd vaccination and 1.9 months (95% CI 1.7–2.1) after heterologous vaccination, reducing the GMT difference between the groups to 3-fold 6 months post vaccination. Peak T-cell responses were stronger in ChAd/BNT vaccinees, but no significant difference was observed 3 months post vaccination. SARS-CoV-2 infection prior to vaccination resulted in substantially higher peak GMTs and IFN-γ levels and enhanced SARS-CoV-2 specific antibody and T cell responses over time. Heterologous primary SARS-CoV-2 immunization with ChAd and BNT elicits a stronger initial immune response compared to homologous vaccination with ChAd. However, although the differences in humoral responses remain over 6 months, the difference in SARS-CoV-2 specific T cell responses are no longer significant three months after vaccination.
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spelling pubmed-89538452022-03-26 Duration of SARS-CoV-2 Immune Responses Up to Six Months Following Homologous or Heterologous Primary Immunization with ChAdOx1 nCoV-19 and BNT162b2 mRNA Vaccines Marking, Ulrika Havervall, Sebastian Greilert-Norin, Nina Ng, Henry Blom, Kim Nilsson, Peter Phillipson, Mia Hober, Sophia Nilsson, Charlotta Mangsbo, Sara Christ, Wanda Klingström, Jonas Gordon, Max Åberg, Mikael Thålin, Charlotte Vaccines (Basel) Article Heterologous primary immunization against SARS-CoV-2 is part of applied recommendations. However, little is known about duration of immune responses after heterologous vaccine regimens. To evaluate duration of immune responses after primary vaccination with homologous adeno-vectored ChAdOx1 nCoV-19 vaccine (ChAd) or heterologous ChAd/BNT162b2 mRNA vaccine (BNT), anti-spike-IgG and SARS-CoV-2 VOC-neutralizing antibody responses were measured in 354 healthcare workers (HCW) at 2 weeks, 3 months, 5 months and 6 months after the second vaccine dose. T-cell responses were investigated using a whole blood interferon gamma (IFN-γ) release assay 2 weeks and 3 months post second vaccine dose. Two hundred and ten HCW immunized with homologous BNT were enrolled for comparison of antibody responses. In study participants naïve to SARS-CoV-2 prior to vaccination, heterologous ChAd/BNT resulted in 6-fold higher peak anti-spike IgG antibody titers compared to homologous ChAd vaccination. The half-life of antibody titers was 3.1 months (95% CI 2.8–3.6) following homologous ChAd vaccination and 1.9 months (95% CI 1.7–2.1) after heterologous vaccination, reducing the GMT difference between the groups to 3-fold 6 months post vaccination. Peak T-cell responses were stronger in ChAd/BNT vaccinees, but no significant difference was observed 3 months post vaccination. SARS-CoV-2 infection prior to vaccination resulted in substantially higher peak GMTs and IFN-γ levels and enhanced SARS-CoV-2 specific antibody and T cell responses over time. Heterologous primary SARS-CoV-2 immunization with ChAd and BNT elicits a stronger initial immune response compared to homologous vaccination with ChAd. However, although the differences in humoral responses remain over 6 months, the difference in SARS-CoV-2 specific T cell responses are no longer significant three months after vaccination. MDPI 2022-02-24 /pmc/articles/PMC8953845/ /pubmed/35334989 http://dx.doi.org/10.3390/vaccines10030359 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Marking, Ulrika
Havervall, Sebastian
Greilert-Norin, Nina
Ng, Henry
Blom, Kim
Nilsson, Peter
Phillipson, Mia
Hober, Sophia
Nilsson, Charlotta
Mangsbo, Sara
Christ, Wanda
Klingström, Jonas
Gordon, Max
Åberg, Mikael
Thålin, Charlotte
Duration of SARS-CoV-2 Immune Responses Up to Six Months Following Homologous or Heterologous Primary Immunization with ChAdOx1 nCoV-19 and BNT162b2 mRNA Vaccines
title Duration of SARS-CoV-2 Immune Responses Up to Six Months Following Homologous or Heterologous Primary Immunization with ChAdOx1 nCoV-19 and BNT162b2 mRNA Vaccines
title_full Duration of SARS-CoV-2 Immune Responses Up to Six Months Following Homologous or Heterologous Primary Immunization with ChAdOx1 nCoV-19 and BNT162b2 mRNA Vaccines
title_fullStr Duration of SARS-CoV-2 Immune Responses Up to Six Months Following Homologous or Heterologous Primary Immunization with ChAdOx1 nCoV-19 and BNT162b2 mRNA Vaccines
title_full_unstemmed Duration of SARS-CoV-2 Immune Responses Up to Six Months Following Homologous or Heterologous Primary Immunization with ChAdOx1 nCoV-19 and BNT162b2 mRNA Vaccines
title_short Duration of SARS-CoV-2 Immune Responses Up to Six Months Following Homologous or Heterologous Primary Immunization with ChAdOx1 nCoV-19 and BNT162b2 mRNA Vaccines
title_sort duration of sars-cov-2 immune responses up to six months following homologous or heterologous primary immunization with chadox1 ncov-19 and bnt162b2 mrna vaccines
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8953845/
https://www.ncbi.nlm.nih.gov/pubmed/35334989
http://dx.doi.org/10.3390/vaccines10030359
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