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Population differences in antibody response to SARS‐CoV‐2 infection and BNT162b2 vaccination
The concentration of SARS‐CoV‐2‐specific serum antibodies, elicited by vaccination or infection, is a primary determinant of anti‐viral immunity, which correlates with protection against infection and COVID‐19. Serum samples were obtained from 25 897 participants and assayed for anti‐SARS‐CoV‐2 spik...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9111330/ https://www.ncbi.nlm.nih.gov/pubmed/35239233 http://dx.doi.org/10.1096/fj.202101492R |
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author | Shapira, Guy Abu Hamad, Ramzia Weiner, Chen Rainy, Nir Sorek‐Abramovich, Reut Benveniste‐Levkovitz, Patricia Rock, Rachel Avnat, Eden Levtzion‐Korach, Osnat Bar Chaim, Adina Shomron, Noam |
author_facet | Shapira, Guy Abu Hamad, Ramzia Weiner, Chen Rainy, Nir Sorek‐Abramovich, Reut Benveniste‐Levkovitz, Patricia Rock, Rachel Avnat, Eden Levtzion‐Korach, Osnat Bar Chaim, Adina Shomron, Noam |
author_sort | Shapira, Guy |
collection | PubMed |
description | The concentration of SARS‐CoV‐2‐specific serum antibodies, elicited by vaccination or infection, is a primary determinant of anti‐viral immunity, which correlates with protection against infection and COVID‐19. Serum samples were obtained from 25 897 participants and assayed for anti‐SARS‐CoV‐2 spike protein RBD IgG antibodies. The cohort was composed of newly vaccinated BNT162b2 recipients, in the first month or 6 months after vaccination, COVID‐19 patients and a general sample of the Israeli population. Antibody levels of BNT162b2 vaccine recipients were negatively correlated with age, with a prominent decrease in recipients over 55 years old, which was most significant in males. This trend was observable within the first month and 6 months after vaccination, while younger participants were more likely to maintain stable levels of serum antibodies. The antibody concentration of participants previously infected with SARS‐CoV‐2 was lower than the vaccinated and had a more complex, non‐linear relation to age, sex and COVID‐19 symptoms. Taken together, our data supports age and sex as primary determining factors for both the magnitude and durability of humoral response to SARS‐CoV‐2 infection and the COVID‐19 vaccine. Our results could inform vaccination policies, prioritizing the most susceptible populations for repeated vaccination. |
format | Online Article Text |
id | pubmed-9111330 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-91113302022-05-17 Population differences in antibody response to SARS‐CoV‐2 infection and BNT162b2 vaccination Shapira, Guy Abu Hamad, Ramzia Weiner, Chen Rainy, Nir Sorek‐Abramovich, Reut Benveniste‐Levkovitz, Patricia Rock, Rachel Avnat, Eden Levtzion‐Korach, Osnat Bar Chaim, Adina Shomron, Noam FASEB J Research Articles The concentration of SARS‐CoV‐2‐specific serum antibodies, elicited by vaccination or infection, is a primary determinant of anti‐viral immunity, which correlates with protection against infection and COVID‐19. Serum samples were obtained from 25 897 participants and assayed for anti‐SARS‐CoV‐2 spike protein RBD IgG antibodies. The cohort was composed of newly vaccinated BNT162b2 recipients, in the first month or 6 months after vaccination, COVID‐19 patients and a general sample of the Israeli population. Antibody levels of BNT162b2 vaccine recipients were negatively correlated with age, with a prominent decrease in recipients over 55 years old, which was most significant in males. This trend was observable within the first month and 6 months after vaccination, while younger participants were more likely to maintain stable levels of serum antibodies. The antibody concentration of participants previously infected with SARS‐CoV‐2 was lower than the vaccinated and had a more complex, non‐linear relation to age, sex and COVID‐19 symptoms. Taken together, our data supports age and sex as primary determining factors for both the magnitude and durability of humoral response to SARS‐CoV‐2 infection and the COVID‐19 vaccine. Our results could inform vaccination policies, prioritizing the most susceptible populations for repeated vaccination. John Wiley and Sons Inc. 2022-03-03 2022-04 /pmc/articles/PMC9111330/ /pubmed/35239233 http://dx.doi.org/10.1096/fj.202101492R Text en © 2022 The Authors. The FASEB Journal published by Wiley Periodicals LLC on behalf of Federation of American Societies for Experimental Biology https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Research Articles Shapira, Guy Abu Hamad, Ramzia Weiner, Chen Rainy, Nir Sorek‐Abramovich, Reut Benveniste‐Levkovitz, Patricia Rock, Rachel Avnat, Eden Levtzion‐Korach, Osnat Bar Chaim, Adina Shomron, Noam Population differences in antibody response to SARS‐CoV‐2 infection and BNT162b2 vaccination |
title | Population differences in antibody response to SARS‐CoV‐2 infection and BNT162b2 vaccination |
title_full | Population differences in antibody response to SARS‐CoV‐2 infection and BNT162b2 vaccination |
title_fullStr | Population differences in antibody response to SARS‐CoV‐2 infection and BNT162b2 vaccination |
title_full_unstemmed | Population differences in antibody response to SARS‐CoV‐2 infection and BNT162b2 vaccination |
title_short | Population differences in antibody response to SARS‐CoV‐2 infection and BNT162b2 vaccination |
title_sort | population differences in antibody response to sars‐cov‐2 infection and bnt162b2 vaccination |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9111330/ https://www.ncbi.nlm.nih.gov/pubmed/35239233 http://dx.doi.org/10.1096/fj.202101492R |
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