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Short-Lived Antibody-Mediated Saliva Immunity against SARS-CoV-2 after Vaccination
Knowledge about the effect of vaccination against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) on immunity reflected in the saliva is sparse. We examined the antibody response in saliva compared to that in serum 2 and 6 months after the first vaccination with the BNT162b2 vaccine. Fo...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10101069/ https://www.ncbi.nlm.nih.gov/pubmed/36877077 http://dx.doi.org/10.1128/spectrum.04947-22 |
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author | Madsen, Johannes Roth Holm, Bettina Eide Pérez-Alós, Laura Bayarri-Olmos, Rafael Rosbjerg, Anne Fogh, Kamille Pries-Heje, Mia Marie Møller, Dina Leth Hansen, Cecilie Bo Heftdal, Line Dam Hasselbalch, Rasmus Bo Hamm, Sebastian Rask Frikke-Schmidt, Ruth Hilsted, Linda Nielsen, Susanne Dam Iversen, Kasper Karmark Bundgaard, Henning Garred, Peter |
author_facet | Madsen, Johannes Roth Holm, Bettina Eide Pérez-Alós, Laura Bayarri-Olmos, Rafael Rosbjerg, Anne Fogh, Kamille Pries-Heje, Mia Marie Møller, Dina Leth Hansen, Cecilie Bo Heftdal, Line Dam Hasselbalch, Rasmus Bo Hamm, Sebastian Rask Frikke-Schmidt, Ruth Hilsted, Linda Nielsen, Susanne Dam Iversen, Kasper Karmark Bundgaard, Henning Garred, Peter |
author_sort | Madsen, Johannes Roth |
collection | PubMed |
description | Knowledge about the effect of vaccination against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) on immunity reflected in the saliva is sparse. We examined the antibody response in saliva compared to that in serum 2 and 6 months after the first vaccination with the BNT162b2 vaccine. Four hundred fifty-nine health care professionals were included in a prospective observational study measuring antibody levels in saliva and corresponding serum samples at 2 and 6 months after BNT162b2 vaccination. Vaccinated, previously SARS-CoV-2-infected individuals (hybrid immunity) had higher IgG levels in saliva at 2 months than vaccinated, infection-naive individuals (P < 0.001). After 6 months, saliva IgG levels declined in both groups (P < 0.001), with no difference between groups (P = 0.37). Furthermore, serum IgG levels declined from 2 to 6 months in both groups (P < 0.001). IgG antibodies in saliva and serum correlated in individuals with hybrid immunity at 2 and 6 months (ρ = 0.58, P = 0.001, and ρ = 0.53, P = 0.052, respectively). In vaccinated, infection-naive individuals, a correlation was observed at 2 months (ρ = 0.42, P < 0.001) but not after 6 months (ρ = 0.14, P = 0.055). IgA and IgM antibodies were hardly detectable in saliva at any time point, regardless of previous infection. In serum, IgA was detected at 2 months in previously infected individuals. BNT162b2 vaccination induced a detectable IgG anti-SARS-CoV-2 RBD response in saliva at both 2 and 6 months after vaccination, being more prominent in previously infected than infection-naive individuals. However, a significant decrease in salivary IgG was observed after 6 months, suggesting a rapid decline in antibody-mediated saliva immunity against SARS-CoV-2, after both infection and systemic vaccination. IMPORTANCE Knowledge about the persistence of salivary immunity after SARS-CoV-2 vaccination is limited, and information on this topic could prove important for vaccine strategy and development. We hypothesized that salivary immunity would wane rapidly after vaccination. We measured anti-SARS-CoV-2 IgG, IgA, and IgM concentrations in saliva and serum in both previously infected and infection-naive individuals, 2 and 6 months after first vaccination with BNT162b2, in 459 hospital employees from Copenhagen University Hospital. We observed that IgG was the primary salivary antibody 2 months after vaccination in both previously infected and infection-naive individuals, but dropped significantly after 6 months. Neither IgA nor IgM was detectable in saliva at either time point. Findings indicate that salivary immunity against SARS-CoV-2 rapidly declines following vaccination in both previously infected and infection-naive individuals. We believe this study shines a light on the workings of salivary immunity after SARS-CoV-2 infection, which could prove relevant for vaccine development. |
format | Online Article Text |
id | pubmed-10101069 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-101010692023-04-14 Short-Lived Antibody-Mediated Saliva Immunity against SARS-CoV-2 after Vaccination Madsen, Johannes Roth Holm, Bettina Eide Pérez-Alós, Laura Bayarri-Olmos, Rafael Rosbjerg, Anne Fogh, Kamille Pries-Heje, Mia Marie Møller, Dina Leth Hansen, Cecilie Bo Heftdal, Line Dam Hasselbalch, Rasmus Bo Hamm, Sebastian Rask Frikke-Schmidt, Ruth Hilsted, Linda Nielsen, Susanne Dam Iversen, Kasper Karmark Bundgaard, Henning Garred, Peter Microbiol Spectr Research Article Knowledge about the effect of vaccination against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) on immunity reflected in the saliva is sparse. We examined the antibody response in saliva compared to that in serum 2 and 6 months after the first vaccination with the BNT162b2 vaccine. Four hundred fifty-nine health care professionals were included in a prospective observational study measuring antibody levels in saliva and corresponding serum samples at 2 and 6 months after BNT162b2 vaccination. Vaccinated, previously SARS-CoV-2-infected individuals (hybrid immunity) had higher IgG levels in saliva at 2 months than vaccinated, infection-naive individuals (P < 0.001). After 6 months, saliva IgG levels declined in both groups (P < 0.001), with no difference between groups (P = 0.37). Furthermore, serum IgG levels declined from 2 to 6 months in both groups (P < 0.001). IgG antibodies in saliva and serum correlated in individuals with hybrid immunity at 2 and 6 months (ρ = 0.58, P = 0.001, and ρ = 0.53, P = 0.052, respectively). In vaccinated, infection-naive individuals, a correlation was observed at 2 months (ρ = 0.42, P < 0.001) but not after 6 months (ρ = 0.14, P = 0.055). IgA and IgM antibodies were hardly detectable in saliva at any time point, regardless of previous infection. In serum, IgA was detected at 2 months in previously infected individuals. BNT162b2 vaccination induced a detectable IgG anti-SARS-CoV-2 RBD response in saliva at both 2 and 6 months after vaccination, being more prominent in previously infected than infection-naive individuals. However, a significant decrease in salivary IgG was observed after 6 months, suggesting a rapid decline in antibody-mediated saliva immunity against SARS-CoV-2, after both infection and systemic vaccination. IMPORTANCE Knowledge about the persistence of salivary immunity after SARS-CoV-2 vaccination is limited, and information on this topic could prove important for vaccine strategy and development. We hypothesized that salivary immunity would wane rapidly after vaccination. We measured anti-SARS-CoV-2 IgG, IgA, and IgM concentrations in saliva and serum in both previously infected and infection-naive individuals, 2 and 6 months after first vaccination with BNT162b2, in 459 hospital employees from Copenhagen University Hospital. We observed that IgG was the primary salivary antibody 2 months after vaccination in both previously infected and infection-naive individuals, but dropped significantly after 6 months. Neither IgA nor IgM was detectable in saliva at either time point. Findings indicate that salivary immunity against SARS-CoV-2 rapidly declines following vaccination in both previously infected and infection-naive individuals. We believe this study shines a light on the workings of salivary immunity after SARS-CoV-2 infection, which could prove relevant for vaccine development. American Society for Microbiology 2023-03-06 /pmc/articles/PMC10101069/ /pubmed/36877077 http://dx.doi.org/10.1128/spectrum.04947-22 Text en Copyright © 2023 Madsen et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Madsen, Johannes Roth Holm, Bettina Eide Pérez-Alós, Laura Bayarri-Olmos, Rafael Rosbjerg, Anne Fogh, Kamille Pries-Heje, Mia Marie Møller, Dina Leth Hansen, Cecilie Bo Heftdal, Line Dam Hasselbalch, Rasmus Bo Hamm, Sebastian Rask Frikke-Schmidt, Ruth Hilsted, Linda Nielsen, Susanne Dam Iversen, Kasper Karmark Bundgaard, Henning Garred, Peter Short-Lived Antibody-Mediated Saliva Immunity against SARS-CoV-2 after Vaccination |
title | Short-Lived Antibody-Mediated Saliva Immunity against SARS-CoV-2 after Vaccination |
title_full | Short-Lived Antibody-Mediated Saliva Immunity against SARS-CoV-2 after Vaccination |
title_fullStr | Short-Lived Antibody-Mediated Saliva Immunity against SARS-CoV-2 after Vaccination |
title_full_unstemmed | Short-Lived Antibody-Mediated Saliva Immunity against SARS-CoV-2 after Vaccination |
title_short | Short-Lived Antibody-Mediated Saliva Immunity against SARS-CoV-2 after Vaccination |
title_sort | short-lived antibody-mediated saliva immunity against sars-cov-2 after vaccination |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10101069/ https://www.ncbi.nlm.nih.gov/pubmed/36877077 http://dx.doi.org/10.1128/spectrum.04947-22 |
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