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Saliva is suitable for SARS-CoV-2 antibodies detection after vaccination: A rapid systematic review

Since the introduction of efficient vaccines anti-SARS-CoV-2, antibody quantification becomes increasingly useful for immunological monitoring and COVID-19 control. In several situations, saliva samples may be an alternative to the serological test. Thus, this rapid systematic review aimed to evalua...

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Autores principales: Guerra, Eliete Neves Silva, de Castro, Vitória Tavares, Amorim dos Santos, Juliana, Acevedo, Ana Carolina, Chardin, Hélène
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9530471/
https://www.ncbi.nlm.nih.gov/pubmed/36203571
http://dx.doi.org/10.3389/fimmu.2022.1006040
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author Guerra, Eliete Neves Silva
de Castro, Vitória Tavares
Amorim dos Santos, Juliana
Acevedo, Ana Carolina
Chardin, Hélène
author_facet Guerra, Eliete Neves Silva
de Castro, Vitória Tavares
Amorim dos Santos, Juliana
Acevedo, Ana Carolina
Chardin, Hélène
author_sort Guerra, Eliete Neves Silva
collection PubMed
description Since the introduction of efficient vaccines anti-SARS-CoV-2, antibody quantification becomes increasingly useful for immunological monitoring and COVID-19 control. In several situations, saliva samples may be an alternative to the serological test. Thus, this rapid systematic review aimed to evaluate if saliva is suitable for SARS-CoV-2 detection after vaccination. For this purpose, search strategies were applied at EMBASE, PubMed, and Web of Science. Studies were selected by two reviewers in a two-phase process. After selection, 15 studies were eligible and included in data synthesis. In total, salivary samples of approximately 1,080 vaccinated and/or convalescent individuals were analyzed. The applied vaccines were mostly mRNA-based (BioNTech 162b2 mRNA/Pfizer and Spikevax mRNA-1273/Moderna), but recombinant viral-vectored vaccines (Ad26. COV2. S Janssen - Johnson & Johnson and Vaxzevria/Oxford AstraZeneca) were also included. Different techniques were applied for saliva evaluation, such as ELISA assay, Multiplex immunoassay, flow cytometry, neutralizing and electrochemical assays. Although antibody titers are lower in saliva than in serum, the results showed that saliva is suitable for antibody detection. The mean of reported correlations for titers in saliva and serum/plasma were moderate for IgG (0.55, 95% CI 0.38-9.73), and weak for IgA (0.28, 95% CI 0.12-0.44). Additionally, six out of nine studies reported numerical titers for immunoglobulins detection, from which the level in saliva reached their reference value in four (66%). IgG but not IgA are frequently presented in saliva from vaccinated anti-COVID-19. Four studies reported lower IgA salivary titers in vaccinated compared to previously infected individuals, otherwise, two reported higher titers of IgA in vaccinated. Concerning IgG, two studies reported high antibody titers in the saliva of vaccinated individuals compared to those previously infected and one presented similar results for vaccinated and infected. The detection of antibodies anti-SARS-CoV-2 in the saliva is available, which suggests this type of sample is a suitable alternative for monitoring the population. Thus, the results also pointed out the possible lack of mucosal immunity induction after anti-SARS-CoV-2 vaccination. It highlights the importance of new vaccination strategies also focused on mucosal alternatives directly on primary routes of SARS-CoV-2 entrance. SYSTEMATIC REVIEW REGISTRATION: https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42022336968, identifier CRD42022336968.
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spelling pubmed-95304712022-10-05 Saliva is suitable for SARS-CoV-2 antibodies detection after vaccination: A rapid systematic review Guerra, Eliete Neves Silva de Castro, Vitória Tavares Amorim dos Santos, Juliana Acevedo, Ana Carolina Chardin, Hélène Front Immunol Immunology Since the introduction of efficient vaccines anti-SARS-CoV-2, antibody quantification becomes increasingly useful for immunological monitoring and COVID-19 control. In several situations, saliva samples may be an alternative to the serological test. Thus, this rapid systematic review aimed to evaluate if saliva is suitable for SARS-CoV-2 detection after vaccination. For this purpose, search strategies were applied at EMBASE, PubMed, and Web of Science. Studies were selected by two reviewers in a two-phase process. After selection, 15 studies were eligible and included in data synthesis. In total, salivary samples of approximately 1,080 vaccinated and/or convalescent individuals were analyzed. The applied vaccines were mostly mRNA-based (BioNTech 162b2 mRNA/Pfizer and Spikevax mRNA-1273/Moderna), but recombinant viral-vectored vaccines (Ad26. COV2. S Janssen - Johnson & Johnson and Vaxzevria/Oxford AstraZeneca) were also included. Different techniques were applied for saliva evaluation, such as ELISA assay, Multiplex immunoassay, flow cytometry, neutralizing and electrochemical assays. Although antibody titers are lower in saliva than in serum, the results showed that saliva is suitable for antibody detection. The mean of reported correlations for titers in saliva and serum/plasma were moderate for IgG (0.55, 95% CI 0.38-9.73), and weak for IgA (0.28, 95% CI 0.12-0.44). Additionally, six out of nine studies reported numerical titers for immunoglobulins detection, from which the level in saliva reached their reference value in four (66%). IgG but not IgA are frequently presented in saliva from vaccinated anti-COVID-19. Four studies reported lower IgA salivary titers in vaccinated compared to previously infected individuals, otherwise, two reported higher titers of IgA in vaccinated. Concerning IgG, two studies reported high antibody titers in the saliva of vaccinated individuals compared to those previously infected and one presented similar results for vaccinated and infected. The detection of antibodies anti-SARS-CoV-2 in the saliva is available, which suggests this type of sample is a suitable alternative for monitoring the population. Thus, the results also pointed out the possible lack of mucosal immunity induction after anti-SARS-CoV-2 vaccination. It highlights the importance of new vaccination strategies also focused on mucosal alternatives directly on primary routes of SARS-CoV-2 entrance. SYSTEMATIC REVIEW REGISTRATION: https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42022336968, identifier CRD42022336968. Frontiers Media S.A. 2022-09-20 /pmc/articles/PMC9530471/ /pubmed/36203571 http://dx.doi.org/10.3389/fimmu.2022.1006040 Text en Copyright © 2022 Guerra, Castro, Amorim dos Santos, Acevedo and Chardin https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Guerra, Eliete Neves Silva
de Castro, Vitória Tavares
Amorim dos Santos, Juliana
Acevedo, Ana Carolina
Chardin, Hélène
Saliva is suitable for SARS-CoV-2 antibodies detection after vaccination: A rapid systematic review
title Saliva is suitable for SARS-CoV-2 antibodies detection after vaccination: A rapid systematic review
title_full Saliva is suitable for SARS-CoV-2 antibodies detection after vaccination: A rapid systematic review
title_fullStr Saliva is suitable for SARS-CoV-2 antibodies detection after vaccination: A rapid systematic review
title_full_unstemmed Saliva is suitable for SARS-CoV-2 antibodies detection after vaccination: A rapid systematic review
title_short Saliva is suitable for SARS-CoV-2 antibodies detection after vaccination: A rapid systematic review
title_sort saliva is suitable for sars-cov-2 antibodies detection after vaccination: a rapid systematic review
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9530471/
https://www.ncbi.nlm.nih.gov/pubmed/36203571
http://dx.doi.org/10.3389/fimmu.2022.1006040
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