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Humoral immunogenicity assessment after receiving three types of SARS-CoV-2 vaccine
Several vaccines have been developed against SARS-CoV-2 and subsequently approved by national/international regulators. Detecting specific antibodies after vaccination enables us to evaluate the vaccine’s effectiveness. We conducted a prospective longitudinal study among members of Tarbiat Modares U...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10657424/ https://www.ncbi.nlm.nih.gov/pubmed/37980441 http://dx.doi.org/10.1038/s41598-023-47611-w |
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author | Najafi, Niloofar Soleimanjahi, Hoorieh Moghaddam-Banaem, Lida Raoufy, Mohammad Reza Shahali, Shadab Kazemnejad, Anoshirvan Nasiri, Zeynab |
author_facet | Najafi, Niloofar Soleimanjahi, Hoorieh Moghaddam-Banaem, Lida Raoufy, Mohammad Reza Shahali, Shadab Kazemnejad, Anoshirvan Nasiri, Zeynab |
author_sort | Najafi, Niloofar |
collection | PubMed |
description | Several vaccines have been developed against SARS-CoV-2 and subsequently approved by national/international regulators. Detecting specific antibodies after vaccination enables us to evaluate the vaccine’s effectiveness. We conducted a prospective longitudinal study among members of Tarbiat Modares University of Tehran, Iran, from 4 September 2021 until 29 December 2021. We aimed to compare the humoral immunogenicity of 3 vaccine types. Participants consisted of 462 adults. Anti-SARS-CoV-2 receptor-binding domain [RBD] IgG titer was compared in 3 groups, each vaccinated by available vaccines in Iran at the time: Oxford/AstraZeneca, COVIran Barekat, and Sinopharm. The median IgG titer was: 91.2, 105.6, 224.0 BAU/ml for Sinopharm, COVIran Barekat and Oxford/AstraZeneca respectively after the first dose; 195.2, 192.0, 337.6 BAU/ml after the second one. We also analyzed the frequency of antibody presence in each vaccine group, in the same order the results were 59.0%, 62.6% and 89.4% after the first dose and 92.1%,89.5% and 98.9% after the second. The comparison of results demonstrated that AstraZeneca vaccine is a superior candidate vaccine for COVID-19 vaccination out of the three. Our data also demonstrated statistically significant higher antibody titer among recipients with an infection history. |
format | Online Article Text |
id | pubmed-10657424 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-106574242023-11-18 Humoral immunogenicity assessment after receiving three types of SARS-CoV-2 vaccine Najafi, Niloofar Soleimanjahi, Hoorieh Moghaddam-Banaem, Lida Raoufy, Mohammad Reza Shahali, Shadab Kazemnejad, Anoshirvan Nasiri, Zeynab Sci Rep Article Several vaccines have been developed against SARS-CoV-2 and subsequently approved by national/international regulators. Detecting specific antibodies after vaccination enables us to evaluate the vaccine’s effectiveness. We conducted a prospective longitudinal study among members of Tarbiat Modares University of Tehran, Iran, from 4 September 2021 until 29 December 2021. We aimed to compare the humoral immunogenicity of 3 vaccine types. Participants consisted of 462 adults. Anti-SARS-CoV-2 receptor-binding domain [RBD] IgG titer was compared in 3 groups, each vaccinated by available vaccines in Iran at the time: Oxford/AstraZeneca, COVIran Barekat, and Sinopharm. The median IgG titer was: 91.2, 105.6, 224.0 BAU/ml for Sinopharm, COVIran Barekat and Oxford/AstraZeneca respectively after the first dose; 195.2, 192.0, 337.6 BAU/ml after the second one. We also analyzed the frequency of antibody presence in each vaccine group, in the same order the results were 59.0%, 62.6% and 89.4% after the first dose and 92.1%,89.5% and 98.9% after the second. The comparison of results demonstrated that AstraZeneca vaccine is a superior candidate vaccine for COVID-19 vaccination out of the three. Our data also demonstrated statistically significant higher antibody titer among recipients with an infection history. Nature Publishing Group UK 2023-11-18 /pmc/articles/PMC10657424/ /pubmed/37980441 http://dx.doi.org/10.1038/s41598-023-47611-w Text en © The Author(s) 2023 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Najafi, Niloofar Soleimanjahi, Hoorieh Moghaddam-Banaem, Lida Raoufy, Mohammad Reza Shahali, Shadab Kazemnejad, Anoshirvan Nasiri, Zeynab Humoral immunogenicity assessment after receiving three types of SARS-CoV-2 vaccine |
title | Humoral immunogenicity assessment after receiving three types of SARS-CoV-2 vaccine |
title_full | Humoral immunogenicity assessment after receiving three types of SARS-CoV-2 vaccine |
title_fullStr | Humoral immunogenicity assessment after receiving three types of SARS-CoV-2 vaccine |
title_full_unstemmed | Humoral immunogenicity assessment after receiving three types of SARS-CoV-2 vaccine |
title_short | Humoral immunogenicity assessment after receiving three types of SARS-CoV-2 vaccine |
title_sort | humoral immunogenicity assessment after receiving three types of sars-cov-2 vaccine |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10657424/ https://www.ncbi.nlm.nih.gov/pubmed/37980441 http://dx.doi.org/10.1038/s41598-023-47611-w |
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