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KINETICS OF ANTI-SARS-COV-2 IGG ANTIBODIES POST-COVID-19 -VACCINATION

INTRO: During the pandemic of COVD-19, several vaccines have been developed and are currently used worldwide. However, head-to-head studies comparing various vaccines are limited. Therefore, This single-center, prospective, realworld study. head-to-head study of compared the effectiveness of BNT162b...

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Autores principales: Kamal, S., Naguib, M., Daador, M., Alanazi, Z., Basalem, A. Abdullah, Alaskar, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier Ltd. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10186921/
http://dx.doi.org/10.1016/j.ijid.2023.04.208
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author Kamal, S.
Naguib, M.
Daador, M.
Alanazi, Z.
Basalem, A. Abdullah
Alaskar, A.
author_facet Kamal, S.
Naguib, M.
Daador, M.
Alanazi, Z.
Basalem, A. Abdullah
Alaskar, A.
author_sort Kamal, S.
collection PubMed
description INTRO: During the pandemic of COVD-19, several vaccines have been developed and are currently used worldwide. However, head-to-head studies comparing various vaccines are limited. Therefore, This single-center, prospective, realworld study. head-to-head study of compared the effectiveness of BNT162b2 (Pfizer BioNTech), mRNA-1273 (Moderna) ChAdOx1-S (Astra Zeneca) vaccines. The kinetics of SARS-CoV2 spike antibodies were monitored post-vaccination and following two booster doses in COVID-19 naïve and previously infected adults. METHODS: The primary outcome was the emergence of virologically positive COVID-19 cases after vaccine completion. The secondary outcome was the occurrence of postvaccination COVID-19-related hospitalizations. The titers of anti-SARS-CoV-2 IgG antibodies against the S1 subunit of the virus's spike protein were measured after the first and second doses of the three vaccines and the booster doses. FINDINGS: The current study enrolled and followed 1550 participants who received ChAdOx1-S or BNT162b2, or mRNA-1273, and 1550 non-vaccinated subjects between March 2021 and February 2022. After completing two vaccine doses, the effectiveness in preventing COVID-19 cases was 89.2%, 95.5%, and 94.6% for ChAdOx1-S or BNT162b2, or mRNA-1273, respectively. Four COVID-19-related hospitalizations (0.26%) were reported in the vaccinated versus 648 (41.81%) non-vaccinated participants (P<0.0001). Following the Pfizer booster dose, no COVID-19-positive cases or hospitalizations were reported. In the three vaccines, SARS-CoV2 antibody titers increased gradually after the first dose, peaked 3-4 weeks after the second dose, then declined after 28-32 weeks. Enhanced antibody response was observed after the booster dose and was maintained until the end of follow-up. Comorbidities were associated with lower antibody titers, particularly diabetes, autoimmune diseases, and advanced renal diseases. CONCLUSION: The study showed that the three COVID-10 vaccines effectively reduced the risk of virologically confirmed COVID-19 disease and prevented severe illness and hospitalizations in COVID-19 naiive and previously infected. Booster doses enhance the SARS-CoV2 antibody response and decrease the incidence of virologically proven severe COVID-19.
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spelling pubmed-101869212023-05-16 KINETICS OF ANTI-SARS-COV-2 IGG ANTIBODIES POST-COVID-19 -VACCINATION Kamal, S. Naguib, M. Daador, M. Alanazi, Z. Basalem, A. Abdullah Alaskar, A. Int J Infect Dis Article INTRO: During the pandemic of COVD-19, several vaccines have been developed and are currently used worldwide. However, head-to-head studies comparing various vaccines are limited. Therefore, This single-center, prospective, realworld study. head-to-head study of compared the effectiveness of BNT162b2 (Pfizer BioNTech), mRNA-1273 (Moderna) ChAdOx1-S (Astra Zeneca) vaccines. The kinetics of SARS-CoV2 spike antibodies were monitored post-vaccination and following two booster doses in COVID-19 naïve and previously infected adults. METHODS: The primary outcome was the emergence of virologically positive COVID-19 cases after vaccine completion. The secondary outcome was the occurrence of postvaccination COVID-19-related hospitalizations. The titers of anti-SARS-CoV-2 IgG antibodies against the S1 subunit of the virus's spike protein were measured after the first and second doses of the three vaccines and the booster doses. FINDINGS: The current study enrolled and followed 1550 participants who received ChAdOx1-S or BNT162b2, or mRNA-1273, and 1550 non-vaccinated subjects between March 2021 and February 2022. After completing two vaccine doses, the effectiveness in preventing COVID-19 cases was 89.2%, 95.5%, and 94.6% for ChAdOx1-S or BNT162b2, or mRNA-1273, respectively. Four COVID-19-related hospitalizations (0.26%) were reported in the vaccinated versus 648 (41.81%) non-vaccinated participants (P<0.0001). Following the Pfizer booster dose, no COVID-19-positive cases or hospitalizations were reported. In the three vaccines, SARS-CoV2 antibody titers increased gradually after the first dose, peaked 3-4 weeks after the second dose, then declined after 28-32 weeks. Enhanced antibody response was observed after the booster dose and was maintained until the end of follow-up. Comorbidities were associated with lower antibody titers, particularly diabetes, autoimmune diseases, and advanced renal diseases. CONCLUSION: The study showed that the three COVID-10 vaccines effectively reduced the risk of virologically confirmed COVID-19 disease and prevented severe illness and hospitalizations in COVID-19 naiive and previously infected. Booster doses enhance the SARS-CoV2 antibody response and decrease the incidence of virologically proven severe COVID-19. Published by Elsevier Ltd. 2023-05 2023-05-16 /pmc/articles/PMC10186921/ http://dx.doi.org/10.1016/j.ijid.2023.04.208 Text en Copyright © 2023 Published by Elsevier Ltd. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Kamal, S.
Naguib, M.
Daador, M.
Alanazi, Z.
Basalem, A. Abdullah
Alaskar, A.
KINETICS OF ANTI-SARS-COV-2 IGG ANTIBODIES POST-COVID-19 -VACCINATION
title KINETICS OF ANTI-SARS-COV-2 IGG ANTIBODIES POST-COVID-19 -VACCINATION
title_full KINETICS OF ANTI-SARS-COV-2 IGG ANTIBODIES POST-COVID-19 -VACCINATION
title_fullStr KINETICS OF ANTI-SARS-COV-2 IGG ANTIBODIES POST-COVID-19 -VACCINATION
title_full_unstemmed KINETICS OF ANTI-SARS-COV-2 IGG ANTIBODIES POST-COVID-19 -VACCINATION
title_short KINETICS OF ANTI-SARS-COV-2 IGG ANTIBODIES POST-COVID-19 -VACCINATION
title_sort kinetics of anti-sars-cov-2 igg antibodies post-covid-19 -vaccination
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10186921/
http://dx.doi.org/10.1016/j.ijid.2023.04.208
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