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Immunogenicity against wild-type and Omicron SARS-CoV-2 after a third dose of inactivated COVID-19 vaccine in healthy adolescents

INTRODUCTION: Two doses of inactivated SARS-CoV-2 vaccine CoronaVac cannot elicit high efficacy against symptomatic COVID-19, especially against the Omicron variant, but that can be improved by a third dose in adults. The use of a third dose of CoronaVac in adolescents may be supported by immunobrid...

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Autores principales: Leung, Daniel, Cohen, Carolyn A., Mu, Xiaofeng, Rosa Duque, Jaime S., Cheng, Samuel M. S., Wang, Xiwei, Wang, Manni, Zhang, Wenyue, Zhang, Yanmei, Tam, Issan Y. S., Lam, Jennifer H. Y., Chan, Sau Man, Chaothai, Sara, Kwan, Kelvin K. H., Chan, Karl C. K., Li, John K. C., Luk, Leo L. H., Tsang, Leo C. H., Chu, Nym Coco, Wong, Wilfred H. S., Mori, Masashi, Leung, Wing Hang, Valkenburg, Sophie, Peiris, Malik, Tu, Wenwei, Lau, Yu Lung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10026957/
https://www.ncbi.nlm.nih.gov/pubmed/36949953
http://dx.doi.org/10.3389/fimmu.2023.1106837
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author Leung, Daniel
Cohen, Carolyn A.
Mu, Xiaofeng
Rosa Duque, Jaime S.
Cheng, Samuel M. S.
Wang, Xiwei
Wang, Manni
Zhang, Wenyue
Zhang, Yanmei
Tam, Issan Y. S.
Lam, Jennifer H. Y.
Chan, Sau Man
Chaothai, Sara
Kwan, Kelvin K. H.
Chan, Karl C. K.
Li, John K. C.
Luk, Leo L. H.
Tsang, Leo C. H.
Chu, Nym Coco
Wong, Wilfred H. S.
Mori, Masashi
Leung, Wing Hang
Valkenburg, Sophie
Peiris, Malik
Tu, Wenwei
Lau, Yu Lung
author_facet Leung, Daniel
Cohen, Carolyn A.
Mu, Xiaofeng
Rosa Duque, Jaime S.
Cheng, Samuel M. S.
Wang, Xiwei
Wang, Manni
Zhang, Wenyue
Zhang, Yanmei
Tam, Issan Y. S.
Lam, Jennifer H. Y.
Chan, Sau Man
Chaothai, Sara
Kwan, Kelvin K. H.
Chan, Karl C. K.
Li, John K. C.
Luk, Leo L. H.
Tsang, Leo C. H.
Chu, Nym Coco
Wong, Wilfred H. S.
Mori, Masashi
Leung, Wing Hang
Valkenburg, Sophie
Peiris, Malik
Tu, Wenwei
Lau, Yu Lung
author_sort Leung, Daniel
collection PubMed
description INTRODUCTION: Two doses of inactivated SARS-CoV-2 vaccine CoronaVac cannot elicit high efficacy against symptomatic COVID-19, especially against the Omicron variant, but that can be improved by a third dose in adults. The use of a third dose of CoronaVac in adolescents may be supported by immunobridging studies in the absence of efficacy data. METHODS: With an immunobridging design, our study (NCT04800133) tested the non-inferiority of the binding and neutralizing antibodies and T cell responses induced by a third dose of CoronaVac in healthy adolescents (N=94, median age 14.2 years, 56% male) compared to adults (N=153, median age 48.1 years, 44% male). Responses against wild-type (WT) and BA.1 SARS-CoV-2 were compared in adolescents. Safety and reactogenicity were also monitored. RESULTS: A homologous third dose of CoronaVac further enhanced antibody response in adolescents compared to just 2 doses. Adolescents mounted non-inferior antibody and T cell responses compared to adults. Although S IgG and neutralizing antibody responses to BA.1 were lower than to WT, they remained detectable in 96% and 86% of adolescents. T cell responses to peptide pools spanning only the mutations of BA.1 S, N and M in adolescents were preserved, increased, and halved compared to WT respectively. No safety concerns were identified. DISCUSSION: The primary vaccination series of inactivated SARS-CoV-2 vaccines for adolescents should include 3 doses for improved humoral immunogenicity.
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spelling pubmed-100269572023-03-21 Immunogenicity against wild-type and Omicron SARS-CoV-2 after a third dose of inactivated COVID-19 vaccine in healthy adolescents Leung, Daniel Cohen, Carolyn A. Mu, Xiaofeng Rosa Duque, Jaime S. Cheng, Samuel M. S. Wang, Xiwei Wang, Manni Zhang, Wenyue Zhang, Yanmei Tam, Issan Y. S. Lam, Jennifer H. Y. Chan, Sau Man Chaothai, Sara Kwan, Kelvin K. H. Chan, Karl C. K. Li, John K. C. Luk, Leo L. H. Tsang, Leo C. H. Chu, Nym Coco Wong, Wilfred H. S. Mori, Masashi Leung, Wing Hang Valkenburg, Sophie Peiris, Malik Tu, Wenwei Lau, Yu Lung Front Immunol Immunology INTRODUCTION: Two doses of inactivated SARS-CoV-2 vaccine CoronaVac cannot elicit high efficacy against symptomatic COVID-19, especially against the Omicron variant, but that can be improved by a third dose in adults. The use of a third dose of CoronaVac in adolescents may be supported by immunobridging studies in the absence of efficacy data. METHODS: With an immunobridging design, our study (NCT04800133) tested the non-inferiority of the binding and neutralizing antibodies and T cell responses induced by a third dose of CoronaVac in healthy adolescents (N=94, median age 14.2 years, 56% male) compared to adults (N=153, median age 48.1 years, 44% male). Responses against wild-type (WT) and BA.1 SARS-CoV-2 were compared in adolescents. Safety and reactogenicity were also monitored. RESULTS: A homologous third dose of CoronaVac further enhanced antibody response in adolescents compared to just 2 doses. Adolescents mounted non-inferior antibody and T cell responses compared to adults. Although S IgG and neutralizing antibody responses to BA.1 were lower than to WT, they remained detectable in 96% and 86% of adolescents. T cell responses to peptide pools spanning only the mutations of BA.1 S, N and M in adolescents were preserved, increased, and halved compared to WT respectively. No safety concerns were identified. DISCUSSION: The primary vaccination series of inactivated SARS-CoV-2 vaccines for adolescents should include 3 doses for improved humoral immunogenicity. Frontiers Media S.A. 2023-03-06 /pmc/articles/PMC10026957/ /pubmed/36949953 http://dx.doi.org/10.3389/fimmu.2023.1106837 Text en Copyright © 2023 Leung, Cohen, Mu, Rosa Duque, Cheng, Wang, Wang, Zhang, Zhang, Tam, Lam, Chan, Chaothai, Kwan, Chan, Li, Luk, Tsang, Chu, Wong, Mori, Leung, Valkenburg, Peiris, Tu and Lau 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
Leung, Daniel
Cohen, Carolyn A.
Mu, Xiaofeng
Rosa Duque, Jaime S.
Cheng, Samuel M. S.
Wang, Xiwei
Wang, Manni
Zhang, Wenyue
Zhang, Yanmei
Tam, Issan Y. S.
Lam, Jennifer H. Y.
Chan, Sau Man
Chaothai, Sara
Kwan, Kelvin K. H.
Chan, Karl C. K.
Li, John K. C.
Luk, Leo L. H.
Tsang, Leo C. H.
Chu, Nym Coco
Wong, Wilfred H. S.
Mori, Masashi
Leung, Wing Hang
Valkenburg, Sophie
Peiris, Malik
Tu, Wenwei
Lau, Yu Lung
Immunogenicity against wild-type and Omicron SARS-CoV-2 after a third dose of inactivated COVID-19 vaccine in healthy adolescents
title Immunogenicity against wild-type and Omicron SARS-CoV-2 after a third dose of inactivated COVID-19 vaccine in healthy adolescents
title_full Immunogenicity against wild-type and Omicron SARS-CoV-2 after a third dose of inactivated COVID-19 vaccine in healthy adolescents
title_fullStr Immunogenicity against wild-type and Omicron SARS-CoV-2 after a third dose of inactivated COVID-19 vaccine in healthy adolescents
title_full_unstemmed Immunogenicity against wild-type and Omicron SARS-CoV-2 after a third dose of inactivated COVID-19 vaccine in healthy adolescents
title_short Immunogenicity against wild-type and Omicron SARS-CoV-2 after a third dose of inactivated COVID-19 vaccine in healthy adolescents
title_sort immunogenicity against wild-type and omicron sars-cov-2 after a third dose of inactivated covid-19 vaccine in healthy adolescents
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10026957/
https://www.ncbi.nlm.nih.gov/pubmed/36949953
http://dx.doi.org/10.3389/fimmu.2023.1106837
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