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Antibody and T-cellular response to COVID-19 booster vaccine in SARS-CoV-1 survivors

The severe acute respiratory syndrome coronavirus 1 (SARS-CoV-1) survivors are more likely to produce a potent immune response to SARS-CoV-2 after booster vaccination. We assessed humoral and T cell responses against SARS-CoV-2 in previously vaccinated SARS-CoV-1 survivors and naïve healthy individu...

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Autores principales: Lu, Bi-Nan, Zhu, Ka-Li, Cui, Xiao-Ming, Yao, Lin, Wang, Xue-Jun, Wang, Guo-Lin, Duan, Li-Jun, Qian, Aruna, Ma, Mai-Juan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9423872/
https://www.ncbi.nlm.nih.gov/pubmed/36049602
http://dx.doi.org/10.1016/j.clim.2022.109103
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author Lu, Bi-Nan
Zhu, Ka-Li
Cui, Xiao-Ming
Yao, Lin
Wang, Xue-Jun
Wang, Guo-Lin
Duan, Li-Jun
Qian, Aruna
Ma, Mai-Juan
author_facet Lu, Bi-Nan
Zhu, Ka-Li
Cui, Xiao-Ming
Yao, Lin
Wang, Xue-Jun
Wang, Guo-Lin
Duan, Li-Jun
Qian, Aruna
Ma, Mai-Juan
author_sort Lu, Bi-Nan
collection PubMed
description The severe acute respiratory syndrome coronavirus 1 (SARS-CoV-1) survivors are more likely to produce a potent immune response to SARS-CoV-2 after booster vaccination. We assessed humoral and T cell responses against SARS-CoV-2 in previously vaccinated SARS-CoV-1 survivors and naïve healthy individuals (NHIs) after a booster Ad5-nCoV dose. Boosted SARS-CoV-1 survivors had a high neutralization of SARS-CoV-2 Wuhan-Hu-1 (WA1), Beta, and Delta but is limited to Omicron subvariants (BA.1, BA.2, BA.2.12.1, and BA.4/BA.5). Most boosted SARS-CoV-1 survivors had robust SARS-CoV-2-specific CD4(+) and CD8(+) T cell responses. While booster vaccination in NHIs elicited less or ineffective neutralization of WA1, Beta, and Delta, and none of them induced neutralizing antibodies against Omicron subvariants. However, they developed comparable SARS-CoV-2-specific T cell responses compared to boosted SARS-CoV-1 survivors. These findings suggest that boosted Ad5-nCoV would not elicit effective neutralizing antibodies against Omicron subvariants in SARS-CoV-1 survivors and NHIs but induced comparable robust T cell responses. Achieving a high antibody titer in SARS-CoV-1 survivors and NHIs is desirable to generate broad neutralization.
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spelling pubmed-94238722022-08-30 Antibody and T-cellular response to COVID-19 booster vaccine in SARS-CoV-1 survivors Lu, Bi-Nan Zhu, Ka-Li Cui, Xiao-Ming Yao, Lin Wang, Xue-Jun Wang, Guo-Lin Duan, Li-Jun Qian, Aruna Ma, Mai-Juan Clin Immunol Article The severe acute respiratory syndrome coronavirus 1 (SARS-CoV-1) survivors are more likely to produce a potent immune response to SARS-CoV-2 after booster vaccination. We assessed humoral and T cell responses against SARS-CoV-2 in previously vaccinated SARS-CoV-1 survivors and naïve healthy individuals (NHIs) after a booster Ad5-nCoV dose. Boosted SARS-CoV-1 survivors had a high neutralization of SARS-CoV-2 Wuhan-Hu-1 (WA1), Beta, and Delta but is limited to Omicron subvariants (BA.1, BA.2, BA.2.12.1, and BA.4/BA.5). Most boosted SARS-CoV-1 survivors had robust SARS-CoV-2-specific CD4(+) and CD8(+) T cell responses. While booster vaccination in NHIs elicited less or ineffective neutralization of WA1, Beta, and Delta, and none of them induced neutralizing antibodies against Omicron subvariants. However, they developed comparable SARS-CoV-2-specific T cell responses compared to boosted SARS-CoV-1 survivors. These findings suggest that boosted Ad5-nCoV would not elicit effective neutralizing antibodies against Omicron subvariants in SARS-CoV-1 survivors and NHIs but induced comparable robust T cell responses. Achieving a high antibody titer in SARS-CoV-1 survivors and NHIs is desirable to generate broad neutralization. Elsevier Inc. 2022-11 2022-08-29 /pmc/articles/PMC9423872/ /pubmed/36049602 http://dx.doi.org/10.1016/j.clim.2022.109103 Text en © 2022 Elsevier Inc. All rights reserved. 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
Lu, Bi-Nan
Zhu, Ka-Li
Cui, Xiao-Ming
Yao, Lin
Wang, Xue-Jun
Wang, Guo-Lin
Duan, Li-Jun
Qian, Aruna
Ma, Mai-Juan
Antibody and T-cellular response to COVID-19 booster vaccine in SARS-CoV-1 survivors
title Antibody and T-cellular response to COVID-19 booster vaccine in SARS-CoV-1 survivors
title_full Antibody and T-cellular response to COVID-19 booster vaccine in SARS-CoV-1 survivors
title_fullStr Antibody and T-cellular response to COVID-19 booster vaccine in SARS-CoV-1 survivors
title_full_unstemmed Antibody and T-cellular response to COVID-19 booster vaccine in SARS-CoV-1 survivors
title_short Antibody and T-cellular response to COVID-19 booster vaccine in SARS-CoV-1 survivors
title_sort antibody and t-cellular response to covid-19 booster vaccine in sars-cov-1 survivors
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9423872/
https://www.ncbi.nlm.nih.gov/pubmed/36049602
http://dx.doi.org/10.1016/j.clim.2022.109103
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