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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc.
2022
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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. |
format | Online Article Text |
id | pubmed-9423872 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
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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