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SARS-CoV-2-specific T cell responses wane profoundly in convalescent individuals 10 months after primary infection
A key question in the coronavirus disease 2019 (COVID-19) pandemic is the duration of specific T cell responses against the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) post primary infection, which is difficult to address due to the large-scale COVID-19 vaccination and re-exposure t...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wuhan Institute of Virology, Chinese Academy of Sciences
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10436107/ https://www.ncbi.nlm.nih.gov/pubmed/37414153 http://dx.doi.org/10.1016/j.virs.2023.06.011 |
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author | Li, Ziwei Xiang, Tiandan Liang, Boyun Liu, Jing Deng, Hui Yang, Xuecheng Wang, Hua Feng, Xuemei Zelinskyy, Gennadiy Trilling, Mirko Sutter, Kathrin Lu, Mengji Dittmer, Ulf Wang, Baoju Yang, Dongliang Zheng, Xin Liu, Jia |
author_facet | Li, Ziwei Xiang, Tiandan Liang, Boyun Liu, Jing Deng, Hui Yang, Xuecheng Wang, Hua Feng, Xuemei Zelinskyy, Gennadiy Trilling, Mirko Sutter, Kathrin Lu, Mengji Dittmer, Ulf Wang, Baoju Yang, Dongliang Zheng, Xin Liu, Jia |
author_sort | Li, Ziwei |
collection | PubMed |
description | A key question in the coronavirus disease 2019 (COVID-19) pandemic is the duration of specific T cell responses against the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) post primary infection, which is difficult to address due to the large-scale COVID-19 vaccination and re-exposure to the virus. Here, we conducted an analysis of the long-term SARS-CoV-2-specific T cell responses in a unique cohort of convalescent individuals (CIs) that were among the first to be infected worldwide and without any possible antigen re-exposure since then. The magnitude and breadth of SARS-CoV-2-specific T cell responses correlated inversely with the time that had elapsed from disease onset and the age of those CIs. The mean magnitude of SARS-CoV-2-specific CD4 and CD8 T cell responses decreased about 82% and 76%, respectively, over the time period of ten months after infection. Accordingly, the longitudinal analysis also demonstrated that SARS-CoV-2-specific T cell responses waned significantly in 75% of CIs during the follow-up. Collectively, we provide a comprehensive characterization of the long-term memory T cell response in CIs, suggesting that robust SARS-CoV-2-specific T cell immunity post primary infection may be less durable than previously expected. |
format | Online Article Text |
id | pubmed-10436107 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Wuhan Institute of Virology, Chinese Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-104361072023-08-19 SARS-CoV-2-specific T cell responses wane profoundly in convalescent individuals 10 months after primary infection Li, Ziwei Xiang, Tiandan Liang, Boyun Liu, Jing Deng, Hui Yang, Xuecheng Wang, Hua Feng, Xuemei Zelinskyy, Gennadiy Trilling, Mirko Sutter, Kathrin Lu, Mengji Dittmer, Ulf Wang, Baoju Yang, Dongliang Zheng, Xin Liu, Jia Virol Sin Research Article A key question in the coronavirus disease 2019 (COVID-19) pandemic is the duration of specific T cell responses against the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) post primary infection, which is difficult to address due to the large-scale COVID-19 vaccination and re-exposure to the virus. Here, we conducted an analysis of the long-term SARS-CoV-2-specific T cell responses in a unique cohort of convalescent individuals (CIs) that were among the first to be infected worldwide and without any possible antigen re-exposure since then. The magnitude and breadth of SARS-CoV-2-specific T cell responses correlated inversely with the time that had elapsed from disease onset and the age of those CIs. The mean magnitude of SARS-CoV-2-specific CD4 and CD8 T cell responses decreased about 82% and 76%, respectively, over the time period of ten months after infection. Accordingly, the longitudinal analysis also demonstrated that SARS-CoV-2-specific T cell responses waned significantly in 75% of CIs during the follow-up. Collectively, we provide a comprehensive characterization of the long-term memory T cell response in CIs, suggesting that robust SARS-CoV-2-specific T cell immunity post primary infection may be less durable than previously expected. Wuhan Institute of Virology, Chinese Academy of Sciences 2023-07-04 /pmc/articles/PMC10436107/ /pubmed/37414153 http://dx.doi.org/10.1016/j.virs.2023.06.011 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Article Li, Ziwei Xiang, Tiandan Liang, Boyun Liu, Jing Deng, Hui Yang, Xuecheng Wang, Hua Feng, Xuemei Zelinskyy, Gennadiy Trilling, Mirko Sutter, Kathrin Lu, Mengji Dittmer, Ulf Wang, Baoju Yang, Dongliang Zheng, Xin Liu, Jia SARS-CoV-2-specific T cell responses wane profoundly in convalescent individuals 10 months after primary infection |
title | SARS-CoV-2-specific T cell responses wane profoundly in convalescent individuals 10 months after primary infection |
title_full | SARS-CoV-2-specific T cell responses wane profoundly in convalescent individuals 10 months after primary infection |
title_fullStr | SARS-CoV-2-specific T cell responses wane profoundly in convalescent individuals 10 months after primary infection |
title_full_unstemmed | SARS-CoV-2-specific T cell responses wane profoundly in convalescent individuals 10 months after primary infection |
title_short | SARS-CoV-2-specific T cell responses wane profoundly in convalescent individuals 10 months after primary infection |
title_sort | sars-cov-2-specific t cell responses wane profoundly in convalescent individuals 10 months after primary infection |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10436107/ https://www.ncbi.nlm.nih.gov/pubmed/37414153 http://dx.doi.org/10.1016/j.virs.2023.06.011 |
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