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T Cell Immunity Evaluation and Immunodominant Epitope T Cell Receptor Identification of Severe Acute Respiratory Syndrome Coronavirus 2 Spike Glycoprotein in COVID-19 Convalescent Patients

A better understanding of the role of T cells in the immune response to Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) is helpful not only for vaccine development but also for the treatment of COVID-19 patients. In this study, we determined the existence of SARS-CoV-2-specific T cells...

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Autores principales: Li, Luo, Chen, Qian, Han, Xiaojian, Shen, Meiying, Hu, Chao, Chen, Siyin, Zhang, Jing, Wang, Yingming, Li, Tingting, Huang, Jingjing, Li, Shenglong, Hao, Yanan, Jin, Aishun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8595245/
https://www.ncbi.nlm.nih.gov/pubmed/34805136
http://dx.doi.org/10.3389/fcell.2021.696662
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author Li, Luo
Chen, Qian
Han, Xiaojian
Shen, Meiying
Hu, Chao
Chen, Siyin
Zhang, Jing
Wang, Yingming
Li, Tingting
Huang, Jingjing
Li, Shenglong
Hao, Yanan
Jin, Aishun
author_facet Li, Luo
Chen, Qian
Han, Xiaojian
Shen, Meiying
Hu, Chao
Chen, Siyin
Zhang, Jing
Wang, Yingming
Li, Tingting
Huang, Jingjing
Li, Shenglong
Hao, Yanan
Jin, Aishun
author_sort Li, Luo
collection PubMed
description A better understanding of the role of T cells in the immune response to Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) is helpful not only for vaccine development but also for the treatment of COVID-19 patients. In this study, we determined the existence of SARS-CoV-2-specific T cells in the blood of COVID-19 convalescents. Meanwhile, the specific T cell response in the non-RBD region was stronger than in the RBD region. We also found that SARS-CoV-2 S-specific reactive CD4(+) T cells exhibited higher frequency than CD8(+) T cells in recovered COVID-19 patients, with greater number of corresponding epitopes presented. Importantly, we isolated the SARS-CoV-2-specific CD4(+) T cell receptors (TCRs) and inserted the TCRs into allogenic CD4(+) T cells. These TCR-T cells can be activated by SARS-CoV-2 spike peptide and produce IFN-γ in vitro. These results might provide valuable information for the development of vaccines and new therapies against COVID-19.
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spelling pubmed-85952452021-11-18 T Cell Immunity Evaluation and Immunodominant Epitope T Cell Receptor Identification of Severe Acute Respiratory Syndrome Coronavirus 2 Spike Glycoprotein in COVID-19 Convalescent Patients Li, Luo Chen, Qian Han, Xiaojian Shen, Meiying Hu, Chao Chen, Siyin Zhang, Jing Wang, Yingming Li, Tingting Huang, Jingjing Li, Shenglong Hao, Yanan Jin, Aishun Front Cell Dev Biol Cell and Developmental Biology A better understanding of the role of T cells in the immune response to Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) is helpful not only for vaccine development but also for the treatment of COVID-19 patients. In this study, we determined the existence of SARS-CoV-2-specific T cells in the blood of COVID-19 convalescents. Meanwhile, the specific T cell response in the non-RBD region was stronger than in the RBD region. We also found that SARS-CoV-2 S-specific reactive CD4(+) T cells exhibited higher frequency than CD8(+) T cells in recovered COVID-19 patients, with greater number of corresponding epitopes presented. Importantly, we isolated the SARS-CoV-2-specific CD4(+) T cell receptors (TCRs) and inserted the TCRs into allogenic CD4(+) T cells. These TCR-T cells can be activated by SARS-CoV-2 spike peptide and produce IFN-γ in vitro. These results might provide valuable information for the development of vaccines and new therapies against COVID-19. Frontiers Media S.A. 2021-11-03 /pmc/articles/PMC8595245/ /pubmed/34805136 http://dx.doi.org/10.3389/fcell.2021.696662 Text en Copyright © 2021 Li, Chen, Han, Shen, Hu, Chen, Zhang, Wang, Li, Huang, Li, Hao and Jin. 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 Cell and Developmental Biology
Li, Luo
Chen, Qian
Han, Xiaojian
Shen, Meiying
Hu, Chao
Chen, Siyin
Zhang, Jing
Wang, Yingming
Li, Tingting
Huang, Jingjing
Li, Shenglong
Hao, Yanan
Jin, Aishun
T Cell Immunity Evaluation and Immunodominant Epitope T Cell Receptor Identification of Severe Acute Respiratory Syndrome Coronavirus 2 Spike Glycoprotein in COVID-19 Convalescent Patients
title T Cell Immunity Evaluation and Immunodominant Epitope T Cell Receptor Identification of Severe Acute Respiratory Syndrome Coronavirus 2 Spike Glycoprotein in COVID-19 Convalescent Patients
title_full T Cell Immunity Evaluation and Immunodominant Epitope T Cell Receptor Identification of Severe Acute Respiratory Syndrome Coronavirus 2 Spike Glycoprotein in COVID-19 Convalescent Patients
title_fullStr T Cell Immunity Evaluation and Immunodominant Epitope T Cell Receptor Identification of Severe Acute Respiratory Syndrome Coronavirus 2 Spike Glycoprotein in COVID-19 Convalescent Patients
title_full_unstemmed T Cell Immunity Evaluation and Immunodominant Epitope T Cell Receptor Identification of Severe Acute Respiratory Syndrome Coronavirus 2 Spike Glycoprotein in COVID-19 Convalescent Patients
title_short T Cell Immunity Evaluation and Immunodominant Epitope T Cell Receptor Identification of Severe Acute Respiratory Syndrome Coronavirus 2 Spike Glycoprotein in COVID-19 Convalescent Patients
title_sort t cell immunity evaluation and immunodominant epitope t cell receptor identification of severe acute respiratory syndrome coronavirus 2 spike glycoprotein in covid-19 convalescent patients
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8595245/
https://www.ncbi.nlm.nih.gov/pubmed/34805136
http://dx.doi.org/10.3389/fcell.2021.696662
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