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Adaptive immune responses to SARS-CoV-2 infection in severe versus mild individuals
The global Coronavirus disease 2019 (COVID-19) pandemic caused by SARS-CoV-2 has affected more than eight million people. There is an urgent need to investigate how the adaptive immunity is established in COVID-19 patients. In this study, we profiled adaptive immune cells of PBMCs from recovered COV...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7426596/ https://www.ncbi.nlm.nih.gov/pubmed/32796814 http://dx.doi.org/10.1038/s41392-020-00263-y |
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author | Zhang, Fan Gan, Rui Zhen, Ziqi Hu, Xiaoli Li, Xiang Zhou, Fengxia Liu, Ying Chen, Chuangeng Xie, Shuangyu Zhang, Bailing Wu, Xiaoke Huang, Zhiwei |
author_facet | Zhang, Fan Gan, Rui Zhen, Ziqi Hu, Xiaoli Li, Xiang Zhou, Fengxia Liu, Ying Chen, Chuangeng Xie, Shuangyu Zhang, Bailing Wu, Xiaoke Huang, Zhiwei |
author_sort | Zhang, Fan |
collection | PubMed |
description | The global Coronavirus disease 2019 (COVID-19) pandemic caused by SARS-CoV-2 has affected more than eight million people. There is an urgent need to investigate how the adaptive immunity is established in COVID-19 patients. In this study, we profiled adaptive immune cells of PBMCs from recovered COVID-19 patients with varying disease severity using single-cell RNA and TCR/BCR V(D)J sequencing. The sequencing data revealed SARS-CoV-2-specific shuffling of adaptive immune repertories and COVID-19-induced remodeling of peripheral lymphocytes. Characterization of variations in the peripheral T and B cells from the COVID-19 patients revealed a positive correlation of humoral immune response and T-cell immune memory with disease severity. Sequencing and functional data revealed SARS-CoV-2-specific T-cell immune memory in the convalescent COVID-19 patients. Furthermore, we also identified novel antigens that are responsive in the convalescent patients. Altogether, our study reveals adaptive immune repertories underlying pathogenesis and recovery in severe versus mild COVID-19 patients, providing valuable information for potential vaccine and therapeutic development against SARS-CoV-2 infection. |
format | Online Article Text |
id | pubmed-7426596 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74265962020-08-14 Adaptive immune responses to SARS-CoV-2 infection in severe versus mild individuals Zhang, Fan Gan, Rui Zhen, Ziqi Hu, Xiaoli Li, Xiang Zhou, Fengxia Liu, Ying Chen, Chuangeng Xie, Shuangyu Zhang, Bailing Wu, Xiaoke Huang, Zhiwei Signal Transduct Target Ther Article The global Coronavirus disease 2019 (COVID-19) pandemic caused by SARS-CoV-2 has affected more than eight million people. There is an urgent need to investigate how the adaptive immunity is established in COVID-19 patients. In this study, we profiled adaptive immune cells of PBMCs from recovered COVID-19 patients with varying disease severity using single-cell RNA and TCR/BCR V(D)J sequencing. The sequencing data revealed SARS-CoV-2-specific shuffling of adaptive immune repertories and COVID-19-induced remodeling of peripheral lymphocytes. Characterization of variations in the peripheral T and B cells from the COVID-19 patients revealed a positive correlation of humoral immune response and T-cell immune memory with disease severity. Sequencing and functional data revealed SARS-CoV-2-specific T-cell immune memory in the convalescent COVID-19 patients. Furthermore, we also identified novel antigens that are responsive in the convalescent patients. Altogether, our study reveals adaptive immune repertories underlying pathogenesis and recovery in severe versus mild COVID-19 patients, providing valuable information for potential vaccine and therapeutic development against SARS-CoV-2 infection. Nature Publishing Group UK 2020-08-14 /pmc/articles/PMC7426596/ /pubmed/32796814 http://dx.doi.org/10.1038/s41392-020-00263-y Text en © The Author(s) 2020, corrected publication 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Zhang, Fan Gan, Rui Zhen, Ziqi Hu, Xiaoli Li, Xiang Zhou, Fengxia Liu, Ying Chen, Chuangeng Xie, Shuangyu Zhang, Bailing Wu, Xiaoke Huang, Zhiwei Adaptive immune responses to SARS-CoV-2 infection in severe versus mild individuals |
title | Adaptive immune responses to SARS-CoV-2 infection in severe versus mild individuals |
title_full | Adaptive immune responses to SARS-CoV-2 infection in severe versus mild individuals |
title_fullStr | Adaptive immune responses to SARS-CoV-2 infection in severe versus mild individuals |
title_full_unstemmed | Adaptive immune responses to SARS-CoV-2 infection in severe versus mild individuals |
title_short | Adaptive immune responses to SARS-CoV-2 infection in severe versus mild individuals |
title_sort | adaptive immune responses to sars-cov-2 infection in severe versus mild individuals |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7426596/ https://www.ncbi.nlm.nih.gov/pubmed/32796814 http://dx.doi.org/10.1038/s41392-020-00263-y |
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