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Long-lived memory T lymphocyte responses against SARS coronavirus nucleocapsid protein in SARS-recovered patients
The nucleocapsid (N) protein is a structural component of severe acute respiratory syndrome (SARS) coronavirus (SARS-CoV) and can induce antibody responses in SARS patients during infection. However, it is not known whether SARS-CoV N protein can induce a long persistence of memory T-cell response i...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc.
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7111820/ https://www.ncbi.nlm.nih.gov/pubmed/16690096 http://dx.doi.org/10.1016/j.virol.2006.03.036 |
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author | Peng, Hui Yang, Li-tao Wang, Ling-yun Li, Jian Huang, Jun Lu, Zhi-qiang Koup, Richard A. Bailer, Robert T. Wu, Chang-you |
author_facet | Peng, Hui Yang, Li-tao Wang, Ling-yun Li, Jian Huang, Jun Lu, Zhi-qiang Koup, Richard A. Bailer, Robert T. Wu, Chang-you |
author_sort | Peng, Hui |
collection | PubMed |
description | The nucleocapsid (N) protein is a structural component of severe acute respiratory syndrome (SARS) coronavirus (SARS-CoV) and can induce antibody responses in SARS patients during infection. However, it is not known whether SARS-CoV N protein can induce a long persistence of memory T-cell response in human. In this study, we found that peripheral blood mononuclear cells (PBMCs) from fully recovered SARS individuals rapidly produced IFN-γ and IL-2 following stimulation with a pool of overlapping peptides that cover the entire N protein sequence. The N-specific IFN-γ(+)CD4(+) T cells were mainly composed of CD45RA(−)CCR7(+)CD62L(−) cells, whereas IFN-γ(+)CD8(+) memory T cells were mostly contained within CD45RA(+)CCR7(−)CD62L(−) cell population. Epitope mapping study indicated that a cluster of overlapping peptides located in the C-terminal region (amino acids [aa] 331 to 362) of N protein contained at least two different T-cell epitopes. The results indicated that human memory T-cell responses specific for SARS-CoV N protein could persist for 2 years in the absence of antigen, which would be a valuable for the design of effective vaccines against SARS-CoV and for basic studies of human T-cell memory. |
format | Online Article Text |
id | pubmed-7111820 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71118202020-04-02 Long-lived memory T lymphocyte responses against SARS coronavirus nucleocapsid protein in SARS-recovered patients Peng, Hui Yang, Li-tao Wang, Ling-yun Li, Jian Huang, Jun Lu, Zhi-qiang Koup, Richard A. Bailer, Robert T. Wu, Chang-you Virology Article The nucleocapsid (N) protein is a structural component of severe acute respiratory syndrome (SARS) coronavirus (SARS-CoV) and can induce antibody responses in SARS patients during infection. However, it is not known whether SARS-CoV N protein can induce a long persistence of memory T-cell response in human. In this study, we found that peripheral blood mononuclear cells (PBMCs) from fully recovered SARS individuals rapidly produced IFN-γ and IL-2 following stimulation with a pool of overlapping peptides that cover the entire N protein sequence. The N-specific IFN-γ(+)CD4(+) T cells were mainly composed of CD45RA(−)CCR7(+)CD62L(−) cells, whereas IFN-γ(+)CD8(+) memory T cells were mostly contained within CD45RA(+)CCR7(−)CD62L(−) cell population. Epitope mapping study indicated that a cluster of overlapping peptides located in the C-terminal region (amino acids [aa] 331 to 362) of N protein contained at least two different T-cell epitopes. The results indicated that human memory T-cell responses specific for SARS-CoV N protein could persist for 2 years in the absence of antigen, which would be a valuable for the design of effective vaccines against SARS-CoV and for basic studies of human T-cell memory. Elsevier Inc. 2006-08-01 2006-05-11 /pmc/articles/PMC7111820/ /pubmed/16690096 http://dx.doi.org/10.1016/j.virol.2006.03.036 Text en Copyright © 2006 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 Peng, Hui Yang, Li-tao Wang, Ling-yun Li, Jian Huang, Jun Lu, Zhi-qiang Koup, Richard A. Bailer, Robert T. Wu, Chang-you Long-lived memory T lymphocyte responses against SARS coronavirus nucleocapsid protein in SARS-recovered patients |
title | Long-lived memory T lymphocyte responses against SARS coronavirus nucleocapsid protein in SARS-recovered patients |
title_full | Long-lived memory T lymphocyte responses against SARS coronavirus nucleocapsid protein in SARS-recovered patients |
title_fullStr | Long-lived memory T lymphocyte responses against SARS coronavirus nucleocapsid protein in SARS-recovered patients |
title_full_unstemmed | Long-lived memory T lymphocyte responses against SARS coronavirus nucleocapsid protein in SARS-recovered patients |
title_short | Long-lived memory T lymphocyte responses against SARS coronavirus nucleocapsid protein in SARS-recovered patients |
title_sort | long-lived memory t lymphocyte responses against sars coronavirus nucleocapsid protein in sars-recovered patients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7111820/ https://www.ncbi.nlm.nih.gov/pubmed/16690096 http://dx.doi.org/10.1016/j.virol.2006.03.036 |
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