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Immune responses against SARS-coronavirus nucleocapsid protein induced by DNA vaccine
The nucleocapsid (N) protein of SARS-coronavirus (SARS-CoV) is the key protein for the formation of the helical nucleocapsid during virion assembly. This protein is believed to be more conserved than other proteins of the virus, such as spike and membrane glycoprotein. In this study, the N protein o...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc.
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7111813/ https://www.ncbi.nlm.nih.gov/pubmed/15582659 http://dx.doi.org/10.1016/j.virol.2004.10.016 |
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author | Zhao, Ping Cao, Jie Zhao, Lan-Juan Qin, Zhao-Lin Ke, Jin-Shan Pan, Wei Ren, Hao Yu, Jian-Guo Qi, Zhong-Tian |
author_facet | Zhao, Ping Cao, Jie Zhao, Lan-Juan Qin, Zhao-Lin Ke, Jin-Shan Pan, Wei Ren, Hao Yu, Jian-Guo Qi, Zhong-Tian |
author_sort | Zhao, Ping |
collection | PubMed |
description | The nucleocapsid (N) protein of SARS-coronavirus (SARS-CoV) is the key protein for the formation of the helical nucleocapsid during virion assembly. This protein is believed to be more conserved than other proteins of the virus, such as spike and membrane glycoprotein. In this study, the N protein of SARS-CoV was expressed in Escherichia coli DH5α and identified with pooled sera from patients in the convalescence phase of SARS. A plasmid pCI-N, encoding the full-length N gene of SARS-CoV, was constructed. Expression of the N protein was observed in COS1 cells following transfection with pCI-N. The immune responses induced by intramuscular immunization with pCI-N were evaluated in a murine model. Serum anti-N immunoglobulins and splenocytes proliferative responses against N protein were observed in immunized BALB/c mice. The major immunoglobulin G subclass recognizing N protein was immunoglobulin G2a, and stimulated splenocytes secreted high levels of gamma interferon and IL-2 in response to N protein. More importantly, the immunized mice produced strong delayed-type hypersensitivity (DTH) and CD8(+) CTL responses to N protein. The study shows that N protein of SARS-CoV not only is an important B cell immunogen, but also can elicit broad-based cellular immune responses. The results indicate that the N protein may be of potential value in vaccine development for specific prophylaxis and treatment against SARS. |
format | Online Article Text |
id | pubmed-7111813 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71118132020-04-02 Immune responses against SARS-coronavirus nucleocapsid protein induced by DNA vaccine Zhao, Ping Cao, Jie Zhao, Lan-Juan Qin, Zhao-Lin Ke, Jin-Shan Pan, Wei Ren, Hao Yu, Jian-Guo Qi, Zhong-Tian Virology Article The nucleocapsid (N) protein of SARS-coronavirus (SARS-CoV) is the key protein for the formation of the helical nucleocapsid during virion assembly. This protein is believed to be more conserved than other proteins of the virus, such as spike and membrane glycoprotein. In this study, the N protein of SARS-CoV was expressed in Escherichia coli DH5α and identified with pooled sera from patients in the convalescence phase of SARS. A plasmid pCI-N, encoding the full-length N gene of SARS-CoV, was constructed. Expression of the N protein was observed in COS1 cells following transfection with pCI-N. The immune responses induced by intramuscular immunization with pCI-N were evaluated in a murine model. Serum anti-N immunoglobulins and splenocytes proliferative responses against N protein were observed in immunized BALB/c mice. The major immunoglobulin G subclass recognizing N protein was immunoglobulin G2a, and stimulated splenocytes secreted high levels of gamma interferon and IL-2 in response to N protein. More importantly, the immunized mice produced strong delayed-type hypersensitivity (DTH) and CD8(+) CTL responses to N protein. The study shows that N protein of SARS-CoV not only is an important B cell immunogen, but also can elicit broad-based cellular immune responses. The results indicate that the N protein may be of potential value in vaccine development for specific prophylaxis and treatment against SARS. Elsevier Inc. 2005-01-05 2004-12-08 /pmc/articles/PMC7111813/ /pubmed/15582659 http://dx.doi.org/10.1016/j.virol.2004.10.016 Text en Copyright © 2004 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 Zhao, Ping Cao, Jie Zhao, Lan-Juan Qin, Zhao-Lin Ke, Jin-Shan Pan, Wei Ren, Hao Yu, Jian-Guo Qi, Zhong-Tian Immune responses against SARS-coronavirus nucleocapsid protein induced by DNA vaccine |
title | Immune responses against SARS-coronavirus nucleocapsid protein induced by DNA vaccine |
title_full | Immune responses against SARS-coronavirus nucleocapsid protein induced by DNA vaccine |
title_fullStr | Immune responses against SARS-coronavirus nucleocapsid protein induced by DNA vaccine |
title_full_unstemmed | Immune responses against SARS-coronavirus nucleocapsid protein induced by DNA vaccine |
title_short | Immune responses against SARS-coronavirus nucleocapsid protein induced by DNA vaccine |
title_sort | immune responses against sars-coronavirus nucleocapsid protein induced by dna vaccine |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7111813/ https://www.ncbi.nlm.nih.gov/pubmed/15582659 http://dx.doi.org/10.1016/j.virol.2004.10.016 |
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