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A combined nucleocapsid vaccine induces vigorous SARS-CD8+ T-cell immune responses

Several studies have shown that cell-mediated immune responses play a crucial role in controlling viral replication. As such, a candidate SARS vaccine should elicit broad CD8+ T-cell immune responses. Several groups of mice were immunized alone or in combination with SARS-nucleocapsid immunogen. A h...

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Autores principales: Azizi, Ali, Aucoin, Susan, Tadesse, Helina, Frost, Rita, Ghorbani, Masoud, Soare, Catalina, Naas, Turaya, Diaz-Mitoma, Francisco
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1249587/
https://www.ncbi.nlm.nih.gov/pubmed/16115319
http://dx.doi.org/10.1186/1479-0556-3-7
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author Azizi, Ali
Aucoin, Susan
Tadesse, Helina
Frost, Rita
Ghorbani, Masoud
Soare, Catalina
Naas, Turaya
Diaz-Mitoma, Francisco
author_facet Azizi, Ali
Aucoin, Susan
Tadesse, Helina
Frost, Rita
Ghorbani, Masoud
Soare, Catalina
Naas, Turaya
Diaz-Mitoma, Francisco
author_sort Azizi, Ali
collection PubMed
description Several studies have shown that cell-mediated immune responses play a crucial role in controlling viral replication. As such, a candidate SARS vaccine should elicit broad CD8+ T-cell immune responses. Several groups of mice were immunized alone or in combination with SARS-nucleocapsid immunogen. A high level of specific SARS-CD8+ T-cell response was demonstrated in mice that received DNA encoding the SARS-nucleocapsid, protein and XIAP as an adjuvant. We also observed that co-administration of a plasmid expressing nucleocapsid, recombinant protein and montanide/CpG induces high antibody titers in immunized mice. Moreover, this vaccine approach merits further investigation as a potential candidate vaccine against SARS.
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spelling pubmed-12495872005-10-08 A combined nucleocapsid vaccine induces vigorous SARS-CD8+ T-cell immune responses Azizi, Ali Aucoin, Susan Tadesse, Helina Frost, Rita Ghorbani, Masoud Soare, Catalina Naas, Turaya Diaz-Mitoma, Francisco Genet Vaccines Ther Research Several studies have shown that cell-mediated immune responses play a crucial role in controlling viral replication. As such, a candidate SARS vaccine should elicit broad CD8+ T-cell immune responses. Several groups of mice were immunized alone or in combination with SARS-nucleocapsid immunogen. A high level of specific SARS-CD8+ T-cell response was demonstrated in mice that received DNA encoding the SARS-nucleocapsid, protein and XIAP as an adjuvant. We also observed that co-administration of a plasmid expressing nucleocapsid, recombinant protein and montanide/CpG induces high antibody titers in immunized mice. Moreover, this vaccine approach merits further investigation as a potential candidate vaccine against SARS. BioMed Central 2005-08-22 /pmc/articles/PMC1249587/ /pubmed/16115319 http://dx.doi.org/10.1186/1479-0556-3-7 Text en Copyright © 2005 Azizi et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Azizi, Ali
Aucoin, Susan
Tadesse, Helina
Frost, Rita
Ghorbani, Masoud
Soare, Catalina
Naas, Turaya
Diaz-Mitoma, Francisco
A combined nucleocapsid vaccine induces vigorous SARS-CD8+ T-cell immune responses
title A combined nucleocapsid vaccine induces vigorous SARS-CD8+ T-cell immune responses
title_full A combined nucleocapsid vaccine induces vigorous SARS-CD8+ T-cell immune responses
title_fullStr A combined nucleocapsid vaccine induces vigorous SARS-CD8+ T-cell immune responses
title_full_unstemmed A combined nucleocapsid vaccine induces vigorous SARS-CD8+ T-cell immune responses
title_short A combined nucleocapsid vaccine induces vigorous SARS-CD8+ T-cell immune responses
title_sort combined nucleocapsid vaccine induces vigorous sars-cd8+ t-cell immune responses
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1249587/
https://www.ncbi.nlm.nih.gov/pubmed/16115319
http://dx.doi.org/10.1186/1479-0556-3-7
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