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

Identifieur interne : 001127 ( Ncbi/Checkpoint ); précédent : 001126; suivant : 001128

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

Auteurs : Ali Azizi ; Susan Aucoin ; Helina Tadesse ; Rita Frost ; Masoud Ghorbani ; Catalina Soare ; Turaya Naas ; Francisco Diaz-Mitoma

Source :

RBID : PMC:1249587

Abstract

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.

Electronic supplementary material

The online version of this article (doi:10.1186/1479-0556-3-7) contains supplementary material, which is available to authorized users.


Url:
DOI: 10.1186/1479-0556-3-7
PubMed: 16115319
PubMed Central: 1249587


Affiliations:


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PMC:1249587

Le document en format XML

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<p>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.</p>
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