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Adenovirus-based vaccine prevents pneumonia in ferrets challenged with the SARS coronavirus and stimulates robust immune responses in macaques.

Identifieur interne : 003927 ( Main/Merge ); précédent : 003926; suivant : 003928

Adenovirus-based vaccine prevents pneumonia in ferrets challenged with the SARS coronavirus and stimulates robust immune responses in macaques.

Auteurs : Gary P. Kobinger [Canada] ; Joanita M. Figueredo ; Thomas Rowe ; Yan Zhi ; Guangping Gao ; Julio C. Sanmiguel ; Peter Bell ; Nelson A. Wivel ; Lois A. Zitzow ; Douglas B. Flieder ; Robert J. Hogan ; James M. Wilson

Source :

RBID : pubmed:17559989

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English descriptors

Abstract

A ferret model of severe acute respiratory syndrome (SARS)-CoV infection was used to evaluate the efficacy of an adenovirus vaccine. Animals were subjected to heterologous prime-boost using vectors from human serotype 5 and chimpanzee derived adenoviruses (human AdHu5 and chimpanzee AdC7) expressing spike protein followed by intranasal challenge with SARS-CoV. Vaccination led to a substantial reduction in viral load and prevented the severe pneumonia seen in unvaccinated animals. The same prime-boost strategy was effective in rhesus macaques in eliciting SARS-CoV specific immune responses. These data indicate that a heterologous adenovirus-based prime-boost vaccine strategy could safely stimulate strong immunity that may be needed for complete protection against SARS-CoV infection.

DOI: 10.1016/j.vaccine.2007.04.065
PubMed: 17559989

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Le document en format XML

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<term>Antigens, Viral (immunology)</term>
<term>B-Lymphocytes (immunology)</term>
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<term>Ferrets</term>
<term>Humans</term>
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<term>Lung (immunology)</term>
<term>Lung (pathology)</term>
<term>Lung (virology)</term>
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<term>SARS Virus (immunology)</term>
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<div type="abstract" xml:lang="en">A ferret model of severe acute respiratory syndrome (SARS)-CoV infection was used to evaluate the efficacy of an adenovirus vaccine. Animals were subjected to heterologous prime-boost using vectors from human serotype 5 and chimpanzee derived adenoviruses (human AdHu5 and chimpanzee AdC7) expressing spike protein followed by intranasal challenge with SARS-CoV. Vaccination led to a substantial reduction in viral load and prevented the severe pneumonia seen in unvaccinated animals. The same prime-boost strategy was effective in rhesus macaques in eliciting SARS-CoV specific immune responses. These data indicate that a heterologous adenovirus-based prime-boost vaccine strategy could safely stimulate strong immunity that may be needed for complete protection against SARS-CoV infection.</div>
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