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Preparation and characterization of a purified influenza virus neuraminidase vaccine

Identifieur interne : 001D06 ( Main/Exploration ); précédent : 001D05; suivant : 001D07

Preparation and characterization of a purified influenza virus neuraminidase vaccine

Auteurs : Michael Hocart [États-Unis] ; Bernardo Grajower [États-Unis] ; Armen Donabedian [États-Unis] ; Barbara Pokorny [États-Unis] ; Charles Whitaker [États-Unis] ; Edwin D. Kilbourne [États-Unis]

Source :

RBID : ISTEX:265463C0F57364D7B4CF0575DCE6B927E7C63F79

English descriptors

Abstract

Abstract: Influenza virus neuraminidase (NA) has been shown to induce protective but infection-permissive immunity in experimental animals. Challenge infection following such immunization is attended by decreased viral replication and disease manifestations but is sufficient to provide antigenic stimulation and definitive immunity to the virus. The present report describes the preparation and characterization of a purified NA vaccine (NAV) used in Phase 1 (immunogenicity and toxicity) trials in humans. In essence, virion NA was isolated from detergent-disrupted virus by affinity chromatography on oxamic acid-agarose, treated with formalin and tested for its enzymatic activity and for its immunogenicity in Balb c mice and New Zealand rabbits. The preparation was essentially free of viral hemagglutinin but contained residual NP and M1 proteins. Both dispersed and aggregated NA tetrameric heads were seen in electron micrographs. Enzymatic activity was preserved, and minimal immunogenic doses in mice and rabbits, respectively, were 3.7 and 0.027 μg per kg.

Url:
DOI: 10.1016/0264-410X(95)00126-L


Affiliations:


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Le document en format XML

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<div type="abstract" xml:lang="en">Abstract: Influenza virus neuraminidase (NA) has been shown to induce protective but infection-permissive immunity in experimental animals. Challenge infection following such immunization is attended by decreased viral replication and disease manifestations but is sufficient to provide antigenic stimulation and definitive immunity to the virus. The present report describes the preparation and characterization of a purified NA vaccine (NAV) used in Phase 1 (immunogenicity and toxicity) trials in humans. In essence, virion NA was isolated from detergent-disrupted virus by affinity chromatography on oxamic acid-agarose, treated with formalin and tested for its enzymatic activity and for its immunogenicity in Balb c mice and New Zealand rabbits. The preparation was essentially free of viral hemagglutinin but contained residual NP and M1 proteins. Both dispersed and aggregated NA tetrameric heads were seen in electron micrographs. Enzymatic activity was preserved, and minimal immunogenic doses in mice and rabbits, respectively, were 3.7 and 0.027 μg per kg.</div>
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