Comparative immunogenicity and cross-clade protective efficacy of mammalian cell-grown inactivated and live attenuated H5N1 reassortant vaccines in ferrets.
Identifieur interne : 000C81 ( Main/Curation ); précédent : 000C80; suivant : 000C82Comparative immunogenicity and cross-clade protective efficacy of mammalian cell-grown inactivated and live attenuated H5N1 reassortant vaccines in ferrets.
Auteurs : Kortney M. Gustin [États-Unis] ; Taronna R. Maines ; Jessica A. Belser ; Neal Van Hoeven ; Xuihua Lu ; Libo Dong ; Irina Isakova-Sivak ; Li-Mei Chen ; J Theo M. Voeten ; Jacco G M. Heldens ; Han Van Den Bosch ; Nancy J. Cox ; Terrence M. Tumpey ; Alexander I. Klimov ; Larisa Rudenko ; Ruben O. Donis ; Jacqueline M. KatzSource :
- The Journal of infectious diseases [ 1537-6613 ] ; 2011.
Descripteurs français
- KwdFr :
- Animaux, Anticorps antiviraux (analyse), Culture virale (), Excrétion virale, Furets, Mâle, Protection croisée (immunologie), Sous-type H5N1 du virus de la grippe A (génétique), Sous-type H5N1 du virus de la grippe A (immunologie), Vaccins antigrippaux (immunologie), Vaccins atténués (génétique), Vaccins atténués (immunologie), Vaccins inactivés (immunologie), Vaccins synthétiques (immunologie).
- MESH :
- analyse : Anticorps antiviraux.
- génétique : Sous-type H5N1 du virus de la grippe A, Vaccins atténués.
- immunologie : Protection croisée, Sous-type H5N1 du virus de la grippe A, Vaccins antigrippaux, Vaccins atténués, Vaccins inactivés, Vaccins synthétiques.
- Animaux, Culture virale, Excrétion virale, Furets, Mâle.
English descriptors
- KwdEn :
- Animals, Antibodies, Viral (analysis), Cross Protection (immunology), Ferrets, Influenza A Virus, H5N1 Subtype (genetics), Influenza A Virus, H5N1 Subtype (immunology), Influenza Vaccines (immunology), Male, Vaccines, Attenuated (genetics), Vaccines, Attenuated (immunology), Vaccines, Inactivated (immunology), Vaccines, Synthetic (immunology), Virus Cultivation (methods), Virus Shedding.
- MESH :
- chemical , analysis : Antibodies, Viral.
- genetics : Influenza A Virus, H5N1 Subtype, Vaccines, Attenuated.
- immunology : Cross Protection, Influenza A Virus, H5N1 Subtype, Influenza Vaccines, Vaccines, Attenuated, Vaccines, Inactivated, Vaccines, Synthetic.
- methods : Virus Cultivation.
- Animals, Ferrets, Male, Virus Shedding.
Abstract
Continued H5N1 virus infection in humans highlights the need for vaccine strategies that provide cross-clade protection against this rapidly evolving virus. We report a comparative evaluation in ferrets of the immunogenicity and cross-protective efficacy of isogenic mammalian cell-grown, live attenuated influenza vaccine (LAIV) and adjuvanted, whole-virus, inactivated influenza vaccine (IIV), produced from a clade 1 H5N1 6:2 reassortant vaccine candidate (caVN1203-Len17rg) based on the cold-adapted A/Leningrad/134/17/57 (H2N2) master donor virus. Two doses of LAIV or IIV provided complete protection against lethal homologous H5N1 virus challenge and a reduction in virus shedding and disease severity after heterologous clade 2.2.1 H5N1 virus challenge and increased virus-specific serum and nasal wash antibody levels. Although both vaccines demonstrated cross-protective efficacy, LAIV induced higher levels of nasal wash IgA and reduction of heterologous virus shedding, compared with IIV. Thus, enhanced respiratory tract antibody responses elicited by LAIV were associated with improved cross-clade protection.
DOI: 10.1093/infdis/jir596
PubMed: 21957153
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<term>Influenza A Virus, H5N1 Subtype (genetics)</term>
<term>Influenza A Virus, H5N1 Subtype (immunology)</term>
<term>Influenza Vaccines (immunology)</term>
<term>Male</term>
<term>Vaccines, Attenuated (genetics)</term>
<term>Vaccines, Attenuated (immunology)</term>
<term>Vaccines, Inactivated (immunology)</term>
<term>Vaccines, Synthetic (immunology)</term>
<term>Virus Cultivation (methods)</term>
<term>Virus Shedding</term>
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<keywords scheme="KwdFr" xml:lang="fr"><term>Animaux</term>
<term>Anticorps antiviraux (analyse)</term>
<term>Culture virale ()</term>
<term>Excrétion virale</term>
<term>Furets</term>
<term>Mâle</term>
<term>Protection croisée (immunologie)</term>
<term>Sous-type H5N1 du virus de la grippe A (génétique)</term>
<term>Sous-type H5N1 du virus de la grippe A (immunologie)</term>
<term>Vaccins antigrippaux (immunologie)</term>
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<term>Vaccins atténués (immunologie)</term>
<term>Vaccins inactivés (immunologie)</term>
<term>Vaccins synthétiques (immunologie)</term>
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<keywords scheme="MESH" qualifier="analyse" xml:lang="fr"><term>Anticorps antiviraux</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Influenza A Virus, H5N1 Subtype</term>
<term>Vaccines, Attenuated</term>
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<term>Vaccins atténués</term>
<term>Vaccins inactivés</term>
<term>Vaccins synthétiques</term>
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<term>Influenza A Virus, H5N1 Subtype</term>
<term>Influenza Vaccines</term>
<term>Vaccines, Attenuated</term>
<term>Vaccines, Inactivated</term>
<term>Vaccines, Synthetic</term>
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<term>Virus Shedding</term>
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<term>Excrétion virale</term>
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<term>Mâle</term>
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<front><div type="abstract" xml:lang="en">Continued H5N1 virus infection in humans highlights the need for vaccine strategies that provide cross-clade protection against this rapidly evolving virus. We report a comparative evaluation in ferrets of the immunogenicity and cross-protective efficacy of isogenic mammalian cell-grown, live attenuated influenza vaccine (LAIV) and adjuvanted, whole-virus, inactivated influenza vaccine (IIV), produced from a clade 1 H5N1 6:2 reassortant vaccine candidate (caVN1203-Len17rg) based on the cold-adapted A/Leningrad/134/17/57 (H2N2) master donor virus. Two doses of LAIV or IIV provided complete protection against lethal homologous H5N1 virus challenge and a reduction in virus shedding and disease severity after heterologous clade 2.2.1 H5N1 virus challenge and increased virus-specific serum and nasal wash antibody levels. Although both vaccines demonstrated cross-protective efficacy, LAIV induced higher levels of nasal wash IgA and reduction of heterologous virus shedding, compared with IIV. Thus, enhanced respiratory tract antibody responses elicited by LAIV were associated with improved cross-clade protection.</div>
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