Monoclonal antibody against N2 neuraminidase of cold adapted A/Leningrad/134/17/57 (H2N2) enables efficient generation of live attenuated influenza vaccines.
Identifieur interne : 000019 ( PubMed/Curation ); précédent : 000018; suivant : 000020Monoclonal antibody against N2 neuraminidase of cold adapted A/Leningrad/134/17/57 (H2N2) enables efficient generation of live attenuated influenza vaccines.
Auteurs : Svetlana Shcherbik [États-Unis] ; Paul Carney [États-Unis] ; Nicholas Pearce [États-Unis] ; James Stevens [États-Unis] ; Vivien G. Dugan [États-Unis] ; David E. Wentworth [États-Unis] ; Tatiana Bousse [États-Unis]Source :
- Virology [ 1096-0341 ] ; 2018.
Descripteurs français
- KwdFr :
- Animaux, Anticorps antiviraux (immunologie), Anticorps antiviraux (isolement et purification), Anticorps monoclonaux (immunologie), Anticorps monoclonaux (isolement et purification), Basse température, Culture virale (), Humains, Lignée cellulaire, Protéines virales (immunologie), Sialidase (immunologie), Sous-type H2N2 du virus de la grippe A (croissance et développement), Sous-type H2N2 du virus de la grippe A (immunologie), Sous-type H2N2 du virus de la grippe A (isolement et purification), Technologie pharmaceutique (), Vaccins antigrippaux (immunologie), Vaccins antigrippaux (isolement et purification), Vaccins atténués (immunologie), Vaccins atténués (isolement et purification), Virus recombinants (croissance et développement), Virus recombinants (immunologie), Virus recombinants (isolement et purification).
- MESH :
- croissance et développement : Sous-type H2N2 du virus de la grippe A, Virus recombinants.
- immunologie : Anticorps antiviraux, Anticorps monoclonaux, Protéines virales, Sialidase, Sous-type H2N2 du virus de la grippe A, Vaccins antigrippaux, Vaccins atténués, Virus recombinants.
- isolement et purification : Anticorps antiviraux, Anticorps monoclonaux, Sous-type H2N2 du virus de la grippe A, Vaccins antigrippaux, Vaccins atténués, Virus recombinants.
- Animaux, Basse température, Culture virale, Humains, Lignée cellulaire, Technologie pharmaceutique.
English descriptors
- KwdEn :
- Animals, Antibodies, Monoclonal (immunology), Antibodies, Monoclonal (isolation & purification), Antibodies, Viral (immunology), Antibodies, Viral (isolation & purification), Cell Line, Cold Temperature, Humans, Influenza A Virus, H2N2 Subtype (growth & development), Influenza A Virus, H2N2 Subtype (immunology), Influenza A Virus, H2N2 Subtype (isolation & purification), Influenza Vaccines (immunology), Influenza Vaccines (isolation & purification), Neuraminidase (immunology), Reassortant Viruses (growth & development), Reassortant Viruses (immunology), Reassortant Viruses (isolation & purification), Technology, Pharmaceutical (methods), Vaccines, Attenuated (immunology), Vaccines, Attenuated (isolation & purification), Viral Proteins (immunology), Virus Cultivation (methods).
- MESH :
- chemical , immunology : Antibodies, Monoclonal, Antibodies, Viral, Influenza Vaccines, Neuraminidase, Vaccines, Attenuated, Viral Proteins.
- chemical , isolation & purification : Antibodies, Monoclonal, Antibodies, Viral, Influenza Vaccines, Vaccines, Attenuated.
- growth & development : Influenza A Virus, H2N2 Subtype, Reassortant Viruses.
- immunology : Influenza A Virus, H2N2 Subtype, Reassortant Viruses.
- isolation & purification : Influenza A Virus, H2N2 Subtype, Reassortant Viruses.
- methods : Technology, Pharmaceutical, Virus Cultivation.
- Animals, Cell Line, Cold Temperature, Humans.
Abstract
Cold adapted influenza virus A/Leningrad/134/17/57 (H2N2) is a reliable master donor virus (Len/17-MDV) for preparing live attenuated influenza vaccines (LAIV). LAIVs are 6:2 reasortants that contain 6 segments of Len/17-MDV and the hemagglutinin (HA) and neuraminidase (NA) of contemporary circulating influenza A viruses. The problem with the classical reassortment procedure used to generate LAIVs is that there is limited selection pressure against NA of the Len/17-MDV resulting in 7:1 reassortants with desired HA only, which are not suitable LAIVs. The monoclonal antibodies (mAb) directed against the N2 of Len/17-MDV were generated. 10C4-8E7 mAb inhibits cell-to-cell spread of viruses containing the Len/17-MDV N2, but not viruses with the related N2 from contemporary H3N2 viruses. 10C4-8E7 antibody specifically inhibited the Len/17-MDV replication in vitro and in ovo but didn't inhibit replication of H3N2 or H1N1pdm09 reassortants. Our data demonstrate that addition of 10C4-8E7 in the classical reassortment improves efficiency of LAIV production.
DOI: 10.1016/j.virol.2018.07.005
PubMed: 30014859
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<term>Antibodies, Viral (isolation & purification)</term>
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<term>Cold Temperature</term>
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<front><div type="abstract" xml:lang="en">Cold adapted influenza virus A/Leningrad/134/17/57 (H2N2) is a reliable master donor virus (Len/17-MDV) for preparing live attenuated influenza vaccines (LAIV). LAIVs are 6:2 reasortants that contain 6 segments of Len/17-MDV and the hemagglutinin (HA) and neuraminidase (NA) of contemporary circulating influenza A viruses. The problem with the classical reassortment procedure used to generate LAIVs is that there is limited selection pressure against NA of the Len/17-MDV resulting in 7:1 reassortants with desired HA only, which are not suitable LAIVs. The monoclonal antibodies (mAb) directed against the N2 of Len/17-MDV were generated. 10C4-8E7 mAb inhibits cell-to-cell spread of viruses containing the Len/17-MDV N2, but not viruses with the related N2 from contemporary H3N2 viruses. 10C4-8E7 antibody specifically inhibited the Len/17-MDV replication in vitro and in ovo but didn't inhibit replication of H3N2 or H1N1pdm09 reassortants. Our data demonstrate that addition of 10C4-8E7 in the classical reassortment improves efficiency of LAIV production.</div>
</front>
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<Abstract><AbstractText>Cold adapted influenza virus A/Leningrad/134/17/57 (H2N2) is a reliable master donor virus (Len/17-MDV) for preparing live attenuated influenza vaccines (LAIV). LAIVs are 6:2 reasortants that contain 6 segments of Len/17-MDV and the hemagglutinin (HA) and neuraminidase (NA) of contemporary circulating influenza A viruses. The problem with the classical reassortment procedure used to generate LAIVs is that there is limited selection pressure against NA of the Len/17-MDV resulting in 7:1 reassortants with desired HA only, which are not suitable LAIVs. The monoclonal antibodies (mAb) directed against the N2 of Len/17-MDV were generated. 10C4-8E7 mAb inhibits cell-to-cell spread of viruses containing the Len/17-MDV N2, but not viruses with the related N2 from contemporary H3N2 viruses. 10C4-8E7 antibody specifically inhibited the Len/17-MDV replication in vitro and in ovo but didn't inhibit replication of H3N2 or H1N1pdm09 reassortants. Our data demonstrate that addition of 10C4-8E7 in the classical reassortment improves efficiency of LAIV production.</AbstractText>
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