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Passive immunization with a recombinant adenovirus expressing an HA (H5)-specific single-domain antibody protects mice from lethal influenza infection

Identifieur interne : 001B14 ( PascalFrancis/Curation ); précédent : 001B13; suivant : 001B15

Passive immunization with a recombinant adenovirus expressing an HA (H5)-specific single-domain antibody protects mice from lethal influenza infection

Auteurs : Irina L. Tutykhina [Russie] ; Elena S. Sedova [Russie] ; Irina Y. Gribova [Russie] ; Tatiana I. Ivanova [Russie] ; Lev A. Vasilev [Russie] ; Marina V. Rutovskaya [Russie] ; Andrei A. Lysenko [Russie] ; Maxim M. Shmarov [Russie] ; Denis Y. Logunov [Russie] ; Boris S. Naroditsky [Russie] ; Sergei V. Tillib [Russie] ; Alexander L. Gintsburg [Russie]

Source :

RBID : Pascal:13-0152042

Descripteurs français

English descriptors

Abstract

One effective method for the prevention and treatment of influenza infection is passive immunization. In our study, we examined the feasibility of creating an antibody-based preparation with a prolonged protective effect against influenza virus. Single-domain antibodies (sdAbs) specific for influenza virus hem-agglutinin were generated. Experiments in mouse models showed 100% survivability for both intranasal sdAbs administration 24 h prior to influenza challenge and 24 h after infection. sdAb-gene delivery by an adenoviral vector led to gene expression for up to 14 days. Protection by a recombinant adenovirus containing the sdAb gene was observed in cases of administration prior to influenza infection (14 d-24 h). We also demonstrated that the single administration of a combined preparation containing sdAb DNA and protein expanded the protection time window from 14 d prior to 48 h after influenza infection. This approach and the application of a broad-spectrum sdAbs will allow the development of efficient drugs for the prevention and treatment of viral infections produced by pandemic virus variants and other infections.
pA  
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A03   1    @0 Antivir. res.
A05       @2 97
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A08 01  1  ENG  @1 Passive immunization with a recombinant adenovirus expressing an HA (H5)-specific single-domain antibody protects mice from lethal influenza infection
A11 01  1    @1 TUTYKHINA (Irina L.)
A11 02  1    @1 SEDOVA (Elena S.)
A11 03  1    @1 GRIBOVA (Irina Y.)
A11 04  1    @1 IVANOVA (Tatiana I.)
A11 05  1    @1 VASILEV (Lev A.)
A11 06  1    @1 RUTOVSKAYA (Marina V.)
A11 07  1    @1 LYSENKO (Andrei A.)
A11 08  1    @1 SHMAROV (Maxim M.)
A11 09  1    @1 LOGUNOV (Denis Y.)
A11 10  1    @1 NARODITSKY (Boris S.)
A11 11  1    @1 TILLIB (Sergei V.)
A11 12  1    @1 GINTSBURG (Alexander L.)
A14 01      @1 Gamaleya Research Institute for Epidemiology and Microbiology, 18, Gamaleya Street @2 Moscow 123098 @3 RUS @Z 1 aut. @Z 2 aut. @Z 3 aut. @Z 7 aut. @Z 8 aut. @Z 9 aut. @Z 10 aut. @Z 12 aut.
A14 02      @1 Institute of Gene Biology, Russian Academy of Sciences, 34/5, Vavilova Street @2 Moscow 119334 @3 RUS @Z 4 aut. @Z 5 aut. @Z 6 aut. @Z 11 aut.
A20       @1 318-328
A21       @1 2013
A23 01      @0 ENG
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A44       @0 0000 @1 © 2013 INIST-CNRS. All rights reserved.
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C01 01    ENG  @0 One effective method for the prevention and treatment of influenza infection is passive immunization. In our study, we examined the feasibility of creating an antibody-based preparation with a prolonged protective effect against influenza virus. Single-domain antibodies (sdAbs) specific for influenza virus hem-agglutinin were generated. Experiments in mouse models showed 100% survivability for both intranasal sdAbs administration 24 h prior to influenza challenge and 24 h after infection. sdAb-gene delivery by an adenoviral vector led to gene expression for up to 14 days. Protection by a recombinant adenovirus containing the sdAb gene was observed in cases of administration prior to influenza infection (14 d-24 h). We also demonstrated that the single administration of a combined preparation containing sdAb DNA and protein expanded the protection time window from 14 d prior to 48 h after influenza infection. This approach and the application of a broad-spectrum sdAbs will allow the development of efficient drugs for the prevention and treatment of viral infections produced by pandemic virus variants and other infections.
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C03 02  X  FRE  @0 Adenoviridae @2 NW @5 02
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C03 03  X  ENG  @0 Human adenovirus @2 NW @5 03
C03 03  X  SPA  @0 Human adenovirus @2 NW @5 03
C03 04  X  FRE  @0 Anticorps @5 04
C03 04  X  ENG  @0 Antibody @5 04
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C03 05  X  FRE  @0 Prévention @5 05
C03 05  X  ENG  @0 Prevention @5 05
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C03 10  X  FRE  @0 Vecteur @5 11
C03 10  X  ENG  @0 Vector @5 11
C03 10  X  SPA  @0 Vector @5 11
C03 11  X  FRE  @0 Forme fatale @4 INC @5 86
C07 01  X  FRE  @0 Virus @2 NW
C07 01  X  ENG  @0 Virus @2 NW
C07 01  X  SPA  @0 Virus @2 NW
C07 02  X  FRE  @0 Mastadenovirus @2 NW
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C07 03  X  FRE  @0 Rodentia @2 NS
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C07 06  X  FRE  @0 Virose
C07 06  X  ENG  @0 Viral disease
C07 06  X  SPA  @0 Virosis
C07 07  X  FRE  @0 Infection
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N21       @1 125
N44 01      @1 OTO
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Pascal:13-0152042

Le document en format XML

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<author>
<name sortKey="Tillib, Sergei V" sort="Tillib, Sergei V" uniqKey="Tillib S" first="Sergei V." last="Tillib">Sergei V. Tillib</name>
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<title level="j" type="main">Antiviral research</title>
<title level="j" type="abbreviated">Antivir. res.</title>
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<date when="2013">2013</date>
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<title level="j" type="main">Antiviral research</title>
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<term>Adenoviridae</term>
<term>Animal</term>
<term>Antibody</term>
<term>Human adenovirus</term>
<term>Influenza</term>
<term>Influenzavirus</term>
<term>Mouse</term>
<term>Passive immunization</term>
<term>Prevention</term>
<term>Vector</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>Immunisation passive</term>
<term>Adenoviridae</term>
<term>Adénovirus humain</term>
<term>Anticorps</term>
<term>Prévention</term>
<term>Animal</term>
<term>Souris</term>
<term>Grippe</term>
<term>Influenzavirus</term>
<term>Vecteur</term>
<term>Forme fatale</term>
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<div type="abstract" xml:lang="en">One effective method for the prevention and treatment of influenza infection is passive immunization. In our study, we examined the feasibility of creating an antibody-based preparation with a prolonged protective effect against influenza virus. Single-domain antibodies (sdAbs) specific for influenza virus hem-agglutinin were generated. Experiments in mouse models showed 100% survivability for both intranasal sdAbs administration 24 h prior to influenza challenge and 24 h after infection. sdAb-gene delivery by an adenoviral vector led to gene expression for up to 14 days. Protection by a recombinant adenovirus containing the sdAb gene was observed in cases of administration prior to influenza infection (14 d-24 h). We also demonstrated that the single administration of a combined preparation containing sdAb DNA and protein expanded the protection time window from 14 d prior to 48 h after influenza infection. This approach and the application of a broad-spectrum sdAbs will allow the development of efficient drugs for the prevention and treatment of viral infections produced by pandemic virus variants and other infections.</div>
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