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CTA1-M2e-DD : A novel mucosal adjuvant targeted influenza vaccine

Identifieur interne : 000466 ( PascalFrancis/Curation ); précédent : 000465; suivant : 000467

CTA1-M2e-DD : A novel mucosal adjuvant targeted influenza vaccine

Auteurs : Dubravka Grdic Eliasson [Suède] ; Karim El Bakkouri [Belgique] ; Karin Schön [Suède] ; Anna Ramne [Suède] ; Els Festjens [Belgique] ; Bjdrn Löwenadler [Suède] ; Walter Fiers [Belgique] ; Xavier Saelens [Belgique] ; Nils Lycke [Suède]

Source :

RBID : Pascal:08-0158301

Descripteurs français

English descriptors

Abstract

At present few vaccine candidates exists against potentially pandemic influenza virus infections. We provide compelling evidence that a targeted fusion protein based on the CTA1-DD adjuvant and containing tandem repeats of the matrix protein 2 (M2e) ectodomain epitope, CTA1-3M2e-DD, confers strong protective immunity against a potentially lethal challenge infection with influenza virus in mice. The formulation was highly effective for mucosal immunizations and promoted high M2e-specific serum IgG and mucosal IgA antibody titers and an hitherto unknown anti-M2e CD4 T cell immunity. This novel CTA1-3M2e-DD fusion protein combines adjuvant and a conserved influenza A antigen in a promising candidate for a universal anti-influenza vaccine.
pA  
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A02 01      @0 VACCDE
A03   1    @0 Vaccine
A05       @2 26
A06       @2 9
A08 01  1  ENG  @1 CTA1-M2e-DD : A novel mucosal adjuvant targeted influenza vaccine
A11 01  1    @1 GRDIC ELIASSON (Dubravka)
A11 02  1    @1 EL BAKKOURI (Karim)
A11 03  1    @1 SCHÖN (Karin)
A11 04  1    @1 RAMNE (Anna)
A11 05  1    @1 FESTJENS (Els)
A11 06  1    @1 LÖWENADLER (Bjdrn)
A11 07  1    @1 FIERS (Walter)
A11 08  1    @1 SAELENS (Xavier)
A11 09  1    @1 LYCKE (Nils)
A14 01      @1 Department of Microbiology and Immunology, Mucosal Immunology and Vaccine Research Center, Institute of Biomedicine, University of Götebors, Box 435 @2 40530 Götebors @3 SWE @Z 1 aut. @Z 3 aut. @Z 9 aut.
A14 02      @1 Department for Molecular Biomedical Research, VIB and University of Ghent @2 Ghent @3 BEL @Z 2 aut. @Z 5 aut. @Z 7 aut. @Z 8 aut.
A14 03      @1 Biovitrum AB @2 Götebory @3 SWE @Z 4 aut.
A14 04      @1 AstraZeneca @2 Götebors @3 SWE @Z 6 aut.
A20       @1 1243-1252
A21       @1 2008
A23 01      @0 ENG
A43 01      @1 INIST @2 20289 @5 354000175098950120
A44       @0 0000 @1 © 2008 INIST-CNRS. All rights reserved.
A45       @0 63 ref.
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A60       @1 P
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C01 01    ENG  @0 At present few vaccine candidates exists against potentially pandemic influenza virus infections. We provide compelling evidence that a targeted fusion protein based on the CTA1-DD adjuvant and containing tandem repeats of the matrix protein 2 (M2e) ectodomain epitope, CTA1-3M2e-DD, confers strong protective immunity against a potentially lethal challenge infection with influenza virus in mice. The formulation was highly effective for mucosal immunizations and promoted high M2e-specific serum IgG and mucosal IgA antibody titers and an hitherto unknown anti-M2e CD4 T cell immunity. This novel CTA1-3M2e-DD fusion protein combines adjuvant and a conserved influenza A antigen in a promising candidate for a universal anti-influenza vaccine.
C02 01  X    @0 002A05F04
C02 02  X    @0 002A05C10
C03 01  X  FRE  @0 Virus grippal A @2 NW @5 01
C03 01  X  ENG  @0 Influenza A virus @2 NW @5 01
C03 01  X  SPA  @0 Influenza A virus @2 NW @5 01
C03 02  X  FRE  @0 Muqueuse @5 05
C03 02  X  ENG  @0 Mucosa @5 05
C03 02  X  SPA  @0 Mucosa @5 05
C03 03  X  FRE  @0 Adjuvant immunologique @5 06
C03 03  X  ENG  @0 Immunological adjuvant @5 06
C03 03  X  SPA  @0 Coadyuvante inmunológico @5 06
C03 04  X  FRE  @0 Vaccin @5 07
C03 04  X  ENG  @0 Vaccine @5 07
C03 04  X  SPA  @0 Vacuna @5 07
C03 05  X  FRE  @0 Vaccination @5 08
C03 05  X  ENG  @0 Vaccination @5 08
C03 05  X  SPA  @0 Vacunación @5 08
C03 06  X  FRE  @0 IgA @5 09
C03 06  X  ENG  @0 IgA @5 09
C03 06  X  SPA  @0 IgA @5 09
C03 07  X  FRE  @0 Immunomodulation @5 10
C03 07  X  ENG  @0 Immunomodulation @5 10
C03 07  X  SPA  @0 Inmunomodulación @5 10
C03 08  X  FRE  @0 Rate @5 11
C03 08  X  ENG  @0 Spleen @5 11
C03 08  X  SPA  @0 Bazo @5 11
C03 09  X  FRE  @0 Ganglion lymphatique @5 12
C03 09  X  ENG  @0 Lymph node @5 12
C03 09  X  SPA  @0 Ganglio linfático @5 12
C03 10  X  FRE  @0 Grippe @5 14
C03 10  X  ENG  @0 Influenza @5 14
C03 10  X  SPA  @0 Gripe @5 14
C03 11  X  FRE  @0 Antigène @5 67
C03 11  X  ENG  @0 Antigen @5 67
C03 11  X  SPA  @0 Antígeno @5 67
C03 12  X  FRE  @0 Peptide @5 68
C03 12  X  ENG  @0 Peptides @5 68
C03 12  X  SPA  @0 Péptido @5 68
C03 13  X  FRE  @0 Déterminant antigénique @5 69
C03 13  X  ENG  @0 Antigenic determinant @5 69
C03 13  X  SPA  @0 Determinante antigénico @5 69
C07 01  X  FRE  @0 Influenzavirus A @2 NW
C07 01  X  ENG  @0 Influenzavirus A @2 NW
C07 01  X  SPA  @0 Influenzavirus A @2 NW
C07 02  X  FRE  @0 Orthomyxoviridae @2 NW
C07 02  X  ENG  @0 Orthomyxoviridae @2 NW
C07 02  X  SPA  @0 Orthomyxoviridae @2 NW
C07 03  X  FRE  @0 Virus @2 NW
C07 03  X  ENG  @0 Virus @2 NW
C07 03  X  SPA  @0 Virus @2 NW
C07 04  X  FRE  @0 Virose
C07 04  X  ENG  @0 Viral disease
C07 04  X  SPA  @0 Virosis
C07 05  X  FRE  @0 Infection
C07 05  X  ENG  @0 Infection
C07 05  X  SPA  @0 Infección
N21       @1 098
N44 01      @1 OTO
N82       @1 OTO

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Pascal:08-0158301

Le document en format XML

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<term>Influenza</term>
<term>Influenza A virus</term>
<term>Lymph node</term>
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<div type="abstract" xml:lang="en">At present few vaccine candidates exists against potentially pandemic influenza virus infections. We provide compelling evidence that a targeted fusion protein based on the CTA1-DD adjuvant and containing tandem repeats of the matrix protein 2 (M2e) ectodomain epitope, CTA1-3M2e-DD, confers strong protective immunity against a potentially lethal challenge infection with influenza virus in mice. The formulation was highly effective for mucosal immunizations and promoted high M2e-specific serum IgG and mucosal IgA antibody titers and an hitherto unknown anti-M2e CD4 T cell immunity. This novel CTA1-3M2e-DD fusion protein combines adjuvant and a conserved influenza A antigen in a promising candidate for a universal anti-influenza vaccine.</div>
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<fA14 i1="03">
<s1>Biovitrum AB</s1>
<s2>Götebory</s2>
<s3>SWE</s3>
<sZ>4 aut.</sZ>
</fA14>
<fA14 i1="04">
<s1>AstraZeneca</s1>
<s2>Götebors</s2>
<s3>SWE</s3>
<sZ>6 aut.</sZ>
</fA14>
<fA20>
<s1>1243-1252</s1>
</fA20>
<fA21>
<s1>2008</s1>
</fA21>
<fA23 i1="01">
<s0>ENG</s0>
</fA23>
<fA43 i1="01">
<s1>INIST</s1>
<s2>20289</s2>
<s5>354000175098950120</s5>
</fA43>
<fA44>
<s0>0000</s0>
<s1>© 2008 INIST-CNRS. All rights reserved.</s1>
</fA44>
<fA45>
<s0>63 ref.</s0>
</fA45>
<fA47 i1="01" i2="1">
<s0>08-0158301</s0>
</fA47>
<fA60>
<s1>P</s1>
</fA60>
<fA61>
<s0>A</s0>
</fA61>
<fA64 i1="01" i2="1">
<s0>Vaccine</s0>
</fA64>
<fA66 i1="01">
<s0>GBR</s0>
</fA66>
<fC01 i1="01" l="ENG">
<s0>At present few vaccine candidates exists against potentially pandemic influenza virus infections. We provide compelling evidence that a targeted fusion protein based on the CTA1-DD adjuvant and containing tandem repeats of the matrix protein 2 (M2e) ectodomain epitope, CTA1-3M2e-DD, confers strong protective immunity against a potentially lethal challenge infection with influenza virus in mice. The formulation was highly effective for mucosal immunizations and promoted high M2e-specific serum IgG and mucosal IgA antibody titers and an hitherto unknown anti-M2e CD4 T cell immunity. This novel CTA1-3M2e-DD fusion protein combines adjuvant and a conserved influenza A antigen in a promising candidate for a universal anti-influenza vaccine.</s0>
</fC01>
<fC02 i1="01" i2="X">
<s0>002A05F04</s0>
</fC02>
<fC02 i1="02" i2="X">
<s0>002A05C10</s0>
</fC02>
<fC03 i1="01" i2="X" l="FRE">
<s0>Virus grippal A</s0>
<s2>NW</s2>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="ENG">
<s0>Influenza A virus</s0>
<s2>NW</s2>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA">
<s0>Influenza A virus</s0>
<s2>NW</s2>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE">
<s0>Muqueuse</s0>
<s5>05</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG">
<s0>Mucosa</s0>
<s5>05</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA">
<s0>Mucosa</s0>
<s5>05</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE">
<s0>Adjuvant immunologique</s0>
<s5>06</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG">
<s0>Immunological adjuvant</s0>
<s5>06</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA">
<s0>Coadyuvante inmunológico</s0>
<s5>06</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE">
<s0>Vaccin</s0>
<s5>07</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG">
<s0>Vaccine</s0>
<s5>07</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA">
<s0>Vacuna</s0>
<s5>07</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE">
<s0>Vaccination</s0>
<s5>08</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG">
<s0>Vaccination</s0>
<s5>08</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA">
<s0>Vacunación</s0>
<s5>08</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE">
<s0>IgA</s0>
<s5>09</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG">
<s0>IgA</s0>
<s5>09</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA">
<s0>IgA</s0>
<s5>09</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE">
<s0>Immunomodulation</s0>
<s5>10</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG">
<s0>Immunomodulation</s0>
<s5>10</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA">
<s0>Inmunomodulación</s0>
<s5>10</s5>
</fC03>
<fC03 i1="08" i2="X" l="FRE">
<s0>Rate</s0>
<s5>11</s5>
</fC03>
<fC03 i1="08" i2="X" l="ENG">
<s0>Spleen</s0>
<s5>11</s5>
</fC03>
<fC03 i1="08" i2="X" l="SPA">
<s0>Bazo</s0>
<s5>11</s5>
</fC03>
<fC03 i1="09" i2="X" l="FRE">
<s0>Ganglion lymphatique</s0>
<s5>12</s5>
</fC03>
<fC03 i1="09" i2="X" l="ENG">
<s0>Lymph node</s0>
<s5>12</s5>
</fC03>
<fC03 i1="09" i2="X" l="SPA">
<s0>Ganglio linfático</s0>
<s5>12</s5>
</fC03>
<fC03 i1="10" i2="X" l="FRE">
<s0>Grippe</s0>
<s5>14</s5>
</fC03>
<fC03 i1="10" i2="X" l="ENG">
<s0>Influenza</s0>
<s5>14</s5>
</fC03>
<fC03 i1="10" i2="X" l="SPA">
<s0>Gripe</s0>
<s5>14</s5>
</fC03>
<fC03 i1="11" i2="X" l="FRE">
<s0>Antigène</s0>
<s5>67</s5>
</fC03>
<fC03 i1="11" i2="X" l="ENG">
<s0>Antigen</s0>
<s5>67</s5>
</fC03>
<fC03 i1="11" i2="X" l="SPA">
<s0>Antígeno</s0>
<s5>67</s5>
</fC03>
<fC03 i1="12" i2="X" l="FRE">
<s0>Peptide</s0>
<s5>68</s5>
</fC03>
<fC03 i1="12" i2="X" l="ENG">
<s0>Peptides</s0>
<s5>68</s5>
</fC03>
<fC03 i1="12" i2="X" l="SPA">
<s0>Péptido</s0>
<s5>68</s5>
</fC03>
<fC03 i1="13" i2="X" l="FRE">
<s0>Déterminant antigénique</s0>
<s5>69</s5>
</fC03>
<fC03 i1="13" i2="X" l="ENG">
<s0>Antigenic determinant</s0>
<s5>69</s5>
</fC03>
<fC03 i1="13" i2="X" l="SPA">
<s0>Determinante antigénico</s0>
<s5>69</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE">
<s0>Influenzavirus A</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="01" i2="X" l="ENG">
<s0>Influenzavirus A</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="01" i2="X" l="SPA">
<s0>Influenzavirus A</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="02" i2="X" l="FRE">
<s0>Orthomyxoviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="02" i2="X" l="ENG">
<s0>Orthomyxoviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="02" i2="X" l="SPA">
<s0>Orthomyxoviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="03" i2="X" l="FRE">
<s0>Virus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="03" i2="X" l="ENG">
<s0>Virus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="03" i2="X" l="SPA">
<s0>Virus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="04" i2="X" l="FRE">
<s0>Virose</s0>
</fC07>
<fC07 i1="04" i2="X" l="ENG">
<s0>Viral disease</s0>
</fC07>
<fC07 i1="04" i2="X" l="SPA">
<s0>Virosis</s0>
</fC07>
<fC07 i1="05" i2="X" l="FRE">
<s0>Infection</s0>
</fC07>
<fC07 i1="05" i2="X" l="ENG">
<s0>Infection</s0>
</fC07>
<fC07 i1="05" i2="X" l="SPA">
<s0>Infección</s0>
</fC07>
<fN21>
<s1>098</s1>
</fN21>
<fN44 i1="01">
<s1>OTO</s1>
</fN44>
<fN82>
<s1>OTO</s1>
</fN82>
</pA>
</standard>
</inist>
</record>

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   |wiki=    Sante
   |area=    PandemieGrippaleV1
   |flux=    PascalFrancis
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   |texte=   CTA1-M2e-DD : A novel mucosal adjuvant targeted influenza vaccine
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