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Screening monoclonal antibodies for cross-reactivity in the ferret model of influenza infection

Identifieur interne : 000526 ( PascalFrancis/Curation ); précédent : 000525; suivant : 000527

Screening monoclonal antibodies for cross-reactivity in the ferret model of influenza infection

Auteurs : John A. Rutigliano [États-Unis] ; Peter C. Doherty [États-Unis, Australie] ; John Franks [États-Unis] ; Melissa Y. Morris [États-Unis] ; Cory Reynolds [États-Unis] ; Paul G. Thomas [États-Unis]

Source :

RBID : Pascal:08-0315453

Descripteurs français

English descriptors

Abstract

Influenza virus infections carry a high public health cost, and pandemics are potentially catastrophic. Though the ferret is generally regarded as the best model for human influenza, few reagents are available for the analysis of cellular immunity. We thus screened monoclonal antibodies (mAbs) made for identifying immune cells in other species to see if any were cross-reactive. Flow cytometric analysis of lymphocytes isolated from blood, spleen, and lung of normal and virus-infected ferrets indicated that several mouse mAbs bound to the corresponding antigens in ferrets. Typing bronchoalveolar lavage populations from pneumonic ferrets with mAb to human CD8 showed the massive CD8+ T cell enrichment characteristic of this infection in mice. The availability of this, and several other mAbs that showed cross-reactivity, should allow us to begin the dissection of cell-mediated immunity in the ferret, which, at least from these early results, looks similar to the situation in mice.
pA  
A01 01  1    @0 0022-1759
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A03   1    @0 J. immunol. methods
A05       @2 336
A06       @2 1
A08 01  1  ENG  @1 Screening monoclonal antibodies for cross-reactivity in the ferret model of influenza infection
A11 01  1    @1 RUTIGLIANO (John A.)
A11 02  1    @1 DOHERTY (Peter C.)
A11 03  1    @1 FRANKS (John)
A11 04  1    @1 MORRIS (Melissa Y.)
A11 05  1    @1 REYNOLDS (Cory)
A11 06  1    @1 THOMAS (Paul G.)
A14 01      @1 Department of Immunology, St. Jude Children's Research Hospital @2 Memphis, TN, 38105 @3 USA @Z 1 aut. @Z 2 aut. @Z 3 aut. @Z 4 aut. @Z 5 aut. @Z 6 aut.
A14 02      @1 Department of Microbiology and Immunology, University of Melbourne @2 Vic 3010 @3 AUS @Z 2 aut.
A20       @1 71-77
A21       @1 2008
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A44       @0 0000 @1 © 2008 INIST-CNRS. All rights reserved.
A45       @0 1/2 p.
A47 01  1    @0 08-0315453
A60       @1 P @3 PR
A61       @0 A
A64 01  1    @0 Journal of immunological methods
A66 01      @0 NLD
C01 01    ENG  @0 Influenza virus infections carry a high public health cost, and pandemics are potentially catastrophic. Though the ferret is generally regarded as the best model for human influenza, few reagents are available for the analysis of cellular immunity. We thus screened monoclonal antibodies (mAbs) made for identifying immune cells in other species to see if any were cross-reactive. Flow cytometric analysis of lymphocytes isolated from blood, spleen, and lung of normal and virus-infected ferrets indicated that several mouse mAbs bound to the corresponding antigens in ferrets. Typing bronchoalveolar lavage populations from pneumonic ferrets with mAb to human CD8 showed the massive CD8+ T cell enrichment characteristic of this infection in mice. The availability of this, and several other mAbs that showed cross-reactivity, should allow us to begin the dissection of cell-mediated immunity in the ferret, which, at least from these early results, looks similar to the situation in mice.
C02 01  X    @0 002A06B06
C03 01  X  FRE  @0 Souris @5 01
C03 01  X  ENG  @0 Mouse @5 01
C03 01  X  SPA  @0 Ratón @5 01
C03 02  X  FRE  @0 Anticorps monoclonal @5 05
C03 02  X  ENG  @0 Monoclonal antibody @5 05
C03 02  X  SPA  @0 Anticuerpo monoclonal @5 05
C03 03  X  FRE  @0 Réaction croisée @5 06
C03 03  X  ENG  @0 Cross reaction @5 06
C03 03  X  SPA  @0 Reacción cruzada @5 06
C03 04  X  FRE  @0 Modèle @5 07
C03 04  X  ENG  @0 Models @5 07
C03 04  X  SPA  @0 Modelo @5 07
C03 05  X  FRE  @0 Lymphocyte T @5 08
C03 05  X  ENG  @0 T-Lymphocyte @5 08
C03 05  X  SPA  @0 Linfocito T @5 08
C03 06  X  FRE  @0 Cytométrie flux @5 09
C03 06  X  ENG  @0 Flow cytometry @5 09
C03 06  X  SPA  @0 Citometría flujo @5 09
C03 07  X  FRE  @0 Méthode immunologique @5 10
C03 07  X  ENG  @0 Immunological method @5 10
C03 07  X  SPA  @0 Método inmunológico @5 10
C03 08  X  FRE  @0 Grippe @5 14
C03 08  X  ENG  @0 Influenza @5 14
C03 08  X  SPA  @0 Gripe @5 14
C07 01  X  FRE  @0 Rodentia @2 NS
C07 01  X  ENG  @0 Rodentia @2 NS
C07 01  X  SPA  @0 Rodentia @2 NS
C07 02  X  FRE  @0 Mammalia @2 NS
C07 02  X  ENG  @0 Mammalia @2 NS
C07 02  X  SPA  @0 Mammalia @2 NS
C07 03  X  FRE  @0 Vertebrata @2 NS
C07 03  X  ENG  @0 Vertebrata @2 NS
C07 03  X  SPA  @0 Vertebrata @2 NS
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       @1 196
N44 01      @1 OTO
N82       @1 OTO

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Pascal:08-0315453

Le document en format XML

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<div type="abstract" xml:lang="en">Influenza virus infections carry a high public health cost, and pandemics are potentially catastrophic. Though the ferret is generally regarded as the best model for human influenza, few reagents are available for the analysis of cellular immunity. We thus screened monoclonal antibodies (mAbs) made for identifying immune cells in other species to see if any were cross-reactive. Flow cytometric analysis of lymphocytes isolated from blood, spleen, and lung of normal and virus-infected ferrets indicated that several mouse mAbs bound to the corresponding antigens in ferrets. Typing bronchoalveolar lavage populations from pneumonic ferrets with mAb to human CD8 showed the massive CD8+ T cell enrichment characteristic of this infection in mice. The availability of this, and several other mAbs that showed cross-reactivity, should allow us to begin the dissection of cell-mediated immunity in the ferret, which, at least from these early results, looks similar to the situation in mice.</div>
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<s0>Linfocito T</s0>
<s5>08</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE">
<s0>Cytométrie flux</s0>
<s5>09</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG">
<s0>Flow cytometry</s0>
<s5>09</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA">
<s0>Citometría flujo</s0>
<s5>09</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE">
<s0>Méthode immunologique</s0>
<s5>10</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG">
<s0>Immunological method</s0>
<s5>10</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA">
<s0>Método inmunológico</s0>
<s5>10</s5>
</fC03>
<fC03 i1="08" i2="X" l="FRE">
<s0>Grippe</s0>
<s5>14</s5>
</fC03>
<fC03 i1="08" i2="X" l="ENG">
<s0>Influenza</s0>
<s5>14</s5>
</fC03>
<fC03 i1="08" i2="X" l="SPA">
<s0>Gripe</s0>
<s5>14</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE">
<s0>Rodentia</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="01" i2="X" l="ENG">
<s0>Rodentia</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="01" i2="X" l="SPA">
<s0>Rodentia</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="02" i2="X" l="FRE">
<s0>Mammalia</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="02" i2="X" l="ENG">
<s0>Mammalia</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="02" i2="X" l="SPA">
<s0>Mammalia</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="03" i2="X" l="FRE">
<s0>Vertebrata</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="03" i2="X" l="ENG">
<s0>Vertebrata</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="03" i2="X" l="SPA">
<s0>Vertebrata</s0>
<s2>NS</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>196</s1>
</fN21>
<fN44 i1="01">
<s1>OTO</s1>
</fN44>
<fN82>
<s1>OTO</s1>
</fN82>
</pA>
</standard>
</inist>
</record>

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