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Mucosal immunisation of african green monkeys (Cercopithecus aethiops) with an attenuated parainfluenza virus expressing the SARS coronavirus spike protein for the prevention of SARS. Commentary

Identifieur interne : 000164 ( PascalFrancis/Curation ); précédent : 000163; suivant : 000165

Mucosal immunisation of african green monkeys (Cercopithecus aethiops) with an attenuated parainfluenza virus expressing the SARS coronavirus spike protein for the prevention of SARS. Commentary

Auteurs : Alexander Bukreyev [États-Unis] ; Elaine W. Lamirande [États-Unis] ; Ursula J. Buchholz [États-Unis] ; Leatrice N. Vogel [États-Unis] ; William R. Elkins [États-Unis] ; Marisa St Claire [États-Unis] ; Brian R. Murphy [États-Unis] ; Kanta Subbarao [États-Unis] ; Peter L. Collins [États-Unis] ; A. R. Foxwell [Australie] ; A. W. Cripps [Australie]

Source :

RBID : Pascal:04-0452239

Descripteurs français

English descriptors

Abstract

Background The outbreak of severe acute respiratory syndrome (SARS) in 2002 was caused by a previously unknown coronavirus-SARS coronavirus (SARS-CoV). We have developed an experimental SARS vaccine for direct immunisation of the respiratory tract, the major site of SARS-coronavirus transmission and disease. Methods We expressed the complete SARS coronavirus envelope spike (S) protein from a recombinant attenuated parainfluenza virus (BHPIV3) that is being developed as a live attenuated, intranasal paediatric vaccine against human parainfluenza virus type 3 (HPIV3). We immunised eight African green monkeys, four with a single dose of BHPIV3/ SARS-S and four with a control, BHPIV3/Ctrl, administered via the respiratory tract. A SARS-coronavirus challenge was given to all monkeys 28 days after immunisation. Findings Immunisation of animals with BHPIV3/SARS-S induced the production of SARS-coronavirus-neutralising serum antibodies, indicating that a systemic immune response resulted from mucosal immunisation. After challenge with SARS coronavirus, all monkeys in the control group shed SARS coronavirus, with shedding lasting 5-8 days. No viral shedding occurred in the group immunised with BHPIV3/SARS-S. Interpretation A vectored mucosal vaccine expressing the SARS-coronavirus S protein alone may be highly effective in a single-dose format for the prevention of SARS.
pA  
A01 01  1    @0 0140-6736
A02 01      @0 LANCAO
A03   1    @0 Lancet : (Br. ed.)
A05       @2 363
A06       @2 9427
A08 01  1  ENG  @1 Mucosal immunisation of african green monkeys (Cercopithecus aethiops) with an attenuated parainfluenza virus expressing the SARS coronavirus spike protein for the prevention of SARS. Commentary
A11 01  1    @1 BUKREYEV (Alexander)
A11 02  1    @1 LAMIRANDE (Elaine W.)
A11 03  1    @1 BUCHHOLZ (Ursula J.)
A11 04  1    @1 VOGEL (Leatrice N.)
A11 05  1    @1 ELKINS (William R.)
A11 06  1    @1 ST CLAIRE (Marisa)
A11 07  1    @1 MURPHY (Brian R.)
A11 08  1    @1 SUBBARAO (Kanta)
A11 09  1    @1 COLLINS (Peter L.)
A11 10  1    @1 FOXWELL (A. R.) @9 comment.
A11 11  1    @1 CRIPPS (A. W.) @9 comment.
A14 01      @1 Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health @2 Bethesda, MD, 20892 @3 USA @Z 1 aut. @Z 2 aut. @Z 3 aut. @Z 4 aut. @Z 5 aut. @Z 7 aut. @Z 8 aut. @Z 9 aut.
A14 02      @1 Bioqual @2 Rockville, MD, 20850 @3 USA @Z 6 aut.
A14 03      @1 Gadi Research Centre for Medical and Health Sciences, University of Canberra @2 Canberra, ACT 2601 @3 AUS @Z 10 aut.
A14 04      @1 School of Medicine, Griffith University, Gold Coast Campus @2 Gold Coast, Queensland @3 AUS @Z 11 aut.
A20       @2 2102-2103,2122-2127 [8 p.]
A21       @1 2004
A23 01      @0 ENG
A43 01      @1 INIST @2 5004 @5 354000110516130030
A44       @0 0000 @1 © 2004 INIST-CNRS. All rights reserved.
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A60       @1 P @3 AR @3 CT
A61       @0 A
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A66 01      @0 GBR
C01 01    ENG  @0 Background The outbreak of severe acute respiratory syndrome (SARS) in 2002 was caused by a previously unknown coronavirus-SARS coronavirus (SARS-CoV). We have developed an experimental SARS vaccine for direct immunisation of the respiratory tract, the major site of SARS-coronavirus transmission and disease. Methods We expressed the complete SARS coronavirus envelope spike (S) protein from a recombinant attenuated parainfluenza virus (BHPIV3) that is being developed as a live attenuated, intranasal paediatric vaccine against human parainfluenza virus type 3 (HPIV3). We immunised eight African green monkeys, four with a single dose of BHPIV3/ SARS-S and four with a control, BHPIV3/Ctrl, administered via the respiratory tract. A SARS-coronavirus challenge was given to all monkeys 28 days after immunisation. Findings Immunisation of animals with BHPIV3/SARS-S induced the production of SARS-coronavirus-neutralising serum antibodies, indicating that a systemic immune response resulted from mucosal immunisation. After challenge with SARS coronavirus, all monkeys in the control group shed SARS coronavirus, with shedding lasting 5-8 days. No viral shedding occurred in the group immunised with BHPIV3/SARS-S. Interpretation A vectored mucosal vaccine expressing the SARS-coronavirus S protein alone may be highly effective in a single-dose format for the prevention of SARS.
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C03 08  X  FRE  @0 Cercopithecus aethiops @2 NS @5 12
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C03 08  X  SPA  @0 Cercopithecus aethiops @2 NS @5 12
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C03 12  X  FRE  @0 Immunisation @5 23
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C03 13  X  SPA  @0 Evaluación @5 24
C03 14  X  FRE  @0 Syndrome respiratoire aigu sévère @4 CD @5 96
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C03 14  X  SPA  @0 Síndrome respiratorio agudo severo @4 CD @5 96
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C07 05  X  FRE  @0 Appareil respiratoire pathologie @5 37
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N21       @1 257
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Pascal:04-0452239

Le document en format XML

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<name sortKey="Subbarao, Kanta" sort="Subbarao, Kanta" uniqKey="Subbarao K" first="Kanta" last="Subbarao">Kanta Subbarao</name>
<affiliation wicri:level="1">
<inist:fA14 i1="01">
<s1>Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health</s1>
<s2>Bethesda, MD, 20892</s2>
<s3>USA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>7 aut.</sZ>
<sZ>8 aut.</sZ>
<sZ>9 aut.</sZ>
</inist:fA14>
<country>États-Unis</country>
</affiliation>
</author>
<author>
<name sortKey="Collins, Peter L" sort="Collins, Peter L" uniqKey="Collins P" first="Peter L." last="Collins">Peter L. Collins</name>
<affiliation wicri:level="1">
<inist:fA14 i1="01">
<s1>Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health</s1>
<s2>Bethesda, MD, 20892</s2>
<s3>USA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>7 aut.</sZ>
<sZ>8 aut.</sZ>
<sZ>9 aut.</sZ>
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<country>États-Unis</country>
</affiliation>
</author>
<author>
<name sortKey="Foxwell, A R" sort="Foxwell, A R" uniqKey="Foxwell A" first="A. R." last="Foxwell">A. R. Foxwell</name>
<affiliation wicri:level="1">
<inist:fA14 i1="03">
<s1>Gadi Research Centre for Medical and Health Sciences, University of Canberra</s1>
<s2>Canberra, ACT 2601</s2>
<s3>AUS</s3>
<sZ>10 aut.</sZ>
</inist:fA14>
<country>Australie</country>
</affiliation>
</author>
<author>
<name sortKey="Cripps, A W" sort="Cripps, A W" uniqKey="Cripps A" first="A. W." last="Cripps">A. W. Cripps</name>
<affiliation wicri:level="1">
<inist:fA14 i1="04">
<s1>School of Medicine, Griffith University, Gold Coast Campus</s1>
<s2>Gold Coast, Queensland</s2>
<s3>AUS</s3>
<sZ>11 aut.</sZ>
</inist:fA14>
<country>Australie</country>
</affiliation>
</author>
</analytic>
<series>
<title level="j" type="main">Lancet : (British edition)</title>
<title level="j" type="abbreviated">Lancet : (Br. ed.)</title>
<idno type="ISSN">0140-6736</idno>
<imprint>
<date when="2004">2004</date>
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<title level="j" type="main">Lancet : (British edition)</title>
<title level="j" type="abbreviated">Lancet : (Br. ed.)</title>
<idno type="ISSN">0140-6736</idno>
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<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>African</term>
<term>Animal</term>
<term>Attenuated strain</term>
<term>Cercopithecus aethiops</term>
<term>Evaluation</term>
<term>Human</term>
<term>Immunization</term>
<term>Medicine</term>
<term>Monkey</term>
<term>Mucosa</term>
<term>Preclinical trial</term>
<term>Prevention</term>
<term>Severe acute respiratory syndrome</term>
<term>Vaccination</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>Muqueuse</term>
<term>Prévention</term>
<term>Vaccination</term>
<term>Africain</term>
<term>Souche atténuée</term>
<term>Animal</term>
<term>Singe</term>
<term>Cercopithecus aethiops</term>
<term>Essai préclinique</term>
<term>Médecine</term>
<term>Homme</term>
<term>Immunisation</term>
<term>Evaluation</term>
<term>Syndrome respiratoire aigu sévère</term>
</keywords>
<keywords scheme="Wicri" type="topic" xml:lang="fr">
<term>Vaccination</term>
<term>Singe</term>
<term>Médecine</term>
<term>Homme</term>
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<front>
<div type="abstract" xml:lang="en">Background The outbreak of severe acute respiratory syndrome (SARS) in 2002 was caused by a previously unknown coronavirus-SARS coronavirus (SARS-CoV). We have developed an experimental SARS vaccine for direct immunisation of the respiratory tract, the major site of SARS-coronavirus transmission and disease. Methods We expressed the complete SARS coronavirus envelope spike (S) protein from a recombinant attenuated parainfluenza virus (BHPIV3) that is being developed as a live attenuated, intranasal paediatric vaccine against human parainfluenza virus type 3 (HPIV3). We immunised eight African green monkeys, four with a single dose of BHPIV3/ SARS-S and four with a control, BHPIV3/Ctrl, administered via the respiratory tract. A SARS-coronavirus challenge was given to all monkeys 28 days after immunisation. Findings Immunisation of animals with BHPIV3/SARS-S induced the production of SARS-coronavirus-neutralising serum antibodies, indicating that a systemic immune response resulted from mucosal immunisation. After challenge with SARS coronavirus, all monkeys in the control group shed SARS coronavirus, with shedding lasting 5-8 days. No viral shedding occurred in the group immunised with BHPIV3/SARS-S. Interpretation A vectored mucosal vaccine expressing the SARS-coronavirus S protein alone may be highly effective in a single-dose format for the prevention of SARS.</div>
</front>
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<s1>Mucosal immunisation of african green monkeys (Cercopithecus aethiops) with an attenuated parainfluenza virus expressing the SARS coronavirus spike protein for the prevention of SARS. Commentary</s1>
</fA08>
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<s1>BUKREYEV (Alexander)</s1>
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<s1>ELKINS (William R.)</s1>
</fA11>
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<s1>ST CLAIRE (Marisa)</s1>
</fA11>
<fA11 i1="07" i2="1">
<s1>MURPHY (Brian R.)</s1>
</fA11>
<fA11 i1="08" i2="1">
<s1>SUBBARAO (Kanta)</s1>
</fA11>
<fA11 i1="09" i2="1">
<s1>COLLINS (Peter L.)</s1>
</fA11>
<fA11 i1="10" i2="1">
<s1>FOXWELL (A. R.)</s1>
<s9>comment.</s9>
</fA11>
<fA11 i1="11" i2="1">
<s1>CRIPPS (A. W.)</s1>
<s9>comment.</s9>
</fA11>
<fA14 i1="01">
<s1>Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health</s1>
<s2>Bethesda, MD, 20892</s2>
<s3>USA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
<sZ>7 aut.</sZ>
<sZ>8 aut.</sZ>
<sZ>9 aut.</sZ>
</fA14>
<fA14 i1="02">
<s1>Bioqual</s1>
<s2>Rockville, MD, 20850</s2>
<s3>USA</s3>
<sZ>6 aut.</sZ>
</fA14>
<fA14 i1="03">
<s1>Gadi Research Centre for Medical and Health Sciences, University of Canberra</s1>
<s2>Canberra, ACT 2601</s2>
<s3>AUS</s3>
<sZ>10 aut.</sZ>
</fA14>
<fA14 i1="04">
<s1>School of Medicine, Griffith University, Gold Coast Campus</s1>
<s2>Gold Coast, Queensland</s2>
<s3>AUS</s3>
<sZ>11 aut.</sZ>
</fA14>
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<s2>2102-2103,2122-2127 [8 p.]</s2>
</fA20>
<fA21>
<s1>2004</s1>
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<s0>ENG</s0>
</fA23>
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<s1>INIST</s1>
<s2>5004</s2>
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<s1>© 2004 INIST-CNRS. All rights reserved.</s1>
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<s0>29 ref.</s0>
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<s0>04-0452239</s0>
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</fA64>
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</fA66>
<fC01 i1="01" l="ENG">
<s0>Background The outbreak of severe acute respiratory syndrome (SARS) in 2002 was caused by a previously unknown coronavirus-SARS coronavirus (SARS-CoV). We have developed an experimental SARS vaccine for direct immunisation of the respiratory tract, the major site of SARS-coronavirus transmission and disease. Methods We expressed the complete SARS coronavirus envelope spike (S) protein from a recombinant attenuated parainfluenza virus (BHPIV3) that is being developed as a live attenuated, intranasal paediatric vaccine against human parainfluenza virus type 3 (HPIV3). We immunised eight African green monkeys, four with a single dose of BHPIV3/ SARS-S and four with a control, BHPIV3/Ctrl, administered via the respiratory tract. A SARS-coronavirus challenge was given to all monkeys 28 days after immunisation. Findings Immunisation of animals with BHPIV3/SARS-S induced the production of SARS-coronavirus-neutralising serum antibodies, indicating that a systemic immune response resulted from mucosal immunisation. After challenge with SARS coronavirus, all monkeys in the control group shed SARS coronavirus, with shedding lasting 5-8 days. No viral shedding occurred in the group immunised with BHPIV3/SARS-S. Interpretation A vectored mucosal vaccine expressing the SARS-coronavirus S protein alone may be highly effective in a single-dose format for the prevention of SARS.</s0>
</fC01>
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<s0>002B05C02C</s0>
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<s5>02</s5>
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<s5>02</s5>
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<s0>Prévention</s0>
<s5>03</s5>
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<s0>Prevention</s0>
<s5>03</s5>
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<s5>03</s5>
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<s0>Vaccination</s0>
<s5>05</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG">
<s0>Vaccination</s0>
<s5>05</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA">
<s0>Vacunación</s0>
<s5>05</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE">
<s0>Africain</s0>
<s5>06</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG">
<s0>African</s0>
<s5>06</s5>
</fC03>
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<s0>Africano</s0>
<s5>06</s5>
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<s0>Souche atténuée</s0>
<s5>08</s5>
</fC03>
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<s0>Attenuated strain</s0>
<s5>08</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA">
<s0>Cepa atenuada</s0>
<s5>08</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE">
<s0>Animal</s0>
<s5>09</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG">
<s0>Animal</s0>
<s5>09</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA">
<s0>Animal</s0>
<s5>09</s5>
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<s0>Singe</s0>
<s5>11</s5>
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<s0>Monkey</s0>
<s5>11</s5>
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<s0>Mono</s0>
<s5>11</s5>
</fC03>
<fC03 i1="08" i2="X" l="FRE">
<s0>Cercopithecus aethiops</s0>
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<s5>12</s5>
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<fC03 i1="08" i2="X" l="ENG">
<s0>Cercopithecus aethiops</s0>
<s2>NS</s2>
<s5>12</s5>
</fC03>
<fC03 i1="08" i2="X" l="SPA">
<s0>Cercopithecus aethiops</s0>
<s2>NS</s2>
<s5>12</s5>
</fC03>
<fC03 i1="09" i2="X" l="FRE">
<s0>Essai préclinique</s0>
<s5>17</s5>
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<s0>Preclinical trial</s0>
<s5>17</s5>
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<s0>Ensayo preclínico</s0>
<s5>17</s5>
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<s0>Médecine</s0>
<s5>19</s5>
</fC03>
<fC03 i1="10" i2="X" l="ENG">
<s0>Medicine</s0>
<s5>19</s5>
</fC03>
<fC03 i1="10" i2="X" l="SPA">
<s0>Medicina</s0>
<s5>19</s5>
</fC03>
<fC03 i1="11" i2="X" l="FRE">
<s0>Homme</s0>
<s5>20</s5>
</fC03>
<fC03 i1="11" i2="X" l="ENG">
<s0>Human</s0>
<s5>20</s5>
</fC03>
<fC03 i1="11" i2="X" l="SPA">
<s0>Hombre</s0>
<s5>20</s5>
</fC03>
<fC03 i1="12" i2="X" l="FRE">
<s0>Immunisation</s0>
<s5>23</s5>
</fC03>
<fC03 i1="12" i2="X" l="ENG">
<s0>Immunization</s0>
<s5>23</s5>
</fC03>
<fC03 i1="12" i2="X" l="SPA">
<s0>Inmunización</s0>
<s5>23</s5>
</fC03>
<fC03 i1="13" i2="X" l="FRE">
<s0>Evaluation</s0>
<s5>24</s5>
</fC03>
<fC03 i1="13" i2="X" l="ENG">
<s0>Evaluation</s0>
<s5>24</s5>
</fC03>
<fC03 i1="13" i2="X" l="SPA">
<s0>Evaluación</s0>
<s5>24</s5>
</fC03>
<fC03 i1="14" i2="X" l="FRE">
<s0>Syndrome respiratoire aigu sévère</s0>
<s4>CD</s4>
<s5>96</s5>
</fC03>
<fC03 i1="14" i2="X" l="ENG">
<s0>Severe acute respiratory syndrome</s0>
<s4>CD</s4>
<s5>96</s5>
</fC03>
<fC03 i1="14" i2="X" l="SPA">
<s0>Síndrome respiratorio agudo severo</s0>
<s4>CD</s4>
<s5>96</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE">
<s0>Primates</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="01" i2="X" l="ENG">
<s0>Primates</s0>
<s2>NS</s2>
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<fC07 i1="01" i2="X" l="SPA">
<s0>Primates</s0>
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<s0>Mammalia</s0>
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<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>
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<fC07 i1="04" i2="X" l="FRE">
<s0>Simioidea</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="04" i2="X" l="ENG">
<s0>Simioidea</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="04" i2="X" l="SPA">
<s0>Simioidea</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="05" i2="X" l="FRE">
<s0>Appareil respiratoire pathologie</s0>
<s5>37</s5>
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<fC07 i1="05" i2="X" l="ENG">
<s0>Respiratory disease</s0>
<s5>37</s5>
</fC07>
<fC07 i1="05" i2="X" l="SPA">
<s0>Aparato respiratorio patología</s0>
<s5>37</s5>
</fC07>
<fC07 i1="06" i2="X" l="FRE">
<s0>Poumon pathologie</s0>
<s5>38</s5>
</fC07>
<fC07 i1="06" i2="X" l="ENG">
<s0>Lung disease</s0>
<s5>38</s5>
</fC07>
<fC07 i1="06" i2="X" l="SPA">
<s0>Pulmón patología</s0>
<s5>38</s5>
</fC07>
<fC07 i1="07" i2="X" l="FRE">
<s0>Virose</s0>
<s2>NM</s2>
<s5>39</s5>
</fC07>
<fC07 i1="07" i2="X" l="ENG">
<s0>Viral disease</s0>
<s2>NM</s2>
<s5>39</s5>
</fC07>
<fC07 i1="07" i2="X" l="SPA">
<s0>Virosis</s0>
<s2>NM</s2>
<s5>39</s5>
</fC07>
<fC07 i1="08" i2="X" l="FRE">
<s0>Infection</s0>
<s2>NM</s2>
</fC07>
<fC07 i1="08" i2="X" l="ENG">
<s0>Infection</s0>
<s2>NM</s2>
</fC07>
<fC07 i1="08" i2="X" l="SPA">
<s0>Infección</s0>
<s2>NM</s2>
</fC07>
<fN21>
<s1>257</s1>
</fN21>
<fN44 i1="01">
<s1>PSI</s1>
</fN44>
<fN82>
<s1>PSI</s1>
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