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Neuraminidase-based recombinant virus-like particles protect against lethal avian influenza A(H5N1) virus infection in ferrets

Identifieur interne : 000807 ( Pmc/Corpus ); précédent : 000806; suivant : 000808

Neuraminidase-based recombinant virus-like particles protect against lethal avian influenza A(H5N1) virus infection in ferrets

Auteurs : Gale E. Smith ; Xiangjie Sun ; Yaohui Bai ; Ye V. Liu ; Michael J. Massare ; Melissa B. Pearce ; Jessica A. Belser ; Taronna R. Maines ; Hannah M. Creager ; Gregory M. Glenn ; David Flyer ; Peter Pushko ; Min Z. Levine ; Terrence M. Tumpey

Source :

RBID : PMC:5788299

Abstract

Avian influenza A (H5N1) viruses represent a growing threat for an influenza pandemic. The presence of widespread avian influenza virus infections further emphasizes the need for vaccine strategies for control of prepandemic H5N1 and other avian influenza subtypes. Influenza neuraminidase (NA) vaccines represent a potential strategy for improving vaccines against avian influenza H5N1 viruses. To evaluate a strategy for NA vaccination, we generated a recombinant influenza virus-like particle (VLP) vaccine comprised of the NA protein of A/Indonesia/05/2005 (H5N1) virus. Ferrets vaccinated with influenza N1 NA VLPs elicited high-titer serum NA-inhibition (NI) antibody titers and were protected from lethal challenge with A/Indonesia/05/2005 virus. Moreover, N1-immune ferrets shed less infectious virus than similarly challenged control animals. In contrast, ferrets administered control N2 NA VLPs were not protected against H5N1 virus challenge. These results provide support for continued development of NA-based vaccines against influenza H5N1 viruses.


Url:
DOI: 10.1016/j.virol.2017.06.006
PubMed: 28624679
PubMed Central: 5788299

Links to Exploration step

PMC:5788299

Le document en format XML

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<name sortKey="Pushko, Peter" sort="Pushko, Peter" uniqKey="Pushko P" first="Peter" last="Pushko">Peter Pushko</name>
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<nlm:aff id="A2">Medigen, Inc., 8420 Gas House Pike, Frederick, MD, USA</nlm:aff>
</affiliation>
</author>
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<name sortKey="Levine, Min Z" sort="Levine, Min Z" uniqKey="Levine M" first="Min Z." last="Levine">Min Z. Levine</name>
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</affiliation>
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<name sortKey="Tumpey, Terrence M" sort="Tumpey, Terrence M" uniqKey="Tumpey T" first="Terrence M." last="Tumpey">Terrence M. Tumpey</name>
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<nlm:aff id="A3">Influenza Division, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA</nlm:aff>
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<p id="P1">Avian influenza A (H5N1) viruses represent a growing threat for an influenza pandemic. The presence of widespread avian influenza virus infections further emphasizes the need for vaccine strategies for control of prepandemic H5N1 and other avian influenza subtypes. Influenza neuraminidase (NA) vaccines represent a potential strategy for improving vaccines against avian influenza H5N1 viruses. To evaluate a strategy for NA vaccination, we generated a recombinant influenza virus-like particle (VLP) vaccine comprised of the NA protein of A/Indonesia/05/2005 (H5N1) virus. Ferrets vaccinated with influenza N1 NA VLPs elicited high-titer serum NA-inhibition (NI) antibody titers and were protected from lethal challenge with A/Indonesia/05/2005 virus. Moreover, N1-immune ferrets shed less infectious virus than similarly challenged control animals. In contrast, ferrets administered control N2 NA VLPs were not protected against H5N1 virus challenge. These results provide support for continued development of NA-based vaccines against influenza H5N1 viruses.</p>
</div>
</front>
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<article-title>Neuraminidase-based recombinant virus-like particles protect against lethal avian influenza A(H5N1) virus infection in ferrets</article-title>
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<contrib contrib-type="author">
<name>
<surname>Smith</surname>
<given-names>Gale E.</given-names>
</name>
<xref ref-type="aff" rid="A1">a</xref>
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<contrib contrib-type="author">
<name>
<surname>Sun</surname>
<given-names>Xiangjie</given-names>
</name>
<xref ref-type="aff" rid="A3">c</xref>
</contrib>
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<name>
<surname>Bai</surname>
<given-names>Yaohui</given-names>
</name>
<xref ref-type="aff" rid="A3">c</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Liu</surname>
<given-names>Ye V.</given-names>
</name>
<xref ref-type="aff" rid="A1">a</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Massare</surname>
<given-names>Michael J.</given-names>
</name>
<xref ref-type="aff" rid="A1">a</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Pearce</surname>
<given-names>Melissa B.</given-names>
</name>
<xref ref-type="aff" rid="A3">c</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Belser</surname>
<given-names>Jessica A.</given-names>
</name>
<xref ref-type="aff" rid="A3">c</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Maines</surname>
<given-names>Taronna R.</given-names>
</name>
<xref ref-type="aff" rid="A3">c</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Creager</surname>
<given-names>Hannah M.</given-names>
</name>
<xref ref-type="aff" rid="A3">c</xref>
<xref ref-type="aff" rid="A4">d</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Glenn</surname>
<given-names>Gregory M.</given-names>
</name>
<xref ref-type="aff" rid="A1">a</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Flyer</surname>
<given-names>David</given-names>
</name>
<xref ref-type="aff" rid="A1">a</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Pushko</surname>
<given-names>Peter</given-names>
</name>
<xref ref-type="aff" rid="A2">b</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Levine</surname>
<given-names>Min Z.</given-names>
</name>
<xref ref-type="aff" rid="A3">c</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Tumpey</surname>
<given-names>Terrence M.</given-names>
</name>
<xref ref-type="aff" rid="A3">c</xref>
<xref rid="FN1" ref-type="author-notes">*</xref>
</contrib>
</contrib-group>
<aff id="A1">
<label>a</label>
Novavax, Inc., 20 Firstfield, Gaithersburg, MD 20878, USA</aff>
<aff id="A2">
<label>b</label>
Medigen, Inc., 8420 Gas House Pike, Frederick, MD, USA</aff>
<aff id="A3">
<label>c</label>
Influenza Division, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA</aff>
<aff id="A4">
<label>d</label>
Microbiology and Molecular Genetics Graduate Program, Emory University, Atlanta, GA, USA</aff>
<author-notes>
<corresp id="FN1">
<label>*</label>
Correspondence to: Influenza Division, MS G-16, 1600 Clifton Rd. NE, Atlanta, GA 30329, USA.
<email>TTumpey@cdc.gov</email>
(T.M. Tumpey)</corresp>
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<pub-date pub-type="nihms-submitted">
<day>24</day>
<month>1</month>
<year>2018</year>
</pub-date>
<pub-date pub-type="epub">
<day>16</day>
<month>6</month>
<year>2017</year>
</pub-date>
<pub-date pub-type="ppub">
<month>9</month>
<year>2017</year>
</pub-date>
<pub-date pub-type="pmc-release">
<day>29</day>
<month>1</month>
<year>2018</year>
</pub-date>
<volume>509</volume>
<fpage>90</fpage>
<lpage>97</lpage>
<pmc-comment>elocation-id from pubmed: 10.1016/j.virol.2017.06.006</pmc-comment>
<abstract>
<p id="P1">Avian influenza A (H5N1) viruses represent a growing threat for an influenza pandemic. The presence of widespread avian influenza virus infections further emphasizes the need for vaccine strategies for control of prepandemic H5N1 and other avian influenza subtypes. Influenza neuraminidase (NA) vaccines represent a potential strategy for improving vaccines against avian influenza H5N1 viruses. To evaluate a strategy for NA vaccination, we generated a recombinant influenza virus-like particle (VLP) vaccine comprised of the NA protein of A/Indonesia/05/2005 (H5N1) virus. Ferrets vaccinated with influenza N1 NA VLPs elicited high-titer serum NA-inhibition (NI) antibody titers and were protected from lethal challenge with A/Indonesia/05/2005 virus. Moreover, N1-immune ferrets shed less infectious virus than similarly challenged control animals. In contrast, ferrets administered control N2 NA VLPs were not protected against H5N1 virus challenge. These results provide support for continued development of NA-based vaccines against influenza H5N1 viruses.</p>
</abstract>
<kwd-group>
<kwd>VLP vaccine</kwd>
<kwd>H5N1 influenza</kwd>
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<kwd>Neuraminidase (NA)</kwd>
</kwd-group>
</article-meta>
</front>
</pmc>
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