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Live Attenuated Influenza Vaccines engineered to express the nucleoprotein of a recent isolate stimulate human influenza CD8+ T cells more relevant to current infections

Identifieur interne : 000E38 ( Ncbi/Merge ); précédent : 000E37; suivant : 000E39

Live Attenuated Influenza Vaccines engineered to express the nucleoprotein of a recent isolate stimulate human influenza CD8+ T cells more relevant to current infections

Auteurs : D. Korenkov [Russie, Australie] ; T. H. O. Nguyen [Australie] ; I. Isakova-Sivak [Russie] ; T. Smolonogina [Russie] ; L. E. Brown [Australie] ; K. Kedzierska [Australie] ; L. Rudenko [Russie]

Source :

RBID : PMC:5893192

Abstract

ABSTRACT

Live attenuated influenza vaccines (LAIV) induce CD8+ T lymphocyte responses that play an important role in killing virus-infected cells. Despite the relative conservation of internal influenza A proteins, the epitopes recognized by T cells can undergo drift under immune pressure. The internal proteins of Russian LAIVs are derived from the master donor virus A/Leningrad/134/17/57 (Len/17) isolated 60 years ago and as such, some CD8+ T cell epitopes may vary between the vaccine and circulating wild-type strains. To partially overcome this issue, the nucleoprotein (NP) gene of wild-type virus can be incorporated into LAIV reassortant virus, along with the HA and NA genes. The present study compares the human CD8+ T cell memory responses to H3N2 LAIVs with the Len/17 or the wild-type NP using an in vitro model.


Url:
DOI: 10.1080/21645515.2017.1417713
PubMed: 29252117
PubMed Central: 5893192

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PMC:5893192

Le document en format XML

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<institution>Department of Virology, Institute of Experimental Medicine</institution>
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<title>ABSTRACT</title>
<p>Live attenuated influenza vaccines (LAIV) induce CD8
<sup>+</sup>
T lymphocyte responses that play an important role in killing virus-infected cells. Despite the relative conservation of internal influenza A proteins, the epitopes recognized by T cells can undergo drift under immune pressure. The internal proteins of Russian LAIVs are derived from the master donor virus A/Leningrad/134/17/57 (Len/17) isolated 60 years ago and as such, some CD8
<sup>+</sup>
T cell epitopes may vary between the vaccine and circulating wild-type strains. To partially overcome this issue, the nucleoprotein (NP) gene of wild-type virus can be incorporated into LAIV reassortant virus, along with the HA and NA genes. The present study compares the human CD8+ T cell memory responses to H3N2 LAIVs with the Len/17 or the wild-type NP using an
<italic>in vitro</italic>
model.</p>
</div>
</front>
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<front>
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<journal-id journal-id-type="nlm-ta">Hum Vaccin Immunother</journal-id>
<journal-id journal-id-type="iso-abbrev">Hum Vaccin Immunother</journal-id>
<journal-id journal-id-type="publisher-id">KHVI</journal-id>
<journal-id journal-id-type="publisher-id">khvi20</journal-id>
<journal-title-group>
<journal-title>Human Vaccines & Immunotherapeutics</journal-title>
</journal-title-group>
<issn pub-type="ppub">2164-5515</issn>
<issn pub-type="epub">2164-554X</issn>
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<title-group>
<article-title>Live Attenuated Influenza Vaccines engineered to express the nucleoprotein of a recent isolate stimulate human influenza CD8
<sup>+</sup>
T cells more relevant to current infections</article-title>
<alt-title alt-title-type="running-authors">D. KORENKOV ET AL.</alt-title>
<alt-title alt-title-type="running-title">HUMAN VACCINES & IMMUNOTHERAPEUTICS</alt-title>
</title-group>
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<contrib contrib-type="author">
<name>
<surname>Korenkov</surname>
<given-names>D.</given-names>
</name>
<xref ref-type="aff" rid="af0001">
<sup>a</sup>
</xref>
<xref ref-type="aff" rid="af0002">
<sup>b</sup>
</xref>
<xref ref-type="corresp" rid="an0001"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Nguyen</surname>
<given-names>T. H. O.</given-names>
</name>
<xref ref-type="aff" rid="af0002">
<sup>b</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<contrib-id contrib-id-type="ORCID">0000-0002-2801-1508</contrib-id>
<name>
<surname>Isakova-Sivak</surname>
<given-names>I.</given-names>
</name>
<xref ref-type="aff" rid="af0001">
<sup>a</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Smolonogina</surname>
<given-names>T.</given-names>
</name>
<xref ref-type="aff" rid="af0001">
<sup>a</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Brown</surname>
<given-names>L. E.</given-names>
</name>
<xref ref-type="aff" rid="af0002">
<sup>b</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Kedzierska</surname>
<given-names>K.</given-names>
</name>
<xref ref-type="aff" rid="af0002">
<sup>b</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Rudenko</surname>
<given-names>L.</given-names>
</name>
<xref ref-type="aff" rid="af0001">
<sup>a</sup>
</xref>
</contrib>
<aff id="af0001">
<label>a</label>
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, Saint Petersburg,
<country>Russia</country>
</aff>
<aff id="af0002">
<label>b</label>
<institution>Department of Microbiology & Immunology, University of Melbourne, at The Peter Doherty Institute for Infection & Immunity</institution>
, Melbourne, VIC,
<country>Australia</country>
</aff>
</contrib-group>
<author-notes>
<corresp id="an0001">
<bold>CONTACT</bold>
D. Korenkov
<email xlink:href="d.korenkov@gmail.com">d.korenkov@gmail.com</email>
</corresp>
<fn>
<p>Supplemental data for this article can be accessed on the
<ext-link ext-link-type="uri" xlink:href="https://doi.org/10.1080/21645515.2017.1417713">publisher's website</ext-link>
.</p>
</fn>
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<year>2018</year>
</pub-date>
<pub-date pub-type="epub">
<day>23</day>
<month>1</month>
<year>2018</year>
</pub-date>
<volume>14</volume>
<issue>4</issue>
<fpage seq="22">941</fpage>
<lpage>946</lpage>
<history>
<date date-type="received">
<day>18</day>
<month>10</month>
<year>2017</year>
</date>
<date date-type="rev-recd">
<day>20</day>
<month>11</month>
<year>2017</year>
</date>
<date date-type="accepted">
<day>8</day>
<month>12</month>
<year>2017</year>
</date>
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<copyright-statement>© 2018 Taylor & Francis</copyright-statement>
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</permissions>
<self-uri content-type="pdf" xlink:href="khvi-14-04-1417713.pdf"></self-uri>
<abstract>
<title>ABSTRACT</title>
<p>Live attenuated influenza vaccines (LAIV) induce CD8
<sup>+</sup>
T lymphocyte responses that play an important role in killing virus-infected cells. Despite the relative conservation of internal influenza A proteins, the epitopes recognized by T cells can undergo drift under immune pressure. The internal proteins of Russian LAIVs are derived from the master donor virus A/Leningrad/134/17/57 (Len/17) isolated 60 years ago and as such, some CD8
<sup>+</sup>
T cell epitopes may vary between the vaccine and circulating wild-type strains. To partially overcome this issue, the nucleoprotein (NP) gene of wild-type virus can be incorporated into LAIV reassortant virus, along with the HA and NA genes. The present study compares the human CD8+ T cell memory responses to H3N2 LAIVs with the Len/17 or the wild-type NP using an
<italic>in vitro</italic>
model.</p>
</abstract>
<kwd-group kwd-group-type="author">
<title>KEYWORDS</title>
<kwd>Antigenic escape</kwd>
<kwd>influenza</kwd>
<kwd>LAIV</kwd>
<kwd>nucleoprotein</kwd>
<kwd>T cell epitope</kwd>
</kwd-group>
<funding-group>
<award-group>
<funding-source>
<named-content content-type="funder-name">Russian Science Foundation Grant</named-content>
</funding-source>
<award-id>14-15-00034</award-id>
</award-group>
<funding-statement>The study was supported by Russian Science Foundation Grant №14–15–00034.</funding-statement>
</funding-group>
<counts>
<fig-count count="2"></fig-count>
<table-count count="1"></table-count>
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<name sortKey="Nguyen, T H O" sort="Nguyen, T H O" uniqKey="Nguyen T" first="T. H. O." last="Nguyen">T. H. O. Nguyen</name>
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