A review of the value of quadrivalent influenza vaccines and their potential contribution to influenza control
Identifieur interne : 000D64 ( Pmc/Curation ); précédent : 000D63; suivant : 000D65A review of the value of quadrivalent influenza vaccines and their potential contribution to influenza control
Auteurs : Riju Ray [Belgique] ; Gaël Dos Santos ; Philip O. Buck [États-Unis] ; Carine Claeys [Belgique] ; Gonçalo Matias [Belgique] ; Bruce L. Innis [États-Unis] ; Rafik Bekkat-Berkani [Belgique]Source :
- Human Vaccines & Immunotherapeutics [ 2164-5515 ] ; 2017.
Abstract
The contribution of influenza B to the seasonal influenza burden varies from year-to-year. Although 2 antigenically distinct influenza B virus lineages have co-circulated since 2001, trivalent influenza vaccines (TIVs) contain antigens from only one influenza B virus. B-mismatch or co-circulation of both B lineages results in increased morbidity and mortality attributable to the B lineage absent from the vaccine. Quadrivalent vaccines (QIVs) contain both influenza B lineages. We reviewed currently licensed QIVs and their value by focusing on the preventable disease burden. Modeling studies support that QIVs are expected to prevent more influenza cases, hospitalisations and deaths than TIVs, although estimates of the case numbers prevented vary according to local specificities. The value of QIVs is demonstrated by their capacity to broaden the immune response and reduce the likelihood of a B-mismatched season. Some health authorities have preferentially recommended QIVs over TIVs in their influenza prevention programmes.
Url:
DOI: 10.1080/21645515.2017.1313375
PubMed: 28532276
PubMed Central: 5512791
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Gaël Dos Santos<affiliation><nlm:aff id="af0002"><institution>Business & Decision Life Sciences</institution>
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Le document en format XML
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<front><div type="abstract" xml:lang="en"><title>ABSTRACT</title>
<p>The contribution of influenza B to the seasonal influenza burden varies from year-to-year. Although 2 antigenically distinct influenza B virus lineages have co-circulated since 2001, trivalent influenza vaccines (TIVs) contain antigens from only one influenza B virus. B-mismatch or co-circulation of both B lineages results in increased morbidity and mortality attributable to the B lineage absent from the vaccine. Quadrivalent vaccines (QIVs) contain both influenza B lineages. We reviewed currently licensed QIVs and their value by focusing on the preventable disease burden. Modeling studies support that QIVs are expected to prevent more influenza cases, hospitalisations and deaths than TIVs, although estimates of the case numbers prevented vary according to local specificities. The value of QIVs is demonstrated by their capacity to broaden the immune response and reduce the likelihood of a B-mismatched season. Some health authorities have preferentially recommended QIVs over TIVs in their influenza prevention programmes.</p>
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<pmc article-type="review-article"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><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>
<publisher><publisher-name>Taylor & Francis</publisher-name>
</publisher>
</journal-meta>
<article-meta><article-id pub-id-type="pmid">28532276</article-id>
<article-id pub-id-type="pmc">5512791</article-id>
<article-id pub-id-type="publisher-id">1313375</article-id>
<article-id pub-id-type="doi">10.1080/21645515.2017.1313375</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Review</subject>
</subj-group>
</article-categories>
<title-group><article-title>A review of the value of quadrivalent influenza vaccines and their potential contribution to influenza control</article-title>
<alt-title alt-title-type="running-authors">R. RAY ET AL.</alt-title>
<alt-title alt-title-type="running-title">HUMAN VACCINES & IMMUNOTHERAPEUTICS</alt-title>
</title-group>
<contrib-group><contrib contrib-type="author"><name><surname>Ray</surname>
<given-names>Riju</given-names>
</name>
<xref ref-type="aff" rid="af0001"><sup>a</sup>
</xref>
<xref ref-type="author-notes" rid="afn0001"><sup>*</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Dos Santos</surname>
<given-names>Gaël</given-names>
</name>
<xref ref-type="aff" rid="af0002"><sup>b</sup>
</xref>
<xref ref-type="author-notes" rid="afn0002"><sup>‡</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Buck</surname>
<given-names>Philip O.</given-names>
</name>
<xref ref-type="aff" rid="af0003"><sup>c</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Claeys</surname>
<given-names>Carine</given-names>
</name>
<xref ref-type="aff" rid="af0001"><sup>a</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Matias</surname>
<given-names>Gonçalo</given-names>
</name>
<xref ref-type="aff" rid="af0001"><sup>a</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Innis</surname>
<given-names>Bruce L.</given-names>
</name>
<xref ref-type="aff" rid="af0003"><sup>c</sup>
</xref>
<xref ref-type="author-notes" rid="afn0003"><sup>#</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Bekkat-Berkani</surname>
<given-names>Rafik</given-names>
</name>
<xref ref-type="aff" rid="af0001"><sup>a</sup>
</xref>
<xref ref-type="corresp" rid="an0001"></xref>
<xref ref-type="author-notes" rid="afn0004"><sup>**</sup>
</xref>
</contrib>
<aff id="af0001"><label>a</label>
<institution>GSK</institution>
, Wavre,<country>Belgium</country>
</aff>
<aff id="af0002"><label>b</label>
<institution>Business & Decision Life Sciences</institution>
, Brussels,<country>Belgium (on behalf of GSK)</country>
</aff>
<aff id="af0003"><label>c</label>
<institution>GSK</institution>
, Philadelphia, PA,<country>USA</country>
</aff>
</contrib-group>
<author-notes><corresp id="an0001"><bold>CONTACT</bold>
Rafik Bekkat-Berkani <email xlink:href="Rafik.X.Bekkat-Berkani@gsk.com">Rafik.X.Bekkat-Berkani@gsk.com</email>
<addr-line>5 Crescent Drive</addr-line>
, Philadelphia, PA 19112, <country>USA</country>
</corresp>
<fn id="afn0001"><label>*</label>
<p>Current affiliation: GSK, Research Triangle Park, NC, USA.</p>
</fn>
<fn id="afn0002"><label>‡</label>
<p>Current affiliation: GSK, Wavre, Belgium.</p>
</fn>
<fn id="afn0003"><label>#</label>
<p>Current affiliation: PATH, Washington, DC, USA.</p>
</fn>
<fn id="afn0004"><label>**</label>
<p>Current affiliation: GSK, Philadelphia, PA, USA.</p>
</fn>
</author-notes>
<pub-date pub-type="collection"><month>6</month>
<year>2017</year>
</pub-date>
<pub-date pub-type="epub"><day>22</day>
<month>5</month>
<year>2017</year>
</pub-date>
<pub-date pub-type="pmc-release"><day>22</day>
<month>5</month>
<year>2017</year>
</pub-date>
<pmc-comment> PMC Release delay is 0 months and 0 days and was based on the . </pmc-comment>
<volume>13</volume>
<issue>7</issue>
<fpage seq="23">1640</fpage>
<lpage>1652</lpage>
<history><date date-type="received"><day>31</day>
<month>1</month>
<year>2017</year>
</date>
<date date-type="rev-recd"><day>20</day>
<month>3</month>
<year>2017</year>
</date>
<date date-type="accepted"><day>25</day>
<month>3</month>
<year>2017</year>
</date>
</history>
<permissions><pmc-comment> © Riju Ray, Gaël Dos Santos, Philip O. Buck, Carine Claeys, Gonçalo Matias, Bruce L. Innis, and Rafik Bekkat-Berkani </pmc-comment>
<copyright-statement>© 2017 The Author(s). Published with license by Taylor & Francis</copyright-statement>
<copyright-year>2017</copyright-year>
<copyright-holder>The Author(s)</copyright-holder>
<license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/3.0/"><license-p>This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by/3.0/">http://creativecommons.org/licenses/by/3.0/</ext-link>
), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.</license-p>
</license>
</permissions>
<self-uri content-type="pdf" xlink:href="khvi-13-07-1313375.pdf"></self-uri>
<abstract><title>ABSTRACT</title>
<p>The contribution of influenza B to the seasonal influenza burden varies from year-to-year. Although 2 antigenically distinct influenza B virus lineages have co-circulated since 2001, trivalent influenza vaccines (TIVs) contain antigens from only one influenza B virus. B-mismatch or co-circulation of both B lineages results in increased morbidity and mortality attributable to the B lineage absent from the vaccine. Quadrivalent vaccines (QIVs) contain both influenza B lineages. We reviewed currently licensed QIVs and their value by focusing on the preventable disease burden. Modeling studies support that QIVs are expected to prevent more influenza cases, hospitalisations and deaths than TIVs, although estimates of the case numbers prevented vary according to local specificities. The value of QIVs is demonstrated by their capacity to broaden the immune response and reduce the likelihood of a B-mismatched season. Some health authorities have preferentially recommended QIVs over TIVs in their influenza prevention programmes.</p>
</abstract>
<kwd-group kwd-group-type="author"><title>KEYWORDS</title>
<kwd>influenza</kwd>
<kwd>influenza B</kwd>
<kwd>mismatch</kwd>
<kwd>quadrivalent influenza vaccine</kwd>
</kwd-group>
<counts><fig-count count="2"></fig-count>
<table-count count="2"></table-count>
<equation-count count="0"></equation-count>
<ref-count count="113"></ref-count>
<page-count count="13"></page-count>
</counts>
</article-meta>
</front>
</pmc>
</record>
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