Evaluation of Multivalent H2 Influenza Pandemic Vaccines in Mice
Identifieur interne : 000238 ( Pmc/Checkpoint ); précédent : 000237; suivant : 000239Evaluation of Multivalent H2 Influenza Pandemic Vaccines in Mice
Auteurs : Brian J. Lenny [États-Unis] ; Stephanie Sonnberg [États-Unis] ; Angela F. Danner [États-Unis] ; Kimberly Friedman [États-Unis] ; Richard J. Webby [États-Unis] ; Robert G. Webster [États-Unis] ; Jeremy C. Jones [États-Unis]Source :
- Vaccine [ 0264-410X ] ; 2017.
Abstract
Subtype H2 Influenza A viruses were the cause of a severe pandemic in the winter of 1957. However, this subtype no longer circulates in humans and is no longer included in seasonal vaccines. As a result, individuals under 50 years of age are immunologically naïve. H2 viruses persist in aquatic birds, which were a contributing source for the 1957 pandemic, and have also been isolated from swine. Reintroduction of the H2 via zoonotic transmission has been identified as a pandemic risk, so pre-pandemic planning should include preparation and testing of vaccine candidates against this subtype. We evaluated the immunogenicity of two inactivated, whole virus influenza vaccines (IVV) in mice: a monovalent IVV containing human pandemic virus A/Singapore/1/1957 (H2N2), and a multivalent IVV containing human A/Singapore/1/1957, avian A/Duck/HongKong/319/1978 (H2N2), and swine A/Swine/Missouri/2124514/2006 (H2N3) viruses. While both vaccines induced protective immunity compared to naïve animals, the
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DOI: 10.1016/j.vaccine.2017.01.026
PubMed: 28189402
PubMed Central: 5336516
Affiliations:
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<front><div type="abstract" xml:lang="en"><p id="P2">Subtype H2 Influenza A viruses were the cause of a severe pandemic in the winter of 1957. However, this subtype no longer circulates in humans and is no longer included in seasonal vaccines. As a result, individuals under 50 years of age are immunologically naïve. H2 viruses persist in aquatic birds, which were a contributing source for the 1957 pandemic, and have also been isolated from swine. Reintroduction of the H2 via zoonotic transmission has been identified as a pandemic risk, so pre-pandemic planning should include preparation and testing of vaccine candidates against this subtype. We evaluated the immunogenicity of two inactivated, whole virus influenza vaccines (IVV) in mice: a monovalent IVV containing human pandemic virus A/Singapore/1/1957 (H2N2), and a multivalent IVV containing human A/Singapore/1/1957, avian A/Duck/HongKong/319/1978 (H2N2), and swine A/Swine/Missouri/2124514/2006 (H2N3) viruses. While both vaccines induced protective immunity compared to naïve animals, the <bold>multivalent</bold>
formulation was advantageous over the monovalent in terms of level and breadth of serological responses, <bold>neutralization of infectious virus</bold>
, and reduction of clinical disease and respiratory tissue replication in mice. Therefore, <bold>multivalent</bold>
pandemic H2 vaccines containing diverse viruses from animal reservoirs, are a potential option to improve the immune responses in a pre-pandemic scenario where antigenic identity cannot be predicted.</p>
</div>
</front>
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<contrib-group><contrib contrib-type="author" equal-contrib="yes"><name><surname>Lenny</surname>
<given-names>Brian J.</given-names>
</name>
<xref ref-type="aff" rid="A1">a</xref>
<xref ref-type="aff" rid="A2">b</xref>
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<contrib contrib-type="author" equal-contrib="yes"><name><surname>Sonnberg</surname>
<given-names>Stephanie</given-names>
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<xref ref-type="aff" rid="A1">a</xref>
<xref ref-type="author-notes" rid="FN1">*</xref>
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<contrib contrib-type="author"><name><surname>Danner</surname>
<given-names>Angela F.</given-names>
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<xref ref-type="aff" rid="A1">a</xref>
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<contrib contrib-type="author"><name><surname>Friedman</surname>
<given-names>Kimberly</given-names>
</name>
<xref ref-type="aff" rid="A1">a</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Webby</surname>
<given-names>Richard J.</given-names>
</name>
<xref ref-type="aff" rid="A1">a</xref>
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<contrib contrib-type="author"><name><surname>Webster</surname>
<given-names>Robert G.</given-names>
</name>
<xref ref-type="aff" rid="A1">a</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Jones</surname>
<given-names>Jeremy C.</given-names>
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<xref ref-type="aff" rid="A1">a</xref>
<xref ref-type="corresp" rid="CR1">#</xref>
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<aff id="A1"><label>a</label>
Department of Infectious Diseases, Division of Virology, St. Jude Children's Research Hospital, 262 Danny Thomas Place, Memphis, TN 38105, USA</aff>
<aff id="A2"><label>b</label>
Department of Biology, Rhodes College, 2000 North Parkway, Memphis, TN 38112, USA</aff>
<author-notes><fn fn-type="present-address" id="FN1"><label>*</label>
<p id="P1">Present Address: Takeda Vaccines Inc., 504 S. Rosa Road, Madison, WI 53719, USA</p>
</fn>
<corresp id="CR1"><label>#</label>
<bold>Corresponding Author</bold>
: Jeremy C. Jones, Department of Infectious Diseases, Virology Division, St. Jude Children's Research Hospital, 262 Danny Thomas Place MS330, Memphis, TN 38120, <email>jeremy.jones@stjude.org</email>
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<pub-date pub-type="nihms-submitted"><day>10</day>
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<pub-date pub-type="ppub"><day>07</day>
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<pub-date pub-type="pmc-release"><day>07</day>
<month>3</month>
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<volume>35</volume>
<issue>10</issue>
<fpage>1455</fpage>
<lpage>1463</lpage>
<pmc-comment>elocation-id from pubmed: 10.1016/j.vaccine.2017.01.026</pmc-comment>
<abstract><p id="P2">Subtype H2 Influenza A viruses were the cause of a severe pandemic in the winter of 1957. However, this subtype no longer circulates in humans and is no longer included in seasonal vaccines. As a result, individuals under 50 years of age are immunologically naïve. H2 viruses persist in aquatic birds, which were a contributing source for the 1957 pandemic, and have also been isolated from swine. Reintroduction of the H2 via zoonotic transmission has been identified as a pandemic risk, so pre-pandemic planning should include preparation and testing of vaccine candidates against this subtype. We evaluated the immunogenicity of two inactivated, whole virus influenza vaccines (IVV) in mice: a monovalent IVV containing human pandemic virus A/Singapore/1/1957 (H2N2), and a multivalent IVV containing human A/Singapore/1/1957, avian A/Duck/HongKong/319/1978 (H2N2), and swine A/Swine/Missouri/2124514/2006 (H2N3) viruses. While both vaccines induced protective immunity compared to naïve animals, the <bold>multivalent</bold>
formulation was advantageous over the monovalent in terms of level and breadth of serological responses, <bold>neutralization of infectious virus</bold>
, and reduction of clinical disease and respiratory tissue replication in mice. Therefore, <bold>multivalent</bold>
pandemic H2 vaccines containing diverse viruses from animal reservoirs, are a potential option to improve the immune responses in a pre-pandemic scenario where antigenic identity cannot be predicted.</p>
</abstract>
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