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Beyond Antigenic Match: Possible Agent-Host and Immuno-epidemiological Influences on Influenza Vaccine Effectiveness During the 2015-2016 Season in Canada.

Identifieur interne : 000120 ( Main/Exploration ); précédent : 000119; suivant : 000121

Beyond Antigenic Match: Possible Agent-Host and Immuno-epidemiological Influences on Influenza Vaccine Effectiveness During the 2015-2016 Season in Canada.

Auteurs : Danuta M. Skowronski [Canada] ; Catharine Chambers [Canada] ; Suzana Sabaiduc [Canada] ; Gaston De Serres [Canada] ; Anne-Luise Winter [Canada] ; James A. Dickinson [Canada] ; Jonathan B. Gubbay [Canada] ; Steven J. Drews [Canada] ; Christine Martineau ; Hugues Charest ; Mel Krajden [Canada] ; Nathalie Bastien [Canada] ; Yan Li [Canada]

Source :

RBID : pubmed:29029166

Descripteurs français

English descriptors

Abstract

Background

Vaccine effectiveness (VE) estimates for 2015-2016 seasonal influenza vaccine are reported from Canada's Sentinel Practitioner Surveillance Network (SPSN). This season was characterized by a delayed 2009 pandemic influenza A(H1N1) virus (A[H1N1]pdm09) epidemic and concurrent influenza B(Victoria) virus activity. Potential influences on VE beyond antigenic match are explored, including viral genomic variation, birth cohort effects, prior vaccination, and epidemic period.

Methods

VE was estimated by a test-negative design comparing the adjusted odds ratio for influenza test positivity among vaccinated compared to unvaccinated participants. Vaccine-virus relatedness was assessed by gene sequencing and hemagglutination inhibition assay.

Results

Analyses included 596 influenza A(H1N1)pdm09 and 305 B(Victoria) cases and 926 test-negative controls. A(H1N1)pdm09 viruses were considered antigenically related to vaccine (unchanged since 2009), despite phylogenetic clustering within emerging clade 6B.1. The adjusted VE against A(H1N1)pdm09 was 43% (95% confidence interval [CI], 25%-57%). Compared to other age groups, VE against A(H1N1)pdm09 was lower for adults born during 1957-1976 (25%; 95% CI, -16%-51%). The VE against A(H1N1)pdm09 was also lower for participants consecutively vaccinated during both the current and prior seasons (41%; 95% CI, 18%-57%) than for those vaccinated during the current season only (75%; 95% CI, 45%-88%), and the VE among participants presenting in March-April 2016 (19%; 95% CI, -15%-44%) was lower than that among those presenting during January-February 2016 (62%; 95% CI, 44%-74%). The adjusted VE for B(Victoria) viruses was 54% (95% CI, 32%-68%), despite lineage-level mismatch to B(Yamagata) vaccine. The further variation in VE as observed for A(H1N1)pdm09 was not observed for B(Victoria).

Conclusions

Influenza VE findings may require consideration of other agent-host and immuno-epidemiologic influences on vaccine performance beyond antigenic match, including viral genomic variation, repeat vaccination, birth (immunological) cohort effects, and potential within-season waning of vaccine protection.


DOI: 10.1093/infdis/jix526
PubMed: 29029166
PubMed Central: PMC5853508


Affiliations:


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<nlm:affiliation>University of Alberta, Edmonton.</nlm:affiliation>
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<name sortKey="Chambers, Catharine" sort="Chambers, Catharine" uniqKey="Chambers C" first="Catharine" last="Chambers">Catharine Chambers</name>
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<nlm:affiliation>Laval University, Québec.</nlm:affiliation>
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<settlement type="city">Québec (ville)</settlement>
<region type="state">Québec</region>
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<name sortKey="Winter, Anne Luise" sort="Winter, Anne Luise" uniqKey="Winter A" first="Anne-Luise" last="Winter">Anne-Luise Winter</name>
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<nlm:affiliation>Public Health Ontario, Toronto.</nlm:affiliation>
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<settlement type="city">Toronto</settlement>
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<wicri:orgArea>Public Health Ontario</wicri:orgArea>
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<name sortKey="Dickinson, James A" sort="Dickinson, James A" uniqKey="Dickinson J" first="James A" last="Dickinson">James A. Dickinson</name>
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<nlm:affiliation>University of Calgary, Calgary.</nlm:affiliation>
<country>Canada</country>
<placeName>
<settlement type="city">Calgary</settlement>
<region type="state">Alberta</region>
</placeName>
<wicri:orgArea>University of Calgary</wicri:orgArea>
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<name sortKey="Gubbay, Jonathan B" sort="Gubbay, Jonathan B" uniqKey="Gubbay J" first="Jonathan B" last="Gubbay">Jonathan B. Gubbay</name>
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<nlm:affiliation>Public Health Ontario, Toronto.</nlm:affiliation>
<country>Canada</country>
<placeName>
<settlement type="city">Toronto</settlement>
<region type="state">Ontario</region>
</placeName>
<wicri:orgArea>Public Health Ontario</wicri:orgArea>
</affiliation>
<affiliation wicri:level="3">
<nlm:affiliation>University of Toronto, Toronto.</nlm:affiliation>
<country>Canada</country>
<placeName>
<settlement type="city">Toronto</settlement>
<region type="state">Ontario</region>
</placeName>
<wicri:orgArea>University of Toronto</wicri:orgArea>
</affiliation>
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<name sortKey="Drews, Steven J" sort="Drews, Steven J" uniqKey="Drews S" first="Steven J" last="Drews">Steven J. Drews</name>
<affiliation wicri:level="3">
<nlm:affiliation>Alberta Provincial Laboratory, Edmonton.</nlm:affiliation>
<country>Canada</country>
<placeName>
<settlement type="city">Edmonton</settlement>
<region type="state">Alberta</region>
</placeName>
<wicri:orgArea>Alberta Provincial Laboratory</wicri:orgArea>
</affiliation>
<affiliation wicri:level="3">
<nlm:affiliation>University of Alberta, Edmonton.</nlm:affiliation>
<country>Canada</country>
<placeName>
<settlement type="city">Edmonton</settlement>
<region type="state">Alberta</region>
</placeName>
<wicri:orgArea>University of Alberta</wicri:orgArea>
</affiliation>
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<name sortKey="Martineau, Christine" sort="Martineau, Christine" uniqKey="Martineau C" first="Christine" last="Martineau">Christine Martineau</name>
<affiliation>
<nlm:affiliation>Institut National de Santé Publique du Québec.</nlm:affiliation>
<wicri:noCountry code="no comma">Institut National de Santé Publique du Québec.</wicri:noCountry>
</affiliation>
</author>
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<name sortKey="Charest, Hugues" sort="Charest, Hugues" uniqKey="Charest H" first="Hugues" last="Charest">Hugues Charest</name>
<affiliation>
<nlm:affiliation>Institut National de Santé Publique du Québec.</nlm:affiliation>
<wicri:noCountry code="no comma">Institut National de Santé Publique du Québec.</wicri:noCountry>
</affiliation>
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<name sortKey="Krajden, Mel" sort="Krajden, Mel" uniqKey="Krajden M" first="Mel" last="Krajden">Mel Krajden</name>
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<nlm:affiliation>British Columbia Centre for Disease Control, Vancouver.</nlm:affiliation>
<country>Canada</country>
<placeName>
<settlement type="city">Vancouver</settlement>
<region type="state">Colombie-Britannique</region>
</placeName>
<wicri:orgArea>British Columbia Centre for Disease Control</wicri:orgArea>
</affiliation>
<affiliation wicri:level="3">
<nlm:affiliation>University of British Columbia, Vancouver.</nlm:affiliation>
<country>Canada</country>
<placeName>
<settlement type="city">Vancouver</settlement>
<region type="state">Colombie-Britannique</region>
</placeName>
<wicri:orgArea>University of British Columbia</wicri:orgArea>
</affiliation>
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<name sortKey="Bastien, Nathalie" sort="Bastien, Nathalie" uniqKey="Bastien N" first="Nathalie" last="Bastien">Nathalie Bastien</name>
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<nlm:affiliation>National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Canada.</nlm:affiliation>
<country xml:lang="fr">Canada</country>
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<name sortKey="Li, Yan" sort="Li, Yan" uniqKey="Li Y" first="Yan" last="Li">Yan Li</name>
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<title level="j">The Journal of infectious diseases</title>
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<term>Adult (MeSH)</term>
<term>Age Factors (MeSH)</term>
<term>Aged (MeSH)</term>
<term>Aged, 80 and over (MeSH)</term>
<term>Antigenic Variation (MeSH)</term>
<term>Antigens, Viral (immunology)</term>
<term>Canada (epidemiology)</term>
<term>Child (MeSH)</term>
<term>Child, Preschool (MeSH)</term>
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<term>Female (MeSH)</term>
<term>Hemagglutination Inhibition Tests (MeSH)</term>
<term>Humans (MeSH)</term>
<term>Immunization (methods)</term>
<term>Immunogenicity, Vaccine (MeSH)</term>
<term>Infant (MeSH)</term>
<term>Influenza A Virus, H1N1 Subtype (classification)</term>
<term>Influenza A Virus, H1N1 Subtype (genetics)</term>
<term>Influenza A Virus, H1N1 Subtype (immunology)</term>
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<term>Influenza Vaccines (immunology)</term>
<term>Influenza, Human (epidemiology)</term>
<term>Influenza, Human (prevention & control)</term>
<term>Influenza, Human (virology)</term>
<term>Male (MeSH)</term>
<term>Middle Aged (MeSH)</term>
<term>Phylogeny (MeSH)</term>
<term>Sequence Analysis, DNA (MeSH)</term>
<term>Sequence Homology (MeSH)</term>
<term>Treatment Outcome (MeSH)</term>
<term>Young Adult (MeSH)</term>
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<term>Adulte (MeSH)</term>
<term>Adulte d'âge moyen (MeSH)</term>
<term>Analyse de regroupements (MeSH)</term>
<term>Analyse de séquence d'ADN (MeSH)</term>
<term>Antigènes viraux (immunologie)</term>
<term>Canada (épidémiologie)</term>
<term>Enfant (MeSH)</term>
<term>Enfant d'âge préscolaire (MeSH)</term>
<term>Facteurs âges (MeSH)</term>
<term>Femelle (MeSH)</term>
<term>Grippe humaine (prévention et contrôle)</term>
<term>Grippe humaine (virologie)</term>
<term>Grippe humaine (épidémiologie)</term>
<term>Humains (MeSH)</term>
<term>Immunisation (méthodes)</term>
<term>Immunogénicité des vaccins (MeSH)</term>
<term>Jeune adulte (MeSH)</term>
<term>Mâle (MeSH)</term>
<term>Nourrisson (MeSH)</term>
<term>Phylogenèse (MeSH)</term>
<term>Résultat thérapeutique (MeSH)</term>
<term>Similitude de séquences (MeSH)</term>
<term>Sous-type H1N1 du virus de la grippe A (classification)</term>
<term>Sous-type H1N1 du virus de la grippe A (génétique)</term>
<term>Sous-type H1N1 du virus de la grippe A (immunologie)</term>
<term>Sous-type H1N1 du virus de la grippe A (isolement et purification)</term>
<term>Sujet âgé (MeSH)</term>
<term>Sujet âgé de 80 ans ou plus (MeSH)</term>
<term>Tests d'inhibition de l'hémagglutination (MeSH)</term>
<term>Vaccins antigrippaux (administration et posologie)</term>
<term>Vaccins antigrippaux (immunologie)</term>
<term>Variation des antigènes (MeSH)</term>
<term>Virus influenza B (classification)</term>
<term>Virus influenza B (génétique)</term>
<term>Virus influenza B (immunologie)</term>
<term>Virus influenza B (isolement et purification)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="administration & dosage" xml:lang="en">
<term>Influenza Vaccines</term>
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<term>Antigens, Viral</term>
<term>Influenza Vaccines</term>
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<term>Canada</term>
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<term>Vaccins antigrippaux</term>
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<term>Influenza A Virus, H1N1 Subtype</term>
<term>Influenza B virus</term>
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<term>Sous-type H1N1 du virus de la grippe A</term>
<term>Vaccins antigrippaux</term>
<term>Virus influenza B</term>
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<term>Influenza B virus</term>
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<term>Influenza B virus</term>
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<term>Grippe humaine</term>
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<term>Age Factors</term>
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<term>Adulte d'âge moyen</term>
<term>Analyse de regroupements</term>
<term>Analyse de séquence d'ADN</term>
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<term>Facteurs âges</term>
<term>Femelle</term>
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<term>Mâle</term>
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<front>
<div type="abstract" xml:lang="en">
<p>
<b>Background</b>
</p>
<p>Vaccine effectiveness (VE) estimates for 2015-2016 seasonal influenza vaccine are reported from Canada's Sentinel Practitioner Surveillance Network (SPSN). This season was characterized by a delayed 2009 pandemic influenza A(H1N1) virus (A[H1N1]pdm09) epidemic and concurrent influenza B(Victoria) virus activity. Potential influences on VE beyond antigenic match are explored, including viral genomic variation, birth cohort effects, prior vaccination, and epidemic period.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>Methods</b>
</p>
<p>VE was estimated by a test-negative design comparing the adjusted odds ratio for influenza test positivity among vaccinated compared to unvaccinated participants. Vaccine-virus relatedness was assessed by gene sequencing and hemagglutination inhibition assay.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>Results</b>
</p>
<p>Analyses included 596 influenza A(H1N1)pdm09 and 305 B(Victoria) cases and 926 test-negative controls. A(H1N1)pdm09 viruses were considered antigenically related to vaccine (unchanged since 2009), despite phylogenetic clustering within emerging clade 6B.1. The adjusted VE against A(H1N1)pdm09 was 43% (95% confidence interval [CI], 25%-57%). Compared to other age groups, VE against A(H1N1)pdm09 was lower for adults born during 1957-1976 (25%; 95% CI, -16%-51%). The VE against A(H1N1)pdm09 was also lower for participants consecutively vaccinated during both the current and prior seasons (41%; 95% CI, 18%-57%) than for those vaccinated during the current season only (75%; 95% CI, 45%-88%), and the VE among participants presenting in March-April 2016 (19%; 95% CI, -15%-44%) was lower than that among those presenting during January-February 2016 (62%; 95% CI, 44%-74%). The adjusted VE for B(Victoria) viruses was 54% (95% CI, 32%-68%), despite lineage-level mismatch to B(Yamagata) vaccine. The further variation in VE as observed for A(H1N1)pdm09 was not observed for B(Victoria).</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>Conclusions</b>
</p>
<p>Influenza VE findings may require consideration of other agent-host and immuno-epidemiologic influences on vaccine performance beyond antigenic match, including viral genomic variation, repeat vaccination, birth (immunological) cohort effects, and potential within-season waning of vaccine protection.</p>
</div>
</front>
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<Title>The Journal of infectious diseases</Title>
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<ArticleTitle>Beyond Antigenic Match: Possible Agent-Host and Immuno-epidemiological Influences on Influenza Vaccine Effectiveness During the 2015-2016 Season in Canada.</ArticleTitle>
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<AbstractText Label="Background">Vaccine effectiveness (VE) estimates for 2015-2016 seasonal influenza vaccine are reported from Canada's Sentinel Practitioner Surveillance Network (SPSN). This season was characterized by a delayed 2009 pandemic influenza A(H1N1) virus (A[H1N1]pdm09) epidemic and concurrent influenza B(Victoria) virus activity. Potential influences on VE beyond antigenic match are explored, including viral genomic variation, birth cohort effects, prior vaccination, and epidemic period.</AbstractText>
<AbstractText Label="Methods">VE was estimated by a test-negative design comparing the adjusted odds ratio for influenza test positivity among vaccinated compared to unvaccinated participants. Vaccine-virus relatedness was assessed by gene sequencing and hemagglutination inhibition assay.</AbstractText>
<AbstractText Label="Results">Analyses included 596 influenza A(H1N1)pdm09 and 305 B(Victoria) cases and 926 test-negative controls. A(H1N1)pdm09 viruses were considered antigenically related to vaccine (unchanged since 2009), despite phylogenetic clustering within emerging clade 6B.1. The adjusted VE against A(H1N1)pdm09 was 43% (95% confidence interval [CI], 25%-57%). Compared to other age groups, VE against A(H1N1)pdm09 was lower for adults born during 1957-1976 (25%; 95% CI, -16%-51%). The VE against A(H1N1)pdm09 was also lower for participants consecutively vaccinated during both the current and prior seasons (41%; 95% CI, 18%-57%) than for those vaccinated during the current season only (75%; 95% CI, 45%-88%), and the VE among participants presenting in March-April 2016 (19%; 95% CI, -15%-44%) was lower than that among those presenting during January-February 2016 (62%; 95% CI, 44%-74%). The adjusted VE for B(Victoria) viruses was 54% (95% CI, 32%-68%), despite lineage-level mismatch to B(Yamagata) vaccine. The further variation in VE as observed for A(H1N1)pdm09 was not observed for B(Victoria).</AbstractText>
<AbstractText Label="Conclusions">Influenza VE findings may require consideration of other agent-host and immuno-epidemiologic influences on vaccine performance beyond antigenic match, including viral genomic variation, repeat vaccination, birth (immunological) cohort effects, and potential within-season waning of vaccine protection.</AbstractText>
<CopyrightInformation>© The Author 2017. Published by Oxford University Press for the Infectious Diseases Society of America.</CopyrightInformation>
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<name sortKey="Li, Yan" sort="Li, Yan" uniqKey="Li Y" first="Yan" last="Li">Yan Li</name>
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