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Establishment of a cohort for deep phenotyping of the immune response to influenza vaccination among elderly individuals recruited from the general population.

Identifieur interne : 000064 ( Main/Exploration ); précédent : 000063; suivant : 000065

Establishment of a cohort for deep phenotyping of the immune response to influenza vaccination among elderly individuals recruited from the general population.

Auteurs : Manas K. Akmatov [Allemagne] ; Peggy Riese [Allemagne] ; Marcus May [Allemagne] ; Leonhard Jentsch [Allemagne] ; Malik W. Ahmed [Allemagne] ; Damaris Werner [Allemagne] ; Anja Rösel [Allemagne] ; Megan Tyler [Allemagne] ; Kevin Pessler [Allemagne] ; Jana Prokein [Allemagne] ; Inga Bernemann [Allemagne] ; Norman Klopp [Allemagne] ; Blair Prochnow [Allemagne] ; Stephanie Trittel [Allemagne] ; Aravind Tallam [Allemagne] ; Thomas Illig [Allemagne] ; Christoph Schindler [Allemagne] ; Carlos A. Guzmán [Allemagne] ; Frank Pessler [Allemagne]

Source :

RBID : pubmed:28394705

Descripteurs français

English descriptors

Abstract

Elderly individuals have the highest burden of disease from influenza infection but also the lowest immune response to influenza vaccination. A better understanding of the host response to influenza vaccination in the elderly is therefore urgently needed. We conducted a biphasic prospective, population-based study from Dec. 2014 to May 2015 (pilot study) and Sept. 2015 to May 2016 (main study). Individuals 65-80 y of age were randomly selected from the residents' registration office in Hannover, Germany, for the pilot (n = 34) and main study (n = 200). The pilot study tested recruitment for study arms featuring 2, 4, or 5 visits/blood draws. The 5-visit (day 0, 1/3, 7, 21, 70 with respect to vaccination) study arm was selected for the main study. Both studies featured vaccination with Fluad™ (Novartis, Italy), a detailed medical history, a physical exam, recording of adverse events, completion of a questionnaire on common infections and an end-of-study questionnaire, and blood samples. Response rates in the pilot and main studies were 3.7% and 4.0%, respectively. Willingness to participate did not differ among the study arms (Fisher's exact test, p = 0.44). In both studies, there were no losses to follow-up. Compliance with study visits, blood sampling and completion of the questionnaires was very high (100%, >97%, 100%, respectively), as were participants' acceptance of and satisfaction with both phases of the study. The low response rates indicate the need for optimized recruitment strategies if the study population is to be representative of the general population. Nonetheless, the complex prospective study design proved to be highly feasible.

DOI: 10.1080/21645515.2017.1299300
PubMed: 28394705
PubMed Central: PMC5512809


Affiliations:


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<name sortKey="Trittel, Stephanie" sort="Trittel, Stephanie" uniqKey="Trittel S" first="Stephanie" last="Trittel">Stephanie Trittel</name>
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<name sortKey="Illig, Thomas" sort="Illig, Thomas" uniqKey="Illig T" first="Thomas" last="Illig">Thomas Illig</name>
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<name sortKey="Guzman, Carlos A" sort="Guzman, Carlos A" uniqKey="Guzman C" first="Carlos A" last="Guzmán">Carlos A. Guzmán</name>
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<name sortKey="Ahmed, Malik W" sort="Ahmed, Malik W" uniqKey="Ahmed M" first="Malik W" last="Ahmed">Malik W. Ahmed</name>
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<name sortKey="Illig, Thomas" sort="Illig, Thomas" uniqKey="Illig T" first="Thomas" last="Illig">Thomas Illig</name>
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<name sortKey="Guzman, Carlos A" sort="Guzman, Carlos A" uniqKey="Guzman C" first="Carlos A" last="Guzmán">Carlos A. Guzmán</name>
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<name sortKey="Pessler, Frank" sort="Pessler, Frank" uniqKey="Pessler F" first="Frank" last="Pessler">Frank Pessler</name>
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<title level="j">Human vaccines & immunotherapeutics</title>
<idno type="eISSN">2164-554X</idno>
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<term>Aged (MeSH)</term>
<term>Aged, 80 and over (MeSH)</term>
<term>Drug-Related Side Effects and Adverse Reactions (epidemiology)</term>
<term>Drug-Related Side Effects and Adverse Reactions (pathology)</term>
<term>Female (MeSH)</term>
<term>Germany (MeSH)</term>
<term>Humans (MeSH)</term>
<term>Influenza Vaccines (administration & dosage)</term>
<term>Influenza Vaccines (adverse effects)</term>
<term>Influenza Vaccines (immunology)</term>
<term>Influenza, Human (prevention & control)</term>
<term>Male (MeSH)</term>
<term>Patient Selection (MeSH)</term>
<term>Prospective Studies (MeSH)</term>
<term>Surveys and Questionnaires (MeSH)</term>
<term>Treatment Outcome (MeSH)</term>
</keywords>
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<term>Allemagne (MeSH)</term>
<term>Effets secondaires indésirables des médicaments (anatomopathologie)</term>
<term>Effets secondaires indésirables des médicaments (épidémiologie)</term>
<term>Enquêtes et questionnaires (MeSH)</term>
<term>Femelle (MeSH)</term>
<term>Grippe humaine (prévention et contrôle)</term>
<term>Humains (MeSH)</term>
<term>Mâle (MeSH)</term>
<term>Résultat thérapeutique (MeSH)</term>
<term>Sujet âgé (MeSH)</term>
<term>Sujet âgé de 80 ans ou plus (MeSH)</term>
<term>Sélection de patients (MeSH)</term>
<term>Vaccins antigrippaux (administration et posologie)</term>
<term>Vaccins antigrippaux (effets indésirables)</term>
<term>Vaccins antigrippaux (immunologie)</term>
<term>Études prospectives (MeSH)</term>
</keywords>
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<term>Influenza Vaccines</term>
</keywords>
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<term>Drug-Related Side Effects and Adverse Reactions</term>
</keywords>
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<div type="abstract" xml:lang="en">Elderly individuals have the highest burden of disease from influenza infection but also the lowest immune response to influenza vaccination. A better understanding of the host response to influenza vaccination in the elderly is therefore urgently needed. We conducted a biphasic prospective, population-based study from Dec. 2014 to May 2015 (pilot study) and Sept. 2015 to May 2016 (main study). Individuals 65-80 y of age were randomly selected from the residents' registration office in Hannover, Germany, for the pilot (n = 34) and main study (n = 200). The pilot study tested recruitment for study arms featuring 2, 4, or 5 visits/blood draws. The 5-visit (day 0, 1/3, 7, 21, 70 with respect to vaccination) study arm was selected for the main study. Both studies featured vaccination with Fluad™ (Novartis, Italy), a detailed medical history, a physical exam, recording of adverse events, completion of a questionnaire on common infections and an end-of-study questionnaire, and blood samples. Response rates in the pilot and main studies were 3.7% and 4.0%, respectively. Willingness to participate did not differ among the study arms (Fisher's exact test, p = 0.44). In both studies, there were no losses to follow-up. Compliance with study visits, blood sampling and completion of the questionnaires was very high (100%, >97%, 100%, respectively), as were participants' acceptance of and satisfaction with both phases of the study. The low response rates indicate the need for optimized recruitment strategies if the study population is to be representative of the general population. Nonetheless, the complex prospective study design proved to be highly feasible.</div>
</front>
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<DateCompleted>
<Year>2018</Year>
<Month>03</Month>
<Day>14</Day>
</DateCompleted>
<DateRevised>
<Year>2018</Year>
<Month>11</Month>
<Day>13</Day>
</DateRevised>
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<Journal>
<ISSN IssnType="Electronic">2164-554X</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>13</Volume>
<Issue>7</Issue>
<PubDate>
<Year>2017</Year>
<Month>07</Month>
<Day>03</Day>
</PubDate>
</JournalIssue>
<Title>Human vaccines & immunotherapeutics</Title>
<ISOAbbreviation>Hum Vaccin Immunother</ISOAbbreviation>
</Journal>
<ArticleTitle>Establishment of a cohort for deep phenotyping of the immune response to influenza vaccination among elderly individuals recruited from the general population.</ArticleTitle>
<Pagination>
<MedlinePgn>1630-1639</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1080/21645515.2017.1299300</ELocationID>
<Abstract>
<AbstractText>Elderly individuals have the highest burden of disease from influenza infection but also the lowest immune response to influenza vaccination. A better understanding of the host response to influenza vaccination in the elderly is therefore urgently needed. We conducted a biphasic prospective, population-based study from Dec. 2014 to May 2015 (pilot study) and Sept. 2015 to May 2016 (main study). Individuals 65-80 y of age were randomly selected from the residents' registration office in Hannover, Germany, for the pilot (n = 34) and main study (n = 200). The pilot study tested recruitment for study arms featuring 2, 4, or 5 visits/blood draws. The 5-visit (day 0, 1/3, 7, 21, 70 with respect to vaccination) study arm was selected for the main study. Both studies featured vaccination with Fluad™ (Novartis, Italy), a detailed medical history, a physical exam, recording of adverse events, completion of a questionnaire on common infections and an end-of-study questionnaire, and blood samples. Response rates in the pilot and main studies were 3.7% and 4.0%, respectively. Willingness to participate did not differ among the study arms (Fisher's exact test, p = 0.44). In both studies, there were no losses to follow-up. Compliance with study visits, blood sampling and completion of the questionnaires was very high (100%, >97%, 100%, respectively), as were participants' acceptance of and satisfaction with both phases of the study. The low response rates indicate the need for optimized recruitment strategies if the study population is to be representative of the general population. Nonetheless, the complex prospective study design proved to be highly feasible.</AbstractText>
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<LastName>Akmatov</LastName>
<ForeName>Manas K</ForeName>
<Initials>MK</Initials>
<AffiliationInfo>
<Affiliation>a TWINCORE, Centre for Experimental and Clinical Infection Research , Hannover , Germany.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>b Helmholtz Centre for Infection Research , Braunschweig , Germany.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>c Centre for Individualized Infection Medicine , Hannover , Germany.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Riese</LastName>
<ForeName>Peggy</ForeName>
<Initials>P</Initials>
<AffiliationInfo>
<Affiliation>d Department of Vaccinology and Applied Microbiology , Helmholtz Centre for Infection Research , Braunschweig , Germany.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>May</LastName>
<ForeName>Marcus</ForeName>
<Initials>M</Initials>
<AffiliationInfo>
<Affiliation>e Clinical Research Center Hannover , Hannover Medical School , Hannover , Germany.</Affiliation>
</AffiliationInfo>
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<LastName>Jentsch</LastName>
<ForeName>Leonhard</ForeName>
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<AffiliationInfo>
<Affiliation>a TWINCORE, Centre for Experimental and Clinical Infection Research , Hannover , Germany.</Affiliation>
</AffiliationInfo>
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<ForeName>Malik W</ForeName>
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</AffiliationInfo>
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<ForeName>Damaris</ForeName>
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<ForeName>Anja</ForeName>
<Initials>A</Initials>
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</AffiliationInfo>
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<Initials>M</Initials>
<AffiliationInfo>
<Affiliation>e Clinical Research Center Hannover , Hannover Medical School , Hannover , Germany.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Pessler</LastName>
<ForeName>Kevin</ForeName>
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<AffiliationInfo>
<Affiliation>a TWINCORE, Centre for Experimental and Clinical Infection Research , Hannover , Germany.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Prokein</LastName>
<ForeName>Jana</ForeName>
<Initials>J</Initials>
<AffiliationInfo>
<Affiliation>f Hannover Unified Biobank , Hannover Medical School , Hannover , Germany.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Bernemann</LastName>
<ForeName>Inga</ForeName>
<Initials>I</Initials>
<AffiliationInfo>
<Affiliation>f Hannover Unified Biobank , Hannover Medical School , Hannover , Germany.</Affiliation>
</AffiliationInfo>
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</AffiliationInfo>
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<LastName>Prochnow</LastName>
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<AffiliationInfo>
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</AffiliationInfo>
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<Author ValidYN="Y">
<LastName>Trittel</LastName>
<ForeName>Stephanie</ForeName>
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<AffiliationInfo>
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</AffiliationInfo>
</Author>
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<LastName>Tallam</LastName>
<ForeName>Aravind</ForeName>
<Initials>A</Initials>
<AffiliationInfo>
<Affiliation>a TWINCORE, Centre for Experimental and Clinical Infection Research , Hannover , Germany.</Affiliation>
</AffiliationInfo>
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<AffiliationInfo>
<Affiliation>f Hannover Unified Biobank , Hannover Medical School , Hannover , Germany.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Schindler</LastName>
<ForeName>Christoph</ForeName>
<Initials>C</Initials>
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</AffiliationInfo>
</Author>
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<LastName>Guzmán</LastName>
<ForeName>Carlos A</ForeName>
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<AffiliationInfo>
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</AffiliationInfo>
<AffiliationInfo>
<Affiliation>d Department of Vaccinology and Applied Microbiology , Helmholtz Centre for Infection Research , Braunschweig , Germany.</Affiliation>
</AffiliationInfo>
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<LastName>Pessler</LastName>
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<AffiliationInfo>
<Affiliation>a TWINCORE, Centre for Experimental and Clinical Infection Research , Hannover , Germany.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>b Helmholtz Centre for Infection Research , Braunschweig , Germany.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>c Centre for Individualized Infection Medicine , Hannover , Germany.</Affiliation>
</AffiliationInfo>
</Author>
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<Month>04</Month>
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<MeshHeading>
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<QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName>
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<MeshHeading>
<DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName>
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<MeshHeading>
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