Serveur d'exploration H2N2

Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.

The composition of immune cells serves as a predictor of adaptive immunity in a cohort of 50‐ to 74‐year‐old adults

Identifieur interne : 000399 ( Main/Exploration ); précédent : 000398; suivant : 000400

The composition of immune cells serves as a predictor of adaptive immunity in a cohort of 50‐ to 74‐year‐old adults

Auteurs : Richard B. Kennedy ; Whitney L. Simon ; Michael J. Gibson ; Krista M. Goergen ; Diane E. Grill ; Ann L. Oberg ; Gregory A. Poland

Source :

RBID : PMC:4913285

Abstract

Summary

Influenza causes significant morbidity and mortality annually. Although vaccination offers a considerable amount of protection, it is far from perfect, especially in aging populations. This is due to age‐related defects in immune function, a process called immunosenescence. To date, there are no assays or methods to predict or explain variations in an individual's level of response to influenza vaccination. In this study, we measured levels of several immune cell subsets at baseline (Day 0) and at Days 3 and 28 post‐vaccination using flow cytometry. Statistical modelling was performed to assess correlations between levels of cell subsets and Day 28 immune responses – haemagglutination inhibition (HAI) assay, virus neutralizing antibody (VNA) assay, and memory B cell ELISPOT. Changes in several groups of cell types from Day 0 to Day 28 and Day 3 to Day 28 were found to be significantly associated with immune response. Baseline levels of several immune cell subsets, including B cells and regulatory T cells, were able to partially explain variation in memory B‐cell ELISPOT results. Increased expression of HLADR on plasmacytoid dendritic cells after vaccination was correlated with increased HAI and VNA responses. Our data suggest that the expression of activation markers (HLADR and CD86) on various immune cell subsets, as well as the relative distribution of cell subsets, both have value in predicting immune responses to influenza vaccination in older individuals.


Url:
DOI: 10.1111/imm.12599
PubMed: 27188667
PubMed Central: 4913285


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

<record>
<TEI>
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en">The composition of immune cells serves as a predictor of adaptive immunity in a cohort of 50‐ to 74‐year‐old adults</title>
<author>
<name sortKey="Kennedy, Richard B" sort="Kennedy, Richard B" uniqKey="Kennedy R" first="Richard B." last="Kennedy">Richard B. Kennedy</name>
<affiliation>
<nlm:aff id="imm12599-aff-0001"></nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Simon, Whitney L" sort="Simon, Whitney L" uniqKey="Simon W" first="Whitney L." last="Simon">Whitney L. Simon</name>
<affiliation>
<nlm:aff id="imm12599-aff-0001"></nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Gibson, Michael J" sort="Gibson, Michael J" uniqKey="Gibson M" first="Michael J." last="Gibson">Michael J. Gibson</name>
<affiliation>
<nlm:aff id="imm12599-aff-0001"></nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Goergen, Krista M" sort="Goergen, Krista M" uniqKey="Goergen K" first="Krista M." last="Goergen">Krista M. Goergen</name>
<affiliation>
<nlm:aff id="imm12599-aff-0002"></nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Grill, Diane E" sort="Grill, Diane E" uniqKey="Grill D" first="Diane E." last="Grill">Diane E. Grill</name>
<affiliation>
<nlm:aff id="imm12599-aff-0002"></nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Oberg, Ann L" sort="Oberg, Ann L" uniqKey="Oberg A" first="Ann L." last="Oberg">Ann L. Oberg</name>
<affiliation>
<nlm:aff id="imm12599-aff-0002"></nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Poland, Gregory A" sort="Poland, Gregory A" uniqKey="Poland G" first="Gregory A." last="Poland">Gregory A. Poland</name>
<affiliation>
<nlm:aff id="imm12599-aff-0001"></nlm:aff>
</affiliation>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">PMC</idno>
<idno type="pmid">27188667</idno>
<idno type="pmc">4913285</idno>
<idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4913285</idno>
<idno type="RBID">PMC:4913285</idno>
<idno type="doi">10.1111/imm.12599</idno>
<date when="2016">2016</date>
<idno type="wicri:Area/Pmc/Corpus">000051</idno>
<idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">000051</idno>
<idno type="wicri:Area/Pmc/Curation">000051</idno>
<idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Curation">000051</idno>
<idno type="wicri:Area/Pmc/Checkpoint">000282</idno>
<idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Checkpoint">000282</idno>
<idno type="wicri:Area/Ncbi/Merge">000C75</idno>
<idno type="wicri:Area/Ncbi/Curation">000C75</idno>
<idno type="wicri:Area/Ncbi/Checkpoint">000C75</idno>
<idno type="wicri:doubleKey">0019-2805:2016:Kennedy R:the:composition:of</idno>
<idno type="wicri:Area/Main/Merge">000399</idno>
<idno type="wicri:Area/Main/Curation">000399</idno>
<idno type="wicri:Area/Main/Exploration">000399</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title xml:lang="en" level="a" type="main">The composition of immune cells serves as a predictor of adaptive immunity in a cohort of 50‐ to 74‐year‐old adults</title>
<author>
<name sortKey="Kennedy, Richard B" sort="Kennedy, Richard B" uniqKey="Kennedy R" first="Richard B." last="Kennedy">Richard B. Kennedy</name>
<affiliation>
<nlm:aff id="imm12599-aff-0001"></nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Simon, Whitney L" sort="Simon, Whitney L" uniqKey="Simon W" first="Whitney L." last="Simon">Whitney L. Simon</name>
<affiliation>
<nlm:aff id="imm12599-aff-0001"></nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Gibson, Michael J" sort="Gibson, Michael J" uniqKey="Gibson M" first="Michael J." last="Gibson">Michael J. Gibson</name>
<affiliation>
<nlm:aff id="imm12599-aff-0001"></nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Goergen, Krista M" sort="Goergen, Krista M" uniqKey="Goergen K" first="Krista M." last="Goergen">Krista M. Goergen</name>
<affiliation>
<nlm:aff id="imm12599-aff-0002"></nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Grill, Diane E" sort="Grill, Diane E" uniqKey="Grill D" first="Diane E." last="Grill">Diane E. Grill</name>
<affiliation>
<nlm:aff id="imm12599-aff-0002"></nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Oberg, Ann L" sort="Oberg, Ann L" uniqKey="Oberg A" first="Ann L." last="Oberg">Ann L. Oberg</name>
<affiliation>
<nlm:aff id="imm12599-aff-0002"></nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Poland, Gregory A" sort="Poland, Gregory A" uniqKey="Poland G" first="Gregory A." last="Poland">Gregory A. Poland</name>
<affiliation>
<nlm:aff id="imm12599-aff-0001"></nlm:aff>
</affiliation>
</author>
</analytic>
<series>
<title level="j">Immunology</title>
<idno type="ISSN">0019-2805</idno>
<idno type="eISSN">1365-2567</idno>
<imprint>
<date when="2016">2016</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc>
<textClass></textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">
<title>Summary</title>
<p>Influenza causes significant morbidity and mortality annually. Although vaccination offers a considerable amount of protection, it is far from perfect, especially in aging populations. This is due to age‐related defects in immune function, a process called immunosenescence. To date, there are no assays or methods to predict or explain variations in an individual's level of response to influenza vaccination. In this study, we measured levels of several immune cell subsets at baseline (Day 0) and at Days 3 and 28 post‐vaccination using flow cytometry. Statistical modelling was performed to assess correlations between levels of cell subsets and Day 28 immune responses – haemagglutination inhibition (
<styled-content style="fixed-case">HAI</styled-content>
) assay, virus neutralizing antibody (
<styled-content style="fixed-case">VNA</styled-content>
) assay, and memory B cell
<styled-content style="fixed-case">ELISPOT</styled-content>
. Changes in several groups of cell types from Day 0 to Day 28 and Day 3 to Day 28 were found to be significantly associated with immune response. Baseline levels of several immune cell subsets, including B cells and regulatory T cells, were able to partially explain variation in memory B‐cell
<styled-content style="fixed-case">ELISPOT</styled-content>
results. Increased expression of
<styled-content style="fixed-case">HLA</styled-content>
<styled-content style="fixed-case">DR</styled-content>
on plasmacytoid dendritic cells after vaccination was correlated with increased
<styled-content style="fixed-case">HAI</styled-content>
and
<styled-content style="fixed-case">VNA</styled-content>
responses. Our data suggest that the expression of activation markers (
<styled-content style="fixed-case">HLA</styled-content>
<styled-content style="fixed-case">DR</styled-content>
and
<styled-content style="fixed-case">CD</styled-content>
86) on various immune cell subsets, as well as the relative distribution of cell subsets, both have value in predicting immune responses to influenza vaccination in older individuals.</p>
</div>
</front>
</TEI>
<affiliations>
<list></list>
<tree>
<noCountry>
<name sortKey="Gibson, Michael J" sort="Gibson, Michael J" uniqKey="Gibson M" first="Michael J." last="Gibson">Michael J. Gibson</name>
<name sortKey="Goergen, Krista M" sort="Goergen, Krista M" uniqKey="Goergen K" first="Krista M." last="Goergen">Krista M. Goergen</name>
<name sortKey="Grill, Diane E" sort="Grill, Diane E" uniqKey="Grill D" first="Diane E." last="Grill">Diane E. Grill</name>
<name sortKey="Kennedy, Richard B" sort="Kennedy, Richard B" uniqKey="Kennedy R" first="Richard B." last="Kennedy">Richard B. Kennedy</name>
<name sortKey="Oberg, Ann L" sort="Oberg, Ann L" uniqKey="Oberg A" first="Ann L." last="Oberg">Ann L. Oberg</name>
<name sortKey="Poland, Gregory A" sort="Poland, Gregory A" uniqKey="Poland G" first="Gregory A." last="Poland">Gregory A. Poland</name>
<name sortKey="Simon, Whitney L" sort="Simon, Whitney L" uniqKey="Simon W" first="Whitney L." last="Simon">Whitney L. Simon</name>
</noCountry>
</tree>
</affiliations>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Sante/explor/H2N2V1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000399 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 000399 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Sante
   |area=    H2N2V1
   |flux=    Main
   |étape=   Exploration
   |type=    RBID
   |clé=     PMC:4913285
   |texte=   The composition of immune cells serves as a predictor of adaptive immunity in a cohort of 50‐ to 74‐year‐old adults
}}

Pour générer des pages wiki

HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Exploration/RBID.i   -Sk "pubmed:27188667" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd   \
       | NlmPubMed2Wicri -a H2N2V1 

Wicri

This area was generated with Dilib version V0.6.33.
Data generation: Tue Apr 14 19:59:40 2020. Site generation: Thu Mar 25 15:38:26 2021