Loading…

Cytokine profiling in healthy children shows association of age with cytokine concentrations

Cytokine-based diagnostic assays are increasingly used in research and clinical practice. Assays developed for adults such as the interferon-gamma release assay for tuberculosis show inferior performance in children. Limited evidence suggests that release of cytokines is influenced by age but normal...

Full description

Saved in:
Bibliographic Details
Published in:Scientific reports 2017-12, Vol.7 (1), p.17842-10, Article 17842
Main Authors: Decker, Marie-Luise, Gotta, Verena, Wellmann, Sven, Ritz, Nicole
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c474t-bbcb73c3451b2d9eeeed9d886b114d75075ecc9c05821258edb8d4564a5ad9893
cites cdi_FETCH-LOGICAL-c474t-bbcb73c3451b2d9eeeed9d886b114d75075ecc9c05821258edb8d4564a5ad9893
container_end_page 10
container_issue 1
container_start_page 17842
container_title Scientific reports
container_volume 7
creator Decker, Marie-Luise
Gotta, Verena
Wellmann, Sven
Ritz, Nicole
description Cytokine-based diagnostic assays are increasingly used in research and clinical practice. Assays developed for adults such as the interferon-gamma release assay for tuberculosis show inferior performance in children. Limited evidence suggests that release of cytokines is influenced by age but normal ranges of cytokines in children are lacking. Whole blood of healthy children (0–12 years) undergoing elective/diagnostic procedures was stimulated with SEB, PHA, Candida albicans for 24 hours or left unstimulated. Concentrations of eight cytokines were measured by multiplex bead-based immunoassays and associations with age and other factors quantified by regression analysis. 271 children (median age 5.2 years) were included. In unstimulated samples IL-1ra, IP-10 and TNF-α concentrations decreased by up to −60% with age. Following antigen stimulation, an age-associated increase (ranging from +90% to +500%) was observed for all cytokines except IL-1ra (significant for IL-4, IFN-γ and TNF-α). Inter-individual variability in cytokine concentrations was large with a coefficient of variation ranging from 42% to 1412%. Despite inter-individual variation age was identified as a strong influencing factor of cytokine concentrations. Age-specific normal values need to be considered for cytokine-based diagnostic purposes. These results are relevant for development of novel cytokine-based diagnostic assays and for optimal dosing of therapeutic agents targeting cytokines.
doi_str_mv 10.1038/s41598-017-17865-2
format article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5736560</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1979174925</sourcerecordid><originalsourceid>FETCH-LOGICAL-c474t-bbcb73c3451b2d9eeeed9d886b114d75075ecc9c05821258edb8d4564a5ad9893</originalsourceid><addsrcrecordid>eNp1kcFqGzEQhkVJqU2aF-ghCHLJZVNJK62kSyCYtikYemlvBaGVZK-cteRI6xi_feWsE5xA56KB-ebXzPwAfMHoBqNafM0UMykqhHmFuWhYRT6AKUG0JDUhZyf5BFzkvEIlGJEUy09gQiRhkuBmCv7O9kN88MHBTYoL3_uwhD7Azul-6PbQdL63yQWYu7jLUOccjdeDjwHGBdRLB3d-6KB5ETExGBeG9Izkz-DjQvfZXRzfc_Dn-7ffs_tq_uvHz9ndvDKU06FqW9Py2tSU4ZZY6UpYaYVoWoyp5Qxx5oyRBjFBMGHC2VZYyhqqmbZSyPoc3I66m227dnacoFeb5Nc67VXUXr2tBN-pZXxSjNcNa1ARuD4KpPi4dXlQa5-N63sdXNxmhSWXmNNytYJevUNXcZtCWa9QoqaknJUUioyUSTHn5Bavw2CkDv6p0T9V_FPP_qlD0-XpGq8tL24VoB6BXEph6dLJ3_-X_Qf3tKg4</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1983422162</pqid></control><display><type>article</type><title>Cytokine profiling in healthy children shows association of age with cytokine concentrations</title><source>Publicly Available Content Database</source><source>PubMed Central</source><source>Free Full-Text Journals in Chemistry</source><source>Springer Nature - nature.com Journals - Fully Open Access</source><creator>Decker, Marie-Luise ; Gotta, Verena ; Wellmann, Sven ; Ritz, Nicole</creator><creatorcontrib>Decker, Marie-Luise ; Gotta, Verena ; Wellmann, Sven ; Ritz, Nicole</creatorcontrib><description>Cytokine-based diagnostic assays are increasingly used in research and clinical practice. Assays developed for adults such as the interferon-gamma release assay for tuberculosis show inferior performance in children. Limited evidence suggests that release of cytokines is influenced by age but normal ranges of cytokines in children are lacking. Whole blood of healthy children (0–12 years) undergoing elective/diagnostic procedures was stimulated with SEB, PHA, Candida albicans for 24 hours or left unstimulated. Concentrations of eight cytokines were measured by multiplex bead-based immunoassays and associations with age and other factors quantified by regression analysis. 271 children (median age 5.2 years) were included. In unstimulated samples IL-1ra, IP-10 and TNF-α concentrations decreased by up to −60% with age. Following antigen stimulation, an age-associated increase (ranging from +90% to +500%) was observed for all cytokines except IL-1ra (significant for IL-4, IFN-γ and TNF-α). Inter-individual variability in cytokine concentrations was large with a coefficient of variation ranging from 42% to 1412%. Despite inter-individual variation age was identified as a strong influencing factor of cytokine concentrations. Age-specific normal values need to be considered for cytokine-based diagnostic purposes. These results are relevant for development of novel cytokine-based diagnostic assays and for optimal dosing of therapeutic agents targeting cytokines.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-017-17865-2</identifier><identifier>PMID: 29259216</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>13/21 ; 692/308/3187 ; 692/700 ; Age ; Chemokine CXCL10 - blood ; Child ; Child, Preschool ; Children ; Coefficient of variation ; Cytokines ; Cytokines - blood ; Female ; Humanities and Social Sciences ; Humans ; Immunoassays ; Interleukin 1 receptor antagonist ; Interleukin 1 Receptor Antagonist Protein - blood ; Interleukin 1 receptors ; Interleukin 4 ; IP-10 protein ; Male ; multidisciplinary ; Regression analysis ; Science ; Science (multidisciplinary) ; Tuberculosis ; Tuberculosis - blood ; Tumor Necrosis Factor-alpha - blood ; Tumor necrosis factor-α ; γ-Interferon</subject><ispartof>Scientific reports, 2017-12, Vol.7 (1), p.17842-10, Article 17842</ispartof><rights>The Author(s) 2017</rights><rights>2017. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-bbcb73c3451b2d9eeeed9d886b114d75075ecc9c05821258edb8d4564a5ad9893</citedby><cites>FETCH-LOGICAL-c474t-bbcb73c3451b2d9eeeed9d886b114d75075ecc9c05821258edb8d4564a5ad9893</cites><orcidid>0000-0002-1498-1685</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1983422162/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1983422162?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,74998</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29259216$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Decker, Marie-Luise</creatorcontrib><creatorcontrib>Gotta, Verena</creatorcontrib><creatorcontrib>Wellmann, Sven</creatorcontrib><creatorcontrib>Ritz, Nicole</creatorcontrib><title>Cytokine profiling in healthy children shows association of age with cytokine concentrations</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>Cytokine-based diagnostic assays are increasingly used in research and clinical practice. Assays developed for adults such as the interferon-gamma release assay for tuberculosis show inferior performance in children. Limited evidence suggests that release of cytokines is influenced by age but normal ranges of cytokines in children are lacking. Whole blood of healthy children (0–12 years) undergoing elective/diagnostic procedures was stimulated with SEB, PHA, Candida albicans for 24 hours or left unstimulated. Concentrations of eight cytokines were measured by multiplex bead-based immunoassays and associations with age and other factors quantified by regression analysis. 271 children (median age 5.2 years) were included. In unstimulated samples IL-1ra, IP-10 and TNF-α concentrations decreased by up to −60% with age. Following antigen stimulation, an age-associated increase (ranging from +90% to +500%) was observed for all cytokines except IL-1ra (significant for IL-4, IFN-γ and TNF-α). Inter-individual variability in cytokine concentrations was large with a coefficient of variation ranging from 42% to 1412%. Despite inter-individual variation age was identified as a strong influencing factor of cytokine concentrations. Age-specific normal values need to be considered for cytokine-based diagnostic purposes. These results are relevant for development of novel cytokine-based diagnostic assays and for optimal dosing of therapeutic agents targeting cytokines.</description><subject>13/21</subject><subject>692/308/3187</subject><subject>692/700</subject><subject>Age</subject><subject>Chemokine CXCL10 - blood</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Children</subject><subject>Coefficient of variation</subject><subject>Cytokines</subject><subject>Cytokines - blood</subject><subject>Female</subject><subject>Humanities and Social Sciences</subject><subject>Humans</subject><subject>Immunoassays</subject><subject>Interleukin 1 receptor antagonist</subject><subject>Interleukin 1 Receptor Antagonist Protein - blood</subject><subject>Interleukin 1 receptors</subject><subject>Interleukin 4</subject><subject>IP-10 protein</subject><subject>Male</subject><subject>multidisciplinary</subject><subject>Regression analysis</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Tuberculosis</subject><subject>Tuberculosis - blood</subject><subject>Tumor Necrosis Factor-alpha - blood</subject><subject>Tumor necrosis factor-α</subject><subject>γ-Interferon</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNp1kcFqGzEQhkVJqU2aF-ghCHLJZVNJK62kSyCYtikYemlvBaGVZK-cteRI6xi_feWsE5xA56KB-ebXzPwAfMHoBqNafM0UMykqhHmFuWhYRT6AKUG0JDUhZyf5BFzkvEIlGJEUy09gQiRhkuBmCv7O9kN88MHBTYoL3_uwhD7Azul-6PbQdL63yQWYu7jLUOccjdeDjwHGBdRLB3d-6KB5ETExGBeG9Izkz-DjQvfZXRzfc_Dn-7ffs_tq_uvHz9ndvDKU06FqW9Py2tSU4ZZY6UpYaYVoWoyp5Qxx5oyRBjFBMGHC2VZYyhqqmbZSyPoc3I66m227dnacoFeb5Nc67VXUXr2tBN-pZXxSjNcNa1ARuD4KpPi4dXlQa5-N63sdXNxmhSWXmNNytYJevUNXcZtCWa9QoqaknJUUioyUSTHn5Bavw2CkDv6p0T9V_FPP_qlD0-XpGq8tL24VoB6BXEph6dLJ3_-X_Qf3tKg4</recordid><startdate>20171219</startdate><enddate>20171219</enddate><creator>Decker, Marie-Luise</creator><creator>Gotta, Verena</creator><creator>Wellmann, Sven</creator><creator>Ritz, Nicole</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-1498-1685</orcidid></search><sort><creationdate>20171219</creationdate><title>Cytokine profiling in healthy children shows association of age with cytokine concentrations</title><author>Decker, Marie-Luise ; Gotta, Verena ; Wellmann, Sven ; Ritz, Nicole</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-bbcb73c3451b2d9eeeed9d886b114d75075ecc9c05821258edb8d4564a5ad9893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>13/21</topic><topic>692/308/3187</topic><topic>692/700</topic><topic>Age</topic><topic>Chemokine CXCL10 - blood</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Children</topic><topic>Coefficient of variation</topic><topic>Cytokines</topic><topic>Cytokines - blood</topic><topic>Female</topic><topic>Humanities and Social Sciences</topic><topic>Humans</topic><topic>Immunoassays</topic><topic>Interleukin 1 receptor antagonist</topic><topic>Interleukin 1 Receptor Antagonist Protein - blood</topic><topic>Interleukin 1 receptors</topic><topic>Interleukin 4</topic><topic>IP-10 protein</topic><topic>Male</topic><topic>multidisciplinary</topic><topic>Regression analysis</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><topic>Tuberculosis</topic><topic>Tuberculosis - blood</topic><topic>Tumor Necrosis Factor-alpha - blood</topic><topic>Tumor necrosis factor-α</topic><topic>γ-Interferon</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Decker, Marie-Luise</creatorcontrib><creatorcontrib>Gotta, Verena</creatorcontrib><creatorcontrib>Wellmann, Sven</creatorcontrib><creatorcontrib>Ritz, Nicole</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection (Proquest)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Decker, Marie-Luise</au><au>Gotta, Verena</au><au>Wellmann, Sven</au><au>Ritz, Nicole</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cytokine profiling in healthy children shows association of age with cytokine concentrations</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2017-12-19</date><risdate>2017</risdate><volume>7</volume><issue>1</issue><spage>17842</spage><epage>10</epage><pages>17842-10</pages><artnum>17842</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>Cytokine-based diagnostic assays are increasingly used in research and clinical practice. Assays developed for adults such as the interferon-gamma release assay for tuberculosis show inferior performance in children. Limited evidence suggests that release of cytokines is influenced by age but normal ranges of cytokines in children are lacking. Whole blood of healthy children (0–12 years) undergoing elective/diagnostic procedures was stimulated with SEB, PHA, Candida albicans for 24 hours or left unstimulated. Concentrations of eight cytokines were measured by multiplex bead-based immunoassays and associations with age and other factors quantified by regression analysis. 271 children (median age 5.2 years) were included. In unstimulated samples IL-1ra, IP-10 and TNF-α concentrations decreased by up to −60% with age. Following antigen stimulation, an age-associated increase (ranging from +90% to +500%) was observed for all cytokines except IL-1ra (significant for IL-4, IFN-γ and TNF-α). Inter-individual variability in cytokine concentrations was large with a coefficient of variation ranging from 42% to 1412%. Despite inter-individual variation age was identified as a strong influencing factor of cytokine concentrations. Age-specific normal values need to be considered for cytokine-based diagnostic purposes. These results are relevant for development of novel cytokine-based diagnostic assays and for optimal dosing of therapeutic agents targeting cytokines.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>29259216</pmid><doi>10.1038/s41598-017-17865-2</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-1498-1685</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2045-2322
ispartof Scientific reports, 2017-12, Vol.7 (1), p.17842-10, Article 17842
issn 2045-2322
2045-2322
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5736560
source Publicly Available Content Database; PubMed Central; Free Full-Text Journals in Chemistry; Springer Nature - nature.com Journals - Fully Open Access
subjects 13/21
692/308/3187
692/700
Age
Chemokine CXCL10 - blood
Child
Child, Preschool
Children
Coefficient of variation
Cytokines
Cytokines - blood
Female
Humanities and Social Sciences
Humans
Immunoassays
Interleukin 1 receptor antagonist
Interleukin 1 Receptor Antagonist Protein - blood
Interleukin 1 receptors
Interleukin 4
IP-10 protein
Male
multidisciplinary
Regression analysis
Science
Science (multidisciplinary)
Tuberculosis
Tuberculosis - blood
Tumor Necrosis Factor-alpha - blood
Tumor necrosis factor-α
γ-Interferon
title Cytokine profiling in healthy children shows association of age with cytokine concentrations
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T04%3A28%3A44IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Cytokine%20profiling%20in%20healthy%20children%20shows%20association%20of%20age%20with%20cytokine%20concentrations&rft.jtitle=Scientific%20reports&rft.au=Decker,%20Marie-Luise&rft.date=2017-12-19&rft.volume=7&rft.issue=1&rft.spage=17842&rft.epage=10&rft.pages=17842-10&rft.artnum=17842&rft.issn=2045-2322&rft.eissn=2045-2322&rft_id=info:doi/10.1038/s41598-017-17865-2&rft_dat=%3Cproquest_pubme%3E1979174925%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c474t-bbcb73c3451b2d9eeeed9d886b114d75075ecc9c05821258edb8d4564a5ad9893%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1983422162&rft_id=info:pmid/29259216&rfr_iscdi=true