CD4+ and CD8+ T Cell Activation in Children with Hepatitis C

Objectives To assess if peripheral T cell populations in children with chronic hepatitis C virus (HCV) infection would show evidence of activation/exhaustion and an attenuated functional response. Study design Compared with adults, children with HCV infection have a higher rate of spontaneous viral...

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Veröffentlicht in:The Journal of pediatrics 2016-03, Vol.170, p.142-148.e1
Hauptverfasser: Sheiko, Melissa A., MD, Golden-Mason, Lucy, PhD, Giugliano, Silvia, PhD, Hurtado, Christine Waasdorp, MD, Mack, Cara L., MD, Narkewicz, Michael R., MD, Rosen, Hugo R., MD
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container_end_page 148.e1
container_issue
container_start_page 142
container_title The Journal of pediatrics
container_volume 170
creator Sheiko, Melissa A., MD
Golden-Mason, Lucy, PhD
Giugliano, Silvia, PhD
Hurtado, Christine Waasdorp, MD
Mack, Cara L., MD
Narkewicz, Michael R., MD
Rosen, Hugo R., MD
description Objectives To assess if peripheral T cell populations in children with chronic hepatitis C virus (HCV) infection would show evidence of activation/exhaustion and an attenuated functional response. Study design Compared with adults, children with HCV infection have a higher rate of spontaneous viral clearance. In adults, chronic HCV has been linked to T cell exhaustion. Little is known of the immune status of children with HCV. Peripheral blood mononuclear cells were isolated from 16 children with HCV (6 males, 10 females; mean age 8.6 years, range 2-17), 16 age- and sex-matched control children without HCV infection, and 20 adults with chronic HCV. Multiparameter flow cytometry was performed to characterize T cell differences across the 3 groups. Results Controls and children with HCV had similar levels of CD4+ , CD8+ , and γδ+ T cells. Children with HCV demonstrated a decrease in naïve T cells compared with control children and increased activation/exhaustion marker expression on both CD8+ and CD4+ T cells. Transcription factor analysis suggested functional activation of T cells in children with HCV; however, only the CD4+ subset had enhanced cytokine production (interferon gamma and interleukin-2) compared with control children. Conclusions The HCV response in children is characterized by several changes in T cell phenotype. Many of these changes, such as increased T cell expression of programmed cell death-1, are similar to responses in adults. Of note, cytokine production by CD4+ helper T cells is increased in children with HCV compared with age- and sex-matched control children, which may influence long-term prognosis in children with HCV.
doi_str_mv 10.1016/j.jpeds.2015.11.055
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Study design Compared with adults, children with HCV infection have a higher rate of spontaneous viral clearance. In adults, chronic HCV has been linked to T cell exhaustion. Little is known of the immune status of children with HCV. Peripheral blood mononuclear cells were isolated from 16 children with HCV (6 males, 10 females; mean age 8.6 years, range 2-17), 16 age- and sex-matched control children without HCV infection, and 20 adults with chronic HCV. Multiparameter flow cytometry was performed to characterize T cell differences across the 3 groups. Results Controls and children with HCV had similar levels of CD4+ , CD8+ , and γδ+ T cells. Children with HCV demonstrated a decrease in naïve T cells compared with control children and increased activation/exhaustion marker expression on both CD8+ and CD4+ T cells. Transcription factor analysis suggested functional activation of T cells in children with HCV; however, only the CD4+ subset had enhanced cytokine production (interferon gamma and interleukin-2) compared with control children. Conclusions The HCV response in children is characterized by several changes in T cell phenotype. Many of these changes, such as increased T cell expression of programmed cell death-1, are similar to responses in adults. Of note, cytokine production by CD4+ helper T cells is increased in children with HCV compared with age- and sex-matched control children, which may influence long-term prognosis in children with HCV.</description><identifier>ISSN: 0022-3476</identifier><identifier>EISSN: 1097-6833</identifier><identifier>DOI: 10.1016/j.jpeds.2015.11.055</identifier><identifier>PMID: 26743497</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adolescent ; Adult ; Case-Control Studies ; CD4-Positive T-Lymphocytes - metabolism ; CD8-Positive T-Lymphocytes - metabolism ; Cells, Cultured ; Child ; Child, Preschool ; Female ; Flow Cytometry ; Hepatitis C, Chronic - blood ; Hepatitis C, Chronic - immunology ; Humans ; Interferon-gamma - metabolism ; Interleukin-2 - metabolism ; Lymphocyte Activation ; Male ; Pediatrics ; Programmed Cell Death 1 Receptor - metabolism ; Receptors, Immunologic - metabolism ; T-Box Domain Proteins - metabolism</subject><ispartof>The Journal of pediatrics, 2016-03, Vol.170, p.142-148.e1</ispartof><rights>2016</rights><rights>Copyright © 2016. Published by Elsevier Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c514t-c29df0fa693b2fc8e454bfc34e7c66eec15091bf4f3a1b62dc4c14e4442350603</citedby><cites>FETCH-LOGICAL-c514t-c29df0fa693b2fc8e454bfc34e7c66eec15091bf4f3a1b62dc4c14e4442350603</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0022347615014675$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26743497$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sheiko, Melissa A., MD</creatorcontrib><creatorcontrib>Golden-Mason, Lucy, PhD</creatorcontrib><creatorcontrib>Giugliano, Silvia, PhD</creatorcontrib><creatorcontrib>Hurtado, Christine Waasdorp, MD</creatorcontrib><creatorcontrib>Mack, Cara L., MD</creatorcontrib><creatorcontrib>Narkewicz, Michael R., MD</creatorcontrib><creatorcontrib>Rosen, Hugo R., MD</creatorcontrib><title>CD4+ and CD8+ T Cell Activation in Children with Hepatitis C</title><title>The Journal of pediatrics</title><addtitle>J Pediatr</addtitle><description>Objectives To assess if peripheral T cell populations in children with chronic hepatitis C virus (HCV) infection would show evidence of activation/exhaustion and an attenuated functional response. Study design Compared with adults, children with HCV infection have a higher rate of spontaneous viral clearance. In adults, chronic HCV has been linked to T cell exhaustion. Little is known of the immune status of children with HCV. Peripheral blood mononuclear cells were isolated from 16 children with HCV (6 males, 10 females; mean age 8.6 years, range 2-17), 16 age- and sex-matched control children without HCV infection, and 20 adults with chronic HCV. Multiparameter flow cytometry was performed to characterize T cell differences across the 3 groups. Results Controls and children with HCV had similar levels of CD4+ , CD8+ , and γδ+ T cells. Children with HCV demonstrated a decrease in naïve T cells compared with control children and increased activation/exhaustion marker expression on both CD8+ and CD4+ T cells. Transcription factor analysis suggested functional activation of T cells in children with HCV; however, only the CD4+ subset had enhanced cytokine production (interferon gamma and interleukin-2) compared with control children. Conclusions The HCV response in children is characterized by several changes in T cell phenotype. Many of these changes, such as increased T cell expression of programmed cell death-1, are similar to responses in adults. Of note, cytokine production by CD4+ helper T cells is increased in children with HCV compared with age- and sex-matched control children, which may influence long-term prognosis in children with HCV.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Case-Control Studies</subject><subject>CD4-Positive T-Lymphocytes - metabolism</subject><subject>CD8-Positive T-Lymphocytes - metabolism</subject><subject>Cells, Cultured</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Female</subject><subject>Flow Cytometry</subject><subject>Hepatitis C, Chronic - blood</subject><subject>Hepatitis C, Chronic - immunology</subject><subject>Humans</subject><subject>Interferon-gamma - metabolism</subject><subject>Interleukin-2 - metabolism</subject><subject>Lymphocyte Activation</subject><subject>Male</subject><subject>Pediatrics</subject><subject>Programmed Cell Death 1 Receptor - metabolism</subject><subject>Receptors, Immunologic - metabolism</subject><subject>T-Box Domain Proteins - metabolism</subject><issn>0022-3476</issn><issn>1097-6833</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU9v1DAQxS0EotvCJ0BCPiJVCZ74TzYSVKrSQpEq9UA5jxxnwjpkncXOLuq3J9stFXDpyYd5857n9xh7AyIHAeZ9n_cbalNeCNA5QC60fsYWIKoyM0spn7OFEEWRSVWaI3acUi-EqJQQL9lRYUolVVUu2If6Qp1yG1peXyxP-S2vaRj4uZv8zk5-DNwHXq_80EYK_JefVvyKNvNk8onXr9iLzg6JXj-8J-zbp8vb-iq7vvn8pT6_zpwGNWWuqNpOdNZUsik6tySlVdM5qah0xhA50KKCplOdtNCYonXKgSKlVCG1MEKesLOD72bbrKl1FKZoB9xEv7bxDkfr8d9J8Cv8Pu5QzRyU1rPBuweDOP7cUppw7ZObL7WBxm1CKE1lYClNOUvlQerimFKk7jEGBO65Y4_33HHPHQFQ3Ae8_fuHjzt_QM-CjwcBzZx2niIm5yk4an0kN2E7-icCzv7bd4MP3tnhB91R6sdtDHMFCJgKFPh1X_2--RktKFNq-RsOaqgZ</recordid><startdate>20160301</startdate><enddate>20160301</enddate><creator>Sheiko, Melissa A., MD</creator><creator>Golden-Mason, Lucy, PhD</creator><creator>Giugliano, Silvia, PhD</creator><creator>Hurtado, Christine Waasdorp, MD</creator><creator>Mack, Cara L., MD</creator><creator>Narkewicz, Michael R., MD</creator><creator>Rosen, Hugo R., MD</creator><general>Elsevier Inc</general><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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20160301</creationdate><title>CD4+ and CD8+ T Cell Activation in Children with Hepatitis C</title><author>Sheiko, Melissa A., MD ; Golden-Mason, Lucy, PhD ; Giugliano, Silvia, PhD ; Hurtado, Christine Waasdorp, MD ; Mack, Cara L., MD ; Narkewicz, Michael R., MD ; Rosen, Hugo R., MD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c514t-c29df0fa693b2fc8e454bfc34e7c66eec15091bf4f3a1b62dc4c14e4442350603</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Case-Control Studies</topic><topic>CD4-Positive T-Lymphocytes - metabolism</topic><topic>CD8-Positive T-Lymphocytes - metabolism</topic><topic>Cells, Cultured</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Female</topic><topic>Flow Cytometry</topic><topic>Hepatitis C, Chronic - blood</topic><topic>Hepatitis C, Chronic - immunology</topic><topic>Humans</topic><topic>Interferon-gamma - metabolism</topic><topic>Interleukin-2 - metabolism</topic><topic>Lymphocyte Activation</topic><topic>Male</topic><topic>Pediatrics</topic><topic>Programmed Cell Death 1 Receptor - metabolism</topic><topic>Receptors, Immunologic - metabolism</topic><topic>T-Box Domain Proteins - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sheiko, Melissa A., MD</creatorcontrib><creatorcontrib>Golden-Mason, Lucy, PhD</creatorcontrib><creatorcontrib>Giugliano, Silvia, PhD</creatorcontrib><creatorcontrib>Hurtado, Christine Waasdorp, MD</creatorcontrib><creatorcontrib>Mack, Cara L., MD</creatorcontrib><creatorcontrib>Narkewicz, Michael R., MD</creatorcontrib><creatorcontrib>Rosen, Hugo R., MD</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of pediatrics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sheiko, Melissa A., MD</au><au>Golden-Mason, Lucy, PhD</au><au>Giugliano, Silvia, PhD</au><au>Hurtado, Christine Waasdorp, MD</au><au>Mack, Cara L., MD</au><au>Narkewicz, Michael R., MD</au><au>Rosen, Hugo R., MD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>CD4+ and CD8+ T Cell Activation in Children with Hepatitis C</atitle><jtitle>The Journal of pediatrics</jtitle><addtitle>J Pediatr</addtitle><date>2016-03-01</date><risdate>2016</risdate><volume>170</volume><spage>142</spage><epage>148.e1</epage><pages>142-148.e1</pages><issn>0022-3476</issn><eissn>1097-6833</eissn><abstract>Objectives To assess if peripheral T cell populations in children with chronic hepatitis C virus (HCV) infection would show evidence of activation/exhaustion and an attenuated functional response. Study design Compared with adults, children with HCV infection have a higher rate of spontaneous viral clearance. In adults, chronic HCV has been linked to T cell exhaustion. Little is known of the immune status of children with HCV. Peripheral blood mononuclear cells were isolated from 16 children with HCV (6 males, 10 females; mean age 8.6 years, range 2-17), 16 age- and sex-matched control children without HCV infection, and 20 adults with chronic HCV. Multiparameter flow cytometry was performed to characterize T cell differences across the 3 groups. Results Controls and children with HCV had similar levels of CD4+ , CD8+ , and γδ+ T cells. Children with HCV demonstrated a decrease in naïve T cells compared with control children and increased activation/exhaustion marker expression on both CD8+ and CD4+ T cells. Transcription factor analysis suggested functional activation of T cells in children with HCV; however, only the CD4+ subset had enhanced cytokine production (interferon gamma and interleukin-2) compared with control children. Conclusions The HCV response in children is characterized by several changes in T cell phenotype. Many of these changes, such as increased T cell expression of programmed cell death-1, are similar to responses in adults. Of note, cytokine production by CD4+ helper T cells is increased in children with HCV compared with age- and sex-matched control children, which may influence long-term prognosis in children with HCV.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>26743497</pmid><doi>10.1016/j.jpeds.2015.11.055</doi><oa>free_for_read</oa></addata></record>
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subjects Adolescent
Adult
Case-Control Studies
CD4-Positive T-Lymphocytes - metabolism
CD8-Positive T-Lymphocytes - metabolism
Cells, Cultured
Child
Child, Preschool
Female
Flow Cytometry
Hepatitis C, Chronic - blood
Hepatitis C, Chronic - immunology
Humans
Interferon-gamma - metabolism
Interleukin-2 - metabolism
Lymphocyte Activation
Male
Pediatrics
Programmed Cell Death 1 Receptor - metabolism
Receptors, Immunologic - metabolism
T-Box Domain Proteins - metabolism
title CD4+ and CD8+ T Cell Activation in Children with Hepatitis C
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