Different core-specific T cell subsets are expanded in chronic hepatitis C with advanced liver disease
•IL-17+IL-6+ T-cells are elevated in HCV patients with advanced liver stiffness.•Lower percentage of CD39+ Tregs in HCV patients with advanced liver stiffness.•HCV-specific PD-1+ CD57+ T cells accumulate in patients with worse hepatic lesions. Chronic hepatitis C (CHC) is frequently related to liver...
Gespeichert in:
Veröffentlicht in: | Cytokine (Philadelphia, Pa.) Pa.), 2019-12, Vol.124, p.154456-154456, Article 154456 |
---|---|
Hauptverfasser: | , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 154456 |
---|---|
container_issue | |
container_start_page | 154456 |
container_title | Cytokine (Philadelphia, Pa.) |
container_volume | 124 |
creator | Cachem, Fabio C.O.F. Dias, Aleida S. Monteiro, Clarice Fernandes, Gabriel Delphim, Letícia Tavares, Felipe Maciel, Alessandra M.A. Amendola-Pires, Marcia M. Brandão-Mello, Carlos Eduardo Andrade, Regis Mariano Bento, Cleonice A.M. |
description | •IL-17+IL-6+ T-cells are elevated in HCV patients with advanced liver stiffness.•Lower percentage of CD39+ Tregs in HCV patients with advanced liver stiffness.•HCV-specific PD-1+ CD57+ T cells accumulate in patients with worse hepatic lesions.
Chronic hepatitis C (CHC) is frequently related to liver fibrosis, and several studies have suggested that the immunological activity of HCV antigens contributes to hepatic damage. In the present study, among structural and non-structural HCV antigens, elevatedIL-1β, IL-6, IL-17 levels were secreted by PBMC cultures obtained from CHC patients following stimulation with core antigen. Moreover, the percentage of core-specific IL-6+IL-17+(CD4+ and CD8+) T cells was significantly higher in patients with worsehepatic lesions, determined on the Metavir scale. When compared with healthy subjects, the percentage of circulating Treg cells was elevated in CHC patients, mainly among those with advanced liver fibrosis. Nevertheless, in this last group of patients, the proportion of CD39+ Treg subsets was very low. Finally, the percentage of senescent (CD57+ CD28−) and exhausted (PD-1+CD28+) core-specific T cells in CHC patients was also found to be a result of fibrotic hepatic status. In summary, imbalances between different core-specific T cell subsets are associated with liver fibrosis severity. |
doi_str_mv | 10.1016/j.cyto.2018.06.023 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2307394295</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1043466618302722</els_id><sourcerecordid>2307394295</sourcerecordid><originalsourceid>FETCH-LOGICAL-c356t-6ac3eafe8d46a9d481e19c9eeb455563a3477ea048599c0ce5cabfc520ed67023</originalsourceid><addsrcrecordid>eNp9kDtPwzAUhS0E4v0HGJBHlgQ7TpxYYkHlKVViKbPlXt-ortok2G6Bf4-jFkame4fvHOl8hFxxlnPG5e0yh-_Y5wXjTc5kzgpxQE45UzJj6T8c_1JkpZTyhJyFsGSMKVHXx-REcCl4I4tT0j64tkWPXaTQe8zCgOBaB3RGAVcrGjbzgDFQ45Hi12A6i5a6jsLC913CFjiY6KILdEI_XVxQY7emgwSt3BY9tS6gCXhBjlqzCni5v-fk_elxNnnJpm_Pr5P7aQaikjGTBgSaFhtbSqNs2XDkChTivKyqSgojyrpGw8qmUgoYYAVm3kJVMLSyTqPPyc2ud_D9xwZD1GsXxiGmw34TdCFYLVRZqCqhxQ4F34fgsdWDd2vjvzVnevSrl3r0q0e_mkmd6lPoet-_ma_R_kV-hSbgbgdgWrl16HUAh6MQ5xGitr37r_8HY1qNTw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2307394295</pqid></control><display><type>article</type><title>Different core-specific T cell subsets are expanded in chronic hepatitis C with advanced liver disease</title><source>Elsevier ScienceDirect Journals</source><creator>Cachem, Fabio C.O.F. ; Dias, Aleida S. ; Monteiro, Clarice ; Fernandes, Gabriel ; Delphim, Letícia ; Tavares, Felipe ; Maciel, Alessandra M.A. ; Amendola-Pires, Marcia M. ; Brandão-Mello, Carlos Eduardo ; Andrade, Regis Mariano ; Bento, Cleonice A.M.</creator><creatorcontrib>Cachem, Fabio C.O.F. ; Dias, Aleida S. ; Monteiro, Clarice ; Fernandes, Gabriel ; Delphim, Letícia ; Tavares, Felipe ; Maciel, Alessandra M.A. ; Amendola-Pires, Marcia M. ; Brandão-Mello, Carlos Eduardo ; Andrade, Regis Mariano ; Bento, Cleonice A.M.</creatorcontrib><description>•IL-17+IL-6+ T-cells are elevated in HCV patients with advanced liver stiffness.•Lower percentage of CD39+ Tregs in HCV patients with advanced liver stiffness.•HCV-specific PD-1+ CD57+ T cells accumulate in patients with worse hepatic lesions.
Chronic hepatitis C (CHC) is frequently related to liver fibrosis, and several studies have suggested that the immunological activity of HCV antigens contributes to hepatic damage. In the present study, among structural and non-structural HCV antigens, elevatedIL-1β, IL-6, IL-17 levels were secreted by PBMC cultures obtained from CHC patients following stimulation with core antigen. Moreover, the percentage of core-specific IL-6+IL-17+(CD4+ and CD8+) T cells was significantly higher in patients with worsehepatic lesions, determined on the Metavir scale. When compared with healthy subjects, the percentage of circulating Treg cells was elevated in CHC patients, mainly among those with advanced liver fibrosis. Nevertheless, in this last group of patients, the proportion of CD39+ Treg subsets was very low. Finally, the percentage of senescent (CD57+ CD28−) and exhausted (PD-1+CD28+) core-specific T cells in CHC patients was also found to be a result of fibrotic hepatic status. In summary, imbalances between different core-specific T cell subsets are associated with liver fibrosis severity.</description><identifier>ISSN: 1043-4666</identifier><identifier>EISSN: 1096-0023</identifier><identifier>DOI: 10.1016/j.cyto.2018.06.023</identifier><identifier>PMID: 31631862</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>HCV ; IL-17 ; IL-6 ; T cells</subject><ispartof>Cytokine (Philadelphia, Pa.), 2019-12, Vol.124, p.154456-154456, Article 154456</ispartof><rights>2018 Elsevier Ltd</rights><rights>Copyright © 2018 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c356t-6ac3eafe8d46a9d481e19c9eeb455563a3477ea048599c0ce5cabfc520ed67023</citedby><cites>FETCH-LOGICAL-c356t-6ac3eafe8d46a9d481e19c9eeb455563a3477ea048599c0ce5cabfc520ed67023</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1043466618302722$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31631862$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cachem, Fabio C.O.F.</creatorcontrib><creatorcontrib>Dias, Aleida S.</creatorcontrib><creatorcontrib>Monteiro, Clarice</creatorcontrib><creatorcontrib>Fernandes, Gabriel</creatorcontrib><creatorcontrib>Delphim, Letícia</creatorcontrib><creatorcontrib>Tavares, Felipe</creatorcontrib><creatorcontrib>Maciel, Alessandra M.A.</creatorcontrib><creatorcontrib>Amendola-Pires, Marcia M.</creatorcontrib><creatorcontrib>Brandão-Mello, Carlos Eduardo</creatorcontrib><creatorcontrib>Andrade, Regis Mariano</creatorcontrib><creatorcontrib>Bento, Cleonice A.M.</creatorcontrib><title>Different core-specific T cell subsets are expanded in chronic hepatitis C with advanced liver disease</title><title>Cytokine (Philadelphia, Pa.)</title><addtitle>Cytokine</addtitle><description>•IL-17+IL-6+ T-cells are elevated in HCV patients with advanced liver stiffness.•Lower percentage of CD39+ Tregs in HCV patients with advanced liver stiffness.•HCV-specific PD-1+ CD57+ T cells accumulate in patients with worse hepatic lesions.
Chronic hepatitis C (CHC) is frequently related to liver fibrosis, and several studies have suggested that the immunological activity of HCV antigens contributes to hepatic damage. In the present study, among structural and non-structural HCV antigens, elevatedIL-1β, IL-6, IL-17 levels were secreted by PBMC cultures obtained from CHC patients following stimulation with core antigen. Moreover, the percentage of core-specific IL-6+IL-17+(CD4+ and CD8+) T cells was significantly higher in patients with worsehepatic lesions, determined on the Metavir scale. When compared with healthy subjects, the percentage of circulating Treg cells was elevated in CHC patients, mainly among those with advanced liver fibrosis. Nevertheless, in this last group of patients, the proportion of CD39+ Treg subsets was very low. Finally, the percentage of senescent (CD57+ CD28−) and exhausted (PD-1+CD28+) core-specific T cells in CHC patients was also found to be a result of fibrotic hepatic status. In summary, imbalances between different core-specific T cell subsets are associated with liver fibrosis severity.</description><subject>HCV</subject><subject>IL-17</subject><subject>IL-6</subject><subject>T cells</subject><issn>1043-4666</issn><issn>1096-0023</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9kDtPwzAUhS0E4v0HGJBHlgQ7TpxYYkHlKVViKbPlXt-ortok2G6Bf4-jFkame4fvHOl8hFxxlnPG5e0yh-_Y5wXjTc5kzgpxQE45UzJj6T8c_1JkpZTyhJyFsGSMKVHXx-REcCl4I4tT0j64tkWPXaTQe8zCgOBaB3RGAVcrGjbzgDFQ45Hi12A6i5a6jsLC913CFjiY6KILdEI_XVxQY7emgwSt3BY9tS6gCXhBjlqzCni5v-fk_elxNnnJpm_Pr5P7aQaikjGTBgSaFhtbSqNs2XDkChTivKyqSgojyrpGw8qmUgoYYAVm3kJVMLSyTqPPyc2ud_D9xwZD1GsXxiGmw34TdCFYLVRZqCqhxQ4F34fgsdWDd2vjvzVnevSrl3r0q0e_mkmd6lPoet-_ma_R_kV-hSbgbgdgWrl16HUAh6MQ5xGitr37r_8HY1qNTw</recordid><startdate>201912</startdate><enddate>201912</enddate><creator>Cachem, Fabio C.O.F.</creator><creator>Dias, Aleida S.</creator><creator>Monteiro, Clarice</creator><creator>Fernandes, Gabriel</creator><creator>Delphim, Letícia</creator><creator>Tavares, Felipe</creator><creator>Maciel, Alessandra M.A.</creator><creator>Amendola-Pires, Marcia M.</creator><creator>Brandão-Mello, Carlos Eduardo</creator><creator>Andrade, Regis Mariano</creator><creator>Bento, Cleonice A.M.</creator><general>Elsevier Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201912</creationdate><title>Different core-specific T cell subsets are expanded in chronic hepatitis C with advanced liver disease</title><author>Cachem, Fabio C.O.F. ; Dias, Aleida S. ; Monteiro, Clarice ; Fernandes, Gabriel ; Delphim, Letícia ; Tavares, Felipe ; Maciel, Alessandra M.A. ; Amendola-Pires, Marcia M. ; Brandão-Mello, Carlos Eduardo ; Andrade, Regis Mariano ; Bento, Cleonice A.M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-6ac3eafe8d46a9d481e19c9eeb455563a3477ea048599c0ce5cabfc520ed67023</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>HCV</topic><topic>IL-17</topic><topic>IL-6</topic><topic>T cells</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cachem, Fabio C.O.F.</creatorcontrib><creatorcontrib>Dias, Aleida S.</creatorcontrib><creatorcontrib>Monteiro, Clarice</creatorcontrib><creatorcontrib>Fernandes, Gabriel</creatorcontrib><creatorcontrib>Delphim, Letícia</creatorcontrib><creatorcontrib>Tavares, Felipe</creatorcontrib><creatorcontrib>Maciel, Alessandra M.A.</creatorcontrib><creatorcontrib>Amendola-Pires, Marcia M.</creatorcontrib><creatorcontrib>Brandão-Mello, Carlos Eduardo</creatorcontrib><creatorcontrib>Andrade, Regis Mariano</creatorcontrib><creatorcontrib>Bento, Cleonice A.M.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Cytokine (Philadelphia, Pa.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cachem, Fabio C.O.F.</au><au>Dias, Aleida S.</au><au>Monteiro, Clarice</au><au>Fernandes, Gabriel</au><au>Delphim, Letícia</au><au>Tavares, Felipe</au><au>Maciel, Alessandra M.A.</au><au>Amendola-Pires, Marcia M.</au><au>Brandão-Mello, Carlos Eduardo</au><au>Andrade, Regis Mariano</au><au>Bento, Cleonice A.M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Different core-specific T cell subsets are expanded in chronic hepatitis C with advanced liver disease</atitle><jtitle>Cytokine (Philadelphia, Pa.)</jtitle><addtitle>Cytokine</addtitle><date>2019-12</date><risdate>2019</risdate><volume>124</volume><spage>154456</spage><epage>154456</epage><pages>154456-154456</pages><artnum>154456</artnum><issn>1043-4666</issn><eissn>1096-0023</eissn><abstract>•IL-17+IL-6+ T-cells are elevated in HCV patients with advanced liver stiffness.•Lower percentage of CD39+ Tregs in HCV patients with advanced liver stiffness.•HCV-specific PD-1+ CD57+ T cells accumulate in patients with worse hepatic lesions.
Chronic hepatitis C (CHC) is frequently related to liver fibrosis, and several studies have suggested that the immunological activity of HCV antigens contributes to hepatic damage. In the present study, among structural and non-structural HCV antigens, elevatedIL-1β, IL-6, IL-17 levels were secreted by PBMC cultures obtained from CHC patients following stimulation with core antigen. Moreover, the percentage of core-specific IL-6+IL-17+(CD4+ and CD8+) T cells was significantly higher in patients with worsehepatic lesions, determined on the Metavir scale. When compared with healthy subjects, the percentage of circulating Treg cells was elevated in CHC patients, mainly among those with advanced liver fibrosis. Nevertheless, in this last group of patients, the proportion of CD39+ Treg subsets was very low. Finally, the percentage of senescent (CD57+ CD28−) and exhausted (PD-1+CD28+) core-specific T cells in CHC patients was also found to be a result of fibrotic hepatic status. In summary, imbalances between different core-specific T cell subsets are associated with liver fibrosis severity.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>31631862</pmid><doi>10.1016/j.cyto.2018.06.023</doi><tpages>1</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1043-4666 |
ispartof | Cytokine (Philadelphia, Pa.), 2019-12, Vol.124, p.154456-154456, Article 154456 |
issn | 1043-4666 1096-0023 |
language | eng |
recordid | cdi_proquest_miscellaneous_2307394295 |
source | Elsevier ScienceDirect Journals |
subjects | HCV IL-17 IL-6 T cells |
title | Different core-specific T cell subsets are expanded in chronic hepatitis C with advanced liver disease |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-05T10%3A51%3A42IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Different%20core-specific%20T%20cell%20subsets%20are%20expanded%20in%20chronic%20hepatitis%20C%20with%20advanced%20liver%20disease&rft.jtitle=Cytokine%20(Philadelphia,%20Pa.)&rft.au=Cachem,%20Fabio%20C.O.F.&rft.date=2019-12&rft.volume=124&rft.spage=154456&rft.epage=154456&rft.pages=154456-154456&rft.artnum=154456&rft.issn=1043-4666&rft.eissn=1096-0023&rft_id=info:doi/10.1016/j.cyto.2018.06.023&rft_dat=%3Cproquest_cross%3E2307394295%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2307394295&rft_id=info:pmid/31631862&rft_els_id=S1043466618302722&rfr_iscdi=true |