Prognostic Significance of the Systemic Inflammatory and Immune Balance in Alcoholic Liver Disease with a Focus on Gender-Related Differences
Mechanisms of immune regulation in alcoholic liver disease (ALD) are still unclear. The aim of our study was to determine an impact of Th17 / regulatory T (Treg) cells balance and its corresponding cytokine profile on the ALD outcome. Possible gender-related differences in the alcohol-induced inflam...
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creator | Kasztelan-Szczerbińska, Beata Surdacka, Agata Celiński, Krzysztof Roliński, Jacek Zwolak, Agnieszka Miącz, Sławomir Szczerbiński, Mariusz |
description | Mechanisms of immune regulation in alcoholic liver disease (ALD) are still unclear. The aim of our study was to determine an impact of Th17 / regulatory T (Treg) cells balance and its corresponding cytokine profile on the ALD outcome. Possible gender-related differences in the alcohol-induced inflammatory response were also assessed.
147 patients with ALD were prospectively recruited, assigned to subgroups based on their gender, severity of liver dysfunction and presence of ALD complications at admission, and followed for 90 days. Peripheral blood frequencies of Th17 and Treg cells together with IL-1beta, IL-6, IL-17A, IL-23, and TGF-beta1 levels were investigated. Flow cytometry was used to identify T cell phenotype and immunoenzymatic ELISAs for the corresponding cytokine concentrations assessment. Multivariable logistic regression was applied in order to select independent predictors of advanced liver dysfunction and the disease complications.
IL-17A, IL-1beta, IL-6 levels were significantly increased, while TGF-beta1 decreased in ALD patients. The imbalance with significantly higher Th17 and lower Treg frequencies was observed in non-survivors. IL-6 and TGF-beta1 levels differed in relation to patient gender in ALD group. Concentrations of IL-6 were associated with the severity of liver dysfunction, development of ALD complications, and turned out to be the only independent immune predictor of 90-day survival in the study cohort.
We conclude that IL-6 revealed the highest diagnostic and prognostic potential among studied biomarkers and was related to the fatal ALD course. Gender-related differences in immune regulation might influence the susceptibility to alcohol-associated liver injury. |
doi_str_mv | 10.1371/journal.pone.0128347 |
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147 patients with ALD were prospectively recruited, assigned to subgroups based on their gender, severity of liver dysfunction and presence of ALD complications at admission, and followed for 90 days. Peripheral blood frequencies of Th17 and Treg cells together with IL-1beta, IL-6, IL-17A, IL-23, and TGF-beta1 levels were investigated. Flow cytometry was used to identify T cell phenotype and immunoenzymatic ELISAs for the corresponding cytokine concentrations assessment. Multivariable logistic regression was applied in order to select independent predictors of advanced liver dysfunction and the disease complications.
IL-17A, IL-1beta, IL-6 levels were significantly increased, while TGF-beta1 decreased in ALD patients. The imbalance with significantly higher Th17 and lower Treg frequencies was observed in non-survivors. IL-6 and TGF-beta1 levels differed in relation to patient gender in ALD group. Concentrations of IL-6 were associated with the severity of liver dysfunction, development of ALD complications, and turned out to be the only independent immune predictor of 90-day survival in the study cohort.
We conclude that IL-6 revealed the highest diagnostic and prognostic potential among studied biomarkers and was related to the fatal ALD course. Gender-related differences in immune regulation might influence the susceptibility to alcohol-associated liver injury.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0128347</identifier><identifier>PMID: 26107937</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Alcohol use ; Alcoholism ; Alcohols ; Bioindicators ; Biomarkers ; Complications ; Cytokines ; Cytokines - blood ; Cytometry ; Diagnostic systems ; Endoscopy ; Ethanol ; Female ; Flow cytometry ; Gastroenterology ; Gender ; Helper cells ; Hepatitis ; Hepatology ; Humans ; Immunology ; Immunoregulation ; Inflammation ; Inflammation - blood ; Inflammation - immunology ; Inflammation - pathology ; Inflammatory response ; Interleukin 1 ; Interleukin 23 ; Interleukin 6 ; Interleukin-6 - blood ; Interleukin-6 - immunology ; Laboratories ; Liver ; Liver - immunology ; Liver - pathology ; Liver diseases ; Liver Diseases, Alcoholic - blood ; Liver Diseases, Alcoholic - immunology ; Liver Diseases, Alcoholic - pathology ; Lymphocytes T ; Male ; Middle Aged ; Patients ; Peripheral blood ; Phenotypes ; Prognosis ; Rodents ; Sex Characteristics ; Sex differences ; Subgroups ; Systematic review ; T-Lymphocytes, Regulatory - immunology ; T-Lymphocytes, Regulatory - pathology ; Th17 Cells - immunology ; Th17 Cells - pathology ; Transforming growth factor-b ; Women</subject><ispartof>PloS one, 2015-06, Vol.10 (6), p.e0128347-e0128347</ispartof><rights>2015 Kasztelan-Szczerbińska et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2015 Kasztelan-Szczerbińska et al 2015 Kasztelan-Szczerbińska et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c526t-e056072d98266a570087753a52bd8efc64513bdfa041ddedb05792aebf5146333</citedby><cites>FETCH-LOGICAL-c526t-e056072d98266a570087753a52bd8efc64513bdfa041ddedb05792aebf5146333</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4480424/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4480424/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2102,2928,23866,27924,27925,53791,53793,79600,79601</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26107937$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Ahlenstiel, Golo</contributor><creatorcontrib>Kasztelan-Szczerbińska, Beata</creatorcontrib><creatorcontrib>Surdacka, Agata</creatorcontrib><creatorcontrib>Celiński, Krzysztof</creatorcontrib><creatorcontrib>Roliński, Jacek</creatorcontrib><creatorcontrib>Zwolak, Agnieszka</creatorcontrib><creatorcontrib>Miącz, Sławomir</creatorcontrib><creatorcontrib>Szczerbiński, Mariusz</creatorcontrib><title>Prognostic Significance of the Systemic Inflammatory and Immune Balance in Alcoholic Liver Disease with a Focus on Gender-Related Differences</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Mechanisms of immune regulation in alcoholic liver disease (ALD) are still unclear. The aim of our study was to determine an impact of Th17 / regulatory T (Treg) cells balance and its corresponding cytokine profile on the ALD outcome. Possible gender-related differences in the alcohol-induced inflammatory response were also assessed.
147 patients with ALD were prospectively recruited, assigned to subgroups based on their gender, severity of liver dysfunction and presence of ALD complications at admission, and followed for 90 days. Peripheral blood frequencies of Th17 and Treg cells together with IL-1beta, IL-6, IL-17A, IL-23, and TGF-beta1 levels were investigated. Flow cytometry was used to identify T cell phenotype and immunoenzymatic ELISAs for the corresponding cytokine concentrations assessment. Multivariable logistic regression was applied in order to select independent predictors of advanced liver dysfunction and the disease complications.
IL-17A, IL-1beta, IL-6 levels were significantly increased, while TGF-beta1 decreased in ALD patients. The imbalance with significantly higher Th17 and lower Treg frequencies was observed in non-survivors. IL-6 and TGF-beta1 levels differed in relation to patient gender in ALD group. Concentrations of IL-6 were associated with the severity of liver dysfunction, development of ALD complications, and turned out to be the only independent immune predictor of 90-day survival in the study cohort.
We conclude that IL-6 revealed the highest diagnostic and prognostic potential among studied biomarkers and was related to the fatal ALD course. Gender-related differences in immune regulation might influence the susceptibility to alcohol-associated liver injury.</description><subject>Alcohol use</subject><subject>Alcoholism</subject><subject>Alcohols</subject><subject>Bioindicators</subject><subject>Biomarkers</subject><subject>Complications</subject><subject>Cytokines</subject><subject>Cytokines - blood</subject><subject>Cytometry</subject><subject>Diagnostic systems</subject><subject>Endoscopy</subject><subject>Ethanol</subject><subject>Female</subject><subject>Flow cytometry</subject><subject>Gastroenterology</subject><subject>Gender</subject><subject>Helper cells</subject><subject>Hepatitis</subject><subject>Hepatology</subject><subject>Humans</subject><subject>Immunology</subject><subject>Immunoregulation</subject><subject>Inflammation</subject><subject>Inflammation - blood</subject><subject>Inflammation - immunology</subject><subject>Inflammation - pathology</subject><subject>Inflammatory response</subject><subject>Interleukin 1</subject><subject>Interleukin 23</subject><subject>Interleukin 6</subject><subject>Interleukin-6 - blood</subject><subject>Interleukin-6 - immunology</subject><subject>Laboratories</subject><subject>Liver</subject><subject>Liver - immunology</subject><subject>Liver - pathology</subject><subject>Liver diseases</subject><subject>Liver Diseases, Alcoholic - blood</subject><subject>Liver Diseases, Alcoholic - immunology</subject><subject>Liver Diseases, Alcoholic - pathology</subject><subject>Lymphocytes T</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Patients</subject><subject>Peripheral blood</subject><subject>Phenotypes</subject><subject>Prognosis</subject><subject>Rodents</subject><subject>Sex Characteristics</subject><subject>Sex differences</subject><subject>Subgroups</subject><subject>Systematic review</subject><subject>T-Lymphocytes, Regulatory - immunology</subject><subject>T-Lymphocytes, Regulatory - pathology</subject><subject>Th17 Cells - immunology</subject><subject>Th17 Cells - pathology</subject><subject>Transforming growth factor-b</subject><subject>Women</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>DOA</sourceid><recordid>eNptkt1uEzEQhVcIREvhDRBY4oabBP_v7g1SKbREigSicG157dnEkddu7d2iPATvjNOkVYu4suX55vjM6FTVa4LnhNXkwyZOKWg_v4oB5pjQhvH6SXVMWkZnkmL29MH9qHqR8wZjwRopn1dHVBJct6w-rv58T3EVYh6dQZduFVzvjA4GUOzRuAZ0uc0jDKW4CL3Xw6DHmLZIB4sWwzAFQJ-0v-VdQKfexHX0BV66G0jos8ugM6Dfblwjjc6jmTKKAV1AsJBmP8DrEWzB-h4SFJH8snrWa5_h1eE8qX6df_l59nW2_HaxODtdzoygcpwBFhLX1LYNlVKLGuOmrgXTgna2gd5ILgjrbK8xJ9aC7bCoW6qh6wXhkjF2Ur3d6175mNVhk1kR2RLMizgvxGJP2Kg36iq5Qaetitqp24eYVkqnsjQPClvathZLZoDwBhvdtUTYput5bZjBXdH6ePht6gawBsKYtH8k-rgS3Fqt4o3iRY7TnZn3B4EUryfIoxpcNuDL5iFOe9-i5YSJgr77B_3_dHxPmRRzTtDfmyFY7dJ116V26VKHdJW2Nw8HuW-6ixP7C9iDzuo</recordid><startdate>20150624</startdate><enddate>20150624</enddate><creator>Kasztelan-Szczerbińska, Beata</creator><creator>Surdacka, Agata</creator><creator>Celiński, Krzysztof</creator><creator>Roliński, Jacek</creator><creator>Zwolak, Agnieszka</creator><creator>Miącz, Sławomir</creator><creator>Szczerbiński, Mariusz</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20150624</creationdate><title>Prognostic Significance of the Systemic Inflammatory and Immune Balance in Alcoholic Liver Disease with a Focus on Gender-Related Differences</title><author>Kasztelan-Szczerbińska, Beata ; Surdacka, Agata ; Celiński, Krzysztof ; Roliński, Jacek ; Zwolak, Agnieszka ; Miącz, Sławomir ; Szczerbiński, Mariusz</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c526t-e056072d98266a570087753a52bd8efc64513bdfa041ddedb05792aebf5146333</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Alcohol use</topic><topic>Alcoholism</topic><topic>Alcohols</topic><topic>Bioindicators</topic><topic>Biomarkers</topic><topic>Complications</topic><topic>Cytokines</topic><topic>Cytokines - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kasztelan-Szczerbińska, Beata</au><au>Surdacka, Agata</au><au>Celiński, Krzysztof</au><au>Roliński, Jacek</au><au>Zwolak, Agnieszka</au><au>Miącz, Sławomir</au><au>Szczerbiński, Mariusz</au><au>Ahlenstiel, Golo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prognostic Significance of the Systemic Inflammatory and Immune Balance in Alcoholic Liver Disease with a Focus on Gender-Related Differences</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2015-06-24</date><risdate>2015</risdate><volume>10</volume><issue>6</issue><spage>e0128347</spage><epage>e0128347</epage><pages>e0128347-e0128347</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Mechanisms of immune regulation in alcoholic liver disease (ALD) are still unclear. The aim of our study was to determine an impact of Th17 / regulatory T (Treg) cells balance and its corresponding cytokine profile on the ALD outcome. Possible gender-related differences in the alcohol-induced inflammatory response were also assessed.
147 patients with ALD were prospectively recruited, assigned to subgroups based on their gender, severity of liver dysfunction and presence of ALD complications at admission, and followed for 90 days. Peripheral blood frequencies of Th17 and Treg cells together with IL-1beta, IL-6, IL-17A, IL-23, and TGF-beta1 levels were investigated. Flow cytometry was used to identify T cell phenotype and immunoenzymatic ELISAs for the corresponding cytokine concentrations assessment. Multivariable logistic regression was applied in order to select independent predictors of advanced liver dysfunction and the disease complications.
IL-17A, IL-1beta, IL-6 levels were significantly increased, while TGF-beta1 decreased in ALD patients. The imbalance with significantly higher Th17 and lower Treg frequencies was observed in non-survivors. IL-6 and TGF-beta1 levels differed in relation to patient gender in ALD group. Concentrations of IL-6 were associated with the severity of liver dysfunction, development of ALD complications, and turned out to be the only independent immune predictor of 90-day survival in the study cohort.
We conclude that IL-6 revealed the highest diagnostic and prognostic potential among studied biomarkers and was related to the fatal ALD course. Gender-related differences in immune regulation might influence the susceptibility to alcohol-associated liver injury.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>26107937</pmid><doi>10.1371/journal.pone.0128347</doi><oa>free_for_read</oa></addata></record> |
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subjects | Alcohol use Alcoholism Alcohols Bioindicators Biomarkers Complications Cytokines Cytokines - blood Cytometry Diagnostic systems Endoscopy Ethanol Female Flow cytometry Gastroenterology Gender Helper cells Hepatitis Hepatology Humans Immunology Immunoregulation Inflammation Inflammation - blood Inflammation - immunology Inflammation - pathology Inflammatory response Interleukin 1 Interleukin 23 Interleukin 6 Interleukin-6 - blood Interleukin-6 - immunology Laboratories Liver Liver - immunology Liver - pathology Liver diseases Liver Diseases, Alcoholic - blood Liver Diseases, Alcoholic - immunology Liver Diseases, Alcoholic - pathology Lymphocytes T Male Middle Aged Patients Peripheral blood Phenotypes Prognosis Rodents Sex Characteristics Sex differences Subgroups Systematic review T-Lymphocytes, Regulatory - immunology T-Lymphocytes, Regulatory - pathology Th17 Cells - immunology Th17 Cells - pathology Transforming growth factor-b Women |
title | Prognostic Significance of the Systemic Inflammatory and Immune Balance in Alcoholic Liver Disease with a Focus on Gender-Related Differences |
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