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Treg/Th17 imbalance and its clinical significance in patients with hepatitis B-associated liver cirrhosis

BACKGROUND: Recent studies have shown that T cell-mediated cellular immune mechanisms play important roles in the progression of hepatitis B to liver cirrhosis, but the underlying mechanisms remain unclear. This present study was aimed to determine the relationship between Treg/Th17 and hepatitis B-...

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Autores principales: Lan, Yong-Ting, Wang, Zhen-li, Tian, Peng, Gong, Xiao-Na, Fan, Yu-Chen, Wang, Kai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6805395/
https://www.ncbi.nlm.nih.gov/pubmed/31639000
http://dx.doi.org/10.1186/s13000-019-0891-4
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author Lan, Yong-Ting
Wang, Zhen-li
Tian, Peng
Gong, Xiao-Na
Fan, Yu-Chen
Wang, Kai
author_facet Lan, Yong-Ting
Wang, Zhen-li
Tian, Peng
Gong, Xiao-Na
Fan, Yu-Chen
Wang, Kai
author_sort Lan, Yong-Ting
collection PubMed
description BACKGROUND: Recent studies have shown that T cell-mediated cellular immune mechanisms play important roles in the progression of hepatitis B to liver cirrhosis, but the underlying mechanisms remain unclear. This present study was aimed to determine the relationship between Treg/Th17 and hepatitis B-associated liver cirrhosis. METHODS: The Treg and Th17 cell frequencies in the peripheral blood of all participants, including 93 patients with hepatitis B-associated liver cirrhosis and 40 healthy subjects, were measured by flow cytometer. Cox regression model and receiver operating characteristic(ROC) curves were applied to investigate the prognostic significance of Treg/Th17 ratio in decompensated liver cirrhosis. RESULTS: We observed the Treg/Th17 imbalance was present in patients with hepatitis B-associated liver cirrhosis, with reduced Treg cells in their peripheral blood, increased Th17 cells and decreased Treg/Th17 ratio. Treg and Th17 cells were negatively correlated. Treg/Th17 imbalance was closely related to the clinical stage of hepatitis B-associated liver cirrhosis. The Virus load, Treg frequencies and the Treg/Th17 ratio were independent factors predicting decompensated liver cirrhosis from a Cox regression model. The ROC analysis showed that the Treg/Th17 ratio was the best marker for predicting decompensated liver cirrhosis. CONCLUSIONS: Treg/Th17 imbalance is involved in the pathogenesis of hepatitis B-associated liver cirrhosis and the Treg/Th17 ratio can be used as a potential marker for predicting decompensated liver cirrhosis.
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spelling pubmed-68053952019-10-24 Treg/Th17 imbalance and its clinical significance in patients with hepatitis B-associated liver cirrhosis Lan, Yong-Ting Wang, Zhen-li Tian, Peng Gong, Xiao-Na Fan, Yu-Chen Wang, Kai Diagn Pathol Research BACKGROUND: Recent studies have shown that T cell-mediated cellular immune mechanisms play important roles in the progression of hepatitis B to liver cirrhosis, but the underlying mechanisms remain unclear. This present study was aimed to determine the relationship between Treg/Th17 and hepatitis B-associated liver cirrhosis. METHODS: The Treg and Th17 cell frequencies in the peripheral blood of all participants, including 93 patients with hepatitis B-associated liver cirrhosis and 40 healthy subjects, were measured by flow cytometer. Cox regression model and receiver operating characteristic(ROC) curves were applied to investigate the prognostic significance of Treg/Th17 ratio in decompensated liver cirrhosis. RESULTS: We observed the Treg/Th17 imbalance was present in patients with hepatitis B-associated liver cirrhosis, with reduced Treg cells in their peripheral blood, increased Th17 cells and decreased Treg/Th17 ratio. Treg and Th17 cells were negatively correlated. Treg/Th17 imbalance was closely related to the clinical stage of hepatitis B-associated liver cirrhosis. The Virus load, Treg frequencies and the Treg/Th17 ratio were independent factors predicting decompensated liver cirrhosis from a Cox regression model. The ROC analysis showed that the Treg/Th17 ratio was the best marker for predicting decompensated liver cirrhosis. CONCLUSIONS: Treg/Th17 imbalance is involved in the pathogenesis of hepatitis B-associated liver cirrhosis and the Treg/Th17 ratio can be used as a potential marker for predicting decompensated liver cirrhosis. BioMed Central 2019-10-21 /pmc/articles/PMC6805395/ /pubmed/31639000 http://dx.doi.org/10.1186/s13000-019-0891-4 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Lan, Yong-Ting
Wang, Zhen-li
Tian, Peng
Gong, Xiao-Na
Fan, Yu-Chen
Wang, Kai
Treg/Th17 imbalance and its clinical significance in patients with hepatitis B-associated liver cirrhosis
title Treg/Th17 imbalance and its clinical significance in patients with hepatitis B-associated liver cirrhosis
title_full Treg/Th17 imbalance and its clinical significance in patients with hepatitis B-associated liver cirrhosis
title_fullStr Treg/Th17 imbalance and its clinical significance in patients with hepatitis B-associated liver cirrhosis
title_full_unstemmed Treg/Th17 imbalance and its clinical significance in patients with hepatitis B-associated liver cirrhosis
title_short Treg/Th17 imbalance and its clinical significance in patients with hepatitis B-associated liver cirrhosis
title_sort treg/th17 imbalance and its clinical significance in patients with hepatitis b-associated liver cirrhosis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6805395/
https://www.ncbi.nlm.nih.gov/pubmed/31639000
http://dx.doi.org/10.1186/s13000-019-0891-4
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