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Changes in cellular proliferation and plasma products are associated with liver failure
AIM: To study the differences in immune response and cytokine profile between acute liver failure and self-limited acute hepatitis. METHODS: Forty-six patients with self-limited acute hepatitis (AH), sixteen patients with acute liver failure (ALF), and twenty-two healthy subjects were involved in th...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5114473/ https://www.ncbi.nlm.nih.gov/pubmed/27917263 http://dx.doi.org/10.4254/wjh.v8.i32.1370 |
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author | Melgaço, Juliana Gil Soriani, Frederico Marianetti Sucupira, Pedro Henrique Ferreira Pinheiro, Leonardo Assaf Vieira, Yasmine Rangel de Oliveira, Jaqueline Mendes Lewis-Ximenez, Lia Laura Araújo, Cristina Carvalho Vianna Pacheco-Moreira, Lúcio Filgueiras Menezes, Gustavo Batista Cruz, Oswaldo Gonçalves Vitral, Claudia Lamarca Pinto, Marcelo Alves |
author_facet | Melgaço, Juliana Gil Soriani, Frederico Marianetti Sucupira, Pedro Henrique Ferreira Pinheiro, Leonardo Assaf Vieira, Yasmine Rangel de Oliveira, Jaqueline Mendes Lewis-Ximenez, Lia Laura Araújo, Cristina Carvalho Vianna Pacheco-Moreira, Lúcio Filgueiras Menezes, Gustavo Batista Cruz, Oswaldo Gonçalves Vitral, Claudia Lamarca Pinto, Marcelo Alves |
author_sort | Melgaço, Juliana Gil |
collection | PubMed |
description | AIM: To study the differences in immune response and cytokine profile between acute liver failure and self-limited acute hepatitis. METHODS: Forty-six patients with self-limited acute hepatitis (AH), sixteen patients with acute liver failure (ALF), and twenty-two healthy subjects were involved in this study. The inflammatory and anti-inflammatory products in plasma samples were quantified using commercial enzyme-linked immunoassays and quantitative real-time PCR. The cellular immune responses were measured by proliferation assay using flow cytometry. The groups were divided into viral- and non-viral-induced self-limited AH and ALF. Thus, we worked with five groups: Hepatitis A virus (HAV)-induced self-limited acute hepatitis (HAV-AH), HAV-induced ALF (HAV-ALF), non-viral-induced self-limited acute hepatitis (non-viral AH), non-viral-induced acute liver failure (non-viral ALF), and healthy subjects (HC). Comparisons among HAV and non-viral-induced AH and ALF were performed. RESULTS: The levels of mitochondrial DNA (mtDNA) and the cytokines investigated [interleukin (IL)-6, IL-8, IL-10, interferon gamma, and tumor necrosis factor] were significantly increased in ALF patients, independently of etiology (P < 0.05). High plasma mtDNA and IL-10 were the best markers associated with ALF [mtDNA: OR = 320.5 (95%CI: 14.42-7123.33), P < 0.0001; and IL-10: OR = 18.8 (95%CI: 1.38-257.94), P = 0.028] and death [mtDNA: OR = 12.1 (95%CI: 2.57-57.07), P = 0.002; and IL-10: OR = 8.01 (95%CI: 1.26-50.97), P = 0.027]. In the cellular proliferation assay, NK(bright), NKT and regulatory T cells (TReg) predominated in virus-specific stimulation in HAV-induced ALF patients with an anergic behavior in the cellular response to mitotic stimulation. Therefore, in non-viral-induced ALF, anergic behavior of activated T cells was not observed after mitotic stimulation, as expected and as described by the literature. CONCLUSION: mtDNA and IL-10 may be predictors of ALF and death. TReg cells are involved in immunological disturbance in HAV-induced ALF. |
format | Online Article Text |
id | pubmed-5114473 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-51144732016-12-02 Changes in cellular proliferation and plasma products are associated with liver failure Melgaço, Juliana Gil Soriani, Frederico Marianetti Sucupira, Pedro Henrique Ferreira Pinheiro, Leonardo Assaf Vieira, Yasmine Rangel de Oliveira, Jaqueline Mendes Lewis-Ximenez, Lia Laura Araújo, Cristina Carvalho Vianna Pacheco-Moreira, Lúcio Filgueiras Menezes, Gustavo Batista Cruz, Oswaldo Gonçalves Vitral, Claudia Lamarca Pinto, Marcelo Alves World J Hepatol Basic Study AIM: To study the differences in immune response and cytokine profile between acute liver failure and self-limited acute hepatitis. METHODS: Forty-six patients with self-limited acute hepatitis (AH), sixteen patients with acute liver failure (ALF), and twenty-two healthy subjects were involved in this study. The inflammatory and anti-inflammatory products in plasma samples were quantified using commercial enzyme-linked immunoassays and quantitative real-time PCR. The cellular immune responses were measured by proliferation assay using flow cytometry. The groups were divided into viral- and non-viral-induced self-limited AH and ALF. Thus, we worked with five groups: Hepatitis A virus (HAV)-induced self-limited acute hepatitis (HAV-AH), HAV-induced ALF (HAV-ALF), non-viral-induced self-limited acute hepatitis (non-viral AH), non-viral-induced acute liver failure (non-viral ALF), and healthy subjects (HC). Comparisons among HAV and non-viral-induced AH and ALF were performed. RESULTS: The levels of mitochondrial DNA (mtDNA) and the cytokines investigated [interleukin (IL)-6, IL-8, IL-10, interferon gamma, and tumor necrosis factor] were significantly increased in ALF patients, independently of etiology (P < 0.05). High plasma mtDNA and IL-10 were the best markers associated with ALF [mtDNA: OR = 320.5 (95%CI: 14.42-7123.33), P < 0.0001; and IL-10: OR = 18.8 (95%CI: 1.38-257.94), P = 0.028] and death [mtDNA: OR = 12.1 (95%CI: 2.57-57.07), P = 0.002; and IL-10: OR = 8.01 (95%CI: 1.26-50.97), P = 0.027]. In the cellular proliferation assay, NK(bright), NKT and regulatory T cells (TReg) predominated in virus-specific stimulation in HAV-induced ALF patients with an anergic behavior in the cellular response to mitotic stimulation. Therefore, in non-viral-induced ALF, anergic behavior of activated T cells was not observed after mitotic stimulation, as expected and as described by the literature. CONCLUSION: mtDNA and IL-10 may be predictors of ALF and death. TReg cells are involved in immunological disturbance in HAV-induced ALF. Baishideng Publishing Group Inc 2016-11-18 2016-11-18 /pmc/articles/PMC5114473/ /pubmed/27917263 http://dx.doi.org/10.4254/wjh.v8.i32.1370 Text en ©The Author(s) 2016. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Basic Study Melgaço, Juliana Gil Soriani, Frederico Marianetti Sucupira, Pedro Henrique Ferreira Pinheiro, Leonardo Assaf Vieira, Yasmine Rangel de Oliveira, Jaqueline Mendes Lewis-Ximenez, Lia Laura Araújo, Cristina Carvalho Vianna Pacheco-Moreira, Lúcio Filgueiras Menezes, Gustavo Batista Cruz, Oswaldo Gonçalves Vitral, Claudia Lamarca Pinto, Marcelo Alves Changes in cellular proliferation and plasma products are associated with liver failure |
title | Changes in cellular proliferation and plasma products are associated with liver failure |
title_full | Changes in cellular proliferation and plasma products are associated with liver failure |
title_fullStr | Changes in cellular proliferation and plasma products are associated with liver failure |
title_full_unstemmed | Changes in cellular proliferation and plasma products are associated with liver failure |
title_short | Changes in cellular proliferation and plasma products are associated with liver failure |
title_sort | changes in cellular proliferation and plasma products are associated with liver failure |
topic | Basic Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5114473/ https://www.ncbi.nlm.nih.gov/pubmed/27917263 http://dx.doi.org/10.4254/wjh.v8.i32.1370 |
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