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Minimal hepatic encephalopathy is associated with expansion and activation of CD(4+)CD28(−), Th22 and Tfh and B lymphocytes
Peripheral inflammation acts synergistically with hyperammonemia in inducing neurological alterations in cirrhotic patients with minimal hepatic encephalopathy (MHE). We hypothesized that appearance of MHE would be associated to some specific qualitative change in peripheral inflammation. The aim of...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5532287/ https://www.ncbi.nlm.nih.gov/pubmed/28751644 http://dx.doi.org/10.1038/s41598-017-05938-1 |
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author | Mangas-Losada, Alba García-García, Raquel Urios, Amparo Escudero-García, Desamparados Tosca, Joan Giner-Durán, Remedios Serra, Miguel Angel Montoliu, Carmina Felipo, Vicente |
author_facet | Mangas-Losada, Alba García-García, Raquel Urios, Amparo Escudero-García, Desamparados Tosca, Joan Giner-Durán, Remedios Serra, Miguel Angel Montoliu, Carmina Felipo, Vicente |
author_sort | Mangas-Losada, Alba |
collection | PubMed |
description | Peripheral inflammation acts synergistically with hyperammonemia in inducing neurological alterations in cirrhotic patients with minimal hepatic encephalopathy (MHE). We hypothesized that appearance of MHE would be associated to some specific qualitative change in peripheral inflammation. The aim of this work was to characterize the changes in peripheral inflammation associated to appearance of MHE. We analyzed it by immunophenotyping and cytokine profile analysis, in cirrhotic patients without or with MHE and controls. The main alterations associated specifically with MHE are: 1) increased activation of all subtypes of CD4(+) T-lymphocytes, with the increased expression of CD69; 2) increased amount of CD4(+)CD28(−) T lymphocytes, associated with increased levels of CX3CL1 and of IL-15; 3) increased differentiation of CD4(+) T lymphocytes to Th follicular and Th22; 4) increased activation of B lymphocytes and serum IgG. This study has identified some specific alterations of the immune system associated with appearance of the neurological alterations in MHE patients. |
format | Online Article Text |
id | pubmed-5532287 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55322872017-08-02 Minimal hepatic encephalopathy is associated with expansion and activation of CD(4+)CD28(−), Th22 and Tfh and B lymphocytes Mangas-Losada, Alba García-García, Raquel Urios, Amparo Escudero-García, Desamparados Tosca, Joan Giner-Durán, Remedios Serra, Miguel Angel Montoliu, Carmina Felipo, Vicente Sci Rep Article Peripheral inflammation acts synergistically with hyperammonemia in inducing neurological alterations in cirrhotic patients with minimal hepatic encephalopathy (MHE). We hypothesized that appearance of MHE would be associated to some specific qualitative change in peripheral inflammation. The aim of this work was to characterize the changes in peripheral inflammation associated to appearance of MHE. We analyzed it by immunophenotyping and cytokine profile analysis, in cirrhotic patients without or with MHE and controls. The main alterations associated specifically with MHE are: 1) increased activation of all subtypes of CD4(+) T-lymphocytes, with the increased expression of CD69; 2) increased amount of CD4(+)CD28(−) T lymphocytes, associated with increased levels of CX3CL1 and of IL-15; 3) increased differentiation of CD4(+) T lymphocytes to Th follicular and Th22; 4) increased activation of B lymphocytes and serum IgG. This study has identified some specific alterations of the immune system associated with appearance of the neurological alterations in MHE patients. Nature Publishing Group UK 2017-07-27 /pmc/articles/PMC5532287/ /pubmed/28751644 http://dx.doi.org/10.1038/s41598-017-05938-1 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Mangas-Losada, Alba García-García, Raquel Urios, Amparo Escudero-García, Desamparados Tosca, Joan Giner-Durán, Remedios Serra, Miguel Angel Montoliu, Carmina Felipo, Vicente Minimal hepatic encephalopathy is associated with expansion and activation of CD(4+)CD28(−), Th22 and Tfh and B lymphocytes |
title | Minimal hepatic encephalopathy is associated with expansion and activation of CD(4+)CD28(−), Th22 and Tfh and B lymphocytes |
title_full | Minimal hepatic encephalopathy is associated with expansion and activation of CD(4+)CD28(−), Th22 and Tfh and B lymphocytes |
title_fullStr | Minimal hepatic encephalopathy is associated with expansion and activation of CD(4+)CD28(−), Th22 and Tfh and B lymphocytes |
title_full_unstemmed | Minimal hepatic encephalopathy is associated with expansion and activation of CD(4+)CD28(−), Th22 and Tfh and B lymphocytes |
title_short | Minimal hepatic encephalopathy is associated with expansion and activation of CD(4+)CD28(−), Th22 and Tfh and B lymphocytes |
title_sort | minimal hepatic encephalopathy is associated with expansion and activation of cd(4+)cd28(−), th22 and tfh and b lymphocytes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5532287/ https://www.ncbi.nlm.nih.gov/pubmed/28751644 http://dx.doi.org/10.1038/s41598-017-05938-1 |
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