Cargando…

The JAK inhibitor tofacitinib ameliorates immune-mediated liver injury in mice

The prevalence of immune-mediated liver diseases such as autoimmune liver disease or viral hepatitis has increased in recent years, and the side effects of pre-existing treatments are a worldwide problem. Regulatory T cells (Tregs) and T helper 17 (Th17) cells play important roles in the development...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Han, Feng, Xinxia, Han, Ping, Lei, Yu, Xia, Yujia, Tian, Dean, Yan, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6854585/
https://www.ncbi.nlm.nih.gov/pubmed/31638166
http://dx.doi.org/10.3892/mmr.2019.10750
_version_ 1783470237698490368
author Wang, Han
Feng, Xinxia
Han, Ping
Lei, Yu
Xia, Yujia
Tian, Dean
Yan, Wei
author_facet Wang, Han
Feng, Xinxia
Han, Ping
Lei, Yu
Xia, Yujia
Tian, Dean
Yan, Wei
author_sort Wang, Han
collection PubMed
description The prevalence of immune-mediated liver diseases such as autoimmune liver disease or viral hepatitis has increased in recent years, and the side effects of pre-existing treatments are a worldwide problem. Regulatory T cells (Tregs) and T helper 17 (Th17) cells play important roles in the development of immune-mediated hepatitis and may serve as potential therapeutic targets. Tofacitinib, a new Janus kinase (JAK) inhibitor, is under investigation for the treatment of rheumatoid arthritis; it is also helpful in treating ulcerative colitis and psoriasis. The roles of tofacitinib were investigated in conferring protection against immune-mediated liver injury in mice. T cell-mediated hepatitis was induced by concanavalin A (ConA). The mice in the treatment groups were administered with tofacitinib intragastrically before the ConA injection. Histopathological examination was performed by hematoxylin and eosin (H&E) staining, and the serum transaminase and inflammatory cytokine levels were determined using an automatic biochemistry analysis apparatus or cytometric bead array (CBA) kits. Flow cytometric analysis was used to detect Tregs and Th17 cells. Tofacitinib significantly decreased the hepatic injury induced by ConA and prominently decreased the liver transaminase level. The secretion of several anti-inflammatory cytokines such as interleukin (IL)-10 was upregulated in mice from the treatment group, compared to that in mice treated with ConA alone, while the expression of interferon-γ (IFN-γ) and tumor necrosis factor-α (TNF-α) decreased. Tofacitinib treatment increased the number of Tregs and reduced the number of Th17 cells. Furthermore, tofacitinib could relieve liver fibrosis under conditions of autoimmune hepatitis (AIH). The present results indicated that tofacitinib improved immune-mediated hepatitis and restored the impaired Treg/Th17 cell ratio, which suggests that it may serve as a novel treatment approach for immune-mediated liver diseases.
format Online
Article
Text
id pubmed-6854585
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher D.A. Spandidos
record_format MEDLINE/PubMed
spelling pubmed-68545852019-11-21 The JAK inhibitor tofacitinib ameliorates immune-mediated liver injury in mice Wang, Han Feng, Xinxia Han, Ping Lei, Yu Xia, Yujia Tian, Dean Yan, Wei Mol Med Rep Articles The prevalence of immune-mediated liver diseases such as autoimmune liver disease or viral hepatitis has increased in recent years, and the side effects of pre-existing treatments are a worldwide problem. Regulatory T cells (Tregs) and T helper 17 (Th17) cells play important roles in the development of immune-mediated hepatitis and may serve as potential therapeutic targets. Tofacitinib, a new Janus kinase (JAK) inhibitor, is under investigation for the treatment of rheumatoid arthritis; it is also helpful in treating ulcerative colitis and psoriasis. The roles of tofacitinib were investigated in conferring protection against immune-mediated liver injury in mice. T cell-mediated hepatitis was induced by concanavalin A (ConA). The mice in the treatment groups were administered with tofacitinib intragastrically before the ConA injection. Histopathological examination was performed by hematoxylin and eosin (H&E) staining, and the serum transaminase and inflammatory cytokine levels were determined using an automatic biochemistry analysis apparatus or cytometric bead array (CBA) kits. Flow cytometric analysis was used to detect Tregs and Th17 cells. Tofacitinib significantly decreased the hepatic injury induced by ConA and prominently decreased the liver transaminase level. The secretion of several anti-inflammatory cytokines such as interleukin (IL)-10 was upregulated in mice from the treatment group, compared to that in mice treated with ConA alone, while the expression of interferon-γ (IFN-γ) and tumor necrosis factor-α (TNF-α) decreased. Tofacitinib treatment increased the number of Tregs and reduced the number of Th17 cells. Furthermore, tofacitinib could relieve liver fibrosis under conditions of autoimmune hepatitis (AIH). The present results indicated that tofacitinib improved immune-mediated hepatitis and restored the impaired Treg/Th17 cell ratio, which suggests that it may serve as a novel treatment approach for immune-mediated liver diseases. D.A. Spandidos 2019-12 2019-10-16 /pmc/articles/PMC6854585/ /pubmed/31638166 http://dx.doi.org/10.3892/mmr.2019.10750 Text en Copyright: © Wang et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Wang, Han
Feng, Xinxia
Han, Ping
Lei, Yu
Xia, Yujia
Tian, Dean
Yan, Wei
The JAK inhibitor tofacitinib ameliorates immune-mediated liver injury in mice
title The JAK inhibitor tofacitinib ameliorates immune-mediated liver injury in mice
title_full The JAK inhibitor tofacitinib ameliorates immune-mediated liver injury in mice
title_fullStr The JAK inhibitor tofacitinib ameliorates immune-mediated liver injury in mice
title_full_unstemmed The JAK inhibitor tofacitinib ameliorates immune-mediated liver injury in mice
title_short The JAK inhibitor tofacitinib ameliorates immune-mediated liver injury in mice
title_sort jak inhibitor tofacitinib ameliorates immune-mediated liver injury in mice
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6854585/
https://www.ncbi.nlm.nih.gov/pubmed/31638166
http://dx.doi.org/10.3892/mmr.2019.10750
work_keys_str_mv AT wanghan thejakinhibitortofacitinibamelioratesimmunemediatedliverinjuryinmice
AT fengxinxia thejakinhibitortofacitinibamelioratesimmunemediatedliverinjuryinmice
AT hanping thejakinhibitortofacitinibamelioratesimmunemediatedliverinjuryinmice
AT leiyu thejakinhibitortofacitinibamelioratesimmunemediatedliverinjuryinmice
AT xiayujia thejakinhibitortofacitinibamelioratesimmunemediatedliverinjuryinmice
AT tiandean thejakinhibitortofacitinibamelioratesimmunemediatedliverinjuryinmice
AT yanwei thejakinhibitortofacitinibamelioratesimmunemediatedliverinjuryinmice
AT wanghan jakinhibitortofacitinibamelioratesimmunemediatedliverinjuryinmice
AT fengxinxia jakinhibitortofacitinibamelioratesimmunemediatedliverinjuryinmice
AT hanping jakinhibitortofacitinibamelioratesimmunemediatedliverinjuryinmice
AT leiyu jakinhibitortofacitinibamelioratesimmunemediatedliverinjuryinmice
AT xiayujia jakinhibitortofacitinibamelioratesimmunemediatedliverinjuryinmice
AT tiandean jakinhibitortofacitinibamelioratesimmunemediatedliverinjuryinmice
AT yanwei jakinhibitortofacitinibamelioratesimmunemediatedliverinjuryinmice