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      Harmful Effects and Potential Benefits of Anti-Tumor Necrosis Factor (TNF)-α on the Liver

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          Abstract

          Anti-tumor necrosis factor (TNF)-α agents represent an effective treatment for chronic inflammatory diseases. However, some concerns about their potentially undesirable effects on liver function have been reported. On the other hand, evidence of their therapeutic effects on certain liver diseases is accumulating. Many data showed the safety of anti-TNF-α in patients with chronic hepatitis B and C and in liver transplanted patients even if a strict follow-up and prophylaxis are recommended in well-defined subgroups. On the other side, anti-TNF-α-induced liver injury is not a rare event. However, it is often reversible after anti-TNF-α withdrawal. Anti-TNF-α agents have been tested in advanced stages of severe alcoholic hepatitis and non-alcoholic fatty liver disease. Limited data on the efficacy of anti-TNF-α in patients with autoimmune hepatitis and primary biliary cholangitis are also available. In this review, we explored the hepatic safety concerns in patients receiving anti-TNF-α agents with and without pre-existent hepatic diseases. In addition, the available evidence on their potential benefits in the treatment of specific hepatic diseases is discussed.

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          Most cited references126

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                Author and article information

                Journal
                Int J Mol Sci
                Int J Mol Sci
                ijms
                International Journal of Molecular Sciences
                MDPI
                1422-0067
                27 July 2018
                August 2018
                : 19
                : 8
                : 2199
                Affiliations
                [1 ]Internal Medicine and Gastroenterology Department, Fondazione Policlinico Universitario A. Gemelli IRCCS-Università Cattolica del Sacro Cuore, 00168 Roma, Italy; lopetusoloris@ 123456libero.it (L.R.L.); manuelamarzo@ 123456gmail.com (M.M.); francesca.dav@ 123456hotmail.it (F.D.); gianludovico.rapaccini@ 123456policlinicogemelli.it (G.L.R.); luisa.guidi@ 123456policlinicogemelli.it (L.G.); alearmuzzi@ 123456yahoo.com (A.A.); antonio.gasbarrini@ 123456unicatt.it (A.G.)
                [2 ]Gastroenterology Unit, Brotzu Hospital, 09121 Cagliari, Italy; giammarco.mocci@ 123456gmail.com
                Author notes
                [* ]Correspondence: Alfredo.Papa@ 123456unicatt.it ; Tel.: +39-06-350-3310
                Author information
                https://orcid.org/0000-0002-5747-2055
                Article
                ijms-19-02199
                10.3390/ijms19082199
                6121684
                30060508
                c2f3fbbe-1ce3-4dcd-adda-120659da4129
                © 2018 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 26 June 2018
                : 24 July 2018
                Categories
                Review

                Molecular biology
                infliximab,adalimumab,etanercept,certolizumab pegol,golimumab,hepatitis b virus,hepatitis c virus,drug-induced liver injury,non-alcoholic fatty liver disease,alcoholic hepatitis,autoimmune hepatitis

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