PMID- 24307780 OWN - NLM STAT- MEDLINE DCOM- 20140502 LR - 20220408 IS - 2219-2840 (Electronic) IS - 1007-9327 (Print) IS - 1007-9327 (Linking) VI - 19 IP - 44 DP - 2013 Nov 28 TI - Tumor necrosis factor-alpha inhibitors and chronic hepatitis C: a comprehensive literature review. PG - 7867-73 LID - 10.3748/wjg.v19.i44.7867 [doi] AB - Tumor necrosis factor-alpha (TNF-alpha) inhibitors are known to increase reactivation of concurrent chronic hepatitis B, but their impact on the hepatitis C virus (HCV) is controversial. Some conditions of immunosuppression, such as liver transplantation, typically cause an increase in the rate of HCV evolution. Inhibition of TNF-alpha, a cytokine involved in the apoptotic signaling pathway of hepatocytes infected by HCV, could potentially increase viral replication. Currently available clinical data appear to contradict this hypothesis. A review of medical literature revealed that a total of 216 patients with HCV were exposed to one or more treatments with TNF-alpha inhibitors, with a median observation time of 1.2 years and 260 cumulative patient-years of exposure. Only three cases of drug withdrawal due to suspected HCV liver disease recrudescence were reported. Treatment with TNF-alpha inhibitors in patients with HCV infection appears to be safe in the short term, but there are insufficient data to assess their long-term safety. Universal screening for HCV before beginning treatment with TNF-alpha inhibitors is currently controversial. The presence of HCV is not a contraindication to therapy with TNF-alpha inhibitors, with the exception of cirrhotic patients. In cases of cirrhosis, the benefit/risk ratio should be evaluated at the individual level. Prior to treatment with TNF-alpha inhibitors, patients with HCV should be referred to a hepatologist to determine the necessity of hepatic disease assessment, using liver biopsy or non-invasive methods, and the potential indication for antiviral therapy. In patients with HCV infection who are treated with TNF-alpha inhibitors, liver function monitoring every three months is advised. FAU - Pompili, Maurizio AU - Pompili M AD - Maurizio Pompili, Marco Biolato, Luca Miele, Antonio Grieco, Department of Internal Medicine, Universita Cattolica del Sacro Cuore, 8-00168 Roma, Italy. FAU - Biolato, Marco AU - Biolato M FAU - Miele, Luca AU - Miele L FAU - Grieco, Antonio AU - Grieco A LA - eng PT - Journal Article PT - Review PL - United States TA - World J Gastroenterol JT - World journal of gastroenterology JID - 100883448 RN - 0 (Antiviral Agents) RN - 0 (Immunosuppressive Agents) RN - 0 (Tumor Necrosis Factor-alpha) SB - IM MH - Animals MH - Antiviral Agents/adverse effects/*therapeutic use MH - Drug Monitoring MH - Hepacivirus/*drug effects MH - Hepatitis C, Chronic/diagnosis/*drug therapy/immunology MH - Humans MH - Immunosuppressive Agents/adverse effects/*therapeutic use MH - Risk Factors MH - Treatment Outcome MH - Tumor Necrosis Factor-alpha/*antagonists & inhibitors/metabolism PMC - PMC3848134 OTO - NOTNLM OT - Adalimumab OT - Etanercept OT - Hepatitis C virus OT - Inflammatory bowel disease OT - Infliximab OT - Psoriasis OT - Rheumatoid arthritis EDAT- 2013/12/07 06:00 MHDA- 2014/05/03 06:00 PMCR- 2013/11/28 CRDT- 2013/12/06 06:00 PHST- 2013/09/27 00:00 [received] PHST- 2013/10/31 00:00 [revised] PHST- 2013/11/12 00:00 [accepted] PHST- 2013/12/06 06:00 [entrez] PHST- 2013/12/07 06:00 [pubmed] PHST- 2014/05/03 06:00 [medline] PHST- 2013/11/28 00:00 [pmc-release] AID - 10.3748/wjg.v19.i44.7867 [doi] PST - ppublish SO - World J Gastroenterol. 2013 Nov 28;19(44):7867-73. doi: 10.3748/wjg.v19.i44.7867.