PMID- 32117698 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20220413 IS - 2231-5047 (Print) IS - 2231-5128 (Electronic) IS - 2231-5047 (Linking) VI - 9 IP - 2 DP - 2019 Jul-Dec TI - Update on Immunosuppression in Liver Transplantation. PG - 96-101 LID - 10.5005/jp-journals-10018-1301 [doi] AB - The standard therapy for decompensated end-stage chronic liver disease of any etiology and acute fulminant hepatic failure is liver transplantation (LT). Advances in immunosuppressive therapy decreased the rates of acute and chronic rejections. Thus, graft and patient survivals have significantly improved. However, long-term adverse effects of prolonged use of immunosuppressive agents such as malignancies, opportunistic infections, metabolic disorders, and other organ toxicities have now become a major concern. Consequently, alternative approaches are needed to deescalate the customary drugs and their side effects. Therapy must be individualized and additional preventive measures should be taken by patients with particular risk factors or predisposed to certain adverse effects. Current opinion favors a combination of agents with different mechanism of actions and toxicity profiles. Corticosteroids are employed in immediate and early postoperative period. Although they have a pronounced side effect profile, calcineurin inhibitors (CNIs) are still the backbone of early and late phase immunosuppressive regimens because of their proved efficacy. Antimetabolites are frequent choices for steroid and/or CNI-sparing strategies. Studies also have established a role for mammalian target of rapamycin (mTOR) inhibitors in specific groups of recipients. Biologic agents are a hot topic of interest and made their way into current strategies for induction. Agents extrapolated from other transplantation or immunologic experience are being evaluated. HOW TO CITE THIS ARTICLE: Tasdogan BE, Ma M, Simsek C, et al. Update on Immunosuppression in Liver Transplantation. Euroasian J Hepato-Gastroenterol 2019;9(2):96-101. CI - Copyright (c) 2019; Jaypee Brothers Medical Publishers (P) Ltd. FAU - Tasdogan, Burcak E AU - Tasdogan BE AD - Department of Gastroenterology and Hepatology, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA. FAU - Ma, Michelle AU - Ma M AD - Department of Gastroenterology and Hepatology, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA. FAU - Simsek, Cem AU - Simsek C AD - Department of Gastroenterology and Hepatology, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA. FAU - Saberi, Behnam AU - Saberi B AD - Department of Liver Diseases, Icahn School of Medicine at Mount Sinai, New York, USA. FAU - Gurakar, Ahmet AU - Gurakar A AD - Department of Gastroenterology and Hepatology, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA. LA - eng PT - Journal Article PT - Review PL - India TA - Euroasian J Hepatogastroenterol JT - Euroasian journal of hepato-gastroenterology JID - 101577625 PMC - PMC7047305 OTO - NOTNLM OT - Adverse effects OT - Immunosuppression OT - Liver transplantation COIS- Source of support: Nil Conflict of interest: None EDAT- 2020/03/03 06:00 MHDA- 2020/03/03 06:01 PMCR- 2019/07/01 CRDT- 2020/03/03 06:00 PHST- 2020/03/03 06:00 [entrez] PHST- 2020/03/03 06:00 [pubmed] PHST- 2020/03/03 06:01 [medline] PHST- 2019/07/01 00:00 [pmc-release] AID - 10.5005/jp-journals-10018-1301 [doi] PST - ppublish SO - Euroasian J Hepatogastroenterol. 2019 Jul-Dec;9(2):96-101. doi: 10.5005/jp-journals-10018-1301.