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Increase of soluble programmed cell death ligand 1 in patients with chronic hepatitis C

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To determine whether the soluble programmed cell death ligand 1 (sPD-L1) levels in patients with chronic hepatitis C (CHC) are associated with the clinical features of the disease and the efficacy of treatment, including interferon (IFN)-α.

Int J Med Sci 2017, Vol 14 Ivyspring International Publisher 403 International Journal of Medical Sciences 2017; 14(5): 403-411 doi: 10.7150/ijms.18784 Research Paper Increase of Soluble Programmed Cell Death Ligand in Patients with Chronic Hepatitis C Satoshi Yamagiwa1, Toru Ishikawa2, Nobuo Waguri3, Soichi Sugitani4, Kenya Kamimura1, Atsunori Tsuchiya1, Masaaki Takamura1, Hirokazu Kawai1, Shuji Terai1 Division of Gastroenterology and Hepatology, Niigata University Graduate School of Medical and Dental Sciences, Niigata 951-8510, Japan; Department of Gastroenterology and Hepatology, Saiseikai Niigata Daini Hospital, Niigata 950-1104, Japan; Department of Gastroenterology and Hepatology, Niigata City General Hospital, Niigata 950-1197, Japan; Department of Gastroenterology and Hepatology, Tachikawa General Hospital, Nagaoka 940-8621, Japan  Corresponding author: Satoshi Yamagiwa, M.D., Ph.D Division of Gastroenterology and Hepatology, Niigata University Graduate School of Medical and Dental Sciences, 1-757 Asahimachi-dori, Chuo-ku, Niigata 951-8510, Japan E-mail address: syamagi@med.niigata-u.ac.jp Telephone: +81-25-227-2207 Fax: +81-25-227-0776 © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/) See http://ivyspring.com/terms for full terms and conditions Received: 2016.12.16; Accepted: 2017.03.01; Published: 2017.04.08 Abstract Objectives: To determine whether the soluble programmed cell death ligand (sPD-L1) levels in patients with chronic hepatitis C (CHC) are associated with the clinical features of the disease and the efficacy of treatment, including interferon (IFN)-α Methods: We investigated the sPD-L1 levels in the sera of 80 genotype 1b Japanese patients with CHC who underwent 12 weeks of telaprevir (TVR)- or simeprevir (SMV)-based triple therapy followed by 12 weeks of dual therapy with pegylated IFN-α plus ribavirin Serum was also obtained from 22 patients with chronic hepatitis B (CHB) and from 10 healthy donors (HC) The sPD-L1 levels were measured using an ELISA kit In addition, we examined the PD-L1 expression on the cell surface of immortalized hepatocytes (HPT1) after incubation with cytokines, including IFN-γ Results: The pretreatment serum sPD-L1 levels were significantly increased in patients with CHC (median 109.3 pg/ml, range 23.1-402.3) compared with patients with CHB (69.2 pg/ml, 15.5-144.8; P

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