Literature DB >> 24845610

Bridging basic science and clinical research: the EASL Monothematic Conference on Translational Research in Viral Hepatitis.

Tobias Boettler1, Darius Moradpour2, Robert Thimme1, Fabien Zoulim3.   

Abstract

The EASL Monothematic Conference on Translational Research in Viral Hepatitis brought together a group of leading scientists and clinicians working on both, basic and clinical aspects of viral hepatitis, thereby building bridges from bench to bedside. This report recapitulates the presentations and discussions at the conference held in Lyon, France on November 29-30, 2013. In recent years, great advances have been made in the field of viral hepatitis, particularly in hepatitis C virus (HCV) infection. The identification of IL28B genetic polymorphisms as a major determinant for spontaneous and treatment-induced HCV clearance was a seminal discovery. Currently, hepatologists are at the doorstep of even greater advances, with the advent of a wealth of directly acting antivirals (DAAs) against HCV. Indeed, promising results have accumulated over the last months and few years, showing sustained virological response (SVR) rates of up to 100% with interferon-free DAA combination therapies. Thus, less than 25 years after its identification, HCV infection may soon be curable in the vast majority of patients, highlighting the great success of HCV research over the last decades. However, viral hepatitis and its clinical complications such as liver cirrhosis and hepatocellular carcinoma (HCC) remain major global challenges. New therapeutic strategies to tackle hepatitis B virus (HBV) and hepatitis D virus (HDV) infection are needed, as current therapies have undeniable limitations. Nucleoside/nucleotide analogues (NUC) can efficiently control HBV replication and reduce or even reverse liver damage. However, these drugs have to be given for indefinite periods in most patients to maintain virological and biochemical responses. Although sustained responses off treatment can be achieved by treatment with (pegylated) interferon-α, only about 10-30% of patients effectively resolve chronic hepatitis B. It was the goal of this conference to review the progress made over the last years in chronic viral hepatitis research and to identify key questions that need to be addressed in order to close the gap between basic and clinical research and to develop novel preventive and treatment approaches for this most common cause of liver cirrhosis and HCC.
Copyright © 2014. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Antivirals; Immunology; Pathogenesis; Virology

Mesh:

Substances:

Year:  2014        PMID: 24845610     DOI: 10.1016/j.jhep.2014.05.016

Source DB:  PubMed          Journal:  J Hepatol        ISSN: 0168-8278            Impact factor:   25.083


  7 in total

1.  Non-nucleoside hepatitis B virus polymerase inhibitors identified by an in vitro polymerase elongation assay.

Authors:  Shogo Nakajima; Koichi Watashi; Kento Fukano; Senko Tsukuda; Kousho Wakae; Hideki Aizaki; Masamichi Muramatsu; Takaji Wakita; Tetsuya Toyoda
Journal:  J Gastroenterol       Date:  2019-11-25       Impact factor: 7.527

Review 2.  Risk for hepatocellular carcinoma in the course of chronic hepatitis B virus infection and the protective effect of therapy with nucleos(t)ide analogues.

Authors:  Irene Rapti; Stephanos Hadziyannis
Journal:  World J Hepatol       Date:  2015-05-18

3.  Comparison Stratagems of Post-Screening Management of Anti-HCV-Positive Community Residents: Simple Notification, Active Referral, or Accessible Medical Care.

Authors:  Yuan-Hung Kuo; Pao-Fei Chen; Jing-Houng Wang; Kuo-Chin Chang; Kwong-Ming Kee; Ming-Chao Tsai; Chun-Yin Lin; Sheng-Che Lin; Lin-San Tsai; Shu-Chuan Chen; Sheng-Nan Lu
Journal:  PLoS One       Date:  2015-05-13       Impact factor: 3.240

4.  Chemical array system, a platform to identify novel hepatitis B virus entry inhibitors targeting sodium taurocholate cotransporting polypeptide.

Authors:  Manabu Kaneko; Yushi Futamura; Senko Tsukuda; Yasumitsu Kondoh; Tomomi Sekine; Hiroyuki Hirano; Kento Fukano; Hirofumi Ohashi; Wakana Saso; Ryo Morishita; Satoko Matsunaga; Fumihiro Kawai; Akihide Ryo; Sam-Yong Park; Ryosuke Suzuki; Hideki Aizaki; Naoko Ohtani; Camille Sureau; Takaji Wakita; Hiroyuki Osada; Koichi Watashi
Journal:  Sci Rep       Date:  2018-02-09       Impact factor: 4.379

5.  The cyclophilin inhibitor CRV431 inhibits liver HBV DNA and HBsAg in transgenic mice.

Authors:  Philippe Gallay; Daren Ure; Michael Bobardt; Udayan Chatterji; James Ou; Daniel Trepanier; Robert Foster
Journal:  PLoS One       Date:  2019-06-10       Impact factor: 3.240

6.  Cyclosporin derivatives inhibit hepatitis B virus entry without interfering with NTCP transporter activity.

Authors:  Satomi Shimura; Koichi Watashi; Kento Fukano; Michael Peel; Ann Sluder; Fumihiro Kawai; Masashi Iwamoto; Senko Tsukuda; Junko S Takeuchi; Takeshi Miyake; Masaya Sugiyama; Yuki Ogasawara; Sam-Yong Park; Yasuhito Tanaka; Hiroyuki Kusuhara; Masashi Mizokami; Camille Sureau; Takaji Wakita
Journal:  J Hepatol       Date:  2016-11-25       Impact factor: 25.083

7.  Tenofovir Disoproxil Fumarate Is Superior to Entecavir in Reducing Hepatitis B Surface Antigen for Chronic Hepatitis B in China: 2-Year Comprehensive Comparative Result of a Matched Comparative Study.

Authors:  Sisi Yang; Xueqing Ma; Chengwei Cai; Huanqiu Wang; Fenqiang Xiao; Chengbo Yu
Journal:  Front Med (Lausanne)       Date:  2021-03-15
  7 in total

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