Literature DB >> 22504920

Management of HBV- and HCV-induced end stage liver disease.

David J Mutimer1, Anna Lok.   

Abstract

Hepatitis B and hepatitis C infections are important causes of end-stage liver disease and primary liver cancer. Successful antiviral treatment prior to the development of cirrhosis will prevent most of the morbidity and mortality associated with those infections. This can be achieved for a high proportion of patients. However, many patients present with end-stage liver disease and ongoing and clinically significant viral replication. Antiviral treatment of HBV can effect recovery of liver function and restores many patients to a state of well compensated cirrhosis. The antiviral treatment of end-stage HCV poses much greater challenges. Interferon remains an essential element of HCV antiviral treatment, but has reduced efficacy and significant toxicity at this stage of cirrhosis. Though yet to be evaluated in the setting of advanced liver disease, the development of direct acting antivirals for HCV offers hope for improved outcomes at this stage of cirrhosis.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22504920     DOI: 10.1136/gutjnl-2012-302076

Source DB:  PubMed          Journal:  Gut        ISSN: 0017-5749            Impact factor:   23.059


  7 in total

1.  Type I IFN augments IL-27-dependent TRIM25 expression to inhibit HBV replication.

Authors:  Guangyun Tan; Qingfei Xiao; Hongxiao Song; Feng Ma; Fengchao Xu; Di Peng; Na Li; Xiaosong Wang; Junqi Niu; Pujun Gao; F Xiao-Feng Qin; Genhong Cheng
Journal:  Cell Mol Immunol       Date:  2017-02-13       Impact factor: 11.530

Review 2.  Virus-related liver cirrhosis: molecular basis and therapeutic options.

Authors:  Ji Lin; Jian-Feng Wu; Qi Zhang; Hong-Wei Zhang; Guang-Wen Cao
Journal:  World J Gastroenterol       Date:  2014-06-07       Impact factor: 5.742

3.  The preventive effect of the impaired liver function for antiemetic therapy against chemotherapy-induced nausea and vomiting in hepatocellular carcinoma patients.

Authors:  Tomohiro Nishikawa; Akira Asai; Norio Okamoto; Hidetaka Yasuoka; Ken Nakamura; Keisuke Yokohama; Hideko Ohama; Yusuke Tsuchimoto; Shinya Fukunishi; Yasuhiro Tsuda; Kazuhiro Yamamoto; Kazuhide Higuchi
Journal:  J Clin Biochem Nutr       Date:  2017-10-19       Impact factor: 3.114

4.  Identification of TRIM14 as a Type I IFN-Stimulated Gene Controlling Hepatitis B Virus Replication by Targeting HBx.

Authors:  Guangyun Tan; Fengchao Xu; Hongxiao Song; Ye Yuan; Qingfei Xiao; Feng Ma; F Xiao-Feng Qin; Genhong Cheng
Journal:  Front Immunol       Date:  2018-08-13       Impact factor: 7.561

Review 5.  Advances in Nanoparticle Drug Delivery Systems for Anti-Hepatitis B Virus Therapy: A Narrative Review.

Authors:  Jing Miao; Peng Gao; Qian Li; Kaifeng He; Liwen Zhang; Junyan Wang; Lingfei Huang
Journal:  Int J Mol Sci       Date:  2021-10-18       Impact factor: 5.923

6.  Bone marrow-derived mesenchymal stem cells inhibit the proliferation of hepatic stellate cells by inhibiting the transforming growth factor β pathway.

Authors:  Li-Ting Zhang; Xue-Qin Fang; Qing-Feng Chen; Hong Chen; Ping Xiao; Xue-Bin Peng; Sheng-Xiang Zhang; Jun-Feng Li; Xiao-Rong Mao
Journal:  Mol Med Rep       Date:  2015-09-25       Impact factor: 2.952

7.  Type-I-IFN-Stimulated Gene TRIM5γ Inhibits HBV Replication by Promoting HBx Degradation.

Authors:  Guangyun Tan; Zhaohong Yi; Hongxiao Song; Fengchao Xu; Feng Li; Roghiyh Aliyari; Hong Zhang; Peishuang Du; Yanhua Ding; Junqi Niu; Xiaosong Wang; Lishan Su; F Xiao-Feng Qin; Genhong Cheng
Journal:  Cell Rep       Date:  2019-12-10       Impact factor: 9.423

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.