| Literature DB >> 26052401 |
Reina Sasaki1, Tatsuo Kanda1, Shingo Nakamoto1, Yuki Haga1, Masato Nakamura1, Shin Yasui1, Xia Jiang1, Shuang Wu1, Makoto Arai1, Osamu Yokosuka1.
Abstract
Chronic hepatitis C virus (HCV) infection can cause liver cirrhosis and hepatocellular carcinoma (HCC). Several studies have demonstrated that the eradication of HCV reduces the occurrence of HCC. In Japan, as many people live to an advanced age, HCV-infected patients are also getting older, and the age at HCC diagnosis has also increased. Although older HCV-infected patients have a risk of developing HCC, the treatment response to peginterferon-alpha plus ribavirin therapy is relatively poor in these patients because of drop-out or discontinuation of this treatment due to adverse events. It is established that the mechanism of action between interferon-alpha and interferon-beta is slightly different. Short-term natural interferon-beta monotherapy is effective for patients with acute hepatitis C and patients infected with HCV genotype 2 and low viral loads. Natural interferon-beta plus ribavirin for 48 wk or for 24 wk are also effective for some patients with HCV genotype 1 or HCV genotype 2. Natural interferon-beta plus ribavirin has been used for certain "difficult-to-treat" HCV-infected patients. In the era of direct-acting anti-virals, natural interferon-beta plus ribavirin may be one of the therapeutic options for special groups of HCV-infected patients. In the near future, signal transduction pathways of interferon-beta will inform further directions.Entities:
Keywords: Hepatitis C virus; Hepatocellular carcinoma; Interferon resistance; Interferon-beta; Ribavirin
Year: 2015 PMID: 26052401 PMCID: PMC4450189 DOI: 10.4254/wjh.v7.i8.1125
Source DB: PubMed Journal: World J Hepatol