Affiliation:
1. VA Palo Alto Health Care System, Palo Alto, CA, USA.
2. Division of Infectious Diseases & Geographic Medicine, Stanford University School of Medicine, Stanford, CA, USA
Abstract
IFN-α has been the cornerstone of chronic hepatitis C virus (HCV) treatment for over a decade. Yet, rates of sustained virologic response of HCV infection to interferon-based therapy, particularly in difficult-to-treat populations, have been disappointingly low. This is particularly true in HIV/HCV coinfection, in which less than a third of patients typically respond to therapy. New HCV protease inhibitors, most of which will need to be administered with pegylated interferon, are in development, but comprehensive, long-term data for their use in coinfected patients is not yet available. Understanding the basis of this population’s poor response to interferon-based therapy is crucial to future exploration of new therapeutic options, immunotherapy and prognosis in HIV/HCV-coinfected population.
Subject
Oncology,Immunology,Immunology and Allergy
Cited by
1 articles.
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