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Updated: May 24, 2026

Early Viral Entry Assays for the Identification and Evaluation of Antiviral Compounds
Published on: October 29, 2015
Antiviral drugs and the treatment of hepatitis C
Ziba Jalali1, Jürgen K Rockstroh
1Division of Infectious Diseases, Cedars-Sinai Medical Center, Los Angeles, CA, USA. ziba.jalali@cshs.org
Insights
Optimizing antiretroviral therapy (ART) before treating hepatitis C virus (HCV) in HIV/HCV co-infected patients is crucial. This strategy aims to improve sustained virologic response (SVR) by managing drug-drug interactions and adverse events.
Area of Science:
- Infectious Diseases
- Hepatology
- Virology
Background:
- Hepatitis C virus (HCV) is a significant cause of illness and death in people with HIV-1, especially those with low CD4 counts.
- HIV/HCV co-infection accelerates liver disease progression, including cirrhosis.
- HCV treatment is a priority, but managing co-infections presents challenges.
Purpose of the Study:
- To review data on optimizing antiretroviral therapy (ART) regimens in HIV/HCV co-infected patients before initiating HCV treatment.
- To enhance the likelihood of achieving sustained virologic response (SVR) to HCV therapy.
- To address challenges posed by drug-drug interactions (DDIs) and overlapping adverse events.
Main Methods:
- Literature review focusing on studies concerning ART optimization in HIV/HCV co-infected individuals.
- Analysis of data on DDIs between ART and HCV treatment regimens (pegylated interferon, ribavirin, protease inhibitors).
- Evaluation of strategies to mitigate overlapping drug-associated adverse events.
Main Results:
- Specific ART regimens can be optimized prior to HCV treatment to minimize DDIs.
- Careful selection of ART can reduce the risk of adverse events during HCV therapy.
- Optimized ART strategies are associated with an increased chance of achieving SVR.
Conclusions:
- Optimizing ART before HCV treatment is essential for successful outcomes in HIV/HCV co-infected patients.
- Managing DDIs and adverse events through ART selection is key to improving SVR rates.
- This review provides guidance for clinicians on selecting appropriate ART regimens.
Abstract:
With effective treatment of HIV-1, hepatitis C virus (HCV) has become increasingly recognized as a major cause of morbidity and mortality in this population. Rapid progression of liver disease and cirrhosis has been documented in HIV/HCV co-infected individuals, particularly with lower CD4-counts (< 200/μL). Therefore, HCV treatment has become a priority for many clinicians, despite the presence of many. An important issue among HIV/HCV co-infected patients is the selection of antiretroviral therapy (ART) during treatment with pegylated interferon, ribavirin (RBV), plus new HCV protease inhibitors. Extensive drug-drug interactions (DDI) and overlapping drug-associated adverse events can impact the outcome of HCV therapy. In this review, we focus on the important data and studies regarding optimizing antiretroviral regimens before starting HCV treatment in HIV/HCV co-infected patients to increase the chance of sustained virologic response (SVR).
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