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Treatment of hepatitis C in HIV-coinfected patients
Christine A Hughes1, Stephen D Shafran
1Faculty of Pharmacy and Pharmaceutical Sciences, HIV, Capital Health Region, Edmonton, Alberta, Canada. christine.hughes@ualberta.ca
Insights
Hepatitis C virus (HCV) treatment with pegylated interferon and ribavirin shows lower sustained virologic response rates in patients coinfected with human immunodeficiency virus (HIV). Careful consideration of risks versus benefits is crucial for managing HCV/HIV coinfection.
Area of Science:
- Hepatology
- Infectious Diseases
- Antiviral Therapy
Background:
- Hepatitis C virus (HCV) coinfection accelerates liver disease progression in individuals with human immunodeficiency virus (HIV).
- Managing HCV/HIV coinfection presents unique challenges due to potential drug interactions and increased risks of adverse events.
Purpose of the Study:
- To review the current management strategies for hepatitis C virus (HCV) in patients coinfected with human immunodeficiency virus (HIV).
- To evaluate the efficacy and safety of antiviral therapies for HCV in the context of HIV coinfection.
Main Methods:
- A comprehensive literature search of MEDLINE (1966-February 2006) was performed using keywords related to HIV, HCV, and antiviral therapies.
- Included studies focused on HCV treatment outcomes and management of HCV/HIV coinfection, supplemented by review of article bibliographies and conference abstracts.
Main Results:
- HCV treatment with pegylated interferon (PEG-IFN) and ribavirin yields sustained virologic response (SVR) rates of 27-40% in coinfected individuals, lower than in HCV monoinfection.
- HCV genotype 1 and increased risks of myelosuppression, drug interactions, and hepatotoxicity complicate treatment in HIV-positive patients.
- Current guidelines recommend considering anti-HCV therapy for all HIV-positive patients with chronic HCV infection due to elevated risk of liver disease progression.
Conclusions:
- Treatment response to PEG-IFN and ribavirin is diminished in HCV/HIV coinfected patients compared to HCV monoinfected patients.
- The benefits of HCV treatment, including viral eradication, must be carefully balanced against potential adverse effects and drug-drug interactions with antiretroviral medications.
Objective:
To review the current management of hepatitis C virus (HCV) in persons coinfected with HIV.
Data Sources:
A MEDLINE search (1966-February 2006) was conducted, using key words such as HIV, human immunodeficiency virus, hepatitis C, interferon, pegylated interferon, and therapy. Article bibliographies and conference abstracts were also reviewed to identify relevant studies.
Study Selection And Data Extraction:
Studies that examined HCV treatment in individuals coinfected with HIV and articles that focused on HCV/HIV coinfection were considered for this review.
Data Synthesis:
Coinfection with HIV leads to a more rapid and severe course of HCV-related liver disease. Treatment of HCV with pegylated interferon (PEG-IFN) and ribavirin therapy is relatively well tolerated in individuals coinfected with HIV, with overall sustained virologic response (SVR) rates of 27-40%. High relapse rates and poor response in HCV-genotype 1 contribute to the lower SVR in coinfected individuals compared with HCV monoinfection. Treatment of HCV is more complicated in HIV-infected persons due to increased risk of myelosuppression, drug interactions, hepatotoxicity of antiretroviral therapy, and the relative contraindication to interferon therapy in advanced HIV disease. Current guidelines recommend that all HIV-positive patients with chronic HCV infection be considered as treatment candidates for anti-HCV therapy due to the higher risk of liver disease progression. Further studies are needed, however, to define the appropriate dose and duration of therapy in HCV/HIV-coinfected individuals.
Conclusions:
Response to treatment with PEG-IFN and ribavirin is poorer in patients coinfected with HCV/HIV than in those infected with HCV alone. The benefits of anti-HCV therapy, including viral eradication, need to be weighed against the risks of adverse effects and drug-drug interactions between anti-HCV and antiretroviral medications.
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Assessment:
