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Therapy of hepatitis C in HIV-coinfection
1Medizinische Universitätsklinik I, Sigmund-Freud-Strasse 25, D-53105 Bonn, Germany. rockstroh@uni-bonn.de
Insights
Approximately one-third of HIV patients have hepatitis C coinfection, leading to accelerated liver disease. Effective treatments are improving outcomes, but careful management is crucial due to potential drug toxicities.
Area of Science:
- Hepatology
- Infectious Diseases
- Immunology
Background:
- Hepatitis C virus (HCV) coinfection affects one-third of European and American HIV patients.
- HIV accelerates HCV liver disease, increasing cirrhosis rates fivefold in coinfected individuals.
- HIV-associated immune deficiency progression exacerbates liver damage in coinfected patients.
Purpose of the Study:
- To review current treatment strategies for HIV/HCV coinfection.
- To highlight the impact of highly active antiretroviral therapy (HAART) on HCV outcomes.
- To emphasize the need for management guidelines considering treatment-related hepatotoxicity.
Main Methods:
- Review of cohort analyses and clinical data on HIV/HCV coinfection.
- Analysis of sustained virological response rates with combination therapy.
- Evaluation of HAART's impact on hepatitis C progression and mortality.
Main Results:
- Pegylated interferon and ribavirin therapy achieves up to 40% sustained virological response in coinfected patients.
- HAART improves the course of hepatitis C and reduces liver disease mortality.
- Current antiretroviral regimens can increase hepatotoxicity in coinfected patients.
Conclusions:
- Combination therapy and HAART offer improved outcomes for HIV/HCV coinfected patients.
- Management of hepatitis C coinfection in HIV requires careful consideration of hepatotoxicity.
- Development of specific treatment strategies and guidelines is essential for this population.
Abstract:
One third of all European and American HIV-patients are coinfected with hepatitis C. HIV accelerates hepatitis C virus liver disease especially when HIV-associated immune deficiency progresses. Indeed, liver cirrhosis rate is five times higher in HIV/HCV-coinfected patients than in HCV-monoinfected patients. With the introduction of pegylated interferon and ribavirin combination therapy sustained virological response rates of up to 40 % could be obtained in HIV/HCV-coinfected individuals. Moreover, cohort analyses could demonstrate that with the use of highly active antiretroviral therapy (HAART) an improved course of hepatitis C and a reduction in liver disease-associated mortality can be achieved. Under consideration of the increased rate of hepatotoxicity due to the presently available antiretroviral treatment regimens in HIV/HCV coinfected patients, however, the development of treatment strategies and guidelines for management of hepatitis coinfection in HIV remains of great clinical significance.
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