Related Experiment Video
Updated: Jun 16, 2026

Stem Cell-Derived Viral Ag-Specific T Lymphocytes Suppress HBV Replication in Mice
Published on: September 25, 2019
The treatment of chronic hepatitis C virus infection in HIV co-infection
Martin Vogel1, Jürgen K Rockstroh
1Department of Internal Medicine I, Bonn university, Bonn, Germany.
Insights
Chronic hepatitis C (HCV) co-infection accelerates liver disease in HIV patients. Treatment with pegylated interferon and ribavirin is recommended, with careful monitoring for drug interactions.
Area of Science:
- Hepatology
- Infectious Diseases
- Virology
Background:
- Chronic hepatitis C virus (HCV) co-infection affects up to one-third of HIV-positive individuals in Europe.
- Sexually transmitted acute HCV infections are increasing among HIV-positive men who have sex with men.
- HCV significantly accelerates liver disease progression in HIV co-infection, leading to end-stage liver disease as a major cause of non-AIDS related death.
Purpose of the Study:
- To emphasize the need for anti-HCV therapy evaluation in all HIV/HCV co-infected patients.
- To highlight the goal of achieving sustained virological response and curing hepatitis C.
- To discuss current treatment standards and considerations for HIV/HCV co-infected patients.
Main Methods:
- Review of current treatment guidelines for chronic HCV in HIV-infected patients.
- Discussion of the standard of care: pegylated interferon plus weight-adapted ribavirin.
- Analysis of drug interactions and toxicities with highly active antiretroviral therapy (HAART).
Main Results:
- Pegylated interferon and ribavirin remain the standard of care for HIV/HCV co-infected patients.
- HAART should not be withheld; it should be initiated first in patients with low CD4 counts.
- Contraindications include concomitant didanosine; zidovudine and stavudine should be avoided due to potential toxicity.
Conclusions:
- All HIV/HCV co-infected patients require evaluation for anti-HCV therapy.
- Current pegylated interferon/ribavirin therapy is recommended over waiting for new drugs.
- Careful management of drug interactions and toxicities is crucial for effective treatment.
Abstract:
Chronic HCV co-infection is present in up to one third of HIV-positive patients in Europe. In recent years, apart from the traditional transmission route of intravenous drug abuse, outbreaks of sexually transmitted acute HCV infections, mainly among HIV-positive men who have sex with men, have contributed to the overall disease burden. - Because the natural course of HCV infection is substantially accelerated in HIV-co-infection, end-stage liver disease has become the most frequent cause of non-AIDS related death in this population. Therefore every HIV/HCV co-infected patient should be evaluated for possible anti-HCV therapy with the goal of reaching a sustained virological response and thus cure of hepatitis C infection. The standard of care for the treatment of chronic HCV infection in HIV-infected remains a pegylated interferon in combination with weight-adapted ribavirin. - HAART should not be withheld from HCV co-infected patients due to concerns of drug related hepatotoxicity and in patients with reduced CD4-cell counts HAART should be started first. Under pegylated interferon and ribavirin combination therapy drug to drug interactions and cumulated toxicity between nucleoside analogues and anti-HCV therapy may be observed and concomitant didanosine use is contraindicated and zidovudine and stavudine should be avoided if possible. - The development of new drugs for the treatment of chronic hepatitis C represents a promising perspective also for HIV positive patients. However, these substances will probably reach clinical routine for HIV patients later than HCV monoinfected patients. Therefore at present waiting for new drugs is not an alternative to a modern pegylated interferon/ribavirin therapy.
Related Concept Videos
Hepatitis
Retrovirus Life Cycles
Viral Hepatitis I: Introduction
Chronic Pancreatitis II: Collaborative Care
Assessment:
Inhibitors of Viral Protein Synthesis
Antiviral Nucleoside Inhibitors
