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Published on: March 30, 2014
HCV chronic hepatitis in patients with HIV: clinical management issues
Raffaele Bruno1, Paolo Sacchi, Massimo Puoti
1Division of Infectious and Tropical Disease, IRCCS S. Matteo Hospital, University of Pavia, Italy.
Insights
HIV-hepatitis C virus (HCV) coinfection accelerates disease progression in both infections. Treating HCV coinfection is crucial, with pegylated interferon and ribavirin as a potential standard of care.
Area of Science:
- Hepatology
- Infectious Diseases
- Immunology
Background:
- HIV-hepatitis C virus (HCV) coinfection affects over one-third of HIV-infected individuals globally.
- Shared risk factors like intravenous drug use (IDU) influence coinfection prevalence.
- Coinfection accelerates the progression of both HIV and HCV, leading to worse clinical outcomes.
Purpose of the Study:
- To highlight the significant clinical implications of HIV-HCV coinfection.
- To discuss the evolving treatment landscape for HCV in coinfected patients.
- To address challenges in managing coinfected individuals and explore future therapeutic options.
Main Methods:
- Review of existing literature on HIV-HCV coinfection.
- Analysis of disease progression in coinfected versus monoinfected patients.
- Evaluation of current and emerging treatment strategies for HCV in the context of HIV.
Main Results:
- HIV accelerates HCV progression to cirrhosis and end-stage liver disease.
- HCV coinfection worsens HIV disease progression and immunological decline.
- Standard interferon-based therapies show limited efficacy; newer combinations are emerging.
Conclusions:
- Effective management of HCV coinfection is increasingly important due to improved HIV prognoses with HAART.
- Pegylated interferon plus ribavirin is a promising standard of care, despite potential overlapping toxicities.
- Liver transplantation is a potential rescue therapy for end-stage liver disease in coinfected patients.
Abstract:
HIV-hepatitis C virus (HCV) coinfection is common and affects more than one-third of all HIV infected persons worldwide. Prevalence among risk categories varies according to shared risk factors for transmission, mainly intravenous drug use (IDU) and hemophiliacs. Chronic HCV infection seems to accelerate the course of HIV disease, resulting in a worsened clinical and immunological progression. At the same time, several studies suggest that HIV disease modifies the natural history of HCV infection, leading to a faster course of progression from active hepatitis to cirrhosis, to end stage liver disease and death. HCV infection mimics opportunistic diseases because its natural history is significantly accelerated in HIV patients. Since highly active antiretroviral therapy (HAART) has slowed the progression of HIV disease and decreased the rate of HIV associated mortality, the prognosis of HIV disease has been modified, and the need to treat HCV coinfection become a significant issue. Because of the poor response rate obtained by either interferon alone or interferon thrice weekly plus ribavirin, the combination of pegylated interferon and ribavirin will probably become the standard of care, although the clinicians should be aware of the overlapping toxicity of nucleoside analogues and ribavirin. Many selected categories of patients pose particular challenges to physicians treating HCV infection: nonresponders to interferon, cirrhotic patients, and patients infected with both HCV and HBV. Liver transplantation in HIV patients is currently under evaluation, but should become the rescue therapy for HIV patients with end stage liver disease.
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