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Hepatitis C in HIV-positive patients--treatment and liver disease outcomes
1Division of Infectious Diseases, CORE Center, Stroger Hospital of Cook County and Rush University Medical Center, Chicago, IL 60612, USA. Oluwatoyin_adeyemi@rush.edu
Insights
Hepatitis C virus (HCV) coinfection in human immunodeficiency virus (HIV) patients leads to significant liver disease. Current treatments offer lower sustained virologic responses (SVRs) in coinfected individuals, necessitating further research into novel therapeutic strategies.
Area of Science:
- Hepatology
- Infectious Diseases
- Immunology
Background:
- Hepatitis C virus (HCV) coinfection is prevalent in human immunodeficiency virus (HIV) positive individuals.
- HCV-related liver disease is a major cause of morbidity and mortality in coinfected patients, even with effective antiretroviral therapy.
- Current treatment guidelines recommend HCV treatment for coinfected patients when feasible.
Purpose of the Study:
- To review the current landscape of HCV treatment in HIV-coinfected patients.
- To discuss challenges and emerging strategies for managing liver disease in this population.
- To highlight the need for improved therapeutic options and earlier inclusion in clinical trials.
Main Methods:
- Review of current clinical guidelines and published literature on HIV/HCV coinfection.
- Analysis of treatment outcomes, including sustained virologic response (SVR) rates.
- Discussion of alternative management strategies for patients unable to receive standard HCV treatment.
Main Results:
- Sustained virologic responses (SVRs) to pegylated interferon-alpha and ribavirin are lower (27%-40%) in coinfected patients compared to HCV mono-infected patients.
- Maintenance interferon strategies are being explored to delay liver disease complications.
- For treatment-refractory or contraindicated patients, highly active antiretroviral therapy (HAART) with careful monitoring and lifestyle counseling may slow fibrosis progression.
Conclusions:
- Optimizing HCV treatment and management in HIV-coinfected individuals remains a critical challenge.
- Early referral for liver transplantation evaluation is crucial for coinfected patients with end-stage liver disease.
- Inclusion of coinfected patients in early-phase clinical trials for new direct-acting antiviral agents is essential for developing more effective therapies.
Abstract:
Many human immunodeficiency virus (HIV) infected persons are coinfected with hepatitis C virus (HCV) and with the use of highly active antiretroviral therapy, liver disease from HCV has become an important cause of morbidity and mortality. The current guidelines recommend that human immunodeficiency virus and HCV coinfected patients be evaluated and treated for HCV if there are no major contraindications to treatment. Coinfected patients treated with pegylated interferon-a and ribavirin have sustained virologic responses (SVRs) of 27% to 40% which for a variety of reasons are lower than those reported in HCV mono-infected patients. Understanding that most patients will not achieve SVRs, strategies to evaluate for the role of maintenance interferon in delaying complications of liver disease are being evaluated. In patients who have failed prior treatment, cannot tolerate treatment, or who have contraindications to HCV treatment, the use of highly active antiretroviral therapy with careful monitoring for hepatotoxicity and aggressive counseling on alcohol and substance abuse may slow down fibrosis progression. As the data on liver transplantation in coinfected patients accumulate, patients with end stage liver disease should be referred early for evaluation in a transplant center. As new drugs for HCV are being developed, it will be of utmost importance to include coinfected patients earlier in the process on new drug trials and therapeutic strategies.
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