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Establishment of the Dual Humanized TK-NOG Mouse Model for HIV-associated Liver Pathogenesis
Published on: September 11, 2019
Therapy of chronic hepatitis C in the setting of HIV co-infection
1University Hospital Antwerp, Wilrijkstraat 10, B-2650 Edegem. peter.michielsen@uza.be
Insights
Hepatitis C virus (HCV) and human immunodeficiency virus (HIV) co-infection is common, particularly in intravenous drug users. While HCV treatment is recommended for stable HIV patients, co-infected individuals show lower sustained viral response rates.
Area of Science:
- Hepatology
- Virology
- Immunology
Background:
- Hepatitis C virus (HCV) and human immunodeficiency virus (HIV) are significant global health concerns.
- Shared transmission routes lead to frequent co-infection, especially among intravenous drug users.
- HIV accelerates HCV-related liver disease progression, and HCV co-infection increases the risk of hepatotoxicity from Highly Active Antiretroviral Therapy (HAART).
Purpose of the Study:
- To review the implications of HCV infection on HIV disease progression and HAART.
- To discuss the current recommendations for HCV treatment in co-infected patients.
- To analyze treatment outcomes and success factors for HCV in co-infected individuals.
Main Methods:
- Literature review of studies on HCV/HIV co-infection and treatment outcomes.
- Analysis of data regarding HCV treatment efficacy in co-infected versus mono-infected patients.
- Examination of factors influencing sustained viral response to therapy.
Main Results:
- HCV co-infection negatively impacts HIV disease progression and increases HAART hepatotoxicity risks.
- HCV treatment is advised for stable HIV patients, with similar schedules to mono-infected individuals (pegylated interferon and ribavirin).
- Co-infected patients demonstrate lower sustained viral response rates compared to HCV mono-infected patients, though success factors are similar.
Conclusions:
- HCV treatment is a critical consideration for patients with stable HIV disease.
- Further research is needed to optimize HCV treatment duration and efficacy in co-infected populations.
- Understanding treatment outcomes is crucial for managing this complex co-infection.
Abstract:
Hepatitis C virus (HCV) and human immunodeficiency virus (HIV) infections are major health problems world-wide. As both viruses partially share routes of transmission, co-infection is common. This is especially the case in patients infected through intravenous drug use. It has been shown that HIV accelerates HCV progression to cirrhosis. The influence of HCV infection on the natural history of HIV disease remains highly controversial. It is also known that HCV co-infection increases the risk of hepatotoxicity of Highly Active Antiretroviral Therapy (HAART). These considerations as well as the improved survival of HIV patients due to HAART leads to increasing numbers of patients undergoing assessment and treatment of HCV infection. HCV treatment should be considered in stable HIV disease. Recent data indicate that HCV treatment schedules should be similar in co-infected and HCV mono-infected individuals, with pegylated interferon combined with ribavirin. For all treatment regimens published, coinfected patients had a lower sustained viral response rate compared to HCV mono-infected patients. Similar predictive factors determine the success rate. The effect of prolonging therapy to 12 months in genotype 2/3 and to 18 months in early viral responders with genotypes 1/4 needs to be assessed in further studies.
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