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Oral Combinational Antiretroviral Treatment in HIV-1 Infected Humanized Mice
Published on: October 6, 2022
[Treatment of chronic hepatitis C in human immunodeficiency virus infected patients]
1Department of HIV/AIDS, Dr Fran Mihaljević University Hospital for Infectious Diseases, Zagreb, Croatia.
Insights
Hepatitis C virus (HCV) and human immunodeficiency virus (HIV) co-infection accelerates liver fibrosis. Treatment with pegylated interferon and ribavirin is recommended for eligible patients, with duration tailored to viral response.
Area of Science:
- Hepatology
- Virology
- Infectious Diseases
Background:
- Hepatitis C virus (HCV) and human immunodeficiency virus (HIV) co-infection increases the risk of advanced liver fibrosis compared to HCV mono-infection.
- HCV treatment can lead to virus eradication, making all individuals with detectable HCV viral load candidates for therapy.
Purpose of the Study:
- To outline treatment recommendations for HCV/HIV co-infected patients.
- To define criteria for initiating and discontinuing HCV treatment in this population.
- To provide guidance on treatment duration and drug interactions.
Main Methods:
- Treatment is recommended for HCV/HIV co-infected patients with elevated aminotransferase levels, F2 fibrosis or higher, or >200 CD4+ T-lymphocytes/microL.
- Treatment involves pegylated interferon and weight-based ribavirin.
- Monitoring HCV RNA levels guides treatment duration and discontinuation.
Main Results:
- Treatment duration varies from 24 to 72 weeks based on HCV genotype and viral response.
- Discontinuation is advised for inadequate viral load decline (<2 log after 12 weeks) or detectable viral load after 24 weeks.
- Caution is advised with hepatotoxic antiretroviral drugs during concurrent treatment.
Conclusions:
- HCV/HIV co-infected patients meeting specific criteria should be considered for HCV treatment.
- Treatment regimens and durations should be individualized based on patient factors and treatment response.
- Careful consideration of drug interactions is crucial for co-infected patients.
Abstract:
Hepatitis C virus (HCV) and human immunodeficiency virus (HIV) co-infected individuals have a higher risk of advanced liver fibrosis compared to those that are HCV mono-infected. Treatment of HCV offers the possibility of virus eradication, thus every person with detectable HCV viral load is a candidate for treatment. Treatment is recommended for all HCV/HIV co-infected patients with: 1) repeatedly elevated aminotransferase levels; 2) F2 stage of liver fibrosis or higher regardless of alanine aminotransferase level; and 3) more than 200 CD4+ T-lymphocytes per microL of blood. Treatment is not recommended for patients that are active injection drug users, consume large amounts of alcohol, or have or had a severe psychiatric disorder. Liver biopsy is generally recommended, however, because of faster progression to liver fibrosis in HIV and HCV co-infected patients, if the patient declines liver biopsy it should not exclude him from treatment. Treatment with a combination of pegylated interferon and weight-based ribavirin (1000 mg/day if <75 kg and 1200 mg/day if >75 kg) is recommended. Pegylated interferon is used as 180 microg for alfa-2a form and 1.5 mg/kg for alfa-2b form once weekly subcutaneously. HCV RNA should be measured after 4 weeks of treatment, and later as needed, in weeks 12, 24, 48 or 72. For evaluation of a sustained viral response, HCV RNA should be measured 24 weeks after the end of treatment. In patients with rapid viral response (undetectable levels of HCV RNA after 4 weeks of treatment), treatment duration is 24 weeks (genotypes 2 and 3) or 48 weeks (genotypes 1 and 4). In patients without rapid viral response but with an adequate response after 12 and 24 weeks, we generally recommend treatment for 48 weeks, however, 72 weeks of treatment can be considered for genotypes 1 and 4. Treatment discontinuation is recommended in patients with <2 log viral load decline after 12 weeks or with a detectable viral load after 24 weeks of treatment. If concurrent treatment of HCV and HIV is necessary, treatment with zidovudine and didanosine should be avoided and caution is needed with the administration of potentially hepatotoxic antiretroviral drugs such as nevirapine and ritonavir.
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