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Oral Combinational Antiretroviral Treatment in HIV-1 Infected Humanized Mice
Published on: October 6, 2022
Ongoing HIV replication in cerebrospinal fluid under successful monotherapy.
Marieke Bierhoff1, Charles A B Boucher, Azzania Fibriani
1Department of Internal Medicine, Kennemer Gasthuis, Haarlem, the Netherlands. m.bierhoff@kg.nl.
Antiviral Therapy
|January 25, 2013
Summary
Ritonavir/lopinavir (r/LPV) monotherapy can lead to HIV drug resistance in the central nervous system. Switching treatment successfully suppressed HIV RNA in both plasma and cerebrospinal fluid.
Area of Science:
- Neurovirology
- Infectious Diseases
- Antiretroviral Therapy
Background:
- Antiretroviral therapy (ART) is crucial for managing HIV infection.
- Ritonavir/lopinavir (r/LPV) has been used as a protease inhibitor-based regimen.
- Monotherapy with ART regimens requires careful monitoring for efficacy and resistance.
Observation:
- A case of an HIV-infected patient on long-term r/LPV monotherapy presented with neurological symptoms.
- High HIV RNA levels were detected in the cerebrospinal fluid (CSF).
- HIV protease gene sequencing from CSF revealed resistance mutations to lopinavir and ritonavir.
Findings:
- HIV RNA levels in plasma and CSF were initially high despite r/LPV monotherapy.
- Drug resistance mutations in the HIV protease gene were identified in the CSF.
- Switching the antiretroviral regimen led to undetectable HIV RNA in both plasma and CSF within two months.
Implications:
- Ritonavir/lopinavir monotherapy may be insufficient for complete viral suppression in the central nervous system (CNS).
- HIV can compartmentalize within the CNS, leading to the selection of drug-resistant strains.
- This case highlights the importance of monitoring viral load and resistance in both plasma and CSF, especially in patients with neurological symptoms on ART.
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