JAIDS Journal of Acquired Immune Deficiency Syndromes · 2010 · 69 citations · 41 references
PharmacyInfectious DiseasesPharmacotherapyImmunology Of Infectious DiseasesNeuroimmunologyVirologyAntiretroviral TherapyAntiviral AgentsAntiviral ImmunityAntiviral PharmacologyAntiviral PharmacotherapyAntiviral TherapyCd4 T-cell DepletionCentral Nervous System Infection TreatmentHiv Antiretroviral TherapyHuman Immunodeficiency Virus PersistenceImmune Reconstitution After Antiretroviral TherapyViral Replication InhibitionViral Replication Kinetics
BACKGROUND: Antiretroviral treatment (ART) significantly reduces cerebrospinal fluid (CSF) HIV-1 RNA levels and residual viremia is less frequently found in CSF than in blood. However, persistent intrathecal immunoactivation is common, even after several years of ART. To investigate whether low-level CSF viremia and residual immunoactivation within the central nervous system (CNS) derive from ongoing local viral replication, we conducted a study of treatment intensification in patients on effective ART. METHODS: Ten patients on ART with plasma HIV RNA <50 copies per milliliter for >18 months were included. Intensification was given for in total 8 weeks: 4 weeks with maraviroc or lopinavir/ritonavir (good CNS penetration), and 4 weeks with enfuvirtide (poor CNS penetration). Lumbar punctures were performed 4 weeks before, at intensification commencement, at switchover after 4 weeks, at the conclusion of, and 4 weeks after the intensification period. RESULTS: No significant changes in HIV RNA, neopterin, β2-microglobulin, immunoglobulin G index, albumin ratio, and CD4(+) T-cell count were observed, either in CSF or blood, neither before, during, nor after the intensification periods. CONCLUSIONS: ART intensification did not reduce residual CSF HIV RNA levels or intrathecal immunoactivation in patients on ART. These findings do not support an ongoing viral replication in CNS.
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