Suppression of Inflammatory Neurotoxins by Highly Active Antiretroviral Therapy in Human Immunodeficiency Virus—Associated Dementia

HE Gendelman, J Zheng, CL Coulter… - The Journal of …, 1998 - academic.oup.com
HE Gendelman, J Zheng, CL Coulter, A Ghorpade, M Che, M Thylin, R Rubocki, Y Persidsky
The Journal of infectious diseases, 1998academic.oup.com
A human immunodeficiency virus type 1 (HIV)—seropositive, antiretroviral-naive patient
presented with significant cognitive dysfunction. Neuropsychologic, neuroradiologic,
immunologic, and virologic studies confirmed HIV-associated dementia (HAD). After 12
weeks of highly active antiretroviral therapy (HAART) with ibuprofen, dramatic improvements
were demonstrated in neurologic function and were sustained for> 1 year. HIV-1 RNA in
cerebrospinal fluid (CSF) decreased from 105 to 104 copies/mL after 4 weeks. After 20 …
Abstract
A human immunodeficiency virus type 1 (HIV)—seropositive, antiretroviral-naive patient presented with significant cognitive dysfunction. Neuropsychologic, neuroradiologic, immunologic, and virologic studies confirmed HIV-associated dementia (HAD). After 12 weeks of highly active antiretroviral therapy (HAART) with ibuprofen, dramatic improvements were demonstrated in neurologic function and were sustained for >1 year. HIV-1 RNA in cerebrospinal fluid (CSF) decreased from 105 to 104 copies/mL after 4 weeks. After 20 weeks of therapy, plasma viremia decreased from 106 copies/mL to undetectable (<96 copies/mL). Assays of neurotoxins (tumor necrosis factor-α, quinolinic acid, and nitric oxide) in plasma and CSF were considerably elevated at presentation and significantly decreased after therapy. Baseline plasma and CSF demonstrated neurotoxic activities in vitro, which also reduced markedly. These data, taken together, support the notion that HAD is a reversible metabolic encephalopathy fueled by viral replication. HAART used with nonsteroidal antiinflammatory agents leads to the suppression of inflammatory neurotoxins and can markedly improve neurologic function in HAD.
Oxford University Press