Hiv And Antiretrovirals In The Central Nervous System: Molecular Mechanisms Of Cognitive Impairment
type: CreativeWork
description: HIV-associated neurocognitive disorder (HAND) describes a wide range of cognitive impairments experienced by up to 55% of HIV+ individuals despite viral suppression by combined antiretroviral therapy. Reasons for the persistence of this disease are unknown, but may be related to both the presence of HIV-infected macrophages in the central nervous system as well as neurotoxicity of antiretroviral drugs. In this thesis, we identified two independent mechanisms of HIV-associated and antiretroviral-associated toxicity that may each contribute distinctly to HAND neuropathogenesis. First, we showed that β-site amyloid precursor protein cleaving enzyme 1 (BACE1), which may play a role in the onset and progression of Alzheimer’s Disease, was both increased in HIV+ patient brains and required for HIV-associated neurotoxicity in vitro. The BACE1 cleavage target amyloid precursor protein (APP) also mediated toxicity and was required for neuroprotective effects of BACE1 inhibition. Second, we showed that two frontline treatment antiretroviral drugs have neurotoxic potential in vitro and that neurotoxicity of antiretrovirals is highly variable both across and within drug classes. Neurotoxicity of one drug, lopinavir, was mediated by oxidative stress. Taken together, these data indicate that HIV and antiretrovirals may contribute to HAND persistence and that both BACE1 inhibitors and drugs targeting oxidative stress may be effective as adjunctive therapeutics in HIV+ patients.
abstract: HIV-associated neurocognitive disorder (HAND) describes a wide range of cognitive impairments experienced by up to 55% of HIV+ individuals despite viral suppression by combined antiretroviral therapy. Reasons for the persistence of this disease are unknown, but may be related to both the presence of HIV-infected macrophages in the central nervous system as well as neurotoxicity of antiretroviral drugs. In this thesis, we identified two independent mechanisms of HIV-associated and antiretroviral-associated toxicity that may each contribute distinctly to HAND neuropathogenesis. First, we showed that β-site amyloid precursor protein cleaving enzyme 1 (BACE1), which may play a role in the onset and progression of Alzheimer’s Disease, was both increased in HIV+ patient brains and required for HIV-associated neurotoxicity in vitro. The BACE1 cleavage target amyloid precursor protein (APP) also mediated toxicity and was required for neuroprotective effects of BACE1 inhibition. Second, we showed that two frontline treatment antiretroviral drugs have neurotoxic potential in vitro and that neurotoxicity of antiretrovirals is highly variable both across and within drug classes. Neurotoxicity of one drug, lopinavir, was mediated by oxidative stress. Taken together, these data indicate that HIV and antiretrovirals may contribute to HAND persistence and that both BACE1 inhibitors and drugs targeting oxidative stress may be effective as adjunctive therapeutics in HIV+ patients.
author: Stern, Anna Louise
language: en
date published: 2017
date modified: 2026-07-24T03:47:17Z
provider: University of Pennsylvania
publisher: Networked Digital Library of Theses and Dissertations
type: WebPage
source organization: University of Pennsylvania