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DOI 10.3390/ijms26146724

Медицинская библиотека · International journal of molecular sciences · 2025

Oxidative Stress in HIV-Associated Neurodegeneration: Mechanisms of Pathogenesis and Therapeutic Targets.

Gagliardi Sophia, Hotchkin Tristan, Hillmer Grace, Engelbride Maeve, Diggs Alexander, Tibebe Hasset, Izumi Coco, Sullivan Cailyn, Cropp Cecelia, Lantz Olive, Marquez Dacia, Chang Jason, Ezaki Jiro, Zestos Alexander George, Riley Anthony L, Izumi Taisuke

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Аннотация

Treatment for HIV infection has become more manageable due to advances in combination antiretroviral therapy (cART). However, HIV still significantly affects the central nervous system (CNS) in infected individuals, even with effective plasma viral suppression, due to persistent viral reservoirs and chronic neuroinflammation. This ongoing inflammation contributes to the development of HIV-associated neurocognitive disorders (HANDs), including dementia and Alzheimer's disease-like pathology. These complications are particularly prevalent among the aging population with HIV. This review aims to provide a comprehensive overview of HAND, with a focus on the contribution of oxidative stress induced by HIV-mediated reactive oxygen species (ROS) production through viral proteins such as gp120, Tat, Nef, Vpr, and reverse transcriptase. In addition, we discuss current and emerging therapeutic interventions targeting HAND, including antioxidant strategies and poly (ADP-ribose) polymerase (PARP) inhibitors. These are potential adjunctive approaches to mitigate neuroinflammation and oxidative damage in the CNS.

Для цитирования: Gagliardi Sophia, Hotchkin Tristan, Hillmer Grace, Engelbride Maeve, Diggs Alexander, Tibebe Hasset, Izumi Coco, Sullivan Cailyn, Cropp Cecelia, Lantz Olive, Marquez Dacia, Chang Jason, Ezaki Jiro, Zestos Alexander George, Riley Anthony L, Izumi Taisuke. Oxidative Stress in HIV-Associated Neurodegeneration: Mechanisms of Pathogenesis and Therapeutic Targets.. International journal of molecular sciences. 2025. DOI: 10.3390/ijms26146724.

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