Brain HIV-1 Infection Modeling in Humanized Mice

The HIV-1-associated neurologic disorders were described earlier in HIV-1 pandemia and are now recognized as a complex of pathologic changes related to the HIV-1 infection of brain perivascular and resident cells, such as microglia. At the same time, the significant contribution to the neurocognitive deficit in humans could be related to the secondary events, such as chronic emotional stress, chronic immune activation due to mucosal barriers deficiency, opportunistic viral and bacterial infections, malnutrition, and other factors that could not be excluded or controlled like on experimental laboratory animals. Animals carrying human hemato-lymphoid tissue and chronically infected with HIV-1 could provide valuable information about the pathogenesis of neurocognitive dysfunction and serve as a model for therapeutic development.