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Published on: January 12, 2016
The shifting patterns of HIV encephalitis neuropathology
I P Everall1, L A Hansen, E Masliah
1Department of Psychiatry, University of California, San Diego, La Jolla, CA 92093-0624, USA.
Highly active antiretroviral therapy (HAART) has altered HIV neuropathology, shifting manifestations from dementia to milder cognitive impairment. New variants of HIV encephalitis (HIVE) are emerging, requiring further study for effective neuroprotection.
Area of Science:
- Neuroscience
- Virology
- Immunology
Background:
- Human Immunodeficiency Virus (HIV) infection involves macrophage infiltration of the nervous system, causing neuropathological changes like HIV encephalitis (HIVE).
- Highly Active Antiretroviral Therapy (HAART) has significantly modified HIV-related neurological disease patterns over the last decade.
- The aging HIV-positive population on HAART may be experiencing an increase in chronic HIVE forms.
Purpose of the Study:
- To characterize proposed variants of HIV-associated neurological conditions.
- To understand the evolving pathogenesis of HIV-related neurological damage.
- To inform the development of targeted neuroprotective treatments.
Main Methods:
- Review and synthesis of existing literature on HIV neuropathology and HAART's impact.
- Pathological and clinical correlation of proposed HIVE variants.
- Identification of factors contributing to emerging HIVE variants.
Main Results:
- Neuropathological alterations in HIV infection include HIVE, leukoencephalopathy, and vacuolar myelopathy, leading to neurodegeneration.
- HAART has decreased opportunistic infections and CNS neoplasms but may be associated with rising chronic HIVE.
- Clinical manifestations have shifted from severe dementia to subtle cognitive impairment, suggesting new classifications.
- Proposed neuropathological variants include aggressive HIVE, lymphocytic infiltration, 'burnt-out' HIVE, and aging-associated changes.
Conclusions:
- Emerging HIVE variants are influenced by viral resistance, immune reconstitution, drug toxicity, and comorbidities.
- Further characterization of these variants is crucial for understanding HIV neurotoxicity.
- Enhanced understanding will facilitate the design of more effective neuroprotective strategies for HIV patients.
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