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Updated: Jan 25, 2026

CD4+ T-Lymphocyte Capture Using a Disposable Microfluidic Chip for HIV
Published on: October 1, 2007
Role of T Lymphocytes in HIV Neuropathogenesis
Caroline Subra1,2, Lydie Trautmann3,4
1Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, MD, USA.
Insights
Human immunodeficiency virus (HIV) invades the central nervous system (CNS) early. This review details how CD4+ T cells facilitate HIV brain infection and how CD8+ T cells combat it, impacting HIV neuropathogenesis.
Area of Science:
- Neuroimmunology
- Virology
- Immunology
Background:
- Human immunodeficiency virus (HIV) frequently targets the central nervous system (CNS) early in infection.
- Neurological impairments persist in HIV-infected individuals despite antiretroviral therapy (ART).
- CD4+ T cells and monocytes facilitate HIV entry into the brain, contributing to viral persistence and neuronal damage.
Purpose of the Study:
- To review the role of CD4+ T lymphocytes in HIV's assault and persistence within the CNS.
- To summarize the mechanisms of HIV-infected CNS resident cell elimination by CD8+ T lymphocytes.
Main Methods:
- Literature review of current knowledge on T cell involvement in HIV CNS infection.
- Analysis of the dual role of CD8+ T cells in HIV neuropathogenesis.
Main Results:
- CD4+ T cells are crucial for initiating and maintaining HIV infection in the CNS.
- CD8+ T cells are recruited to the CNS to control viral replication but struggle to eliminate infected cells.
- The precise role of CD8+ T cells in HIV neuropathogenesis remains complex, potentially involving both beneficial clearance and detrimental inflammation.
Conclusions:
- Understanding T cell dynamics in the CNS is critical for addressing HIV-related neurological complications.
- Further research is needed to fully elucidate the beneficial and detrimental roles of CD8+ T cells in HIV CNS disease.
Purpose Of Review:
The purpose of this review is to summarize the current knowledge on the role of CD4+ T lymphocytes leading to HIV assault and persistence in the central nervous system (CNS) and the elimination of HIV-infected CNS resident cells by CD8+ T lymphocytes.
Recent Findings:
HIV targets the CNS early in infection, and HIV-infected individuals suffer from mild forms of neurological impairments even under antiretroviral therapy (ART). CD4+ T cells and monocytes mediate HIV entry into the brain and constitute a source for HIV persistence and neuronal damage. HIV-specific CD8+ T cells are also massively recruited in the CNS in acute infection to control viral replication but cannot eliminate HIV-infected cells within the CNS. This review summarizes the involvement of CD4+ T cells in seeding and maintaining HIV infection in the brain and describes the involvement of CD8+ T cells in HIV neuropathogenesis, playing a role still to be deciphered, either beneficial in eliminating HIV-infected cells or deleterious in releasing inflammatory cytokines.
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