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Updated: Aug 23, 2025

Assessment of the Synaptic Interface of Primary Human T Cells from Peripheral Blood and Lymphoid Tissue
Published on: July 30, 2018
The immune synapses reveal aberrant functions of CD8 T cells during chronic HIV infection
Nadia Anikeeva1, Maria Steblyanko1, Leticia Kuri-Cervantes2
1Department of Microbiology and Immunology, Thomas Jefferson University, Philadelphia, PA, USA.
Insights
Chronic HIV infection impairs CD8 T cell function by causing premature immune aging. Aberrant naive T cells develop into abnormal effector cells, reducing the capacity to control HIV and other infections.
Area of Science:
- Immunology
- Virology
- Cellular Biology
Background:
- Chronic human immunodeficiency virus (HIV) infection leads to persistent inflammation and premature immune system aging.
- This immune aging particularly affects CD8 T cells, diminishing their functional capacity over time.
Purpose of the Study:
- To investigate the mechanisms behind the reduced potency of CD8 T cells in individuals with chronic HIV.
- To analyze how HIV infection impacts T cell synapse formation and degranulation patterns.
Main Methods:
- CD8 T cells from people living with HIV were exposed to artificial lipid bilayers presenting T-cell receptor and integrin ligands.
- Analysis included cellular morphology, synaptic interface dynamics, and degranulation patterns.
Main Results:
- A significant proportion of phenotypically naive T cells from HIV-infected individuals formed mature synapses with focused degranulation.
- This synapse formation and degranulation is typically a characteristic of differentiated, effector T cells.
Conclusions:
- HIV infection can induce aberrant differentiation in naive T cells, leading to the development of anomalous effector T cells.
- These anomalous effector T cells may have a compromised ability to control HIV and other opportunistic infections.
Abstract:
Chronic HIV infection causes persistent low-grade inflammation that induces premature aging of the immune system including senescence of memory and effector CD8 T cells. To uncover the reasons of gradually diminished potency of CD8 T cells from people living with HIV, here we expose the T cells to planar lipid bilayers containing ligands for T-cell receptor and a T-cell integrins and analyze the cellular morphology, dynamics of synaptic interface formation and patterns of the cellular degranulation. We find a large fraction of phenotypically naive T cells from chronically infected people are capable to form mature synapse with focused degranulation, a signature of a differentiated T cells. Further, differentiation of aberrant naive T cells may lead to the development of anomalous effector T cells undermining their capacity to control HIV and other pathogens that could be contained otherwise.
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