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Updated: Apr 5, 2026

In Vitro Assay to Evaluate the Impact of Immunoregulatory Pathways on HIV-specific CD4 T Cell Effector Function
Published on: October 15, 2013
Persistent HIV Type 1 Seronegative Status Is Associated With Lower CD8+ T-Cell Activation
Peter J Kuebler1, Megha L Mehrotra2, Brian I Shaw1
1Division of Experimental Medicine, University of California-San Francisco.
Increased T-cell activation, specifically CD8+ T cells expressing CD38 and HLA-DR, was linked to a higher risk of human immunodeficiency virus type 1 (HIV-1) infection in a global trial. This finding suggests T-cell activation may serve as an early biomarker for HIV-1 risk.
Area of Science:
- Immunology
- Virology
- Clinical Trials
Background:
- Pre-exposure prophylaxis (PrEP) is a key strategy for preventing human immunodeficiency virus type 1 (HIV-1) infection.
- Understanding factors associated with HIV-1 acquisition risk is crucial for refining prevention strategies.
Purpose of the Study:
- To compare T-cell activation levels between individuals who acquired HIV-1 and those who remained uninfected during the iPrEx PrEP trial.
- To investigate whether T-cell activation serves as a potential biomarker for elevated HIV-1 infection risk.
Main Methods:
- Analysis of T-cell activation markers, specifically CD38(+)HLA-DR(+) CD8(+) T cells, in participants of the Preexposure Prophylaxis Initiative (iPrEx) trial.
- Comparison of T-cell activation frequencies between HIV-1 seroconverters and HIV-1 seronegative participants.
Main Results:
- A significantly greater frequency of CD38(+)HLA-DR(+) CD8(+) T cells was observed in individuals who seroconverted to HIV-1 compared to those who remained uninfected (1.30% vs. 0.82%, P = .005).
- An odds ratio of 4.26 (95% CI, 1.54-11.78) indicated a strong association between elevated CD8+ T-cell activation and HIV-1 infection.
Conclusions:
- CD8+ T-cell activation is significantly higher in individuals who acquire HIV-1 infection.
- T-cell activation may function as a valuable biomarker for identifying individuals at increased risk of HIV-1 acquisition.
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