Longitudinal T-Cell Phenotypic Dynamics During Sustained Antiretroviral Therapy in People With HIV

Long-term ART promotes partial immune normalization, including reduced activation and reversal of CD4⁺ T-cell exhaustion. However, persistent expression of CD8⁺ T-cell surrogate markers of exhaustion and stable cytotoxic profiles suggest ongoing antigenic stimulation, potentially driven by HIV or chronic coinfections.

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Publication Details

Journal
Open Forum Infectious Diseases
Published
2025-12-24
DOI
https://doi.org/10.1093/ofid/ofaf775
Primary Topic
HIV Research and Treatment
Type
article
Field-Weighted Citation Impact
0.00
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article

Longitudinal T-Cell Phenotypic Dynamics During Sustained Antiretroviral Therapy in People With HIV

Victor DeGruttola, Noah C. Gaitan, Eileen P. Scully, Alan Landay et al.
Open Forum Infectious Diseases
HIV Research and Treatment
article

Longitudinal T-Cell Phenotypic Dynamics During Sustained Antiretroviral Therapy in People With HIV

Victor DeGruttola, Noah C. Gaitan, Eileen P. Scully, Alan Landay, Antoine Chaillon, Miranda L. Lynch, Brendon Woodworth, Jonathan Karn, Stephen A. Rawlings, A. F. Wells, Sara Gianella, Christophe Guy Éric Vanpouille, Xinlian Zhang, Kathleen M Weber, Xin Tu
article en

Abstract

Long-term ART promotes partial immune normalization, including reduced activation and reversal of CD4⁺ T-cell exhaustion. However, persistent expression of CD8⁺ T-cell surrogate markers of exhaustion and stable cytotoxic profiles suggest ongoing antigenic stimulation, potentially driven by HIV or chronic coinfections.

Open Forum Infectious DiseasesVol. 13(1)
Johns Hopkins University (US), Johns Hopkins Medicine (US), University of California San Diego (US), Hektoen Institute (US), Human Longevity (United States) (US), Eunice Kennedy Shriver National Institute of Child Health and Human Development (US), The University of Texas Medical Branch at Galveston (US), Case Western Reserve University (US), University at Buffalo, State University of New York (US)
Openalex Percentile: Top 34%
HIV Research and Treatment
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