Increased frequency of Foxp3 + CD8 + T cells is associated with disease progression during HIV infection
- PMID: 40116077
- DOI: 10.1097/QAD.0000000000004185
Increased frequency of Foxp3 + CD8 + T cells is associated with disease progression during HIV infection
Abstract
Objectives: Recent years have witnessed unprecedented strides in comprehending non-CD4 regulatory T cells (Tregs), such as CD8 + Tregs and double-negative T cells (DNT cells), and their role in sustaining immune tolerance and restricting immune activation. This study investigates the role of Foxp3 + CD8 + T cells during HIV infection and assess the markers associated with CD4 + Tregs.
Design: This study was designed as a cross-sectional cohort study, comprising 21 age-matched healthy controls, 122 treatment-naive participants, and 60 people with HIV (PWH) receiving successful treatment (antiretroviral therapies, ARTs).
Methods: The frequency of Foxp3 + CD8 + T cells was assessed alongside CD4 + Treg-associated markers and plasma inflammatory factor levels.
Results: Foxp3 + CD8 + T cells were enriched in PWH with CD4 + T cell count less than 350 cells/μl and persisted after ART. Moreover, the Foxp3 + CD8 + T cells were correlated with CD4 + T cell count, CD4/CD8 ratio, and the parameters of activation and systematic inflammation in PWH. Moreover, Foxp3 + CD8 + T cells expressed different levels of Tregs related markers compared to CD4 + Tregs and Foxp3 + DNT cells.
Conclusion: The Foxp3 + CD8 + T cells are associated with HIV disease progression and employ distinct mechanisms to exert their functions.
Keywords: Foxp3; HIV; immune activation; immune regulation.
Copyright © 2025 Wolters Kluwer Health, Inc. All rights reserved.
Similar articles
-
Severe immune dysregulation affects CD4⁺CD25(hi)FoxP3⁺ regulatory T cells in HIV-infected patients with low-level CD4 T-cell repopulation despite suppressive highly active antiretroviral therapy.J Infect Dis. 2012 May 15;205(10):1501-9. doi: 10.1093/infdis/jis230. Epub 2012 Mar 28. J Infect Dis. 2012. PMID: 22457273
-
Elevated Foxp3+ double-negative T cells are associated with disease progression during HIV infection.Front Immunol. 2022 Jul 28;13:947647. doi: 10.3389/fimmu.2022.947647. eCollection 2022. Front Immunol. 2022. PMID: 35967422 Free PMC article.
-
FOXP3+Helios+ Regulatory T Cells, Immune Activation, and Advancing Disease in HIV-Infected Children.J Acquir Immune Defic Syndr. 2016 Aug 15;72(5):474-84. doi: 10.1097/QAI.0000000000001000. J Acquir Immune Defic Syndr. 2016. PMID: 27003495 Free PMC article.
-
[The subpopulation CD4(+); CD25(+); Foxp3(+);/CD127(low/-); regulatory T cells in peripheral blood of HIV-infected patients correlated with disease progression].Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2012 Nov;28(11):1188-91. Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2012. PMID: 23127412 Chinese.
-
Thymic function in HIV-infection.Dan Med J. 2013 Apr;60(4):B4622. Dan Med J. 2013. PMID: 23651726 Review.
References
-
- Lv T, Cao W, Li T. HIV-related immune activation and inflammation: current understanding and strategies . J Immunol Res 2021; 2021:7316456.
-
- Sokoya T, Steel HC, Nieuwoudt M, Rossouw TM. HIV as a cause of immune activation and immunosenescence . Mediators Inflamm 2017; 2017:6825493.
-
- García F, Fumero E, Gatell JM. Immune modulators and treatment interruption . Curr Opin HIV AIDS 2008; 3:124–130.
-
- Goswami TK, Singh M, Dhawan M, Mitra S, Emran TB, Rabaan AA, et al. Regulatory T cells (Tregs) and their therapeutic potential against autoimmune disorders - advances and challenges . Hum Vaccin Immunother 2022; 18:2035117.
-
- Rodríguez-Perea AL, Arcia ED, Rueda CM, Velilla PA. Phenotypical characterization of regulatory T cells in humans and rodents . Clin Exp Immunol 2016; 185:281–291.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials