Association between discordant immunological response to highly active anti-retroviral therapy, regulatory T cell percentage, immune cell activation and very low-level viraemia in HIV-infected patients
- PMID: 24460818
- PMCID: PMC4008985
- DOI: 10.1111/cei.12278
Association between discordant immunological response to highly active anti-retroviral therapy, regulatory T cell percentage, immune cell activation and very low-level viraemia in HIV-infected patients
Abstract
The mechanisms sustaining the absence of complete immune recovery in HIV-infected patients upon long-term effective highly active anti-retroviral therapy (HAART) remain elusive. Immune activation, regulatory T cells (T(regs)) or very low-level viraemia (VLLV) have been alternatively suspected, but rarely investigated simultaneously. We performed a cross-sectional study in HIV-infected aviraemic subjects (mean duration of HAART: 12 years) to concomitantly assess parameters associated independently with inadequate immunological response. Patients were classified as complete immunological responders (cIR, n = 48) and inadequate immunological responders (iIR, n = 39), depending on the CD4(+) T cell count (> or < 500/mm(3)). Clinical and virological data (including very low-level viraemia) were collected. In parallel, immunophenotyping of CD4(+) lymphocytes, including T(reg) subsets, and CD8(+) T cells was performed. Percentages of activated CD4(+) T cells, T(regs), effector T(regs) and terminal effector T(regs) were found to be significantly elevated in iIR. Neither the percentage of activated CD8(+) T cells nor VLLV were found to be associated with iIR. In the multivariate analysis, nadir of CD4(+) T cell count and percentage of T(regs) were the only two parameters associated independently with iIR [odds ratio (OR) = 2·339, P = 0·001, and OR = 0·803, P = 0·041]. We present here the largest study investigating simultaneously the immune response to long-term HAART, activation of CD4(+) and CD8(+) T cells, T(reg) percentages and very low-level viraemia. Causative interactions between T(regs) and CD4(+) T cells should now be explored prospectively in a large patients cohort.
Keywords: HAART; immune activation; immunological response; regulatory T cells; very low-level viraemia.
© 2014 British Society for Immunology.
Figures



Similar articles
-
Relationship between discordant response to HAART, Tregs, immune activation and low-level viraemia.J Int AIDS Soc. 2014 Nov 2;17(4 Suppl 3):19672. doi: 10.7448/IAS.17.4.19672. eCollection 2014. J Int AIDS Soc. 2014. PMID: 25397422 Free PMC article.
-
Regulatory T cells in human immunodeficiency virus-infected patients are elevated and independent of immunological and virological status, as well as initiation of highly active anti-retroviral therapy.Clin Exp Immunol. 2008 Oct;154(1):80-6. doi: 10.1111/j.1365-2249.2008.03725.x. Clin Exp Immunol. 2008. PMID: 18821942 Free PMC article.
-
Increase in frequencies of circulating Th-17 cells correlates with microbial translocation, immune activation and exhaustion in HIV-1 infected patients with poor CD4 T-cell reconstitution.Immunobiology. 2016 May;221(5):670-8. doi: 10.1016/j.imbio.2016.01.002. Epub 2016 Jan 15. Immunobiology. 2016. PMID: 26817581
-
Thymic function in HIV-infection.Dan Med J. 2013 Apr;60(4):B4622. Dan Med J. 2013. PMID: 23651726 Review.
-
The role of T regulatory cells in the immunopathogenesis of HIV: Clinical implications.Braz J Infect Dis. 2024 Sep-Oct;28(5):103866. doi: 10.1016/j.bjid.2024.103866. Epub 2024 Aug 18. Braz J Infect Dis. 2024. PMID: 39163991 Free PMC article. Review.
Cited by
-
Low CD4/CD8 Ratio Is Associated with Non AIDS-Defining Cancers in Patients on Antiretroviral Therapy: ANRS CO8 (Aproco/Copilote) Prospective Cohort Study.PLoS One. 2016 Aug 22;11(8):e0161594. doi: 10.1371/journal.pone.0161594. eCollection 2016. PLoS One. 2016. PMID: 27548257 Free PMC article.
-
Maraviroc intensification in patients with suppressed HIV viremia has limited effects on CD4+ T cell recovery and gene expression.Antiviral Res. 2014 Jul;107:42-9. doi: 10.1016/j.antiviral.2014.04.005. Epub 2014 Apr 24. Antiviral Res. 2014. PMID: 24769244 Free PMC article.
-
Stimulation of PBMC and Monocyte-Derived Macrophages via Toll-Like Receptor Activates Innate Immune Pathways in HIV-Infected Patients on Virally Suppressive Combination Antiretroviral Therapy.Front Immunol. 2016 Dec 19;7:614. doi: 10.3389/fimmu.2016.00614. eCollection 2016. Front Immunol. 2016. PMID: 28066424 Free PMC article.
-
Current views on HIV-1 latency, persistence, and cure.Folia Microbiol (Praha). 2017 Jan;62(1):73-87. doi: 10.1007/s12223-016-0474-7. Epub 2016 Oct 5. Folia Microbiol (Praha). 2017. PMID: 27709447 Review.
-
Systemic Cytokine Levels Do Not Predict CD4(+) T-Cell Recovery After Suppressive Combination Antiretroviral Therapy in Chronic Human Immunodeficiency Virus Infection.Open Forum Infect Dis. 2016 Feb 8;3(1):ofw025. doi: 10.1093/ofid/ofw025. eCollection 2016 Jan. Open Forum Infect Dis. 2016. PMID: 26966697 Free PMC article.
References
-
- Grabar S, Le Moing V, Goujard C, et al. Clinical outcome of patients with HIV-1 infection according to immunologic and virologic response after 6 months of highly active antiretroviral therapy. Ann Intern Med. 2000;133:401–410. - PubMed
-
- Piketty C, Weiss L, Thomas F, Mohamed AS, Belec L, Kazatchkine MD. Long-term clinical outcome of human immunodeficiency virus-infected patients with discordant immunologic and virologic responses to a protease inhibitor-containing regimen. J Infect Dis. 2001;183:1328–1335. - PubMed
-
- Gilson RJ, Man SL, Copas A, et al. Discordant responses on starting highly active antiretroviral therapy: suboptimal CD4 increases despite early viral suppression in the UK Collaborative HIV Cohort (UK CHIC) Study. HIV Med. 2010;11:152–160. - PubMed
-
- Li T, Wu N, Dai Y, et al. Reduced thymic output is a major mechanism of immune reconstitution failure in HIV-infected patients after long-term antiretroviral therapy. Clin Infect Dis. 2005;53:944–951. - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials