The persistence of low CD4/CD8 ratio in chronic HIV-infection, despite ART suppression and normal CD4 levels, is associated with pre-therapy values of inflammation and thymic function.

Garrido-Rodríguez, VanesaBulnes-Ramos, ÁngelOlivas-Martínez, IsraelPozo-Balado, María Del MarÁlvarez-Ríos, Ana IsabelGutiérrez, FélixIzquierdo Miguel, RebecaGarcía, FedericoTiraboschi, Juan ManuelVera-Méndez, FranciscoPeraire, JoaquimRull, AnnaPacheco, Yolanda MaríaCoRIS Cohort2025-02-032025-02-032024-12Garrido-Rodríguez V, Bulnes-Ramos Á, Olivas-Martínez I, Pozo-Balado MDM, Álvarez-Ríos AI, Gutiérrez F, Izquierdo R, García F, Tiraboschi JM, Vera-Méndez F, Peraire J, Rull A, Pacheco YM; CoRIS cohort. The persistence of low CD4/CD8 ratio in chronic HIV-infection, despite ART suppression and normal CD4 levels, is associated with pre-therapy values of inflammation and thymic function. J Microbiol Immunol Infect. 2024 Dec;57(6):854-867.1684-1182https://hdl.handle.net/20.500.12105/26245Background: Persistence of a low CD4/CD8 ratio is associated with an increased morbimortality in people living with HIV (PLWH) under effective antiretroviral therapy. We aimed to explore the immunological significance of a persistently low CD4/CD8 ratio, even despite normal CD4 levels, and assess whether these features vary from those associated to a low nadir-CD4, another well-established predictor of disease progression. Methods: CD4-recovered PLWH were classified by CD4/CD8 ratio after three-years of ART (viral suppression, CD4≥500; R < 0.8, n = 24 and R > 1.2, n = 28). sj/β-TRECs ratio and inflammatory-related markers were quantified. PBMCs were immunophenotyped by CyTOF and functionally characterized by ELISPOT. Subjects were also reclassified depending on nadir-CD4 (N ≤ 350/N > 350). Results: R < 0.8 showed a differential inflammatory profile compared to R > 1.2 (increased β2-microglobulin, D-dimers and IP-10 before ART). R < 0.8 presented lower baseline thymic function, being inversely correlated with post-ART inflammation. R < 0.8 at follow-up showed most alterations in CD8 subsets (increasing frequency and exhibiting a senescent phenotype [e.g., CD57+, CD95+]) and enhanced T-cell IFNγ/IL-2 secretion. However, comparing N ≤ 350 to N > 350, the main features were altered functional markers in CD4 T-cells, despite no differences in maturational subsets, together with a restricted T-cell cytokine secretion pattern. Conclusion: Persistence of low CD4/CD8 ratio in successfully-treated PLWH, with normal CD4 counts, is associated with baseline inflammation and low thymic function, and it features post-therapy alterations specific to CD8 T-cells. Differently, subjects recovered from low nadir-CD4 in this setting feature post-therapy alterations on CD4 T-cells. Hence, different mechanisms of disease progression could underlie these biomarkers, potentially requiring different clinical approaches.engVoRhttp://creativecommons.org/licenses/by-nc-nd/4.0/CD4/CD8 ratioHIV-InfectionImmunological dysfunctionNadir-CD4 T-cellsj/β-TRECsAdultAntiretroviral Therapy, Highly ActiveBiomarkersCD4 Lymphocyte CountCD4-CD8 RatioCD4-Positive T-LymphocytesDisease ProgressionFemaleHIV InfectionsHumansInflammationMaleMiddle AgedThymus GlandViral LoadThe persistence of low CD4/CD8 ratio in chronic HIV-infection, despite ART suppression and normal CD4 levels, is associated with pre-therapy values of inflammation and thymic function.Attribution-NonCommercial-NoDerivatives 4.0 International39209566576854-86710.1016/j.jmii.2024.08.0071995-9133Journal of microbiology, immunology, and infection = Wei mian yu gan ran za zhiopen access