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               <mods:identifier type="citation">Garrido-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.</mods:identifier>
               <mods:identifier type="doi">10.1016/j.jmii.2024.08.007</mods:identifier>
               <mods:identifier type="e-issn">1995-9133</mods:identifier>
               <mods:identifier type="issn">1684-1182</mods:identifier>
               <mods:identifier type="journal">Journal of microbiology, immunology, and infection = Wei mian yu gan ran za zhi</mods:identifier>
               <mods:identifier type="pubmedID">39209566</mods:identifier>
               <mods:identifier type="uri">https://hdl.handle.net/20.500.12105/26245</mods:identifier>
               <mods:abstract>Background: 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 &lt; 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 &lt; 0.8 showed a differential inflammatory profile compared to R > 1.2 (increased β2-microglobulin, D-dimers and IP-10 before ART). R &lt; 0.8 presented lower baseline thymic function, being inversely correlated with post-ART inflammation. R &lt; 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.</mods:abstract>
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                  <mods:topic>CD4/CD8 ratio</mods:topic>
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                  <mods:topic>HIV-Infection</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Immunological dysfunction</mods:topic>
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               <mods:subject>
                  <mods:topic>Nadir-CD4 T-cell</mods:topic>
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               <mods:subject>
                  <mods:topic>sj/β-TRECs</mods:topic>
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                  <mods:title>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.</mods:title>
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