Frontiers in immunology · 2026
Increased CD95+ or CD160+ double-negative T-cell subsets are associated with incomplete immune reconstitution in ART-treated people living with HIV.
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Peng Jingli, Li Yanyan, Xi Jiale, Xia Zihao, Luo Ping, Yang Shuo, Lu Lianfeng, Chen Chen, Cai Rentian, Wang Qin, Wei Hongxia
Аннотация
OBJECTIVE: To investigate the expression patterns of CD95 and CD160 on double-negative T (DN T) cells and their association with incomplete immune reconstitution in people living with HIV.
METHODS: In this cross-sectional study, people living with HIV (PLWH) receiving long-term antiretroviral therapy (ART) with sustained viral suppression were classified as immunological non-responders (INR) or immunological responders (IR). Flow cytometry was used to characterize double-negative T (DN T) cells and their CD95+ and CD160+ subsets. Associations between DN T-cell phenotypes and INR were evaluated using univariable and multivariable logistic regression analyses, with odds ratios (ORs) calculated per 10% increase in cell percentages. Receiver operating characteristic (ROC) curves were used to assess discriminatory ability.
RESULTS: The frequency of DN T cells was significantly higher in the INR group than in the IR group (P = 0.022). The frequencies of CD95+ DN T cells and CD160+ DN T cells were increased in INR participants (P < 0.001 and P = 0.003, respectively) and were negatively correlated with CD4+ T-cell counts (CD95: r = -0.447, P < 0.001; CD160: r = -0.281, P = 0.008). After adjustment for age, ART duration, and baseline CD4+ T-cell counts, multivariable analysis showed that CD95+ DN T cells and CD160+ DN T cells were independently associated with INR. ROC analysis showed moderate discriminatory ability for CD95+ DN T cells (AUC = 0.788), whereas CD160+ DN T cells demonstrated lower discriminatory performance (AUC = 0.687). Adding DN T-cell phenotypic parameters to a baseline clinical model modestly improved discriminatory performance.
CONCLUSION: Incomplete immune reconstitution in PLWH is associated with phenotypic alterations of DN T cells characterized by increased CD95 and CD160 expression. These findings provide a phenotypic characterization of DN T-cell alterations associated with immune dysregulation in INR and may offer insights for further mechanistic investigation.
METHODS: In this cross-sectional study, people living with HIV (PLWH) receiving long-term antiretroviral therapy (ART) with sustained viral suppression were classified as immunological non-responders (INR) or immunological responders (IR). Flow cytometry was used to characterize double-negative T (DN T) cells and their CD95+ and CD160+ subsets. Associations between DN T-cell phenotypes and INR were evaluated using univariable and multivariable logistic regression analyses, with odds ratios (ORs) calculated per 10% increase in cell percentages. Receiver operating characteristic (ROC) curves were used to assess discriminatory ability.
RESULTS: The frequency of DN T cells was significantly higher in the INR group than in the IR group (P = 0.022). The frequencies of CD95+ DN T cells and CD160+ DN T cells were increased in INR participants (P < 0.001 and P = 0.003, respectively) and were negatively correlated with CD4+ T-cell counts (CD95: r = -0.447, P < 0.001; CD160: r = -0.281, P = 0.008). After adjustment for age, ART duration, and baseline CD4+ T-cell counts, multivariable analysis showed that CD95+ DN T cells and CD160+ DN T cells were independently associated with INR. ROC analysis showed moderate discriminatory ability for CD95+ DN T cells (AUC = 0.788), whereas CD160+ DN T cells demonstrated lower discriminatory performance (AUC = 0.687). Adding DN T-cell phenotypic parameters to a baseline clinical model modestly improved discriminatory performance.
CONCLUSION: Incomplete immune reconstitution in PLWH is associated with phenotypic alterations of DN T cells characterized by increased CD95 and CD160 expression. These findings provide a phenotypic characterization of DN T-cell alterations associated with immune dysregulation in INR and may offer insights for further mechanistic investigation.