Journal of Capital Medical University ›› 2025, Vol. 46 ›› Issue (6): 1118-1125.doi: 10.3969/j.issn.1006-7795.2025.06.020

Previous Articles     Next Articles

Correlation between CD4+ and CD8+ T cells, mitochondrial mass, and depression

Sun Xuejiao 1,2, Liu Yanru 3,Wang Zhiren 2*   

  1. 1. School of Psychiatry and Psychology, North China University of Science and Technology, Tangshan 063200,Hebei Province ,China;2.Department of Science and Technology,Beijing Huilongguan Hospital, Beijing 100096, China;3.Department of Psychosomatic Medicine, Beijing Children’s Hospital, Capital Medical University, Beijing 100045, China
  • Received:2025-02-21 Revised:2025-10-06 Online:2025-12-21 Published:2025-12-19
  • Supported by:
    This study was supported by the Capital Health Development Research Special-Independent Innovation Program (2022-2-2133).

Abstract: Objective  To investigate the characteristics of changes in CD4+ and CD8+ T cell counts and mitochondrial mass(mean fluorescence intensity, MFI) in the peripheral blood of patients with depression, and to analyze their association with depression severity as assessed by the Hamilton Depression Rating  Scale(HAMD) .Methods  A total of 31 major depressive disorder (MDD) patients and 50 healthy controls were enrolled. Flow cytometry was used to assess T-cell subsets and mitochondrial quality. Welch’s t-tests and Mann-Whitney U tests were applied for group comparisons; Pearson correlation and FDR correction were used for association analyses. Multiple linear regression evaluated independent predictors of HAMD scores.  Results  CD4+ and CD8+ T-cell counts and MFI values were significantly reduced in MDD patients (P<0.01). CD8+T-cell MFI showed the strongest negative correlation with HAMD scores (R=-0.570, P<0.001). Regression analysis identified CD8+ MFI and CD4+ T-cell count as independent negative predictors of depression severity. Conclusion  Reduced T-cell counts and mitochondrial quality are associated with depressive symptoms, suggesting that mitochondrial dysfunction and T-cell imbalance may contribute to MDD pathogenesis.

Key words: depression, CD4+T cells, CD8+ T cells, mitochondrial mass, immunometabolism, biomarkers

CLC Number: