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PD-1 high expression in T lymphocytes correlates with decreased survival in childhood B-cell precursor acute lymphoblastic leukemia

Year: 2026
Type: article
Study design: Observational Study
Abstract: B-cell precursor acute lymphoblastic leukemia (BCP-ALL) is the most common in pediatric malignancy. Despite high cure rates, relapse and treatment resistance remain major causes of mortality. Immune checkpoint molecules such as programmed death-1 (PD-1) have been implicated in T-cell dysfunction and immune evasion in cancer. In this study, we evaluated PD-1 expression on bone marrow CD4 + and CD8 + T lymphocytes from pediatric patients with BCP-ALL at diagnosis and investigated its association with clinical outcome. Flow cytometry analysis demonstrated significantly increased PD-1 expression, assessed as relative mean fluorescence intensity and as percentages of PD-1 low-density (PD-1 LD ) and high-density (PD-1 HD ) subsets, in patients compared with non-leukemic subjects. Survival analyses revealed that high frequencies of PD-1 HD CD4 + and CD8 + T lymphocytes were significantly associated with inferior overall survival, whereas higher proportions of PD-1 LD CD4 + T cells were associated with improved survival. Thus, our study identified two distinguishable T-cell populations in the bone marrow of pediatric patients with BCP-ALL: PD-1 LD and PD-1 HD . Furthermore, it demonstrated a correlation between high PD-1 expression on CD4 and CD8 T lymphocytes and survival in pediatric BCP-ALL. These results suggest that PD-1 may serve as a prognostic biomarker and a potential target for immune-based therapeutic strategies in BCP-ALL.
Language: English
Field: Medicine
Open Access status: hybrid
Estimated APC paid: $3,600
OpenAlex ID: W7154090167
FWCI:
Cites: 21
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