食管癌明确放化疗前后T淋巴细胞亚群及相关免疫指标PD-1表达的变化

Annals of medicine Pub Date : 2025-12-01 Epub Date: 2024-12-23 DOI:10.1080/07853890.2024.2445190
Xueling Shi, Hongyu Zhao, Jiaqi Yu, Peng Cai, Shixiang Zhou, Ning Yang, Duojie Li
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引用次数: 0

摘要

目的:本研究旨在观察首发食管鳞状细胞癌(ESCC)患者放化疗(CRT)前后T淋巴细胞、自然杀伤细胞(NK)和PD-1表达的动态变化,并评价外周血PD-1表达对ESCC患者近期预后的影响。患者和方法:73例ESCC患者接受了明确的CRT治疗。CRT前后采用流式细胞术检测外周血pd -1表达及相关免疫指标。选取10例健康人外周血作为对照。结果:CD3+百分比(p = 0.018)、CD4+百分比(p = 0.009);CD4+/CD8+比值(p +CD3+ (p +CD4+ (p +CD8+ (p +CD8+ (p +CD8+) T细胞在单独放疗组与CRT组间差异有统计学意义(p +、CD4+ (p +CD8+) T细胞在达到总有效率的患者中显著降低(CR组p +CD8+ T细胞均显著降低)p结论:CRT加重了ESCC患者的免疫抑制,增加了T淋巴细胞亚群PD-1的表达,可能与放疗场有关。T淋巴细胞亚群中PD-1的表达可预测患者的短期预后,为放化疗后PD-1免疫抑制剂的序贯应用提供理论依据。
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Changes in PD-1 expression on T lymphocyte subsets and related immune indicators before and after definitive chemoradiotherapy for esophageal squamous cell carcinoma.

Objective: This study aimed to observe the dynamic changes in the expression of T lymphocytes, natural killer (NK) cells, and PD-1 in patients with first-diagnosed esophageal squamous cell carcinoma (ESCC) before and after chemoradiotherapy (CRT) and evaluate the impact of PD-1 expression in peripheral blood on the short-term outcome of patients with ESCC.

Patients and methods: Seventy-three patients with ESCC who were treated with definitive CRT were enrolled. Before and after CRT, flow cytometry was used to detect thePD-1 expression in the peripheral blood and related immune indicators. Peripheral blood from 10 healthy individuals was used as control.

Results: The percentages of CD3+ (p = 0.018), CD4+ (p < 0.001), and CD8+ T cells (p < 0.001); NK cells (p = 0.009); and the CD4+/CD8+ ratio (p < 0.001), as well as PD-1+CD3+ (p < 0.001), PD-1+CD4+ (p < 0.001), and PD-1+CD8+ (p < 0.001) T cells, before CRT significantly differed from those in the post-CRT group. The percentages of PD-1+CD8+ T cells differed significantly between the radiotherapy alone and CRT groups (p < 0.05). PD-1 expression in CD3+, CD4+, and CD8+ T cells significantly decreased in patients achieving overall response rate (all p < 0.05). Compared with those in the incomplete response group, PD-1+CD8+ T cells significantly decreased in the CR group (p < 0.05).

Conclusion: CRT aggravated immunosuppression and increased PD-1 expression in T lymphocyte subsets in patients with ESCC, possibly related to the radiation field. PD-1 expression in T lymphocyte subsets can predict short-term outcomes in patients and provide a theoretical basis for the sequential application of PD-1 immunosuppressants after radiotherapy and chemotherapy.

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