[PD-1和ICOS在原发性免疫性血小板减少症中的表达及意义]。

Zi Fu, Wen Qu, Zong-Hong Shao, Hua-Quan Wang, Li-Min Xing, Xi-Feng Dong, Zhao-Yun Liu, Xiao-Na Li, Yang Zhang, Shao-Xue Ding
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引用次数: 0

摘要

目的:观察原发性免疫性血小板减少症(ITP)患者外周血CD8+ T细胞表面程序性死亡受体-1 (PD-1)和诱导共刺激因子(ICOS)的表达情况,探讨PD-1和ICOS在ITP发生发展中的作用。方法:选取2020年9月至12月在天津医科大学总医院就诊的ITP患者28例,其中新诊断ITP患者13例,慢性ITP患者15例,健康志愿者22例作为对照组。流式细胞术检测PD-1和ICOS的表达水平,并评价其与临床指标的相关性。结果:慢性组ITP患者的CD8 + T细胞百分比高于新诊断组和对照组(新诊断组和慢性组ITP患者的P+ T细胞百分比均显著低于对照组(PPD-1=-0.4374;rico = -0.4492)。结论:ITP患者体内PD-1和ICOS表达不平衡可能干扰机体免疫稳态,可作为ITP患者的治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Expression and Significance of PD-1 and ICOS in Patients with Primary Immune Thrombocytopenia].

Objective: To investigate the expression of programmed death receptor-1 (PD-1) and inducible costimulator (ICOS) on the surface of CD8+ T cells in peripheral blood of patients with primary immune thrombocytopenia (ITP), and explore the roles of PD-1 and ICOS in the occurrence and development of ITP.

Methods: A total of 28 ITP patients treated in Tianjin Medical University General Hospital from September to December 2020 were selected, including 13 patients with newly diagnosed ITP, 15 patients with chronic ITP, and 22 healthy volunteers were recruited as control group. Flow cytometry was used to detect the expression levels of PD-1 and ICOS, and evaluate their correlation with clinical indicators.

Results: The percentage of CD8 + T cells in ITP patients of chronic group was higher than that of the newly diagnosed group and the control group (P<0.05). The expression level of PD-1 on CD8+ T cells in ITP patients of newly diagnosed group and chronic group were significantly lower than that of the control group (P<0.05), while the expression level of ICOS were significantly higher (P<0.05). In ITP patients, PD-1 was negatively correlated with platelet count (r=-0.4942, P<0.01), but positively with ICOS (r=0.4342). PD-1 and ICOS were both negatively correlated with lymphocyte count (rPD-1=-0.4374; rICOS=-0.4492).

Conclusion: In ITP patients, the unbalanced expression of PD-1 and ICOS may interfere with the immune homeostasis of the body, which can be used as a therapeutic target for ITP patients.

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