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[原发性免疫性血小板减少症患者脾脏单个核细胞中TIM-1和TIM-3的表达及其在Th1极化中的作用]

[Expression of TIM-1 and TIM-3 in spleen mononuclear cells and their role in Th1 polarization in primary immune thrombocytopenia patients].

作者信息

Zhang Xiao-Mei, Shan Ning-Ning, Hu Yu, Wang Xin

机构信息

Department of Hematology, Provincial Hospital Affiliated to Shandong University, Jinan 250021, China.

出版信息

Zhonghua Xue Ye Xue Za Zhi. 2013 Jul;34(7):614-7. doi: 10.3760/cma.j.issn.0253-2727.2013.07.012.

DOI:10.3760/cma.j.issn.0253-2727.2013.07.012
PMID:23906457
Abstract

OBJECTIVE

To explore the expression and clinical significance of T cell immunoglobulin mucin (TIM)-1, TIM-3 and T cell-specific transcription factors T-bet and GATA-3 in spleen mononuclear cells in patients with primary immune thrombocytopenia (ITP).

METHODS

The spleen samples were obtained from 17 active ITP patients and 10 controls with spleen traumatic rupture. By using real-time quantitative polymerase chain reaction, the mRNA expressions of TIM-3, TIM1, T-bet and GATA-3 were studied in all subjects.

RESULTS

TIM-3 mRNA levels of active ITP patients were significantly decreased to (29 ± 16)% of that of control, TIM-1 mRNA levels of active ITP patients increased to (3.20 ± 2.18) folds of that of control, but the difference was not significant. The ratio of TIM-1/ TIM-3 was elevated in active ITP patients. T-bet mRNA levels were up-regulated in ITP patients by (2.82 ± 1.57) folds (P<0.05) and the expression of GATA3 was decreased by 14% folds (P<0.05) compared to controls. The ratio of T-bet/GATA3 were significantly elevated in ITP patients.

CONCLUSION

The imbalance between TIM-3 and TIM-1 expression might play an important role in pathogenesis of ITP.

摘要

目的

探讨原发性免疫性血小板减少症(ITP)患者脾脏单个核细胞中T细胞免疫球蛋白黏蛋白(TIM)-1、TIM-3及T细胞特异性转录因子T-bet和GATA-3的表达及临床意义。

方法

收集17例活动性ITP患者及10例脾脏外伤性破裂患者的脾脏标本,采用实时定量聚合酶链反应检测所有研究对象中TIM-3、TIM-1、T-bet和GATA-3的mRNA表达。

结果

活动性ITP患者TIM-3 mRNA水平显著降低至对照组的(29±16)%,活动性ITP患者TIM-1 mRNA水平升高至对照组的(3.20±2.18)倍,但差异无统计学意义。活动性ITP患者TIM-1/TIM-3比值升高。与对照组相比,ITP患者T-bet mRNA水平上调(2.82±1.57)倍(P<0.05),GATA3表达下降14%(P<0.05)。ITP患者T-bet/GATA3比值显著升高。

结论

TIM-3与TIM-1表达失衡可能在ITP发病机制中起重要作用。

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