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艾曲泊帕通过上调慢性免疫性血小板减少性紫癜患者糖蛋白VI的表达来增强血小板黏附。

Eltrombopag enhances platelet adhesion by upregulating the expression of glycoprotein VI in patients with chronic immune thrombocytopenic purpura.

作者信息

Chiou Tzeon-Jye, Chang Yi-Fang, Wang Ming-Chung, Kao Chen-Wei, Lin Hsuan-Yu, Chen Tsai-Yun, Hsueh Erh-Jung, Lan Yii-Jenq, Sung Yung-Chuan, Lin Sheng-Feng, Bai Li-Yuan, Chen Caleb G

机构信息

Department of Hematology, Taipei Veterans General Hospital, Taipei, Taiwan.

Department of Hematology, GCRC Laboratory, Mackay Memorial Hospital, Taipei, Taiwan.

出版信息

Transl Res. 2015 Dec;166(6):750-761.e4. doi: 10.1016/j.trsl.2015.09.005. Epub 2015 Sep 30.

Abstract

Eltrombopag, a thrombopoietin receptor agonist, has been approved for the treatment of patients with immune thrombocytopenia because of its abilities to enhance platelet production and reduce hemorrhage. Both platelet count and platelet adhesion are crucial to stop bleeding. Although eltrombopag is known to improve platelet counts, its effects on platelet adhesion are not yet known. This study aimed to assess the efficacy of eltrombopag on platelet production and platelet adhesive affinity. To evaluate the efficacy of low-dose eltrombopag (25 mg) for patients with chronic refractory immune thrombocytopenic purpura (ITP) and to determine the ex vivo platelet adhesion ability before and after treatment with eltrombopag, we conducted an open-label, multicenter study in which 25 Taiwanese patients with chronic ITP were enrolled. During the 6-month evaluation, the starting and maximum doses of eltrombopag were 25 and 50 mg, respectively, to maintain the platelet count of ≥50,000 per μL. Flow-based adhesion assay was used to detect the percentage of platelets adhering to immobilized von Willebrand factor-collagen on microslides. Of the enrolled patients, 48% achieved a platelet count of ≥50,000 per μL. Interestingly, 83% of all responders required 25 mg of eltrombopag daily to achieve the target platelet count. In addition, the percentage of bleeding patients was significantly reduced in both responders and nonresponders by 50% from the baseline level throughout the treatment period. The ex vivo platelet adhesion capacity was elevated after the 6-month eltrombopag treatment in both responders and nonresponders. Furthermore, glycoprotein VI (GPVI) expression was significantly upregulated after treatment with eltrombopag. Low-to-intermediate dose of eltrombopag showed good efficacy to expedite platelet production and augment platelet adhesion. These 2 factors might explain the efficacy of eltrombopag in ameliorating hemorrhage in patients with ITP.

摘要

艾曲波帕是一种血小板生成素受体激动剂,因其具有增强血小板生成和减少出血的能力,已被批准用于治疗免疫性血小板减少症患者。血小板计数和血小板黏附对于止血都至关重要。虽然已知艾曲波帕可改善血小板计数,但其对血小板黏附的影响尚不清楚。本研究旨在评估艾曲波帕对血小板生成和血小板黏附亲和力的疗效。为了评估低剂量艾曲波帕(25毫克)对慢性难治性免疫性血小板减少性紫癜(ITP)患者的疗效,并确定艾曲波帕治疗前后的体外血小板黏附能力,我们进行了一项开放标签、多中心研究,纳入了25名台湾慢性ITP患者。在6个月的评估期间,艾曲波帕的起始剂量和最大剂量分别为25毫克和50毫克,以维持血小板计数≥每微升50,000个。采用基于流式细胞术的黏附试验检测血小板黏附在微玻片上固定的血管性血友病因子 - 胶原蛋白上的百分比。在纳入的患者中,48%的患者血小板计数达到≥每微升50,000个。有趣的是,所有有反应的患者中83%每天需要25毫克艾曲波帕来达到目标血小板计数。此外,在整个治疗期间,有反应者和无反应者的出血患者百分比均较基线水平显著降低了50%。在接受6个月艾曲波帕治疗后,有反应者和无反应者体外血小板黏附能力均有所提高。此外,用艾曲波帕治疗后糖蛋白VI(GPVI)表达显著上调。低至中等剂量的艾曲波帕在加速血小板生成和增强血小板黏附方面显示出良好疗效。这两个因素可能解释了艾曲波帕在改善ITP患者出血方面的疗效。

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