Karakantza Marina, Giannakoulas Nikolaos C, Zikos Panagiotis, Sakellaropoulos George, Kouraklis Alexandra, Aktypi Anthi, Metallinos Ioannis C, Theodori Eleni, Zoumbos Nicholas C, Maniatis Alice
Laboratory Hematology and Transfusion Medicine, Medical School, University of Patras, Patras GR-26110, Greece.
Int J Hematol. 2004 Apr;79(3):253-9. doi: 10.1532/ijh97.e0316.
We investigated endothelial and in vivo platelet activation in a cohort of 52 patients with essential thrombocythemia (ET) and polycythemia vera (PV) before and after cytoreductive treatment, 22 healthy controls, and 17 patients with acute cerebrovascular ischemia (ACVI) and normal platelet counts. We measured platelet expression of CD62P and CD63 antigens and levels of soluble vascular cell adhesion molecule 1 (sVCAM-1). We found increased in vivo platelet activation in all patients with ET and PV, both before and after cytoreductive treatment, compared with controls. In patients with arterial thrombosis, platelet expression of CD62P, and in patients with erythromelalgia, expression of both markers was higher compared with expression in patients without thrombotic complications. In patients with ET and PV before and after treatment, sVCAM-1 expression was increased compared with expression in controls but also compared with expression in patients with ACVI and normal platelet counts. In patients with arterial thrombosis and erythromelalgia, in vivo platelet activation correlated with the level of sVCAM-1. Our findings indicated that in vivo platelet activation reflects intrinsic platelet defects in patients with ET and PV, persists after cytoreductive treatment, and results in endothelial damage, probably through release of angiogenic factors and/or activation of white blood cells.
我们调查了52例原发性血小板增多症(ET)和真性红细胞增多症(PV)患者在进行细胞减灭治疗前后的内皮细胞和体内血小板活化情况,22名健康对照者,以及17例急性脑血管缺血(ACVI)且血小板计数正常的患者。我们检测了血小板CD62P和CD63抗原的表达以及可溶性血管细胞黏附分子1(sVCAM-1)的水平。我们发现,与对照组相比,所有ET和PV患者在细胞减灭治疗前后体内血小板活化均增加。在动脉血栓形成患者中,CD62P在血小板上的表达增加;在红斑性肢痛症患者中,这两种标志物的表达均高于无血栓并发症患者。在ET和PV患者治疗前后,sVCAM-1的表达与对照组相比增加,与ACVI且血小板计数正常的患者相比也增加。在动脉血栓形成和红斑性肢痛症患者中,体内血小板活化与sVCAM-1水平相关。我们的研究结果表明,体内血小板活化反映了ET和PV患者内在的血小板缺陷,在细胞减灭治疗后持续存在,并可能通过血管生成因子的释放和/或白细胞的激活导致内皮损伤。