Meyer Oliver, Herzig Eric, Salama Abdulgabar
Institut für Transfusionsmedizin, Abteilung Innere Medizin und Poliklinik, Charité - Universitätsmedizin Berlin, Germany.
Transfus Med Hemother. 2012 Feb;39(1):5-8. doi: 10.1159/000335553. Epub 2011 Dec 23.
Thrombopoietin receptor agonists (Tpo RA) increase platelet counts in the majority of chronic autoimmune thrombocytopenia (idiopathic thrombocytopenic purpura; ITP) patients. It is unknown whether this treatment may also improve platelet survival (PS) in these patients. METHODS: In order to determine platelet survival (PS), autologous platelets were labeled with (111)In oxine and retransfused in six patients under treatment with Tpo RA (romiplostim n = 3; eltrombopag n = 3). RESULTS: Stable platelet counts of greater than 100 × 10(3)/μl were observed in all 6 patients. Platelet survival was decreased in all cases (mean 2.10 days; range 0.13-3.73 days). No correlation was found between platelet count and PS. Similarly, there was no significant relationship between platelet turnover and platelet count. However, a high platelet turnover, exceeding 25 or three times the norm was observed in 2 patients who presented the lowest PS (0.13 or 0.83 days). Two patients had a moderately shortened PS (1.91 or 2.42 days), and, correspondingly, a moderately increased platelet turnover rate (63,072 or 72,872 platelets/μl/day). CONCLUSION: These results indicate that Tpo RA may not only overcompensate platelet destruction in ITP, but may interfere with other mechanisms, which, in some cases, results in a reduced platelet destruction rate.
血小板生成素受体激动剂(Tpo RA)可使大多数慢性自身免疫性血小板减少症(特发性血小板减少性紫癜;ITP)患者的血小板计数增加。目前尚不清楚这种治疗是否也能改善这些患者的血小板生存期(PS)。方法:为了确定血小板生存期(PS),对自体血小板用(111)铟喷替酸盐进行标记,并回输给6例接受Tpo RA治疗的患者(罗米司亭3例;艾曲泊帕3例)。结果:所有6例患者的血小板计数均稳定在大于100×10³/μl。所有病例的血小板生存期均缩短(平均2.10天;范围0.13 - 3.73天)。未发现血小板计数与PS之间存在相关性。同样,血小板周转率与血小板计数之间也无显著关系。然而,在2例PS最短(0.13或0.83天)的患者中观察到高血小板周转率,超过正常水平的25倍或三倍。2例患者的PS中度缩短(1.91或2.42天),相应地,血小板周转率中度增加(63,〇72或72,872个血小板/μl/天)。结论:这些结果表明,Tpo RA不仅可能过度补偿ITP中的血小板破坏,还可能干扰其他机制,在某些情况下,这会导致血小板破坏率降低。