Department of Hematology, The First Affiliated Hospital of Harbin Medical University, Harbin, 150001, People's Republic of China.
Department of Hematology, The Fourth Affiliated Hospital of Harbin Medical University, Harbin, 150001, People's Republic of China.
Ann Hematol. 2021 Jun;100(6):1473-1483. doi: 10.1007/s00277-021-04533-9. Epub 2021 Apr 24.
Acute promyelocytic leukemia (APL) cells constitutively express a large amount of tissue factor (TF) antigen, most of which is present in the cytoplasm. Coagulopathy may persist after induction therapy. We evaluated the overall role of circulating microparticles (MPs) in coagulation activation in APL-associated coagulopathy before and during induction therapy. Eleven adult patients with ≥ World Health Organization's (WHO) grade 2 bleeding events and 11 sex- and age-matched healthy controls were selected. All patients received arsenic trioxide alone as induction therapy. MP-associated TF (MP-TF) activity and MP procoagulant activity (MP-PCA) and 12 coagulation- and anticoagulation-associated indexes were measured before, during, and after induction therapy. Correlation between MP-associated indexes and the other 12 indexes was analyzed in patients. The MP-TF activity was negligible in controls, whereas it markedly increased in patients, dropped rapidly after treatment, and returned to normal at the end of induction therapy. The MP-PCA was similar between patients and controls. The correlation analysis revealed that TF-bearing MPs in patients mainly originated from APL cells. Partially differentiated APL cells could also release TF-bearing MPs, and the higher the degree of APL cell differentiation, the lower the ability of APL cells to release TF-bearing MPs. MP-TF was the main source of active TF in plasma and an important contributor for the coagulation activation in APL-associated coagulopathy. It was MPs released by APL cells/partially differentiated APL cells that served as the vehicle to transfer the large amount of TF to plasma to activate coagulation.
急性早幼粒细胞白血病(APL)细胞持续表达大量组织因子(TF)抗原,其中大部分存在于细胞质中。诱导治疗后可能会持续存在凝血功能障碍。我们评估了循环微粒(MPs)在诱导治疗前后 APL 相关凝血功能障碍中的凝血激活中的总体作用。选择了 11 名≥世界卫生组织(WHO)2 级出血事件的成年患者和 11 名性别和年龄匹配的健康对照者。所有患者均接受单独三氧化二砷作为诱导治疗。在诱导治疗前、治疗中和治疗后测量了 MP 相关 TF(MP-TF)活性和 MP 促凝活性(MP-PCA)以及 12 个凝血和抗凝相关指标。对患者的 MP 相关指标与其他 12 个指标之间的相关性进行了分析。对照者的 MP-TF 活性可以忽略不计,而患者的 MP-TF 活性明显增加,治疗后迅速下降,在诱导治疗结束时恢复正常。患者和对照者的 MP-PCA 相似。相关性分析表明,患者中带 TF 的 MPs 主要来源于 APL 细胞。部分分化的 APL 细胞也可以释放带 TF 的 MPs,并且 APL 细胞的分化程度越高,释放带 TF 的 MPs 的能力越低。带 TF 的 MPs 是血浆中活性 TF 的主要来源,也是 APL 相关凝血功能障碍中凝血激活的重要因素。是 APL 细胞/部分分化的 APL 细胞释放的 MPs 将大量 TF 转移到血浆中以激活凝血。