Haemostasis Department and Haemophilia Centre, Blood Transfusion Institute of Serbia, Belgrade, Serbia.
Int J Lab Hematol. 2012 Feb;34(1):35-40. doi: 10.1111/j.1751-553X.2011.01349.x. Epub 2011 Jun 27.
Thrombin activatable fibrinolysis inhibitor (TAFI) down-regulates fibrinolysis after activation by thrombin/thrombomodulin. We investigated the effect of treatment with FVIII concentrate on plasma levels of pro-TAFI and activated TAFI in haemophilia A patients.
Samples were collected pre and posttreatment from patients treated prophylactically or on-demand. Pro-TAFI, TAFI/TAFIi and FVIII levels were measured in all samples.
Treatment had no effect on pro-TAFI levels. Pro-TAFI was similar in both patient groups but higher than in controls. Patients from the prophylactic treatment group had measurable FVIII levels pretreatment while in the treatment-on-demand group FVIII levels were ≤0.01 IU/mL. In the prophylactic treatment group, the levels of TAFI/TAFIi were significantly lower pre- and posttreatment (4.31 ± 3.14 and 3.48 ± 2.65 ng/mL respectively) than in the on-demand group (13.02 ± 3.47 and 14.87 ± 3.47 ng/mL respectively). This difference may be due to release of tissue factor at the injury site in the on-demand group. This could induce thrombin and TAFI activation within the clot counterbalancing fibrinolysis in these patients. In the prophylactic group, no injury existed, thus there was insufficient thrombin generation within the clot to activate TAFI.
These findings suggest that in patients to whom FVIII is administered on demand the fibrinolysis activity is more down regulated than in patients following a prophylactic treatment regime.
凝血酶激活的纤溶抑制物(TAFI)在被凝血酶/血栓调节蛋白激活后下调纤溶。我们研究了 FVIII 浓缩物治疗对血友病 A 患者血浆中前 TAFI 和活化 TAFI 水平的影响。
采集预防性或按需治疗的患者治疗前后的样本。所有样本均测量前 TAFI、TAFI/TAFIi 和 FVIII 水平。
治疗对前 TAFI 水平没有影响。两组患者的前 TAFI 水平相似,但均高于对照组。预防性治疗组患者在治疗前有可测量的 FVIII 水平,而按需治疗组的 FVIII 水平≤0.01 IU/mL。在预防性治疗组,治疗前后 TAFI/TAFIi 水平(分别为 4.31±3.14 和 3.48±2.65 ng/mL)明显低于按需治疗组(分别为 13.02±3.47 和 14.87±3.47 ng/mL)。这种差异可能是由于按需治疗组在损伤部位释放组织因子,从而在这些患者的血栓中诱导凝血酶和 TAFI 激活,抵消了纤溶作用。在预防性治疗组,不存在损伤,因此血栓中没有足够的凝血酶生成来激活 TAFI。
这些发现表明,与接受预防性治疗方案的患者相比,按需给予 FVIII 的患者的纤溶活性受到更大的抑制。