Burnouf-Radosevich M, Burnouf T
Centre Régional de Transfusion Sanguine de Lille, France.
Transfusion. 1992 Nov-Dec;32(9):861-7. doi: 10.1046/j.1537-2995.1992.32993110761.x.
A highly purified factor XI (FXI) concentrate was prepared from human plasma by a process comprising a filter adsorption step and chromatography on a cation exchange resin. The freeze-dried FXI, which solubilized quickly, had high specific activity (130-150 U/mg protein), high potency (approx. 100 U/mL), and excellent stability for at least 24 hours at room temperature in the liquid state. The overall recovery was about 220 U of FXI per liter of plasma. Minor protein contaminants (C1-inhibitor, fibronectin, IgG, and alpha-2-macroglobulin) were found to be between 0.13 and 0.46 mg per 1000 U of FXI. Fibrinogen and relevant coagulation factors (factors II, V, VII, IX, X, XII, XIII, and VIII/von Willebrand factor) were undetectable, as evidenced by immunologic and immunoelectrophoretic data. Components of the kinin system were present in trace amounts or were undetectable. No evidence of activated factors such as factors Xa and IXa was found. Proteolytic activity, as assessed by S-2288 chromogenic substrate, was negligible and thrombin was undetectable. A solvent-detergent treatment was included prior to chromatographic purification to enhance viral safety against lipid-enveloped viruses. In vitro and in vivo animal studies demonstrated the absence of thrombogenic, hypotensive, or toxic effects. No thrombogenic activity was found in the Wessler model in rabbits at doses of 900 to 1100 U of FXI per kg of body weight. This FXI preparation could be beneficial in substitution therapy of congenital or acquired FXI deficiency, especially as a way to avoid the use of fresh-frozen plasma.
通过包括过滤吸附步骤和阳离子交换树脂色谱法的工艺,从人血浆中制备了一种高度纯化的凝血因子 XI(FXI)浓缩物。冻干的 FXI 溶解迅速,具有高比活性(130 - 150 U/mg 蛋白质)、高效能(约 100 U/mL),并且在室温下液态至少 24 小时具有出色的稳定性。总体回收率约为每升血浆 220 U 的 FXI。发现每 1000 U 的 FXI 中微量蛋白质污染物(C1 抑制剂、纤连蛋白、IgG 和 α-2-巨球蛋白)在 0.13 至 0.46 mg 之间。通过免疫学和免疫电泳数据证明,未检测到纤维蛋白原和相关凝血因子(因子 II、V、VII、IX、X、XII、XIII 和 VIII/血管性血友病因子)。激肽系统的成分含量微量或未检测到。未发现活化因子如因子 Xa 和 IXa 的证据。通过 S - 2288 显色底物评估的蛋白水解活性可忽略不计,且未检测到凝血酶。在色谱纯化之前进行了溶剂 - 去污剂处理,以增强针对脂包膜病毒的病毒安全性。体外和体内动物研究表明不存在血栓形成、降压或毒性作用。在兔的韦氏模型中,每千克体重给予 900 至 1100 U 的 FXI 剂量时未发现血栓形成活性。这种 FXI 制剂可能对先天性或获得性 FXI 缺乏的替代治疗有益,特别是作为避免使用新鲜冷冻血浆的一种方法。