Brettler D B, Forsberg A D, Levine P H, Petillo J, Lamon K, Sullivan J L
Department of Medicine, Worcester Memorial Hospital, MA 01605.
Blood. 1989 May 15;73(7):1859-63.
Conventional clotting factor concentrates have, until recently, been "of intermediate purity," containing less than 1% of the coagulation factor, and greater than 99% extraneous plasma proteins such as fibrinogen, fibronectin, gamma globulins, and traces of many others. We report here the results of a new factor VIII concentrate that is purified from human plasma using a mouse monoclonal antibody to factor VIII:vWF in an affinity chromatography system. The resultant concentrate has an activity of between 3,000 and 5,000 U/mg protein before albumin is added as a stabilizer. Seven patients with severe hemophilia A and no inhibitor who were positive for antibody to human immunodeficiency virus (HIV) have been treated solely with this concentrate for over 24 months. Factor usage in these patients has ranged from 611 U/kg/yr to 2,022 U/kg/yr. These patients have infused approximately once per week on the average, most often for joint hemorrhages. The efficacy of the concentrate is excellent. No allergic reactions have occurred and no factor VIII antibodies have developed. In these seven patients mean CD4 counts stabilized (856 +/- 619 at screen v 778 +/- 686 at 24 months) and there was reversal of skin test anergy. In a comparison group on conventional intermediate purity concentrate chosen retrospectively decreases in mean CD4 cell counts similarly did not occur. However, the number of the comparison patients who were anergic increased over the course of the study. These observations indicate the possibility that more highly purified concentrates may stabilize immune function in HIV seropositive patients.
直到最近,传统的凝血因子浓缩物一直是“中等纯度”的,含有不到1%的凝血因子,以及超过99%的外来血浆蛋白,如纤维蛋白原、纤连蛋白、γ球蛋白和许多其他物质的痕量。我们在此报告一种新型的凝血因子VIII浓缩物的结果,该浓缩物是在亲和色谱系统中使用针对凝血因子VIII:血管性血友病因子(vWF)的小鼠单克隆抗体从人血浆中纯化得到的。在添加白蛋白作为稳定剂之前,所得浓缩物的活性为3000至5000 U/mg蛋白质。七名重度甲型血友病且无抑制剂的患者,他们对人类免疫缺陷病毒(HIV)抗体呈阳性,仅使用这种浓缩物治疗了超过24个月。这些患者的因子使用量范围为611 U/kg/年至2022 U/kg/年。这些患者平均每周输注约一次,最常见的原因是关节出血。该浓缩物的疗效极佳。未发生过敏反应,也未产生凝血因子VIII抗体。在这七名患者中,平均CD4细胞计数稳定(筛查时为856±619,24个月时为778±686),皮肤试验无反应性得到逆转。在一个回顾性选择的使用传统中等纯度浓缩物的对照组中,平均CD4细胞计数同样没有下降。然而,在研究过程中,无反应性的对照患者数量增加了。这些观察结果表明,更高纯度的浓缩物可能稳定HIV血清阳性患者免疫功能的可能性。