Garcia V V, Coppola R, Mannucci P M
Blood. 1982 Dec;60(6):1402-6.
Organ transplantation and perfusion studied indicate that the spleen plays an important role in the regulation of plasma levels of factor VIII-von Willebrand's factor (FVIII-vWF). To better understand the mechanisms that regulate the FVIII-vWF increases after infusion of 1-deamino-8-D-arginine vasopressin (DDAVP), we have measured factor VIII coagulant activity (FVIII:C) and antigen (FVIII:CAg) and von Willebrand's factor antigen (vWF:Ag) and ristocetin cofactor (vWF:RCof) in 9 asplenic subjects with normal baseline concentrations, in 7 asplenic subjects with high concentrations, and in 14 normal controls with intact spleens. In "normal" aasplenics, all the FVIII-vWF-related measurements increased significantly over baseline values, indicating that responsiveness to DDAVP is not abolished by splenectomy. The maximal vWF:Ag and vWF:RCof responses were no different from those of normal controls, suggesting that DDAVP releases vWF from storage sites other than the spleen. The FVIII:C response was significantly lower than in normal controls, but FVIII:CAg did not differ, making FVIII:CAg higher than FVIII:CAg in "normal" asplenics. These findings suggest that the spleen, rather than being a storage site for FVIII, is the organ in which a partially inactive form of FVIII acquires full coagulant activity. In "high" asplenics, all the FVIII-vWF-related measurements increased less than in "normal" splenics, indicating that long-term elevations of plasma concentrations of FVIII-vWF are accompanied by decreased release from those storage pool(s) mobilized by DDAVP.
器官移植及灌注研究表明,脾脏在调节血浆中第八因子 - 血管性血友病因子(FVIII - vWF)水平方面发挥着重要作用。为了更好地理解输注1 - 去氨基 - 8 - D - 精氨酸加压素(DDAVP)后调节FVIII - vWF升高的机制,我们测定了9名基线浓度正常的无脾受试者、7名高浓度的无脾受试者以及14名脾脏完整的正常对照者的第八因子凝血活性(FVIII:C)、抗原(FVIII:CAg)、血管性血友病因子抗原(vWF:Ag)和瑞斯托霉素辅因子(vWF:RCof)。在“正常”无脾者中,所有与FVIII - vWF相关的测量值均较基线值显著升高,表明脾切除并未消除对DDAVP的反应性。最大vWF:Ag和vWF:RCof反应与正常对照者无异,提示DDAVP从脾脏以外的储存部位释放vWF。FVIII:C反应显著低于正常对照者,但FVIII:CAg无差异,使得“正常”无脾者中的FVIII:CAg高于FVIII:C。这些发现表明,脾脏并非FVIII的储存部位,而是FVIII的部分无活性形式获得完全凝血活性的器官。在“高浓度”无脾者中,所有与FVIII - vWF相关测量值的升高幅度均小于“正常”无脾者,表明FVIII - vWF血浆浓度的长期升高伴随着DDAVP动员的那些储存池释放减少。