Department of Pediatrics, Medical College of Wisconsin Blood Research Institute, BloodCenter of Wisconsin Children's Research Institute, Children's Hospital of Wisconsin, Milwaukee, WI, USA.
J Thromb Haemost. 2012 Nov;10(11):2328-37. doi: 10.1111/j.1538-7836.2012.04902.x.
The important association between von Willebrand factor (VWF) and factor VIII (FVIII) has been investigated for decades, but the effect of VWF on the reactivity of FVIII inhibitory antibodies, referred to as inhibitors, is still controversial.
To investigate the interaction among VWF, FVIII and FVIII inhibitory antibodies.
Three sources of inhibitors were used for in vitro studies, including the plasma from immunized VWF(null) FVIII(null) mice, purified plasma IgG from human inhibitor patients, or human monoclonal antibody from inhibitor patients' B-cell clones. Inhibitors were incubated with recombinant human FVIII (rhFVIII) either with or without VWF. The remaining FVIII activity was determined by chromogenic assay and inhibitor titers were determined. For in vivo studies, inhibitors and rhFVIII were infused into FVIII(null) or VWF(null) FVIII(null) mice followed by a tail clip survival test.
VWF has a dose-dependent protective effect on FVIII, limiting inhibitor inactivation of FVIII in both mouse and human samples. A preformed complex of VWF with FVIII provides more effective protection from inhibitors than competitive binding of antibodies and VWF to FVIII. The protective effect of VWF against FVIII inactivation by inhibitors was further confirmed in vivo by infusing inhibitors and FVIII into FVIII(null) or VWF(null) FVIII(null) mice followed by a tail clip survival test.
Our results demonstrate that VWF exerts a protective effect, reducing inhibitor inactivation of FVIII, both in vitro and in vivo.
血管性血友病因子(VWF)与因子 VIII(FVIII)之间的重要关联已被研究了几十年,但 VWF 对 FVIII 抑制性抗体(即抑制剂)反应性的影响仍存在争议。
研究 VWF、FVIII 和 FVIII 抑制性抗体之间的相互作用。
使用三种抑制剂来源进行体外研究,包括免疫 VWF(null)FVIII(null) 小鼠的血浆、来自人类抑制剂患者的纯化血浆 IgG 或来自抑制剂患者 B 细胞克隆的人单克隆抗体。抑制剂与重组人 FVIII(rhFVIII)孵育,无论是否存在 VWF。通过显色测定法测定剩余的 FVIII 活性,并测定抑制剂滴度。对于体内研究,将抑制剂和 rhFVIII 输注到 FVIII(null)或 VWF(null)FVIII(null)小鼠中,然后进行尾部夹闭存活试验。
VWF 对 FVIII 具有剂量依赖性的保护作用,限制了抑制剂在小鼠和人类样本中对 FVIII 的失活。VWF 与 FVIII 的预形成复合物比抗体和 VWF 与 FVIII 的竞争性结合提供了更有效的保护作用,以防止抑制剂对 FVIII 的失活。通过将抑制剂和 FVIII 输注到 FVIII(null)或 VWF(null)FVIII(null)小鼠中,然后进行尾部夹闭存活试验,进一步在体内证实了 VWF 对 FVIII 免受抑制剂失活的保护作用。
我们的研究结果表明,VWF 在体外和体内均发挥保护作用,降低抑制剂对 FVIII 的失活作用。