血管性血友病因子中和抗体AJW200在兔栓塞性脑卒中后低剂量(0.9 mg/mg)溶栓治疗中的协同作用

Paul A Lapchak, Sarina Doyan, Xiaomin Fan, Catherine M Woods
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引用次数: 16

摘要

血管性血液病因子(vWF)是一种急性卒中反应蛋白,参与缺血性卒中后发生的血小板聚集、粘附、炎症和血栓形成等反应。我们假设抗vwf抗体(抗vwf - ab)的使用可能作为组织型纤溶酶原激活剂(tPA)的辅助治疗,以促进栓塞性卒中后的行为改善。在这项采用盲法和随机设计的概念验证研究中,我们以兔小血栓栓塞性卒中模型(RSCEM)为主要临床相关终点,研究了抗vwf - ab, AJW200 (0.30 mg/kg)单独或联合兔低剂量tPA (0.9 mg/kg)的延迟治疗。为评价脑血块负荷与临床评分之间的定量关系,计算脑卒中有效剂量(P50),构建logistic s型定量分析曲线。与对照组相比,有益治疗显著增加P50。将抗体单独或低剂量tPA给药的效果与“阳性对照”(标准兔最佳tPA剂量(3.3 mg/kg))进行比较,以衡量RSCEM的最大改善潜力。栓塞后1小时静脉注射抗vwf - ab、AJW200或对照IgG, 48小时后测量行为。AJW200加低剂量tPA可显著提高P50值74% (p0.05)。与对照组相比,AJW200使P50值提高了28% (p < 0.05)。标准剂量tPA使P50值增加154% (p
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Synergistic Effect of AJW200, a von Willebrand Factor Neutralizing Antibody with Low Dose (0.9 mg/mg) Thrombolytic Therapy Following Embolic Stroke in Rabbits.

The von Willebrand factor (vWF) is an acute stroke response protein involved in platelet aggregation, adhesion, inflammation, and thrombus formation, responses that occur following an ischemic stroke. We hypothesize that administration of an anti-vWF antibody (anti-vWF-Ab) may be used as adjunctive therapy with tissue plasminogen activator (tPA) to promote behavioral improvement following an embolic stroke. In this proof-of-concept study, which used a blinded and randomized design, we studied delayed treatment with the anti-vWF-Ab, AJW200 (0.30 mg/kg), alone or in combination with a rabbit low-dose of tPA (0.9 mg/kg) using the rabbit small clot embolic stroke model (RSCEM) with behavioral function as the primary clinically relevant endpoint. To evaluate the quantitative relationship between clot burden in brain and clinical scores, so that an effective stroke dose (P50) could be calculated, logistic sigmoidal quantal analysis curves were constructed. A beneficial treatment significantly increases P50 compared to control. The effect of antibody administration, either alone or with low dose tPA was compared to a "positive control", a standard rabbit optimized dose of tPA (3.3 mg/kg), as a measure of the maximum improvement potential in the RSCEM. The anti-vWF-Ab, AJW200, or control IgG were administered IV 1 hour following embolization, and behavior was measured 48 hours later. AJW200 plus low-dose tPA significantly increased the P50 value by 74% (p<0.05, t=2.612) and 81% (p<0.05, t=2.519) compared to low dose tPA or IgG, respectively, but not the AJW200 group (p>0.05). AJW200 increased the P50 value by 28%, (p>0.05) compared to the control IgG-treated group. Standard dose tPA increased the P50 value by 154% (p<0.05). Statistically, the combination response for AJW200 plus low-dose tPA was not significantly different from standard dose tPA (p=0.26). This study shows that the concomitant administration of the anti-vWF-Ab AJW200 with low dose tPA is synergistic and results in significantly improved behavioral function following embolic stroke. We postulate that neutralization of vWF may suppress or attenuate one or more aspects of the acute phase stroke cascade response including suppression of inflammatory response and reduced leukocyte adhesion.

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