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Blocking von willebrand factor for treatment of cutaneous inflammation

机译:阻断血管性假血友病因子治疗皮肤炎症

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Von Willebrand factor (VWF), a key player in hemostasis, is increasingly recognized as a proinflammatory protein. Here, we found a massive accumulation of VWF in skin biopsies of patients suffering from immune complex (IC)-mediated vasculitis (ICV). To clarify the impact of VWF on cutaneous inflammation, we induced experimental ICV either in mice treated with VWF-blocking antibodies or in VWF-/- mice. Interference with VWF led to a significant inhibition of the cutaneous inflammatory response. We confirmed the major findings in irritative contact dermatitis, a second model of cutaneous inflammation. In vivo imaging of cutaneous inflammation in the dorsal skinfold chamber revealed unaffected leukocyte rolling on anti-VWF treatment. However, we identified that reduced leukocyte recruitment is accompanied by reduced vascular permeability. Although VWF-mediated neutrophil recruitment to the peritoneum was described to require the VWF receptor on platelets (glycoprotein Ibα (GPIbα)), the VWF/GPIbα axis was dispensable for cutaneous inflammation. As assessed in tail bleeding assays, we could exclude interference of VWF blockade with hemostasis. Of particular importance, anti-VWF treatment was effective both in prophylactic and therapeutic administration. Thus, VWF represents a promising target for the treatment of cutaneous inflammation, e.g., leukocytoclastic vasculitis.
机译:止血的关键因素Von Willebrand因子(VWF)被越来越多地认为是促炎蛋白。在这里,我们发现在患有免疫复合物(IC)介导的血管炎(ICV)的患者的皮肤活检中大量积累了VWF。为了阐明VWF对皮肤炎症的影响,我们在用VWF阻断抗体治疗的小鼠中或在VWF-/-小鼠中诱导了实验性ICV。对VWF的干扰导致皮肤炎症反应的显着抑制。我们证实了刺激性接触性皮炎的主要发现,这是皮肤炎症的第二种模型。背部皮褶腔内皮肤炎症的体内成像显示抗VWF治疗后白细胞滚动不受影响。但是,我们发现白细胞募集减少伴随着血管渗透性降低。尽管描述了VWF介导的嗜中性白细胞募集进入腹膜需要血小板上的VWF受体(糖蛋白Ibα(GPIbα)),但VWF /GPIbα轴对于皮肤炎症是必不可少的。如在尾巴出血分析中评估的那样,我们可以排除VWF阻滞对止血的干扰。特别重要的是,抗VWF治疗在预防和治疗方面均有效。因此,VWF代表了治疗皮肤炎症例如白细胞碎裂性血管炎的有希望的靶标。

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