Biafine应用于人表皮创面对巨噬细胞具有趋化作用,可提高IL-1/IL-6比值。

B Coulomb, L Friteau, L Dubertret
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引用次数: 26

摘要

我们利用正常人体志愿者的纯表皮创面模型,首先研究了Biafine乳剂在创面24小时内对炎症细胞迁移、血管通透性和细胞因子释放的影响,其次通过测量第1天至第7天经皮失水对表皮创面愈合的影响。在这些情况下,比芬不能改善表皮愈合,与出血的皮表皮伤口相反。我们的结果表明,比芬的影响基本上是在真皮水平。对表皮创面渗出物的分析也得出了同样的结论。事实上,我们证明了Biafine对巨噬细胞具有趋化作用,主要通过减少IL-6的分泌来增加IL-1/IL-6的比值。这项研究允许逐步澄清比芬的作用模式,它似乎位于肉芽组织形成水平而不是表皮水平。
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Biafine applied on human epidermal wounds is chemotactic for macrophages and increases the IL-1/IL-6 ratio.

Using a model of pure epidermal wounds in normal human volunteers, we have studied the effects of Biafine emulsion firstly on inflammatory cell migration, vascular permeability and cytokine release during the first 24 h, and secondly on epidermal wound healing by measuring transepidermal water loss from day 1 to day 7. Under these conditions, Biafine does not improve epidermal healing, in contrast to what is observed with bleeding dermoepidermal wounds. Our results suggest that the effects of Biafine are essentially at the dermis level. The analysis of epidermal wound exudates leads to the same conclusion. As a matter of fact, we demonstrated that Biafine is chemotactic for macrophages and increases the IL-1/IL-6 ratio, chiefly by reducing the secretion of IL-6. This study permits to progressively clarify the mode of action of Biafine, that seems to be located at the level of granulation tissue formation and not at the epidermal level.

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