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首页> 外文期刊>Wound repair and regeneration: official publication of the Wound Healing Society [and] the European Tissue Repair Society >Short-term treatment of equine wounds with orf virus IL-10 and VEGF-E dampens inflammation and promotes repair processes without accelerating closure
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Short-term treatment of equine wounds with orf virus IL-10 and VEGF-E dampens inflammation and promotes repair processes without accelerating closure

机译:用orf病毒IL-10和VEGF-E短期治疗马伤口可在不加速闭合的情况下减轻炎症并促进修复过程

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摘要

Healing is delayed in limb wounds relative to body wounds of horses, partly because of sustained inflammation and inefficient angiogenesis. In laboratory animals, proteins derived from orf virus modulate these processes and enhance healing. We aimed to compare immune cell trafficking and the inflammatory, vascular, and epidermal responses in body and limb wounds of horses and then to investigate the impact of orf virus interleukin-10 and vascular endothelial growth factor-E on these processes. Standardized excisional wounds were created on the body and forelimb of horses and their progression monitored macroscopically until healed. Tissue samples were harvested to measure the expression of genes regulating inflammation and repair (quantitative polymerase chain reaction) and to observe epithelialization (histology), innate immune cell infiltration, and angiogenesis (immunofluorescence). Delayed healing of limb wounds was characterized by intensified and extended pro-inflammatory signaling and exacerbated innate immune response, concomitant with the absence of anti-inflammatory eIL-10. Blood vessels were initially more permeable and then matured belatedly, concomitant with retarded production of angiogenic factors. Epithelial coverage was achieved belatedly in limb wounds. Viral proteins were administered to wounds of one body and one limb site/horse at days 1-3, while wounds at matching sites served as controls. Treatment dampened pro-inflammatory gene expression and the innate immune response in all wounds. It also improved angiogenic gene expression, but primarily in body wounds, where it altered blood vessel density and myofibroblast persistence. Moreover, the viral proteins increased epithelialization of all wounds. The short-term viral protein therapy did not, however, improve the healing rate of wounds in either location, likely due to suboptimal dosing. In conclusion, we have further detailed the processes contributing to protracted healing in limb wounds of horses and shown that short-term administration of viral proteins exerts several promising though transient effects that, if optimized, may positively influence healing.
机译:相对于马的身体伤口,肢体伤口的愈合延迟,部分原因是持续的炎症和无效的血管生成。在实验动物中,源自orf病毒的蛋白质可调节这些过程并增强愈合。我们旨在比较免疫细胞的运输以及马的身体和肢体伤口的炎症,血管和表皮反应,然后研究orf病毒白介素10和血管内皮生长因子E对这些过程的影响。在马的身体和前肢上创建了标准化的切除伤口,并对其肉眼的进展进行了宏观监测,直至愈合。收获组织样品以测量调节炎症和修复的基因的表达(定量聚合酶链反应),并观察上皮形成(组织学),先天免疫细胞浸润和血管生成(免疫荧光)。肢体伤口延迟愈合的特点是增强和延长了促炎信号传导,加重了先天免疫反应,同时缺乏抗炎eIL-10。血管最初具有较高的渗透性,但后来才成熟,并伴有血管生成因子的产生受阻。上肢伤口迟来获得上皮覆盖。在第1-3天将病毒蛋白施用于一个身体和一个肢体部位/马的伤口,而在匹配部位的伤口用作对照。治疗减弱了所有伤口的促炎基因表达和先天免疫反应。它也改善了血管生成基因的表达,但主要是在身体伤口中,它改变了血管密度和成肌纤维细胞的持久性。此外,病毒蛋白增加了所有伤口的上皮形成。但是,短期的病毒蛋白治疗可能无法达到最佳剂量,因此不能提高任一部位伤口的愈合速度。总而言之,我们进一步详细描述了导致马肢体伤口持久愈合的过程,并表明,短期施用病毒蛋白会产生一些有希望的但短暂的影响,如果优化,可能会积极影响愈合。

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