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Understanding Systemic Immune Dysregulation in Severe Trauma and the Effects of Biomaterial-based Interventions

机译:了解严重创伤中的全身免疫失调和基于生物材料的干预措施的影响

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Complications in bone defect healing, especially in immune dysregulated patients, remains a significant clinical challenge. Our preliminary results show strong evidence of immune dysregulation and suppression at 8 weeks post-injury in our clinically-relevant rat model. Even with treatment at week 8 using two different biomaterial-mediated BMP-2 delivery strategies, immune dysregulation persisted, and possibly even worsened. Despite this, radiographs showed evidence of early mineralization, but this could be attributed to the high dosage of BMP-2 used. Further detailed analyses will provide a more complete interpretation of the links between bone healing, biomaterial delivery strategies, and the immune system status. Understanding the immune response to biomaterial-mediated treatment strategies in the context of immune dysregulation will guide improvements in future therapeutics.
机译:骨缺损愈合中的并发症,尤其是免疫失调的患者,仍然是一项重大的临床挑战。我们的初步结果显示了在与临床相关的大鼠模型中,损伤后8周免疫功能失调和抑制的有力证据。即使在第8周使用两种不同的生物材料介导的BMP-2递送策略进行治疗,免疫失调仍然持续,甚至可能恶化。尽管如此,射线照片显示了早期矿化的证据,但这可能归因于所用的BMP-2剂量很高。进一步的详细分析将对骨骼愈合,生物材料输送策略和免疫系统状态之间的联系提供更完整的解释。在免疫失调的背景下了解对生物材料介导的治疗策略的免疫反应将指导未来治疗方法的改进。

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