Regenerative Medicine Department, Naval Medical Research Center, Silver Spring, MD, USA.
J Transl Med. 2011 Jun 15;9:92. doi: 10.1186/1479-5876-9-92.
Trauma is one of the leading causes of death in young adult patients. Many pre-clinical and clinical studies attempt to investigate the immunological pathways involved, however the true mediators remain to be elucidated. Herein, we attempt to describe the immunologic response to systemic trauma in the context of the Danger model.
A literature search using PubMed was used to identify pertinent articles describing the Danger model in relation to trauma.
Our knowledge of Danger signals in relation to traumatic injury is still limited. Danger/alarmin signals are the most proximal molecules in the immune response that have many possibilities for effector function in the innate and acquired immune systems. Having a full understanding of these molecules and their pathways would give us the ability to intervene at such an early stage and may prove to be more effective in blunting the post-injury inflammatory response unlike previously failed cytokine experiments.
创伤是导致年轻成年患者死亡的主要原因之一。许多临床前和临床研究试图研究涉及的免疫学途径,但真正的介质仍有待阐明。在此,我们试图描述全身性创伤的免疫反应在危险模型中的情况。
使用 PubMed 进行文献检索,以确定描述与创伤相关的危险模型的相关文章。
我们对危险信号与创伤的关系的了解仍然有限。危险/警报信号是免疫反应中最接近的分子,它们在先天和获得性免疫系统中具有许多效应功能的可能性。充分了解这些分子及其途径将使我们能够在如此早期阶段进行干预,并且可能比以前失败的细胞因子实验更有效地抑制损伤后的炎症反应。