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创伤性脑损伤的免疫反应。

The immunological response to traumatic brain injury.

机构信息

Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.

Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.

出版信息

J Neuroimmunol. 2019 Jul 15;332:112-125. doi: 10.1016/j.jneuroim.2019.04.005. Epub 2019 Apr 11.

Abstract

Traumatic brain injury (TBI) is the leading cause of death and disability in young adults in the developed world. The accuracy of early outcome-prediction remains poor even when all known prognostic factors are considered, suggesting important currently unidentified variables. In addition, whilst survival and neurological outcomes have improved markedly with the utilisation of therapies that optimise physiology, no treatments specifically modulate the underlying pathophysiology. The immunological response to TBI represents both a potential contributor to outcome heterogeneity and a therapeutically tractable component of the acute disease process. Furthermore, chronic inflammation has been linked with neurodegeneration, and may mark a bridge between acute brain injury and the subsequent neurodegenerative process seen in a proportion of patients following TBI. Given the complexity of the immune response and its varying functions ranging from repair of injury to bystander damage of healthy tissue, attempts at immunomodulatory intervention must necessarily be highly targeted towards the maladaptive facets of the inflammatory process. In this review we aim to provide an integrated description of the immunological processes triggered by TBI in both humans and animal models, in particular considering the interplay between the innate immune system, danger-associated molecular patterns and loss of self-tolerance leading to adaptive autoimmunity.

摘要

创伤性脑损伤 (TBI) 是发达国家年轻人死亡和残疾的主要原因。即使考虑了所有已知的预后因素,早期预后的准确性仍然很差,这表明存在重要的、目前尚未确定的变量。此外,尽管通过利用优化生理学的治疗方法,生存和神经学结果有了明显改善,但没有专门的治疗方法可以调节潜在的病理生理学。TBI 的免疫反应既是导致结果异质性的潜在因素,也是急性疾病过程中具有治疗潜力的组成部分。此外,慢性炎症与神经退行性变有关,并且可能标志着急性脑损伤与 TBI 后部分患者随后发生的神经退行性过程之间的桥梁。鉴于免疫反应的复杂性及其从损伤修复到健康组织旁观者损伤的不同功能,免疫调节干预的尝试必然需要针对炎症过程的适应不良方面进行高度靶向。在这篇综述中,我们旨在提供 TBI 在人类和动物模型中引发的免疫过程的综合描述,特别是考虑到先天免疫系统、危险相关分子模式和自身耐受丧失之间的相互作用,导致适应性自身免疫。

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