Center for Brain and Spinal Cord Repair, Department of Neuroscience, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
Curr Opin Neurol. 2018 Jun;31(3):334-344. doi: 10.1097/WCO.0000000000000550.
In adult mammals, a traumatic spinal cord injury (SCI) elicits a chronic unregulated neuroinflammatory response accompanied by seemingly paradoxical suppression of systemic immunity. These SCI-induced changes in immune function contribute to poor neurological outcomes and enhanced morbidity or mortality. Nonspecific anti-inflammatory or proinflammatory therapies are ineffective and can even worsen outcomes. Therefore, recent experimental SCI research has advanced the understanding of how neuroimmune cross-talk contributes to spinal cord and systemic pathology.
It is now appreciated that the immune response caused by injury to the brain or spinal cord encompasses heterogeneous elements that can drive events on the spectrum between exacerbating pathology and promoting tissue repair, within the spinal cord and throughout the body. Recent novel discoveries regarding the role and regulation of soluble factors, monocytes/macrophages, microRNAs, lymphocytes and systemic immune function are highlighted in this review.
A more nuanced understanding of how the immune system responds and reacts to nervous system injury will present an array of novel therapeutic opportunities for clinical SCI and other forms of neurotrauma.
在成年哺乳动物中,外伤性脊髓损伤 (SCI) 会引发慢性、不受调节的神经炎症反应,同时伴有全身免疫的明显抑制。这些 SCI 引起的免疫功能变化导致不良的神经学结果,并增加发病率或死亡率。非特异性抗炎或促炎治疗无效,甚至可能使病情恶化。因此,最近的实验性 SCI 研究提高了对神经免疫相互作用如何导致脊髓和全身病理的理解。
现在人们已经认识到,大脑或脊髓损伤引起的免疫反应包含异质成分,这些成分可以在脊髓内和全身范围内,在加剧病理和促进组织修复之间的谱上驱动事件。本文重点介绍了关于可溶性因子、单核细胞/巨噬细胞、microRNAs、淋巴细胞和全身免疫功能的作用和调节的新发现。
对免疫系统如何对神经系统损伤做出反应的更细致的理解,将为临床 SCI 和其他形式的神经创伤提供一系列新的治疗机会。