Department of Biology, University of Texas at San Antonio, San Antonio, TX, 78249, USA.
J Neural Transm (Vienna). 2018 May;125(5):781-795. doi: 10.1007/s00702-017-1732-9. Epub 2017 May 22.
It is becoming increasingly clear that neuroinflammation has a causal role in the pathogenesis of central nervous system (CNS)-related diseases, and therefore therapeutic strategies targeting the regulation or availability of inflammatory mediators can be used to prevent or mitigate pathology. Interestingly, the proinflammatory cytokine, interleukin-1 beta (IL-1β), has been implicated in perpetuating immune responses and contributing to disease severity in a variety of CNS diseases ranging from multiple sclerosis, neurodegenerative diseases, traumatic brain injury, and diabetic retinopathy. Moreover, pharmacological blockade of IL-1 signaling has shown to be beneficial in some autoimmune and autoinflammatory diseases, making IL-1β a promising therapeutic target in neuroinflammatory conditions. This review highlights recent advances of our understanding on the multifaceted roles of IL-1β in neuroinflammatory diseases.
神经炎症在中枢神经系统(CNS)相关疾病的发病机制中起着因果关系,因此针对炎症介质的调节或可用性的治疗策略可用于预防或减轻病理。有趣的是,促炎细胞因子白细胞介素-1β(IL-1β)在多种 CNS 疾病中持续免疫反应并导致疾病严重程度,这些疾病包括多发性硬化症、神经退行性疾病、创伤性脑损伤和糖尿病性视网膜病变。此外,IL-1 信号的药理学阻断已被证明在一些自身免疫和自身炎症性疾病中是有益的,这使得 IL-1β 成为神经炎症条件下有前途的治疗靶点。这篇综述强调了我们对 IL-1β 在神经炎症性疾病中的多方面作用的最新认识。