Department of Neurology, The Affiliated Suzhou Hospital, Nanjing Medical University, Suzhou, China.
Neurochem Res. 2018 Jul;43(7):1454-1463. doi: 10.1007/s11064-018-2560-5. Epub 2018 Jun 8.
IL-35 has been identified as a novel anti-inflammatory cytokine that belongs to the IL-12 cytokine family and has been verified to play a protective role in autoimmune diseases. In this study, we investigated the protective effects of IL-35 on cerebral ischemia/reperfusion (I/R) injury in a middle cerebral artery occlusion mouse model. We determined that the expression of IL-35 was initially decreased and subsequently increased in I/R injury. Moreover, IL-35 (i.c.v.) pre- and posttreatment significantly reduced the infarct volume and improved neurological deficits after 45 min of ischemia and 24 h of reperfusion. Importantly, IL-35 treatment improved neurological function recovery, particularly in balance ability, at 14 days after treatment. Finally, our results showed that IL-35 treatment reduced the expression of IL-6 and IL-1β, which are confirmed proinflammatory cytokines, thus indicating that these cytokines have both been linked to the anti-inflammatory mechanisms of IL-35. Therefore, IL-35 may be a key immune mediator in brain ischemic injury and appears to have promising potential for clinical trials.
IL-35 已被确定为一种新型抗炎细胞因子,属于 IL-12 细胞因子家族,已被证实在自身免疫性疾病中发挥保护作用。在本研究中,我们在大脑中动脉闭塞小鼠模型中研究了 IL-35 对脑缺血/再灌注(I/R)损伤的保护作用。我们发现,在 I/R 损伤中,IL-35 的表达最初降低,随后增加。此外,IL-35(脑室内)预处理和后处理可显著减少缺血 45 分钟和再灌注 24 小时后的梗死体积,并改善神经功能缺损。重要的是,IL-35 治疗可改善治疗后 14 天的神经功能恢复,特别是平衡能力。最后,我们的结果表明,IL-35 治疗可降低 IL-6 和 IL-1β 的表达,这两种细胞因子被证实为促炎细胞因子,表明这些细胞因子均与 IL-35 的抗炎机制有关。因此,IL-35 可能是脑缺血损伤的关键免疫介质,似乎具有临床试验的巨大潜力。