Department of Neurology, Renji Hospital, Shanghai Jiao Tong University School of Medicine, 160 Pujian Road, Pudong, Shanghai, 200127, China.
J Neuroinflammation. 2022 Jun 17;19(1):157. doi: 10.1186/s12974-022-02502-1.
Multiple sclerosis (MS), as an autoimmune neurological disease with both genetic and environmental contribution, still lacks effective treatment options among progressive patients, highlighting the need to re-evaluate disease innate properties in search for novel therapeutic targets. Fatty acids (FA) and MS bear an interesting intimate connection. FA and FA metabolism are highly associated with autoimmunity, as the diet-derived circulatory and tissue-resident FAs level and composition can modulate immune cells polarization, differentiation and function, suggesting their broad regulatory role as "metabokines". In addition, FAs are indeed protective factors for blood-brain barrier integrity, crucial contributors of central nervous system (CNS) chronic inflammation and progressive degeneration, as well as important materials for remyelination. The remaining area of ambiguity requires further exploration into this arena to validate the existed phenomenon, develop novel therapies, and confirm the safety and efficacy of therapeutic intervention targeting FA metabolism.
多发性硬化症(MS)是一种自身免疫性神经系统疾病,既有遗传因素又有环境因素的影响。对于进展期患者,目前仍缺乏有效的治疗方法,这凸显了需要重新评估疾病的固有特性,以寻找新的治疗靶点。脂肪酸(FA)和多发性硬化症之间存在着有趣的密切联系。FA 和 FA 代谢与自身免疫密切相关,因为饮食来源的循环和组织驻留 FA 水平和组成可以调节免疫细胞的极化、分化和功能,这表明它们作为“代谢因子”具有广泛的调节作用。此外,FA 确实是血脑屏障完整性的保护因素,也是中枢神经系统(CNS)慢性炎症和进行性退化的重要贡献者,也是髓鞘再生的重要物质。这一领域仍存在一些不明确的问题,需要进一步探索,以验证已有的现象,开发新的治疗方法,并确认针对 FA 代谢的治疗干预的安全性和有效性。