Avila Mirla, Bansal Arpana, Culberson John, Peiris Alan N
Department of Neurology, Texas Tech University Health Sciences Center, Lubbock, Texas, USA.
Texas Tech University Health Sciences Center, School of Medicine, Lubbock, Texas,
Eur Neurol. 2018;80(1-2):93-99. doi: 10.1159/000494262. Epub 2018 Oct 19.
Multiple sclerosis (MS) is a chronic inflammatory demyelination disorder with an immune-mediated pathophysiology that affects the central nervous system (CNS). Like other autoimmune conditions, it has a predilection for female gender. This suggests a gender bias and a possible hormonal association. Inflammation and demyelination are hallmarks of MS. Oligodendrocytes are the myelinating cells of the CNS and these continue to be generated by oligodendrocyte precursor cells (OPCs). The process of remyelination represents a major form of plasticity in the developing adult CNS. Remyelination does occur in MS, but the process is largely inadequate and/or incomplete. Current treatment strategies primarily focus on reducing inflammation or immunosuppression, but there is a need for more extensive research on re-myelination as a possible mechanism of treatment. Previous studies have shown that pregnancy leads to an increase in OPC proliferation, oligodendrocyte generation and the number of myelinated axons in the maternal CNS. Studies have also suggested that this remyelination is possibly mediated by estriol. Sex hormones in particular have been shown to have an immuno-protective effect in TH1-driven autoimmunity diseases. The aim of our article is to review the available research on sex hormone-specific immune modulatory effects, assess its remyelination potential in MS, and suggest a future path for more extensive research on sex hormone as a target for therapeutics in MS.
多发性硬化症(MS)是一种慢性炎症性脱髓鞘疾病,其病理生理过程由免疫介导,会影响中枢神经系统(CNS)。与其他自身免疫性疾病一样,它在女性中更为常见。这表明存在性别偏见以及可能的激素关联。炎症和脱髓鞘是MS的特征。少突胶质细胞是中枢神经系统的髓鞘形成细胞,这些细胞继续由少突胶质前体细胞(OPC)产生。再髓鞘化过程是成年中枢神经系统发育过程中可塑性的一种主要形式。MS中确实会发生再髓鞘化,但这个过程在很大程度上是不充分和/或不完全的。目前的治疗策略主要集中在减轻炎症或免疫抑制,但需要对再髓鞘化作为一种可能的治疗机制进行更广泛的研究。先前的研究表明,怀孕会导致母体中枢神经系统中OPC增殖、少突胶质细胞生成以及有髓轴突数量增加。研究还表明,这种再髓鞘化可能是由雌三醇介导的。特别是性激素已被证明在TH1驱动的自身免疫性疾病中具有免疫保护作用。我们文章的目的是综述关于性激素特异性免疫调节作用的现有研究,评估其在MS中的再髓鞘化潜力,并为将性激素作为MS治疗靶点进行更广泛研究提出未来的方向。