Xie Zhong-Xiang, Zhang Hong-Liang, Wu Xiu-Juan, Zhu Jie, Ma Di-Hui, Jin Tao
Neuroscience Center, Department of Neurology, The First Hospital of Jilin University, Changchun 130021, China.
Neuroscience Center, Department of Neurology, The First Hospital of Jilin University, Changchun 130021, China ; Department of Neurobiology, Care Sciences and Society, Karolinska Institute, 141 86 Stockholm, Sweden.
Mediators Inflamm. 2015;2015:513295. doi: 10.1155/2015/513295. Epub 2015 Jan 29.
Multiple sclerosis (MS) is an immune-mediated disorder in the central nervous system (CNS) characterized by inflammation and demyelination as well as axonal and neuronal degeneration. So far effective therapies to reverse the disease are still lacking; most therapeutic drugs can only ameliorate the symptoms or reduce the frequency of relapse. Dendritic cells (DCs) are professional antigen presenting cells (APCs) that are key players in both mediating immune responses and inducing immune tolerance. Increasing evidence indicates that DCs contribute to the pathogenesis of MS and might provide an avenue for therapeutic intervention. Here, we summarize the immunogenic and tolerogenic roles of DCs in MS and review medicinal drugs that may affect functions of DCs and have been applied in clinic for MS treatment. We also describe potential therapeutic molecules that can target DCs by inducing anti-inflammatory cytokines and inhibiting proinflammatory cytokines in MS.
多发性硬化症(MS)是一种中枢神经系统(CNS)的免疫介导性疾病,其特征为炎症、脱髓鞘以及轴突和神经元变性。迄今为止,仍缺乏有效的逆转该疾病的疗法;大多数治疗药物只能缓解症状或降低复发频率。树突状细胞(DCs)是专职抗原呈递细胞(APCs),在介导免疫反应和诱导免疫耐受方面均发挥关键作用。越来越多的证据表明,DCs参与了MS的发病机制,可能为治疗干预提供途径。在此,我们总结了DCs在MS中的免疫原性和耐受性作用,并综述了可能影响DCs功能且已应用于MS临床治疗的药物。我们还描述了可通过在MS中诱导抗炎细胞因子和抑制促炎细胞因子来靶向DCs的潜在治疗分子。