From the Department of Multiple Sclerosis Therapeutics (K.F.), Fukushima Medical University School of Medicine; and Multiple Sclerosis and Neuromyelitis Optica Center, Southern TOHOKU Research Institute for Neuroscience, Koriyama, Japan; Departments of Neurology and Ophthalmology (J.L.B.), Programs in Neuroscience and Immunology, School of Medicine, University of Colorado, Aurora; Department of Neurology (J.S.), Hôpital de Hautepierre, Strasbourg Cedex, France; Chugai Pharmaceutical Co. (M.H.), Ltd, Tokyo, Japan; Department of Neurology (I.K.), St. Josef Hospital, Ruhr University Bochum; Marianne-Strauß-Klinik (I.K.), Behandlungszentrum Kempfenhausen für Multiple Sklerose Kranke gGmbH, Berg, Germany; Department of Neurology (B.G.W.), Mayo Clinic, Rochester, MN; ApotheCom (D.K., T.M.), London, UK; and Department of Immunology (T.Y.), National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo, Japan.
Neurol Neuroimmunol Neuroinflamm. 2020 Aug 20;7(5). doi: 10.1212/NXI.0000000000000841. Print 2020 Sep 3.
Neuromyelitis optica spectrum disorder (NMOSD) is a rare autoimmune disorder that preferentially affects the spinal cord and optic nerve. Most patients with NMOSD experience severe relapses that lead to permanent neurologic disability; therefore, limiting frequency and severity of these attacks is the primary goal of disease management. Currently, patients are treated with immunosuppressants. Interleukin-6 (IL-6) is a pleiotropic cytokine that is significantly elevated in the serum and the CSF of patients with NMOSD. IL-6 may have multiple roles in NMOSD pathophysiology by promoting plasmablast survival, stimulating the production of antibodies against aquaporin-4, disrupting blood-brain barrier integrity and functionality, and enhancing proinflammatory T-lymphocyte differentiation and activation. Case series have shown decreased relapse rates following IL-6 receptor (IL-6R) blockade in patients with NMOSD, and 2 recent phase 3 randomized controlled trials confirmed that IL-6R inhibition reduces the risk of relapses in NMOSD. As such, inhibition of IL-6 activity represents a promising emerging therapy for the management of NMOSD manifestations. In this review, we summarize the role of IL-6 in the context of NMOSD.
视神经脊髓炎谱系疾病(NMOSD)是一种罕见的自身免疫性疾病,优先影响脊髓和视神经。大多数 NMOSD 患者经历严重的复发,导致永久性神经功能障碍;因此,限制这些发作的频率和严重程度是疾病管理的主要目标。目前,患者接受免疫抑制剂治疗。白细胞介素-6(IL-6)是一种多效细胞因子,在 NMOSD 患者的血清和脑脊液中显著升高。IL-6 可能通过促进浆母细胞存活、刺激针对水通道蛋白-4 的抗体产生、破坏血脑屏障完整性和功能、增强促炎 T 淋巴细胞分化和激活,在 NMOSD 发病机制中发挥多种作用。病例系列研究表明,NMOSD 患者接受 IL-6 受体(IL-6R)阻断后复发率降低,最近的两项 3 期随机对照试验证实 IL-6R 抑制可降低 NMOSD 复发风险。因此,抑制 IL-6 活性代表了 NMOSD 表现的一种有前途的新兴治疗方法。在这篇综述中,我们总结了 IL-6 在 NMOSD 中的作用。