Department of Neurology, School of Medicine, Technical University Munich, Klinikum Rechts der Isar, Ismaninger Str. 22, 81675 Muenchen, Germany.
Int J Mol Sci. 2022 Apr 9;23(8):4154. doi: 10.3390/ijms23084154.
Neuromyelitis optica spectrum disorders (NMOSD) are rare neurologic autoimmune diseases that have a poor prognosis if left untreated. For many years, generic oral immunosuppressants and repurposed monoclonal antibodies that target the interleukin-6 pathway or B cells were the mainstays of drug treatment. Recently, these drug treatments have been complemented by new biologics developed and approved specifically for NMOSD. In principle, all of these drugs are effective, but treatment recommendations that take this into account are still pending. Instead, the choice of a drug may depend on other criteria such as drug safety or tolerability. In this review, we summarise current knowledge on the adverse effects of azathioprine, mycophenolate mofetil, rituximab, tocilizumab, eculizumab, satralizumab, and inebilizumab in NMOSD. Infections, cytopenias, and infusion-related reactions are most common, but the data are as heterogeneous as the manifestations are diverse. Nevertheless, knowledge of safety issues may facilitate treatment choices for individual patients.
视神经脊髓炎谱系疾病(NMOSD)是罕见的神经自身免疫性疾病,如果不治疗,预后很差。多年来,通用的口服免疫抑制剂和靶向白细胞介素-6 途径或 B 细胞的重新定位的单克隆抗体一直是药物治疗的主要方法。最近,专门为 NMOSD 开发和批准的新型生物制剂补充了这些药物治疗。原则上,所有这些药物都有效,但仍在等待考虑到这一点的治疗建议。相反,药物的选择可能取决于其他标准,如药物安全性或耐受性。在这篇综述中,我们总结了目前关于硫唑嘌呤、霉酚酸酯、利妥昔单抗、托珠单抗、依库珠单抗、satralizumab 和 inebilizumab 在 NMOSD 中的不良反应的知识。感染、血细胞减少和输注相关反应最常见,但数据与临床表现一样多样,具有异质性。然而,对安全问题的了解可能有助于为个别患者做出治疗选择。