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视神经脊髓炎谱系疾病的造血干细胞移植。能否重新建立免疫耐受?

Hematopoietic stem cell transplantation for neuromyelitis optica spectrum disorder. Can immune tolerance be reestablished?

机构信息

Department of Medicine, Scripps Health Care, La Jolla, CA, United States; Genani Corporation, Chicago, IL, United States.

Department of Medical Sciences, Uppsala University, Uppsala, Sweden.

出版信息

Handb Clin Neurol. 2024;202:169-197. doi: 10.1016/B978-0-323-90242-7.00009-2.

Abstract

Neuromyelitis optica (NMO), which is also referred to as Devic's disease, was originally considered an aggressive subtype of multiple sclerosis (MS) presenting as optic neuritis and/or extensive transverse myelitis in which 50% of patients become blind or in a wheelchair within 5 years of onset. Subsequently, NMO was categorized as one of a spectrum of inflammatory and demyelinating autoimmune disorders that are distinct from multiple sclerosis and termed neuromyelitis optica spectrum disorder (NMOSD). NMOSD differs from multiple sclerosis by its clinical course, presentation, magnetic resonance imaging findings, clinical presentation, serum biomarker prognosis, and response to treatment. More recently, NMOSD has been subdivided according to auto-antibody status as aquaporin 4 (AQP4) seropositive NMO, myelin oligodendrocyte glycoprotein (MOG) antibody-associated disease (MOGAD), and seronegative NMOSD. The only treatment to date that has resulted in treatment-free remissions, now lasting for more than 5-10 years with posttreatment disappearance of anti-AQP4 antibodies, is hematopoietic stem cell transplantation (HSCT) using either an allogeneic (matched sibling or unrelated) donor with a reduced toxicity conditioning regimen or an autologous stem cell source using a nonmyeloablative conditioning regimen of plasmapheresis (PLEX), cyclophosphamide (Cytoxan®), rabbit antithymocyte (ATG), and rituximab (Rituxan®). Post-HSCT long-term resolution of disease activity and disappearance of AQP4 antibodies is consistent with HSCT-induced immune tolerance.

摘要

视神经脊髓炎(NMO),也称为 Devic 病,最初被认为是多发性硬化症(MS)的一种侵袭性亚型,表现为视神经炎和/或广泛的横贯性脊髓炎,其中 50%的患者在发病后 5 年内失明或坐上轮椅。随后,NMO 被归类为一组炎症性和脱髓鞘自身免疫性疾病之一,与多发性硬化症不同,并被称为视神经脊髓炎谱系障碍(NMOSD)。NMOSD 与多发性硬化症在临床病程、表现、磁共振成像结果、临床表现、血清生物标志物预后和治疗反应方面存在差异。最近,NMOSD 根据自身抗体状态进一步细分,包括水通道蛋白 4(AQP4)阳性 NMO、髓鞘少突胶质细胞糖蛋白(MOG)抗体相关疾病(MOGAD)和血清阴性 NMOSD。迄今为止,唯一能够实现无治疗缓解的治疗方法是造血干细胞移植(HSCT),使用异基因(匹配的兄弟姐妹或无关供体)或自体干细胞来源,采用降低毒性的预处理方案或非清髓性预处理方案,包括血浆置换(PLEX)、环磷酰胺(Cytoxan®)、兔抗胸腺细胞(ATG)和利妥昔单抗(Rituxan®)。HSCT 后疾病活动的长期缓解和 AQP4 抗体的消失与 HSCT 诱导的免疫耐受一致。

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