Nikolay Blokhin National Medical Research Center of Oncology, Moscow, Russia.
Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
Handb Clin Neurol. 2024;202:249-258. doi: 10.1016/B978-0-323-90242-7.00004-3.
Autologous hematopoietic stem cell transplantation (aHSCT) may be effective in carefully selected pediatric patients with multiple sclerosis (MS), neuromyelitis optica (NMO), and chronic inflammatory demyelinating polyneuropathy (CIDP). aHSCT for pediatric MS (same as for adults) is performed to eradicate inflammatory autoreactive cells with lympho-ablative regimens and restore immune tolerance. Its therapeutic effect in MS relies on various mechanisms: (1) the immunosuppressive conditioning regimen prior to aHSCT was able to eradicate the autoreactive cells and (2) the regeneration/renewal of the immune system to reset the aberrant immune response against self-antigens. The aHSCT procedure includes the following different steps, as described in this chapter: patient selection through careful pretransplant screening, "wash-out" period from previous treatments, mobilization of hematopoietic stem cells (HSC), conditioning regimen, HSC infusion, and posttransplant monitoring for early and late complications. Moreover, specific aspects of pediatric population undergoing aHSCT are described. According to the available evidence, aHSCT appears to be safe in pediatric MS, obtaining disease control for a prolonged time after the procedure. A reasonable approach in this setting includes the application of less toxic treatments while reserving aHSCT procedure for patients with severe/refractory forms of the disease. The EBMT considers MS, NMO, and CIDP in pediatric patients within the category of the clinical option (CO), where candidates for aHSCT can be selected on the basis of careful consideration of individual case history in the multidisciplinary setting.
自体造血干细胞移植(aHSCT)可能对精心挑选的多发性硬化症(MS)、视神经脊髓炎(NMO)和慢性炎症性脱髓鞘性多发性神经病(CIDP)儿科患者有效。aHSCT 用于儿科 MS(与成人相同)是为了用淋巴清除方案消除炎症性自身反应性细胞,并恢复免疫耐受。其在 MS 中的治疗作用依赖于多种机制:(1)aHSCT 前的免疫抑制性预处理方案能够消除自身反应性细胞,(2)免疫系统的再生/更新以重置针对自身抗原的异常免疫反应。aHSCT 程序包括以下不同步骤,如本章所述:通过仔细的移植前筛选选择患者,“清洗”先前治疗的时间,动员造血干细胞(HSC),预处理方案,HSC 输注,以及移植后早期和晚期并发症的监测。此外,还描述了接受 aHSCT 的儿科人群的具体方面。根据现有证据,aHSCT 在儿科 MS 中似乎是安全的,在手术后能获得长时间的疾病控制。在这种情况下,合理的方法包括应用毒性较小的治疗方法,同时为疾病严重/难治型患者保留 aHSCT 方案。EBMT 将儿科患者的 MS、NMO 和 CIDP 归类为临床选择(CO),可以在多学科环境下根据对个体病史的仔细考虑选择 aHSCT 候选人。