自体造血干细胞移植治疗小儿自身免疫性神经系统疾病。

Kirill Kirgizov, Joachim Burman, John A Snowden, Raffaella Greco
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引用次数: 0

摘要

自体造血干细胞移植(aHSCT)对精心挑选的多发性硬化症(MS)、视神经炎(NMO)和慢性炎症性脱髓鞘性多发性神经病(CIDP)小儿患者可能有效。它对多发性硬化症的治疗效果依赖于多种机制:(1)aHSCT 前的免疫抑制调理方案能够根除自体反应细胞;(2)免疫系统的再生/更新能够重置针对自身抗原的异常免疫反应。如本章所述,造血干细胞移植过程包括以下不同步骤:通过仔细的移植前筛查选择患者、先前治疗的 "冲洗期"、动员造血干细胞、调理方案、造血干细胞输注以及移植后早期和晚期并发症监测。此外,还介绍了接受造血干细胞移植的儿科患者的具体情况。根据现有证据,接受造血干细胞移植对小儿多发性硬化症似乎是安全的,术后可长期控制病情。在这种情况下,合理的方法包括应用毒性较小的治疗方法,同时为重症/难治性疾病患者保留 aHSCT 程序。EBMT 认为,多发性硬化症、NMO 和 CIDP 儿童患者属于临床选择(CO)的范畴,可在多学科环境中根据个体病史进行仔细考虑后选择接受 aHSCT 的候选者。
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Autologous hematopoietic stem cell transplantation for pediatric autoimmune neurologic disorders.

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.

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来源期刊
Handbook of clinical neurology
Handbook of clinical neurology Medicine-Neurology (clinical)
CiteScore
4.10
自引率
0.00%
发文量
302
期刊介绍: The Handbook of Clinical Neurology (HCN) was originally conceived and edited by Pierre Vinken and George Bruyn as a prestigious, multivolume reference work that would cover all the disorders encountered by clinicians and researchers engaged in neurology and allied fields. The first series of the Handbook (Volumes 1-44) was published between 1968 and 1982 and was followed by a second series (Volumes 45-78), guided by the same editors, which concluded in 2002. By that time, the Handbook had come to represent one of the largest scientific works ever published. In 2002, Professors Michael J. Aminoff, François Boller, and Dick F. Swaab took on the responsibility of supervising the third (current) series, the first volumes of which published in 2003. They have designed this series to encompass both clinical neurology and also the basic and clinical neurosciences that are its underpinning. Given the enormity and complexity of the accumulating literature, it is almost impossible to keep abreast of developments in the field, thus providing the raison d''être for the series. The series will thus appeal to clinicians and investigators alike, providing to each an added dimension. Now, more than 140 volumes after it began, the Handbook of Clinical Neurology series has an unparalleled reputation for providing the latest information on fundamental research on the operation of the nervous system in health and disease, comprehensive clinical information on neurological and related disorders, and up-to-date treatment protocols.
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