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用于治疗多发性硬化症的T细胞去除自体造血干细胞移植:前三例患者报告

T cell-depleted autologous hematopoietic stem cell transplantation for multiple sclerosis: report on the first three patients.

作者信息

Burt R K, Traynor A E, Cohen B, Karlin K H, Davis F A, Stefoski D, Terry C, Lobeck L, Russell E J, Goolsby C, Rosen S, Gordon L I, Keever-Taylor C, Brush M, Fishman M, Burns W H

机构信息

Department of Medicine, Northwestern University Medical School, Chicago, IL, USA.

出版信息

Bone Marrow Transplant. 1998 Mar;21(6):537-41. doi: 10.1038/sj.bmt.1701129.

Abstract

Multiple sclerosis (MS) is a disease of the central nervous system characterized by immune-mediated destruction of myelin. In patients with progressive deterioration, we have intensified immunosuppression to the point of myeloablation. Subsequently, a new hematopoietic and immune system is generated by infusion of CD34-positive hematopoietic stem cells (HSC). Three patients with clinical MS and a decline of their Kurtzke extended disability status scale (EDSS) by 1.5 points over the 12 months preceding enrollment and a Kurtzke EDSS of 8.0 at the time of enrollment were treated with hematopoietic stem cell (HSC) transplantation using a myeloablative conditioning regimen of cyclophosphamide (120 mg/kg), methylprednisolone (4 g) and total body irradiation (1200 cGy). Reconstitution of hematopoiesis was achieved with CD34-enriched stem cells. The average time of follow-up is 8 months (range 6-10 months). Despite withdrawal of all immunosuppressive medications, functional improvements have occurred in all three patients. We conclude that T cell-depleted hematopoietic stem cell transplantation can be performed safely in patients with severe and debilitating multiple sclerosis. Stem cell transplantation has resulted in modest neurologic improvements for the first time since onset of progressive disease although no significant changes in EDSS or NRS scales are evident at this time.

摘要

多发性硬化症(MS)是一种中枢神经系统疾病,其特征是髓鞘受到免疫介导的破坏。对于病情逐渐恶化的患者,我们强化免疫抑制至骨髓消融的程度。随后,通过输注CD34阳性造血干细胞(HSC)生成新的造血和免疫系统。三名临床确诊为MS的患者,在入组前12个月内其库尔特克扩展残疾状态量表(EDSS)下降了1.5分,入组时库尔特克EDSS为8.0,采用环磷酰胺(120mg/kg)、甲泼尼龙(4g)和全身照射(1200cGy)的骨髓消融预处理方案进行造血干细胞(HSC)移植治疗。使用富集CD34的干细胞实现了造血重建。平均随访时间为8个月(范围6 - 10个月)。尽管停用了所有免疫抑制药物,但所有三名患者的功能均有改善。我们得出结论,对于患有严重且致残性多发性硬化症的患者,可以安全地进行去除T细胞的造血干细胞移植。自疾病进展开始以来,干细胞移植首次使神经功能有了适度改善,尽管此时EDSS或NRS量表尚无明显变化。

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