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多发性硬化症患者自体造血干细胞移植后的MRI及脑脊液寡克隆带

MRI and CSF oligoclonal bands after autologous hematopoietic stem cell transplantation in MS.

作者信息

Saiz A, Carreras E, Berenguer J, Yagüe J, Martínez C, Marín P, Rovira M, Pujol T, Arbizu T, Graus F

机构信息

Services of Neurology, Hospital Clínic, Institut d'Investigació Biomèdica August Pi i Sunyer (IDIBAPS), University of Barcelona, Spain.

出版信息

Neurology. 2001 Apr 24;56(8):1084-9. doi: 10.1212/wnl.56.8.1084.

Abstract

OBJECTIVE

To analyze the MRI and CSF oligoclonal bands (OB) changes in patients with MS who underwent an autologous hematopoietic stem cell transplantation (AHSCT).

BACKGROUND

AHSCT is evaluated as an alternative therapy in severe MS. In previous series of AHSCT for MS, data on MRI or OB outcome were limited or not provided.

METHODS

Five patients with a median Kurtzke's EDSS score of 6.5, more than two attacks, and confirmed worsening of the EDSS in the previous year received an AHSCT. Hematopoietic stem cells were mobilized with cyclophosphamide (3 g/m2) and granulocyte colony-stimulating factor (5 microg/kg/d). The graft was T cell depleted by positive CD 34+ selection. Conditioning regimen included BCNU (300 mg/m(2)), cyclophosphamide (150 mg/kg in 3 days), and antithymocyte globulin (60 mg/kg in 4 days). MRI scans were scheduled at baseline and 1, 3, 6, and 12 months and OB analysis at baseline and 3 and 12 months post-AHSCT.

RESULTS

Four patients had a stable or improved EDSS after a median follow-up of 18 months (range, 12 to 24 months). The fifth patient's condition deteriorated during AHSCT. She partially improved and remained stable after month 3 after AHSCT. The baseline CSF OB persisted 1 year after AHSCT. MRI studies after AHSCT showed no enhanced T1 lesions and no new or enlarging T2 lesions. The median percentage change of T2 lesion load was -11.8% (range, -26.6 to -4.0%). All patients had a decrease of corpus callosum area at 1 year (median, 12.4%; range, 7.8% to 20.5%) that did not progress in the two patients evaluated at 2 years after AHSCT.

CONCLUSIONS

Although the persistence of CSF OB suggests the lymphocytes were not eliminated from the CNS, the follow-up MRI studies showed no enhanced T1 brain lesions and a reduction in the T2 lesion load that correlated with the clinical stabilization of MS after AHSCT.

摘要

目的

分析接受自体造血干细胞移植(AHSCT)的多发性硬化症(MS)患者的MRI及脑脊液寡克隆区带(OB)变化。

背景

AHSCT被评估为重度MS的一种替代疗法。在既往一系列针对MS的AHSCT研究中,关于MRI或OB结果的数据有限或未提供。

方法

5例患者接受了AHSCT,其Kurtzke扩展残疾状态量表(EDSS)评分中位数为6.5,发作超过两次,且上一年度EDSS确有恶化。采用环磷酰胺(3 g/m2)和粒细胞集落刺激因子(5 μg/kg/d)动员造血干细胞。通过阳性CD 34+分选去除移植物中的T细胞。预处理方案包括卡莫司汀(300 mg/m²)、环磷酰胺(150 mg/kg,分3天给药)和抗胸腺细胞球蛋白(60 mg/kg,分4天给药)。在基线、1、3、6和12个月时安排MRI扫描,并在基线以及AHSCT后3个月和12个月进行OB分析。

结果

中位随访18个月(范围12至24个月)后,4例患者的EDSS稳定或改善。第5例患者在AHSCT期间病情恶化。她在AHSCT后3个月后部分改善并保持稳定。AHSCT后1年,基线脑脊液OB持续存在。AHSCT后的MRI研究显示无强化T1病变,也无新的或扩大的T2病变。T2病变负荷的中位百分比变化为-11.8%(范围-26.6%至-4.0%)。所有患者在1年时胼胝体面积均减小(中位数为12.4%;范围7.8%至20.5%),在AHSCT后2年评估的2例患者中未进一步进展。

结论

尽管脑脊液OB持续存在提示淋巴细胞未从CNS中清除,但随访MRI研究显示无脑强化T1病变,且T2病变负荷降低,这与AHSCT后MS的临床稳定相关。

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