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甲基泼尼松龙和环磷酰胺治疗多发性硬化症复发患者的临床实验室研究

Clinico-laboratory study of methylprednisolone and cyclophosphamide treatment in patients with multiple sclerosis relapse.

作者信息

Manova M G, Kostadinova I I, Rangelov A A

机构信息

Higher Medical Institute, Department of Neurology, 15A Vassil Aprilov St., 4000 Plovdiv, Bulgaria.

出版信息

Folia Med (Plovdiv). 2000;42(3):20-5.

Abstract

INTRODUCTION

The effect of combined treatment (methylprednisolone and cyclophosphamide) of multiple sclerosis relapse within one year was investigated in an open clinical trial study of 70 patients. The sample comprised subjects shown to have clinically proven multiple sclerosis according to the criteria of C Poser and degree of neurological deficit according to EDSS rating from 2.5 to 6.0 points.

MATERIAL AND METHODS

Methylprednisolone (200 mg, i.v., every other day, 10 doses, total course dose 2 g) was administered to 35 patients (mean age 31.34 +/- 1.53 years). Methylprednisolone using the same schedule and cyclophosphamide (200 mg, i.v.) given in the methylprednisolone-free day, 10 doses plus 200 mg i.v. once a month in the first three consecutive months (total course dose 2.6 g) were applied in another 35 patients (mean age 33.22 +/- 1.32 years).

RESULTS AND DISCUSSION

The changes of EDSS ratings at the end of months 1 and 12, of the CD+ T-lymphocytes subpopulations and B-lymphocytes from peripheral blood--prior to treatment and between the 5th and 9th week of treatment were compared. The neurological deficit degree according to EDSS dropped significantly (P < 0.01; P < 0.001) after one month of treatment in both groups. At the end of month 12 this indicator reached its baseline value in the group treated only with methylprednisolone while remaining significantly lower in the combined therapy group (P < 0.01). After methylprednisolone and cyclophosphamide application the suppressor/inducer CD8+ T-cells increased significantly in percentage (P < 0.05), while the values of B-lymphocytes decrease significantly (P < 0.05), in contrast to the results from the methylprednisolone-only treatment.

CONCLUSIONS

The results clearly indicate the greater efficaciousness of treatment by combining two immunosuppressive drugs.

摘要

引言

在一项针对70名患者的开放性临床试验研究中,对联合治疗(甲基强的松龙和环磷酰胺)在一年内对多发性硬化症复发的影响进行了调查。样本包括根据C·波泽标准临床确诊为多发性硬化症的受试者,以及根据扩展残疾状态量表(EDSS)评分为2.5至6.0分的神经功能缺损程度的受试者。

材料与方法

35名患者(平均年龄31.34±1.53岁)接受甲基强的松龙(200毫克,静脉注射,隔日一次,共10剂,总疗程剂量2克)治疗。另外35名患者(平均年龄33.22±1.32岁)接受相同疗程的甲基强的松龙治疗,并在无甲基强的松龙治疗日给予环磷酰胺(200毫克,静脉注射),共10剂,在前三个月连续每月额外静脉注射200毫克(总疗程剂量2.6克)。

结果与讨论

比较了治疗前以及治疗第5至9周外周血中CD+T淋巴细胞亚群和B淋巴细胞在第1个月和第12个月末的EDSS评分变化。两组治疗1个月后,根据EDSS评定的神经功能缺损程度均显著下降(P<0.01;P<0.001)。在第12个月末,仅接受甲基强的松龙治疗的组该指标恢复到基线值,而联合治疗组仍显著低于基线值(P<0.01)。与仅接受甲基强的松龙治疗的结果相比,应用甲基强的松龙和环磷酰胺后,抑制/诱导性CD8+T细胞百分比显著增加(P<0.05),而B淋巴细胞值显著降低(P<0.05)。

结论

结果清楚地表明两种免疫抑制药物联合治疗具有更高的疗效。

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