Janiec K, Wajgt A, Kondera-Anasz Z
Department of Neurology, Silesian Medical University, Katowice, Poland.
Med Sci Monit. 2001 Jan-Feb;7(1):93-8.
Multiple sclerosis is presumably cell-mediated autoimmune disorder with immune abnormalities as presence of activated T-cells and increase interleukin 2 (IL-2) and soluble IL-2 receptor (sIL-2R) levels in central nervous system and peripheral blood of patients. The aim of immunosuppressive treatment is to diminish such activation. The aim of this study was to evaluate the influence of immunosuppressive cladribine treatment with total dose of 2.1 mg/kg b.w. administered in 7 cycles for 12 months, on serum leucocytes in 34 chronic progressive multiple sclerosis (CPMS) patients observed for 2 years as well as IL-2 and sIL-2R serum levels assessed before and right after the treatment.
The study was designed as a randomised, placebo-controlled, double-blind trial. The patients were divided in two groups: group I, cladribine-treated, n = 34; group II, placebo-treated, n = 35. Group III were healthy controls, n = 20. Leucocyte levels were determined with flow-cytometry. IL-2 and sIL-2R levels were assessed with enzyme-linked immunosorbent assay.
Statistically significant gradual decrease of lymphocyte level was observed from 7th week to 12th month after the beginning of treatment. During the following 12 months, lymphocyte levels remained decreased in comparison to baseline. Mean values of IL-2 and sIL-2R levels measured 12 months after the treatment were found to be lowered by 20% (p. = 0.01) and by 24% (p. = 0.0005), respectively.
The results obtained indicate fast and long-lasting decrease of serum leucocyte level and suppressive influence of cladribine treatment on immune processes in multiple sclerosis patients.
多发性硬化症可能是一种细胞介导的自身免疫性疾病,其免疫异常表现为患者中枢神经系统和外周血中存在活化的T细胞以及白细胞介素2(IL-2)和可溶性IL-2受体(sIL-2R)水平升高。免疫抑制治疗的目的是减少这种活化。本研究的目的是评估总剂量为2.1mg/kg体重、分7个周期给药共12个月的免疫抑制性克拉屈滨治疗对34例慢性进展性多发性硬化症(CPMS)患者血清白细胞的影响,这些患者被观察了2年,同时评估治疗前和治疗刚结束时的血清IL-2和sIL-2R水平。
本研究设计为随机、安慰剂对照、双盲试验。患者分为两组:第一组,接受克拉屈滨治疗,n = 34;第二组,接受安慰剂治疗,n = 35。第三组为健康对照,n = 20。采用流式细胞术测定白细胞水平。采用酶联免疫吸附测定法评估IL-2和sIL-2R水平。
治疗开始后第7周直至12个月,观察到淋巴细胞水平有统计学意义的逐渐下降。在接下来的12个月中,与基线相比,淋巴细胞水平仍持续下降。治疗12个月后测得的IL-2和sIL-2R水平平均值分别降低了20%(p = 0.01)和24%(p = 0.0005)。
所得结果表明血清白细胞水平快速且持久下降,以及克拉屈滨治疗对多发性硬化症患者免疫过程有抑制作用。