Rentzos Michael, Nikolaou Chryssoula, Rombos Antonis, Evangelopoulos M Eleftheria, Kararizou Evangelia, Koutsis George, Zoga Margarita, Dimitrakopoulos Antonis, Tsoutsou Anthousa, Sfangos Costas
Department of Neurology, Aeginition Hospital, Athens National University, School of Medicine, Greece.
Clin Neurol Neurosurg. 2008 Dec;110(10):992-6. doi: 10.1016/j.clineuro.2008.06.005. Epub 2008 Jul 25.
Interleukin-12 (IL-12), a proinflammatory cytokine produced by Th1 cells, and interleukin-10 (IL-10), a product of Th2 cells, are involved in the pathogenetic mechanisms of multiple sclerosis (MS). CCL2 chemokine expression is induced by Th2 cytokines and is decreased in MS relapse. The mechanisms responsible for the beneficial effects of IVmethylprednisolone in attacks are not clearly established and the duration of the effect of this treatment remains controversial.
We measured by enzyme-like immunosorbent assay (ELISA) serum levels of IL-12, IL-10 and CCL2 before, 5 days and 1 month after the initiation of treatment with IVMP in 20 patients with MS in relapse.
A significant increase of IL-10 and decrease of CCL2 serum levels was observed (p=0.0028 and 0.045 respectively) five days after the onset of steroid treatment but not after one month. Steroid treatment had no influence in serum levels of IL-12.
The clinical improvement of our MS patients with relapse following the treatment with methylprednisolone may be associated with an immediate but not a long-term modification of serum levels of IL-10 and CCL2. IL-12 may not be influenced by steroid treatment.
白细胞介素 - 12(IL - 12)是一种由Th1细胞产生的促炎细胞因子,白细胞介素 - 10(IL - 10)是Th2细胞的产物,它们都参与了多发性硬化症(MS)的发病机制。CCL2趋化因子的表达由Th2细胞因子诱导,且在MS复发时降低。静脉注射甲基泼尼松龙在发作期产生有益作用的机制尚未明确确立,且这种治疗效果的持续时间仍存在争议。
我们采用酶联免疫吸附测定(ELISA)法,对20例复发型MS患者在静脉注射甲基泼尼松龙治疗前、治疗开始后5天及1个月时的血清IL - 12、IL - 10和CCL2水平进行了检测。
在类固醇治疗开始后5天观察到IL - 10血清水平显著升高,CCL2血清水平显著降低(p值分别为0.0028和0.045),但1个月后未出现这种情况。类固醇治疗对IL - 12的血清水平没有影响。
我们的复发型MS患者在接受甲基泼尼松龙治疗后临床症状改善,可能与血清IL - 10和CCL2水平的即刻而非长期改变有关。IL - 12可能不受类固醇治疗的影响。