Bomprezzi Roberto
Department of Neurology, University of Massachusetts, 55 Lake Avenue North, Worcester, MA 01655, USA.
Ther Adv Neurol Disord. 2015 Jan;8(1):20-30. doi: 10.1177/1756285614564152.
Multiple sclerosis (MS) shares an immune-mediated origin with psoriasis. Long-term safety and efficacy data generated in Europe from usage of fumaric acid formulations in the latter disease constituted grounds to investigate their effects in MS patients. Dimethyl fumarate (DMF) was found to be the active principle in those formulations and in vitro studies have demonstrated that DMF has immune-modulatory properties exerted through abilities to divert cytokine production toward a Th2 profile, both on lymphocytes and microglial cells. More importantly, DMF was discovered to impact the anti-oxidative stress cell machinery promoting the transcription of genes downstream to the activation of the nuclear factor (erythroid derived 2)-like2 (NRF2). DMF exposure increases the cytosol concentrations of NRF2, which besides immune regulatory effects, has the potential for cytoprotection on glial cells, oligodendrocytes and neurons. Extensive and rigorous clinical trials have assessed the efficacy and safety of DMF at the dose of 240 mg twice and three times a day in relapsing-remitting MS patients during one phase IIb and two phase III trials. Robust, positive results were obtained across a number of clinical and paraclinical parameters. In one study (DEFINE), the relative reductions of the adjusted annualized relapse rate of the low and high dose regimens in comparison with placebo were 53% and 48%, respectively (p < 0.001 for both comparisons). In the other trial (CONFIRM), DMF decreased the annualized relapse rate in comparison with placebo by 44% in the lower and by 51% in higher dosage group (also p < 0.001). The number and size of lesions as detected by magnetic resonance imaging were also significantly decreased in comparison with the patients receiving DMF at every dosage. Multiple post hoc and subgroup analyses corroborated the clinical data, rendering DMF an appealing medication whose potential for impacting the degenerative aspects of MS remains to be explored.
多发性硬化症(MS)与银屑病有着共同的免疫介导起源。欧洲针对后者使用富马酸制剂所产生的长期安全性和有效性数据,为研究其对MS患者的影响提供了依据。已发现富马酸二甲酯(DMF)是这些制剂中的活性成分,体外研究表明,DMF具有免疫调节特性,可通过使淋巴细胞和小胶质细胞的细胞因子产生转向Th2型来发挥作用。更重要的是,人们发现DMF会影响抗氧化应激细胞机制,促进核因子(红系衍生2)样2(NRF2)激活下游基因的转录。DMF暴露会增加NRF2的胞质溶胶浓度,NRF2除了具有免疫调节作用外,还具有对神经胶质细胞、少突胶质细胞和神经元进行细胞保护的潜力。在一项IIb期和两项III期试验中,广泛而严格的临床试验评估了每天两次和三次服用240mg剂量的DMF对复发缓解型MS患者的疗效和安全性。在许多临床和临床前参数方面都获得了有力的阳性结果。在一项研究(DEFINE)中,与安慰剂相比,低剂量和高剂量方案调整后的年化复发率相对降低分别为53%和48%(两项比较的p均<0.001)。在另一项试验(CONFIRM)中,与安慰剂相比,DMF在较低剂量组使年化复发率降低了44%,在较高剂量组降低了51%(p也<0.001)。与接受各剂量DMF的患者相比,通过磁共振成像检测到的病灶数量和大小也显著减少。多项事后分析和亚组分析证实了临床数据,使DMF成为一种有吸引力的药物,其对MS退行性方面的影响潜力仍有待探索。