Brochet B
Service de Neurologie, Hôpital Pellegrin, CHRU de Bordeaux.
Rev Neurol (Paris). 1998 Sep;154(8-9):629-34.
Several series of arguments favor at least partial efficacy of immunosuppression in multiple sclerosis. Immunosuppression can often treat experimental autoimmune encephalitis, and imperfect model of multiple sclerosis. Certain agents have been shown to affect the pathophysiological processes seen indirectly on magnetic resonance imaging (mitoxantrone and Campath, for example). Therapeutic trials have their methodological weaknesses but do allow certain conclusions. The progressive forms of multiple sclerosis are the most widely studied. Massive but short-term immunosuppression does not appear to affect the course of progression but prolonged immunosuppression would appear to slow down the process, at least in responders. The effect on disease progression is modest and preference should go to well-tolerated treatments. Immunosuppression appears to effectively decrease the number of acute episodes and reduce the number of new lesions detectable by magnetic resonance imaging. The effect of immunosuppression is limited however by the fact that the clinical course of progressive forms depends less on the development of new lesions than on an aggravation of the demyelinization process and possible axon loss within constituted lesions. This is a further argument favoring early immunosuppressive treatment at a stage when it can be most effective.
有一系列论据支持免疫抑制在多发性硬化症中至少具有部分疗效。免疫抑制通常能够治疗实验性自身免疫性脑脊髓炎,这是多发性硬化症的一种不完美模型。某些药物已被证明会影响磁共振成像间接观察到的病理生理过程(例如米托蒽醌和阿仑单抗)。治疗试验存在方法学上的弱点,但确实能得出某些结论。多发性硬化症的进展型是研究最为广泛的类型。大规模但短期的免疫抑制似乎不会影响疾病进展过程,但长期免疫抑制似乎会减缓这一进程,至少对有反应者是这样。对疾病进展的影响较为适度,应优先选择耐受性良好的治疗方法。免疫抑制似乎能有效减少急性发作的次数,并减少磁共振成像可检测到的新病灶数量。然而,免疫抑制的效果受到限制,因为进展型的临床病程较少依赖新病灶的形成,而更多取决于脱髓鞘过程的加重以及既定病灶内可能出现的轴突损失。这是支持在最有效阶段进行早期免疫抑制治疗的又一论据。