Ozawa Kyoko
Department of Neurology, Utano National Hospital.
Nihon Rinsho. 2003 Aug;61(8):1449-54.
Immunological treatments of progressive multiple sclerosis are discussed. Recent trials of interferon-beta 1b(IFN beta-1b) and IFN beta-1a in secondary progressive MS (SPMS) have demonstrated treatment benefits on relapse rate and accumulation of MRI lesions, and one trial of IFN beta-1b showed significant slowing of disability progression. In another recent study, mitoxantrone, a potent immunosuppressive agent, was reported to reduce progression of disability in SPMS. As regards primary progressive MS, there is currently no convincing disease-modifying treatment. Pathologic studies have revealed that axonal injury is prominent in MS and may be the explanation for irreversible disability. It is hoped that therapeutic strategies will be aimed at axonal loss as well as inflammation and demyelination.
本文讨论了进展性多发性硬化症的免疫治疗方法。近期针对继发性进展性多发性硬化症(SPMS)进行的β-干扰素1b(IFNβ-1b)和β-干扰素1a试验表明,这些治疗方法在降低复发率和减少磁共振成像(MRI)病灶累积方面具有益处,且一项IFNβ-1b试验显示其能显著减缓残疾进展。在另一项近期研究中,据报道,强效免疫抑制剂米托蒽醌可减缓SPMS患者的残疾进展。至于原发性进展性多发性硬化症,目前尚无令人信服的疾病改善治疗方法。病理研究表明,轴突损伤在多发性硬化症中较为突出,这可能是导致不可逆残疾的原因。人们希望治疗策略能够针对轴突损失以及炎症和脱髓鞘病变。