Fukaura Hikoaki
Nihon Rinsho. 2014 Nov;72(11):2015-22.
The purpose of this section is to introduce the clinical utility of several disease-modifying agents including natalizumab and immunosuppressive treatments that are currently available in Japan, and glatiramer acetate that will be probably available in Japan within a few years. Immunosuppressive therapy has been used to treat multiple sclerosis(MS) for over 30 years based on the hypothesis that MS is a T cell-mediated autoimmune disease. The most commonly used immunosuppressive agents in MS are azathioprine, cyclophosphamide, methotrexate, and mitoxantrone. Like the interferons and glatiramer acetate, immunosuppressive drugs are most efficacious in stages of MS that have an inflammatory component as evidenced by relapses and/or gadolinium-enhancing lesions on MRI or in patients in earlier stages of disease where inflammation predominates over degenerative processes in the CNS. There is no evidence of efficacy in primary progressive MS or later stages of secondary progressive MS. It is appropriate to consider glatiramer acetate for treatment in any patient who has relapsing remitting MS (RRMS), and glatiramer acetate may be helpful in patients with progressive disease. Because of the possibility that natalizumab therapy may be responsible for the increased risk of primary progressive leukoencephalopathy (PML), it is recommended that natalizumab be reserved for use in selected patients with relapsing remitting disease who have failed other therapies either through continued disease activity or medication intolerance, or who have a particularly aggressive initial disease course.
本节的目的是介绍几种疾病修正药物的临床应用,包括目前在日本可用的那他珠单抗和免疫抑制治疗药物,以及可能在未来几年内在日本上市的醋酸格拉替雷。基于多发性硬化症(MS)是一种T细胞介导的自身免疫性疾病这一假设,免疫抑制疗法已被用于治疗MS超过30年。MS中最常用的免疫抑制药物是硫唑嘌呤、环磷酰胺、甲氨蝶呤和米托蒽醌。与干扰素和醋酸格拉替雷一样,免疫抑制药物在MS具有炎症成分的阶段最为有效,这可通过复发和/或MRI上钆增强病变来证明,或在疾病早期阶段炎症占中枢神经系统退行性过程主导地位的患者中。没有证据表明其对原发性进行性MS或继发性进行性MS后期有效。对于任何复发缓解型MS(RRMS)患者,考虑使用醋酸格拉替雷进行治疗是合适的,醋酸格拉替雷可能对进行性疾病患者有帮助。由于那他珠单抗治疗可能导致原发性进行性白质脑病(PML)风险增加,建议仅将那他珠单抗用于选定的复发缓解型疾病患者,这些患者因疾病持续活动或药物不耐受而对其他治疗无效,或有特别侵袭性的初始病程。