Palace Jacqueline, Leite Maria Isabel, Nairne Angela, Vincent Angela
DM, Department of Clinical Neurology, John Radcliffe Hospital, University of Oxford, Level 3 West Wing, Oxford OX3 9DU, England.
Arch Neurol. 2010 Aug;67(8):1016-7. doi: 10.1001/archneurol.2010.188.
To describe a patient with neuromyelitis optica (NMO) whose aquaporin 4 (AQP4) antibody levels increased following treatment with interferon beta.
Prospective clinical and laboratory case report.
Institutional referral center for multiple sclerosis (MS). Patient One patient with an initial diagnosis of MS that was later revised to NMO.
A course of interferon beta-1a followed by conventional immunosuppression. Blood samples were collected from the onset of treatment, and clinical and laboratory assessment was performed.
Serum levels of AQP4 antibody and number and characteristics of neurological relapses.
After 3 relapses during a 10-month period despite interferon beta-1a treatment, the diagnosis of AQP4 antibody-positive NMO was made and treatment was switched to prednisolone and methotrexate. The AQP4 antibody titers rose dramatically during treatment with interferon beta, and then fell when conventional immunosuppressive therapy was substituted; the patient has remained relapse-free for the subsequent years.
Although previous articles have suggested that interferon beta may increase relapses in NMO, this is the first to illustrate an increase in AQP4 antibodies associated with such treatment.
描述一名视神经脊髓炎(NMO)患者,其水通道蛋白4(AQP4)抗体水平在接受β-干扰素治疗后升高。
前瞻性临床及实验室病例报告。
多发性硬化症(MS)机构转诊中心。患者 一名最初诊断为MS,后来修订为NMO的患者。
一个疗程的β-1a干扰素治疗,随后进行常规免疫抑制治疗。从治疗开始时采集血样,并进行临床及实验室评估。
AQP4抗体血清水平以及神经复发的次数和特征。
尽管接受了β-1a干扰素治疗,但在10个月内仍复发3次,之后确诊为AQP4抗体阳性NMO,并将治疗改为泼尼松龙和甲氨蝶呤。在使用β-干扰素治疗期间,AQP4抗体滴度急剧上升,而在改用常规免疫抑制治疗后则下降;该患者在随后几年中一直未复发。
尽管之前的文章表明β-干扰素可能会增加NMO的复发率,但本文首次阐明了这种治疗与AQP4抗体增加有关。