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血浆置换对水通道蛋白4抗体阳性视神经脊髓炎患者的治疗效果

Therapeutic efficacy of plasma exchange in NMO-IgG-positive patients with neuromyelitis optica.

作者信息

Watanabe S, Nakashima I, Misu T, Miyazawa I, Shiga Y, Fujihara K, Itoyama Y

机构信息

Department of Neurology, Tohoku University School of Medicine, 1-1 Seiryomachi, Aobaku, Sendai 980-8574, Japan.

出版信息

Mult Scler. 2007 Jan;13(1):128-32. doi: 10.1177/1352458506071174.

Abstract

Neuromyelitis optica (NMO) is an inflammatory demyelinating disease of the central nervous system (CNS) with a poor prognosis in terms of the optic-spinal function. Recently, a serum autoantibody (NMO-IgG) binding to the blood-brain barrier region was detected exclusively in patients with NMO and its high risk group. We treated six NMO-IgG-positive patients (all female; age 21-67 years old, median 41; three with optic neuritis and three with myelitis) who were unresponsive to high-dose intravenous methylprednisolone (HIMP), with plasma exchange (PE) (three to five exchanges, 2-3 L each). Three of the patients (one with optic neuritis and two with myelitis) showed definite functional improvement following PE. The clinical improvement started to appear after one or two exchanges, while there was little or no improvement in the other three patients. Such quick clinical responses to PE suggest a pathogenetic role of humoral immune factors in NMO, although delayed responses to the corticosteroid therapy might have contributed to the therapeutic efficacy, in part. Further clinical and in vitro studies are needed to determine whether the removal of NMO-IgG is directly relevant to the therapeutic efficacy. PE may hasten the functional recovery from corticosteroid-resistant relapses in some NMO-IgG-positive patients with NMO.

摘要

视神经脊髓炎(NMO)是一种中枢神经系统(CNS)的炎性脱髓鞘疾病,就视神经脊髓功能而言预后较差。最近,在NMO患者及其高危人群中专门检测到一种与血脑屏障区域结合的血清自身抗体(NMO-IgG)。我们对6例对大剂量静脉注射甲基强的松龙(HIMP)无反应的NMO-IgG阳性患者(均为女性;年龄21-67岁,中位数41岁;3例患有视神经炎,3例患有脊髓炎)进行了血浆置换(PE)(3至5次置换,每次2-3升)治疗。其中3例患者(1例视神经炎和2例脊髓炎)在PE后显示出明确的功能改善。临床改善在1次或2次置换后开始出现,而其他3例患者几乎没有改善。对PE如此快速的临床反应表明体液免疫因素在NMO发病机制中起作用,尽管对皮质类固醇治疗的延迟反应可能在一定程度上促成了治疗效果。需要进一步的临床和体外研究来确定去除NMO-IgG是否与治疗效果直接相关。PE可能会加速一些NMO-IgG阳性的NMO患者从皮质类固醇抵抗性复发中的功能恢复。

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