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Therapeutic efficacy of plasma exchange in NMO-IgG-positive patients with neuromyelitis optica
被引:191
作者:

Watanabe, S.
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Tohoku Univ, Sch Med, Dept Neurol, Sendai, Miyagi 9808574, Japan Tohoku Univ, Sch Med, Dept Neurol, Sendai, Miyagi 9808574, Japan

Nakashima, I.
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Tohoku Univ, Sch Med, Dept Neurol, Sendai, Miyagi 9808574, Japan Tohoku Univ, Sch Med, Dept Neurol, Sendai, Miyagi 9808574, Japan

Misu, T.
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Tohoku Univ, Sch Med, Dept Neurol, Sendai, Miyagi 9808574, Japan Tohoku Univ, Sch Med, Dept Neurol, Sendai, Miyagi 9808574, Japan

Miyazawo, I.
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Tohoku Univ, Sch Med, Dept Neurol, Sendai, Miyagi 9808574, Japan Tohoku Univ, Sch Med, Dept Neurol, Sendai, Miyagi 9808574, Japan

Shiga, Y.
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Tohoku Univ, Sch Med, Dept Neurol, Sendai, Miyagi 9808574, Japan Tohoku Univ, Sch Med, Dept Neurol, Sendai, Miyagi 9808574, Japan

Fujihara, K.
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机构:
Tohoku Univ, Sch Med, Dept Neurol, Sendai, Miyagi 9808574, Japan Tohoku Univ, Sch Med, Dept Neurol, Sendai, Miyagi 9808574, Japan

Itoyama, Y.
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Tohoku Univ, Sch Med, Dept Neurol, Sendai, Miyagi 9808574, Japan Tohoku Univ, Sch Med, Dept Neurol, Sendai, Miyagi 9808574, Japan
机构:
[1] Tohoku Univ, Sch Med, Dept Neurol, Sendai, Miyagi 9808574, Japan
关键词:
aquaporin-4;
Devic's disease;
neuromyelitis optica;
NMO-IgG;
plasma exchange;
therapy;
D O I:
10.1177/1352458506071174
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
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.
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页码:128 / 132
页数:5
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