Koski Carol Lee
GBS/CIDP Foundation International, 104 ½ Forrest Avenue, Narberth, PA, 19072, USA,
J Clin Immunol. 2014 Jul;34 Suppl 1:S127-31. doi: 10.1007/s10875-014-0016-5. Epub 2014 Apr 5.
Multifocal motor neuropathy (MMN) is a rare inflammatory, chronically progressive, unremitting disorder affecting the peripheral nervous system. Although the etiology of this condition is not known, high titers of IgM Ab to GM1 may serve as a biomarker for this disease. Clinical findings of motor weakness are associated with focal conduction blocks and with time, axonal destruction. Evidence supporting an immune etiology as well as the use of intravenous immunoglobulin to limit the disease progression is reviewed.
多灶性运动神经病(MMN)是一种罕见的、影响周围神经系统的炎症性、慢性进行性、持续性疾病。尽管这种疾病的病因尚不清楚,但高滴度的抗GM1 IgM抗体可作为该疾病的生物标志物。运动无力的临床发现与局灶性传导阻滞有关,随着时间推移还与轴索破坏有关。本文综述了支持免疫病因以及使用静脉注射免疫球蛋白来限制疾病进展的证据。