Nuffield Department of Clinical Neurosciences, Level 6, West Wing, John Radcliffe Hospital, Headley Way, Oxford OX39DS, UK.
Curr Neurol Neurosci Rep. 2011 Jun;11(3):298-304. doi: 10.1007/s11910-011-0186-y.
N-methyl-D-aspartate receptor (NMDAR) antibody encephalitis is a recently described immunotherapy-responsive panencephalitis with characteristic features that include a psychiatric onset and a later movement disorder. This entity was first described as a paraneoplastic phenomenon in young women with ovarian teratomata. However, more recently it has become clear that the majority of patients, particularly children, do not harbor a tumor and that males can also be affected. With the development of the NMDAR antibody assay, now available worldwide, a few patients with classical limbic encephalitis and early psychosis and epilepsy have also been found to harbor these antibodies. Early diagnosis followed by immunotherapies and tumor removal, when relevant, expedite recovery from the condition. Antibody levels correlate with the clinical severity of the disease in individual patients, and the antibodies have been shown to substantially reduce NMDA receptors on hippocampal neurons both in vitro and in vivo, supporting the likely direct pathogenicity of the NMDAR antibodies.
N-甲基-D-天冬氨酸受体(NMDAR)抗体脑炎是一种新近描述的免疫治疗反应性全脑炎,具有特征性表现,包括精神发病和后期运动障碍。该病症最初被描述为年轻女性伴卵巢畸胎瘤的副肿瘤现象。然而,最近越来越清楚的是,大多数患者,尤其是儿童,没有肿瘤,男性也可能受到影响。随着 NMDAR 抗体检测的发展,现已在全球范围内可用,一些具有经典边缘性脑炎和早期精神病和癫痫的患者也被发现携带这些抗体。早期诊断后进行免疫治疗和肿瘤切除(如有)可加快病情恢复。抗体水平与个体患者疾病的临床严重程度相关,并且抗体已被证明在体外和体内大量减少海马神经元上的 NMDA 受体,支持 NMDAR 抗体的可能直接致病性。