Venkatesan Arun, Adatia Krishma
Johns Hopkins Encephalitis Center, Division of Neuroimmunology and Neuroinfectious Diseases, Department of Neurology, Johns Hopkins University School of Medicine , Baltimore, Maryland 21287, United States.
ACS Chem Neurosci. 2017 Dec 20;8(12):2586-2595. doi: 10.1021/acschemneuro.7b00319. Epub 2017 Nov 7.
NMDAR encephalitis is a common cause of autoimmune encephalitis, predominantly affecting young adults. Current data supports the idea that autoantibodies targeting NMDARs are responsible for disease pathogenesis. While these autoantibodies occur in the setting of underlying malignancy in approximately half of all patients, initiating factors for the autoimmune response in the remainder of patients are unclear. While there is increasing evidence supporting viral triggers such as herpes simplex encephalitis, this association and the mechanism of action have not yet been fully described. Although the majority of patients achieve good outcomes, those without an underlying tumor consistently show worse outcomes, prolonged recovery, and more frequent relapses. The cloning of patient-specific autoantibodies from affected individuals has raised important questions as to disease pathophysiology and clinical heterogeneity. Further advances in our understanding of this disease and underlying triggers are necessary to develop treatments which improve outcomes in patients presenting in the absence of tumors.
N-甲基-D-天冬氨酸受体(NMDAR)脑炎是自身免疫性脑炎的常见病因,主要影响年轻成年人。目前的数据支持这样一种观点,即靶向NMDAR的自身抗体是疾病发病机制的原因。虽然这些自身抗体在大约一半的患者中出现在潜在恶性肿瘤的背景下,但其余患者自身免疫反应的起始因素尚不清楚。虽然越来越多的证据支持病毒触发因素,如单纯疱疹性脑炎,但这种关联和作用机制尚未完全阐明。尽管大多数患者预后良好,但那些没有潜在肿瘤的患者始终表现出更差的预后、恢复时间延长和复发更频繁。从受影响个体中克隆患者特异性自身抗体引发了关于疾病病理生理学和临床异质性方面的重要问题。为了开发能够改善无肿瘤患者预后的治疗方法,有必要进一步深入了解这种疾病及其潜在触发因素。