Giannoccaro Maria Pia, Verde Federico, Morelli Luana, Rizzo Giovanni, Ricciardiello Fortuna, Liguori Rocco
IRCCS Istituto delle Scienze Neurologiche di Bologna, 40139 Bologna, Italy.
Dipartimento di Scienze Biomediche e Neuromotorie, Università di Bologna, 40126 Bologna, Italy.
Biomedicines. 2023 Feb 22;11(3):666. doi: 10.3390/biomedicines11030666.
Autoimmune encephalitis and neurodegenerative disorders share several clinical features, including behavioural and psychiatric manifestations, cognitive impairment, sleep and movement disorders. Therefore, it is not surprising that autoimmune encephalitis is one of the main differential diagnoses of rapidly progressive dementia. However, more chronic presentations of autoimmune disorders have been reported and can lead to the misdiagnosis of a neurodegenerative disease. On the other hand, antibodies against neuronal proteins, such as those directed against NMDAR, can occur during established neurogenerative disorders, and their role in this context is still unclear. They might be simple bystanders or modify the disease course and phenotype. Indeed, autoimmune encephalitis can leave long-term cognitive sequelae and specific antibodies to neuronal surface antigens are associated with clinical and pathological neurodegenerative features. Here we review the link between these antibodies and neurodegeneration. In particular we discuss: (a) the possibility that autoimmune encephalitis presents as a neurodegenerative disease, identifying the red flags that can help in the differential diagnosis between antibody-mediated and neurodegenerative disorders; (b) the occurrence of antibodies against neuronal surface antigens in patients with neurodegenerative disorders and their possible role in the disease course; and (c) the long-term cognitive and neuroradiological changes associated with autoimmune encephalitis, as well as the biomarkers that can help to predict the cognitive outcome. Finally, we review the clinical and pathological features of IgLON5 antibodies-related encephalitis, a unique model of the relationship between antibodies and neurodegeneration.
自身免疫性脑炎和神经退行性疾病具有若干共同的临床特征,包括行为和精神表现、认知障碍、睡眠和运动障碍。因此,自身免疫性脑炎是快速进展性痴呆的主要鉴别诊断之一也就不足为奇了。然而,已有报道称自身免疫性疾病存在更慢性的表现,可能导致神经退行性疾病的误诊。另一方面,针对神经元蛋白的抗体,如针对NMDAR的抗体,可在已确诊的神经退行性疾病过程中出现,其在这种情况下的作用仍不清楚。它们可能只是旁观者,也可能改变疾病进程和表型。事实上,自身免疫性脑炎可留下长期的认知后遗症,针对神经元表面抗原的特异性抗体与临床和病理神经退行性特征相关。在此,我们综述这些抗体与神经退行性变之间的联系。特别是我们将讨论:(a)自身免疫性脑炎表现为神经退行性疾病的可能性,确定有助于鉴别抗体介导性疾病和神经退行性疾病的警示信号;(b)神经退行性疾病患者中针对神经元表面抗原的抗体的出现及其在疾病进程中的可能作用;(c)与自身免疫性脑炎相关的长期认知和神经放射学改变,以及有助于预测认知结果的生物标志物。最后,我们综述与IgLON5抗体相关脑炎的临床和病理特征,这是抗体与神经退行性变关系的一个独特模型。