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NMDA and AMPA Receptor Autoantibodies in Brain Disorders: From Molecular Mechanisms to Clinical Features

机译:脑病中的NMDA和AMPA受体自身抗体:从分子机制到临床特征

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摘要

The role of autoimmunity in central nervous system (CNS) disorders is rapidly expanding. In the last twenty years, different types of autoantibodies targeting subunits of ionotropic glutamate receptors have been found in a variety of patients affected by brain disorders. Several of these antibodies are directed against NMDA receptors (NMDAR), mostly in autoimmune encephalitis, whereas a growing field of research has identified antibodies against AMPA receptor (AMPAR) subunits in patients with different types of epilepsy or frontotemporal dementia. Several in vitro and in vivo studies performed in the last decade have dramatically improved our understanding of the molecular and functional effects induced by both NMDAR and AMPAR autoantibodies at the excitatory glutamatergic synapse and, consequently, their possible role in the onset of clinical symptoms. In particular, the method by which autoantibodies can modulate the localization at synapses of specific target subunits leading to functional impairments and behavioral alterations has been well addressed in animal studies. Overall, these preclinical studies have opened new avenues for the development of novel pharmacological treatments specifically targeting the synaptic activation of ionotropic glutamate receptors.
机译:自身免疫中的作用在中枢神经系统(CNS)紊乱迅速扩展。在过去的二十年中,已发现各种受脑疾病影响的各种患者的不同类型的自身抗体靶向离子型谷氨酸受体的亚基。这些抗体中的几种针对NMDA受体(NMDAR),主要是在自身免疫性脑炎中,而越来越多的研究领域已经鉴定了不同类型的癫痫或额定痴呆症患者的针对AMPA受体(AMPAR)亚基的抗体。在过去十年中进行了几种体外和体内研究已经大大改善了我们对鼻咽癌和氨分解突触的肿瘤和AMPAR自身抗体诱导的分子和功能作用的理解,因此,它们在临床症状发作中的可能作用。特别地,自身抗体可以调节特定目标亚基突触的定位的方法,该方法导致功能损伤和行为改变在动物研究中已经很好地解决。总的来说,这些临床前研究已经开辟了新型药理学治疗的新途径,具体靶向离子型谷氨酸受体的突触激活。

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