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自身抗体介导的中枢神经系统疾病

Autoantibody-mediated disorders of the central nervous system.

作者信息

Irani Sarosh, Lang Bethan

机构信息

Neurosciences Group, Department of Clinical Neurology, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, Headington, Oxford, UK.

出版信息

Autoimmunity. 2008 Feb;41(1):55-65. doi: 10.1080/08916930701619490.

Abstract

Autoimmunity has been demonstrated in a diverse range of peripheral neurological disorders, such as myasthenia gravis and acquired neuromyotonia. Serum antibodies found in these conditions are directed against ion channels and receptors situated on the cell surface and have been shown to produce pathogenic effects. The symptoms of these peripheral disorders have been transferred to animals by passive or active immunisation and, in humans, treated successfully with immunomodulatory therapy. Recently, a number of central nervous system disorders (CNS), such as limbic encephalitis, certain forms of epilepsy, neuromyelitis optica and cerebellar ataxia, have been hypothesised to associate with specific serum autoantibodies. In this article we consider this rapidly expanding field of CNS disorders, discuss evidence for their proposed autoimmune aetiology and review whether the antibodies detected have been shown to be pathogenic or if they are secondary to preceding neuronal damage.

摘要

自身免疫已在多种周围神经系统疾病中得到证实,如重症肌无力和获得性神经性肌强直。在这些疾病中发现的血清抗体针对位于细胞表面的离子通道和受体,并已显示出致病作用。这些周围神经系统疾病的症状已通过被动或主动免疫转移到动物身上,并且在人类中通过免疫调节疗法成功治疗。最近,一些中枢神经系统疾病(CNS),如边缘性脑炎、某些形式的癫痫、视神经脊髓炎和小脑共济失调,被认为与特定的血清自身抗体有关。在本文中,我们将探讨这个迅速扩展的中枢神经系统疾病领域,讨论其提出的自身免疫病因的证据,并回顾所检测到的抗体是否已被证明具有致病性,或者它们是否继发于先前的神经元损伤。

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