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自身免疫性神经病中的抗体:检测什么、如何检测以及为何检测。

Antibodies in Autoimmune Neuropathies: What to Test, How to Test, Why to Test.

作者信息

Pascual-Goñi Elba, Caballero-Ávila Marta, Querol Luis

机构信息

From the Neuromuscular Diseases Unit (E.P.-G., M.C.-Á., L.Q.), Department of Neurology, Hospital de la Santa Creu i Sant Pau, Universitat Autònoma de Barcelona; ERN (European Reference Network) EURO-NMD (Neuromuscular Disorders); and Centro para la Investigación Biomédica en Red en Enfermedades Raras (CIBERER) (E.P.-G., L.Q.), Madrid, Spain.

出版信息

Neurology. 2024 Aug 27;103(4):e209725. doi: 10.1212/WNL.0000000000209725. Epub 2024 Aug 1.

Abstract

Autoimmune neuropathies are a heterogeneous group of immune-mediated disorders of the peripheral nerves. Guillain-Barré syndrome (GBS) and chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) are the archetypal acute and chronic forms. Over the past few decades, pathogenic antibodies targeting antigens of the peripheral nervous system and driving peripheral nerve damage in selected patients have been described. Moreover, the detection of these antibodies has diagnostic and therapeutic implications that have prompted a modification of the GBS and CIDP diagnostic algorithms. GBS diagnosis is based in clinical criteria, and systematic testing of anti-ganglioside antibodies is not required. Nonetheless, a positive anti-ganglioside antibody test may support the clinical suspicion when diagnosis of GBS (GM1 IgG), Miller Fisher (GQ1b IgG), or acute sensory-ataxic (GD1b IgG) syndromes is uncertain. Anti-myelin-associated glycoprotein (MAG) IgM and anti-disialosyl IgM antibodies are key in the diagnosis of anti-MAG neuropathy and chronic ataxic neuropathy, ophthalmoplegia, M-protein, cold agglutinins, and disialosyl antibodies spectrum neuropathies, respectively, and help differentiating these conditions from CIDP. Recently, the field has been boosted by the discovery of pathogenic antibodies targeting proteins of the node of Ranvier contactin-1, contactin-associated protein 1, and nodal and paranodal isoforms of neurofascin (NF140, NF186, or NF155). These antibodies define subgroups of patients with specific clinical (most importantly poor or partial response to conventional therapies and excellent response to anti-CD20 therapy) and pathologic (node of Ranvier disruption in the absence of inflammation) features that led to the definition of the "autoimmune nodopathy" diagnostic category and to the incorporation of nodal/paranodal antibodies to clinical routine testing. The purpose of this review was to provide a practical vision for the general neurologist of the use of antibodies in the clinical assessment of autoimmune neuropathies.

摘要

自身免疫性神经病是一组由免疫介导的外周神经异质性疾病。吉兰 - 巴雷综合征(GBS)和慢性炎症性脱髓鞘性多发性神经根神经病(CIDP)分别是典型的急性和慢性形式。在过去几十年中,已经描述了针对外周神经系统抗原并在特定患者中导致外周神经损伤的致病性抗体。此外,这些抗体的检测具有诊断和治疗意义,促使对GBS和CIDP诊断算法进行修改。GBS的诊断基于临床标准,不需要系统检测抗神经节苷脂抗体。尽管如此,当GBS(GM1 IgG)、米勒 - 费希尔综合征(GQ1b IgG)或急性感觉性共济失调(GD1b IgG)综合征的诊断不确定时,抗神经节苷脂抗体检测呈阳性可能支持临床怀疑。抗髓鞘相关糖蛋白(MAG)IgM和抗二唾液酸IgM抗体分别是抗MAG神经病和慢性共济失调性神经病、眼肌麻痹、M蛋白、冷凝集素和二唾液酸抗体谱神经病诊断的关键,有助于将这些疾病与CIDP区分开来。最近,针对郎飞结接触蛋白 - 1、接触蛋白相关蛋白1以及神经束蛋白的节点和旁节点异构体(NF140、NF186或NF155)的致病性抗体的发现推动了该领域的发展。这些抗体定义了具有特定临床(最重要的是对传统疗法反应不佳或部分反应以及对抗CD20疗法反应良好)和病理(无炎症时郎飞结破坏)特征的患者亚组,这导致了“自身免疫性结节病”诊断类别的定义,并将节点/旁节点抗体纳入临床常规检测。本综述的目的是为普通神经科医生提供关于抗体在自身免疫性神经病临床评估中应用的实用观点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6d5/11319070/c81d170a8470/WNL-2024-100982f1.jpg

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