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原发性自身免疫性神经病不断变化的格局。

The changing landscape of primary autoimmune neuropathies.

作者信息

Caballero-Ávila Marta, Pascual-Goñi Elba, Lleixà Cinta, Martín-Aguilar Lorena, Collet-Vidiella Roger, Querol Luis

机构信息

Neuromuscular Diseases Unit, Department of Neurology, Hospital de la Santa Creu i Sant Pau (IR SANT PAU), Universitat Autònoma de Barcelona, Barcelona, Spain.

Centro para la Investigación Biomédica en Red en Enfermedades Raras (CIBERER), Madrid, Spain.

出版信息

Nat Rev Neurol. 2025 Sep 5. doi: 10.1038/s41582-025-01133-3.

Abstract

Autoimmune neuropathies, such as Guillain-Barré syndrome (GBS) and chronic inflammatory demyelinating polyradiculoneuropathy (CIDP), are rare, disabling disorders. Diagnosis, follow-up and treatment of autoimmune neuropathies rely almost exclusively on clinical parameters, and the available therapies, such as intravenous immunoglobulins and corticosteroids, date from >30 years ago. The lack of therapeutic progress in autoimmune neuropathies has resulted from a combination of limited understanding of their pathophysiology, disease heterogeneity and challenges in trial design. However, advances in the past 5 years are set to change the rate of progress. The discovery of pathogenic autoantibodies that target cell-adhesion molecules at the node of Ranvier, thereby defining the new diagnostic category of autoimmune nodopathies, has provided a new perspective on disease pathophysiology. In addition, better definitions of the diagnostic criteria for GBS and CIDP, FDA approval of efgartigimod for the treatment of CIDP, promising results in trials of complement inhibitors in CIDP, GBS and multifocal motor neuropathy and the identification of biomarkers with the potential to optimize prognostication and monitoring are moving us towards targeted and precise therapeutic approaches to improve outcomes of autoimmune neuropathies. In this Review, we summarize the latest developments in autoimmune neuropathies, including discoveries in disease mechanisms, the implications of new diagnostic guidelines, identification of new biomarkers and the status of the most promising clinical trials.

摘要

自身免疫性神经病,如吉兰-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),是罕见的致残性疾病。自身免疫性神经病的诊断、随访和治疗几乎完全依赖于临床参数,而现有的治疗方法,如静脉注射免疫球蛋白和皮质类固醇,可追溯到30多年前。自身免疫性神经病治疗进展的缺乏是由于对其病理生理学的理解有限、疾病异质性以及试验设计中的挑战共同导致的。然而,过去5年的进展有望改变进展速度。针对郎飞结处细胞粘附分子的致病性自身抗体的发现,从而定义了自身免疫性结节病这一新的诊断类别,为疾病病理生理学提供了新的视角。此外,对GBS和CIDP诊断标准的更好定义、FDA批准依加西莫德用于治疗CIDP、CIDP、GBS和多灶性运动神经病补体抑制剂试验的 promising 结果以及具有优化预后和监测潜力的生物标志物的鉴定,正推动我们朝着有针对性和精确的治疗方法发展,以改善自身免疫性神经病的预后。在本综述中,我们总结了自身免疫性神经病的最新进展,包括疾病机制的发现、新诊断指南的影响、新生物标志物的鉴定以及最有前景的临床试验的现状。

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