Gross Simone, Fischer Andrea, Rosati Marco, Matiasek Lara, Corlazzoli Daniele, Cappello Rodolfo, Porcarelli Laura, Harcourt-Brown Tom, Jurina Konrad, Garosi Laurent, Flegel Thomas, Quitt Pia, Molin Jessica, Huelsmeyer Velia-Isabel, Schenk Henning, Gandini Gualtiero, Gnirs Kirsten, Blot Stéphane, Jeandel Aurélien, Baroni Massimo, Loderstedt Shenja, Abbiati Gianluca, Leithaeuser Carola, Schulze Sabine, Kornberg Marion, Lowrie Mark, Matiasek Kaspar
Section of Clinical & Comparative Neuropathology, Centre for Clinical Veterinary Medicine, Ludwig-Maximilians-Universität München, Munich, Germany.
Section of Neurology, Clinic of Small Animal Medicine, Centre for Clinical Veterinary Medicine, Ludwig-Maximilians-Universität, München, Munich, Germany.
Neuromuscul Disord. 2016 Dec;26(12):825-836. doi: 10.1016/j.nmd.2016.08.015. Epub 2016 Sep 1.
Recent views on Guillain-Barré syndrome (GBS) question the accuracy of classification into axonal and demyelinating subtypes that represent convergent neurophysiological phenotypes rather than immunological targets. Instead it has been proposed to clarify the primarily affected fibre subunit in nerve biopsies. As nerve biopsies rarely are part of routine work-up in human patients we evaluated tissues taken from companion animals affected by GBS-like polyradiculoneuropathy to screen for distribution of immune cells, targeted fibre components and segregating non-inflammatory lesions. We identified that immune responses were directed either at Schmidt-Lanterman clefts, the paranode-node complex or both. Based on infiltrative and non-inflammatory changes, four subtypes and/or stages were distinguished, some of which indicate localisation of primary target antigens while others represent convergent late stage pictures, as a consequence to epitope spreading. The impact of histological subtyping onto clinical management and prognosis remains to be evaluated in future clinical trials. Natural development and clinical manifestation of large animal dysimmune neuropathy may reflect human Guillain-Barré syndrome more accurately than experimental models and therefore provide complementary clues for translational research.
近期关于吉兰-巴雷综合征(GBS)的观点对将其分类为轴索性和脱髓鞘性亚型的准确性提出了质疑,因为这两种亚型代表的是趋同的神经生理学表型,而非免疫靶点。相反,有人提议在神经活检中明确主要受影响的纤维亚单位。由于神经活检很少作为人类患者常规检查的一部分,我们评估了从患有类GBS多神经根神经病的伴侣动物身上获取的组织,以筛查免疫细胞的分布、靶向纤维成分和分离出的非炎症性病变。我们发现免疫反应要么针对施密特-兰特尔曼切迹、结旁-结复合体,要么针对两者。基于浸润性和非炎症性变化,区分出了四种亚型和/或阶段,其中一些表明主要靶抗原的定位,而另一些则代表由于表位扩展导致的趋同晚期图像。组织学亚型对临床管理和预后的影响仍有待未来临床试验进行评估。大型动物免疫性神经病的自然发展和临床表现可能比实验模型更准确地反映人类吉兰-巴雷综合征,因此为转化研究提供了补充线索。