| Literature DB >> 27743643 |
Simone Gross1, Andrea Fischer2, Marco Rosati1, Lara Matiasek3, Daniele Corlazzoli4, Rodolfo Cappello5, Laura Porcarelli4, Tom Harcourt-Brown6, Konrad Jurina2, Laurent Garosi7, Thomas Flegel8, Pia Quitt2, Jessica Molin1, Velia-Isabel Huelsmeyer2, Henning Schenk9, Gualtiero Gandini10, Kirsten Gnirs11, Stéphane Blot12, Aurélien Jeandel12, Massimo Baroni13, Shenja Loderstedt14, Gianluca Abbiati15, Carola Leithaeuser16, Sabine Schulze17, Marion Kornberg18, Mark Lowrie19, Kaspar Matiasek20.
Abstract
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.Entities:
Keywords: Canine; Coonhound paralysis; Feline; Immune-mediated; Peripheral nerve; Polyneuritis; Polyradiculoneuritis; Subtype; Teasing
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Year: 2016 PMID: 27743643 DOI: 10.1016/j.nmd.2016.08.015
Source DB: PubMed Journal: Neuromuscul Disord ISSN: 0960-8966 Impact factor: 4.296