Autoantibody screening in Guillain-Barré Syndrome

Author:

Lleixà Cinta,Martín-Aguilar Lorena,Pascual-Goñi Elba,Franco Teresa,Caballero Marta,Diaz-Manera Jordi,Rojas-García RicardORCID,de Luna Noemí,Gallardo Eduard,Cortés-Vicente Elena,Turón Joana,Suárez-Calvet XavierORCID,Casasnovas Carlos,Homedes Christian,Gutiérrez-Gutiérrez GerardoORCID,Jimeno-Montero María Concepción,Berciano José,Sedano Tous Maria José,Garcia-Sobrino Tania,Pardo-Fernandez Julio,Márquez-Infante Celedonio,Rojas-Marcos IñigoORCID,Jericó-Pascual Ivonne,Martínez-Hernández Eugenia,Morís de la Tassa GermánORCID,Domínguez-González CristinaORCID,Martínez-Martínez Laura,Juárez Cándido,Illa Isabel,Querol LuisORCID

Abstract

AbstractGuillain-Barré Syndrome (GBS) is an acute inflammatory neuropathy with a heterogeneous presentation and pathogenesis. Serum antibodies against various gangliosides can be found in less than half of all patients in the acute phase of GBS but the target antigens remain unknown for the remaining half. Our work describes a comprehensive screening for serum autoantibodies targeting peripheral nerve tissue, cells, and purified antigens in a prospective GBS cohort including 100 patients. Our study confirms that (1) GBS patients display a very heterogeneous repertoire of autoantibodies targeting nerve cells and structures, (2) gangliosides are the most frequent antigens in GBS patients and have prognostic value, (3) a small subset of patients display antibodies targeting the myelin sheath, and (4) further antigen-discovery experiments are needed to elucidate other potential disease-specific autoantibodies in GBS.

Publisher

Cold Spring Harbor Laboratory

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