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Autoantibody screening in Guillain-Barre syndrome.


ABSTRACT:

Background

Guillain-Barré syndrome (GBS) is an acute inflammatory neuropathy with a heterogeneous presentation. Although some evidences support the role of autoantibodies in its pathogenesis, the target antigens remain unknown in a substantial proportion of GBS patients. The objective of this study is to screen for autoantibodies targeting peripheral nerve components in Guillain-Barré syndrome.

Methods

Autoantibody screening was performed in serum samples from all GBS patients included in the International GBS Outcome study by 11 different Spanish centres. The screening included testing for anti-ganglioside antibodies, anti-nodo/paranodal antibodies, immunocytochemistry on neuroblastoma-derived human motor neurons and murine dorsal root ganglia (DRG) neurons, and immunohistochemistry on monkey peripheral nerve sections. We analysed the staining patterns of patients and controls. The prognostic value of anti-ganglioside antibodies was also analysed.

Results

None of the GBS patients (n = 100) reacted against the nodo/paranodal proteins tested, and 61 (61%) were positive for, at least, one anti-ganglioside antibody. GBS sera reacted strongly against DRG neurons more frequently than controls both with IgG (6% vs 0%; p = 0.03) and IgM (11% vs 2.2%; p = 0.02) immunodetection. No differences were observed in the proportion of patients reacting against neuroblastoma-derived human motor neurons. Reactivity against monkey nerve tissue was frequently detected both in patients and controls, but specific patterns were only detected in GBS patients: IgG from 13 (13%) patients reacted strongly against Schwann cells. Finally, we confirmed that IgG anti-GM1 antibodies are associated with poorer outcomes independently of other known prognostic factors.

Conclusion

Our study confirms that (1) GBS patients display a heterogeneous repertoire of autoantibodies targeting nerve cells and structures; (2) gangliosides are the most frequent antigens in GBS patients and have a prognostic value; (3) further antigen-discovery experiments may elucidate other potential antigens in GBS.

SUBMITTER: Lleixa C 

PROVIDER: S-EPMC8559393 | biostudies-literature | 2021 Nov

REPOSITORIES: biostudies-literature

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Autoantibody screening in Guillain-Barré syndrome.

Lleixà Cinta C   Martín-Aguilar Lorena L   Pascual-Goñi Elba E   Franco Teresa T   Caballero Marta M   de Luna Noemí N   Gallardo Eduard E   Suárez-Calvet Xavier X   Martínez-Martínez Laura L   Diaz-Manera Jordi J   Rojas-García Ricard R   Cortés-Vicente Elena E   Turón Joana J   Casasnovas Carlos C   Homedes Christian C   Gutiérrez-Gutiérrez Gerardo G   Jimeno-Montero María Concepción MC   Berciano José J   Sedano-Tous Maria José MJ   García-Sobrino Tania T   Pardo-Fernández Julio J   Márquez-Infante Celedonio C   Rojas-Marcos Iñigo I   Jericó-Pascual Ivonne I   Martínez-Hernández Eugenia E   Morís de la Tassa Germán G   Domínguez-González Cristina C   Juárez Cándido C   Illa Isabel I   Querol Luis L  

Journal of neuroinflammation 20211101 1


<h4>Background</h4>Guillain-Barré syndrome (GBS) is an acute inflammatory neuropathy with a heterogeneous presentation. Although some evidences support the role of autoantibodies in its pathogenesis, the target antigens remain unknown in a substantial proportion of GBS patients. The objective of this study is to screen for autoantibodies targeting peripheral nerve components in Guillain-Barré syndrome.<h4>Methods</h4>Autoantibody screening was performed in serum samples from all GBS patients inc  ...[more]

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