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dc.contributor.authorFreire Dapena, Maria del Carmen 
dc.contributor.authorAndrade Piña, Ariadna Helena
dc.contributor.authorSopeña Perez-Argüelles, Bernardo
dc.contributor.authorLópez Rodríguez, María 
dc.contributor.authorVarela García, Pablo Manuel 
dc.contributor.authorCacabelos Pérez, Purificación
dc.contributor.authorEsteban Cartelle, Helena 
dc.contributor.authorGonzález Quintela, Arturo 
dc.date.accessioned2026-01-23T13:49:57Z
dc.date.available2026-01-23T13:49:57Z
dc.date.issued2021-08
dc.identifier.urihttp://hdl.handle.net/20.500.11940/22482
dc.description.abstractThe disease caused by the coronavirus SARS-CoV-2 (COVID-19), which emerged in China in December 2019, has become a global pandemic in just a few months. The concomitant presentation of COVID-19 and some autoimmune diseases has also been reported, among which is Guillain Barr´e Syndrome (GBS). GBS is considered an immune mediated neuropathy preceded 1 to 6 weeks in 70% of cases by a bac terial or a viral infection. In many cases associated with Campylobacter jejuni (the predominant pathogen) the presence of antiganglioside an tibodies is observed. This supports a post-infectious mechanism, with molecular mimicry and antibody cross-response. However, in GBS associated with Zika virus infection, an earlier onset is seen, and asso ciated antiganglioside antibodies are rarely present, suggesting a para infectious pathogenetic mechanism. There is contradictory infor mation on whether GB associated with COVID-19 has also characteris tics that may indicate a para-infectious pathogenetic process. To review the accumulated evidence about the pathogenic mechanism of this association, we carried out a review of the literature with a selection of the clinical cases reported until February 1st 2021, adding one owncase. We selected studies reporting adult patients with all: Guillain-Barr´e syndrome, according to diagnostic criteria of the GBS Classification Group [8]; SARS-CoV-2 infection confirmed by nasopharyngeal reverse transcription polymerase chain reaction, antigen-detecting rapid diag nostic tests or serum antibody test; Detailed individual clinical description; A minimum of 6/8 points using the Joanna Briggs Institute Critical Appraisal Checklist for Case Reports and for Case Series studies.es
dc.language.isoenges
dc.subject.meshPandemics *
dc.subject.meshGuillain-Barre Syndrome *
dc.subject.meshSevere Acute Respiratory Syndrome *
dc.subject.meshCoronavirus *
dc.subject.meshSARS-CoV-2 *
dc.subject.meshHumans *
dc.subject.meshCOVID-19 *
dc.subject.meshLiterature *
dc.subject.meshAutoimmunity *
dc.subject.meshMiller Fisher Syndrome *
dc.titleGuillain Barré syndrome associated with COVID-19- lessons learned about its pathogenesis during the first year of the pandemic, a systematic review.es
dc.typeArtigoes
dc.identifier.doi10.1016/j.autrev.2021.102875
dc.identifier.essn1873-0183
dc.identifier.pmid34119673
dc.issue.number8es
dc.journal.titleAutoimmunity reviewses
dc.organizationServizo Galego de Saúde::Áreas Sanitarias (A.S.)::Área Sanitaria de Santiago de Compostela - Complexo Hospitalario Universitario de Santiago de Compostelaes
dc.page.initial102875es
dc.rights.accessRightsopenAccesses
dc.subject.decscoronavirus *
dc.subject.decsautoinmunidad *
dc.subject.decshumanos *
dc.subject.decssíndrome de Guillain-Barre *
dc.subject.decspandemias *
dc.subject.decssíndrome de Miller Fisher *
dc.subject.decssíndrome respiratorio agudo grave *
dc.subject.keywordCHUSes
dc.typefidesArtigo Científico (inclue Orixinal, Orixinal breve, Revisión Sistemática e Meta-análisis)es
dc.typesophosArtículo Originales
dc.volume.number20es


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