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An immunoassay that distinguishes realneuromyelitis optica signals from a labelingdetected in patients receiving natalizumab

dc.contributor.authorSanchez-Gomar, Ismael
dc.contributor.authorDiaz Sanchez, Maria
dc.contributor.authorUcles Sanchez, Antonio Jose
dc.contributor.authorCasado Chocan, Jose Luis
dc.contributor.authorRamirez-Lorca, Reposo
dc.contributor.authorSerna, Ana
dc.contributor.authorVilladiego, Javier
dc.contributor.authorToledo-Arahal, Juan Jose
dc.contributor.authorEchevarria, Miriam
dc.date.accessioned2025-01-22T08:46:12Z
dc.date.available2025-01-22T08:46:12Z
dc.date.issued2014-07-01
dc.identifier.citationSánchez Gomar, I., Díaz Sánchez, M., Uclés Sánchez, A.J. et al. An immunoassay that distinguishes real neuromyelitis optica signals from a labeling detected in patients receiving natalizumab. BMC Neurol 14, 139 (2014). https://doi.org/10.1186/1471-2377-14-139es
dc.identifier.issn1471-2377
dc.identifier.urihttps://hdl.handle.net/20.500.12412/6371
dc.description.abstractThis study aimed to develop a sensitive quantitative method for detecting anti-aquaporin 4 (AQP4) antibodies to improve neuromyelitis optica (NMO) diagnosis and distinguish false positives caused by natalizumab treatment. Using sera from 167 individuals, including NMO patients and various controls, an immunofluorescence assay on HEK cells transfected with the M23 isoform of human AQP4 was performed. Results showed that NMO patients' sera were 100% positive for anti-AQP4 antibodies, while other sera were negative. The assay significantly increased signal specificity and reduced false diagnoses, especially in natalizumab-treated patients, with frozen pretreated cells allowing faster detection.es
dc.language.isoenges
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titleAn immunoassay that distinguishes realneuromyelitis optica signals from a labelingdetected in patients receiving natalizumabes
dc.typearticlees
dc.identifier.doi10.1186/1471-2377-14-139
dc.issue.number139es
dc.journal.titleBMC Neurologyes
dc.page.initial1es
dc.page.final11es
dc.rights.accessRightsopenAccesses
dc.subject.keywordImmunohistochemistryes
dc.subject.keywordNatalizumabes
dc.subject.keywordAQP4-EGFPes
dc.subject.keywordNMO.IgGes
dc.subject.keywordHEK cellses
dc.volume.number14es


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
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