Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/34608
Title: Anti-aquaporin-4 antibodies in the context of assorted immune-mediated diseases
Authors: Dellavance, A.
Alvarenga, R. R. [UNIFESP]
Rodrigues, S. H. [UNIFESP]
Kok, F.
Souza, A. W. S. de [UNIFESP]
Andrade, L. E. C. [UNIFESP]
Universidade Federal de São Paulo (UNIFESP)
Fleury Grp
Universidade de São Paulo (USP)
Keywords: AQP4 antibody
aquaporin-4
myasthenia gravis
neuromyelitis Optica
NMO-IgG
Sjogren's syndrome
systemic lupus erythematosus
Issue Date: 1-Feb-2012
Publisher: Wiley-Blackwell
Citation: European Journal of Neurology. Malden: Wiley-Blackwell, v. 19, n. 2, p. 248-252, 2012.
Abstract: Background and purposes: Anti-aquaporin 4 antibodies are specific markers for Devics disease. This study aimed to test if this high specificity holds in the context of a large spectrum of systemic autoimmune and non-autoimmune diseases.Methods: Anti-aquaporin-4 antibodies (NMO-IgG) were determined by indirect immunofluorescence (IIF) on mouse cerebellum in 673 samples, as follows: group I (clinically defined Devic's disease, n = 47); group II [ inflammatory/demyelinating central nervous system (CNS) diseases, n = 41]; group III (systemic and organ-specific autoimmune diseases, n = 250); group IV (chronic or acute viral diseases, n = 35); and group V (randomly selected samples from a general clinical laboratory, n = 300).Results: MNO-IgG was present in 40/47 patients with classic Devic's disease (85.1% sensitivity) and in 13/22 (59.1%) patients with disorders related to Devic's disease. the latter 13 positive samples had diagnosis of longitudinally extensive transverse myelitis (n = 10) and isolated idiopathic optic neuritis (n = 3). One patient with multiple sclerosis and none of the remaining 602 samples with autoimmune and miscellaneous diseases presented NMO-IgG (99.8% specificity). the autoimmune disease subset included five systemic lupus erythematosus individuals with isolated or combined optic neuritis and myelitis and four primary Sjogren's syndrome (SS) patients with cranial/peripheral neuropathy.Conclusions: the available data clearly point to the high specificity of anti-aquaporin-4 antibodies for Devic's disease and related syndromes also in the context of miscellaneous non-neurologic autoimmune and non-autoimmune disorders.
URI: http://repositorio.unifesp.br/handle/11600/34608
ISSN: 1351-5101
Other Identifiers: http://dx.doi.org/10.1111/j.1468-1331.2011.03479.x
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