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Detection of Autoantibodies against Aquaporin-1 in the Sera of Patients with Primary Sjögren's Syndrome
Immune Network ; : 103-109, 2017.
Artigo em Inglês | WPRIM | ID: wpr-51911
ABSTRACT
The pathophysiology of glandular dysfunction in Sjögren's syndrome (SS) has not been fully elucidated. Previously, we reported the presence of autoantibodies to AQP-5 in patients with SS, which was associated with a low resting salivary flow. The purpose of this study was to investigate the presence of anti-AQP1 autoantibodies. To detect anti-AQP1 autoantibodies, cell-based indirect immunofluorescence assay was developed using MDCK cells that overexpressed human AQP1. By screening 112 SS and 52 control sera, anti-AQP1 autoantibodies were detected in 27.7% of the SS but in none of the control sera. Interestingly, the sera that were positive for anti-AQP1 autoantibodies also contained anti-AQP5 autoantibodies in the previous study. Different from anti-AQP5 autoantibodies, the presence of anti-AQP1 autoantibodies was not associated with the salivary flow rate. Although anti-AQP1 autoantibodies are not useful as a diagnostic marker, the presence of autoantibodies to AQP1 may be an obstacle to AQP1 gene therapy for SS.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Autoanticorpos / Terapia Genética / Programas de Rastreamento / Imunofluorescência / Técnica Indireta de Fluorescência para Anticorpo / Aquaporina 1 / Células Madin Darby de Rim Canino Tipo de estudo: Estudo diagnóstico / Estudo de rastreamento Limite: Humanos Idioma: Inglês Revista: Immune Network Ano de publicação: 2017 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Autoanticorpos / Terapia Genética / Programas de Rastreamento / Imunofluorescência / Técnica Indireta de Fluorescência para Anticorpo / Aquaporina 1 / Células Madin Darby de Rim Canino Tipo de estudo: Estudo diagnóstico / Estudo de rastreamento Limite: Humanos Idioma: Inglês Revista: Immune Network Ano de publicação: 2017 Tipo de documento: Artigo