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10.4110/in.2017.17.2.103

http://scihub22266oqcxt.onion/10.4110/in.2017.17.2.103
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C5407981!5407981!28458621
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suck abstract from ncbi


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pmid28458621      Immune+Netw 2017 ; 17 (2): 103-9
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  • Detection of Autoantibodies against Aquaporin-1 in the Sera of Patients with Primary Sjögren s Syndrome #MMPMID28458621
  • Alam J; Choi YS; Koh JH; Kwok SK; Park SH; Song YW; Park K; Choi Y
  • Immune Netw 2017[Apr]; 17 (2): 103-9 PMID28458621show ga
  • 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.
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