| Literature DB >> 26235378 |
Anamika Basu1, Leanne Woods-Burnham1, Greisha Ortiz1, Leslimar Rios-Colon1, Johnny Figueroa1, Roger Albesa2, Luis E Andrade3, Michael Mahler2, Carlos A Casiano4.
Abstract
Human antinuclear autoantibodies (ANAs) targeting the dense fine speckled (DFS) nuclear protein DFS70, commonly known as lens epithelium derived growth factor p75 (LEDGFp75), present a clinical puzzle since their significance remains elusive. While their frequencies are low in ANA-positive autoimmune rheumatic diseases, they are relatively elevated in clinical laboratory referrals, diverse inflammatory conditions, and 'apparently' healthy individuals. We reported previously that DFS70/LEDGFp75 is an autoantigen in prostate cancer that closely interacts with another 70kD DFS nuclear protein, methyl CpG binding protein 2 (MeCP2). This led us to investigate if anti-DFS sera exclusively target DFS70/LEDGFp75 or also recognize MeCP2. Using several complementary autoantibody detection platforms and cellular/molecular approaches we evaluated 65 human sera producing anti-DFS autoantibodies. Our results show that these antibodies are highly specific for DFS70/LEDGFp75 and do not target MeCP2. Establishing the specificity of anti-DFS autoantibodies has implications for increasing our understanding of their biological significance and clinical utility.Entities:
Keywords: Autoantibodies; Autoimmunity; DFS70; Dense fine speckles; LEDGFp75; MeCP2
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Year: 2015 PMID: 26235378 PMCID: PMC4712632 DOI: 10.1016/j.clim.2015.07.014
Source DB: PubMed Journal: Clin Immunol ISSN: 1521-6616 Impact factor: 3.969