Specificity of antinuclear autoantibodies recognizing the dense fine speckled nuclear pattern: Preferential targeting of DFS70/LEDGFp75 over its interacting partner MeCP2

被引:29
作者
Basu, Anamika [1 ]
Woods-Burnham, Leanne [1 ]
Ortiz, Greisha [1 ]
Rios-Colon, Leslimar [1 ]
Figueroa, Johnny [1 ]
Albesa, Roger [2 ]
Andrade, Luis E. [3 ,4 ]
Mahler, Michael [2 ]
Casiano, Carlos A. [1 ,5 ]
机构
[1] Loma Linda Univ, Sch Med, Ctr Hlth Dispar & Mol Med, Dept Basic Sci, Loma Linda, CA 92350 USA
[2] Inova Diagnost Inc, Dept Res, San Diego, CA USA
[3] Univ Fed Sao Paulo, Div Rheumatol, Div Immunol, Fleury Med Lab, Sao Paulo, Brazil
[4] Univ Fed Sao Paulo, Div Rheumatol, Div Immunol, Hlth Lab, Sao Paulo, Brazil
[5] Loma Linda Univ, Sch Med, Div Rheumatol, Dept Med, Loma Linda, CA 92350 USA
关键词
Autoantibodies; Autoimmunity; Dense fine speckles; DFS70; LEDCFp75; MeCP2; AUTOIMMUNE RHEUMATIC-DISEASES; GROWTH-FACTOR; PROSTATE-CANCER; ANTI-DFS70; ANTIBODIES; OXIDATIVE STRESS; COACTIVATOR P75; HIV-1; INTEGRASE; TRANSCRIPTIONAL REGULATION; HEALTHY-INDIVIDUALS; ATOPIC-DERMATITIS;
D O I
10.1016/j.clim.2015.07.014
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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 70 kD 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. (C) 2015 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license.
引用
收藏
页码:241 / 250
页数:10
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