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Identification of an anti‐aldolase autoantibody as a diagnostic marker for diabetic retinopathy by immunoproteomic analysis
Author(s) -
Ahn BoYoung,
Song EunSun,
Cho Yang Je,
Kwon Oh Woong,
Kim Jin Kook,
Lee Na Gyong
Publication year - 2006
Publication title -
proteomics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.26
H-Index - 167
eISSN - 1615-9861
pISSN - 1615-9853
DOI - 10.1002/pmic.200500457
Subject(s) - autoantibody , aldolase a , identification (biology) , diabetic retinopathy , proteomics , medicine , immunology , biology , antibody , diabetes mellitus , genetics , endocrinology , biochemistry , enzyme , botany , gene
Circulating autoantibodies specific for retinal proteins are associated with retinal destruction in patients with diabetic retinopathy (DR). In this study, we screened diabetic sera for the presence of anti‐retinal autoantibodies with an aim of developing diagnostic markers for DR. Immunoblot analysis of DR patients' sera with human retinal cytosolic proteins revealed a higher incidence of anti‐retinal autoantibodies, compared to normal blood donors or diabetic patients without DR. Anti‐retinal protein autoantibody profiles of DR patient sera were obtained by 2‐DE immunoblot analysis. Specifically, 20 protein spots reactive with DR patient sera were identified by ESI‐MS/MS. Of these spots, 14 were specific for DR patients, and 4 reacted with both non‐proliferative DR (non‐PDR) and PDR sera. The anti‐aldolase autoantibody was selected as a DR marker candidate, and specific reactivity of DR patient sera was confirmed by immunoblot analysis with rabbit aldolase. The serum anti‐aldolase autoantibody level was measured by ELISA. DR patients showed significantly higher autoantibody levels than normal donors or diabetic patients without retinopathy. However, no significant differences were observed between non‐PDR and PDR patients, suggesting that the level of anti‐aldolase autoantibody is not determined by the severity of retinopathy in diabetic patients. Our data collectively demonstrate that the anti‐aldolase autoantibody serves as a useful marker for DR diagnosis.