Identification of Novel Autoantibodies in Type 1 Diabetic Patients Using a High-Density Protein Microarray

Author:

Koo Bo Kyung12,Chae Sehyun3,Kim Kristine M.4,Kang Min Jueng5,Kim Eunhee G.4,Kwak Soo Heon1,Jung Hye Seung1,Cho Young Min1,Choi Sung Hee1,Park Young Joo1,Shin Choong Ho6,Jang Hak C.1,Shin Chan Soo1,Hwang Daehee37,Yi Eugene C.5,Park Kyong Soo15

Affiliation:

1. Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea

2. Department of Internal Medicine, Boramae Medical Center, Seoul, Korea

3. School of Interdisciplinary Bioscience and Bioengineering, Pohang University of Science and Technology, Pohang, Korea

4. Department of Systems Immunology, College of Biomedical Science, and Institute of Bioscience and Biotechnology, Kangwon National University, Chuncheon, Korea

5. Department of Molecular Medicine and Biopharmaceutical Sciences, Graduate School of Convergence Science and Technology, and College of Medicine or College of Pharmacy, Seoul National University, Seoul, Korea

6. Department of Pediatrics, Seoul National University College of Medicine, Seoul, Korea

7. Center for Systems Biology of Plant Aging Research, Institute for Basic Science, Daegu Gyeongbuk Institute of Science and Technology, Daegu, Korea

Abstract

Autoantibodies can facilitate diagnostic and therapeutic means for type 1 diabetes (T1DM). We profiled autoantibodies from serum samples of 16 T1DM patients, 16 type 2 diabetic (T2DM) patients, and 27 healthy control subjects with normal glucose tolerance (NGT) by using protein microarrays containing 9,480 proteins. Two novel autoantibodies, anti-EEF1A1 and anti-UBE2L3, were selected from microarrays followed by immunofluorescence staining of pancreas. We then tested the validity of the candidates by ELISA in two independent test cohorts: 1) 95 adults with T1DM, 49 with T2DM, 11 with latent autoimmune diabetes in adults (LADA), 20 with Graves disease, and 66 with NGT and 2) 33 children with T1DM and 34 healthy children. Concentrations of these autoantibodies were significantly higher in T1DM patients than in NGT and T2DM subjects (P < 0.01), which was also confirmed in the test cohort of children (P < 0.05). Prevalence of anti-EEF1A1 and anti-UBE2L3 antibodies was 29.5% and 35.8% in T1DM, respectively. Of note, 40.9% of T1DM patients who lack anti-GAD antibodies (GADA) had anti-EEF1A1 and/or anti-UBE2L3 antibodies. These were also detected in patients with fulminant T1DM but not LADA. Our approach identified autoantibodies that can provide a new dimension of information indicative of T1DM independent of GADA and new insights into diagnosis and classification of T1DM.

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

Reference48 articles.

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2. Islet-cell antibodies in diabetes mellitus with autoimmune polyendocrine deficiencies;Bottazzo;Lancet,1974

3. Islet cell antigen 512 is a diabetes-specific islet autoantigen related to protein tyrosine phosphatases;Rabin;J Immunol,1994

4. The cation efflux transporter ZnT8 (Slc30A8) is a major autoantigen in human type 1 diabetes;Wenzlau;Proc Natl Acad Sci U S A,2007

5. Fulminant type 1 diabetes: a nationwide survey in Japan;Imagawa;Diabetes Care,2003

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