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A Korean Patient With Fulminant Autoantibody-Negative Type 1 Diabetes

  1. Tae S. Jung, MD1,
  2. Soon I. Chung, MD, PHD12,
  3. Me A. Kim, MD, PHD23,
  4. Sun J. Kim, MD, PHD23,
  5. Myoung H. Park, MD, PHD4,
  6. Deok R. Kim, PHD5,
  7. Mi Y. Kang, MD1 and
  8. Jong R. Hahm, MD, PHD12
  1. 1Department of Internal Medicine, College of Medicine, Gyeongsang National University, Jinju, Korea
  2. 2Gyeongsang Institute of Health Science, Jinju, Korea
  3. 3Department of Laboratory Medicine, College of Medicine, Gyeongsang National University, Jinju, Korea
  4. 4Department of Laboratory Medicine, Seoul National University, Seoul, Korea
  5. 5Department of Biochemistry, College of Medicine, Gyeongsang National University, Jinju, Korea
  1. Address correspondence to Jong R. Hahm, MD, PhD, Gyeongsang National University Hospital, 90, Chilamdong, Jinju, Korea. E-mail: jrhahm{at}gshp.gsnu.ac.kr

Since 11 novel cases of fulminant autoantibody-negative type 1 diabetes were introduced by Imagawa and colleagues (1,2), about 150 additional cases have been reported. The development of typical fulminant autoantibody-negative type 1 diabetes is strictly confined to Japan. Although the pathogenetic mechanism still remains unclear, there is some evidence supporting the immunogenetic predisposition mechanism in the development of this subtype. A fulminant autoantibody-negative type 1 diabetic patient with insulitis and exocrine pancreatitis showed infiltration of a large number of CD8+ T-cell and peripheral GAD-reactive interferon-γ-producing CD4+ T-cell (3). According to previous reports, some HLA haplotypes, DRB1*0405-DQB1*0401, DQA1*0303-DQB1*0401, DQA1*0302-DQB1*0303, and DRB*0901 are closely associated with fulminant autoantibody-negative …

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