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      Specific HLA genotypes confer susceptibility to acute necrotizing encephalopathy.

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          Abstract

          Acute necrotizing encephalopathy (ANE) is a rare and severe syndrome of acute encephalopathy triggered by viral infections. Cytokine storm is considered as the main pathogenetic mechanism of ANE. ANE is prevalent in East Asia, suggesting the association of host genetic factors. To elucidate the genetic background of Japanese ANE, we examined genotypes of human leukocyte antigen (HLA)-A, C, B, DRB1, DQB1 and DPB1 in 31 patients. Significant positive association was observed in both the allele frequency and positivity of DRB1*09:01 (P=0.043 and 0.025, respectively), as well as those of DQB1*03:03 (P=0.034 and 0.026, respectively). The carrier frequency of DRB1*09:01 and DQB1*03:03 alleles was higher in the patients (45.16%) than in controls (28.57%). These alleles are more common in East Asian than in European populations, and are reportedly associated with various autoimmune diseases in Japanese patients. Our data provide further evidence that altered immune response based on individual HLA genotypes may contribute to ANE pathogenesis.

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          Author and article information

          Journal
          Genes Immun.
          Genes and immunity
          Springer Science and Business Media LLC
          1476-5470
          1466-4879
          September 2016
          : 17
          : 6
          Affiliations
          [1 ] Department of Developmental Medical Sciences, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
          [2 ] Department of Pediatrics, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
          [3 ] Department of Human Genetics, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
          [4 ] Sleep Disorders Project, Department of Psychiatry and Behavioral Sciences, Tokyo Metropolitan Institute of Medical Science, Tokyo, Japan.
          [5 ] Division of Neurology, National Center for Child Health and Development, Tokyo, Japan.
          [6 ] Department of Pediatrics, Tokyo Women's Medical University Yachiyo Medical Center, Yachiyo, Japan.
          [7 ] Department of Pediatrics, Asahikawa Habilitation Center for Disabled Children, Asahikawa, Japan.
          Article
          gene201632
          10.1038/gene.2016.32
          27467284
          aa09abe7-0543-481b-9bcf-ce50677403ef
          History

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