Immunopathogenesis of juvenile dermatomyositis

Sahil Khanna, Ann M. Reed

Research output: Contribution to journalReview article

32 Scopus citations

Abstract

There is increasing evidence for involvement of the mechanisms of the innate immune system in the pathogenesis of idiopathic inflammatory myopathies (IIMs), especially in the adult and juvenile forms of dermatomyositis. Juvenile dermatomyositis (JDM) is the most common form of childhood IIM, and this review focuses on recent advances in understanding the actions of the innate immune system in this condition. Over the last few years, great strides have been made in understanding immune dysregulation in IIM, including JDM. Novel autoantibodies have been identified, and new genetic contributions have been described. Among the most striking findings is type I interferon activity in JDM tissue and peripheral blood. This is in conjunction with the description of dysregulation of the major histocompatibility complex (MHC) class I gene and identification of plasmacytoid dendritic infiltrates as the possible cellular source of type I interferons. These findings also point toward the potential prognostic value of muscle biopsies and have helped expand our understanding of the etiopathogenesis of IIM.

Original languageEnglish (US)
Pages (from-to)581-592
Number of pages12
JournalMuscle and Nerve
Volume41
Issue number5
DOIs
StatePublished - May 1 2010

Keywords

  • B cells
  • Human leukocyte antigens
  • Idiopathic inflammatory myopathies
  • Juvenile dermatomyositis
  • Plasmacytoid dendritic cells
  • T cells
  • Type I interferons

ASJC Scopus subject areas

  • Physiology
  • Clinical Neurology
  • Cellular and Molecular Neuroscience
  • Physiology (medical)

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