Skip to main navigation Skip to search Skip to main content

Multiple target autoantigens on endothelial cells identified in juvenile dermatomyositis using proteomics

  • Rie Karasawa
  • , Mayumi Tamaki
  • , Toshiko Sato
  • , Megumi Tanaka
  • , Makiko Nawa
  • , Kazuo Yudoh
  • , James N. Jarvis
  • St. Marianna University School of Medicine
  • Institute of Science Tokyo

Research output: Contribution to journalArticlepeer-review

18 Scopus citations

Abstract

Objective. Although generally classified within the group of inflammatory myopathies, JDM displays many pathological features of vasculitis. Previous work has shown that AECA are abundant in other forms of vasculitis. We therefore investigated whether such antibodies might also be detected in JDM. Methods. We screened plasma from children with JDM for the presence of AECA by western blotting and 2D gel electrophoresis (2DE) using proteins extracted from human aortic endothelial cells as the substrate. We performed mass spectrometry to identify candidate antigens from 2DE gels and used ELISA to confirm the presence of specific antibodies. Results. We identified 22 candidate target autoantigens for AECA probed with JDM plasma. Interestingly, 17 of these 22 target antigens were proteins associated with antigen processing and protein trafficking. ELISA confirmed the presence of antibodies to heat shock cognate 71 kDa protein in JDM plasma, particularly in children with active, untreated disease. Conclusion. Children with JDM express antibodies to autoantigens in endothelial cells. The clinical and pathological significance of such autoantibodies require further investigation.

Original languageEnglish
Pages (from-to)671-676
Number of pages6
JournalRheumatology
Volume57
Issue number4
DOIs
StatePublished - Apr 1 2018

Keywords

  • Anti-endothelial cell antibodies
  • Autoantibodies
  • Chaperone proteins
  • Endothelium
  • Heat shock cognate 71 kDa protein
  • Juvenile dermatomyositis
  • Proteomics

Fingerprint

Dive into the research topics of 'Multiple target autoantigens on endothelial cells identified in juvenile dermatomyositis using proteomics'. Together they form a unique fingerprint.

Cite this