Selective screening of secretory vesicle-associated proteins for autoantigens in type 1 diabetes: VAMP2 and NPY are new minor autoantigens

Hiroki Hirai, Junnosuke Miura, Yafang Hu, Helena Larsson, Karin Larsson, Åke Lernmark, Sten Ivarsson, Tianxia Wu, Albert Kingman, Athanasios G Tzioufas, Abner L Notkins

Research output: Contribution to journalArticlepeer-review

Abstract

The four major autoantigens (IA-2, IA-2 beta, GAD65 and insulin) of type 1 diabetes are all associated with dense core or synaptic vesicles. This raised the possibility that other secretory vesicle-associated proteins might be targets of the autoimmune response in type 1 diabetes. To test this hypothesis 56 proteins, two-thirds of which are associated with secretory vesicles, were prepared by in vitro transcription/translation and screened for autoantibodies by liquid phase radioimmunoprecipitation. Two secretory vesicle-associated proteins, VAMP2 and NPY, were identified as new minor autoantigens with 21% and 9%, respectively, of 200 type 1 diabetes sera reacting positively. These findings add support to the hypothesis that secretory vesicle-associated proteins are particularly important, but not the exclusive, targets of the autoimmune response in type 1 diabetes. Selective screening of the human proteome offers a useful approach for identifying new autoantigens in autoimmune diseases.
Original languageEnglish
Pages (from-to)366-374
JournalClinical Immunology
Volume127
Issue number3
DOIs
Publication statusPublished - 2008

Subject classification (UKÄ)

  • Immunology in the medical area

Free keywords

  • type 1 diabetes
  • secretory vesicles
  • proteome
  • phosphatase
  • protein tyrosine
  • IA-2
  • GAD65
  • autoantibodies
  • autoantigens

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