Title of article :
Selective screening of secretory vesicle-associated proteins for autoantigens in type 1 diabetes: VAMP2 and NPY are new minor autoantigens
Author/Authors :
Hirai، نويسنده , , Hiroki and Miura، نويسنده , , Junnosuke and Hu، نويسنده , , Yafang and Larsson، نويسنده , , Helena and Larsson، نويسنده , , Karin and Lernmark، نويسنده , , Ake and Ivarsson، نويسنده , , Sten-A. and Wu، نويسنده , , Tianxia and Kingman، نويسنده , , Albert and Tzioufas، نويسنده , , Athanasios G. and Notkins، نويسنده , , Abner L. and Bich-Thuy، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2008
Abstract :
The four major autoantigens (IA-2, IA-2β, 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.
Keywords :
IA-2 , Protein tyrosine phosphatase , Proteome , Secretory vesicles , Type 1 diabetes , autoantibodies , GAD65 , Autoantigens
Journal title :
Clinical Immunology
Journal title :
Clinical Immunology