Originally published In Press as doi:10.1074/mcp.M500352-MCP200 on May 11, 2006.
Molecular & Cellular Proteomics 5:1462-1470, 2006.
© 2006 by The American Society for Biochemistry and Molecular Biology, Inc.
Research
Identification and Functional Validation of Novel Autoantigens in Equine Uveitis* ,S
Cornelia A. Deeg , ,
Dirk Pompetzki ,
Albert J. Raith ,
Stefanie M. Hauck¶,
Barbara Amann ,
Sabine Suppmann¶,
Thomas W. F. Goebel ,
Ursula Olazabal¶,
Hartmut Gerhards||,
Sven Reese**,
Manfred Stangassinger ,
Bernd Kaspers and
Marius Ueffing¶
From the Institute of Animal Physiology, || Department of Equine Surgery and Medicine, and ** Institute of Veterinary Anatomy I, Ludwig Maximilians University (LMU) Munich, Veterinärstr. 13, D-80539 Munich, Germany and ¶ Institute of Human Genetics, National Research Center for Environment and Health (GSF) Neuherberg, Ingolstädter Landstr. 1, D-85764 Neuherberg, Germany
The development, progression, and recurrence of autoimmune diseases are frequently driven by a group of participatory autoantigens. We identified and characterized novel autoantigens by analyzing the autoantibody binding pattern from horses affected by spontaneous equine recurrent uveitis to the retinal proteome. Cellular retinaldehyde-binding protein (cRALBP) had not been described previously as autoantigen, but subsequent characterization in equine recurrent uveitis horses revealed B and T cell autoreactivity to this protein and established a link to epitope spreading. We further immunized healthy rats and horses with cRALBP and observed uveitis in both species with typical tissue lesions at cRALBP expression sites. The autoantibody profiling outlined here could be used in various autoimmune diseases to detect autoantigens involved in the dynamic spreading cascade or serve as predictive markers.
To whom correspondence should addressed. Tel.: 498921801630; Fax: 498921802554; E-mail: deeg{at}tiph.vetmed.uni-muenchen.de

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Copyright © 2006 by the American Society for Biochemistry and Molecular Biology.
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