Identification of a peptide inducing experimental autoimmune uveoretinitis (EAU) in H-2Ak-carrying mice

Author:

Namba K12,Ogasawara K1,Kitaichi N12,Matsuki N1,Takahashi A1,Sasamoto Y2,Kotake S2,Matsuda H2,Iwabuchi K1,Ohno S3,Onoé K1

Affiliation:

1. Section of Pathology, Institute of Immunological Science

2. Department of Ophthalmology, School of Medicine, Hokkaido University, Sapporo

3. Department of Ophthalmology, Yokohama City University School of Medicine, Yokohama, Japan

Abstract

SUMMARY When certain strains of mice bearing H-2Ak are immunized with the interphotoreceptor retinoid-binding protein (IRBP), EAU is induced. Thus far uveitogenic determinant(s) has not been determined in the H-2Ak mouse system. In addition it is hard to prepare purified IRBP. In the present study, to circumvent these problems we attempted to identify uveitogenic peptides derived from bovine IRBP in H-2Ak haplotype mice. Six peptides which had been selected according to the H-2Ak binding motif (Dxxxxxxxx[A, R, T]) were synthesized. We report here that all the peptides are immunogenic but only one peptide, K2, which consisted of IRBP201–216 residues, induces EAU in various mice carrying H-2Ak. Amino acid substitution of K2 revealed that the core region interacted with both H-2Ak and T cell antigen receptor (TCR). The amino acid sequence of the core region derived from bovine IRBP was identical to the corresponding region of mouse IRBP. In addition, K2 appeared to be a natural peptide antigen processed from bovine IRBP. Altogether, we concluded that K2 is one of the natural autoantigens involved in induction of EAU in H-2Ak mice.

Publisher

Oxford University Press (OUP)

Subject

Immunology,Immunology and Allergy

Reference25 articles.

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3. Basic Mechanisms in Immune-mediated Uveitic Disease

4. Adoptive transfer of experimental autoimmune uveoretinitis in rats: immunopathogenic mechanisms and histologic features;Mochizuki;Invest Opthalmol Vis Sci,1985

5. T cell lines mediating experimental autoimmune uveoretinitis (EAU) in the rat;Caspi;J Immunol,1986

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