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

机译:在携带H-2Ak的小鼠中鉴定诱导实验性自身免疫性葡萄膜视网膜炎(EAU)的肽

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摘要

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.
机译:当某些带有H-2Ak的小鼠品系用感光细胞间的类维生素A结合蛋白(IRBP)进行免疫时,会诱发EAU。迄今为止,尚未在H-2Ak小鼠系统中确定葡萄膜决定簇。另外,难以制备纯化的IRBP。在本研究中,为了避免这些问题,我们尝试在H-2Ak单倍型小鼠中鉴定出源自牛IRBP的葡萄胎生成肽。合成了根据H-2Ak结合基序选择的六个肽(Dxxxxxxxx [A,R,T])。我们在这里报告所有的肽都是免疫原性的,但是只有一种肽,即由IRBP201–216残基组成的K2,可以在携带H-2Ak的各种小鼠中诱导EAU。 K2的氨基酸取代表明核心区域与H-2Ak和T细胞抗原受体(TCR)相互作用。源自牛IRBP的核心区域的氨基酸序列与小鼠IRBP的相应区域相同。另外,K2似乎是由牛IRBP加工的天然肽抗原。总之,我们得出结论,K2是参与诱导H-2Ak小鼠EAU的天然自身抗原之一。

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