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源自视网膜S抗原葡萄膜致病位点的三至五个残基的寡肽可在Lewis大鼠中诱发实验性自身免疫性葡萄膜炎(EAU)。

Oligopeptides of three to five residues derived from uveitopathogenic sites of retinal S-antigen induce experimental autoimmune uveitis (EAU) in Lewis rats.

作者信息

Sunil S, Eto K, Singh V K, Shinohara T

机构信息

Molecular Biology Section, National Eye Institute, National Institutes of Health, Bethesda, Maryland 20892.

出版信息

Cell Immunol. 1993 Apr 15;148(1):198-207. doi: 10.1006/cimm.1993.1102.

Abstract

We have previously reported that microbial peptides having 3 to 6 amino acid sequence homology with uveitopathogenic peptide of retinal S-antigen (S-Ag) are capable of inducing experimental autoimmune uveitis (EAU) in Lewis rats and subhuman primates. T-cells obtained from animals immunized with these microbial peptides proliferate when stimulated with S-Ag peptide in culture and vice versa. We were interested to know whether these 3 to 6 identical amino acid residues by themselves were sufficient to induce EAU in susceptible animals under optimal conditions. For this purpose we have determined the response of synthetic oligopeptides of 3 to 18 amino acid residues for their ability to indice EAU. Here, we report that small synthetic oligopeptides of 3 to 5 amino acid residues of the two uveitopathogenic peptides of S-Ag induced EAU in Lewis rats, although with a higher dose (2000 micrograms/rat) than that of the larger peptides (50 micrograms/rat). These results define the core sequences in the uveitopathogenic peptides of retinal S-Ag.

摘要

我们之前曾报道,与视网膜S抗原(S-Ag)的葡萄膜致病肽具有3至6个氨基酸序列同源性的微生物肽,能够在Lewis大鼠和非人灵长类动物中诱发实验性自身免疫性葡萄膜炎(EAU)。用这些微生物肽免疫的动物所获得的T细胞,在培养中用S-Ag肽刺激时会增殖,反之亦然。我们想知道,在最佳条件下,这些3至6个相同的氨基酸残基本身是否足以在易感动物中诱发EAU。为此,我们测定了3至18个氨基酸残基的合成寡肽诱发EAU的能力。在此,我们报告,S-Ag的两种葡萄膜致病肽的3至5个氨基酸残基的小合成寡肽,在Lewis大鼠中诱发了EAU,尽管其剂量(2000微克/只大鼠)高于较大肽段(50微克/只大鼠)。这些结果确定了视网膜S-Ag葡萄膜致病肽中的核心序列。

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