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用IRBP衍生的合成肽免疫的灵长类动物中的葡萄膜炎和免疫反应。

Uveitis and immune responses in primates immunized with IRBP-derived synthetic peptides.

作者信息

Sanui H, Redmond T M, Kotake S, Wiggert B, Tanaka T, Chader G J, Gery I

机构信息

Laboratory of Immunology, National Eye Institute, National Institutes of Health, Bethesda, MD 20892.

出版信息

Curr Eye Res. 1990 Feb;9(2):193-9. doi: 10.3109/02713689008995206.

Abstract

Monkeys immunized with bovine IRBP-derived synthetic peptides R4 (sequence 1158-1180) or R14 (1169-1191) developed EAU which was detected by both clinical and histological examinations. The inflammation localized mainly in the choroid, with only minor changes being noticed in the adjacent retinal tissue. EAU developed in only one of the two monkeys immunized with each of the peptides and the animals with disease also showed higher levels of cellular immunity toward the immunizing peptide than did the monkeys with no disease. The cellular immune responses, measured by the lymphocyte proliferation assay, were specific toward the immunizing peptides, with no cross responsiveness to whole IRBP. This finding suggests that the two uveitogenic peptides were non-immunodominant in the tested monkeys. In contrast, peptide R14 is highly immunodominant in the Lewis rat. Also, the fine specificity of the monkey response to R14 differed from that of the Lewis rat. The possible genetic control of the monkey susceptibility to EAU induction by the peptides is discussed and the unique finding of an autoimmune disease induction by a non-immunodominant peptide is underscored.

摘要

用牛视网膜间质抗原结合蛋白(IRBP)衍生的合成肽R4(序列1158 - 1180)或R14(1169 - 1191)免疫的猴子发生了实验性自身免疫性葡萄膜炎(EAU),通过临床和组织学检查均能检测到。炎症主要局限于脉络膜,相邻视网膜组织仅有轻微变化。在用每种肽免疫的两只猴子中,只有一只发生了EAU,患病动物对免疫肽的细胞免疫水平也高于未患病的猴子。通过淋巴细胞增殖试验测定的细胞免疫反应对免疫肽具有特异性,对完整的IRBP无交叉反应性。这一发现表明,在受试猴子中,这两种致葡萄膜炎肽是非免疫显性的。相比之下,肽R14在Lewis大鼠中具有高度免疫显性。此外,猴子对R14反应的精细特异性与Lewis大鼠不同。文中讨论了猴子对肽诱导EAU易感性的可能遗传控制,并强调了非免疫显性肽诱导自身免疫性疾病这一独特发现。

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