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主要屋尘螨变应原中鼠类MHC I类表位的预测及T1型CD8 + T细胞应答的诱导

Prediction of murine MHC class I epitopes in a major house dust mite allergen and induction of T1-type CD8+ T cell responses.

作者信息

Harris S J, Roth J F, Savage N, Woodrow S A, Hemingway I K, Hoyne G F, Lamb J R, Layton G T

机构信息

British Biotech Pharmaceuticals Ltd, Oxford, UK.

出版信息

Int Immunol. 1997 Feb;9(2):273-80. doi: 10.1093/intimm/9.2.273.

Abstract

The group I (Der p 1) allergen of Dermatophagoides pteronyssinus (house dust mite, HDM) contains several T helper (Th) epitopes recognized by C57BL/6 mice, with the peptide (111-139) containing a dominant MHC class II-restricted epitope (113-127). Since CD8+ T cells are thought to play a role in the regulation of allergic disease, we examined the Der p 1 sequence for potential MHC class I-binding motifs and observed that residues 111-119 (FGISNYCQI) contain motifs for H-2Db and Kb. Furthermore, immunization of C57BL/6 mice with unadjuvanted Ty virus-like particles (VLP) carrying Der p 1 (111-139), a method known to induce murine cytotoxic T lymphocyte (CTL) responses, primed Der p 1 (111-119)-specific Db-restricted CTL which produce high levels of IFN-gamma and low levels of IL-5 and IL-6 in vitro (T1-type CTL). VLP carrying the minimal epitope (FGISNYCQI) also induced a CTL response following immunization without adjuvant by various routes. Der p 1 (111-139)-VLP adjuvanted with alum did not prime CTL in C57BL/6 mice but were found to prime Th1-type CD4+ T cells that recognize the overlapping peptide (113-127) and native protein. The ability to successfully predict allergen-specific CD8+ T cell epitopes and prime CD8+ and/or CD4+ T cell responses provides an opportunity to dissect the relative roles of these T cells in the regulation of allergic responses and may offer therapeutic potential for reprogramming Th2-type allergic responses.

摘要

屋尘螨(HDM)的第I组(Der p 1)变应原包含几个被C57BL/6小鼠识别的辅助性T细胞(Th)表位,其中肽段(111 - 139)含有一个主要的MHC II类限制性表位(113 - 127)。由于认为CD8 + T细胞在过敏性疾病的调节中起作用,我们检查了Der p 1序列中潜在的MHC I类结合基序,发现111 - 119位残基(FGISNYCQI)含有与H - 2Db和Kb结合的基序。此外,用携带Der p 1(111 - 139)的无佐剂Ty病毒样颗粒(VLP)免疫C57BL/6小鼠,这是一种已知可诱导鼠细胞毒性T淋巴细胞(CTL)反应的方法,可引发Der p 1(111 - 119)特异性的Db限制性CTL,其在体外产生高水平的IFN - γ和低水平的IL - 5及IL - 6(T1型CTL)。携带最小表位(FGISNYCQI)的VLP通过各种途径无佐剂免疫后也诱导了CTL反应。用明矾佐剂的Der p 1(111 - 139) - VLP在C57BL/6小鼠中未引发CTL,但发现可引发识别重叠肽段(113 - 127)和天然蛋白的Th1型CD4 + T细胞。成功预测变应原特异性CD8 + T细胞表位并引发CD8 +和/或CD4 + T细胞反应的能力为剖析这些T细胞在过敏性反应调节中的相对作用提供了机会,并可能为重新编程Th2型过敏反应提供治疗潜力。

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