Suppr超能文献

人类过敏和非过敏受试者对蜂毒磷脂酶A2的T细胞表位特异性

T cell epitope specificity in human allergic and nonallergic subjects to bee venom phospholipase A2.

作者信息

Carballido J M, Carballido-Perrig N, Kägi M K, Meloen R H, Wüthrich B, Heusser C H, Blaser K

机构信息

Swiss Institute of Allergy and Asthma Research, Davos.

出版信息

J Immunol. 1993 Apr 15;150(8 Pt 1):3582-91.

PMID:7682244
Abstract

Phospholipase A2 (PLA) is a biochemically fully defined glycoprotein, representing the main allergen of bee venom. We have established CD4+ T cell clones specific to PLA from subjects allergic and nonallergic to bee sting. By screening the epitope specificity of these clones with 62 synthetic overlapping dodecapeptides representing the PLA molecule, two immunogenic epitopes, PLA81-92 and PLA113-124, were identified. Additional screening, using longer peptides of up to 18 residues, revealed a third epitope at position PLA 45-62. These epitopes are recognized by specific T cell clones in association with HLA-DP and -DQ molecules, although HLA-DR-associated responses to PLA exist. Primary in vitro proliferation of unfractionated PBMC from bee sting allergic, hyposensitized, or hyperimmune subjects to PLA-derived peptides revealed the same immunogenic sites as found in the T cell clones. Among the different groups of individuals, proliferative responses to the PLA molecule and fragments thereof were generally higher in allergic patients than in nonallergic subjects. Thus, at least three linear epitopes are involved in T cell recognition of PLA, independently whether or not subjects are allergic.

摘要

磷脂酶A2(PLA)是一种生化特性完全明确的糖蛋白,是蜂毒的主要过敏原。我们从对蜂蜇过敏和不过敏的受试者中建立了针对PLA的CD4 + T细胞克隆。通过用代表PLA分子的62种合成重叠十二肽筛选这些克隆的表位特异性,鉴定出两个免疫原性表位,即PLA81 - 92和PLA113 - 124。使用长达18个残基的更长肽进行的进一步筛选,在PLA 45 - 62位置发现了第三个表位。这些表位与HLA - DP和 - DQ分子结合时可被特异性T细胞克隆识别,尽管存在与HLA - DR相关的对PLA的反应。来自蜂蜇过敏、进行减敏治疗或免疫过强的受试者的未分级外周血单核细胞(PBMC)对PLA衍生肽的体外初次增殖显示出与T细胞克隆中相同的免疫原性位点。在不同个体组中,过敏患者对PLA分子及其片段的增殖反应通常高于非过敏受试者。因此,至少三个线性表位参与了T细胞对PLA的识别,无论受试者是否过敏。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验