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人类T细胞对豚草过敏原的反应:Amb V同源物

Human T-cell responses to ragweed allergens: Amb V homologues.

作者信息

Huang S K, Marsh D G

机构信息

Johns Hopkins Asthma and Allergy Center, Johns Hopkins University School of Medicine, Baltimore, Maryland 21224.

出版信息

Immunology. 1991 Jul;73(3):363-5.

Abstract

Specific IgE and IgG responses to highly purified Ambrosia (ragweed) allergens, Amb a V, Amb t V and Amb p V from the artemisiifolia (short), trifida (giant) and psilostachya (western) species are strongly associated with HLA-DR2 and Dw2 (DR2.2) in allergic Caucasoid individuals. To investigate the molecular basis of these HLA associations, we examined the human T-cell responses to these Amb V homologues using three Amb a V-specific, DR alpha beta I 2.2-restricted T-cell clones from an atopic patient. We first examined the cross-reactivity of Amb a V-specific T-cell clones upon challenge with the Amb a V homologues, Amb t V and Amb p V, in the presence of autologous antigen-presenting cells (APC). Neither Amb t V nor Amb p V was able to stimulate the T-cell clones directly. However, both Amb t V and Amb p V specifically blocked, in a dose-dependent fashion, the ability of APC to present Amb a V to all three T-cell clones. Taken together, these results suggest that Amb t V and Amb p V possess distinct T-cell epitopes, but that all Amb V homologues share similar or identical regions (agretopes) interacting with the DR alpha beta I 2.2 (DR alpha beta I 1501) heterodimer. The agretope was potentially localized to a 14-residue C-terminal Amb a V peptide (with Ala-Cys substitutions), which was able to block presentation of native Amb a V by the APC to the T-cell clones.

摘要

在过敏性高加索个体中,针对来自豚草(短叶豚草)、三裂叶豚草(巨型豚草)和西部豚草的高度纯化的豚草过敏原Amb a V、Amb t V和Amb p V的特异性IgE和IgG反应与HLA - DR2和Dw2(DR2.2)密切相关。为了研究这些HLA关联的分子基础,我们使用来自一名特应性患者的三个Amb a V特异性、DRαβI 2.2限制性T细胞克隆,检测了人类T细胞对这些Amb V同源物的反应。我们首先在自体抗原呈递细胞(APC)存在的情况下,用Amb a V同源物Amb t V和Amb p V刺激Amb a V特异性T细胞克隆,检测其交叉反应性。Amb t V和Amb p V都不能直接刺激T细胞克隆。然而,Amb t V和Amb p V都以剂量依赖性方式特异性地阻断了APC将Amb a V呈递给所有三个T细胞克隆的能力。综上所述,这些结果表明Amb t V和Amb p V具有不同的T细胞表位,但所有Amb V同源物都共享与DRαβI 2.2(DRαβI 1501)异二聚体相互作用的相似或相同区域(抗原结合位)。抗原结合位可能定位于一个14个残基的Amb a V C末端肽(有Ala - Cys替换),它能够阻断APC将天然Amb a V呈递给T细胞克隆。

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