Glycation of a food allergen by the Maillard reaction enhances its T-cell immunogenicity: Role of macrophage scavenger receptor class A type I and II

被引:97
作者
Ilchmann, Anne [1 ]
Burgdorf, Sven [4 ]
Scheurer, Stephan [3 ]
Waibler, Zoe [2 ]
Nagai, Ryoji [5 ]
Wellner, Anne [6 ]
Yamamoto, Yasuhiko [7 ]
Yamamoto, Hiroshi [7 ]
Henle, Thomas [6 ]
Kurts, Christian [4 ]
Kalinke, Ulrich [8 ]
Vieths, Stefan [3 ]
Toda, Masako [1 ]
机构
[1] Paul Ehrlich Inst, Jr Res Grp Expt Allergol 1, D-63225 Langen, Germany
[2] Paul Ehrlich Inst, Jr Res Grp Novel Vaccinat Strategies & Early Immu, D-63225 Langen, Germany
[3] Paul Ehrlich Inst, Div Allergol, D-63225 Langen, Germany
[4] Univ Bonn, Inst Mol Med & Expt Immunol, D-5300 Bonn, Germany
[5] Japan Womens Univ, Dept Food & Nutr, Lab Biochem & Nutr Sci, Tokyo, Japan
[6] Tech Univ Dresden, Inst Food Chem, Dresden, Germany
[7] Kanazawa Univ, Grad Sch Med Sci, Dept Biochem & Mol Vasc Biol, Kanazawa, Ishikawa 9201192, Japan
[8] Ctr Expt & Clin Infect Res, TWINCORE, Hannover, Germany
关键词
Food allergy; food allergen; Maillard reaction; T-cell immunogenicity; dendritic cells; macrophage scavenger receptor; GLYCOSYLATION END-PRODUCTS; HEATED PECAN NUT; DENDRITIC CELLS; ANTIGEN PRESENTATION; MATURATION; PROTEINS; ENDPRODUCTS; BINDING; RAGE; ATHEROSCLEROSIS;
D O I
10.1016/j.jaci.2009.08.013
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: The Maillard reaction occurs between reducing sugars and proteins during thermal processing of foods. It produces chemically glycated proteins termed advanced glycation end products (AGEs). The glycation structures of AGES are suggested to function as pathogenesis-related immune epitopes in food allergy. Objective: This study aimed at defining the T-cell immunogenicity of food AGES by using ovalbumin (OVA) as a model allergen. Methods: AGE-OVA was prepared by means of thermal processing of OVA in the presence of glucose. Activation of OVA-specific CD4(+) T cells by AGE-OVA was evaluated in cocultures with bone marrow-derived murine myeloid dendritic cells (mDCs) as antigen-presenting cells. The uptake mechanisms of mDCs for AGE-OVA were investigated by using inhibitors of putative cell-surface receptors for AGES, as well as mDCs deficient for these receptors. Results: Compared with the controls (native OVA and OVA thermally processed without glucose), AGE-OVA enhanced the activation of OVA-specific CD4(+) T cells on coculture with mDCs, indicating that the glycation of OVA enhanced the T-cell immunogenicity of the allergen. The mDC uptake of AGE-OVA was significantly higher than that of the controls. We identified scavenger receptor class A type I and II (SR-AI/II) as a mediator of the AGE-OVA uptake, whereas the receptor for AGEs and galectin-3 were not responsible. Importantly, the activation of OVA-specific CD4(+) T cells by AGE-OVA was attenuated on coculture with SR-AI/II-deficient mDCs. Conclusion: SR-AI/II targets AGE-OVA to the MHC class II loading pathway in mDCs, leading to an enhanced CD4(+) T-cell activation. The Maillard reaction might thus play an important role in the T-cell immunogenicity of food allergens. (J Allergy Clin Immunol 2010;125:175-83.)
引用
收藏
页码:175 / 183
页数:9
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