HLA-DQ Molecules as Affinity Matrix for Identification of Gluten T Cell Epitopes

被引:19
|
作者
Dorum, Siri [1 ,2 ]
Bodd, Michael [3 ]
Fallang, Lars-Egil [1 ]
Bergseng, Elin [1 ]
Christophersen, Asbjorn [1 ]
Johannesen, Marie K. [1 ]
Qiao, Shuo-Wang [1 ]
Stamnaes, Jorunn [1 ]
de Souza, Gustavo A. [1 ,2 ]
Sollid, Ludvig M. [1 ,3 ]
机构
[1] Univ Oslo, Dept Immunol, Ctr Immune Regulat, N-0424 Oslo, Norway
[2] Oslo Univ Hosp, Rikshosp, Prote Core Facil, N-0027 Oslo, Norway
[3] Oslo Univ Hosp, RIKEN, Dept Immunol, Ctr Immune Regulat, N-0424 Oslo, Norway
来源
JOURNAL OF IMMUNOLOGY | 2014年 / 193卷 / 09期
基金
欧洲研究理事会;
关键词
CELIAC-DISEASE; TISSUE TRANSGLUTAMINASE; GLIADIN PEPTIDES; DISSOCIATION; DEAMIDATION; HLA-DQ2.2; GENETICS; BINDING; RISK; DM;
D O I
10.4049/jimmunol.1301466
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Even though MHC class II is a dominant susceptibility factor for many diseases, culprit T cell epitopes presented by diseaseassociated MHC molecules remain largely elusive. T cells of celiac disease lesions recognize cereal gluten epitopes presented by the disease-associated HLA molecules DQ2.5, DQ2.2, or DQ8. Employing celiac disease and complex gluten Ag digests as a model, we tested the feasibility of using DQ2.5 and DQ2.2 as an affinity matrix for identification of disease-relevant T cell epitopes. Known gluten T cell epitope peptides were enriched by DQ2.5, whereas a different set of peptides was enriched by DQ2.2. Of 86 DQ2.2-enriched peptides, four core sequences dominated. One of these core sequences is a previously known epitope and two others are novel epitopes. The study provides insight into the selection of gluten epitopes by DQ2.2. Furthermore, the approach presented is relevant for epitope identification in other MHC class II-associated disorders.
引用
收藏
页码:4497 / 4506
页数:10
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