Celiac disease association with CD8+ T cell responses:: Identification of a novel gliadin-derived HLA-A2-restricted epitope

被引:64
作者
Gianfrani, C
Troncone, R
Mugione, P
Cosentini, E
De Pascale, M
Faruolo, C
Senger, S
Terrazzano, G
Southwood, S
Auricchio, S
Sette, A
机构
[1] CNR, Inst Food Sci & Technol, I-83100 Avellino, Italy
[2] Univ Naples Federico II, Dept Pediat, Naples, Italy
[3] Univ Naples Federico II, European Lab Invest Food Induced Dis, Naples, Italy
[4] Univ Naples Federico II, Dept Mol & Cellular Biol & Pathol, Naples, Italy
[5] Univ Naples Federico II, Dept Immunohematol & Transfus Med, Naples, Italy
[6] Epimmune, San Diego, CA 92121 USA
[7] La Jolla Inst Allergy & Immunol, San Diego, CA 92121 USA
关键词
D O I
10.4049/jimmunol.170.5.2719
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
One of the diagnostic hallmarks of the histological lesions associated with celiac disease is the extensive infiltration of the small intestinal epithelium by CD8(+) T cells of unknown Ag specificity. In this study, we report recognition of the gliadin-derived peptide (A-gliadin 123-132) by CD8(+) T lymphocytes from celiac patients. A-gliadin 123-132-specific IFN-gamma production and cytotoxic activity were detected in PBMCs derived from patients on gluten-free diet, but not from either celiac patients on gluten-containing diet or healthy controls. In contrast, A-gliadin 123-132-specific cells were isolated from small intestine biopsies of patients on either gluten-free or gluten-containing diets. Short-term T cell lines derived from the small intestinal mucosa and specific for the 123-132 epitope recognized human APC pulsed with either whole recombinant a-gliadin or a partial pepsin-trypsin gliadin digest. Finally, we speculate on a possible mechanism leading to processing and presentation of class I-restricted gliadin-derived epitopes in celiac disease patients.
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收藏
页码:2719 / 2726
页数:8
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