Recognition of a subregion of human proinsulin by class I-restricted T cells in type 1 diabetic patients

被引:100
作者
Toma, A
Haddouk, S
Briand, JP
Camoin, L
Gahery, H
Connan, F
Dubois-Laforgue, D
Caillat-Zucman, S
Guillet, JG
Care, JC
Muller, S
Choppin, J
Boitard, C [1 ]
机构
[1] Univ Paris 05, Hop Cochin St Vincent Paul, INSERM, U561, F-75014 Paris, France
[2] CNRS, UPR 9021, Inst Biol Mol & Cellulaire, F-67000 Strasbourg, France
[3] Univ Paris 05, CNRS, INSERM, U567,UMR 8104,Inst Cochin, F-75014 Paris, France
[4] Hop Cochin St Vincent Paul, Serv Immunol Clin, F-75014 Paris, France
关键词
autoimmunity; beta cell; CD8 T cells; human autoantigens; proteasome;
D O I
10.1073/pnas.0504230102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Proinsulin is a key autoantigen in type 1 diabetes. Evidence in the mouse has underscored the importance of the insulin B chain region in autoimmunity to pancreatic beta cells. In man, a majority of proteasome cleavage sites are predicted by proteasome cleavage algorithms within this region. To study CD8(+) T cell responses to the insulin B chain and adjacent C peptide, we selected 8- to 11-mer peptides according to proteasome cleavage patterns obtained by digestion of two peptides covering proinsulin residues 28 to 64. We studied their binding to purified HLA class 1 molecules and their recognition by T cells from diabetic patients. Peripheral blood mononuclear cells from 17 of 19 recent-onset and 12 of 13 long-standing type 1 diabetic patients produced IFN-gamma in response to proinsulin peptides as shown by using an ELISPOT assay. In most patients, the response was against several class I-restricted peptides. Nine peptides were recognized within the proinsulin region covering residues 34 to 61. Four yielded a high frequency of recognition in HLA-A1 and -B8 patients. Three peptides located in the proinsulin region 41-51 were shown to bind several HLA molecules and to be recognized in a high percentage of diabetic patients.
引用
收藏
页码:10581 / 10586
页数:6
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