PS13 - 66. The type 1 diabetes associated HLA-DQ8-transdimer accommodates a unique islet peptide repertoire

被引:0
|
作者
Menno van Lummel
Peter A. van Veelen
Arnaud Zaldumbide
Arnoud de Ru
George M.C. Janssen
Antonis K. Moustakas
George K. Papadopoulos
Jan W. Drijfhout
Bart O. Roep
Frits Koning
机构
[1] Leiden University Medical Center,Department of Immunohematology and Blood Transfusion
[2] Leiden University Medical Center,Department of Molecular Cell Biology
[3] Technological Educational Institute of Ionian Islands,Department of Organic Farming
[4] Faculty of Agricultural Technology,Laboratory of Biochemistry and Biophysics
[5] Epirus Institute of Technology,undefined
关键词
Peptide; Binding Assay; Binding Motif; Genetic Research; Peptide Binding;
D O I
10.1007/s12467-011-0091-7
中图分类号
学科分类号
摘要
In spite of the promise of decades of genetic research and the recently hyped expectations following genome-wide association studies in T1D, it remains unknown why HLADQ2 and HLA-DQ8 are strongly predisposing haplotypes for T1D. We understand even less why HLA-DQ2/8 heterozygous individuals have a synergistically increased risk compared to HLA-DQ2 or HLA-DQ8 homozygote subjects that may result from the presence of a transdimer formed between the α-chain of HLA-DQ2 (DQA1*0501) and the β-chain of HLA-DQ8 (DQB1*0302) that may bind and present unique autoantigen derived diabetogenic epitopes.
引用
收藏
页码:135 / 136
页数:1
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