Beijing Computing Center Beijing China

Beijing China, China

Beijing Computing Center Beijing China

Beijing China, China
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Xie L.-J.,Guangxi Medical University | Cui Z.,Peking University | Chen F.-J.,Peking University | Pei Z.-Y.,Beijing Computing Center Beijing China | And 10 more authors.
Immunology | Year: 2017

Goodpasture's disease is closely associated with HLA, particularly DRB1*1501. Other susceptible or protective HLA alleles are not clearly elucidated. The presentation models of epitopes by susceptible HLA alleles are also unclear. We genotyped 140 Chinese patients and 599 controls for four-digit HLA II genes, and extracted the encoding sequences from the IMGT/HLA database. T-cell epitopes of α3(IV)NC1 were predicted and the structures of DR molecule-peptide-T-cell receptor were constructed. We confirmed DRB1*1501 (OR = 4·6, P = 5·7 × 10-28) to be a risk allele for Goodpasture's disease. Arginine at position 13 (ARG13) (OR = 4·0, P = 1·0 × 10-17) and proline at position 11 (PRO11) (OR = 4·0, P = 2·0 × 10-17) on DRβ1, encoded by DRB1*1501, were associated with disease susceptibility. α134-148 (HGWISLWKGFSFIMF) was predicted as a T-cell epitope presented by DRB1*1501. Isoleucine137, tryptophan140, glycine142, phenylalanine143 and phenylalanine145, were presented in peptide-binding pockets 1, 4, 6, 7 and 9 of DR2b, respectively. ARG13 in pocket 4 interacts with tryptophan140 and forms a hydrogen bond. In conclusion, we propose a mechanism for DRB1*1501 susceptibility for Goodpasture's disease through encoding ARG13 and PRO11 on MHC-DRβ1 chain and presenting T-cell epitope, α134-148, with five critical residues. © 2017 John Wiley & Sons Ltd.

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