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Principal contribution of HLA-DQ alleles, DQB106:04 and DQB103:01, to disease resistance against primary biliary cholangitis in a Japanese population
Identification of the primary allele(s) in HLA class II associated diseases remains challenging because of a tight linkage between alleles of HLA-DR and -DQ loci. In the present study, we determined the genotypes of seven HLA loci ( HLA-A , -B , -DRB1 , -DQA1 , -DQB1 , -DPA1 and -DPB1 ) for 1200 Jap...
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Published in: | Scientific reports 2017-09, Vol.7 (1), p.11093-10, Article 11093 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Identification of the primary allele(s) in
HLA class II
associated diseases remains challenging because of a tight linkage between alleles of
HLA-DR
and
-DQ
loci. In the present study, we determined the genotypes of seven
HLA
loci (
HLA-A
,
-B
,
-DRB1
,
-DQA1
,
-DQB1
,
-DPA1
and
-DPB1
) for 1200 Japanese patients with primary biliary cholangitis and 1196 controls. Observation of recombination derivatives facilitated an evaluation of the effects of individual
HLA
alleles consisting of disease-prone/disease-resistant
HLA
haplotypes. Consequently, a primary contribution of
DQB1*06:04
(odds ratio: 0.19, p = 1.91 × 10
−22
),
DQB1*03:01
(odds ratio: 0.50, p = 6.76 × 10
−10
),
DRB1*08:03
(odds ratio: 1.75, p = 1.01 × 10
−7
) and
DQB1*04:01
(odds ratio: 1.50, p = 9.20 × 10
−6
) was suggested. Epistasis of the protective
DQB1*06:04
to risk conferred by
DRB1*08:03
was demonstrated by subpopulation analysis, implicating the presence of an active immunological mechanism that alleviates pathogenic autoimmune reactions. Further, the contribution of the aforementioned
HLA
alleles as well as an
HLA-DP
allele,
DPB1*02:01
to the association signals of 304 loci among 4103 SNPs in the
HLA
region at the genome-wide level of significance (p values less than 5 × 10
−8
) was demonstrated by the stepwise exclusion of the individuals possessing these
HLA
alleles from the comparison. |
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ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/s41598-017-11148-6 |