Human leukocyte antigen class II (DRB1 and DQB1) alleles and haplotypes frequencies in patients with pemphigus vulgaris among the Serbian population

被引:11
|
作者
Zivanovic, D. [1 ]
Bojic, S. [2 ]
Medenica, L. [1 ,3 ]
Andric, Z. [4 ]
Popadic, D. [5 ]
机构
[1] Clin Ctr Serbia, Clin Dermatovenereol, 2 Pasterova St, Belgrade 11000, Serbia
[2] Univ Belgrade, Fac Biol, Belgrade, Serbia
[3] Univ Belgrade, Sch Med, Dept Dermatovenereol, Belgrade, Serbia
[4] Blood Transfus Inst Serbia, Tissue Typing Dept, Belgrade, Serbia
[5] Univ Belgrade, Inst Microbiol & Immunol, Sch Med, Belgrade, Serbia
关键词
HLA class II alleles; HLA haplotypes; Pemphigus vulgaris; ITALIAN PATIENTS; HLA-A; JAPANESE PATIENTS; JEWISH PATIENTS; ASSOCIATION; HLA-DRB1; SUSCEPTIBILITY; FOLIACEUS; PEPTIDES; MARKERS;
D O I
10.1111/tan.12796
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The etiology of pemphigus vulgaris (PV) is multifactorial and includes genetic, environmental, hormonal, and immunological factors. Inheritance of certain Human class II leukocyte antigen (HLA) alleles is by far the best-established predisposing factor for the development of PV. Class II HLA alleles vary among racial/ethnic backgrounds. We have determined an association between HLA class II alleles and PV among the Serbian population. A total of 72 patients with confirmed diagnosis of PV were genotyped for HLA class II alleles. HLA frequencies were compared with unrelated healthy bone marrow donors. The statistical significance of differences between patients and controls was evaluated using Fisher's exact test. The DRB1*04 and DRB1*14 allelic groups were associated with PV (P adj = 4.45 x 10(-13) and 4.06 x 10(-19) respectively), while HLA-DRB1*11 was negatively associated with PV (P adj = 0.0067) suggesting a protective role. DRB1*04:02, DRB1*14:04, DQB1*03:02 and DQB1*05:03 alleles were shown to be strongly associated with PV (P adj = 1.63 x 10(-12), 5.20 x 10(-7), 1.28 x 10(-6), and 4.44 x 10(-5), respectively). The frequency of HLA DRB1*04-DQB1*03 and HLA DRB1*14-DQB1*05 haplotypes in PV patients was significantly higher than in controls (31.3% vs 8.8%, P adj = 7.66 x 10(-8) and 30.6% vs 6.3%, P adj = 3.22 x 10(-10), respectively). At high-resolution level, statistical significance was observed in HLA-DRB1*04:02-DQB1*03:02 and HLA-DRB1*14:04-DQB1*05:03 haplotypes (P adj = 5.55 x 10(-12), and P adj = 3.91 x 10(-6), respectively). Our findings suggest that HLA-DRB1*04:02, DRB1*14:04, HLA-DQB1*03:02 and DQB1*05:03 alleles and HLA-DRB1*04:02-DQB1*03:02 and HLA-DRB1*14:04-DQB1*05:03 haplotypes are genetic markers for susceptibility for PV, while DRB1*11 allelic group appears protective in Serbian population.
引用
收藏
页码:367 / 374
页数:8
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