期刊论文详细信息
BMC Nephrology
The association of HLA-DQB1, -DQA1 and -DPB1 alleles with anti- glomerular basement membrane (GBM) disease in Chinese patients
Ming-Hui Zhao1  Xu-Jie Zhou1  Peng-Cheng Xu1  Rui Yang1  Zhao Cui1  Min Chen1  Huan Luo1 
[1] Renal Division, Department of Medicine, Peking University First Hospital; Institute of Nephrology, Peking University; Key Laboratory of Renal Disease, Ministry of Health of China; Beijing 100034, China
关键词: Chinese;    HLA-DPB1*0401;    Anti-GBM disease;   
Others  :  1083262
DOI  :  10.1186/1471-2369-12-21
 received in 2010-12-04, accepted in 2011-05-13,  发布年份 2011
PDF
【 摘 要 】

Background

Human leukocyte antigen (HLA) alleles are associated with many autoimmune diseases, including anti-glomerular basement membrane (GBM) disease. In our previous study, it was demonstrated that HLA-DRB1*1501 was strongly associated with anti-GBM disease in Chinese. However, the association of anti-GBM disease and other HLA class II genes, including HLA-DQB1, -DQA1,-DPB1 alleles, has rarely been investigated in Asian, especially Chinese patients. The present study further analyzed the association between anti-GBM disease and HLA-DQB1, -DQA1, and -DPB1 genes. Apart from this, we tried to locate the potential risk amino acid residues of anti-GBM disease.

Methods

This study included 44 Chinese patients with anti-GBM disease and 200 healthy controls. The clinical and pathological data of the patients were collected and analyzed. Typing of HLA-DQB1, -DQA1 and -DPB1 alleles were performed by bi-directional sequencing of exon 2 using the SeCoreTM Sequencing Kits.

Results

Compared with normal controls, the prevalence of HLA-DPB1*0401 was significantly lower in patients with anti-GBM disease (3/88 vs. 74/400, p = 4.4 × 10-4, pc = 0.039). Comparing with normal controls, the combination of presence of DRB1*1501 and absence of DPB1*0401 was significantly prominent among anti-GBM patients (p = 2.0 × 10-12, pc = 1.7 × 10-10).

Conclusions

HLA-DPB1*0401 might be a protective allele to anti-GBM disease in Chinese patients. The combined presence of DRB1*1501 and absence of DPB1*0401 might have an even higher risk to anti-GBM disease than HLA-DRB1*1501 alone.

【 授权许可】

   
2011 Luo et al; licensee BioMed Central Ltd.

【 预 览 】
附件列表
Files Size Format View
20150101013829315.pdf 143KB PDF download
【 参考文献 】
  • [1]Saus J, Wieslander J, Langeveld JP, Quinones S, Hudson BG: Identification of the Goodpasture antigen as the alpha 3(IV) chain of collagen IV. J Biol Chem 1988, 263:13374-13380.
  • [2]Shiina T, Inoko H, Kulski JK: An update of the HLA genomic region, locus information and disease associations: 2004. Tissue Antigens 2004, 64:631-649.
  • [3]Phelps RG, Rees AJ: The HLA complex in Goodpasture's disease: a model for analyzing susceptibility to autoimmunity. Kidney Int 1999, 56:1638-1653.
  • [4]Kitagawa W, Imai H, Komatsuda A, Maki N, Wakui H, Hiki Y, Sugiyama S: The HLA-DRB1*1501 allele is prevalent among Japanese patients with anti-glomerular basement membrane antibody-mediated disease. Nephrol Dial Transplant 2008, 23:3126-3129.
  • [5]Yang R, Cui Z, Zhao J, Zhao MH: The role of HLA-DRB1 alleles on susceptibility of Chinese patients with anti-GBM disease. Clin Immunol 2009, 133:245-250.
  • [6]Cui Z, Zhao J, Jia XY, Zhu SN, Zhao MH: Clinical features and outcomes of anti-glomerular basement membrane disease in older patients. Am J Kidney Dis 2011, 57:575-582.
  • [7]Pusey CD: Anti-glomerular basement membrane disease. Kidney Int 2003, 64:1535-1550.
  • [8]Cui Z, Zhao MH: Avidity of anti-glomerular basement membrane autoantibodies was associated with disease severity. Clin Immunol 2005, 116:77-82.
  • [9]Miller SA, Dykes DD, Polesky HF: A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 1988, 16:1215.
  • [10]Kanterakis S, Magira E, Rosenman KD, Rossman M, Talsania K, Monos DS: SKDM human leukocyte antigen (HLA) tool: A comprehensive HLA and disease associations analysis software. Hum Immunol 2008, 69:522-525.
  • [11]Huey B, McCormick K, Capper J, Ratliff C, Colombe BW, Garovoy MR, Wilson CB: Associations of HLA-DR and HLA-DQ types with anti-GBM nephritis by sequence-specific oligonucleotide probe hybridization. Kidney Int 1993, 44:307-312.
  • [12]Fisher M, Pusey CD, Vaughan RW, Rees AJ: Susceptibility to anti-glomerular basement membrane disease is strongly associated with HLA-DRB1 genes. Kidney Int 1997, 51:222-229.
  • [13]Toussirot E, Auge B, Tiberghien P, Chabod J, Cedoz JP, Wendling D: HLA-DRB1 alleles and shared amino acid sequences in disease susceptibility and severity in patients from eastern France with rheumatoid arthritis. J Rheumatol 1999, 26:1446-1451.
  • [14]DeLuca GC, Ramagopalan SV, Herrera BM, Dyment DA, Lincoln MR, Montpetit A, Pugliatti M, Barnardo MC, Risch NJ, Sadovnick AD, Chao M, Sotgiu S, Hudson TJ, Ebers GC: An extremes of outcome strategy provides evidence that multiple sclerosis severity is determined by alleles at the HLA-DRB1 locus. Proc Natl Acad Sci USA 2007, 104:20896-20901.
  • [15]Kotb M, Norrby-Teglund A, McGeer A, El-Sherbini H, Dorak MT, Khurshid A, Green K, Peeples J, Wade J, Thomson G, Schwartz B, Low DE: An immunogenetic and molecular basis for differences in outcomes of invasive group A streptococcal infections. Nat Med 2002, 8:1398-1404.
  • [16]Ooi JD, Holdsworth SR, Kitching AR: Advances in the pathogenesis of Goodpasture's disease: from epitopes to autoantibodies to effector T cells. J Autoimmun 2008, 31:295-300.
  • [17]Phelps RG, Jones V, Turner AN, Rees AJ: Properties of HLA class II molecules divergently associated with Goodpasture's disease. Int Immunol 2000, 12:1135-1143.
  文献评价指标  
  下载次数:5次 浏览次数:11次