Strong Influence of Human Leukocyte Antigen (HLA)-DP Gene Variants on Development of Persistent Chronic Hepatitis B Virus Carriers in the Han Chinese Population

被引:145
作者
Guo, Xiuchan [1 ,2 ,3 ]
Zhang, Yong [2 ]
Li, Ji [3 ]
Ma, Jingchen [4 ]
Wei, Zuli [5 ]
Tan, Wenjie [6 ]
O'Brien, Stephen J. [3 ]
机构
[1] Wenzhou Med Coll, Zhejiang Prov Key Lab Med Genet, Sch Lab Med & Life Sci, Wenzhou, Zhejiang, Peoples R China
[2] Chinese Ctr Dis Control & Prevent, State Key Lab Infect Dis Prevent & Control, Inst Viral Dis Control & Prevent, Beijing, Peoples R China
[3] NCI, Lab Genom Divers, Ctr Canc Res, NIH, Frederick, MD 21701 USA
[4] Hebei Prov Ctr Dis Control & Prevent, Shijiazhuang, Peoples R China
[5] Luohes Ctr Dis Control & Prevent, Luohe City, Henan, Peoples R China
[6] Chinese Ctr Dis Control & Prevent, Biotech Ctr Viral Dis Emergency, Inst Viral Dis Control & Prevent, Beijing, Peoples R China
基金
美国国家卫生研究院;
关键词
CHRONIC VIRAL-HEPATITIS; HEPATOCELLULAR-CARCINOMA; INFECTIOUS-DISEASES; ASSOCIATION; HLA; POLYMORPHISMS; CLEARANCE; SUSCEPTIBILITY; BINDING; KOREA;
D O I
10.1002/hep.24048
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Chronic hepatitis B virus (HBV) infection is a major health issue, especially in Asia. A recent genome-wide association study (GWAS) implicated genetic variants in the human leukocyte antigen (HLA)-DP locus associated with chronic hepatitis B in Japanese and Thai populations. To confirm whether the polymorphisms at the HLA-DP genes are associated with persistent chronic HBV infection in Han Chinese, we conducted an independent casecontrol study using 521 persistent chronic HBV carriers and 819 controls that included 571 persons with HBV natural clearance and 248 never HBV-infected (healthy) individuals. Eleven single nucleotide polymorphisms (SNPs) in a region including HLA-DPA and HLA-DPB and an adjacent SNP in strong linkage disequilibrium (LD) with a neighboring HLA-DR13 locus were genotyped using the TaqMan SNP genotyping assay. Eleven variants at HLA-DP showed a strong association with persistent chronic HBV carrier status (P = 1.82 X 10(-12) to 0.01). We also stratified the analysis by HBV clearance status to test the association between these polymorphisms and HBV natural clearance; similar results were obtained (P = 2.70 x 10(-1)1 to 0.003). Included SNPs define highly structured haplotypes that were also strongly associated with HBV chronic infection (block 1: odds ratio [OR] = 0.54, P = 8.73 x 10(-7); block 2: OR = 1.98, P = 1.37 x 10(-10)). These results further confirm that genetic variants in the HLA-DP locus are strongly associated with persistent HBV infection in the Han Chinese population. (HEPATOLOGY 2011;53:422-428)
引用
收藏
页码:422 / 428
页数:7
相关论文
共 25 条
[1]
Association between hepatitis B virus infection and HLA-DR type in Korea [J].
Ahn, SH ;
Han, KH ;
Park, JY ;
Lee, CK ;
Kang, SW ;
Chon, CY ;
Kim, YS ;
Park, K ;
Kim, DK ;
Moon, YM .
HEPATOLOGY, 2000, 31 (06) :1371-1373
[2]
Haploview: analysis and visualization of LD and haplotype maps [J].
Barrett, JC ;
Fry, B ;
Maller, J ;
Daly, MJ .
BIOINFORMATICS, 2005, 21 (02) :263-265
[3]
Tuberculosis and chronic hepatitis B virus infection in Africans and variation in the vitamin D receptor gene [J].
Bellamy, R ;
Ruwende, C ;
Corrah, T ;
McAdam, KPWJ ;
Thursz, M ;
Whittle, HC ;
Hill, AVS .
JOURNAL OF INFECTIOUS DISEASES, 1999, 179 (03) :721-724
[4]
Ben-Ari Z, 2003, AM J GASTROENTEROL, V98, P144, DOI 10.1111/j.1572-0241.2003.07179.x
[5]
HLA and Infectious Diseases [J].
Blackwell, Jenefer M. ;
Jamieson, Sarra E. ;
Burgner, David .
CLINICAL MICROBIOLOGY REVIEWS, 2009, 22 (02) :370-+
[6]
Clinical significance of hepatitis B virus genotypes [J].
Chu, CJ ;
Lok, ASF .
HEPATOLOGY, 2002, 35 (05) :1274-1276
[7]
Association of estrogen receptor α polymorphisms with susceptibility to chronic hepatitis B virus infection [J].
Deng, GH ;
Zhou, GQ ;
Zhai, Y ;
Li, SQ ;
Li, XH ;
Li, Y ;
Zhang, RF ;
Yao, ZJ ;
Shen, Y ;
Qiang, BQ ;
Wang, YM ;
He, FC .
HEPATOLOGY, 2004, 40 (02) :318-326
[8]
Functional analysis of HLA-DP polymorphism:: a crucial role for DPβ residues 9, 11, 35, 55, 56, 69 and 84-87 in T cell allorecognition and peptide binding [J].
Díaz, G ;
Amicosante, M ;
Jaraquemada, D ;
Butler, RH ;
Guillén, MV ;
Sánchez, M ;
Nombela, C ;
Arroyo, J .
INTERNATIONAL IMMUNOLOGY, 2003, 15 (05) :565-576
[9]
Genetics of infectious diseases [J].
Frodsham, AJ ;
Hill, AVS .
HUMAN MOLECULAR GENETICS, 2004, 13 :R187-R194
[10]
Molecular analysis of HLA class II associations with hepatitis B virus clearance and vaccine non responsiveness [J].
Godkin, A ;
Davenport, M ;
Hill, AVS .
HEPATOLOGY, 2005, 41 (06) :1383-1390