Human leukocyte antigen class II DQB1*0301, DRB1*1101 alleles and spontaneous clearance of hepatitis C virus infection: A meta-analysis

被引:67
作者
Hong, Xin [1 ]
Yu, Rong-Bin [1 ]
Sun, Nan-Xiong [2 ]
Wang, Bin [3 ]
Xu, Yao-Chu [1 ]
Wu, Guan-Ling [4 ]
机构
[1] Nanjing Med Univ, Sch Publ Hlth, Dept Epidemiol & Biostat, Nanjing 210029, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Res Lab Infect Dis, Affiliated Hosp 1, Nanjing 210029, Jiangsu, Peoples R China
[3] Nanjing Med Univ, Dept Pharmacol, Nanjing 210029, Jiangsu, Peoples R China
[4] Nanjing Med Univ, Dept Microbiol, Nanjing 210029, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Human leukocyte antigen; Genetic polymorphism; DQB1*0301; DRB1*1101; Hepatitis C virus; Spontaneous clearance; Meta-analysis;
D O I
10.3748/wjg.v11.i46.7302
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To assess the associations of human leukocyte antigen (HLA) class II DQB1*0301 and/or DRB1*1101 allele with spontaneous hepatitis C virus (HCV) clearance by meta-analysis of individual dataset from all studies published till date. METHODS: To clarify the impact of HLA class II polymorphisms on viral clearance, we performed a meta-analysis of the published data from 11 studies comparing the frequencies of DQB1*0301 and DRB1*1101 alleles in individuals with spontaneous resolution to those with persistent infection. As we identified the heterogeneity between studies, summary statistical data were calculated based on a random-effect model. RESULTS: Meta-analyses yielded summary estimates-odds ratio (OR) of 2.36 [95% CI (1.62, 3.43), P < 0.00001] and 2.02 [95% CI (1.56, 2.62), P < 0.00001] for the effects of DQB1*0301 and DRB1*1101 alleles on spontaneous clearance of HCV, respectively. CONCLUSION: These results support the hypothesis that specific HLA class II alleles might influence the susceptibility or resistance to persistent HCV infection. Both DQB1*0301 and DRB1*1101 are protective alleles and present HCV epitopes more effectively to CD4(+)T lymphocytes than others, and subjects with these two alleles are at a lower risk of developing chronic HCV infection. Large, multi-ethnic confirmatory and well-designed studies are needed to determine the host genetic determinants of HCV infection. (C) 2005 The WJG Press and Elsevier Inc. All rights reserved.
引用
收藏
页码:7302 / 7307
页数:6
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