Abstract | 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.
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Authors | Xin Hong, Rong-Bin Yu, Nan-Xiong Sun, Bin Wang, Yao-Chu Xu, Guan-Ling Wu |
Journal | World journal of gastroenterology
(World J Gastroenterol)
Vol. 11
Issue 46
Pg. 7302-7
(Dec 14 2005)
ISSN: 1007-9327 [Print] United States |
PMID | 16437632
(Publication Type: Journal Article, Meta-Analysis, Research Support, Non-U.S. Gov't)
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Chemical References |
- HLA-DQ Antigens
- HLA-DQ beta-Chains
- HLA-DQB1 antigen
- HLA-DR Antigens
- HLA-DRB1 Chains
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Topics |
- Alleles
- HLA-DQ Antigens
(genetics)
- HLA-DQ beta-Chains
- HLA-DR Antigens
(genetics)
- HLA-DRB1 Chains
- Hepacivirus
(isolation & purification)
- Hepatitis C
(genetics, immunology, virology)
- Humans
- Polymorphism, Genetic
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