A meta-analysis of the relation of polymorphism at sites-1082 and-592 of the IL-10 gene promoter with susceptibility and clearance to persistent hepatitis B virus infection in the Chinese population

被引:27
作者
Zhang, T. -C. [1 ]
Pan, F. -M. [1 ]
Zhang, L. -Z. [2 ]
Gao, Y. -F. [2 ]
Zhang, Z. -H. [2 ]
Gao, J. [1 ]
Ge, R. [1 ]
Mei, Y. [1 ]
Shen, B. -B. [1 ]
Duan, Z. -H. [1 ]
Li, X. [2 ]
机构
[1] Anhui Med Univ, Acad Publ Hlth, Dept Epidemiol & Biostat, Hefei 230032, Anhui, Peoples R China
[2] Anhui Med Univ, Affiliated Hosp 1, Dept Infect Dis, Hefei 230032, Anhui, Peoples R China
关键词
Hepatitis B virus; IL-10; gene; Polymorphism; Meta-analysis; CYTOTOXIC T-LYMPHOCYTES; INTERLEUKIN-10; GENE; HEPATOCELLULAR-CARCINOMA; DISEASE PROGRESSION; IN-VIVO; ASSOCIATION; EXPRESSION; HAPLOTYPES; ALLELES; RISK;
D O I
10.1007/s15010-010-0075-3
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Up to now, many publications about the Chinese population have evaluated the correlation between interleukin-10 (IL-10) -1082 and -592 polymorphisms and persistent hepatitis B virus (HBV) infection. However, the results remain inconclusive. In order to resolve this conflict, a meta-analysis was performed. Seven studies were included and dichotomous data are presented as the odds ratio (OR) with a 95% confidence interval (CI). The results of our study suggest that carriers of the IL-10 -592A allele were more likely to clear HBV spontaneously in the Chinese pooled population (A vs. C: OR = 0.799, 95% CI = 0.678-0.941, P = 0.007; AC vs. AA: OR = 1.343, 95% CI = 1.017-1.684, P = 0.011; AA vs. AC + CC: OR = 0.736, 95% CI = 0.594-0.912; AA + AC vs. CC: OR = 0.588, 95% CI = 0.408-0.848, P = 0.004) and the IL-10 -1082A allele was associated with significantly reduced persistent HBV infection risk in Chinese (A vs. G: OR = 0.701, 95% CI = 0.494-0.996, P = 0.047; AA vs. GG + GA: OR = 0.684, 95% CI = 0.476-0.982, P = 0.040). Persistent HBV infection susceptibility is associated with the gene polymorphism IL-10 -1082GA in the Chinese population and the clearance of HBV is associated with the gene polymorphism IL-10 -592CA in the Chinese population.
引用
收藏
页码:21 / 27
页数:7
相关论文
共 30 条
[1]   Association of TNF-α-308 polymorphism with the outcome of hepatitis B virus infection in Turkey [J].
Basturk, Bilkay ;
Karasu, Zeki ;
Kilic, Murat ;
Ulukaya, Sezgin ;
Boyacioglu, Sedat ;
Oral, Barbaros .
INFECTION GENETICS AND EVOLUTION, 2008, 8 (01) :20-25
[2]  
Ben-Ari Z, 2003, AM J GASTROENTEROL, V98, P144, DOI 10.1111/j.1572-0241.2003.07179.x
[3]   Interleukin-10 determines viral clearance or persistence in vivo [J].
Brooks, David G. ;
Trifilo, Matthew J. ;
Edelmann, Kurt H. ;
Teyton, Luc ;
McGavern, Dorian B. ;
Oldstone, Michael B. A. .
NATURE MEDICINE, 2006, 12 (11) :1301-1309
[4]   Association of Candidate Susceptible Loci With Chronic Infection With Hepatitis B Virus in a Chinese Population [J].
Chen, Ding-Qiang ;
Zeng, Yong ;
Zhou, Jie ;
Yang, Ling ;
Jiang, Shibo ;
Huang, Jian-Dong ;
Lu, Liwei ;
Zheng, Bo-Jian .
JOURNAL OF MEDICAL VIROLOGY, 2010, 82 (03) :371-378
[5]  
Crawley E, 1999, ARTHRITIS RHEUM-US, V42, P1101, DOI 10.1002/1529-0131(199906)42:6<1101::AID-ANR6>3.0.CO
[6]  
2-Y
[7]   Microsatellite alleles and single nucleotide polymorphisms (SNP) combine to form four major haplotype families at the human interleukin-10 (IL-10) locus [J].
Eskdale, J ;
Keijsers, V ;
Huizinga, T ;
Gallagher, G .
GENES AND IMMUNITY, 1999, 1 (02) :151-155
[8]   Polymorphisms of some cytokines and chronic hepatitis B and C virus infection [J].
Gao, Qiu-Ju ;
Liu, Dian-Wu ;
Zhang, Shi-Yong ;
Jia, Min ;
Wang, Li-Min ;
Wu, Li-Hong ;
Wang, Shu-Yun ;
Tong, Li-Xin .
WORLD JOURNAL OF GASTROENTEROLOGY, 2009, 15 (44) :5610-5619
[9]   CYTOTOXIC T-LYMPHOCYTES INHIBIT HEPATITIS-B VIRUS GENE-EXPRESSION BY A NONCYTOLYTIC MECHANISM IN TRANSGENIC MICE [J].
GUIDOTTI, LG ;
ANDO, K ;
HOBBS, MV ;
ISHIKAWA, T ;
RUNKEL, L ;
SCHREIBER, RD ;
CHISARI, FV .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (09) :3764-3768
[10]   Intracellular inactivation of the hepatitis B virus by cytotoxic T lymphocytes [J].
Guidotti, LG ;
Ishikawa, T ;
Hobbs, MV ;
Matzke, B ;
Schreiber, R ;
Chisari, FV .
IMMUNITY, 1996, 4 (01) :25-36