Source:http://linkedlifedata.com/resource/pubmed/id/17033822
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11
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pubmed:dateCreated |
2006-11-23
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pubmed:abstractText |
In general, cytokines encoded by different genes of human genome might strongly influence host cell-mediated immune responses, which play an important role in the clearance of virus by the infected host. Interferon gamma (IFN-gamma) produced by T lymphocytes and natural killer cells plays an essential role in affecting cellular immune responses. A functional study demonstrated that two single nucleotide polymorphisms located in the IFN-gamma gene intron (at positions +874 and +2109) were involved in its transcriptional regulation. The aim of this study was to evaluate whether IFN-gamma gene polymorphisms or its haplotypes might be associated with predisposition to hepatitis B virus (HBV) infection in the Chinese population. The study included 181 cases with HBV infection and 272 gender, age-matched healthy controls. All genotyping were identified by polymerase chain reaction in association with the measurement of amplification refractory mutation system. A significant difference was observed between case and control groups. The frequency of +874A allele was significantly higher in patients than in controls (OR = 2.25, 95%CI = 1.69-2.99, P < 0.0001). However, no significant difference was found in the allelic frequencies of IFN-gamma +2109A/G between cases and controls (P > 0.05). By haplotype analysis, the frequency of haplotype AG (+874A and +2109G) revealed a significant difference in the cases in comparison to controls (P < 0.0001). Multiple logistic regression analysis showed that individuals possessing haplotype AG had an increased likelihood of HBV infection (OR = 8.14, 95%CI = 4.98-13.30). Our results suggest that haplotype AG containing +874A and +2109G may be a crucial risk factor of genetic susceptibility to HBV infection in the Chinese population.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0093-7711
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
58
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
859-64
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:17033822-Adolescent,
pubmed-meshheading:17033822-Adult,
pubmed-meshheading:17033822-Asian Continental Ancestry Group,
pubmed-meshheading:17033822-China,
pubmed-meshheading:17033822-Female,
pubmed-meshheading:17033822-Haplotypes,
pubmed-meshheading:17033822-Hepatitis B,
pubmed-meshheading:17033822-Hepatitis B virus,
pubmed-meshheading:17033822-Humans,
pubmed-meshheading:17033822-Interferon-gamma,
pubmed-meshheading:17033822-Linkage Disequilibrium,
pubmed-meshheading:17033822-Male,
pubmed-meshheading:17033822-Middle Aged,
pubmed-meshheading:17033822-Polymorphism, Genetic,
pubmed-meshheading:17033822-Population
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pubmed:year |
2006
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pubmed:articleTitle |
Association of interferon-gamma gene haplotype in the Chinese population with hepatitis B virus infection.
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pubmed:affiliation |
Medical College, Shandong University, Jinan, Shandong Province, China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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