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前炎性细胞因子基因多态性与乙型肝炎病毒感染的关系
引用本文:邢培祥,ZOU Ming-jin,邹明瑾,邢全台,王洪春,汪运山.前炎性细胞因子基因多态性与乙型肝炎病毒感染的关系[J].山东大学学报(医学版),2007,45(12):1229-1233.
作者姓名:邢培祥  ZOU Ming-jin  邹明瑾  邢全台  王洪春  汪运山
作者单位:1. 山东大学齐鲁医院检验科,济南,250012
2. 山东大学齐鲁医院感染科,济南,250012
3. 山东大学临床医学院济南市中心医院,中心实验室,济南,250013
摘    要:目的探讨肿瘤坏死因子-α(TNF-α)和白细胞介素-6(IL-6)基因单核苷酸多态性(SNP)与乙型肝炎病毒(HBV)感染的关系。方法采用基因芯片技术检测150例HBV感染患者(病例组)和不相关联的100例急性乙型肝炎病毒感染自行恢复后对照人群(对照组)中TNF-α-238G/A,-308G/A和IL-6-597G/A,-174G/C,-572G/C位点SNP。结果TNF-α-308GG基因型和G等位基因频率,病例组明显高于对照组(P<0.01,相对危险度[OR]=6.71及P<0.01,OR=2.22);TNF 308AA基因型与抗病毒治疗具有协同作用(P<0.05,OR=2.91)。未见IL -6和TNF-α其他位点的SNP与病例组有任何相关性。结论TNF-308GG基因型及其等位基因G与乙型肝炎病毒感染易感性相关,而TNF-308AA基因型则与抗病毒治疗具有协同抗病毒作用。

关 键 词:细胞因子  多态性  单核苷酸  基因芯片  乙型肝炎病毒
文章编号:1671-7554(2007)12-1229-05
收稿时间:2006-11-28
修稿时间:2006年11月28

Relationship between proinflammatory cytokine gene polymorphisms and diseases of HBV infection
XING Pei-xiang,ZOU Ming-jin,XING Quan-tai,WANG Hong-chun,WANG Yun-shan.Relationship between proinflammatory cytokine gene polymorphisms and diseases of HBV infection[J].Journal of Shandong University:Health Sciences,2007,45(12):1229-1233.
Authors:XING Pei-xiang  ZOU Ming-jin  XING Quan-tai  WANG Hong-chun  WANG Yun-shan
Institution:1. Qilu Hospital of Shandong University, a. Department of Clinical Laboratory, b. Department of Epidemiology; 2. Central Laboratory, Jinan Central Hospital, School of Clinical Medicine, Shandong University
Abstract:ObjectiveTo investigate relationships between the single nucleotide polymorphisms(SNPs) of tumor necrosis factor-α(TNFα) or interleukin-6(IL-6)promoter genes and susceptibility to patients with chronic hepatitis B (HB)in Jinan area. MethodsThe SNPs of the TNF-α(-238G/A and -308G/A) and IL-6(-597G/A, -174G/C and -572G/C) were determined by gene chips in 150 patients infected with hepatitis B virus(HBV) and 100 unrelated healthy controls of self limited HBV infection. ResultFrequencies of TNF-α-308GG genotype and G allele in patients with HBV infection were significantly higher than those in healthy controls(P<0.01,OR=6.71, and P<0.01,OR=2.22, respectively). TNF-308AA genotype had a cooperative effect on the antiviral therapy (P<0.05,OR=2.91). No association was found between any of the other polymorphisms and patients with HBV infection. Conclusion TNF-α-308GG genotype and G allele are significantly related to patients with HBV infection, and TNF-308AA genotype is associated with the response to antiviral therapy.
Keywords:Hepatitis B vires  Cytokine  Polymorphism  single nucleotide  Gene chip
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