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细胞因子基因多态性与乙型肝炎病毒宫内感染易感性的研究
引用本文:朱启镕,顾绍庆,俞惠,王建设,顾新焕,董左权,费林娥.细胞因子基因多态性与乙型肝炎病毒宫内感染易感性的研究[J].中华流行病学杂志,2005,26(4):236-239.
作者姓名:朱启镕  顾绍庆  俞惠  王建设  顾新焕  董左权  费林娥
作者单位:200032,上海,复旦大学附属儿科医院传染科
基金项目:国家自然科学基金资助项目(30271365)
摘    要:目的对前期研究发现宫内乙型肝炎病毒(HBV)感染免疫失败儿童表达异常的细胞因子TNFα、IFNγ、IL4和IL10,研究其相关基因位点单核苷酸多态性与HBV宫内感染易感性的关系。方法在确定时限内选择乙型肝炎疫苗随访门诊中符合纳入标准的高危儿童,系宫内感染HBV经免疫接种失败者为Ⅰ组,免疫接种有效者为Ⅱ组和非携带HBV母亲所生健康儿童作对照。应用实时荧光定量PCR技术检测TNFα基因-238位点、IFNγ基因+874位点、IL4基因-590位点和IL10基因-1082位点的单核苷酸多态性。结果TNFα基因-238位点A等位基因频率Ⅰ组显著高于Ⅱ组(χ2=6.797,P<0.05),并与对照组相比较差异有显著性(χ2=9.513,P<0.05),而Ⅱ组与对照组比较χ2=0.047,P>0.05;IFNγ基因+874位点A基因频率Ⅰ组与Ⅱ组比较χ2=7.238,P<0.05,与对照组比较χ2=5.199,P<0.05,Ⅱ组与对照组比较χ2=0.602,P>0.05;IL4基因-590位点C/T等位基因频率Ⅰ组与Ⅱ组比较χ2=0.632,P>0.05,Ⅰ组与对照组比较χ2=0.584,P>0.05,Ⅱ组与对照组比较χ2=0.004,P>0.05;IL10基因-1082位点G等位基因频率Ⅱ组与Ⅰ组比较χ2=10.359,P<0.001,Ⅱ组与对照组比较χ2=35.418,P<0.001,但是Ⅰ组与对照组比较差异无显著性(χ2=1.759,P>0.05)。结论TNFα基因-238位点A等位基因和IFNγ基因+874位

关 键 词:感染易感性  细胞因子基因多态性  乙型肝炎病毒(HBV)  单核苷酸多态性  IFN-γ基因  IL-10基因  P〉0.05  IL-4基因  等位基因频率  PCR技术检测  TNF-α基因  乙型肝炎疫苗  免疫接种失败  实时荧光定量  宫内感染  对照组  表达异常
收稿时间:2005/12/5 0:00:00
修稿时间:2004年12月5日

Relationship between cytokine gene polymorphism and susceptibility to hepatitis B virus intrauterine infection
ZHU Qi-rong,GU Shao-qing,YU Hui,WANG Jian-she,GU Xin-huan,DONG Zuo-quan and FEI Lin-e.Relationship between cytokine gene polymorphism and susceptibility to hepatitis B virus intrauterine infection[J].Chinese Journal of Epidemiology,2005,26(4):236-239.
Authors:ZHU Qi-rong  GU Shao-qing  YU Hui  WANG Jian-she  GU Xin-huan  DONG Zuo-quan and FEI Lin-e
Institution:Department of Infectious Disease, Children's Hospital, Fudan University, Shanghai 200032, China.
Abstract:OBJECTIVE: To explore the possible relationship between cytokines (TNF-alpha, IFN-gamma, IL-4 and IL-10), which were expressed abnormal quantity in the peripheral blood to intrauterine HBV infectious children, gene single nucleotide polymorphism (SNP) and susceptibility to HBV intrauterine infection. METHODS: A cross sectional study on molecular epidemiology was carried out. The subjects were selected from outpatients of the hepatitis B vaccine special clinics of our hospital. According to intrant criteria, children under high risk of HBV intrauterine infection were divided into immuno-failure group (group I) and immuno-effective group (group II) while children without high risk were included in the control group. Four gene SNP sites of TNF-alpha-238, IFN-gamma + 874, IL-4-590 and IL-10-1082 region were determined by real-time quantitative fluorescent PCR. RESULTS: Significant differences of TNF-alpha-238 A allele frequency were found between group I and group II (chi(2) = 6.797, P < 0.05) as well as between group I and control group (chi(2) = 9.513, P < 0.05). No evident difference of TNF-alpha-238 A was found between group II and control group (chi(2) = 0.047, P > 0.05). Significant differences of IFN-gamma + 874 A allele frequency were found between group I and group II (chi(2) = 7.238, P < 0.05), and between group I and the controls (chi(2) = 5.199, P < 0.05) but no significant difference was found between group II and control group (chi(2) = 0.602, P > 0.05). Significant differences of IL-4-590 C/T allele frequency were not found between group I and group II (chi(2) = 0.632, P > 0.05), group I and control group (chi(2) = 0.584, P > 0.05), or between group II and control group (chi(2) = 0.004, P > 0.05) respectively. Significant differences of IL-10-1082 G allele frequency were found between group II and group I (chi(2) = 10.359, P < 0.001), and between group II and the controls (chi(2) = 35.418, P < 0.001), but not found between group I and control group (chi(2) = 1.759, P > 0.05). CONCLUSION: This study suggested the possibility that TNF-alpha-238 A allele and IFN-gamma + 874 A allele were associated with HBV intrauterine infection. There was no evident relationship between IL-4-590 C/T allele SNP and susceptibility to HBV intrauterine infection, but the IL-10-1082 G allele seemed to be associated with preventive efficacy to HBV intrauterine infection.
Keywords:Hepatitis B virus  Intrauterine infection  Cytokine  Gene polymorphism
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