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母婴传播中慢性乙型重型肝炎病毒相关变异的研究
引用本文:刘敏,李自雄,路卫,李怀芳,曹广文. 母婴传播中慢性乙型重型肝炎病毒相关变异的研究[J]. 同济大学学报(医学版), 2017, 38(4): 49-54, 59
作者姓名:刘敏  李自雄  路卫  李怀芳  曹广文
作者单位:同济大学附属同济医院妇产科,上海 200065,第二军医大学海军医学系流行病学教研室,上海 200433,第二军医大学长海医院全军烧伤中心,上海 200433,同济大学附属同济医院妇产科,上海 200065,第二军医大学海军医学系流行病学教研室,上海 200433
基金项目:国家自然科学基金重点国际合作项目(81520108021)
摘    要:目的 研究乙型肝炎病毒基因(HBV DNA)preS区内与慢性乙型重型肝炎(chronic severe hepatitis B, CSHB)相关变异在母婴传播过程中的进化趋势。方法收集879例HBsAg阳性孕妇外周血,孕妇分娩后将其新生儿脐带血、完成乙肝疫苗注射后的7月龄婴儿外周血亦纳入队列。通过基因分型和系统发育分析鉴定HBV的母婴传播情况,运用单克隆测序方式检测母子体内HBV preS区中CSHB相关突变情况。结果 HBV B/C基因型中CSHB相关变异C2875T、C2980T、G2988A、C3067T、C3097A、T25G、A76C、A79G、T100C、C102T、C106A、T109G、C135T、T147C、A148G,可通过宫内感染途径传播给新生儿;C2基因型中变异A3097C/G、G132C在HBV宫内感染中存在明显优势(P<0.05;P<0.05)。B2基因型中,变异C3057G、T3060C、C3097A、T3169A、A20G、A76C、C129T,能够通过MCTC途径由母亲传播给7月龄婴儿;C2基因型中以上变异突变率低。结论 在母婴传播过程中,HBV B2基因型中CSHB相关变异较多;婴儿完成接种免疫后,野生型HBV在母婴传播中具有感染优势,进化具有保守性。

关 键 词:乙型肝炎病毒   慢性乙型重型肝炎   变异   宫内感染   母婴传播
收稿时间:2017-02-09

Evolutionary tendency of chronic severe hepatitis B-related mutations in mother-to-child transmission of hepatitis B virus
LIU Min,LI Zi-xiong,LU Wei,LI Huai-fang and CAO Guang-wen. Evolutionary tendency of chronic severe hepatitis B-related mutations in mother-to-child transmission of hepatitis B virus[J]. Journal of Tongji University(Medical Science), 2017, 38(4): 49-54, 59
Authors:LIU Min  LI Zi-xiong  LU Wei  LI Huai-fang  CAO Guang-wen
Affiliation:Dept.of Obstetrics and Gynecology, Tongji Hospital, Tongji University, Shanghai 200065, China,Dept.of Epidemiology, Faculty of Navy Medicine, Second Military Medical University, Shanghai 200433, China,Burn Trauma Center of Changhai Hospital, Second Military Medical University, Shanghai 200433, China,Dept.of Obstetrics and Gynecology, Tongji Hospital, Tongji University, Shanghai 200065, China and Dept.of Epidemiology, Faculty of Navy Medicine, Second Military Medical University, Shanghai 200433, China
Abstract:Objective To study the evolutionary tendency of chronic severe hepatitis B (CSHB)-related mutations in the preS region of hepatitis B virus (HBV) during mother-to-child transmission. Methods Peripheral blood from HBsAg-positive mothers, umbilical cord blood from newborns, and peripheral blood from 7-month old infants who received intact vaccination were collected. Cloning sequencing was conducted to detect the viral mutations. Genotyping and phylogenetics analysis were conducted to determine the mother-to-child transmission of HBV. The Pearson Chi-square test and continuity correction were applied to evaluate the categorical variables. ResultsHBV strains with CSHB-related mutations C2875T, C2980T, G2988A, C3067T, C3097A, T25G, A76C, A79G, T100C, C102T, C106A, T109G, C135T, T147C and A148G could be transmitted to newborns through intrauterine pathway. HBV mutations includingA3097C/G and G132C had survival advantages in intrauterine transmission and chronicity (P<0.05; P<0.05). Genotype B2 HBV strains with mutations C3057G, T3060C, C3097A, T3169A, A20G, A76C, and C129T could be transmitted to 7-month old infants through mother to child transmission, while the similar phenomenon was not observed in genotype C2 HBV strains. Conclusion More CSHB-related mutations could be detected in genotype B2 HBV during mother-to-child transmission. After the immunization, HBV without the CSHB-related mutations has advantage of infecting infants and reflects the conservative nature on evolution perspectives of HBV.
Keywords:hepatitis B virus   chronic severe hepatitis B   mutations   trans-placental HBV transmission   mother-to-child transmission
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