首页> 外文期刊>Journal of Hepatology: The Journal of the European Association for the Study of the Liver >Precore stop codon mutant in chronic hepatitis B virus infection in children: its relation to hepatitis B e seroconversion and maternal hepatitis B surface antigen.
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Precore stop codon mutant in chronic hepatitis B virus infection in children: its relation to hepatitis B e seroconversion and maternal hepatitis B surface antigen.

机译:儿童慢性乙型肝炎病毒感染中的Precor终止密码子突变:与乙型肝炎e血清转化和孕妇乙型肝炎表面抗原的关系。

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BACKGROUND/AIMS: The aims of this study were to investigate the significance of the precore stop codon mutant in the natural course of hepatitis B virus infection in children, and the influence of maternal transmission. METHODS: Sequential sera from 80 hepatitis B virus carrier children both before and after e seroconversion during long-term follow-up were studied using the polymerase chain reaction-amplification created restriction site method. Direct sequencing of the precore region was performed in 89 sera from 32 of the 80 children. RESULTS: The precore stop codon mutant coexisting with wild strain was found in 10% of children initially, and later in 25% of children before e seroconversion. After e seroconversion, wild type was still present in 75% and mutant in 39% of children at the end of follow-up. The mutant alone was present in 15% of anti-HBe positive children without concomitant aminotransferase elevation. Children with earlier emergence of this mutant tended to have higher peak aminotransferase levels. This mutant emerged less frequently in children of hepatitis B virus carrier mothers (37.5%) than in those of non-carrier mothers (65%) (p<0.05). CONCLUSIONS: These observations suggest that this mutant is selected by host immune pressure, but is not an initiator in the loss of immune tolerance during childhood chronic hepatitis B virus infection.
机译:背景/目的:这项研究的目的是调查前核心终止密码子突变体在儿童感染乙型肝炎病毒的自然过程中的意义以及母体传播的影响。方法:采用聚合酶链反应-扩增限制性酶切位点法研究了80例乙型肝炎病毒携带者患儿在长期随访中进行血清学转换前后的序贯血清。在80名儿童中的32名儿童的89个血清中对前核心区进行了直接测序。结果:最初在10%的儿童中发现了与野生菌株共存的前核心终止密码子突变体,随后在进行血清转换之前在25%的儿童中发现了。血清转换后,随访结束时仍有75%的儿童存在野生型,有39%的儿童存在突变型。仅突变体存在于15%的抗HBe阳性儿童中,而不会伴随氨基转移酶升高。具有此突变体较早出现的儿童往往具有较高的峰值氨基转移酶水平。该突变体在乙型肝炎病毒携带者母亲的孩子中出现的频率较低(37.5%),比非携带者母亲的孩子中出现频率较低(65%)(p <0.05)。结论:这些观察结果表明,该突变体是通过宿主免疫压力选择的,但不是儿童慢性乙型肝炎病毒感染期间免疫耐受丧失的引发剂。

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