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Characterization of the basal core promoter and precore regions in anti-HBe-positive inactive carriers of hepatitis B virus

机译:乙型肝炎病毒抗HBe阳性惰性携带者的基础核心启动子和前核心区域的特征

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SummaryBackground The study of hepatitis B virus (HBV) genomic heterogeneity has become a major issue in investigations aimed at understanding the relationship between {HBV} mutants and the wide spectrum of clinical and pathological conditions associated with {HBV} infection. Although most chronically infected {HBV} patients are inactive carriers, several virological aspects of this state remain unclear. Methods In order to determine the prevalence and clinical significance of mutations in the basal core promoter (BCP) and precore (pC) regions among inactive carriers, the nucleotide sequences from 41 inactive carriers were analyzed and compared with those from 29 individuals with chronic active hepatitis. Results Genotypes A (24.3%), D (37.1%), {F1b} (12.9%), and {F4} (18.6%) were the most prevalent. Mutations in the BCP/pC regions were observed in most of the inactive carriers (92.7%) and in most of the patients with chronic active hepatitis (93.1%). The prevalence of mutation 1764A was significantly higher in patients with chronic active hepatitis (65.5%) than in inactive carriers (36.6%) (p?=?0.038), whereas the prevalences of mutations at the other positions analyzed were not significantly different. Older patients (>50 years) showed BCP/pC patterns with a higher number of substitutions. Mutations were found to be biased by genotype: the 1896A mutation was highly prevalent in genotypes D and F4, while alternative substitutions in the pC region were more prevalent in genotypes A and F1b. Conclusions Mutations in the BCP/pC regions are the hallmark of chronic anti-HBe-positive individuals; nevertheless, the even distribution of mutations in active and inactive carriers suggests that BCP/pC mutations may occur during {HBV} infection not strictly related to the {HBV} infection activity.
机译:概述背景乙肝病毒(HBV)基因组异质性的研究已成为旨在了解 {HBV }突变体与 {HBV }感染相关的广泛临床和病理状况之间关系的调查中的一个主要问题。尽管大多数慢性感染的 {HBV }患者是不活跃的携带者,但这种状态的几个病毒学方面仍不清楚。方法为确定无活性携带者中基础核心启动子(BCP)和前核心(pC)区域突变的发生率和临床意义,分析了41种无活性携带者的核苷酸序列,并与29例慢性活动性肝炎患者进行了比较。 。结果基因型A(24.3%),D(37.1%), {F1b }(12.9%)和 {F4 }(18.6%)最为流行。在大多数非活动性携带者(92.7%)和大多数慢性活动性肝炎患者(93.1%)中观察到BCP / pC区突变。慢性活动性肝炎患者中1764A突变的患病率(65.5%)显着高于非活动性肝炎患者(36.6%)(p?=?0.038),而其他分析位置的突变患病率无显着差异。年龄较大的患者(> 50岁)表现出BCP / pC模式,具有更高的替代数量。发现突变受基因型影响:1896A突变在基因型D和F4中非常普遍,而在pC区的替代取代在基因型A和F1b中更为普遍。结论BCP / pC区突变是慢性抗HBe阳性个体的标志。然而,突变在活性和非活性携带者中的均匀分布表明BCP / pC突变可能发生在 {HBV }感染过程中,而与 {HBV }感染活动并不严格相关。

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