Bozkaya H, Akarca U S, Ayola B, Lok A S
Section of Gastroenterology and Hepatology, Tulane University, New Orleans, LA, USA.
J Hepatol. 1997 Mar;26(3):508-16. doi: 10.1016/s0168-8278(97)80415-1.
Mutations in the hepatitis B virus genome have been implicated in the persistence of hepatitis B virus infection and the pathogenesis of hepatitis B virus related liver disease. In view of the heterogeneity in published sequences, data from cross-sectional studies of unrelated subjects cannot differentiate true mutations from infections with variant sequences.
AIMS/METHODS: We compared the hepatitis B virus core gene sequences of 42 HBsAg positive subjects from 11 Chinese families with those of the index patients (maternal carriers) to determine the frequency and rate of true hepatitis B virus core gene mutations in patients with chronic hepatitis B virus infection.
Completely identical nucleotide sequences were present in all the family members and index patients in two families, suggesting that the hepatitis B virus core gene can be conserved for more than 20 years. The high degree of sequence conservation in these families is related to the young age of the subjects (mean 19.2+/-8.9 years), the fact that they were all HBeAg positive and that 75% of them had persistently normal aminotransferase levels. Longitudinal studies confirmed that mutations were rare in those who remained HBeAg positive with normal aminotransferase levels (immune tolerant phase), but significantly more common in HBeAg positive subjects who had elevated aminotransferase levels and in those who cleared HBeAg (immune clearance phase), the rates of nucleotide and amino acid changes were respectively: 0.28+/-0.12 vs 1.30+/-0.26/10(3) nt position/yr and 0.04+/-0.01 vs 0.18+/-0.5/10(2) codon/yr.
Identical nucleotide differences could be found in the sequences of all the subjects in some families. These differences were more likely to be due to intra-familial transmission of stable variants. Sequence analysis based on comparisons with published sequences would have led to over-reporting of mutations. The hepatitis B virus core gene can remain highly conserved for more than two decades during the immune tolerant phase of perinatally acquired chronic hepatitis B virus infection. However, significant changes can occur within 2-3 years during the immune clearance phase.
乙肝病毒基因组中的突变与乙肝病毒感染的持续存在以及乙肝相关肝病的发病机制有关。鉴于已发表序列的异质性,来自无关受试者横断面研究的数据无法区分真正的突变与变异序列感染。
目的/方法:我们比较了来自11个中国家庭的42名HBsAg阳性受试者与索引患者(母亲携带者)的乙肝病毒核心基因序列,以确定慢性乙肝病毒感染患者中真正的乙肝病毒核心基因突变的频率和速率。
两个家庭的所有家庭成员和索引患者中均存在完全相同的核苷酸序列,这表明乙肝病毒核心基因可以保持20多年不变。这些家庭中高度的序列保守性与受试者的年轻年龄(平均19.2±8.9岁)、他们均为HBeAg阳性以及其中75%的人转氨酶水平持续正常有关。纵向研究证实,在转氨酶水平正常且仍为HBeAg阳性的患者(免疫耐受期)中突变很少见,但在转氨酶水平升高的HBeAg阳性受试者以及清除HBeAg的受试者(免疫清除期)中更为常见,核苷酸和氨基酸变化的速率分别为:0.28±0.12对1.30±0.26/10³核苷酸位置/年以及0.04±0.01对0.18±0.5/10²密码子/年。
在一些家庭的所有受试者序列中可以发现相同的核苷酸差异。这些差异更可能是由于稳定变异体的家族内传播所致。基于与已发表序列比较的序列分析会导致突变报告过度。在围产期获得的慢性乙肝病毒感染的免疫耐受期,乙肝病毒核心基因可以在二十多年间保持高度保守。然而,在免疫清除期的2 - 3年内会发生显著变化。