Chen Bing-Fang, Liu Chun-Jen, Jow Guey-Mei, Chen Pei-Jer, Kao Jia-Horng, Chen Ding-Shinn
School of Medicine, Fu Jen Catholic University, Taipei, Taiwan.
Gastroenterology. 2006 Apr;130(4):1153-68. doi: 10.1053/j.gastro.2006.01.011.
BACKGROUND & AIMS: The interactions among pre-S deletion, precore (PC) mutation, and basal core promoter (BCP) mutation in various stages of chronic hepatitis B virus (HBV) infection remain unclear and were thus investigated in this study.
The sequences of the pre-S region and the BCP (A1762T, G1764A) and PC (G1896A) mutations were determined in 46 HBV chronic carriers (CC) and 106 age-matched carriers with different stages of liver diseases, including 38 chronic hepatitis (CH), 18 cirrhosis (LC), and 50 hepatocellular carcinoma (HCC).
A higher prevalence of pre-S deletion and BCP and PC mutations was found in carriers with progressive liver diseases compared with the CC group. By logistic regression analysis, patients with pre-S deletion and BCP mutation were significantly associated with the development of progressive liver diseases than those without. Combination of mutations rather than single mutation was associated with the development of progressive liver diseases, especially in combination with pre-S deletion. Sequencing analysis showed that the deleted regions were more often in the 3' terminus of pre-S1 and the 5' terminus of pre-S2. Further mapping of these pre-S deletion sequences found that all the deletion regions encompassed T- and B-cell epitopes, and most of them lost 1 or more functional sites.
Our data indicate that patients with progressive liver diseases have a higher frequency of pre-S deletion.
慢性乙型肝炎病毒(HBV)感染不同阶段中前S区缺失、前核心(PC)突变和基本核心启动子(BCP)突变之间的相互作用仍不清楚,因此本研究对此进行了调查。
测定了46例HBV慢性携带者(CC)和106例年龄匹配的不同肝病阶段携带者的前S区序列以及BCP(A1762T、G1764A)和PC(G1896A)突变情况,其中包括38例慢性肝炎(CH)、18例肝硬化(LC)和50例肝细胞癌(HCC)。
与CC组相比,进展性肝病携带者中前S区缺失以及BCP和PC突变的发生率更高。通过逻辑回归分析,与无前S区缺失和BCP突变的患者相比,有这些突变的患者与进展性肝病的发生显著相关。突变组合而非单一突变与进展性肝病的发生相关,尤其是与前S区缺失组合时。测序分析表明,缺失区域更常见于前S1的3'末端和前S2的5'末端。对这些前S区缺失序列的进一步定位发现,所有缺失区域都包含T细胞和B细胞表位,并且其中大多数失去了1个或更多功能位点。
我们的数据表明,进展性肝病患者前S区缺失的频率更高。