Hur G M, Lee Y I, Suh D J, Lee J H, Lee Y I
Biomedicine Research Group, Korea Institute of Science and Technology, Taejeon.
J Med Virol. 1996 Jan;48(1):38-46. doi: 10.1002/(SICI)1096-9071(199601)48:1<38::AID-JMV6>3.0.CO;2-M.
The sequence in the precore and core region of the hepatitis B virus (HBV) genome in the serum of five chronic active hepatitis patients at four different stages in each individual were studied by polymerase chain reaction and DNA sequencing to determine the prevalence and type of precore and core mutants in each chronic active hepatitis (CAH) patient. Gradual changes of the virus genome in each CAH patient in precore and core regions were identified. Except for the virus from one patient, the mutant viruses showed gradual changes of genome sequences, which resulted in the generation of stop codons at the precore and core region, causing the association of active hepatitis in each patient even in the presence of anti-HBe. Mutational hot spots in the core region, which includes a clustering of changes in a small region of 14 amino acids (codons 84-97 from the start of the core gene) were found in all patients. This region of mutational hot spots in the core might be a major target of cytotoxic T lymphocytes (CTL), which has evolved under the pressure of immune selections, and these mutants might play a important role in the pathogenesis of viral hepatitis.
采用聚合酶链反应和DNA测序技术,对5例慢性活动性肝炎患者在4个不同阶段血清中乙型肝炎病毒(HBV)基因组的前核心区和核心区序列进行研究,以确定各慢性活动性肝炎(CAH)患者前核心突变体和核心突变体的流行情况及类型。在每个CAH患者中,均发现前核心区和核心区病毒基因组存在渐进性变化。除1例患者的病毒外,突变病毒的基因组序列均呈现渐进性变化,导致在前核心区和核心区产生终止密码子,即使在抗HBe存在的情况下,也致使每位患者发生活动性肝炎。在所有患者中均发现核心区存在突变热点,该区域包括在14个氨基酸的小区域(核心基因起始处的密码子84 - 97)内的一系列变化。核心区的这一突变热点区域可能是细胞毒性T淋巴细胞(CTL)的主要靶点,它在免疫选择压力下发生了进化,这些突变体可能在病毒性肝炎的发病机制中起重要作用。