Loriot M A, Marcellin P, Talbodec N, Guigonis V, Gigou M, Boyer N, Bezeaud A, Erlinger S, Benhamou J P
Unité de Recherches de Physiopathologie Hépatique, Hôpital Beaujon, Clichy, France.
Hepatology. 1995 Mar;21(3):627-31.
The objective of this study was to evaluate the role of hepatitis B virus (HBV) precore mutations in patients with anti-HBe-positive chronic hepatitis B with or without previous known HBe antigen (HBeAg) viremic phase, and to assess the potential implication of precore mutants in HBeAg-negative reactivation after loss of HBeAg. Nineteen patients were studied: 7 had a previous HBeAg-positive phase and had spontaneous or therapeutically induced loss of HBeAg (group A); 12 had no previous HBeAg-positive phase (group B). Direct sequencing of PCR products was performed on serum collected during the anti-HBe-positive phase in the two groups. In group A, precore sequencing showed that 5 patients were infected by wild-type virus, 1 patient was infected with a precore mutant, and 1 patient was found to be infected by a mixture of wild-type and precore mutant viruses. In group B, precore sequencing showed that only 1 patient was infected with wild-type virus and that 11 were infected with precore mutants. In a few patients, the presence of HBeAg within immune complexes may explain HBeAg negativity. In conclusion, our results show that, in patients with anti-HBe-positive chronic hepatitis B: (1) precore mutations creating a stop codon are more frequently found in those without known previous HBeAg positivity; (2) after loss of HBeAg, the patients who have anti-HBe-positive reactivation are infected by wild-type virus, which suggests that reactivation is not related to precore mutations; (3) HBeAg negativity may be caused by immune complexes formation.
本研究的目的是评估乙肝病毒(HBV)前核心区突变在抗HBe阳性慢性乙型肝炎患者中的作用,这些患者有无既往已知的HBe抗原(HBeAg)病毒血症期,并评估前核心区突变体在HBeAg阴性后HBeAg阴性再激活中的潜在影响。研究了19例患者:7例有既往HBeAg阳性期,且有自发或经治疗诱导的HBeAg消失(A组);12例无既往HBeAg阳性期(B组)。对两组抗HBe阳性期采集的血清进行PCR产物直接测序。在A组中,前核心区测序显示5例患者感染野生型病毒,1例患者感染前核心区突变体,1例患者感染野生型和前核心区突变体病毒的混合物。在B组中,前核心区测序显示仅1例患者感染野生型病毒,11例感染前核心区突变体。在少数患者中,免疫复合物中HBeAg的存在可能解释了HBeAg阴性。总之,我们的结果表明,在抗HBe阳性慢性乙型肝炎患者中:(1)在无既往已知HBeAg阳性的患者中更频繁地发现产生终止密码子的前核心区突变;(2)在HBeAg消失后,抗HBe阳性再激活的患者感染野生型病毒,这表明再激活与前核心区突变无关;(3)HBeAg阴性可能由免疫复合物形成引起。