Geng Yan, Wang Xiangling, Lu Xiaolan, Wu Xiaokang, Xu Nan, Han Lei, Xu Jiru
From the Department of Laboratory (YG, XW, XW, NX); Department of Digestive, The Second Affiliated Hospital (XL); and Department of Immunology and Pathogenic Biology, Health Science Center, Xi'an Jiaotong University, Xi'an, People's Republic of China (LH, JX).
Medicine (Baltimore). 2016 Feb;95(5):e2657. doi: 10.1097/MD.0000000000002657.
To study the changes in 3 mutations related with hepatitis B e antigen (HBeAg) in patients with HBeAg-positive chronic hepatitis B (CHB) during interferon therapy.HBeAg seroconversion is a major therapeutic milestone for patients with HBeAg-positive CHB. The precore mutation G1896A and the basal core promoter mutations A1762T/G1764A are 3 important mutations that affect the expression of HBeAg; however, the change of these 3 mutations in CHB patients during interferon therapy has not yet been evaluated.Sixty-four treatment-naive patients with HBeAg-positive CHB were treated with interferon for 48 weeks and followed up for 24 weeks. Serum samples were collected from all of the participants at different time points and then subjected to viral DNA extraction. The precore and basal core promoter sequences were determined using nested PCR and direct sequencing. The treatment outcomes were confirmed both at the end of therapy and the follow-up period, and the results were compared between patients with mutant and wild-type virus.No significant difference in HBeAg loss and HBeAg seroconversion was observed between patients with mutant versus wild-type virus although the portion of patients who achieved HBeAg loss/seroconversion with mutant virus was a little higher than in patients with wild-type virus. Once a mutation exists, it is not replaced with the wild-type sequence during interferon therapy and follow-up; moreover, our results show that mutants stably coexist with the wild-type virus during interferon therapy.This study shows the changes in 3 mutations affecting the expression of HBeAg during interferon therapy. However, additional studies with a larger sample size and more sensitive detection methods are needed to uncover the underlying mechanism and clinical significance of these results.
研究HBeAg阳性慢性乙型肝炎(CHB)患者在干扰素治疗期间与乙肝e抗原(HBeAg)相关的3种突变的变化情况。HBeAg血清学转换是HBeAg阳性CHB患者治疗的一个主要里程碑。前核心区突变G1896A和核心启动子区突变A1762T/G1764A是影响HBeAg表达的3个重要突变;然而,CHB患者在干扰素治疗期间这3种突变的变化情况尚未得到评估。64例未经治疗的HBeAg阳性CHB患者接受干扰素治疗48周,并随访24周。在不同时间点从所有参与者中采集血清样本,然后进行病毒DNA提取。使用巢式PCR和直接测序法测定前核心区和核心启动子区序列。在治疗结束时和随访期确认治疗结果,并比较突变型和野生型病毒患者的结果。尽管携带突变型病毒实现HBeAg消失/血清学转换的患者比例略高于野生型病毒患者,但在突变型与野生型病毒患者之间,未观察到HBeAg消失和HBeAg血清学转换有显著差异。一旦存在突变,在干扰素治疗和随访期间不会被野生型序列取代;此外,我们的结果表明,在干扰素治疗期间,突变体与野生型病毒稳定共存。本研究显示了干扰素治疗期间影响HBeAg表达的3种突变的变化情况。然而,需要更多样本量和更灵敏检测方法的进一步研究来揭示这些结果的潜在机制和临床意义。