[Relationship between core gene mutations of hepatitis B virus and response to alpha interferon therapy in chronic hepatitis B].

Byung Chul Yoo, Hyung Joon Kim, Jae Hyuk Do, Sill Moo Park
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Abstract

Background/aims: Treatment of chronic hepatitis B with interferon results in a sustained loss of hepatitis B virus DNA and hepatitis B e antigen (HBeAg) and remission of liver disease only in a proportion of cases. Recently, mutations of hepatitis B virus (HBV) core gene have been reported as being related to the failure of interferon treatment in chronic hepatitis B. This study investigated whether core gene mutations of HBV are related to non-response to interferon therapy and whether the recurrence of HBeAg and HBV DNA in initial responders to interferon therapy is associated with the emergence of HBV core gene mutants.

Methods: The precore/core gene sequence was determined by polymerase chain reaction (PCR) and direct sequencing of PCR product in serum samples obtained before interferon treatment from 10 responders and 10 non-responders to interferon therapy. In addition, precore/core gene sequence was determined in serum samples obtained before interferon treatment and after recurrence from 10 patients who showed recurrence of HBeAg and HBV DNA after initial response to interferon therapy.

Results: In samples from 10 responders, there were 7 missense mutations and 71 silent mutations. However, there were 43 missense mutations and 109 silent mutations in samples from 10 non-responders. In samples obtained before interferon treatment from the 10 patients who showed recurrence after initial response, 8 missense mutations and 74 silents mutations were found. The nucleotide sequences from the samples obtained after the recurrence showed 6 silent nucleotide substitutions compared with the sequences from the samples obtained before interferon treatment.

Conclusions: Mutations in the core protein of HBV occur more frequently in non-responders than responders to interferon therapy of chronic hepatitis B and may be a factor responsible for the failure of interferon treatment. The recurrence of HBeAg and HBV-DNA in initial responders to interferon therapy is not associated with the emergence of the HBV core gene mutants.

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乙型肝炎病毒核心基因突变与慢性乙型肝炎患者对α -干扰素治疗反应的关系
背景/目的:用干扰素治疗慢性乙型肝炎可导致乙型肝炎病毒DNA和乙型肝炎e抗原(HBeAg)的持续丢失,仅在一部分病例中肝脏疾病得到缓解。最近,乙型肝炎病毒(HBV)核心基因突变被报道为与干扰素治疗慢性乙型肝炎失败有关。本研究探讨了HBV核心基因突变是否与干扰素治疗无反应有关,以及干扰素治疗初始应答者HBeAg和HBV DNA的复发是否与HBV核心基因突变的出现有关。方法:对10例对干扰素治疗有反应的患者和10例对干扰素治疗无反应的患者,采用聚合酶链反应(PCR)和PCR产物直接测序法测定干扰素治疗前血清样品的前核/核心基因序列。此外,在干扰素治疗初期出现HBeAg和HBV DNA复发的10例患者中,测定了干扰素治疗前和复发后获得的血清样本的preore /core基因序列。结果:在10名应答者的样本中,有7个错义突变和71个沉默突变。然而,在10个无应答者的样本中有43个错义突变和109个沉默突变。在干扰素治疗前获得的10例初始缓解后出现复发的患者的样本中,发现8个错义突变和74个沉默突变。复发后样品的核苷酸序列与干扰素治疗前样品的核苷酸序列相比,有6个沉默核苷酸取代。结论:慢性乙型肝炎干扰素治疗无应答者比应答者更容易发生HBV核心蛋白突变,这可能是干扰素治疗失败的一个因素。在干扰素治疗的初始应答者中,HBeAg和HBV- dna的复发与HBV核心基因突变的出现无关。
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