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乙型肝炎病毒基因型分析有什么价值吗?

Is there any value to hepatitis B virus genotype analysis?

作者信息

Tanwar Sudeep, Dusheiko Geoffrey

机构信息

Centre for Hepatology, University College London Royal Free Campus, Rowland Hill Street Hampstead, London, NW3 2PF, UK.

出版信息

Curr Gastroenterol Rep. 2012 Feb;14(1):37-46. doi: 10.1007/s11894-011-0233-5.

Abstract

Hepatitis B may cause a varying spectrum of diseases ranging from an asymptomatic or mild anicteric acute illness, to severe or fulminant hepatitis. Similarly, the outcome of chronic hepatitis B is variable. Viral factors associated with outcome of chronic hepatitis B virus (HBV) infection include hepatitis B e antigen status, HBV DNA, genotype, and HBV variants. HBV genotypes and subgenotypes have been associated with differences in clinical and virological characteristics, indicating that they may play a role in the virus-host relationship. A total of ten hepatitis B virus genotypes have been defined with a distinct geographical distribution. Hitherto, genotypes A, B, C and D have been studied most extensively. The HBV genotype appears to influence not only the natural history of HBV related liver disease but also the response to HBV treatment. HBV genotypes are also linked with both core promoter and BCP mutations. Progression to chronic infection appears to occur more frequently following acute infection with genotypes A and D than with the other studied genotypes. Genotypes A and B appear to have higher rates of spontaneous HBeAg seroconversion. More advanced liver disease and progression to HCC is more often seen in chronic infection with genotypes C and D in contrast to genotypes A and B. More specifically, genotypes A1, C, B2-B5 and H appear to be associated with more serious complications than genotypes A2, B1 and B6. These observations suggest important pathogenic differences between HBV genotypes. Genotypes A and B have higher response rates to interferon based therapy than genotypes C and D. Knowledge of HBV genotype enables clinicians to identify those patients at increased risk of disease progression whilst aiding the selection of appropriate antiviral therapy. Genotyping and monoclonal subtyping can provide useful information for epidemiological studies. In conclusion, genotyping of chronic HBV infections can help practicing physicians identify those at risk of disease progression and determine optimal anti-viral therapy.

摘要

乙型肝炎可导致一系列不同的疾病,从无症状或轻度无黄疸型急性疾病到严重或暴发性肝炎。同样,慢性乙型肝炎的结局也各不相同。与慢性乙型肝炎病毒(HBV)感染结局相关的病毒因素包括乙肝e抗原状态、HBV DNA、基因型和HBV变异体。HBV基因型和亚基因型与临床和病毒学特征的差异有关,表明它们可能在病毒与宿主的关系中发挥作用。总共已确定了十种乙型肝炎病毒基因型,具有独特的地理分布。迄今为止,A、B、C和D基因型研究最为广泛。HBV基因型似乎不仅影响HBV相关肝病的自然史,还影响对HBV治疗的反应。HBV基因型还与核心启动子和BCP突变有关。与其他研究的基因型相比,急性感染A和D基因型后进展为慢性感染的情况似乎更常见。A和B基因型的HBeAg自发血清学转换率似乎更高。与A和B基因型相比,C和D基因型的慢性感染中更常出现更严重的肝病和进展为肝癌的情况。更具体地说,与A2、B1和B6基因型相比,A1、C、B2 - B5和H基因型似乎与更严重的并发症有关。这些观察结果表明HBV基因型之间存在重要的致病差异。A和B基因型对基于干扰素的治疗的反应率高于C和D基因型。了解HBV基因型使临床医生能够识别那些疾病进展风险增加的患者,同时有助于选择合适的抗病毒治疗。基因分型和单克隆亚型分析可为流行病学研究提供有用信息。总之,慢性HBV感染的基因分型可帮助执业医生识别那些有疾病进展风险的患者,并确定最佳抗病毒治疗方案。

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