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Persistent human hepatitis B virus infection in cynomolgus monkeys: A novel animal model in the search for a cure?

机译:食蟹猴中持久性人类乙型肝炎病毒感染:寻求治疗的新型动物模型?

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摘要

Worldwide, human hepatitis B virus (HBV) infection causes liver-related death in more than 600 thousand people annually (www. who.int/mediacentre/factsheets/fs204/en/). Approximately 400 million people are persistently infected with HBV with dramatically increased risk of developing liver cirrhosis, end-stage liver disease, and hepatocellular carcinoma. Thus, over half of the 700 thousand annual liver cancer cases are caused by HBV. However, current therapy of chronic HBV is suboptimal and expensive and, in most treated patients, does not lead to a cure.1 Treatment options include nucleos(t)ide analogs teno-fovir and entecavir, which are highly effective in lowering viremia level, but only rarely lead to sustained clearance or long-term suppression of viral load. Another option is treatment with pegylated interferon-alpha (PEG-IFN-alpja), which, in a small number of cases, has been associated with late viral clearance, thus suggesting that induction of relevant immune responses might lead to a cure for persistent HBV. Taken together, there is a great need for studies of alternative and less-expensive treatment options, and it would be highly relevant to have a readily available immunocompetent animal model for human HBV.
机译:在世界范围内,人类乙型肝炎病毒(HBV)感染每年导致超过60万人与肝脏相关的死亡(www。who.int/mediacentre/factsheets/fs204/en/)。大约有4亿人持续感染HBV,从而显着增加发生肝硬化,晚期肝病和肝细胞癌的风险。因此,在每年70万例肝癌病例中,超过一半是由HBV引起的。但是,当前的慢性HBV治疗并不理想且昂贵,并且在大多数接受治疗的患者中无法治愈。1治疗选择包括核苷酸(t)ide类似物替诺福韦和恩替卡韦,它们在降低病毒血症水平方面非常有效,但很少会导致持续清除或长期抑制病毒载量。另一个选择是用聚乙二醇化干扰素-α(PEG-IFN-alpja)治疗,在少数情况下,它与晚期病毒清除有关,因此表明诱导相关的免疫反应可能会治愈持久性HBV 。综上所述,迫切需要研究替代性和廉价的治疗方案,因此,对于人类HBV建立易于获得的具有免疫能力的动物模型将具有重大意义。

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