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‘Double-hit’ pegylated interferon-alpha successfully treats Hepatitis B and Hepatitis D co-infection

机译:'双击'聚乙二醇化干扰素-α成功治疗乙型肝炎和丙型肝炎的共感染

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Hepatitis delta (HDV) infection is either acquired simultaneously with, or as a superinfection to, existing Hepatitis B (HBV). It leads to a serious form of chronic viral hepatitis and accelerated liver-related morbidity and mortality including hepatocellular carcinoma. Current treatment regimes propose Pegylated interferon-alpha for 48?weeks however sustained virological response (SVR) rates remain low. We report a patient who initially responded to Pegylated interferon treatment for HBV-HDV co-infection. Although initial improvement in viraemia from both virsues was seen, SVR was not achieved with ongoing progression of liver injury biochemically. However, the summative effect of a second course of Pegylated interferon 2?years later led to HDV cure (SVR 12?months post-treatment), very low level HBV carrier status (with persistently undetectable viral load) and ongoing biochemical normalization. This case illustrates a successful treatment strategy for persistent HBV-HDV co-infection where proposed treatment regimes elicit an initial response but SVR is not achieved.
机译:肝炎δ(HDV)感染是与现有乙型肝炎(HBV)同时获得的或作为过度染色的。它导致严重形式的慢性病毒性肝炎和加速肝癌的发病率和死亡率,包括肝细胞癌。目前的处理制度提出了聚乙二醇化的干扰素-α48?周,但持续的病毒学响应(SVR)率保持低。我们报告了一个初始应对聚乙二醇化干扰素治疗的患者,用于HBV-HDV共感染。虽然从两种病毒素中出现初始改善来自血症的病毒性症,但在肝损伤的持续进展中没有实现SVR。然而,第二级聚乙二醇干扰素2的总结效应2?年后的效果导致HDV固化(后处理后的SVR 12?持续),非常低水平的HBV载体状态(具有持续无检测的病毒载荷)和持续的生物化学归一化。这种情况说明了持久性HBV-HDV共同感染的成功治疗策略,其中建议的治疗制度引发了初始反应,但没有实现SVR。

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