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“双靶点”聚乙二醇化干扰素α成功治疗乙肝和丁肝合并感染。

'Double-hit' pegylated interferon-alpha successfully treats Hepatitis B and Hepatitis D co-infection.

作者信息

Bhuva Meha, Moore Marie, Sen Sambit

机构信息

Hepatology Department, Luton and Dunstable University Hospital, Luton, UK.

出版信息

Oxf Med Case Reports. 2020 Oct 23;2020(10):omaa084. doi: 10.1093/omcr/omaa084. eCollection 2020 Oct.

Abstract

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.

摘要

丁型肝炎病毒(HDV)感染可与现有的乙型肝炎病毒(HBV)感染同时发生,或作为重叠感染发生。它会导致一种严重的慢性病毒性肝炎,并加速与肝脏相关的发病率和死亡率,包括肝细胞癌。目前的治疗方案建议使用聚乙二醇化干扰素-α治疗48周,但持续病毒学应答(SVR)率仍然很低。我们报告了一名最初对聚乙二醇化干扰素治疗HBV-HDV合并感染有反应的患者。虽然两种病毒的病毒血症最初有所改善,但随着肝脏损伤生化指标的持续进展,未实现SVR。然而,两年后第二个疗程的聚乙二醇化干扰素的累积效应导致HDV治愈(治疗后12个月SVR)、极低水平的HBV携带状态(病毒载量持续检测不到)以及持续的生化指标正常化。该病例说明了一种针对持续性HBV-HDV合并感染的成功治疗策略,即所提出的治疗方案引发了初始反应,但未实现SVR。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57f4/7733525/927d6b65063f/omaa084f1.jpg

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