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综述文章:对丁型肝炎病毒的免疫病理学、临床和治疗方面的新见解。

Review article: emerging insights into the immunopathology, clinical and therapeutic aspects of hepatitis delta virus.

机构信息

Centre for Immunobiology, Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK.

The Royal London Hospital, Barts Health NHS Trust, London, UK.

出版信息

Aliment Pharmacol Ther. 2022 Apr;55(8):978-993. doi: 10.1111/apt.16807. Epub 2022 Mar 16.

Abstract

BACKGROUND

Hepatitis delta virus (HDV), which causes the most severe form of viral hepatitis, is an obligated hepatitis B (HBV) satellite virus that can either infect naïve subjects simultaneously with HBV (co-infection), or chronically infect HBV carriers (super-infection). An estimated 12 million people are infected by HDV worldwide.

AIMS

To summarise the most relevant aspects of the molecular biology of HDV, and to discuss the latest understanding of the induced pathology, interactions with the immune system, as well as both approved and investigational treatment options.

METHODS

References for this review were identified through searches of PubMed with the terms "HDV" "viral hepatitis" "co-infection" and "super-infection," published between 1980 and October 2021 RESULTS: The limited access to the HDV-infected liver has hampered the investigation of the intrahepatic compartment and our understanding of the mechanisms of HDV pathogenesis. In the absence of standardised and sensitive diagnostic tools, HDV is often underdiagnosed and owing to its strong dependence on host cellular factors, the development of direct antiviral agents has been challenging. New therapeutic agents targeting different steps of the viral cycle have recently been investigated, among which bulevirtide (which was conditionally approved by EMA in July 2020) and lonafarnib; both drugs having received orphan drug designation from both the EMA and FDA.

CONCLUSIONS

The HBV cure programme potentially offers a unique opportunity to enhance HDV treatment strategies. In addition, a more comprehensive analysis of the intrahepatic compartment is mandated to better understand any liver-confined interaction of HDV with the host immune system.

摘要

背景

乙型肝炎 Delta 病毒(HDV)是一种强制性乙型肝炎(HBV)卫星病毒,可导致最严重的病毒性肝炎,可同时感染未感染的个体(合并感染),或慢性感染 HBV 携带者(重叠感染)。据估计,全世界有 1200 万人感染 HDV。

目的

总结 HDV 分子生物学的最相关方面,并讨论最新的诱导病理学、与免疫系统的相互作用以及已批准和正在研究的治疗选择的认识。

方法

通过在 PubMed 中搜索术语“HDV”、“病毒性肝炎”、“合并感染”和“重叠感染”,对本综述的参考文献进行了检索,检索时间为 1980 年至 2021 年 10 月。

结果

HDV 感染肝脏的获取途径有限,阻碍了对肝内区室的研究,也阻碍了我们对 HDV 发病机制的理解。由于缺乏标准化和敏感的诊断工具,HDV 经常被漏诊,而且由于其强烈依赖宿主细胞因子,直接抗病毒药物的开发具有挑战性。最近已经研究了针对病毒周期不同步骤的新治疗药物,其中包括 bulevirtide(2020 年 7 月 EMA 有条件批准)和 lonafarnib;这两种药物都获得了 EMA 和 FDA 的孤儿药指定。

结论

HBV 治愈计划为增强 HDV 治疗策略提供了独特的机会。此外,需要对肝内区室进行更全面的分析,以更好地了解 HDV 与宿主免疫系统在肝脏内的任何相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd4f/9314912/56398b80d6ed/APT-55-978-g006.jpg

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