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丁型肝炎病毒感染:病理生理学、流行病学与治疗。2024年第三届德尔塔治疗会议报告。

Hepatitis D Virus Infection: Pathophysiology, Epidemiology and Treatment. Report From the Third Delta Cure Meeting 2024.

作者信息

Degasperi Elisabetta, Sandmann Lisa, Wedemeyer Heiner, Lampertico Pietro

机构信息

Division of Gastroenterology and Hepatology, Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.

D-SOLVE Consortium, an EU Horizon Europe Funded Project (No 101057917), Hannover, Germany.

出版信息

Liver Int. 2025 Jul;45(7):e70189. doi: 10.1111/liv.70189.

Abstract

Chronic infection with hepatitis delta virus (HDV) leads to rapid progression of liver disease, cirrhosis and complications such as end-stage liver disease and hepatocellular carcinoma. In recent years, understanding of the HDV life cycle has increased significantly; however, much remains unknown about the pathogenesis, host-virus interactions and the role of the immune system in HDV persistence and control. Challenges remain in the diagnosis of HDV, not only because of the lack of standardised assays, but also because of limited access and availability in resource-limited countries. The improved knowledge of the HDV life cycle has led to the development and approval of the first HDV-direct antiviral, Bulevirtide (BLV). Treatment with BLV shows high rates of viral suppression in clinical trials and real-world studies. Questions remain about the duration of treatment with BLV and the potential benefits of combination therapy with pegylated interferon alpha (PegIFNα). First data from the Phase III study in which BLV was stopped after 3 years of treatment have recently been presented at congresses. Results from the Phase II study evaluating the combination of BLV and PegIFNα, as well as real-world experiences, have been published. Despite recent advances in antiviral treatment, strategies to achieve HBsAg loss, which most closely resembles HDV cure, are not available and antiviral treatment for patients with advanced liver disease is limited. The third international Delta Cure meeting, held in Milan in October 2024, aimed to share the latest findings, and this review highlights key takeaways from the lectures and research on HDV.

摘要

丁型肝炎病毒(HDV)的慢性感染会导致肝病迅速进展、肝硬化以及诸如终末期肝病和肝细胞癌等并发症。近年来,对HDV生命周期的了解有了显著增加;然而,关于其发病机制、宿主与病毒的相互作用以及免疫系统在HDV持续存在和控制中的作用,仍有许多未知之处。HDV的诊断仍然面临挑战,这不仅是因为缺乏标准化检测方法,还因为资源有限的国家获取检测的途径和可用性受限。对HDV生命周期认识的提高促成了首款直接抗HDV药物布立维亭(BLV)的研发和获批。在临床试验和真实世界研究中,使用BLV治疗显示出较高的病毒抑制率。关于BLV的治疗持续时间以及与聚乙二醇化干扰素α(PegIFNα)联合治疗的潜在益处,仍存在疑问。最近在大会上公布了一项III期研究的首批数据,该研究在治疗3年后停用了BLV。评估BLV与PegIFNα联合使用的II期研究结果以及真实世界经验已发表。尽管抗病毒治疗最近取得了进展,但实现HBsAg消失(这最接近HDV治愈)的策略尚不可用,晚期肝病患者的抗病毒治疗也很有限。2024年10月在米兰举行的第三届国际HDV治愈会议旨在分享最新研究成果,本综述重点介绍了关于HDV的讲座和研究中的关键要点。

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