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用于治疗丁型肝炎的新兴药物。

Emerging drugs for hepatitis D.

机构信息

Department of Gastroenterology, Hacettepe University, Ankara, Turkey.

Department of Gastroenterology & Hepatology, Koc University Medical School, Istanbul, Turkey.

出版信息

Expert Opin Emerg Drugs. 2023 Dec;28(2):55-66. doi: 10.1080/14728214.2023.2205639. Epub 2023 Apr 27.

Abstract

INTRODUCTION

Chronic hepatitis delta (CHD) is the most severe form of chronic viral hepatitis. Until recently, its treatment consisted of pegylated interferon alfa (pegIFN) use.

AREAS COVERED

Current and new drugs for treating CHD. Virus entry inhibitor bulevirtide has received conditional approval by the European Medicines Agency. Prenylation inhibitor lonafarnib and pegIFN lambda are in phase 3 and nucleic acid polymers in phase 2 of drug development.

EXPERT OPINION

Bulevirtide appears to be safe. Its antiviral efficacy increases with treatment duration. Combining bulevirtide with pegIFN has the highest antiviral efficacy short-term. The prenylation inhibitor lonafarnib prevents hepatitis D virus assembly. It is associated with dose-dependent gastrointestinal toxicity and is better used with ritonavir which increases liver lonafarnib concentrations. Lonafarnib also possesses immune modulatory properties which explains some post-treatment beneficial flare cases. Combining lonafarnib/ritonavir with pegIFN has superior antiviral efficacy. Nucleic acid polymers are amphipathic oligonucleotides whose effect appears to be a consequence of phosphorothioate modification of internucleotide linkages. These compounds led to HBsAg clearance in a sizable proportion of patients. PegIFN lambda is associated with less IFN typical side effects. In a phase 2 study it led to 6 months off treatment viral response in one third of patients.

摘要

简介

慢性丁型肝炎(CHD)是最严重的慢性病毒性肝炎。直到最近,其治疗方法还包括聚乙二醇干扰素 alfa(pegIFN)的使用。

涵盖领域

目前和用于治疗 CHD 的新药。病毒进入抑制剂布乐韦肽已获得欧洲药品管理局有条件批准。前蛋白转化酶枯草溶菌素 1(PCSK9)抑制剂 lonafarnib 和 pegIFN lambda 处于 3 期临床试验,核酸聚合物处于 2 期临床试验。

专家意见

布乐韦肽似乎是安全的。其抗病毒疗效随治疗时间的延长而增加。将布乐韦肽与 pegIFN 联合使用具有短期最高的抗病毒疗效。前蛋白转化酶枯草溶菌素 1 抑制剂 lonafarnib 可阻止乙型肝炎病毒组装。它与剂量相关的胃肠道毒性有关,最好与利托那韦合用,因为利托那韦可增加肝脏 lonafarnib 浓度。Lonafarnib 还具有免疫调节特性,这可以解释一些治疗后有益的爆发案例。Lonafarnib/利托那韦联合 pegIFN 具有更高的抗病毒疗效。核酸聚合物是具有两亲性的寡核苷酸,其作用似乎是通过对核苷酸间键进行硫代磷酸酯修饰而产生的。这些化合物使相当一部分患者的 HBsAg 得到清除。pegIFN lambda 与较少的 IFN 典型副作用相关。在一项 2 期研究中,它使三分之一的患者在 6 个月的治疗后病毒得到缓解。

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