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慢性乙型肝炎的新型治疗策略。

Novel therapeutic strategies for chronic hepatitis B.

机构信息

Institute of Hepatology Foundation for Liver Research London UK, School of Immunology and Microbial Sciences King's College London, London, UK.

出版信息

Virulence. 2022 Dec;13(1):1111-1132. doi: 10.1080/21505594.2022.2093444.

Abstract

The last few years have seen a resurgence of activity in the hepatitis B drug pipeline, with many compounds in various stages of development. This review aims to provide a comprehensive overview of the latest advances in therapeutics for chronic hepatitis B (CHB). We will discuss the broad spectrum of direct-acting antivirals in clinical development, including capsids inhibitors, siRNA, HBsAg and polymerase inhibitors. In addition, host-targeted therapies (HTT) will be extensively reviewed, focusing on the latest progress in immunotherapeutics such as toll-like receptors and RIG-1 agonists, therapeutic vaccines and immune checkpoints modulators. A growing number of HTT in pre-clinical development directly target the key to HBV persistence, namely the covalently closed circular DNA (cccDNA) and hold great promise for HBV cure. This exciting area of HBV research will be highlighted, and molecules such as cyclophilins inhibitors, APOBEC3 deaminases and epigenetic modifiers will be discussed.

摘要

近年来,乙型肝炎药物研发领域再次活跃起来,许多化合物处于不同的研发阶段。本综述旨在全面概述慢性乙型肝炎(CHB)治疗的最新进展。我们将讨论处于临床开发阶段的广谱直接作用抗病毒药物,包括衣壳抑制剂、siRNA、HBsAg 和聚合酶抑制剂。此外,还将广泛综述宿主靶向治疗(HTT),重点介绍免疫治疗如 Toll 样受体和 RIG-1 激动剂、治疗性疫苗和免疫检查点调节剂的最新进展。越来越多的处于临床前开发阶段的 HTT 直接针对乙型肝炎病毒持续存在的关键,即共价闭合环状 DNA(cccDNA),为乙型肝炎病毒的治愈带来了巨大希望。本文将重点介绍这一令人兴奋的乙型肝炎病毒研究领域,并讨论亲环素抑制剂、APOBEC3 脱氨酶和表观遗传修饰剂等分子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88d1/9272843/448770dd2279/KVIR_A_2093444_F0001_OC.jpg

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