Sneller Laura, Lin Christine, Price Angie, Kottilil Shyam, Chua Joel V
Division of Clinical Care and Research, Institute of Human Virology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Microorganisms. 2024 Mar 17;12(3):599. doi: 10.3390/microorganisms12030599.
Chronic hepatitis B (CHB) is a global health challenge that can result in significant liver-related morbidity and mortality. Despite a prophylactic vaccine being available, patients already living with CHB often must engage in lifelong therapy with nucleoside analogues. However, the potential of RNA interference (RNAi) therapeutics as a promising avenue for CHB treatment is being explored. RNAi, particularly using small interfering RNA (siRNA), targets viral RNA that can be used to inhibit hepatitis B virus (HBV) replication. Several candidates are currently being studied and have exhibited varying success in reducing hepatitis B surface antigen (HBsAg) levels, with some showing sustained HBsAg loss after cessation of therapy. The dynamic evolution of RNAi therapy presents a promising trajectory for the development of effective and sustained treatments for CHB. This review highlights recent findings on RNAi therapeutics, including modifications for stability, various delivery vectors, and specific candidates currently in development.
慢性乙型肝炎(CHB)是一项全球性的健康挑战,可导致严重的肝脏相关发病和死亡。尽管有预防性疫苗可用,但已感染CHB的患者通常必须接受核苷类似物的终身治疗。然而,RNA干扰(RNAi)疗法作为一种有前景的CHB治疗途径正在被探索。RNAi,特别是使用小干扰RNA(siRNA),靶向可用于抑制乙型肝炎病毒(HBV)复制的病毒RNA。目前有几种候选药物正在研究中,并且在降低乙肝表面抗原(HBsAg)水平方面取得了不同程度的成功,有些药物在治疗停止后显示出持续的HBsAg消失。RNAi疗法的动态发展为开发有效且持久的CHB治疗方法提供了一条有前景的途径。本综述重点介绍了RNAi疗法的最新研究成果,包括稳定性修饰、各种递送载体以及目前正在开发的特定候选药物。