乙型肝炎表面抗原
清脆的
cccDNA
病毒学
乙型肝炎病毒
质粒
反式激活crRNA
生物
乙型肝炎病毒β前体
核糖核酸
分子生物学
病毒
病毒复制
Cas9
DNA
遗传学
基因
乙型肝炎病毒DNA聚合酶
作者
Laura C. McCoullough,Mohamed Fareh,Wenxin Hu,Vitina Sozzi,Christina Makhlouf,Yianni Droungas,Chee Leng Lee,Mina Takawy,Stewart A. Fabb,Thomas J. Payne,Colin W. Pouton,Hans Netter,Sharon R. Lewin,Damian F. J. Purcell,Jacinta A. Holmes,Joseph A. Trapani,Margaret Littlejohn,Peter Revill
标识
DOI:10.1016/j.jhep.2024.05.025
摘要
Owing to the limitations of current antiviral therapies for hepatitis B, there is an urgent need for new treatments that target multiple aspects of the HBV replication cycle to improve rates of functional cure. Here, we present CRISPR-Cas13b as a novel strategy to target HBV replication and protein expression, paving the way for its development as a potential new treatment option for patients living with chronic hepatitis B.
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