病毒学
小干扰RNA
核糖核酸
医学
病毒
乙型肝炎病毒
生物
基因
遗传学
作者
Emily P. Thi,Xin Ye,Nicholas M. Snead,Amy C. H. Lee,Holly M. Micolochick Steuer,Andrzej Ardzinski,Ingrid Graves,Christine Espiritu,Andrea Cuconati,Cory Abbott,Agnes Jarosz,Xiaowei Teng,Bhavna Paratala,Kevin McClintock,Troy O. Harasym,René Rijnbrand,Angela M. Lam,Michael J. Sofia
出处
期刊:ACS Infectious Diseases
[American Chemical Society]
日期:2024-09-22
被引量:1
标识
DOI:10.1021/acsinfecdis.4c00514
摘要
Chronic hepatitis B is a global health concern with a high risk of end-stage liver disease. Current standard-of-care agents have low cure rates, and new therapies are needed. Small interfering RNAs (siRNAs) that target viral RNAs fulfill a gap not addressed by standard-of-care agents and may contribute to a functional cure. Here, we describe the preclinical characterization of imdusiran (AB-729), a novel, pan-genotypic siRNA therapeutic that effectively reduces HBsAg, viral antigens, and viral replication in chronic hepatitis B patients and is currently in Phase 2 clinical studies. In hepatitis B virus (HBV) cell-based systems, imdusiran possessed pan-genotypic nanomolar potency and retained activity against HBV target site polymorphisms. Imdusiran was active against nucleos(t)ide analogue- and capsid assembly modulator-resistant HBV isolates, and combination with standard-of-care agents was additive. In an HBV adeno-associated virus mouse model, HBsAg was reduced up to 3.7 log
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