Kostyushev Dmitry, Kostyusheva Anastasiya, Ponomareva Natalia, Brezgin Sergey, Chulanov Vladimir
National Medical Research Center of Tuberculosis and Infectious Diseases, Ministry of Health, Moscow, Russia.
Division of Biotechnology, Scientific Center for Genetics and Life Sciences, Sirius University of Science and Technology, Sochi, Russia.
Nucleic Acid Ther. 2022 Feb;32(1):14-28. doi: 10.1089/nat.2021.0075. Epub 2021 Nov 19.
After almost a decade of using CRISPR/Cas9 systems to edit target genes, CRISPR/Cas9 and related technologies are rapidly moving to clinical trials. Hepatitis B virus (HBV), which causes severe liver disease, cannot be cleared by modern antivirals, but represents an ideal target for CRISPR/Cas9 systems. Early studies demonstrated very high antiviral potency of CRISPR/Cas9 and supported its use for developing a cure against chronic HBV infection. This review discusses the key issues that must be solved to make CRISPR/Cas9 an anti-HBV therapy.
在使用CRISPR/Cas9系统编辑目标基因近十年后,CRISPR/Cas9及相关技术正迅速进入临床试验阶段。导致严重肝脏疾病的乙型肝炎病毒(HBV)无法被现代抗病毒药物清除,但却是CRISPR/Cas9系统的理想靶点。早期研究表明CRISPR/Cas9具有很高的抗病毒效力,并支持将其用于开发治愈慢性HBV感染的方法。本文综述了使CRISPR/Cas9成为抗HBV疗法必须解决的关键问题。