HBcAg
乙型肝炎表面抗原
病毒学
乙型肝炎病毒
抗原
抗体
表位
生物
乙型肝炎
肝细胞癌
病毒
免疫学
癌症研究
作者
Chongwei Xie,Bing Zhou,Da Yao,Xin Wang,Lihong Zhou,Chuanghua Qiu,Junfang Zhang
出处
期刊:Virus Research
[Elsevier BV]
日期:2025-01-31
卷期号:353: 199531-199531
标识
DOI:10.1016/j.virusres.2025.199531
摘要
Hepatitis B virus (HBV) represents one of the major pathogenic factor that leads to chronic liver diseases and the development of hepatocellular carcinoma (HCC). The currently approved anti-HBV drugs cannot eradicate the virus or block the development of HCC. HBV nucleocapsid consists of the hepatitis B core antigen (HBcAg) and the HBV relaxed-circular partially double-stranded DNA (rcDNA), indispensable in virus replication. The present study reported a cell-penetrating bispecific antibody targeting HBcAg and preS1, fused with the cell-penetrating peptide R9TAT, named Anti-preS1 × Anti-HBcAg-R9TAT. The antibody could recognize preS1 and HBcAg and internalize into living cells efficiently, suppressing the extracellular hepatitis B surface antigen (HBsAg) and hepatitis B envelope antigen, and the intracellular HBsAg and HBcAg in vitro. This cell-penetrating bispecific antibody is a novel approach to suppressing HBV replication and secretion and is a promising anti-HBV therapeutic antibody candidate.
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