Ritonavir Blocks Hepatitis E Virus Internalization and Clears Hepatitis E Virus In Vitro with Ribavirin

被引:7
|
作者
Primadharsini, Putu Prathiwi [1 ]
Nagashima, Shigeo [1 ]
Takahashi, Masaharu [1 ]
Murata, Kazumoto [1 ]
Okamoto, Hiroaki [1 ]
机构
[1] Jichi Med Univ, Dept Infect & Immun, Div Virol, Sch Med, Shimotsuke, Tochigi 3290498, Japan
来源
VIRUSES-BASEL | 2022年 / 14卷 / 11期
基金
日本学术振兴会;
关键词
hepatitis E virus; ritonavir; virus internalization; ribavirin; drug combination; in vitro; virus growth; CELL-CULTURE-SYSTEM; MONOCLONAL-ANTIBODIES; STRAIN JE03-1760F; ORF3; PROTEIN; OPEN-LABEL; INFECTION; HEV; RELEASE; PARITAPREVIR; OMBITASVIR;
D O I
10.3390/v14112440
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Hepatitis E virus (HEV) is increasingly recognized as the leading cause of acute hepatitis. Although HEV infections are mostly self-limiting, a chronic course can develop especially in those with immunocompromised state. Ribavirin is currently used to treat such patients. According to various reports on chronic HEV infections, a sustained virological response (SVR) was achieved in approximately 80% of patients receiving ribavirin monotherapy. To increase the SVR rate, drug combination might be a viable strategy, which we attempted in the current study. Ritonavir was identified in our previous drug screening while searching for candidate novel anti-HEV drugs. It demonstrated potent inhibition of HEV growth in cultured cells. In the present study, ritonavir blocked HEV internalization as shown through time-of-addition and immunofluorescence assays. Its combination with ribavirin significantly increased the efficiency of inhibiting HEV growth compared to that shown by ribavirin monotherapy, even in PLC/PRF/5 cells with robust HEV production, and resulted in viral clearance. Similar efficiency was seen for HEV genotypes 3 and 4, the main causes of chronic infection. The present findings provide insight concerning the advantage of combination therapy using drugs blocking different steps in the HEV life cycle (internalization and RNA replication) as a potential novel treatment strategy for chronic hepatitis E.
引用
收藏
页数:18
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