Molnupiravir is effective against hepatitis E virus infection in an animal model
BACKGROUND: There are few treatment options for patients with chronic hepatitis E unresponsive to ribavirin. Drug repurposing is required to identify new treatments. Molnupiravir, a nucleoside analogue, is approved for the treatment of coronavirus disease 2019 (COVID-19). This study evaluated the activity of molnupiravir against hepatitis E virus (HEV) in cell culture and animal models. METHODS: Cytotoxicity and antiviral efficacy of molnupiravir, ribavirin, and sofosbuvir were investigated using infectious cDNA clones and wild-type HEV isolates in PLC/PRF/5 cells and primary rat hepatocytes. Immunosuppressed rats were infected with HEV and treated with molnupiravir and ribavirin. The effectiveness of molnupiravir in clearing HEV in serum, feces, and liver tissue was compared with that of untreated and ribavirin-treated animals. Mutations arising in virus populations during treatment were assessed using next-generation sequencing. RESULTS: The antiviral effect of molnupiravir was comparable to that of ribavirin and superior to that of sofosbuvir against HEV strains in vitro, with decreased HEV RNA in supernatant (p<0.05) and cytoplasmic viral protein expression. No additive effect with sofosbuvir was observed. Rats (n=14 per group) treated with 400 mg/kg/d molnupiravir cleared viremia within 4 weeks of treatment, and 9/14 of these animals also cleared viral shedding in stool. Mean viremia and fecal viral loads were reduced compared with untreated and ribavirin-treated animals (p≤0.005). Partial effectiveness was apparent at the lower 250 mg/kg/d molnupiravir dose. Molnupiravir-treated rats had improved liver histology compared with control animals. Frequent transition mutations were observed in HEV from molnupiravir-treated animals. CONCLUSIONS: Molnupiravir limits HEV infection in cell culture and animal models. Molnupiravir could be an alternative for ribavirin-refractory chronic hepatitis E.
Authors
- Weihui Ma
- X. Ma
- Longchao Zhu
- Feifei Yin (ORCID: https://orcid.org/0000-0001-9942-0395)
- Nicholas Foo‐Siong Chew (ORCID: https://orcid.org/0000-0002-9479-1493)
- Kelvin Kai‐Wang To (ORCID: https://orcid.org/0000-0002-1921-5824)
- Estie Hon-Kiu Shun (ORCID: https://orcid.org/0009-0000-5112-2276)
- James Yiu-Hung Tsoi (ORCID: https://orcid.org/0000-0002-0045-637X)
- Jasper Fuk‐Woo Chan (ORCID: https://orcid.org/0000-0001-6336-6657)
- K. L. Chen
- Jonathan Daniel Ip (ORCID: https://orcid.org/0000-0002-9549-7384)
- Jianwen Situ
- Shusheng Wu (ORCID: https://orcid.org/0000-0001-8280-2960)
- Yaowei Huang (ORCID: https://orcid.org/0009-0006-7462-562X)
- Yan Liang
- Su Ling Ho
- Shuofeng Yuan
- Anna Jinxia Zhang
- Weiwei Mao
- Siddharth Sridhar
- Can Li
Institutions
- South China Agricultural University (CN)
- Dongguan University of Technology (CN)
- Hong Kong Science and Technology Parks Corporation (HK)
- Hainan Medical University (CN)
- University of Hong Kong (HK)
Publication Details
- Journal
- Hepatology Communications
- Published
- 2026-04-13
- DOI
- https://doi.org/10.1097/hc9.0000000000000944
- Primary Topic
- Hepatitis Viruses Studies and Epidemiology
- Type
- article
- Field-Weighted Citation Impact
- 0.00