Oral 4’fluorouridine provides postexposure protection against lethal Nipah virus infection

There are no approved medical countermeasures for combatting Nipah virus (NiV) which causes regular outbreaks in humans and animals in South and Southeast Asia with mortality rates in humans ranging from 40% to more than 90%. Recently, it was shown that 4'-fluorouridine (4'-FlU; EIDD-2749), an orally available ribonucleoside analog, protected guinea pigs and nonhuman primates from lethal challenge with Lassa virus and that 4'-FlU has <i>in vitro</i> antiviral activity against NiV. Here, we assessed the postexposure protective efficacy of 4'-FlU in a lethal hamster model of NiV infection. Daily treatment with 4'-FlU beginning 3 days after exposure to NiV resulted in complete protection from lethal infection. Our findings support the further development of 4'-FlU as a therapy for NiV disease.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-02-22
DOI
https://doi.org/10.64898/2026.02.21.707194
Primary Topic
Virology and Viral Diseases
Type
article
Field-Weighted Citation Impact
0.00
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article

Oral 4’fluorouridine provides postexposure protection against lethal Nipah virus infection

Mack B. Harrison, Krystle N. Agans, Robert W. Cross, Viktoriya Borisevich et al.
bioRxiv (Cold Spring Harbor Laboratory)
Virology and Viral Diseases
article

Oral 4’fluorouridine provides postexposure protection against lethal Nipah virus infection

Mack B. Harrison, Krystle N. Agans, Robert W. Cross, Viktoriya Borisevich, Declan D. Pigeaud, Thomas W Geisbert, Rachel O'Toole, Abhishek N Prasad
article en

Abstract

There are no approved medical countermeasures for combatting Nipah virus (NiV) which causes regular outbreaks in humans and animals in South and Southeast Asia with mortality rates in humans ranging from 40% to more than 90%. Recently, it was shown that 4'-fluorouridine (4'-FlU; EIDD-2749), an orally available ribonucleoside analog, protected guinea pigs and nonhuman primates from lethal challenge with Lassa virus and that 4'-FlU has <i>in vitro</i> antiviral activity against NiV. Here, we assessed the postexposure protective efficacy of 4'-FlU in a lethal hamster model of NiV infection. Daily treatment with 4'-FlU beginning 3 days after exposure to NiV resulted in complete protection from lethal infection. Our findings support the further development of 4'-FlU as a therapy for NiV disease.

bioRxiv (Cold Spring Harbor Laboratory)
The University of Texas Medical Branch at Galveston (US)
Good health and well-being
Openalex Percentile: Top 47%
Virology and Viral Diseases
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