4.7 Article

Late remdesivir treatment initiation partially protects African green monkeys from lethal Nipah virus infection

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ANTIVIRAL RESEARCH
卷 216, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.antiviral.2023.105658

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Nipah virus; Antiviral; Remdesivir; Nonhuman primate; Nucleotide analog

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The study found that delayed administration of remdesivir by 3 days still had some efficacy against Nipah virus infection, but it had limited preventive effects on clinical disease.
Remdesivir is a nucleotide prodrug with preclinical efficacy against lethal Nipah virus infection in African green monkeys when administered 1 day post inoculation (dpi) (Lo et al., 2019). Here, we determined whether remdesivir treatment was still effective when treatment administration initiation was delayed until 3 dpi. Three groups of six African green monkeys were inoculated with a lethal dose of Nipah virus, genotype Bangladesh. On 3 dpi, one group received a loading dose of 10 mg/kg remdesivir followed by daily dosing with 5 mg/kg for 11 days, one group received 10 mg/kg on 12 consecutive days, and the remaining group received an equivalent volume of vehicle solution. Remdesivir treatment initiation on 3 dpi provided partial protection from severe Nipah virus disease that was dose dependent, with 67% of animals in the high dose group surviving the chal-lenge. However, remdesivir treatment did not prevent clinical disease, and surviving animals showed histologic lesions in the brain. Thus, early administration seems critical for effective remdesivir treatment during Nipah virus infection.

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