Prophylactic and therapeutic remdesivir (GS-5734) treatment in the rhesus macaque model of MERS-CoV infection

Emmie de Wit(National Institute of Allergy and Infectious Diseases), Friederike Feldmann(National Institute of Allergy and Infectious Diseases), Jacqueline Cronin(National Institute of Allergy and Infectious Diseases), Robert Jordan(National Institute of Allergy and Infectious Diseases), Atsushi Okumura(National Institute of Allergy and Infectious Diseases), Tina Thomas(National Institute of Allergy and Infectious Diseases), Dana Scott(National Institute of Allergy and Infectious Diseases), Tomáš Cihlář(National Institute of Allergy and Infectious Diseases), Heinz Feldmann(National Institute of Allergy and Infectious Diseases)
Proceedings of the National Academy of Sciences
February 13, 2020
Cited by 944Open Access
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Abstract

The continued emergence of Middle East Respiratory Syndrome (MERS) cases with a high case fatality rate stresses the need for the availability of effective antiviral treatments. Remdesivir (GS-5734) effectively inhibited MERS coronavirus (MERS-CoV) replication in vitro, and showed efficacy against Severe Acute Respiratory Syndrome (SARS)-CoV in a mouse model. Here, we tested the efficacy of prophylactic and therapeutic remdesivir treatment in a nonhuman primate model of MERS-CoV infection, the rhesus macaque. Prophylactic remdesivir treatment initiated 24 h prior to inoculation completely prevented MERS-CoV-induced clinical disease, strongly inhibited MERS-CoV replication in respiratory tissues, and prevented the formation of lung lesions. Therapeutic remdesivir treatment initiated 12 h postinoculation also provided a clear clinical benefit, with a reduction in clinical signs, reduced virus replication in the lungs, and decreased presence and severity of lung lesions. The data presented here support testing of the efficacy of remdesivir treatment in the context of a MERS clinical trial. It may also be considered for a wider range of coronaviruses, including the currently emerging novel coronavirus 2019-nCoV.


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