Abstract

With continued expansion of the coronavirus disease (COVID-19) pandemic, caused by severe acute respiratory syndrome 2 (SARS-CoV-2), both antiviral drugs as well as effective vaccines are desperately needed to treat patients at high risk of life-threatening disease. Here, we present in vitro evidence for significant inhibition of SARS-CoV-2 by oleandrin and a defined extract of N. oleander (designated as PBI-06150). Using Vero cells, we found that prophylactic (pre-infection) oleandrin (as either the pure compound or as the active principal ingredient in PBI-06150) administration at concentrations as low as 0.05 µg/ml exhibited potent antiviral activity against SARS-CoV-2, with an 800-fold reduction in virus production, and a 0.1 µg/ml concentration resulted in a greater than 3000-fold reduction in infectious virus production. The half maximal effective concentration (EC50) values were 11.98 ng/ml when virus output was measured at 24 h post-infection, and 7.07 ng/ml measured at 48 h post-infection. Therapeutic (post-infection) treatment up to 24 h after SARS-CoV-2 infection of Vero cells also reduced viral titers, with 0.1 µg/ml and 0.05 µg/ml concentrations causing greater than 100-fold reduction as measured at 48 h, and the 0.05 µg/ml concentration resulting in a 78-fold reduction. Concentrations of oleandrin up to 10 µg/ml were well tolerated in Vero cells. We also present in vivo evidence of the safety and efficacy of defined N. oleander extract (PBI-06150), which was administered to golden Syrian hamsters in a preparation containing as high as 130 µg/ml of oleandrin. In comparison to administration of control vehicle, PBI-06150 provided a statistically significant reduction of the viral titer in the nasal turbinates (nasal conchae). The potent prophylactic and therapeutic antiviral activities demonstrated here, together with initial evidence of its safety and efficacy in a relevant hamster model of COVID-19, support the further development of oleandrin and/or defined extracts containing this molecule for the treatment of SARS-CoV-2 and associated COVID-19 disease and potentially also for reduction of virus spread by persons diagnosed early after infection.

Highlights

  • After its emergence in late 2019, an epidemic of coronavirus disease termed coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was first recognized in the city of Wuhan, China, quickly spread to pandemic pro­ portions [1]

  • The emergency COVID-19 pandemic situation calls for rapid screening of potential therapeutic or prophylactic drugs already shown in prior clinical trials to be safely tolerated

  • The prophylactic and therapeutic in vitro efficacy of oleandrin, a cardiac glycoside extracted from the N. oleander plant, against SARS-CoV-2 was tested

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Summary

Introduction

After its emergence in late 2019, an epidemic of coronavirus disease termed coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was first recognized in the city of Wuhan, China, quickly spread to pandemic pro­ portions [1]. As of January 2021, over 93 million cases have been identified with nearly every country involved worldwide. Hospitals and other health care systems were overwhelmed in Wuhan, Italy, Spain and New York City before cases peaked in these locations. While several approved vaccines are available, their dissemination around the world and administration remain a significant challenge. It is possible that vaccines may require continuous redevelopment due to the ongoing mutation of coronavirus into different variants; in addition, the rate of reduction in the titer of neutralizing antibodies remains unclear. Identification of safe and effective therapeutic agents that can be effective against SARS-CoV-2 remains an unmet need

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