A single-dose live-attenuated YF17D-vectored SARS-CoV2 vaccine candidate
Lorena Sanchez Felipe, Thomas Vercruysse, Sapna Sharma, Ji Ma, Viktor LemmensiD, Dominique van Looveren, Mahadesh Prasad Arkalagud Javarappa, Robbert BoudewijnsiD, Bert Malengier-Devlies, Suzanne F. Kaptein, Laurens LiesenborghsiD, Carolien De Keyzer, Lindsey Bervoets, Madina RasulovaiD, Laura SeldeslachtsiD, Sander Jansen, Michael Bright Yakass, Osbourne Quaye, Li-Hsin Li, Xin ZhangiD, Sebastiaan ter HorstiD, Niraj Mishra, Lotte Coelmont, Christopher CawthorneiD, Koen Van LaereiD, , Kai D
Abstract
The explosively expanding COVID-19 pandemic urges the development of safe, efficacious and fast-acting vaccines to quench the unrestrained spread of SARS-CoV-2. Several promising vaccine platforms, developed in recent years, are leveraged for a rapid emergency response to COVID-191. We employed the live-attenuated yellow fever 17D (YF17D) vaccine as a vector to express the prefusion form of the SARS-CoV-2 Spike antigen. In mice, the vaccine candidate, tentatively named YF-S0, induces high levels of SARS-CoV-2 neutralizing antibodies and a favorable Th1 cell-mediated immune response. In a stringent hamster SARS-CoV-2 challenge model2, vaccine candidate YF-S0 prevents infection with SARS-CoV-2. Moreover, a single dose confers protection from lung disease in most vaccinated animals even within 10 days. These results warrant further development of YF-S0 as a potent SARS-CoV-2 vaccine candidate.
02 /Specification & Classification
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