A multiantigenic Orf virus-based vaccine efficiently protects hamsters and nonhuman primates against SARS-CoV-2

一种基于多抗原羊痘病毒的疫苗能有效保护仓鼠和非人灵长类动物免受SARS-CoV-2感染。

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作者:Alena Reguzova # ,Melanie Müller # ,Felix Pagallies ,Dominique Burri ,Ferdinand Salomon ,Hanns-Joachim Rziha ,Zsofia Bittner-Schrader ,Babs E Verstrepen ,Kinga P Böszörményi ,Ernst J Verschoor ,Ingo Gerhauser ,Knut Elbers ,Meral Esen ,Alessandro Manenti ,Martina Monti ,Hans-Georg Rammensee ,Madiha Derouazi ,Markus W Löffler ,Ralf Amann

Abstract

Among the common strategies to design next-generation COVID-19 vaccines is broadening the antigenic repertoire thereby aiming to increase efficacy against emerging variants of concern (VoC). This study describes a new Orf virus-based vector (ORFV) platform to design a multiantigenic vaccine targeting SARS-CoV-2 spike and nucleocapsid antigens. Vaccine candidates were engineered, either expressing spike protein (ORFV-S) alone or co-expressing nucleocapsid protein (ORFV-S/N). Mono- and multiantigenic vaccines elicited comparable levels of spike-specific antibodies and virus neutralization in mice. Results from a SARS-CoV-2 challenge model in hamsters suggest cross-protective properties of the multiantigenic vaccine against VoC, indicating improved viral clearance with ORFV-S/N, as compared to equal doses of ORFV-S. In a nonhuman primate challenge model, vaccination with the ORFV-S/N vaccine resulted in long-term protection against SARS-CoV-2 infection. These results demonstrate the potential of the ORFV platform for prophylactic vaccination and represent a preclinical development program supporting first-in-man studies with the multiantigenic ORFV vaccine.

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