Frontiers in Immunology (Mar 2022)

Poxvirus MVA Expressing SARS-CoV-2 S Protein Induces Robust Immunity and Protects Rhesus Macaques From SARS-CoV-2

  • Petra Mooij,
  • Juan García-Arriaza,
  • Juan García-Arriaza,
  • Patricia Pérez,
  • Patricia Pérez,
  • Adrian Lázaro-Frías,
  • Adrian Lázaro-Frías,
  • Babs E. Verstrepen,
  • Kinga P. Böszörményi,
  • Daniella Mortier,
  • Zahra Fagrouch,
  • Gwendoline Kiemenyi-Kayere,
  • Henk Niphuis,
  • Roja Fidel Acar,
  • Lisette Meijer,
  • Marieke A. Stammes,
  • Ivanela Kondova,
  • Ernst J. Verschoor,
  • Corine H. GeurtsvanKessel,
  • Erwin de Bruin,
  • Reina S. Sikkema,
  • Joanna Luczkowiak,
  • Rafael Delgado,
  • Rafael Delgado,
  • Dolores Montenegro,
  • Eugenia Puentes,
  • Esteban Rodríguez,
  • Willy M. J. M. Bogers,
  • Gerrit Koopman,
  • Mariano Esteban

DOI
https://doi.org/10.3389/fimmu.2022.845887
Journal volume & issue
Vol. 13

Abstract

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Novel safe, immunogenic, and effective vaccines are needed to control the COVID-19 pandemic, caused by SARS-CoV-2. Here, we describe the safety, robust immunogenicity, and potent efficacy elicited in rhesus macaques by a modified vaccinia virus Ankara (MVA) vector expressing a full-length SARS-CoV-2 spike (S) protein (MVA-S). MVA-S vaccination was well tolerated and induced S and receptor-binding domain (RBD)-binding IgG antibodies and neutralizing antibodies against SARS-CoV-2 and several variants of concern. S-specific IFNγ, but not IL-4, -producing cells were also elicited. After SARS-CoV-2 challenge, vaccinated animals showed a significant strong reduction of virus loads in bronchoalveolar lavages (BAL) and decreased levels in throat and nasal mucosa. Remarkably, MVA-S also protected macaques from fever and infection-induced cytokine storm. Computed tomography and histological examination of the lungs showed reduced lung pathology in MVA-S-vaccinated animals. These findings favor the use of MVA-S as a potential vaccine for SARS-CoV-2 in clinical trials.

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