iScience (Jun 2022)

COH04S1 and beta sequence-modified vaccine protect hamsters from SARS-CoV-2 variants

  • Felix Wussow,
  • Mindy Kha,
  • Katelyn Faircloth,
  • Vu H. Nguyen,
  • Angelina Iniguez,
  • Joy Martinez,
  • Yoonsuh Park,
  • Jenny Nguyen,
  • Swagata Kar,
  • Hanne Andersen,
  • Mark G. Lewis,
  • Flavia Chiuppesi,
  • Don J. Diamond

Journal volume & issue
Vol. 25, no. 6
p. 104457

Abstract

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Summary: COVID-19 vaccine efficacy is threatened by emerging SARS-CoV-2 variants of concern (VOC) with the capacity to evade protective neutralizing antibody responses. We recently developed clinical vaccine candidate COH04S1, a synthetic modified vaccinia Ankara vector (sMVA) co-expressing spike and nucleocapsid antigens based on the Wuhan-Hu-1 reference strain that showed potent efficacy to protect against ancestral SARS-CoV-2 in Syrian hamsters and non-human primates and was safe and immunogenic in healthy volunteers. Here, we demonstrate that intramuscular immunization of Syrian hamsters with COH04S1 and an analogous Beta variant-adapted vaccine candidate (COH04S351) elicits potent cross-reactive antibody responses and protects against weight loss, lower respiratory tract infection, and lung pathology following challenge with major SARS-CoV-2 VOC, including Beta and the highly contagious Delta variant. These results demonstrate efficacy of COH04S1 and a variant-adapted vaccine analog to confer cross-protective immunity against SARS-CoV-2 and its emerging VOC, supporting clinical investigation of these sMVA-based COVID-19 vaccine candidates.

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