Mucosal administration of a live attenuated recombinant COVID-19 vaccine protects nonhuman primates from SARS-CoV-2

  • Mariana F. Tioni
  • , Robert Jordan
  • , Angie Silva Pena
  • , Aditya Garg
  • , Danlu Wu
  • , Shannon I. Phan
  • , Christopher M. Weiss
  • , Xing Cheng
  • , Jack Greenhouse
  • , Tatyana Orekov
  • , Daniel Valentin
  • , Swagata Kar
  • , Laurent Pessaint
  • , Hanne Andersen
  • , Christopher C. Stobart
  • , Melissa H. Bloodworth
  • , R. Stokes Peebles
  • , Yang Liu
  • , Xuping Xie
  • , Pei Yong Shi
  • Martin L. Moore, Roderick S. Tang

Research output: Contribution to journalArticlepeer-review

Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the causative agent of the COVID-19 global pandemic. SARS-CoV-2 is an enveloped RNA virus that relies on its trimeric surface glycoprotein spike for entry into host cells. Here we describe the COVID-19 vaccine candidate MV-014-212, a live, attenuated, recombinant human respiratory syncytial virus expressing a chimeric SARS-CoV-2 spike as the only viral envelope protein. MV-014-212 was attenuated and immunogenic in African green monkeys (AGMs). One mucosal administration of MV-014-212 in AGMs protected against SARS-CoV-2 challenge, reducing by more than 200-fold the peak shedding of SARS-CoV-2 in the nose. MV-014-212 elicited mucosal immunoglobulin A in the nose and neutralizing antibodies in serum that exhibited cross-neutralization against virus variants of concern Alpha, Beta, and Delta. Intranasally delivered, live attenuated vaccines such as MV-014-212 entail low-cost manufacturing suitable for global deployment. MV-014-212 is currently in Phase 1 clinical trials as an intranasal COVID-19 vaccine.

Original languageEnglish (US)
Article number85
Journalnpj Vaccines
Volume7
Issue number1
DOIs
StatePublished - Dec 2022

ASJC Scopus subject areas

  • Immunology
  • Pharmacology
  • Infectious Diseases
  • Pharmacology (medical)

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