Abstract

Safe and effective vaccines against coronavirus disease 2019 (COVID-19) are essential for ending the ongoing pandemic. Although impressive progress has been made with several COVID-19 vaccines already approved, it is clear that those developed so far cannot meet the global vaccine demand alone. We describe a COVID-19 vaccine based on a replication-defective gorilla adenovirus expressing the stabilized prefusion severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein named GRAd-COV2. We assessed the safety and immunogenicity of a single-dose regimen of this vaccine in healthy younger and older adults to select the appropriate dose for each age group. For this purpose, a phase 1, dose-escalation, open-labeled trial was conducted including 90 healthy participants (45 aged 18 to 55 years old and 45 aged 65 to 85 years old) who received a single intramuscular administration of GRAd-COV2 at three escalating doses. Local and systemic adverse reactions were mostly mild or moderate and of short duration, and no serious adverse events were reported. Four weeks after vaccination, seroconversion to spike protein and receptor binding domain was achieved in 43 of 44 young volunteers and in 45 of 45 older participants. Consistently, neutralizing antibodies were detected in 42 of 44 younger-age and 45 of 45 older-age volunteers. In addition, GRAd-COV2 induced a robust and T helper 1 cell (TH1)–skewed T cell response against the spike protein in 89 of 90 participants from both age groups. Overall, the safety and immunogenicity data from the phase 1 trial support the further development of this vaccine.

Highlights

  • The coronavirus disease 2019 (COVID-19) pandemic is one of the most major international public health emergencies that have occurred over the last century

  • We describe a COVID-19 vaccine based on a replication-defective gorilla adenovirus expressing the stabilized pre-fusion SARS-CoV-2 spike protein, named GRAd-COV2

  • One participant who was vaccinated in arm 4 was found to be positive at baseline for anti-spike protein IgG by chemiluminescent immunoassay (CLIA), the primary serology assay per the study protocol for the evaluation of vaccine-induced spike proteinspecific antibody responses

Read more

Summary

Introduction

The coronavirus disease 2019 (COVID-19) pandemic is one of the most major international public health emergencies that have occurred over the last century. COVID-19 is caused by severe acute respiratory syndrome coronavirus 2 (SARSCoV-2), which emerged in the People Republic of China at the end of 2019. The COVID-19 pandemic has already caused hundreds of millions of infections with several million fatalities worldwide. This unprecedented global health emergency has boosted international efforts to develop a vaccine targeting SARS-CoV-2. A multitude of innovative platforms have been used, including genetic vaccines based on mRNA, DNA and viral vectors. As of September 2021, there are as many as 315 vaccine candidates still in development.

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call