4.5 Article

Covax-19/Spikogen® vaccine based on recombinant spike protein extracellular domain with Advax-CpG55.2 adjuvant provides single dose protection against SARS-CoV-2 infection in hamsters

Journal

VACCINE
Volume 40, Issue 23, Pages 3182-3192

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.vaccine.2022.04.041

Keywords

COVID-19; SARS-Cov-2; Vaccine; Adjuvant; Advax; Pandemic; Coronavirus

Funding

  1. National Institute of Allergy and Infectious Diseases of the National Institutes of Health [HHS-N272201400053C, HHSN272201800044C, HHSN272201800024C]
  2. MTPConnect Biomedical Translation Bridge Program
  3. Fast Grant

Ask authors/readers for more resources

This study compares the immunogenicity and protective efficacy of several recombinant SARS-CoV-2 spike protein candidates expressed in insect cells. The soluble secreted spike protein extracellular domain (ECD) formulated with adjuvants elicited robust immune responses and showed good protective effects in animal experiments. There was a strong correlation between serum neutralizing antibody levels and lung protection. Based on these findings, the spike protein ECD formulated with Advax-CpG55.2 was selected for human clinical development.
COVID-19 presents an ongoing global health crisis. Protein-based COVID-19 vaccines that are well-tolerated, safe, highly-protective and convenient to manufacture remain of major interest. We therefore sought to compare the immunogenicity and protective efficacy of a number of recombinant SARS-CoV-2 spike protein candidates expressed in insect cells. By comparison to a full length (FL) spike protein detergent-extracted nanoparticle antigen, the soluble secreted spike protein extracellular domain (ECD) generated higher protein yields per liter of culture and when formulated with either Alum-CpG55.2 or Advax-CpG55.2 combination adjuvants elicited robust antigen-specific humoral and cellular immunity in mice. In hamsters, the spike ECD when formulated with either adjuvant induced high serum neutralizing antibody titers even after a single dose. When challenged with the homologous SARS-CoV-2 virus, hamsters immunized with the adjuvanted spike ECD exhibited reduced viral load in day 1-3 oropharyngeal swabs and day 3 nasal turbinate tissue and had no recoverable infectious virus in day 3 lung tissue. The reduction in lung viral load correlated with less weight loss and lower lung pathology scores. The formulations of spike ECD with Alum-CpG55.2 or Advax-CpG55.2 were protective even after just a single dose, although the 2-dose regimen performed better overall and required only half the total amount of antigen. Pre-challenge serum neutralizing antibody levels showed a strong correlation with lung protection, with a weaker correlation seen with nasal or oropharyngeal protection. This suggests that serum neutralizing antibody levels may correlate more closely with systemic, rather than mucosal, protection. The spike protein ECD with Advax-CpG55.2 formulation (Covax-19 (R) vaccine) was selected for human clinical development. (C) 2022 Elsevier Ltd. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available