Immunological and pathological outcomes of SARS-CoV-2 challenge after formalin-inactivated vaccine immunisation of ferrets and rhesus macaques
Author:
Bewley Kevin R., Gooch Karen, Thomas Kelly M., Longet Stephanie, Wiblin Nathan, Hunter Laura, Chan Kin, Brown Phillip, Russell Rebecca A., Ho Catherine, Slack Gillian, Humphries Holly E., Alden Leonie, Allen Lauren, Aram Marilyn, Baker Natalie, Brunt Emily, Cobb Rebecca, Fotheringham Susan, Harris Debbie, Kennard Chelsea, Leung Stephanie, Ryan Kathryn, Tolley Howard, Wand Nadina, White Andrew, Sibley Laura, Sarfas Charlotte, Pearson Geoff, Rayner Emma, Xue Xiaochao, Lambe Teresa, Charlton Sue, Gilbert SarahORCID, Sattentau Quentin J., Gleeson Fergus, Hall Yper, Funnell SimonORCID, Sharpe Sally, Salguero Francisco J., Gorringe AndrewORCID, Carroll Miles
Abstract
AbstractThere is an urgent requirement for safe and effective vaccines to prevent novel coronavirus disease (COVID-19) caused by SARS-CoV-2. A concern for the development of new viral vaccines is the potential to induce vaccine-enhanced disease (VED). This was reported in several preclinical studies with both SARS-CoV-1 and MERS vaccines but has not been reported with SARS-CoV-2 vaccines. We have used ferret and rhesus macaques challenged with SARS-CoV-2 to assess the potential for VED in animals vaccinated with formaldehyde-inactivated SARS-CoV-2 (FIV) formulated with Alhydrogel, compared to a negative control vaccine in ferrets or unvaccinated macaques. We showed no evidence of enhanced disease in ferrets or rhesus macaques given FIV except for mild transient enhanced disease seen at seven days post infection in ferrets. This increased lung pathology was observed early in the infection (day 7) but was resolved by day 15. We also demonstrate that formaldehyde treatment of SARS-CoV-2 reduces exposure of the spike receptor binding domain providing a mechanistic explanation for suboptimal immunity.
Publisher
Cold Spring Harbor Laboratory
Cited by
4 articles.
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