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Int Immunopharmacol . Safety and immunogenicity of the ChAdOx1, MVA-MERS-S, and GLS-5300 DNA MERS-CoV vaccines

tetano

Editor, Senior Moderator
Int Immunopharmacol


. 2023 Mar 29;118:109998.
doi: 10.1016/j.intimp.2023.109998. Online ahead of print.
Safety and immunogenicity of the ChAdOx1, MVA-MERS-S, and GLS-5300 DNA MERS-CoV vaccines


Mahmoud Kandeel[SUP] 1 [/SUP], Mohamed A Morsy[SUP] 2 [/SUP], Hany M Abd El-Lateef[SUP] 3 [/SUP], Mohamed Marzok[SUP] 4 [/SUP], Hossam S El-Beltagi[SUP] 5 [/SUP], Khalid M Al Khodair[SUP] 6 [/SUP], Ibrahim Albokhadaim[SUP] 7 [/SUP], Katharigatta N Venugopala[SUP] 8 [/SUP]



Affiliations

Abstract

Background: The Middle East respiratory syndrome coronavirus (MERS-CoV) is a pathogen associated with an acute respiratory infection that has a high mortality rate in humans. It was first identified in June of 2012 in the Arabian Peninsula. The success of the COVID-19 vaccines has shown that it is possible to take advantage of medical and scientific advances to produce safe and effective vaccines for coronaviruses. This study aimed to examine the safety and immunogenicity of MERS-CoV vaccines.
Methods: The research method Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) was used as the guideline for this study. RevMan 5.4 software was used to perform a meta-analysis of the included studies. The safety was assessed by recording adverse events following vaccination, and the immunogenicity was assessed by using seroconversion.
Results: The study included five randomized controlled trials that met the inclusion criteria after screening. The studies had 173 participants and were performed in four countries. The vaccines examined were the ChAdOx1 MERS vaccine, MVA-MERS-S vaccine, and GLS-5300 DNA MERS-CoV vaccine. The meta-analysis showed no significant differences in local adverse effects (all local adverse effects and pain) or systemic adverse effects (all systemic adverse effects, fatigue, and headache) among participants in groups receiving a high-dose vaccine or a low-dose vaccine. There were, however, higher levels of seroconversion in high-dose groups than in low-dose groups (OR 0.16 [CI 0.06, 0.42, p = 0.0002]).
Conclusion: The findings showed that high doses of current MERS-CoV vaccine candidates conferred better immunogenicity than low doses and that there were no differences in the safety of the vaccines.

Keywords: ChAdOx1 MERS; GLS-5300; MERS-CoV; MVA-MERS-S; Vaccine.
 
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