Vaccines (Nov 2023)

Pre-Clinical Safety and Immunogenicity Study of a Coronavirus Protein-Based Subunit Vaccine for COVID-19

  • Kamshat Shorayeva,
  • Aziz Nakhanov,
  • Ainur Nurpeisova,
  • Olga Chervyakova,
  • Kuanysh Jekebekov,
  • Zhandos Abay,
  • Nurika Assanzhanova,
  • Sandugash Sadikaliyeva,
  • Elina Kalimolda,
  • Aibol Terebay,
  • Sabina Moldagulova,
  • Zharkinay Absatova,
  • Ali Tulendibayev,
  • Syrym Kopeyev,
  • Gulnur Nakhanova,
  • Aisha Issabek,
  • Sergazy Nurabayev,
  • Aslan Kerimbayev,
  • Lespek Kutumbetov,
  • Yergali Abduraimov,
  • Markhabat Kassenov,
  • Mukhit Orynbayev,
  • Kunsulu Zakarya

DOI
https://doi.org/10.3390/vaccines11121771
Journal volume & issue
Vol. 11, no. 12
p. 1771

Abstract

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Creating an effective and safe vaccine is critical to fighting the coronavirus infection successfully. Several types of COVID-19 vaccines exist, including inactivated, live attenuated, recombinant, synthetic peptide, virus-like particle-based, DNA and mRNA-based, and sub-unit vaccines containing purified immunogenic viral proteins. However, the scale and speed at which COVID-19 is spreading demonstrate a global public demand for an effective prophylaxis that must be supplied more. The developed products promise a bright future for SARS-CoV-2 prevention; however, evidence of safety and immunogenicity is mandatory before any vaccine can be produced. In this paper, we report on the results of our work examining the safety, toxicity, immunizing dose choice, and immunogenicity of QazCoVac-P, a Kazakhstan-made sub-unit vaccine for COVID-19. First, we looked into the product’s safety profile by assessing its pyrogenicity in vaccinated rabbit models and using the LAL (limulus amebocyte lysate) test. We examined the vaccine’s acute and sub-chronic toxicity on BALB/c mice and rats. The vaccine did not cause clinically significant toxicity-related changes or symptoms in our toxicity experiments. Finally, we performed a double immunization of mice, ferrets, Syrian hamsters, and rhesus macaques (Macaca mulatta). We used ELISA to measure antibody titers with the maximum mean geometric titer of antibodies in the animals’ blood sera totaling approximately 8 log2. The results of this and other studies warrant recommending the QazCoVac-P vaccine for clinical trials.

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