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Immunogenicity and Safety of Heterologous Boost Immunization With Pastocovac Plus Against Covid-19 in Chadox1-S or Bbibp-Corv Primed Individuals Publisher Pubmed



Eybpoosh S1 ; Biglari A2 ; Sorouri R3, 4 ; Ashrafian F5 ; Larijani MS5 ; Verezbencomo V6 ; Toledoromani ME7 ; Silva CV8 ; Salehivaziri M9 ; Dahmardeh S10 ; Doroud D11 ; Banifazl M12 ; Mostafavi E1 ; Bavand A5 Show All Authors
Authors
  1. Eybpoosh S1
  2. Biglari A2
  3. Sorouri R3, 4
  4. Ashrafian F5
  5. Larijani MS5
  6. Verezbencomo V6
  7. Toledoromani ME7
  8. Silva CV8
  9. Salehivaziri M9
  10. Dahmardeh S10
  11. Doroud D11
  12. Banifazl M12
  13. Mostafavi E1
  14. Bavand A5
  15. Ramezani A5
Show Affiliations
Authors Affiliations
  1. 1. Department of Epidemiology and Biostatistics, Research Centre for Emerging and Reemerging Infectious Diseases, Pasteur Institute of Iran, Tehran, Iran
  2. 2. School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. IPI Directorate, Pasteur Institute of Iran, Tehran, Iran
  4. 4. Department of Microbiology, Faculty of Medicine, Baqiyatallah University of Medical Sciences, Tehran, Iran
  5. 5. Clinical Research Department, Pasteur Institute of Iran, Tehran, Iran
  6. 6. Finlay Vaccine Institute, Havana, Cuba
  7. 7. Pedro Kouri Tropical Medicine Institute, Havana, Cuba
  8. 8. Cybernetics, Mathematics and Physics Institute, Havana, Cuba
  9. 9. COVID-19 National Reference Laboratory, Pasteur Institute of Iran, Tehran, Iran
  10. 10. Vaccination Department, Pasteur Institute of Iran, Tehran, Iran
  11. 11. Quality Control Department, Production and research Complex, Pasteur Institute of Iran, Tehran, Iran
  12. 12. Iranian Society for Support of Patients with Infectious Disease, Tehran, Iran

Source: PLoS Pathogens Published:2023


Abstract

Background This study aimed at evaluation and comparison of PastoCovac Plus protein-subunit vaccine in parallel with ChAdOx1-S (AstraZeneca) and BBIBP-CorV (Sinopharm) in primarily vaccinated volunteers with two doses of ChAdOx1-S or BBIBP-CorV. Materials and methods 194 volunteers enrolled the study who were previously primed with 2 doses of ChAdOx1-S or BBIBP-CorV vaccines. They were divided into two heterologous regimens receiving a third dose of PastoCovac Plus, and two parallel homologous groups receiving the third dose of BBIBP-CorV or ChAdOx1-S. Serum samples were obtained just before and 4 weeks after booster dose. Anti-spike IgG and neutralizing antibodies were quantified and the conventional live-virus neutralization titer, (cVNT50) assay was done against Omicron BA.5 variant. Moreover, the adverse events data were recorded after receiving booster doses. Results ChAdOx1-S/PastoCovac Plus group reached 73.0 units increase in anti-Spike IgG rise compared to the ChAdOx1-S/ ChAdOx1-S (P: 0.016). No significant difference was observed between the two groups regarding neutralizing antibody rise (P: 0.256), indicating equivalency of both booster types. Adjusting for baseline titers, the BBIBP-CorV/PastoCovac Plus group showed 135.2 units increase (P<0.0001) in anti-Spike IgG, and 3.1 (P: 0.008) unit increase in mean rise of neutralizing antibodies compared to the homologous group. Adjustment for COVID-19 history, age, underlying diseases, and baseline antibody titers increased the odds of anti-Spike IgG fourfold rise both in the ChAdOx1-S (OR: 1.9; P: 0.199) and BBIBP CorV (OR: 37.3; P< 0.0001) heterologous groups compared to their corresponding homologous arms. The odds of neutralizing antibody fourfold rise, after adjustment for the same variables, was 2.4 (P: 0.610) for the ChAdOx1-S heterologous group and 5.4 (P: 0.286) for the BBIBP CorV heterologous groups compared to their corresponding homologous groups. All the booster types had the potency to neutralize BA.5 variant with no significant difference. The highest rate of adverse event incidence was recorded for ChAdOx1-S homologous group. Conclusions PastoCovac Plus booster application in primed individuals with BBIBP-CorV or ChAdOx1-S successfully increased specific antibodies’ levels without any serious adverse events. This vaccine could be administrated in the heterologous regimen to effectively boost humoral immune responses. Copyright: © 2023 Eybpoosh et al.