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Vlp-Based Covid-19 Vaccines: An Adaptable Technology Against the Threat of New Variants Publisher



Pratessyed WA1, 2 ; Chaves LCS3 ; Crema KP1, 2 ; Vuitika L1 ; Lira A1, 2 ; Cortes N1, 2 ; Kersten V1 ; Guimaraes FEG4 ; Sadraeian M4, 5 ; Barroso Da Silva FL6, 7 ; Cabralmarques O1, 8, 9 ; Barbuto JAM1, 10 ; Russo M1 ; Camara NOS1 Show All Authors
Authors
  1. Pratessyed WA1, 2
  2. Chaves LCS3
  3. Crema KP1, 2
  4. Vuitika L1
  5. Lira A1, 2
  6. Cortes N1, 2
  7. Kersten V1
  8. Guimaraes FEG4
  9. Sadraeian M4, 5
  10. Barroso Da Silva FL6, 7
  11. Cabralmarques O1, 8, 9
  12. Barbuto JAM1, 10
  13. Russo M1
  14. Camara NOS1
  15. Cabralmiranda G1, 2
Show Affiliations
Authors Affiliations
  1. 1. Department of Immunology, Institute of Biomedical Sciences, University of Sao Paulo (ICB/USP), Sao Paulo, SP, 05508000, Brazil
  2. 2. Institute of Research and Education in Child Health (PENSI), Sao Paulo, SP, 01228200, Brazil
  3. 3. Department of Microbiology and Immunology, School of Medicine, Emory University, Claudia Nance Rollins Building, Atlanta, 30329, GA, United States
  4. 4. Sao Carlos Institute of Physics, IFSC-USP, Sao Carlos, SP, 13566590, Brazil
  5. 5. Institute for Biomedical Materials & Devices (IBMD), Faculty of Science, University of Technology, Sydney, 2007, NSW, Australia
  6. 6. Department of Biomolecular Sciences, School of Pharmaceutical Sciences of Ribeirao Preto, University of Sao Paulo, Ribeirao Preto, SP, 14040903, Brazil
  7. 7. Department of Chemical and Biomolecular Engeneering, North Carolina State University, Raleigh, 276957905, NC, United States
  8. 8. Department of Clinical and Toxicological Analyses, School of Pharmaceutical Sciences, University of Sao Paulo, Sao Paulo, SP, 05508000, Brazil
  9. 9. Network of Immunity in Infection, Malignancy and Autoimmunity (NIIMA), Universal Scientific Education and Research Network (USERN), Children’s Medical Center, Tehran, 1419733151, Iran
  10. 10. Laboratory of Medical Investigation in Pathogenesis and Targeted Therapy in Onco-Immuno-Hematology (LIM-31), Department of Hematology, Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, SP, 0124690, Brazil

Source: Vaccines Published:2021


Abstract

Virus-like particles (VLPs) are a versatile, safe, and highly immunogenic vaccine platform. Recently, there are developmental vaccines targeting SARS-CoV-2, the causative agent of COVID-19. The COVID-19 pandemic affected humanity worldwide, bringing out incomputable human and financial losses. The race for better, more efficacious vaccines is happening almost simultaneously as the virus increasingly produces variants of concern (VOCs). The VOCs Alpha, Beta, Gamma, and Delta share common mutations mainly in the spike receptor-binding domain (RBD), demonstrat-ing convergent evolution, associated with increased transmissibility and immune evasion. Thus, the identification and understanding of these mutations is crucial for the production of new, op-timized vaccines. The use of a very flexible vaccine platform in COVID-19 vaccine development is an important feature that cannot be ignored. Incorporating the spike protein and its variations into VLP vaccines is a desirable strategy as the morphology and size of VLPs allows for better presentation of several different antigens. Furthermore, VLPs elicit robust humoral and cellular immune responses, which are safe, and have been studied not only against SARS-CoV-2 but against other coronaviruses as well. Here, we describe the recent advances and improvements in vaccine development using VLP technology. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.
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