Immunogenicity of a spike protein subunit-based COVID-19 vaccine with broad protection against various SARS-CoV-2 variants in animal studies

• Published in: PloS one Vol. 18; no. 3; p. e0283473
• Main Authors: Yang, Ming-Chen, Wang, Chun-Chung, Tang, Wei-Chien, Chen, Kuan-Ming, Chen, Chu-Ying, Lin, Hsiao-Han, Hsieh, Yin-Cheng, Wang, Nan-Hsuan, Kuo, Yin-Chieh, Chu, Ping-Tzu, Tung, Hsin-Yi, Wu, Yi-Chen, Sun, Juo-Ling, Liu, Sheng-Yu, Li, Wan-Fen, Lee, Wei-Han, Lai, Jiann-Shiun, Chang, Michael, Lai, Ming-Tain
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 24.03.2023; Public Library of Science (PLoS)
• Subjects: Adjuvants, Immunologic; Adjuvants, Pharmaceutic; Aluminum; Aluminum hydroxide; Analysis; Animal experimentation; Animals; Animals, Laboratory; Antibodies, Neutralizing; Antibodies, Viral; Antigens; Biology and Life Sciences; Coronaviruses; COVID-19 - prevention & control; COVID-19 Vaccines; Epidemics; Evaluation; Global economy; Health aspects; Humans; Immunity; Immunization; Immunogenicity; Immunoglobulin G; Infections; ISCOMS; Lymphocytes T; Medicine and Health Sciences; Molecular weight; Nanoparticles; Neutralization; Pandemics; Physical Sciences; Protein Subunits; Proteins; Research and Analysis Methods; SARS-CoV-2; Severe acute respiratory syndrome coronavirus 2; Spike Glycoprotein, Coronavirus - genetics; Spike protein; Vaccination; Vaccines; Viral diseases; Taiwan
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0283473

SARS-CoV-2 pandemic has profound impacts on human life and global economy since the outbreak in 2019. With the new variants continue to emerge with greater immune escaping capability, the protectivity of the available vaccines is compromised. Therefore, development a vaccine that is capable of inducing immunity against variants including omicron strains is in urgent need. In this study, we developed a protein-based vaccine BCVax that is consisted of antigen delta strain spike protein and QS21-based adjuvant AB801 in nanoparticle immune stimulation complex format (AB801-ISCOM). Results from animal studies showed that high level of anti-S protein IgG was induced after two doses of BCVax and the IgG was capable of neutralizing multiple variants of pseudovirus including omicron BA.1 or BA.2 strains. In addition, strong Th1 response was stimulated after BCVax immunization. Furthermore, BCvax with AB801-ISCOM as the adjuvant showed significant stronger immunity compared with the vaccine using aluminum hydroxide plus CpG 1018 as the adjuvant. BCVax was also evaluated as a booster after two prior vaccinations, the IgG titers and pseudovirus neutralization activities against BA.2 or BA.4/BA.5 were further enhanced suggesting BCVax is a promising candidate as booster. Taken together, the pre-clinical data warrant BCVax for further development in clinic.