PRE-CLINICAL IMMUNE RESPONSE AND SAFETY EVALUATION OF THE PROTEIN SUBUNIT VACCINE NANOCOVAX FOR COVID-19
T. N. M. Tran, B. May, T. T. Ung, M. K. Nguyen, T. T. Nguyen, V. L. Dinh, T. V. Tran, H. Khong, T. T. Nguyen, H. Q. H. Hua, V. A. Nguyen, T. P. Ha, D. L. Phan, T. A. Nguyen, T. N. Bui, T. M. Tu, T. T. Nguyen, T. H. Le, T. L. Dong, T. H. Huynh, C. T. Truong, L. Nie, M. N. Cao, D. K. Nguyen, T. H. Trinh, M. S. Do
Abstract
The Coronavirus disease-2019 (COVID-19) pandemic caused by the Severe Acute Respiratory Syndrome coronavirus 2 (SARS-CoV-2), has become a dire global health concern. The development of vaccines with high immunogenicity and safety is crucial for control of the global COVID-19 pandemic and prevention of further illness and fatalities. Here, we report development of SARS-CoV-2 vaccine candidate, Nanocovax, based on recombinant protein production of the extracellular (soluble) portion of the S protein of SARS-CoV-2. The results showed that Nanocovax induced high levels of S protein-specific IgG, as well neutralizing antibody in three animal models including Balb/C mice, Syrian hamsters, and non-human primate (Macaca leonina). In addition, the viral challenge study using the hamster model showed that Nanocovax protected the upper respiratory tract from SARS-CoV-2 infection. No adverse effects were induced by Nanocovax in swiss mice (Musmusculus var. Albino), Rats (Rattus norvegicus), and New Zealand rabbits. These pre-clinical results indicated that Nanocovax is safe and effective.
02 /Specification & Classification
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