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  • Preclinical Immune Response...
    Tran, Thi Nhu Mai; May, Bruce Pearson; Ung, Trong Thuan; Nguyen, Mai Khoi; Nguyen, Thi Thuy Trang; Dinh, Van Long; Doan, Chinh Chung; Tran, The Vinh; Khong, Hiep; Nguyen, Thi Thanh Truc; Hua, Hoang Quoc Huy; Nguyen, Viet Anh; Ha, Tan Phat; Phan, Dang Luu; Nguyen, Truong An; Bui, Thi Ngoc; Tu, Tieu My; Nguyen, Thi Theo; Le, Thi Thuy Hang; Dong, Thi Lan; Huynh, Trong Hieu; Ho, Phien Huong; Le, Nguyen Thanh Thao; Truong, Cong Thao; Pham, Hoang Phi; Luong, Cong Y; Y, Nie Lim; Cao, Minh Ngoc; Nguyen, Duy Khanh; Le, Thi Thanh; Vuong, Duc Cuong; Nguyen, Le Khanh Hang; Do, Minh Si

    Frontiers in immunology, 12/2021, Letnik: 12
    Journal Article

    The coronavirus disease 2019 (COVID-19) pandemic caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has become a global health concern. The development of vaccines with high immunogenicity and safety is crucial for controlling the global COVID-19 pandemic and preventing further illness and fatalities. Here, we report the development of a SARS-CoV-2 vaccine candidate, Nanocovax, based on recombinant protein production of the extracellular (soluble) portion of the spike (S) protein of SARS-CoV-2. The results showed that Nanocovax induced high levels of S protein-specific IgG and neutralizing antibodies in three animal models: BALB/c mouse, Syrian hamster, and a non-human primate ( ). In addition, a viral challenge study using the hamster model showed that Nanocovax protected the upper respiratory tract from SARS-CoV-2 infection. Nanocovax did not induce any adverse effects in mice ( var. albino) and rats ( ). These preclinical results indicate that Nanocovax is safe and effective.