“…To date, researchers have expressed partial S protein, including the collagenase equivalent domain (COE), receptor binding domain (RBD) and S1, or the full-length S protein of individual SECs using E. coli , Lactobacillus , Bacillus subtilis , yeast, 293T cells, virus expression system (e.g., vesicular stomatitis virus, swinepox virus, pseudorabies virus, baculovirus, and human adenovirus), or transgenic plant expression systems ( Table 3 ). Among them, the immunogenicity of 14 vaccine candidates was evaluated in mice [ 103 , 104 , 105 , 106 , 107 , 108 , 109 , 110 , 111 , 112 , 113 , 114 , 115 , 116 ]. All these vaccine candidates induced high levels of the virus-specific IgG and VN antibodies in serum and cytokines in splenocytes.…”