With the relatively serious global
epidemic outbreak of SARS-CoV-2 infection, public concerns focus on not only clinical
therapeutic measures and public
quarantine for this
disease but also the development of
vaccines. The technical design of our
SARS-CoV-2 inactivated vaccine provides a
viral antigen that enables the exposure of more than one structural
protein based upon the antibody composition of COVID-19
patients convalescent
serum. This design led to valid
immunity with increasing
neutralizing antibody titers and a CTL response detected post-
immunization of this
vaccine by two
injections in
rhesus macaques. Further, this elicited immunoprotection in
macaques enables not only to restrain completely
viral replication in
tissues of immunized
animals, compared to the adjuvant
control and those immunized by an RBD
peptide vaccine, but also to significantly alleviate inflammatory lesion in
lung tissues in histo-pathologic
detection, compared to the adjuvant
control with developed
interstitial pneumonia. The data obtained from these
macaques immunized with the
inactivated vaccine or RBD
peptide vaccine suggest that
immunity with a clinically protective effect against SARS-CoV-2 infection should include not only specific
neutralizing antibodies but also specific CTL responses against at least the S and N
antigens.