Inactivated virus vaccines |
Virus particles are inactivated by heat, chemicals, or radiation |
Whole virus, with or without adjuvant (promote an effective immune response against the inactivated pathogen) [93,94] |
Whole virus, with or without adjuvant (promote an effective immune response against the inactivated pathogen) [91,95] |
Maintained virus particles structure; rapidly develop; easy to prepare; safety; high-titer neutralizing antibodies [93]; protection with adjuvant [96,97]. |
Potential inappropriate for highly immunosuppressed individuals; possible TH2 cell-distortive immune response [98,99]. |
Live-attenuated virus vaccines |
Attenuated the virulence, but still keeping it viable by mutagenesis or targeted deletions |
Envelope protein deletion [100]; non-structural protein 14 (nsp14) and exonuclease (ExoN) inactivation [101] |
Full-length infectious cDNA clone or mutant viruses [102] |
Inexpensive; quick immunity; less adverse effect; activates all phases of the immune system [103]; more durable immunity; more targeted [77]. |
Phenotypic or genotypic reversion possible; need sufficient viral replication [77]. |
Viral vector vaccines |
Genetically engineered unrelated viral genome with deficient packaging elements for encoding targeted gene |
Spike and nucleocapsid proteins [100,104] |
Spike and nucleocapsid proteins [87,88] |
Safety; stronger and specific cellular and humoral immune responses [77]. |
Varies inoculation routes may produce different immune responses [96]; possibly incomplete protection; may fail in aged vaccinees; possible TH2 cell-distortive immune response [105]. |
Subunit vaccines |
Antigenic components inducing the immune system without introducing viral particles, whole or otherwise. |
Spike and nucleocapsid proteins [53,59,106] |
Spike and nucleocapsid proteins [85,86,107,108] |
High safety; consistent production; can induce cellular and humoral immune responses; high-titer neutralizing antibodies [109]. |
Uncertain cost-effectiveness; relatively lower immunogenicity; need appropriate adjuvants [77]. |
DNA vaccines |
Genetically engineered DNA for directly producing an antigen |
Spike and nucleocapsid proteins [110,111] |
Spike and nucleocapsid proteins [89,90] |
Easier to design; high safety; high-titer neutralizing antibodies [110]. |
Lower immune responses; potential TH2 cell-distortive immune response results; potential ineffective; possibly delayed-type hypersensitivity [112]. |