Table 1.
Vaccine Platform | Coronavirus | Description | Mechanism of immune stimulation | Clinical trial | Ref |
---|---|---|---|---|---|
Live Attenuated vaccine |
SARS-CoV | SARS-CoV envelope spike proteinrecom- binant attenuated influenza virus. | Antibody-based immune responses | Pre-clinical | [82] |
Attenuated vesicular stomatitis virus (VSV) expressing SARS-CoV spike protein |
Antibody-based immune responses | Pre-clinical | [83] | ||
Live attenuated with deletion of the E protein and accessory proteins |
Induction of T cell and antibody responses | Pre-clinical | [84] | ||
Engineered inactivated of SARS-CoV- 2 virus |
Induce neutralizing antibodies responses | Pre-clinical | [85] | ||
Live attenuated recombinant measles vaccine |
High-titre neutralizing antibodies and Th-1 based immune response | Pre-clinical | [86] | ||
Inactivated vaccine | SARS-CoV | SARS-CoV virus inactivated by use of β-propiolactone | Antibody-based immune responses | Phase I | [89,90,93,130] |
SARS-CoV UV- inactivated with or without an adjuvant | Induce T-cell responses and cytokine production such as IFN-γ, TNF-α, IL-5, IL-4, IL-2. | Pre-clinical | [91] | ||
SARS-CoV inactivated by UV and formalin | Immune response (IgG and IL-4 generation) |
Pre-clinical | [131] | ||
MERS-CoV | Inactivated MERS-CoV | Antibody-based immune responses | Pre-clinical | [132] | |
Subunit vaccine | SARS-CoV | A recombinant subunit vaccine contained S protein severe acute respiratory syndrome (SARS) and aluminum hydroxide adjuvant (Alhydrogel®) | Inducing the neutralizing antibody responses | Phase I | [133] |
Recombinant fusion protein consists of 318-510 residues and IgG1-Fc fragment | Antibody-based immune responses | Pre-clinical | [39] | ||
Recombinant S2 fragment with amino acid residues with Freund’s adjuvant | Antibodies, Th1-and Th-2 type responses | Pre-clinical | [95] | ||
Consists of spike protein amino acids S318-510 with alum+CpG oligodeoxynucleotides adjuvants | IgG2 antibodies and cellular immune response | Pre-clinical | [43] | ||
Trimeric recombinant spike protein | Antibody-based immune responses | Pre-clinical | [134] | ||
MERS-CoV | Protein containing amino-acid residues from 377 to 588 of receptor binding domain | Induce humoral and cellular responses | Pre-clinical | [135] | |
Different epitopes of receptor binding domain with a glycan. | Pre-clinical | [96] | |||
MERS-CoV- S1 subunit | Antibody-based immune responses | Pre-clinical | [136] | ||
Vector-based vaccine | SARS-CoV | Adenovirus carrying N-terminal segment of S1gene of SARS-CoV | Induce humoral responses | Pre-clinical | [98] |
MERS-CoV | Recombinant adenovirus encoding the spike S1 subunit | Induce humoral and cellular responses | Pre-clinical | [99] | |
Adenovirus-vectored consist of full length spike glycoprotein MERS-CoV (ChAdOx1 MERS) | Induce humoral and cellular responses | Phase I | [137] | ||
Nucleic acid vaccine | SARS-CoV, | Full spike (S) glycoprotein or fragments | Specific CD4+ and CD8+ T-cell and neutralizing antibody responses. | Phase I | [107] |
Plasmid pCI-N, encodes full-length N gene. | cytotoxic T lymphocytes and CD8+ response and cytokine production such as IFN-γ and IL-2 | Pre-clinical | [104] | ||
Designed DNA vaccine by encoding S1 and S2 subunit | Antibody-based immune responses | Pre-clinical | [138] | ||
Utilized three fragments of N proteins (N1, N2 and N3) to express in E. coli for designing of DNA vaccine |
Antibody-based immune responses (IgG and IgG-1 antibodies) | Pre-clinical | [103] | ||
Open reading frame SARS-3a gene and bat like SARSCoV open reading frame 3a gene | Antibody and Th-1 responses and cytokine production such as IFN-γ and IL-2 | Pre-clinical | [106] | ||
MERS-CoV | GLS-5300 is a DNA plasmid vaccine that expresses the MERS CoV spike (S) glycoprotein | Induce the strong neutralizing antibodies and T-cell responses | Phase I | [139] | |
DNA vaccine encodes the 725 S amino-acid residues of MERS-CoV | Induce CD4 and CD8 T cells and cytokine production such as IFN-γ | Pre-clinical | [105] | ||
Nano- based vaccine | SARS-CoV | S protein of SARS-CoV on polyethylenimine nanocarrier | Induce humoral and immune response (IgG, IgA, IFN-γ, IL-2) | Pre-clinical | [108] |
Plasmid DNA loaded biotinylated chitosan nanoparticles as a carrier for N protein of (SARS-CoV) | Induces mucosal IgG and IgA antibodies |
Pre-clinical | [109] |