From: Coronavirus vaccine development: from SARS and MERS to COVID-19
Vaccine platform | Advantages | Disadvantages | Clinically approved examples |
---|---|---|---|
Whole inactivated virus vaccine | Stronger immune response; Safer than live attenuated virus | Potential epitope alteration by inactivation process | Typhoid, Cholera, Hepatitis AÂ virus, Plague, Rabies, Influenza, Polio (Salk) |
Live attenuated virus vaccine | Stronger immune response; Preservation of native antigen; Mimicking natural infection | Risk of residual virulence, especially for immunocompromised people | Measles, Mumps, Polio (Sabin), Rota virus, Yellow Fever, Bacillus Calmette–Guérin (BCG), Rubella, Varicella |
Viral vector vaccine | Stronger immune response; Preservation of native antigen; Mimicking natural infection | More complicated manufacturing process; Risk of genomic integration; Response dampened by pre-existing immunity against vector | Ebola virus |
Subunit vaccine | Safe and well-tolerated | Lower immunogenicity; Requirement of adjuvant or conjugate to increase immunogenicity | Pertussis, Influenza, Streptococcus pneumoniae, Haemophilus influenzae type b |
Viral-like particle vaccine | Safe and well-tolerated; mimicking native virus conformation | Lower immunogenicity; More complicated manufacturing process | Hepatitis B virus, Human Papillomavirus |
DNA vaccine | Safe and well-tolerated; Stable under room temperature; Highly adaptable to new pathogen; Native antigen expression | Lower immunogenicity; Difficult administration route; Risk of genomic integration | NA |
RNA vaccine | Safe and well-tolerated; Highly adaptable to new pathogen; Native antigen expression | Lower immunogenicity; Requirement of low temperature storage and transportation; Potential risk of RNA-induced interferon response | NA |