Whole inactivated virus vaccine |
Stronger immune response; Safer than live attenuated virus |
Potential epitope alteration by inactivation process |
Typhoid, Cholera, Hepatitis A 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 |