Table 1.
Vaccine type | COVID-19 vaccines furthest in development/approved | Advantages | Disadvantages |
---|---|---|---|
Inactivated virus |
SinoVac (CoronaVac + aluminum) SinoPharm (Inactivated whole virus SARS-CoV-2 + aluminum) |
Entire virus, with all antigens presented Prior experience and technology – e.g., quadrivalent influenza vaccine Easier storage – does not need to be frozen |
Need adjuvants to boost Poor inducers of CD8 + T-cell immunity Hard to mass-produce Large batches of live virus pose biosecurity risk |
Protein subunits |
Novavax (NVX-CoV2373) Vector Institute (EpiVacCorona) |
Can focus on antigens that generate neutralizing antibodies Does not introduce intact pathogen |
Produced ex vivo, may not retain post-translational modifications or conformation Not efficiently presented Lower humoral and cellular response Require adjuvants to boost |
Replication incompetent adenoviral vector |
AstraZeneca (ChAdOx1 nCoV-19; AZD1222) Johnson & Johnson (Ad26.COV2.S) CanSino Biologics (Ad5-nCoV) Gamaleya (Sputnik V) |
Replication-defective, no new viral particles Avoids intact pathogen Mimics natural infection Elicits humoral and cellular immunity |
Anti-vector immunity may interfere Lower efficacy if prior anti-vector immunity exists |
DNA | Inovio (INO-4800) |
Mimic natural infection Elicits strong humoral and cellular immunity Avoids introducing pathogen Easier to mass-produce |
Delivery into cell nucleus |
mRNA |
Moderna (mRNA-1273) Pfizer-BioNTech (BNT162b2) |
Delivery into cytoplasm Unable to integrate into host genome Elicit strong humoral and cellular immunity Avoids anti-vector immunity Avoids introducing pathogen Easier to mass-produce |
Fragile – easily degraded Needs lipid nanoparticle for delivery Frozen for storage |