Preclinical and clinical studies for viral vector-based COVID-19 vaccines

VectorConstructFindingsRef
ChAdOx1ChAdOx1 nCoV-19Protection against SARS-CoV-2 in macaques[11]
ChAdOx1ChAdOx1 nCoV-19Protection after intranasal injection in mice[11]
ChAdOx1ChAdOx1 nCoV-19Phase I/II: safety, strong immune responses[12]
ChAdOx1ChAdOx1 nCoV-19Phase II/III: high Ab titers in all age groups[13]
ChAdOx1ChAdOx1 nCoV-19Phase III: > 30,000 healthy volunteers[14]
ChAdOx1ChAdOx1 nCoV-19Phase III: 62.1–90.0% vaccine efficacy[15]
ChAdOx1ChAdOx1 nCoV-19EUA in the UK in December 2020[16]
Ad26Ad26.COV2.SProtection of hamsters after single injection[18]
Ad26Ad26.COV2.SProtection of macaques after single injection[19]
Ad26Ad26.COV2.SPhase I: single injection > immune response[20]
Ad26Ad26.COV2.SPhase I/II: strong immune response[21]
Ad26Ad26.COV2.SPhase III: > 60,000 healthy volunteers[22]
Ad26Ad26.COV2.SEUA by the FDA in February 2021[23]
Ad26/Ad5rAd26-S/rAd5-S100% protection in mice, hamsters & primates[24]
Ad26/Ad5rAd26-S/rAd5-SPhase I/II: safety, strong immune response[25]
Ad26/Ad5rAd26-S/rAd5-SPhase III: 91.6% vaccine efficacy[26]
Ad26/Ad5rAd26-S/rAd5-SEUA in Russia in July 2020[27]
Ad5Ad5-S-nb2SARS-CoV-2 protection in mice & ferrets[28]
Ad5Ad5-S.nb2SARS-CoV-2 protection in macaques[29]
Ad5Ad5-S.nb2Phase I: binding and neutralization Abs[30]
Ad5Ad5-S.nb2Phase II: Abs dependent on age, pre-existing Ad5[31]
Ad5Ad5-S.nb290.1% efficacy of preventing severe COVID-19[32]
Ad5Ad5-S.nb2EUA in China in February 2021[33]
Ad5Ad5-S nb2Protection in macaques after i.n. administration[29]
Ad5AdCOVID-RBDSystemic & mucosal immunity after i.n. delivery[59]
Ad5VXA-COV2-1Strong immune response after i.n. delivery in mice[66]
Ad5VXA-COV2-1Phase I: oral delivery, strong immunogenicity[69]
GRAdGRAd-COV2Robust immune responses in mice & macaques[34]
GradGRAd-COV2Phase I: study in progress[35]
ChAd68ChAdV68 + SAMPhase I: study in progress[37]
AAVCOVID-1AAV2-CoV-2 SProtection in primates after single administration[38]
MVAMVA-CoV-2 S/NHumoral & cellular immune responses in mice[40]
MVAMVA-COV-2 SProtection in mice[41]
MVAMVA-COV-2Phase I: study in progress[42]
MVAMVA-COV-2Phase I: study in progress[43]
NDVNDV-SARS-CoV-2 SProtection in mice and hamsters[45]
NDVNDV-SARS-CoV-2 SProtection in mice[46]
NDVNDV-HXP-SPhase I/II: study in progress[47]
MVMV-SARS-CoV-2-STh1-biased and T-cell immune responses in mice[49]
MVMV-SARS-CoV-2-SPhase I: weak immunogenicity, trial discontinued[51]
VSVVSV-SARS-CoV-2-SProtection against SARS-CoV-2 pathogenesis in mice[52]
VSVVSV-SARS-CoV-2-SPhase I: weak immunogenicity, trial discontinued[53]
VSVVSV-ΔGProtection against SARS-CoV-2 in hamsters[55]
VSVVSV-ΔGPhase I/II: study in progress[56]
VEE RNAVEE-SARS-CoV-2 STh1-biased immune response in mice[58]
VEE RNAVEE-SARS-CoV-2 SPhase I: dose-escalation study in progress[59]
LVLV-SARS-COV-2-SReduced viral load after i.n. delivery in mice[61]
LVLV-SMENP + CTLPhase I/II: s.c. delivery of LV-DCs. i.v. CTLs[62]
InfluenzaΔNA(RBD)-FluSingle i.n. dose: strong immune response[63]
InfluenzaIFV-COV-2 S RBDPhase I: registered trial for intranasal spray[64]
InfluenzaIFV-COV-2 S RBDPhase II: registered trial for intranasal spray[65]

AAV: adeno-associated virus; Ab: antibodies; CTLs: cytotoxic T cell lymphocytes; DCs: dendritic cells; FDA: Food and Drug Administration; GRAd: gorilla adenovirus; i.n.: intranasal; IFV: influenza virus; i.v.: intravenous; LV: lentivirus; LV-SMENP: lentivirus vector expressing SARS-CoV-2 minigene; MV: measles virus; MVA: modified vaccinia virus Ankara; NDV: Newcastle disease virus; RBD: receptor binding domain; SAM: self-amplifying mRNA; s.c.: subcutaneous; VEE: Venezuelan equine encephalitis virus; VSV: vesicular stomatitis virus; VSV-ΔG: VSV G protein