Preclinical and clinical studies for viral vector-based COVID-19 vaccines
Vector | Construct | Findings | Ref |
---|---|---|---|
ChAdOx1 | ChAdOx1 nCoV-19 | Protection against SARS-CoV-2 in macaques | [11] |
ChAdOx1 | ChAdOx1 nCoV-19 | Protection after intranasal injection in mice | [11] |
ChAdOx1 | ChAdOx1 nCoV-19 | Phase I/II: safety, strong immune responses | [12] |
ChAdOx1 | ChAdOx1 nCoV-19 | Phase II/III: high Ab titers in all age groups | [13] |
ChAdOx1 | ChAdOx1 nCoV-19 | Phase III: > 30,000 healthy volunteers | [14] |
ChAdOx1 | ChAdOx1 nCoV-19 | Phase III: 62.1–90.0% vaccine efficacy | [15] |
ChAdOx1 | ChAdOx1 nCoV-19 | EUA in the UK in December 2020 | [16] |
Ad26 | Ad26.COV2.S | Protection of hamsters after single injection | [18] |
Ad26 | Ad26.COV2.S | Protection of macaques after single injection | [19] |
Ad26 | Ad26.COV2.S | Phase I: single injection > immune response | [20] |
Ad26 | Ad26.COV2.S | Phase I/II: strong immune response | [21] |
Ad26 | Ad26.COV2.S | Phase III: > 60,000 healthy volunteers | [22] |
Ad26 | Ad26.COV2.S | EUA by the FDA in February 2021 | [23] |
Ad26/Ad5 | rAd26-S/rAd5-S | 100% protection in mice, hamsters & primates | [24] |
Ad26/Ad5 | rAd26-S/rAd5-S | Phase I/II: safety, strong immune response | [25] |
Ad26/Ad5 | rAd26-S/rAd5-S | Phase III: 91.6% vaccine efficacy | [26] |
Ad26/Ad5 | rAd26-S/rAd5-S | EUA in Russia in July 2020 | [27] |
Ad5 | Ad5-S-nb2 | SARS-CoV-2 protection in mice & ferrets | [28] |
Ad5 | Ad5-S.nb2 | SARS-CoV-2 protection in macaques | [29] |
Ad5 | Ad5-S.nb2 | Phase I: binding and neutralization Abs | [30] |
Ad5 | Ad5-S.nb2 | Phase II: Abs dependent on age, pre-existing Ad5 | [31] |
Ad5 | Ad5-S.nb2 | 90.1% efficacy of preventing severe COVID-19 | [32] |
Ad5 | Ad5-S.nb2 | EUA in China in February 2021 | [33] |
Ad5 | Ad5-S nb2 | Protection in macaques after i.n. administration | [29] |
Ad5 | AdCOVID-RBD | Systemic & mucosal immunity after i.n. delivery | [59] |
Ad5 | VXA-COV2-1 | Strong immune response after i.n. delivery in mice | [66] |
Ad5 | VXA-COV2-1 | Phase I: oral delivery, strong immunogenicity | [69] |
GRAd | GRAd-COV2 | Robust immune responses in mice & macaques | [34] |
Grad | GRAd-COV2 | Phase I: study in progress | [35] |
ChAd68 | ChAdV68 + SAM | Phase I: study in progress | [37] |
AAVCOVID-1 | AAV2-CoV-2 S | Protection in primates after single administration | [38] |
MVA | MVA-CoV-2 S/N | Humoral & cellular immune responses in mice | [40] |
MVA | MVA-COV-2 S | Protection in mice | [41] |
MVA | MVA-COV-2 | Phase I: study in progress | [42] |
MVA | MVA-COV-2 | Phase I: study in progress | [43] |
NDV | NDV-SARS-CoV-2 S | Protection in mice and hamsters | [45] |
NDV | NDV-SARS-CoV-2 S | Protection in mice | [46] |
NDV | NDV-HXP-S | Phase I/II: study in progress | [47] |
MV | MV-SARS-CoV-2-S | Th1-biased and T-cell immune responses in mice | [49] |
MV | MV-SARS-CoV-2-S | Phase I: weak immunogenicity, trial discontinued | [51] |
VSV | VSV-SARS-CoV-2-S | Protection against SARS-CoV-2 pathogenesis in mice | [52] |
VSV | VSV-SARS-CoV-2-S | Phase I: weak immunogenicity, trial discontinued | [53] |
VSV | VSV-ΔG | Protection against SARS-CoV-2 in hamsters | [55] |
VSV | VSV-ΔG | Phase I/II: study in progress | [56] |
VEE RNA | VEE-SARS-CoV-2 S | Th1-biased immune response in mice | [58] |
VEE RNA | VEE-SARS-CoV-2 S | Phase I: dose-escalation study in progress | [59] |
LV | LV-SARS-COV-2-S | Reduced viral load after i.n. delivery in mice | [61] |
LV | LV-SMENP + CTL | Phase I/II: s.c. delivery of LV-DCs. i.v. CTLs | [62] |
Influenza | ΔNA(RBD)-Flu | Single i.n. dose: strong immune response | [63] |
Influenza | IFV-COV-2 S RBD | Phase I: registered trial for intranasal spray | [64] |
Influenza | IFV-COV-2 S RBD | Phase 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