VOC | Vaccine name | Neutralization capacity against wild-type/D614G strain/Victoria virus | Assays used | References | Original Trial | References | |
---|---|---|---|---|---|---|---|
B.1.1.7 | BNT162b2 | Single mutation- (=) Full spike mutation- (↓) to (↓↓) CE: Against infection: 87.0% to 95.3%; Against symptomatic infection: 97%; Against hospitalization: 97.5% | VSV based pseudovirus assay | Pfizer | 1. Multinational, placebo-controlled, observer-blinded, efficacy trial 2. 43, 548 participants with 21, 720 vaccine recipients 3. Only 8 cases of COVID-19 among vaccine recipients after 7 days of 2nd dose 4. Vaccine efficacy 95% | [77] | |
mRNA-1273 | Full spike mutation: (↓) | VSV-based pseudovirus assay | [55] | ||||
Chadox1nCov | B.1.1.7: (↓↓↓) CE: Against symptomatic infection: 70.4% | Live virus microneutralization assay | [56] | ||||
B.1.351 | BNT162b2 | Triple mutation: (↓↓↓) Full spike variant: (↓↓) E484K mutation: (↓↓) B.1.351 lineage: v1: (↓↓↓); v2: (↓↓↓); v3: (↓↓↓) B.1.351: (↓↓) CE: Against infection: 72.1% to 75.0%; Against severe disease: 86% | In vitro FRENT assay | ||||
Moderna | 1. Randomized, observer-blinded, placebo-controlled 2. Study site: USA 3. 30, 420 volunteers with 15,210 in vaccine recipient group 4. Only 11 cases of COVID 19 in vaccine recipient group 5. Vaccine efficacy: 94.1% | [78] | |||||
mRNA-1273 | For B.1.351 lineage: v1: (↓↓↓); v2: (↓↓↓); v3: (↓↓↓) For B.1.351: (↓↓↓) | In vitro FRENT assay | |||||
Chadox1nCov | Triple mutation: (↓↓↓) B.1.351: (↓↓↓) Triple mutants: drop-in neutralization titer to 85 B.1.351: drop in neutralization titer to 74 In live virus, assay titer ranged from (= to ↓↓↓) CE: Against infection: 10.4%, with no severe cases | In vitro FRENT assay; Pseudovirus assay; Live virus neutralization assay; clinical trial | [79] | ||||
Oxford-Astrazeneca | 1. Blinded, randomized, controlled trial across the UK, Brazil, South Africa 2. Two standard-dose vaccine efficacy 62.1% 3. low dose/ standard-dose vaccine efficacy 90.4% 4. Overall vaccine efficacy 70.4% 5. Dosing interval 21 days | [80] | |||||
P.1 | BNT162b2 | Triple mutation: (↓) P.2 with E484K: (↓↓) P.1 with triple mutants: (↓↓) | In vitro FRENT assay | [63] | |||
mRNA-1273 | P.2 with E484K: (↓) P.1 with triple mutants: (↓↓) | In vitro FRENT assay | [63] | ||||
Chadox1nCov | Triple mutation: (↓) CE: Against infection: 77.9%; against hospitalization: 87.6%; against death: 93.6% | In vitro FRENT assay | |||||
B.1.671 | BNT162b2 | GMT 164 (↓↓) E484K: (↓↓↓) CE: Against symptomatic infection: 88% | FRNT50 assay |  |  |  | |
mRNA-1273 | GMT 190 (↓↓) | FRNT50 assay | [68] |  |  |  | |
Chadox1nCov | CE: Against symptomatic infection: 60%; Against moderate to severe disease: 79.2% | Â | Â | Â | Â | ||
Covaxin | GMT ratio for B.1.617: 1.84, while for B.1.1.7 and D614G: 1.06 | Pseudovirus assay | [69] | Â | Â | Â |