Table 1.
MNT | sVNT Genscript | ELISA Euroimmun (IgG/IgA; Spike & IgG; N) | ELISA Wantai (IgM; RBD) | In‐house ELISA (IgM/IgA/IgG; RBD/Spike) | Chaotropic‐based dissociation assays | Multiplex | |
---|---|---|---|---|---|---|---|
Test time | 5 days | 65 min | 120 min (S); 105 min (N) | 75 min | 48 h | 48 h | 24 h per detector (antibody isotype or FcR) |
Hands‐on user time | 7 h | 30 min | 30 min | 30 min | ~2.5 h (6 plates) | ~3 h (6 plates) | ~4 h per detector |
Capacity; samples/run | 96 samples | 96 samples | 96 samples | 96 samples | 10 samples per plate | 5 samples per plate | 384 samples per detector |
Volume of sample per test | 28 µL | 10 µL | 10 µL | 10 µL | 7.3 µL | 7.3 µL | 1 µL per detector |
Plasma vs serum | Either a | Either | Either | Either | Either | Either | Either |
Samples run in duplicate or singularly | Duplicate in independent assays | Singularly (duplicate for samples within the equivocal zone) | Singularly (duplicate for samples within the equivocal zone) | Singularly (duplicate for samples within the equivocal zone) | Singularly | Singularly | Duplicate in independent assays |
Cost per sample (AUD) | – | ~$14 | ~$8 | ~$8 | ~$1.60–$2.20 | ~$1.80–$2.40 | ~$16 |
TGA approval 42 | – | Emergency access scheme | Emergency access scheme | Emergency access scheme | – | – | – |
FDA approval 43 | – | Emergency use authorisation | Emergency use authorisation (IgG) | – | – | – | – |
Biosafety level | BSL 3 | BSL 2 | BSL 2 | BSL 2 | BSL 2 | BSL 2 | BSL 2 |
Antigen specificity | Whole virus | RBD | S or N | RBD | S, RBD | S, RBD | S, S1, S2, RBD, N |
Class switching | No | No | Yes | Yes | Yes | No | Yes |
Antibody avidity | No | No | No | No | No | Yes | Yes |
Level of expertise | High | Moderate | Moderate | Moderate | Moderate | Moderate | High |
Standardisation | Run specific | Yes | Yes | Yes | Yes | Yes | Bead set specific |
Result readout | End‐point titre | % inhibition | Index value | Index value | End‐point titre | Avidity Index | MFI |
Serum preferred.