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. 2022 Jun 14;10(4):e00926-22. doi: 10.1128/spectrum.00926-22

TABLE 1.

Descriptive overview of the neutralizing susceptibility assays and the MAbs undergoing testing

Author(s) (reference[s]) Virus typea Cell lineb Inoculumc Hoursd Control Variant(s) MAb(s)e
Aggarwal21 (33) Infectious Vero 104 24 A.2.2 BA.1 BAM, CAS/IMD, SOT, CIL/TIX
Boschi22 (9) Infectious Vero NAg 48 B.1 BA.1 BAM/ETE, CAS/IMD, CIL/TIX
Cameroni21 (11) Infectious Vero NA 20 B.1 BA.1 SOT
Dejnirattisai22 (14) Infectious Vero 102 NA B BA.1 BAM/ETE, CAS/IMD, SOT, CIL/TIX, ADI
Duty22 (39) Infectious Vero 102 NA A BA.1 CIL/TIX, SOT
Fenwick22 (40) Infectious Vero 103 48 Delta BA.1, BA.2 CAS/IMD, CIL/TIX, SOT, ADI
Ma22 (43) Infectious Vero 102 96 A BA.1 BAM/ETE, CAS/IMD, SOT
Case22 (36) Infectious Vero-TMPRSS2 102 60 B.1 BA.1, BA.1.1, BA.2 CIL/TIX, SOT
Ohashi22 (44) Infectious Vero-TMPRSS2 NA 24 A BA.1, BA.2 CAS/IMD, SOT
Takashita22 and Takashita22b (30, 31) Infectious Vero-TMPRSS2 103 24 A BA.1, BA.2 BAM/ETE, CAS/IMD, SOT, CIL/TIX
Touret22 (25); Touret22b (48) Infectious Vero-TMPRSS2 NA 48 B.1 BA.1, BA.2 BAM/ETE, CAS/IMD, SOT, CIL/TIX, REG
VanBlargan22-1 (26) Infectious Vero-TMPRSS2 102 70 B.1 BA.1 BAM/ETE, CAS/IMD, SOT, CIL/TIX, REG
VanBlargan22-2 (26) Infectious Vero-ACE2-TMPRSS2 102 24 B.1 BA.1 BAM/ETE, CAS/IMD, SOT, CIL/TIX, REG
Meng22 (21) Infectious HOS-ACE2-TMPRSS2 102 24 Delta BA.1 CAS/IMD
Planas21 (22); Bruel22 (10) Infectious U2OS-ACE2 NA 20 Delta BA.1, BA.2 BAM/ETE, CAS/IMD, SOT, CIL/TIX, REG, ADI
Wilhelm21 (51) Infectious NA 4 × 103 48 B BA.1 CAS/IMD
FDA21, FDA21b, and FDA22 (5557) Infectious NA NA NA NA BA.1, BA.2, BA.1.1 CIL/TIX, SOT, BEB
Ai22 (34) PV (VSV) Vero NA 24 B BA.1, BA.1.1, BA.2 BAM/ETE, CAS/IMD, SOT, CIL/TIX, BEB, REG, AMU, ADI
Cameroni21 (11) PV (VSV) Vero NA 20 B.1 BA.1, BA.1.1 BAM/ETE, CAS/IMD, SOT, CIL/TIX, REG
Cathcart22 (37) PV (VSV) Vero 2 × 103 6 - BA.1, BA.1.1, BA.2 SOT
Hoffmann22 (16); Schulz22 (23) PV (VSV) Vero NA 16 B.1 BA.1 BAM/ETE, CAS/IMD, SOT, CIL/TIX
Rothenberger21 (46) PV (VSV) Vero 250 16 B BA.1 BAM/ETE, CAS/IMD, SOT, CIL/TIX, AMU/ROM
Wang22 (28) PV (VSV) Vero NA 24 B.1 BA.1 BAM/ETE, CAS/IMD, SOT, CIL/TIX, REG, ADI
Iketani22 and Liu21 (17, 19) PV (VSV) Vero NA 10 B.1 BA.1, BA.1.1, BA.2 BAM/ETE, CAS/IMD, SOT, CIL/TIX, AMU/ROM, ADI, BEB
Duty22 (39) PV (VSV) 293T-ACE2-TMPRSS2 NA NA B.1 BA.1, BA.1.1 CIL/TIX
Cao21, Cao22, and Cui22 (12, 13, 35) PV (VSV) Huh-7 103 24 B.1 BA.1, BA.1.1, BA.2 BAM/ETE, CAS/IMD, SOT, CIL/TIX, BEB, ADI, AMU/ROM, C144
Wang22c (27) PV (VSV) Huh-7 NA 24 B BA.1 ETE, IMD, TIX, SOT
Westendorf21 (50); FDA22 (56) PV (VSV) 293T-ACE2/ACE2-TMPRSS2 NA 72 B.1 BA.1, BA.2 BAM/ETE, CAS/IMD, SOT, CIL/TIX, BEB, REG, ADI, C135/C144
FDA21, FDA21b, and FDA22 (5557) PV 293T-ACE2-TMPRSS2 NA 48 B BA.1, BA.1.1, BA.2 CIL/TIX, SOT, BEB
NIH-NCATS21-2 (AstraZeneca) (Monogram) (58) PV 293T-ACE2-TMPRSS2 1 × 104–5 × 105 RLU 72 B BA.1 CIL/TIX
Lusvarghi22 (20) PV (HIV) 293T-ACE2-TMPRSS2 1 × 105–5 × 105 RLU 48 B.1 BA.1 BAM/ETE, CAS/IMD, SOT, CIL/TIX, BEB, AMU/ROM, ADI, C144
Chen22 (38) PV (HIV) 293T-ACE2-TMPRSS2 NA 72 A BA.1 BAM/ETE, CAS/IMD
Zhou21 (29)f PV (HIV) 293T-ACE2-TMPRSS2 NA 72 B.1 BA.1 BAM/ETE, CAS/IMD, SOT, CIL/TIX, BEB, REG, ADI, C135/C144
Gruell22 and Gruell22b (15, 41) PV (HIV) 293T-ACE2 NA 48 B BA.1, BA.1.1, BA.2 BAM/ETE, CAS/IMD, CIL/TIX, SOT, BEB, REG, ADI, AMU, C135/C144
Ju22 (18) PV (HIV) 293T-ACE2 NA 48 B BA.1 ETE, CAS/IMD, SOT, C144
Pelzek22 (45) PV (HIV) 293T-ACE2 NA 60 B BA.1 SOT
Sheward22 (24) PV (HIV) 293T-ACE2 5 × 104 RLU 48 B.1 BA.1 BAM/ETE, CAS/IMD, SOT
Tada22 and Zhou22 (32, 54) PV (HIV) 293T-ACE2 2 × 103 48 B.1 BA.1, BA.2 BAM/ETE, CAS/IMD, SOT, CIL/TIX
Wang22b (49) PV (HIV) 293T-ACE2 NA 48 B BA.1 IMD, SOT
Ikemura21 (42) PV (HIV) 293T-ACE2 NA 48 B BA.1 CAS/IMD, SOT
Yamasoba22 (52) PV (HIV) HOS-ACE2-TMPRSS2 2 × 104 RLU 48 B.1 BA.1, BA.2 CAS/IMD, SOT
NIH-NCATS21 (Brii Biosciences) (59) PV (HIV) NA NA NA B BA.1 AMU/ROM
Yuan22 (53) PV (MLV) Vero NA 120 B BA.1 BAM/ETE, CAS/IMD, CIL/TIX, SOT, ADI, C144
a

The reference is indicated by the first author’s surname followed by the year of publication. For authors that have more than one publication in the same year, a lower case letter has been added. For publications with more than one assay, a dash followed by a number has been added. PV, pseudotyped virus; HIV, human immunodeficiency virus; VSV, vesicular stomatitis virus; MLV, murine leukemia virus. A study using virus-like particles is not shown (47).

b

Cell line followed by ACE2 and/or TMPRSS2 indicates cells modified to stably express these surface proteins.

c

Studies using infectious viruses reported the inoculum as 50% tissue culture infectious doses (TCID50), focus-forming units (FFU), infectious units (IU), or multiplicity of infection (MOI). This column treats the TCID50, FFU, and IU similarly. MOI was used to calculate the inoculum if the number of cells per well was available. Studies using PVs inconsistently reported the virus inoculum, and when reported, it was reported as a TCID50 or as relative light units (RLU).

d

The endpoint for the infectious virus assays was cytopathic effect usually augmented by immunostaining of virally infected cells, with the exception of two studies which used RNA yield (25, 48). PV assays measured RLU produced by luciferase-encoding reporter genes.

e

BAM, bamlanivimab; ETE, etesevimab; CAS, casirivimab; IMD, imdevimab; SOT, sotrovimab; CIL, cilgavimab; TIX, tixagevimab; BEB, bebtelovimab; REG, regdanvimab; ADI, adintrevimab; AMU, amubarvimab; ROM, romlusevimab. The presence of two MAbs separated by “/” indicates the combination was tested and/or that each individual MAb in the combination was also tested. Not all MAbs were tested for activity against each of the Omicron variants. A dash indicates that the relevant data were not identified.

f

293T-ACE2 cells were used for TIX and 293T-ACE2-TMPRSS2 used for CIL. Several of the results in this study overlap results in Westendorf21 (50).

g

NA, not available.