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. 2022 Jun 1;11(1):1488–1499. doi: 10.1080/22221751.2022.2079426

Figure 3.

Figure 3.

Analysis of antigenicity of SARS-CoV-2 variants using a panel of engineered ACE2 and neutralizing monoclonal antibodies. (a) The inhibition effect of WT-sACE2 (black) and C4-1 (pink) in SARS-CoV-2 variants entrance into ACE2 expressing HEK-293T cell lines. (b) The inhibition effect of monoclonal antibodies. Dashed lines indicate the neutralizing range of C4-1. Therapeutic effects for cocktails of C4-1 and monoclonal antibodies against beta (c), gamma (d), delta (e), and omicron (f) variants. Unpaired t-test was used to analyse differences between groups. *p<0.05, ** p<0.01, ***p<0.001, ****p<0.0001. EC 50 was calculated based on all dilutions of soluble ACE2 protein. The limit of EC 50 detection was 0–12000 ng/mL for panel A and 0–10000 ng/mL for panel b, c, d, e, and f. All results were obtained from three independent experiments. In each experiment, the infection assay was performed in duplicate wells. Data are mean ±SEM, n = 2 replicates.