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. 2023 Mar;23(3):278-280.
doi: 10.1016/S1473-3099(23)00010-5. Epub 2023 Feb 3.

ACE2 binding and antibody evasion in enhanced transmissibility of XBB.1.5

Affiliations

ACE2 binding and antibody evasion in enhanced transmissibility of XBB.1.5

Can Yue et al. Lancet Infect Dis. 2023 Mar.
No abstract available

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Conflict of interest statement

YC is a cofounder of Singlomics Biopharmaceuticals and inventor of provisional patents associated with SARS-CoV-2 neutralising antibodies, including SA55 and SA58. All other authors declare no competing interests. CY and WS contributed equally.

Figures

Figure
Figure
Comparison of antibody evasiveness and hACE2 binding affinity of XBB.1 and XBB.1.5 (A) NT50 against SARS-CoV-2 B.1 (Asp614Gly), XBB.1, and XBB.1.5 pseudovirus using plasma from patients with BA.1 (n=50), BA.5 (n=36), or BF.7 (n=30) breakthrough infection convalescents who had received three doses of CoronaVac, and those with a BA.5 breakthrough infection convalescents who had received three or four vaccinations, including at least two doses of mRNA vaccines (BNT162b2 or mRNA-1273; n=10). p values were calculated using two-tailed Wilcoxon signed rank tests. (B) Pseudovirus IC50 of therapeutic neutralising antibodies. (C) Surface plasmon resonance sensorgrams measuring the hACE2-binding affinity of SARS-CoV-2 BQ.1.1, XBB and XBB.1, and XBB.1.5 receptor-binding domain. Surface plasmon resonance data were fitted to a 1:1 binding model using Biacore 8K Evaluation Software (version 3.0.12; Cytiva, Uppsala, Sweden). All neutralisation assays were done in at least two independent experiments. hACE2=human ACE2. IC50=50% inhibition concentration. ka=fitted association rate constant. kd=fitted dissociation rate constant. KD=dissociation equilibrium constant. *10 000 was the upper limit of detect; these analyses gave values more than 10 000.

References

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