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Data · dataset · 2026

<p>Mechanism and functional activity of V1WT_06, V1WT_41, and VA14_26.</p>

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<p>Neutralisation of sarbecoviruses through entry via different host ACE2s.

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Neutralisation of <b>A)</b> Rc-o319 and <b>B)</b> RhGB07 was measured against entry via <i>Rh. cornutus</i> ACE2 and <i>Rh. alcyone</i> ACE2, respectively, which were transiently expressed in HEK293T/17 cells. <b>C)</b> Neutralisation of WIV-1 was compared between entry via hu-ACE2 (dotted line and closed symbols) and <i>Rh. alcyone</i> ACE2 (full line and closed symbols).

Neutralisation was measured using HEK 293T cells transiently expressing either <i>Human</i> ACE2 or <i>Rh. alcyone</i> ACE2. For A-C, mean values are plotted with error bars showing ± standard deviation (s.d.). <b>D)</b> Ability of IgGs to inhibit the interaction between cell surface ACE2 (including hu-ACE2, <i>Rh. cornutus</i> ACE2 and <i>Rh. alcyone</i> ACE2) and soluble RBD (including SARS-CoV-2, WIV-1, Rs4231, RhBG07, and Rc-o319 RBDs).

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IgGs were pre-incubated with fluorescently labelled RBD before addition to ACE2 expressing cells. N.B = No binding of IgG to the RBD. The percentage reduction in mean fluorescence intensity is reported.

Experiments were performed in duplicate. <b>E)</b> Antibody dependant cellular cytotoxicity (ADCC) of IgGs measured through the surface expression of CD107a on activated NK cells (NK-92 cells expressing CD16) [<a href="plosbiology.org/article/info:doi/10.1371/journal.pbio.3003882#pbio.3003882.ref041" target="_blank">41</a>]. HIV-1 specific neutralising antibody, PGT128 is used as a negative control [<a href="plosbiology.org/article/info:doi/10.1371/journal.pbio.3003882#pbio.3003882.ref031" target="_blank">31</a>].

The data underlying this Figure can be found in <a href="plosbiology.org/article/info:doi/10.1371/journal.pbio.3003882#pbio.3003882.s010" target="_blank">S1 Data</a>.</p>

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