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January 6, 2022Science164 citationsOpen Access

Antibody-mediated broad sarbecovirus neutralization through ACE2 molecular mimicry

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YPYoung‐Jun ParkAMAnna De MarcoTSTyler N. Starr

Structured PICO

Does the human monoclonal antibody S2K146 neutralize sarbecoviruses and protect against SARS-CoV-2 challenge in hamsters?

P
Population
Hamsters (for in vivo challenge) and in vitro viral models (SARS-CoV- and SARS-CoV-2-related sarbecovirus clades)
I
Intervention
Human monoclonal antibody S2K146
O
Outcome
Viral neutralization, receptor attachment inhibition, protection against SARS-CoV-2 Beta challenge, and viral escape mutant emergencesurrogate

The human monoclonal antibody S2K146 broadly neutralizes sarbecoviruses through ACE2 molecular mimicry and protects against SARS-CoV-2 Beta challenge in hamsters, presenting a candidate for clinical development.

Abstract

Understanding broadly neutralizing sarbecovirus antibody responses is key to developing countermeasures against SARS-CoV-2 variants and future zoonotic sarbecoviruses. We describe the isolation and characterization of a human monoclonal antibody, designated S2K146, that broadly neutralizes viruses belonging to SARS-CoV- and SARS-CoV-2-related sarbecovirus clades which use ACE2 as an entry receptor. Structural and functional studies show that most of the virus residues that directly bind S2K146 are also involved in binding to ACE2. This allows the antibody to potently inhibit receptor attachment. S2K146 protects against SARS-CoV-2 Beta challenge in hamsters and viral passaging experiments reveal a high barrier for emergence of escape mutants, making it a good candidate for clinical development. The conserved ACE2-binding residues present a site of vulnerability that might be leveraged for developing vaccines eliciting broad sarbecovirus immunity.

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Cite This Study

Park et al. (2022) studied this question.

synapsesocial.com/papers/69d81417ba18484428d1862fhttps://doi.org/10.1126/science.abm8143
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