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July 1, 2025Cell ReportsOpen Access

Broadly neutralizing antibodies targeting a conserved silent face of spike RBD resist extreme SARS-CoV-2 antigenic drift

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Why the study?

Developing broad coronavirus vaccines requires identifying and understanding the molecular basis of conserved spike epitopes targeted by broadly neutralizing antibodies.

Design

Structural and neutralization study

Key result

Group 1 and 2 broadly neutralizing antibodies retain neutralizing activity against highly mutated SARS-CoV-2 variants like BA.2.86 and JN.1 by targeting conserved spike receptor-binding domain epitopes.

Authors

GSGe SongMYMeng YuanHLHejun Liu

Discussion

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Overview

Animal data extend conserved RBD epitopes as vaccine targets; human efficacy remains unproven.

Structured PICO

P
Population
sarbecovirus receptor-binding domain (RBD) group 1 and 2 broadly neutralizing antibodies (bnAbs) and highly mutated SARS-CoV-2 variants, including BA.2.86 and JN.1
I
Intervention
Broadly neutralizing antibodies (bnAbs) targeting sarbecovirus RBD group 1 and 2
O
Outcome
Neutralizing activity against highly mutated SARS-CoV-2 variants and structural interactionssurrogate

Identification of conserved spike RBD epitopes targeted by broadly neutralizing antibodies provides a potential target for broad coronavirus vaccines.

Cite This Study

Song et al. (2025) studied SARS-CoV-2. Broadly neutralizing antibodies (group 1 and 2 bnAbs) was evaluated on Neutralizing activity against SARS-CoV-2 variants and structural interactions. Group 1 and 2 broadly neutralizing antibodies retain neutralizing activity against highly mutated SARS-CoV-2 variants like BA.2.86 and JN.1 by targeting conserved spike receptor-binding domain epitopes.

synapsesocial.com/papers/6a9aed13d23b4b438634a847https://doi.org/10.1016/j.celrep.2025.115948
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