# Induction of neutralizing antibodies against SARS-CoV-2 variants by a multivalent mRNA-lipid nanoparticle vaccine encoding SARS-CoV-2/SARS-CoV Spike protein receptor-binding domains in mice

**Authors:** Qiong Zhang, Shashi Tiwari, Jing Wen, Shaobo Wang, Lingling Wang, Wanyu Li, Lingzhi Zhang, Stephen Rawling, Yong Cheng, Jesse Jokerst, Tariq M. Rana

PMC · DOI: 10.1371/journal.pone.0300524 · 2024-04-18

## TL;DR

This study shows that a multivalent mRNA vaccine can induce antibodies that neutralize multiple SARS-CoV and SARS-CoV-2 variants in mice.

## Contribution

A novel multivalent mRNA-lipid nanoparticle vaccine design that induces cross-neutralizing antibodies against multiple coronaviruses and variants.

## Key findings

- All vaccine constructs induced strong anti-RBD antibody responses in mice.
- The heterodimeric vaccine elicited cross-neutralizing IgG against SARS-CoV, Wuhan-Hu-1, B.1.351, and B.1.617.2 variants.

## Abstract

To address the need for multivalent vaccines against Coronaviridae that can be rapidly developed and manufactured, we compared antibody responses against SARS-CoV, SARS-CoV-2, and several variants of concern in mice immunized with mRNA-lipid nanoparticle vaccines encoding homodimers or heterodimers of SARS-CoV/SARS-CoV-2 receptor-binding domains. All vaccine constructs induced robust anti-RBD antibody responses, and the heterodimeric vaccine elicited an IgG response capable of cross-neutralizing SARS-CoV, SARS-CoV-2 Wuhan-Hu-1, B.1.351 (beta), and B.1.617.2 (delta) variants.

## Linked entities

- **Diseases:** SARS-CoV-2 (MONDO:0100096)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** S (surface glycoprotein) [NCBI Gene 43740568] {aka spike glycoprotein}
- **Species:** Severe acute respiratory syndrome-related coronavirus (no rank) [taxon 694009], Mus musculus (house mouse, species) [taxon 10090], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11025929/full.md

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Source: https://tomesphere.com/paper/PMC11025929