# Trivalent coronavirus vaccines elicit broad-spectrum immunity in mice and attenuate respiratory viral load in golden hamsters

**Authors:** Xiuli Shen, Jiangshan He, Maoshun Liu, Xinyu Zhang, Peijia Wang, Yiming Shao

PMC · DOI: 10.3389/fimmu.2026.1734382 · Frontiers in Immunology · 2026-01-26

## TL;DR

A trivalent coronavirus vaccine induces broad immunity in mice and reduces viral load in hamsters, offering potential for future outbreaks.

## Contribution

A trivalent vaccine using S proteins of SARS-CoV-1, MERS-CoV, and SARS-CoV-2 elicits broad-spectrum immunity and protects against variants.

## Key findings

- Trivalent vaccines induce robust humoral and cellular immune responses against multiple coronaviruses in mice.
- The vaccine provides protection against the SARS-CoV-2 XBB variant in golden hamsters.
- The heterologous DNA-prime/VTT-boost regimen enhances immune response breadth and efficacy.

## Abstract

Coronaviruses frequently undergo genomic mutation and recombination in nature. Through cross-species infection and sporadic spillover events, novel coronaviruses may periodically emerge in humans. SARS-CoV-1, MERS-CoV, and SARS-CoV-2 all cause severe, predominantly respiratory diseases with moderate to high pathogenicity, posing a substantial threat to public health. To prepare for potential future coronavirus outbreaks, there is a need for universal vaccines capable of eliciting broad-spectrum humoral and cellular immunity.

In this study, we constructed DNA- and replicating Vaccinia virus TianTan (VTT)-vectored monovalent and trivalent vaccines, using the spike (S) proteins of the aforementioned wild-type viruses as immunogens in a heterologous DNA-prime/VTT-boost regimen.

Compared with monovalent vaccines, the trivalent candidate induced robust, broad-spectrum humoral and cellular immune responses against the S proteins of SARS-CoV-1, MERS-CoV, and SARS-CoV-2 in mice. Notably, it also conferred protection against challenge with the SARS-CoV-2 XBB variant.

These findings offer important insights for developing practical multivalent coronavirus vaccines that could help mitigate transmission and mortality early in future coronavirus outbreaks. Such an initial countermeasure could buy critical time for the development of variant-specific vaccines and further inform the design of universal coronavirus vaccines.

## Linked entities

- **Diseases:** SARS (MONDO:0005091), MERS (MONDO:0100116), SARS-CoV-2 (MONDO:0100096)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** S (surface glycoprotein) [NCBI Gene 43740568] {aka spike glycoprotein}
- **Diseases:** infection (MESH:D007239), respiratory diseases (MESH:D012140)
- **Species:** Middle East respiratory syndrome-related coronavirus (no rank) [taxon 1335626], Homo sapiens (human, species) [taxon 9606], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Gammacoronavirus (genus) [taxon 694013], Mus musculus (house mouse, species) [taxon 10090], Cricetinae (hamsters, subfamily) [taxon 10026]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12883751/full.md

## References

50 references — full list in the complete paper: https://tomesphere.com/paper/PMC12883751/full.md

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Source: https://tomesphere.com/paper/PMC12883751