# A broad-spectrum SARS-CoV-2 RBD vaccine with selected high-impact mutations and novel adjuvant induces durable T cell response and broad protection in mice

**Authors:** Xianying Chen, Yuzhen Zhang, Shimin Yang, Yan Chen, Shengnan Qian, Zhen Zhang, Qianyun Liu, Chengbao Ma, Weiyi Yu, Jiangpeng Feng, Jiejie Liu, Ming Guo, Zhixiang Huang, Xin Wang, Jie Chen, Haiyan Zhao, Huan Yan, Ke Lan, Yu Chen, Li Zhou

PMC · DOI: 10.3389/fcimb.2025.1690554 · Frontiers in Cellular and Infection Microbiology · 2026-01-30

## TL;DR

A new SARS-CoV-2 vaccine with key mutations and a novel adjuvant induces strong and lasting immunity against multiple variants in mice.

## Contribution

A novel RBD vaccine with selected high-impact mutations and a new adjuvant provides broad protection against multiple SARS-CoV-2 variants.

## Key findings

- M5-RBD vaccine induces high titers of neutralizing antibodies against multiple SARS-CoV-2 variants.
- Combining M5-RBD with HP007 adjuvant enhances durable T cell responses and protects mice from lethal infections.
- N440K or G446S mutations reduce immune response effectiveness.

## Abstract

The emergence of new SARS-CoV-2 variants with immune evasion capabilities underscores the importance of developing a broad-spectrum and effective vaccine. The receptor binding domain (RBD) of the Spike protein has been widely utilized in vaccine due to its high immunogenicity. However, the Spike protein, particularly the RBD region, exhibits significant variability in the evolution of SARS-CoV-2, leading to viral immune evasion and reduced vaccine effectiveness.

A broad-spectrum antigen (M5-RBD) was developed via mutation patching, incorporating key high-impact mutation sites (K417T, L452R, T478K, E484K, N501Y). Additionally, extra mutations (N440K or G446S) were introduced into M5-RBD to evaluate their impact on immune response. M5-RBD was further combined with a novel CpG adjuvant HP007 for immunization.

M5-RBD elicited high titers of broad-spectrum neutralizing antibodies against SARS-CoV-2 wild-type and various variants (Delta, Omicron BA.1, BA.2, BA.2.75, BA.5, BF.7, BQ.1.1, XBB, EG.5, JN.1, KP.3 strains). Introduction of N440K or G446S significantly diminished the immune response to viral strains. When combined with HP007 adjuvant, M5-RBD induced efficient and durable T cell responses, providing protection to K18-hACE2 KI mice against lethal infections with both wild-type and Omicron BA.2 strains.

Rationally designed with key high-impact mutation sites, M5-RBD effectively overcomes SARS-CoV-2 variant immune evasion and elicits broad-spectrum neutralizing antibodies. The combination with HP007 adjuvant enhances immune protection, providing a promising strategy for the development of next-generation COVID-19 vaccines.

## Linked entities

- **Proteins:** CHMP5 (charged multivesicular body protein 5), l(3)62Bi (lethal (3) 62Bi)
- **Chemicals:** CpG (PubChem CID 145459096)
- **Diseases:** SARS-CoV-2 (MONDO:0100096), COVID-19 (MONDO:0100096)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** KRT18 (keratin 18) [NCBI Gene 3875] {aka CK-18, CYK18, K18}
- **Diseases:** COVID-19 (MESH:D000086382)
- **Chemicals:** HP007 (-)
- **Species:** Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Mus musculus (house mouse, species) [taxon 10090]
- **Mutations:** E484K, K417T, N501Y, G446S, L452R, T478K, N440K

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12901505/full.md

## References

41 references — full list in the complete paper: https://tomesphere.com/paper/PMC12901505/full.md

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Source: https://tomesphere.com/paper/PMC12901505