# A single-dose MCMV-based vaccine elicits long-lasting immune protection in mice against distinct SARS-CoV-2 variants

**Authors:** Kristin Metzdorf, Henning Jacobsen, Yeonsu Kim, Luiz Gustavo Teixeira Alves, Upasana Kulkarni, Maja Cokarić Brdovčak, Jelena Materljan, Kathrin Eschke, M. Zeeshan Chaudhry, Markus Hoffmann, Federico Bertoglio, Maximilian Ruschig, Michael Hust, Marko Šustić, Astrid Krmpotić, Stipan Jonjić, Marek Widera, Sandra Ciesek, Stefan Pöhlmann, Markus Landthaler, Luka Čičin-Šain

PMC · DOI: 10.3389/fimmu.2024.1383086 · Frontiers in Immunology · 2024-07-25

## TL;DR

A single-dose MCMV-based vaccine provides long-lasting protection in mice against multiple SARS-CoV-2 variants, including Omicron.

## Contribution

A recombinant MCMV vaccine vector was shown to elicit durable and broad immune responses against SARS-CoV-2 variants in mice.

## Key findings

- A single dose of MCMVS conferred rapid virus clearance and controlled Beta and Omicron variants.
- Spike-specific immunity increased over six months, with enhanced antibody avidity and breadth against distant variants.
- MCMVS vaccination elicited robust and lasting protection in both young and aged mice.

## Abstract

Current vaccines against COVID-19 elicit immune responses that are overall strong but wane rapidly. As a consequence, the necessary booster shots have contributed to vaccine fatigue. Hence, vaccines that would provide lasting protection against COVID-19 are needed, but are still unavailable. Cytomegaloviruses (CMVs) elicit lasting and uniquely strong immune responses. Used as vaccine vectors, they may be attractive tools that obviate the need for boosters. Therefore, we tested the murine CMV (MCMV) as a vaccine vector against COVID-19 in relevant preclinical models of immunization and challenge. We have previously developed a recombinant MCMV vaccine vector expressing the spike protein of the ancestral SARS-CoV-2 (MCMVS). In this study, we show that the MCMVS elicits a robust and lasting protection in young and aged mice. Notably, spike-specific humoral and cellular immunity was not only maintained but also even increased over a period of at least 6 months. During that time, antibody avidity continuously increased and expanded in breadth, resulting in neutralization of genetically distant variants, like Omicron BA.1. A single dose of MCMVS conferred rapid virus clearance upon challenge. Moreover, MCMVS vaccination controlled two variants of concern (VOCs), the Beta (B.1.135) and the Omicron (BA.1) variants. Thus, CMV vectors provide unique advantages over other vaccine technologies, eliciting broadly reactive and long-lasting immune responses against COVID-19.

## Linked entities

- **Proteins:** CHMP5 (charged multivesicular body protein 5)
- **Diseases:** COVID-19 (MONDO:0100096), SARS-CoV-2 (MONDO:0100096)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Diseases:** fatigue (MESH:D005221), CMV (MESH:D003586), COVID-19 (MESH:D000086382)
- **Chemicals:** VOCs (-)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11306140/full.md

## References

82 references — full list in the complete paper: https://tomesphere.com/paper/PMC11306140/full.md

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Source: https://tomesphere.com/paper/PMC11306140