# A selective C5a-derived peptidomimetic enhances IgG response following inactivated SARS-CoV-2 immunization and confers rapid disease resolution following murine coronavirus infection

**Authors:** Andrew J. Neville, Mackenzie E. Conrin, Thomas T. Schulze, Paul H. Davis

PMC · DOI: 10.3389/fimmu.2025.1470034 · Frontiers in Immunology · 2025-04-04

## TL;DR

A new peptidomimetic called EP67 boosts immune responses to SARS-CoV-2 vaccines and speeds recovery from coronavirus infections in mice.

## Contribution

EP67 is shown to enhance IgG responses as an adjuvant and accelerate recovery when administered post-infection.

## Key findings

- EP67 combined with inactivated SARS-CoV-2 increases nucleocapsid-specific IgG antibodies in rodents.
- Intranasal EP67 improves health outcomes in mice infected with MHV-A59 coronavirus.
- EP67 shows efficacy as both an adjuvant and a therapeutic for betacoronaviruses.

## Abstract

The host complement system is a critical component of innate immunity and serves as a principal mechanism of pathogen defense in mammals. EP67 is an engineered decapeptide derived from the C terminus of human complement protein C5a, which displays selective immunostimulatory activity. EP67 preferentially activates phagocyte mononuclear cells but shows minimal activity towards inflammatory granulocytes, including neutrophils. Previous studies of viral infection showed that EP67 possessed antiviral efficacy when used following infection and enhanced antibody responses to antigen challenges when used as an adjuvant. Here, we show in a rodent model that immunization with inactivated γ-irradiated SARS-CoV-2 in combination with EP67 can produce elevated nucleocapsid-specific IgG antibodies compared to viral lysate alone, supporting an enhanced adaptive immune response. Additionally, intranasal administration of EP67 following infection with live MHV-A59 coronavirus resulted in a rapid health improvement in symptomatic infections compared to PBS vehicle controls. Taken together, these results suggest EP67 shows efficacy towards betacoronaviruses when used as an adjuvant during immunization or as a therapeutic during active infections. Moreover, these findings continue to support the capability of EP67 as an antiviral agent and a useful immunostimulatory peptide.

## Linked entities

- **Proteins:** C5 (complement C5)
- **Diseases:** SARS-CoV-2 (MONDO:0100096)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** C5AR1 (complement C5a receptor 1) [NCBI Gene 728] {aka C5A, C5AR, C5R1, CD88}, N (nucleocapsid phosphoprotein) [NCBI Gene 43740575]
- **Diseases:** coronavirus infection (MESH:D018352), viral infection (MESH:D014777), inflammatory (MESH:D007249), infection (MESH:D007239)
- **Chemicals:** EP67 (-)
- **Species:** Homo sapiens (human, species) [taxon 9606], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Mus musculus (house mouse, species) [taxon 10090], Betacoronavirus (genus) [taxon 694002]

## Full text

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## Figures

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## References

21 references — full list in the complete paper: https://tomesphere.com/paper/PMC12006086/full.md

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Source: https://tomesphere.com/paper/PMC12006086