# Protection Against Rabbit Hemorrhagic Disease Virus Strains: Efficacy of a New Commercial Recombinant RHDV2 Capsid Protein VP60 Vaccine

**Authors:** Mireia Fontseca, Eva Perozo, Guillem Nadal, Sandra Gascón-Torrens, Jordi Montané, Ricard March, Marta Sitjà

PMC · DOI: 10.3390/vaccines14020123 · Vaccines · 2026-01-27

## TL;DR

A new vaccine effectively protects rabbits from multiple strains of the deadly rabbit hemorrhagic disease virus, including the highly virulent variant.

## Contribution

The first recombinant vaccine to demonstrate durable protection against RHDV2, hvRHDV2, and classical RHDV strains.

## Key findings

- Vaccinated rabbits showed significantly lower mortality compared to placebo when challenged with all three RHDV strains.
- Antibody levels in vaccinated rabbits were higher than controls as early as seven days post-vaccination and remained elevated for at least 12 months.
- The vaccine provided robust and long-lasting immunity against both classical and emerging RHDV strains.

## Abstract

Background/Objectives: Rabbit hemorrhagic disease (RHD) is an incurable, highly contagious disease caused by different RHD virus (RHDV) strains, such as the coexisting RHDV2 and classical RHDV. Disease control is based on vaccination using different or polyvalent vaccines. This study assessed the protective efficacy, onset of immunity (OOI), and duration of immunity (DOI) of a new recombinant vaccine containing a single active substance developed to target both strains: against RDHV2, highly virulent RDHV2 (hvRHDV2), and classical RDHV strains. Methods: This study included six randomized, controlled, blinded trials in clinically healthy New Zealand White rabbits. Rabbits were grouped to receive the recombinant vaccine or placebo (1:1 ratio) and challenged with RHDV2 (215 hemagglutination [HA], infective dose; n = 39 for duration and n = 43 for onset), hvRHDV2 (215 HA; n = 48 and n = 40), or classical RHDV (212 hemagglutination [HA], infective dose; n = 20 and n = 22) strains to evaluate OOI and DOI. Results: Rabbits receiving the vaccine showed a lower mortality than those receiving placebo upon challenge with any of the three strains. OOI trials showed that vaccinated rabbits exhibited higher levels of antibodies against RHDV2 than controls seven days post-vaccination. DOI trials revealed that, compared with controls, vaccinated rabbits had increased levels of antibodies against RHDV2 across all time points assessed, at least until the day of the viral challenge with any of the RHDV strains (approximately 12 months post-vaccination). Conclusions: This recombinant vaccine is the first to show a durable and robust protection against all tested strains, including the RHDV2, hvRHDV2, and classical RHDV strains, underscoring its potential as a comprehensive tool for RHD prevention.

## Full-text entities

- **Diseases:** injury to (MESH:D014947), coccidiosis (MESH:D003048), deaths (MESH:D003643), RHDV (MESH:D014777), dyspnea (MESH:D004417), infection (MESH:D007239), myxomatosis (MESH:D009234), nephropathy (MESH:D007674), depression (MESH:D003866), RHD (MESH:D006470), hepatitis (MESH:D056486), paralysis (MESH:D010243), diarrhea (MESH:D003967), disseminated intravascular coagulation (MESH:D004211)
- **Chemicals:** VP60 (-), phosphate (MESH:D010710), tiletamine (MESH:D013992), mineral oil (MESH:D008899), xylazine (MESH:D014991), BEI (MESH:C478655), sodium thiosulphate (MESH:C017717), oil (MESH:D009821), sodium pentobarbital (MESH:D010424), water (MESH:D014867), zolazepam (MESH:D015041)
- **Species:** Myxoma virus (no rank) [taxon 10273], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Homo sapiens (human, species) [taxon 9606], Oryctolagus cuniculus (domestic rabbit, species) [taxon 9986], Rabbit hemorrhagic disease virus (no rank) [taxon 11976], Lagovirus (genus) [taxon 95339]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12945178/full.md

## References

22 references — full list in the complete paper: https://tomesphere.com/paper/PMC12945178/full.md

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Source: https://tomesphere.com/paper/PMC12945178