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New foot-and-mouth vaccine marks a significant milestone
Scientists hope the vaccine will address the current shortfall in availability.

Vaccine less reliant on cold-chain transport and storage

A new affordable vaccine to protect livestock against several serotypes of foot-and-mouth-disease (FMD) has been granted for development by The Pirbright Institute.

Researchers say the new vaccine is more stable than existing FMD vaccines and less reliant on a cold-chain during vaccine distribution - characteristics that give the vaccine greater potential to relieve the burden placed on regions where the disease is endemic.

The vaccine is the result of a long-standing collaboration between Pirbright, the University of Oxford, Diamond Light Source, the University of Reading and MSD Animal Health, who will now be taking the technology into development.


It also marks a significant milestone in years of research to develop a new synthetic vaccine.

“We are proud and excited that our research has resulted in a vaccine that is undergoing commercial development and will have a major impact on the health and wellbeing of those people whose livelihoods have been most severely affected by this devastating disease,” said Professor Bryan Charleston, director of The Pirbright Institute. 


“The vaccine’s properties allow for a greater degree of flexibility during production, storage and transportation, which will result in a more affordable solution and therefore better access to those living in areas such as Asia and Africa.”


The vaccine is comprised of small, synthetic protein shells called ‘virus-like particles’ (VLPs). These VLPs mimic the outer shell of FMDV, stimulating an immune response.

Unlike inactivated FMD vaccines, the VLPs do not require high containment facilities for production and have been designed to remain stable up to temperatures of 56 degrees celsius, therefore reducing reliance on cold-chain transport and storage.

It is hoped that these factors combined will revolutionise vaccination in areas of Africa and Asia, where the disease continues to circulate.

Defra chief veterinary officer Christine Middlemiss said: “This is a major milestone in tackling the foot-and-mouth disease in the developing countries where it is endemic.

“The increased robustness of this new vaccine has the potential to not only protect livestock but to transform the lives of people whose livelihoods have previously been threatened by this disease. Many people have worked for years to get to this point, and I am delighted to see the vaccine receive its commercial licence.”

 

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Defra shares new Sanitary and Phytosanitary guidance

News Story 1
 Defra has published guidance for the vet sector ahead of a proposed UK-EU Sanitary and Phytosanitary agreement.

The agreement, which will change the movement and trade of animals and related products, could see reductions in checks, paperwork and certification. As well as describing regulatory developments, the advice highlights the importance of animal ID, registration and traceability in disease control and other compliance arrangements.

The guidance can be found here. More detail is expected as negotiations progress. 

Click here for more...
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Lords Committee opens Pet Parasite Medication inquiry

The House of Lords Environment and Climate Change Committee will launch its inquiry into Pet Parasite Medication (PPM) on Wednesday (3 June).

Focusing on treatments containing fipronil and imidacloprid, the inquiry will seek to understand distribution pathways and the impacts of PPM use and non-use on biodiversity and human health. It will also cover current regulation, monitoring, and the potential implications for pets and their owners.

The committee will hear evidence from environmental non-governmental organisations and research institutes. The public can follow the proceedings live on Parliament TV or in person in the Palace of Westminster.