Award details

21-ICRAD - Novel strategies to enhance vaccine immunity in neonatal livestock (NEOVACC)

ReferenceBB/V019856/1
Principal Investigator / Supervisor Professor Simon Graham
Co-Investigators /
Co-Supervisors
Professor John Hammond, Dr Julian Seago
Institution The Pirbright Institute
DepartmentPRRS Immunology
Funding typeResearch
Value (£) 474,536
StatusCurrent
TypeResearch Grant
Start date 30/03/2021
End date 29/03/2024
Duration36 months

Abstract

Infectious diseases of livestock continue to cause a major financial impact globally, threatening food security and public health. Vaccination remains the most cost-effective tool to prevent, manage and even eradicate diseases. Maternally derived antibodies (MDA) play a critical role in protecting neonatal livestock against infectious diseases during their early life. However, MDA can dampen immune responses of neonates to vaccination through a number of distinct mechanisms. Thus, as MDA wanes immunised animals remain vulnerable to pathogen challenge. In this project, we will test vaccine strategies designed to enhance immune responses in neonatal animals with MDA. Our state-of-the-art approaches to this challenge span improved immunogen design, antigen delivery configuration and immunopotentiators. We will focus on two major endemic viral diseases: bovine respiratory syncytial virus (BRSV) in cattle and porcine reproductive and respiratory syndrome virus (PRRSV) in pigs, for which the consortium has developed preliminary tools and knowledge of strategies to counteract different mechanisms of MDA interference. The project is structured with three complementary work-packages that aim to: (1) Design BSRV immunogens to exploit differences in antibody repertoires between adult and neonatal cattle; (2) Evaluate a DNA vaccine-based approach against PRRSV designed to counteract MDA interference; and (3) Engineer peptide-based immune checkpoint inhibitors into live PRRSV vaccines to enhance neonatal responses to vaccination. The outputs from this project will directly benefit the development of improved vaccines against these two key diseases but also as a concept since the approaches may be exploited in the context of other pathogens, livestock species and humans.

Summary

NA
Committee Not funded via Committee
Research TopicsAnimal Health, Immunology, Microbiology
Research PriorityX – Research Priority information not available
Research Initiative ICRAD ERA-NET [2020]
Funding SchemeX – not Funded via a specific Funding Scheme
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