The study of efficacy and immune correlates to an inactivated H5N1 vaccine in non-human primates

Lead Research Organisation: MRC Human Immunology Unit
Department Name: UNLISTED

Abstract

An effective vaccine would be the first choice for protection against future pandemic influenza infection. Hundreds of millions of vaccine doses would be required to prevent the first wave of the disease in a pandemic. However, because influenza virus can mutate quickly, one cannot predict exactly which strain of influenza virus will be next the pandemic virus. Therefore, a vaccine would not only have to be effective but would also have to be made in a very short period of time. Avian influenza viruses have the potential to initiate the next flu pandemics in humans. The current avian flu vaccine (H5N1) is poorly immunogenic in humans and has to be used at a 10-fold higher doses than the seasonal influenza vaccines and more than one immunization is needed to reach protective levels of antibody response. The amount of the vaccine required is therefore far beyond the present worldwide manufacturing capacity and current candidate vaccines may be too slow in stimulating protection. The simplest way to solve this problem would be to lower the dose and number of shots required for protection by increasing the immunogenicity of the vaccine. This research project aims to study how to enhance the immune responses to avian influenza vaccines in non-human primates as a model. The outcome of this study will help to develop an effective vaccine requiring a lower dose to protect against H5N1 infection.

Technical Summary

The highly pathogenic strains of avian influenza (H5N1) virus from Asia, which have a near 50% death rate in infected humans, pose a potential threat to the public health should they start transmitting between humans. An effective vaccine that induces a long-lasting protective immunity against this virus is urgently needed. However, our knowledge of the mechanism governing protective immunity to influenza A virus is incomplete, particularly the immunogenicity of avian influenza virus in humans. The aim of this proposal, involving collaboration with two Chinese research institutes, is to study the efficacy and protective immunity of an inactivated H5N1 vaccine in non-human primates. Our results will provide novel and invaluable information for designing safe and cost-effective vaccines for future pandemic influenza.

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Publications

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Title T cell epitopes in human influenza infections 
Description Database of T cell epitopes in human influenza infections, including pandemic H1N1, seasonal H1N1, H3N2, and H5N1 subtypes. 
Type Of Material Model of mechanisms or symptoms - human 
Provided To Others? No  
Impact Development of T cell-based vaccine and reagents to study antigen-specific responses. 
 
Title T cell epitopes in human influenza infections 
Description Database of T cell epitopes in human influenza infections, including pandemic H1N1, seasonal H1N1, H3N2, and H5N1 subtypes. 
Type Of Material Model of mechanisms or symptoms - human 
Provided To Others? No  
Impact Development of T cell-based vaccine and reagents to study antigen-specific responses. 
 
Description Avian Flu vaccine -NHP 
Organisation Chinese Academy of Agricultural Sciences
Department Harbin Veterinary Research Institute (HVRI)
Country China 
Sector Public 
PI Contribution Antibody and T cell responses
Collaborator Contribution vaccine development and animal model
Impact One publication
Start Year 2006
 
Description SARS 
Organisation Beijing Huilongguan Hospital
Country China 
Sector Hospitals 
PI Contribution performing T cell responses to whole SARS genome
Collaborator Contribution SARS cohort recruitment
Impact four publications