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Glycoengineered erythrocytes for better influenza vaccines

Project description

Glycoengineered red blood cells for characterisation of influenza viruses

The antigenic characterisation of influenza A/H3N2 viruses by the standard hemagglutination inhibition (HI) assay is not possible anymore as a result of virus evolution. The EU-funded Sugar-enabledVAC project is developing glycan-engineered red blood cells for antigenic characterisation of circulating A/H3N2 viruses. The current objective of the project is to perform a technical and commercial feasibility study of the developed technology. The antigenic characterisation of the influenza A virus is essential for the development of seasonal vaccines. The developed glycoengineered erythrocytes will make possible the return to the standard antigenic viruses’ characterisation by the HI assay.

Objective

The objective of this ERC PoC project is to establish technical and commercial feasibility of our recently developed glycan-engineered red blood cells (RBCs) for antigenic characterization of circulating influenza A/H3N2 viruses. Due to the rapid evolution of influenza A/H3N2 viruses, antigenic characterization by the widely used hemagglutination inhibition (HI) assay is not possible anymore. Continuous antigenic characterization of influenza A viruses is, however, essential for the development of protective seasonal vaccines. The ERC program “sugar-enable” has developed glycoengineered RBCs that make it possible again to antigenically characterize circulating A/H3N2 viruses by the standard HI assay, and it is expected that the cells will find application in hundreds of laboratories worldwide.

Fields of science (EuroSciVoc)

Programme(s)

Topic(s)

Funding Scheme

HORIZON-ERC-POC - HORIZON ERC Proof of Concept Grants

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Call for proposal

(opens in new window) ERC-2022-POC2

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Host institution

UNIVERSITEIT UTRECHT
Net EU contribution
€ 150 000,00
Address
HEIDELBERGLAAN 8
3584 CS Utrecht
Netherlands
Activity type
Higher or Secondary Education Establishments
Links
Total cost
No data

Beneficiaries (1)