Emerging Microbes & InfectionsImmunologyPeer-reviewed journal article
Digitally immune optimised haemagglutinin with nanocage plug-and-display elicits broadly neutralising pan-H5 influenza subtype vaccine responses
Chloe Qingzhou HuangiD, Rory A. HillsiD, George CarnelliD, Sneha VishwanathiD, Ernest T. AguinamiD, Andrew C. Y. ChaniD, Phil PalmeriD, Laura O’Reilly, Paul TonksiD, Nigel James TempertoniD, Simon D. W. FrostiD, Laurence S. TileyiD, Mark R. HowarthiD, Jonathan Luke HeeneyiD
Abstract
The increasing global spread of the highly pathogenic avian influenza (HPAI) A/H5 viruses poses a serious public health threat. Circulating clade 2.3.4.4b viruses have demonstrated rapid transcontinental dissemination, extensive reassortment, epizootic spread and potential sustained mammal-to-mammal transmission, signifying a heightened risk of becoming a human pathogen of high consequence. A broadly protective, future-proof vaccine against multiple clades of H5 influenza is urgently needed for pandemic preparedness. Here, we combine two novel vaccine technologies to generate a Digitally Immune Optimised and Selected H5 antigen (DIOSvax-H5inter) displayed multivalently on the mi3 nanocage using the SpyTag003/SpyCatcher003 conjugation system. Mice immunised with DIOSvax-H5inter Homotypic Nanocages at low doses demonstrate potent, cross-clade neutralising antibody and T cell responses against diverse H5 strains. DIOSvax-H5inter Homotypic Nanocages provide a scalable vaccine candidate with the potential for pan-H5 protection against drifted or newly emergent H5 strains. This World Health Organization preferred product characteristic is essential for prospective strategic stockpiling in the pre-pandemic phase.
- organism: mouse
- assay: proteomics
- research focus: drug response / drug discovery
- research focus: variant calling
- approach: experimental assay
- Citations
- 8
- FWCI
- 4.89
- Field percentile
- top 4%
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