Projektbeschreibung
Forschung zu Glykanen und funktionellen Virusrezeptoren für neuartige antivirale Impfstoffe
Mit herkömmlichen Tests können bislang weder Rezeptorspezifität noch Effizienz von Impfstoffen gegen das Influenza A-Virus bestimmt werden, da sie unspezifisch für Rezeptoren der menschlichen oberen Atemwege sind. Da Laborversuchstiere diese Rezeptoren nicht besitzen, ist die Ausbeute bei der Impfstoffherstellung signifikant niedrig, sodass der Impfstoff nicht gezielt entwickelt werden kann und die Antigendrift verstärkt wird. Schwerpunkt des EU-finanzierten Projekts Sugar-Enable ist daher der funktionelle Rezeptor menschlicher Influenza-A-Viren. Untersucht wird, wie der Immundruck die Glykanspezifität verändert. Auf diese Weise soll das Glykan identifiziert werden, dessen sich alle menschlichen Influenza-A-Viren bedienen. Letztlich sollen dadurch Überwachungstechniken, Zellkulturmodelle und strukturbasierte Inhibitoren verbessert und neue Wege zur Herstellung Glykan-analoger Inhibitoren und wirksamerer Impfstoffe geebnet werden.
Ziel
Our current assays to determine the receptor specificity and vaccine efficiency of influenza A virus fail as they do not represent receptors available in the human upper respiratory tract. The lack of these receptors in our laboratory hosts to create vaccines significantly dampen yields, the resulting mismatched vaccines do not afford proper protection and further drive antigenic drift.
The objective of this proposal is to elucidate the functional receptor of human influenza A viruses. By using antigenically drifted viruses, we expect to understand how glycan specificity changes due to immune pressure but it will also lead to the identification of a glycan that is utilized by all human IAV viruses. With this knowledge, better surveillance techniques, culture models and structure-based inhibitors can be developed. Using a novel and sophisticated cell-engineering tool, based on lipidated sugars, we will show functional glycan receptor usage. In addition, I will create cell lines in which human influenza A vaccine viruses grow to high titers without adaptation, thus providing superior protection.
To achieve this goal, I propose to enzymatically synthesize complex glycans (AIM 1), including sialic acid modifications that are found on the respiratory tract epithelial cells of humans and other IAV hosts. Several enzymatic methods and glycan array tools are in place, and thus the chance of success is high. I already set-up preliminary methods for the use of lipidated N-glycan structures and extensive knowledge on SEEL is present in the department (AIM 2). For creating super vaccine producing cell lines I will use genetic approaches that previously have shown to be successful (AIM3).
The systems dealing with sugars enabling function, either for infection or vaccine research, I term sugar-enable, will provide new endeavors to create glycan-analog inhibitors and will bring us steps closer to better vaccines.
Wissenschaftliches Gebiet
- natural sciencesbiological sciencesmicrobiologyvirology
- medical and health scienceshealth sciencesinfectious diseasesRNA virusesinfluenza
- medical and health sciencesbasic medicinepharmacology and pharmacypharmaceutical drugsvaccines
- natural sciencesbiological sciencesbiochemistrybiomoleculescarbohydrates
Schlüsselbegriffe
Programm/Programme
Thema/Themen
Finanzierungsplan
ERC-STG - Starting GrantGastgebende Einrichtung
3584 CS Utrecht
Niederlande