Abstract
Influenza A viruses are a public-health concern as they cause annual epidemics and may initiate a pandemic. Common inactivated influenza A vaccines induce a serum antibody response, which may not be protective against virus variation in the field. In contrast to conventional vaccines, the intranasally administered live influenza vaccine may have the potential to induce long-lived and heterosubtypic immunity. In this perspective, attenuated hemagglutinin cleavage-site mutants are discussed in view of usage as influenza live vaccines. This approach allows the convertion of any influenza A strain into an attenuated vaccine virus. The mutated hemagglutinin can serve as a component of a multiple live-attenuated influenza vaccine and would prevent reassortment into circulating viruses.
Acknowledgements
For very fruitful collaboration and support during the projects on HA cleavage-site mutants, I am very grateful to H Garn, M Wegmann, A Spies, A Wensing, H Renz, R Wagner, A Herwig, J Klärig, M Abram, S Jung, G Gabriel, O Stech, H-D Klenk, S Berthel, U Lanzinger, G Schemken, Philipps-University Marburg, Germany, and THC Mettenleiter, Friedrich-Loeffler-Institut, Greifswald, Insel Riems, Germany.
Financial & competing interests disclosure
The author has no relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript. This includes employment, consultancies, honoraria, stock ownership or options, expert testimony, grants or patents received or pending, or royalties.
No writing assistance was utilized in the production of this manuscript.