Abstract
H5N1 viruses are widely considered to be a probable cause of the next influenza pandemic. Influenza vaccines are considered to form the main prophylactic measure against pandemic influenza. The world’s population is expected to have no pre-existing immunity against the pandemic virus strain and will need two vaccine doses to acquire protective immunity. A pandemic outbreak will spread much faster than it will take for pandemic vaccines to be produced and distributed. Therefore, increasing efforts are being made to develop prepandemic vaccines that can induce broad cross-protective responses and that can be administered as soon as a pandemic is declared or even before, in order to successfully prime the immune system and allow for a rapid and protective antibody response with one dose of the pandemic vaccine. Several vaccine manufacturers have developed candidate pandemic and prepandemic vaccines, predominantly based on reverse-genetics reference strains and have improved the immunogenicity by formulating these vaccines with different adjuvants. Clinical studies with inactivated split-virion or whole-virion vaccines based on H5N1 indicate that two immunizations appear necessary to elicit the level of immunity required to meet licensure criteria. A detailed overview is given of the most successful candidate vaccines developed by seven vaccine manufacturers.
Financial & competing interests disclosure
Geert Leroux-Roels was principal investigator of clinical studies of seasonal and (pre)pandemic influenza vaccines for the following manufacturers: Baxter, GlaxoSmithKline Biologicals, Novartis and Sanofi Pasteur. The Ghent University and University Hospital received sponsoring for the conduct of these studies. Geert Leroux-Roels also performed consulting services for the following manufacturers: GlaxoSmithKline Biologicals and Novartis. Isabel Leroux-Roels assisted in the conduct of clinical studies of seasonal and (pre)pandemic influenza vaccines for the following manufacturers: GlaxoSmithKline Biologicals and Sanofi Pasteur. Isabel Leroux-Roels also received travel and speaker fees from the following manufacturers: GlaxoSmithKline Biologicals and Sanofi Pasteur. The authors have no other 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 apart from those disclosed.
No writing assistance was utilized in the production of this manuscript.