New vaccine against deadliest strain of avian flu tested by scientists

A vaccine against the most common and deadliest strain of avian flu, H5N1, has been engineered and tested by researchers at the University of Pittsburgh’s Center for Vaccine Research and Rockville, Maryland-based Novavax. A future flu pandemic is inevitable because of the virus’s ability to continually reinvent itself and the lack of broad immunity in humans, according to Dr. Ted Ross, lead author of the study and an assistant professor at Pitt’s vaccine research center. Influenza pandemics have occurred three times throughout modern history with deadly consequences. The first, the Spanish Flu of 1918, caused more deaths than the First World War. Unlike other avian flu vaccines, which are partially developed from live viruses, the vaccine uses a virus-like particle, or VLP, that is recognized by the immune system as a real virus but lacks genetic information to reproduce, making it a potentially safer alternative for a human vaccine. Given the evolving nature of H5N1, the vaccine was engineered to encode genes for three influenza viral proteins to offer enhanced protection against possible new strains of the virus.

To test the vaccine, researchers administered it to mice in one-dose and two-dose regimens. Mice immunized twice with the vaccine developed protective antibodies against H5N1 and were protected from disease and death when directly exposed to the virus. The researchers also compared modes of vaccine administration by delivering the vaccine to the muscle or the nose. Both methods of vaccine administration were equally effective. However, mice injected with the vaccine through the muscle developed more antibodies in the blood, while mice that received the nasal administration had more antibodies in their lungs. “VLPs may be advantageous over other vaccine strategies because they are easy to develop, produce and manufacture,” said Ross. “Using recombinant technologies, within ten weeks, we could generate a vaccine most effective towards the current circulating strain of virus, making it a cost-effective counter-measure to the threat of an avian influenza pandemic.”

-read more in Rick A. Bright et al., “Cross-Clade Protective Immune Responses to Influenza Viruses with H5N1 HA and NA Elicited by an Influenza Virus-Like Particle,” PLoS ONE 3, no. 1 (30 January 2008) (doi:10.1371/journal.pone.0001501): e1501