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Scientists develop potential pandemic influenza vaccine in mice

US researchers have genetically engineered a vaccine that can protect mice from different human strains of the H5N1 influenza virus. They report their findings online today (Thursday February 2, 2006) in The Lancet.

Effective vaccines against highly pathogenic avian influenza H5N1 viruses are an urgent and global public-health priority. However, there are a number of problems with current vaccine manufacturing strategies. To produce a H5N1 vaccine using standard methods would involve first growing a virus strain in millions of fertilised chicken eggs and then harvesting, purifying, and killing the virus. It takes at least 6 months to make a conventional egg-derived vaccine and scientists estimate that 4 billion fertilised eggs would be needed to produce enough pandemic vaccine for 1.2 billion people worldwide at high-risk. However, in the event of a pandemic, ensuring the availability of fertilised chicken eggs would be problematic since H5N1 viruses are highly virulent in poultry. An egg-based vaccine would also not be useful for stockpiling, as it would not be able to protect against different strains of the virus. Therefore, alternative vaccine-manufacturing strategies are needed.

Suryaprakash Sambhara (The Centers for Disease Control and Prevention, Atlanta, GA, USA), Suresh Mittal (Purdue University, West Lafayette, IN, USA), and their colleagues genetically engineered an adenovirus (a common cold virus) to produce a protein called haemugglutinin subtype 5 (H5HA)--a component of the H5N1 influenza virus. The team injected one group of mice with the H5HA vaccine and another with saline as a negative control. They found that the immunised mice, despite having low or no neutralising antibodies against H5N1 viruses, were nonetheless protected from death and weight loss when infected with H5N1 viruses isolated from people in 2003 and 2004. The researchers found that unlike the conventional H5N1 vaccines, which do not activate the cellular arm of t
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Contact: Joe Santangelo
j.santangelo@elsevier.com
212-633-3810
Lancet
1-Feb-2006


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