Vaccine breakthroughs create hope for millions
Announced this month, two major advances in the development and
technology of vaccine delivery could result in millions of lives being
saved in the next decade.
Published in the Lancet on October 16th, the results of a major
trial on more than 2000 children have created real hope for families
living in malaria endemic countries, demonstrating the best results
ever for a candidate malaria vaccine. The trial vaccine, RTS,S/AS02A
has been developed through a public/private partnership between GlaxoSmithKline
Biologicals and the Malaria Vaccine Initiative (MVI) of the Program for
Appropriate Technology in Health (PATH). It completed its first major
clinical trial involving more than 2000 children aged between one and
four living in Maputo province, in southern Mozambique, an area with
perennial malaria transmission due to the most deadly and common type
of malaria infection, the Plasmodium falciparum malaria parasite.
Results show that, although not reaching the efficacy of classical
childhood vaccines, which is often greater than 80%, the vaccine did reduce
new episodes of severe malaria by 57.7%. Amongst the under two year olds,
the vaccine was reported to be 77% effective against severe malaria.
With resistance to anti-malarial drugs now a growing problem, this level
of efficacy has the potential to make a huge impact as one weapon in an
armoury of malaria control tools, none of which is 100% effective.
Although further trials are needed before licensing, hopes are
for the general availability of a commercial malaria vaccine by 2010.
Meanwhile, in the UK, came the announcement of a new technology
that could revolutionise the international vaccine programme by eliminating
the need for refrigeration. Based on processes two billion years old, this
new 'stable liquid' technology should enable vaccines to be stored for long
periods in a range of environmental conditions, without the need for
refrigeration and reconstitution.
Manufacturer, Cambridge Biostability Ltd estimates that today, some
50% of all vaccines are wasted partly due to suspected or real temperature
damage. Savings from removing the 'cold chain' from the vaccination process
could enable the vaccination of 10 million additional children worldwide within
existing health budgets. Of the 132 million children born each year, almost one
third are not reached by routine vaccination. Two million die each year from
preventable diseases.
The availability of stable vaccines will also give hope to children
in remote areas of the world, currently excluded from traditional vaccination
programmes. They also create an opportunity for emergency response teams to
store vaccines in preparation for an outbreak and business travellers and
military personnel to carry vaccines as part of a standard medical kit.
A first initiative is underway using this new technique to develop
a five in one vaccine for diphtheria, tetanus, pertussis, hib and hepatitis B,
expected to be completed in three years. In theory the technology can be used
on any vaccine. The Department for International Development (DFID) has awarded
£950,000 funding to the project.
For more information visit www.biostability.com.
20 October, 2004
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