Developments in genetic engineering have enabled scientists to create the
potential for a malaria vaccine to be carried in goats' milk.

A vaccine must not only be effective, it must be cheap to
manufacture if it is to be used in those countries hit hardest by
malaria

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Anthony Stowers, malaria researcher
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Scientists hope it could lead to the
production of an effective vaccine at a fraction of the cost of
manufacturing it in laboratories.
Researchers developed transgenic mice which could secrete an
experimental malaria vaccine into their milk. When a purified form of this
vaccine was injected into monkeys, it protected four out of five animals
from a normally lethal dose of malaria.
The researchers are trying to scale up their process from mice to
larger animals such as goats and other livestock, in the hope they could
become inexpensive, high-yield producers of malaria vaccine.
Malaria infects 300-500 million people every year and kills one
million, according to World Health Organization (WHO) estimates.
Ninety per cent of cases are in sub-Saharan Africa where many nations
are also struggling to cope with HIV.
'Exciting possibility'
The results of this development are published online in the Proceedings
of the National Academy of Sciences.
"A vaccine must not only be effective, it must be cheap to manufacture
if it is to be used in those countries hit hardest by malaria," said lead
author Anthony Stowers, PhD, a malaria researcher at the National
Institute of Allergy and Infectious Diseases (NIAID) in the USA.
He added: "Using transgenic animals to achieve both ends is an exciting
possibility.
"If it works, a herd of several goats could conceivably produce
proteins for all of Africa."
Practical potential
Previously, scientists have introduced genes encoding specific proteins
into animals to produce large quantities of those proteins for medical
use.
Dr Stowers and his colleagues investigated whether transgenic animals
could produce proteins specifically for use in malaria vaccines.
They produced two transgenic mice strains, each carrying a form of the
gene for a surface protein from the deadliest malaria parasite,
Plasmodium falciparum.
They designed the transgenes to be switched on by the cells that line
the mammary glands, so that the resulting proteins would be secreted into
the animals' milk.
Both mouse strains produced large quantities of the desired vaccine
protein, which was used on the monkeys.
Malaria kills one million people annually
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Only one of the five immunised animals
contracted the disease.
Six out of seven unvaccinated animals had to be treated for virulent
malaria.
Preliminary results of using the same technique in goats, which have
not yet been published, suggest the procedure works well in larger
animals.
This offers a far more practical option for large-scale vaccine
production.
Professor David Warhurst, from the Public Health Laboratory Service in
London, said: "It sounds very interesting. Four out of five isn't a
brilliant result, but it's a nice approach and it might be a good way of
producing large quantities of the material."