British scientists say they have taken the first major steps towards
finding a way of vaccinating against a type of leukaemia.
The team has identified a way that should theoretically boost the
capacity of the immune system to fight a form of the disease called
Chronic Myeloid Leukaemia (CML).

This is a very important discovery

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Professor Alejandro Madrigal
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CML affects mainly adults over the age
of 30. It claims about 1,000 victims a year in the UK. Without a bone
marrow transplant and chemotherapy, survival is normally less than five
years.
The international scientific community has been looking for something
on which to base a vaccine against the disease.
Protein
A US group has synthesised an artificial peptide - a piece of a protein
- which shows promise.
But the British team is the first to identify the actual peptide
produced by leukaemic cells that is targeted by the immune system.
This will greatly accelerate work to develop the first practical
vaccine against CML.
Professor Alejandro Madrigal, scientific director at the Anthony Nolan
Bone Marrow Trust, who led the research, said: "This is a very important
discovery.
"In just a few years there could be a vaccine for CML. It could be used
to treat individual patients, but there's no reason why you couldn't
extend it to the general population to prevent the disease."
Natural reaction
Scientists know that the immune system naturally reacts to CML - but
usually the response is not strong enough to conquer the leukaemia.
White blood cells called T-cells, which attack foreign bodies, lock on
to a specific peptide which appears on the surface of the cancerous cells.
It took seven years of work before the peptide, made up of a small
number of linked amino acids, was identified.
Professor Madrigal's team at the Anthony Nolan Research Institute
laboratories in Hampstead, north London, collaborated with scientists at
Nottingham Trent and Liverpool universities.
A simple vaccine could be made using the peptide to trigger an immune
system reaction against the cancer.
Alternatively, said Prof Madrigal, T-cells could be grown in the
laboratory and "trained" to recognise the molecule.
They could then be used as a treatment in their own right. The cells
would not have to be returned to the patient they came from.
They could be stored and given to any patient who provides a close
enough match, just as bone marrow transplants are carried out today.
Professor Robert Rees, from Nottingham Trent University, said: "These
results demonstrate that we have identified key components of leukaemia
cells against which we might be able to develop a vaccine."