Monday 18 January 2010

Stem cell therapy found for leukaemia

In a ray of hope for millions of leukaemia patients, American scientists have claimed to have developed a technique which multiplies the small number of stem cells in the donor blood, making it much more potent for the treatment of the fatal disease.

It also eliminates the need for a matching donor, whose bone marrow is usually transplanted to the patient, according to a study which appeared in the journal Nature Medicine. Traditionally, there was always a risk that the patient’s body may reject the new cells from a donor. The alternate path was to introduce cells extracted from umbilical cords as these cells do not have characteristics which would normally trigger immune rejection. So these cells can be used in any patient, without the need for matching. However, the only disadvantage of this process was that a single cord would not have enough cells to meet the needs of an adult patient.

Now, researchers at Fred Hutchinson Cancer Research Center in Seattle have developed a process in which using a protein they multiply the stem cells in the blood from the umbilical cord before they are transplanted to the patient. The technique has been tested on humans after successful trials on animals.

leukaemia is a cancer of the blood or bone marrow and is characterised by an abnormal proliferation of blood cells, usually white blood cells — leukocytes. As part of the treatment, the infected bone marrow cells of the patient are killed off and new cells are introduced in their place.

Hailing the development, UK-based charity Leukaemia Research said this could be the “holy grail” for doctors. “This is a promising development towards this because the concern has been that once stem cells start ‘growing’ they lose their stem cell properties and progress to ordinary blood cells with a very limited lifespan,” said Dr David Grant, Scientific Director of the charity.

“The holy grail is to have an ‘off the peg’ source of unlimited numbers of ‘neutral’ stem cells which can be given to any patient safe in the knowledge that they will not cause the very difficult ‘graft versus host’ problems that lead to rejection and often the death of the patient,” Grant said.link

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