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Preliminary success of fetal Brain-Cell Transplantation in Huntington's
disease
A preliminary study published on The Lancet's website - www.thelancet.com -
outlines a surgical technique involving transplantation of fetal brain cells
which could be of future benefit to people with Huntington's disease.
Huntington's disease is a genetic neurodegenerative disease that mainly
affects the area of the brain called the striatum. It has severe motor and
cognitive consequences and, up to now, no treatment. Motor and cognitive
functions can be restored in experimental animal models by means of
transplantation of fetal brain cells. Marc Peschanski and colleagues from
INSERM, Paris, France, explored whether grafts of human fetal striatal tissue
could survive and have detectable effects in five patients with mild to
moderate Huntington's disease.
After 2 years of preoperative assessment, patients were grafted with human
fetal nerve cells into the right then, after a year, the left striatum. Final
results were assessed 1 year later. Assessment of the effects was done by a
range of neurological and psychiatric tests. These results were compared with
a control group of 22 untreated patients at similar stages of the disease who
were followed up in parallel. Repeated magnetic resonance imaging (MRI) and
positron emission tomography (PET) scanning was also done to assess metabolic
activity.
donate to HDA  The final PET-scan assessment showed increased metabolic
activity in various parts of the striatum in three of five patients,
contrasting with the progressive decline recorded in the two other patients
in the series, as seen in patients with untreated Huntington's disease. As a
result, motor and cognitive functions were improved or maintained within the
normal range, and functional benefits were seen in daily-life activities in
these three patients, but not in the other two.
In an accompanying Commentary, Olle Lindvall and Anders Bjorklund from Lund
University, Sweden, comments: "Although the findings reported by Peschanski
and colleagues are promising, the clinical usefulness of cell-replacement
therapy for Huntington's disease remains unclear". They conclude: "The
encouraging results reported by Peschanski and co-workers indicate that this
strategy may work in Huntington's disease. Future studies will have to
clarify whether cell therapy can be developed into a clinically useful
treatment for patients with this disease".
The decision to publish the paper early on The Lancet's website ahead of the
scheduled print publication date of December 9 was made after some of the
research findings were made public by French Government officials on Monday
27 November. The full research study and accompanying Commentary are freely
available to doctors, patients, journalists and the general public on the
journal's website (www.thelancet.com).

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