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I found this article following links from Patrik's NECTAR page. Sounds like
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Brain disorder treatment hailed

Los Angeles Times

Thursday, March 28, 1996
(Page A 3 and continued on page A 24)

Health:  Fetal cell transplants halted progression of fatal
Huntington's disease in three patients, L.A. researchers
say.

By Thomas H. Maugh II,  Times Medical Writer

Researchers at Good Samaritan Hospital on Wednesday reported the
first successful use of fetal cell transplants to treat Huntington's
disease, offering hope for the first effective treatment of the
fatal brain disorder.

Dr. Deane B. "Skip" Jacques and his colleagues told
a meeting of the American Academy of Neurology in San Francisco
that the transplants halted progression of the disease in the
three patients treated and reversed some of the deterioration
that had occurred.

Although the patients need to be studied longer to ensure the
survival of the grafts, "I think we could impact Huntington's
in a revolutionary way," said Dr. Matthias Kurth of the Barrow
Neurosciences Institute in Phoenix, who evaluated the patients.


Matthew Hopson, a 24-year-old from Phoenix who received the first
graft in July, put it more succinctly:"It saved my life."


Huntington's is one of the more common inherited brain disorders.
 About 25,000 Americans have it, and an additional 60,000 carry
the defective gene and will develop the disorder as they age.
 The slowly progressive condition, which killed folk singer Woody
Guthrie, usually comes on between the ages of 30 and 50 and causes
the degeneration of brain cells.

It is characterized by jerky, involuntary movements called chorea,
loss of control of bodily functions, and dementia, a progressive
deterioration of memory and thought processes.  Children of patients
have a 50% chance of developing the disorder, which is invariably
fatal within 10 to 15 years after onset.

Although researchers hope to develop therapies based upon the
discovery three years ago of the defective gene that causes Huntington's,
no effective therapy exists.  Success with transplants would represent
a major step forward in improving the condition of Huntington's
patients.

Fetal cell transplants are being widely studied as a treatment
of Parkinson's disease, and the Good Samaritan group is one of
the leaders in that effort.

Jacques' team has performed the procedure on 40 patents and reports
in this month's Journal of Cell Transplantation that 70% of them
have shown significant improvement in neurological functions.
 The remaining 30% are now taking less medication for their Parkinson's
and none have deteriorated as a result of the transplant.

Animal experiments suggest that Huntington's may be a much better
prospect for transplants than Parkinson's, said Dr. Oleg V. Kopyov
of Good Samaritan. In Parkinson's, the transplanted cells serve
simply as a source of brain hormones, particularly dopamine and
growth factors.

But in animal models of Huntington's, the transplanted cells actually
become integrated into the brains's structure, restoring neural
circuitry that was destroyed by the disease. "It lends itself
better to transplants than anything else in the brain," Kurth
said.  Although several groups have talked about performing the
transplants, no one has yet reported any results.


The Good Samaritan team actually performed their first transplant
a little sooner than they had planned when Kurth told them about
Hopson.  He is an unusual Huntington's patient in that his first
symptoms appeared early, at age 20, and the disease progressed
very rapidly.

Researchers now know that this early onset is a function of the=7F
degree of mutation in the Huntington's gene, and Hopson's gene
is, in fact, severely mutated -- much more so than the gene carried
by his father.  The elder Hopson, 48, has not yet developed the
disease.

By the time that Hopson underwent surgery in July, he was bed-bound,
said his mother, Sherry Cauldwell.

If he tried to walk, he fell, and he had bruises and cuts=7F
all over his body," Cauldwell said. "We had to spoon-feed
him.  He had tremors in his voice so bad that his speech was=
 incomprehensible,
which really made it difficult because he also couldn't write."


Kurth was examining Hopson every month and it became apparent
that he was declining rapidly. "He had maybe five years
of life left, which weren't going to be very pretty", Kurth
said.  He discussed the case with Jacques and Skip said,
"`Why don't we do a transplant?"


The results from the surgery surprised even the research team.
"Our expectations were exceeded a lot",Kopyov said.
"We couldn't expect what we obtained."

Within 10 days after the surgery," Kopyov said, "Hopson was walking
and talking and had no chorea. We thought it was a placebo
effect, but we now know that it isn't" the doctor said.
"But we still don't know how to explain such immediate improvement."

The two other male patients operated on in January showed the
same type of immediate improvement, but "It was even more
pronounced" Kopyov said.

Hopson has continued improving and is now living independently
with a roommate.  He uses a wheelchair, but can walk short distances
and rides an exercise bicycle.

"I miss playing Frisbee and all that stuff ... but I can
go anyplace I really want to," he said," I'm slowly
but surely getting better."

"What we can say with confidence," Kopyov said, "Is
that the disease is not progressing any more."

The team plans no more transplants for perhaps another year while
they evaluate the current patients' progress.  They also do not
have funds to perform further surgeries.  "But if the patients
continue to show improvement, " Kopyov said," that problem will probably
resolve itself."

Transcribed from The Los Angeles Times