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which this article appears: Genetics
BMJ 2002;325:10 ( 6 July )
News
Scientists use gene therapy to cure immune deficient child
Judy Siegel-Itzkovich, Jerusalem
An international team of scientists has managed to cure a child with severe
combined immunodeficiency (SCID) using genetherapy.
Patients with SCID are usually treated by replacing an essential enzyme,
adenosine deaminase, which is lacking in such people.But this
treatment is effective for only a couple of days at atime and is
expensive. Some patients can have a bone marrow transplant,but only
if a good match can befound.
The team was headed by Professor Shimon Slavin, of the Hadassah University
Hospital in Jerusalem, and his colleagues Dr ShoshanaMorecki and Dr
Memet Aker. They collaborated with Dr AllesandroAiuti and other
staff from the San Raffaele Institute for GeneTherapy in Milan,
Italy. They published their results in the journalScience
last week (2002;296:2410-3).
The patient, whose first name is Salsabil, is a baby Arab girl from east
Jerusalem who had to live for the first seven monthsof her life
inside a plastic bubble to protect her from all pathogensbecause she
totally lacked an immunesystem.
Although the condition is diagnosed in only a few dozen infants around the
world each year (in most cases the babies die beforea diagnosis is
made and they can be treated), Professor Slavinsaid the treatment
can be used to cure other genetic diseasesin which patients are born
lacking a vitalenzyme.
"Among these are Gaucher's syndrome, metachromatic leukodystrophy, and
Hurler's syndrome," hesaid.
A decade ago scientists began treating SCID by using gene therapy to alter T
cells and stem cells. Although a theoreticalsuccess, these
experiments failed to have a real impact on thebabies' condition
because only a tiny amount of the geneticallyabnormal bone marrow
products was repaired, Professor Slavinexplained.
The patients still required adenosine deaminase replacement treatment to
survive because the "good" cells were overwhelmedby the much larger
number of genetically abnormal cells remainingin the
host.
Professor Slavin believed that if he could give the genetically treated cells
a "biological advantage," they could overcomethe more numerous
abnormal cells. He asked Dr Claudio Bordigan,head of the San
Raffaele Institute, to supply adenosine deaminaseretroviralvector.
At Hadassah University Hospital 15 months ago, Professor Slavin's team gave
Salsabil a mild form of chemotherapy, called non-myeloblative
conditioning, to suppress her defective bone marrow cells, and
prepare the ground for the transfused cells to multiply. The team
then introduced, using a genetically engineered virus, a healthycopy
of the missing gene for adenosine deaminase into her purifiedbone
marrow stemcells.
No enzyme replacement had been given at any stage, showing that the gene
alteration treatment was responsible for thecure.
The baby recovered quickly, and within a few weeks the number of lymphocytes
in her blood rose dramatically. Within a monthshe was out of
isolation and went home perfectlywell.
She is the third baby with SCID born to her parents. The first child died
from the condition and the second, Salsabil's oldersister Tasmin,
survived after receiving a transplantation of allogeneicumbilical
cord blood from a youngerbrother.
After the first child died, Hadassah doctors froze umbilical cord blood cells
from each successive baby for possible treatmentof subsequentsiblings.
Salsabil's immune system is thought to be working properly, because after she
was exposed to chickenpox in the family shedeveloped antibodies
against the disease.
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