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James Ciment The Food and Drug Administration (FDA) temporarily shut down a
series of human gene therapy experiments at the University of
Pennsylvania last month following the death of Jesse Gelsinger, an 18 year old man from Arizona who was being treated for a liver disorder.
The order to place the university's entire gene therapy programme on
indefinite "clinical hold" came two days after inspectors issued a
report noting 18 specific violations of government protocols.
The administration said that the hold would not be lifted until the
university's Institute for Gene Therapy showed that it could follow
procedures that protect volunteers from harm.
Among the evidence gathered by the administration was the institute's
failure to consider Mr Gelsinger's eligibility for the treatment, in
the light of reports of serious effects in other patients.
This violation was made public in a report issued during a December
meeting of the recombinant DNA advisory committee, the National
Institutes of Health's panel established to oversee gene therapy research.
But the final report included numerous other violations. The FDA said
that the informed consent process "was not well documented" and
thus it was difficult to determine who had conducted or attended the
discussions on informed consent.
Meanwhile, Paul Gelsinger, Jesse's father, who supported the
experiments even after last month's advisory committee report, has
said that he has now changed his mind and hired a lawyer. So far no
suit has been filed.
Jesse Gelsinger was undergoing treatment for ornithine transcarbamylase
deficiency, a disorder that prevents the liver from effectively
processing ammonia, a toxin produced in the breakdown of proteins. He
died of multiple organ failure triggered by a severe immune reaction to
an infusion of corrective genes.
Adding to the controversy was the fact that the inherited disorder is
relatively mild and that the patient had previously kept the problem in
check through diet modification and prescription drugs.
Mr Gelsinger's death is believed to be the first directly resulting
from gene therapy. The episode
widely reported in the media
has sent
shock waves through the gene therapy research
establishment.

The artist Alexa Wright collaborated with the dermatologist
Professor Irene Leigh to create this image of a woman with vitiligo.
The photograph is part of the Invisible Body exhibition at the Atrium
Gallery, Whiteleys Shopping Centre, London, until 13 February.