Download Gene Therapy, Successful Against Parkinson`s, Continues on the

Gene Therapy, Successful Against Parkinson's,
Continues on the Road to Redemption
By Patrick Morgan | March 17, 2011 3:27 pm
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Back in the 1980s, gene therapy was one of science’s
greatest hopes and hypes, and researchers predicted the
technique would be used to cure a huge range of
illnesses. During the 90s, many early gene therapy trials
were effective or downright dangerous, some causing
cancer or even death. But more recently, scientists who
stuck with gene therapy have started to see positive
results, with promising treatments for malformed
hemoglobin, color blindness, and depression. (See the
DISCOVER magazine feature “The Second Coming of Gene Therapy” for more.) Now,
researchers have announced that they’ve successfully treated the symptoms of
Parkinson’s disease in a small group of people—a far cry from a cure, but still a step in
the right direction.
I Once Was Blind but Now I See
The theory behind gene therapy is simple: A healthy gene hitches a ride into the
patient’s genome on a virus, replacing the genes responsible for some genetic disease or
disorder. Actually doing this is more difficult, because humans have a little thing called
an immune system that’s remarkably efficient at finding and destroying foreign bodies.
After the first U.S. death from gene therapy in 1999, and leukemia cases in France the
same year, many started to think that gene therapy was more of a problem than an
answer.
The early and awful failures forced all of the researchers in the field to retreat and
reconsider the staggering complexity that challenged them. They could not just replace a
bad gene with a good gene, as some early pundits had hoped—they also had to
orchestrate the nuanced and elaborate dance between the gene products (proteins) and
the patient’s immune system, which could recognize a foreign body and viciously attack
it. After that was settled, gene therapists still had to find a suitable virus, or vector, to
carry replacement genes into human cells without inciting a damaging or deadly
immune response…. It was this new perspective more than anything else that turned
gene therapy from a simple but failed and frustrated hope into, once again, medicine’s
next big thing—a stunning spectacle of hubris, ignominy, and redemption on the
scientific stage. [DISCOVER]
New: Gene Therapy and Parkinson’s Disease
While there’s no cure for Parkinson’s as of yet, doctors have an arsenal of methods,
ranging from drugs, brain stimulation, and (now) gene therapy that help reduce the
disease’s symptoms. Hopes for using gene therapy to alleviate Parkinson’s effects aren’t
new. What is new is that scientists have successfully completed the first randomized,
controlled, double-blind trial of treating Parkison’s patients with gene therapy—and
they found that it significantly improved debilitating symptoms such as tremors, motor
skill problems, and rigidity.The basic premise is that Parkison’s patients’ movement
problems is caused from an overactive brain region: the subthalamic nucleus. If
scientists could introduce a gene into that region of the brain that would produce
GABA—an inhibitory chemical—then they could potentially quiet that brain region and
alleviate tremors.
The therapy, which was done with local anesthesia, used a harmless, inactive virus
[AAV-2 GAD] to deliver the GAD gene into each patient’s subthalamic nucleus, a key
brain region involving motor function. The gene instructs cells to begin making GABA
neurotransmitters to re-establish the normal chemical balance that becomes
dysfunctional as the disease progresses. [US News]
After injecting the virus into the brains of 22 patients and administering a placebo to 23
others, the scientists discovered 6 months later (when the patients’ motor skills were
assessed), that the gene therapy group’s motor abilities improved by 23.1%, while the
placebo group only improved by 12.7%.
As the researchers told the BBC, this technique “shows the promise of gene therapy for
other neurological disorders,” but they urged caution because the relative improvement
of 10.4% is “rather small.” Importantly, it doesn’t match the most effective method
currently used: Deep brain stimulation has about twice the rate of clinical improvement
than gene therapy does.
On a Hot Streak
This latest triumph of gene therapy is merely one cobble in the long road to redemption.
As 80beats covered previously, a similar brain-related gene therapy method has been
used to treat depression in mice. Just like the Parkinson’s treatment, it involves
piggybacking a gene on a virus and changing a neurotransmitter system:
The gene in question creates a protein called p11 that helps carry serotonin receptors up
to the surface of a brain cell where they can receive signals from other brain cells. Poor
serotonin signaling may be one of the major drivers behind depression, and a dearth of
p11 could worsen the problem, according to study author Michael Kaplitt. [80beats]
Another promising gene therapy technique seeks to mitigate the HIV virus’s weakening
of the immune system:
Carl June and colleagues tested six male patients who already had HIV and were taking
a standard antiviral regimen. Like many HIV patients, the drugs helped them, but their
counts of immune cells stayed low. June’s team tested a therapy created by Sangamo
BioSciences in Richmond, California, that alters a patient’s actual white blood cells to
make them more HIV-resistant. [80beats]
Researchers removed a sample of CD4+ T cells, the type of immune cells affected by
HIV, from each man and used Sangamo’s enzyme to disrupt the CCR5 gene, which
encodes a protein that HIV uses to enter CD4+ cells. The engineered cells were then
infused back into the patients. Immune-cell counts subsequently rose for five of the six
patients who received the therapy. “It’s very exciting,” says John Rossi, a molecular
biologist at the City of Hope’s Beckman Research Institute in Duarte, California. “If they
did this several times in a given patient, you could establish a high percentage of
resistant cells.” [Nature]
But as in the other cases, we shouldn’t get too excited about these humble starts: There’s
a big difference between alleviating symptoms and curing a disease, and in the case of
HIV, those promising results were only in a population of six patients.
Oddly enough, modified viruses in the same family as HIV serve as the gene-shuttles for
some gene therapies, including those aimed at people with beta-thalassaemia, a
condition that results in faulty hemoglobin. In this case, by shoving a gene into a
tweaked lentivirus (a group that includes HIV), the scientists were able to edit the
defective genes, allowing the patient’s body to create working hemoglobin.
Gene therapy has also been used for rather less debilitating conditions, like color
blindness. In one case, researchers used gene therapy to cure red-green color blindness
in two adult monkeys:
In the new study, published in Nature, the researchers used a type of squirrel monkey in
which the males lack a visual pigment called L-opsin. Its absence renders the monkeys
color-blind, unable to distinguish reds and green. Most of the females, on the other
hand, see in full color. So the scientists got to wondering: what would happen if they
gave a boy squirrel monkey the same opsin that girls have [Scientific American]. They
used a harmless virus to ferry in the gene that makes opsin, injecting the virus behind
the monkeys’ retinas. [80beats]
Though they target different genes for different reasons, all of these gene therapy
techniques share the same fundamental methods, and study by study, they’re redeeming
a once-tarnished discipline—but all the same it’ll be many years before these specific
methods become standard medical procedures.