Genetically engineered
immune cells are saving the lives of cancer patients. That may be just the
start
W hether you've watched 28 days, Resident Evil, or I am Legend, the story line is a familiar one. A desperate young child is at death's door when suddenly, a doctor takes a leap of faith and tries a experimental cure that uses DNA altered T cells to target malignant cells. The net, zombie proliferation that threatens the world.
However, in this case, no zombies, just promising medicine. Seriously, as if right out of the pages of a Marvel comic...
Doctors looking at Layla Richards, a 12 month old baby desperately ill. Despite bags and bags of chemotherapy and a
bone marrow transplant, the cancer still thrived. By last June, the
12-month-old was desperately ill. Her parents pleaded to the Doctors at the London hospital. The prognosis did not look good; however, one Doctor knew that sitting in a vial on a shelf in her freezer at the hospital, was an experimental treatment. A treatment was white blood cells that had been altered genetically to search and destroy leukemia. The issue? The hospital hadn't yet sough permission to test this protocol. They were the most extensively engineered cells ever proposed as a therapy, with a total of four genetic changes, two of them introduced by the new technique of genome editing.
There was. In a
freezer at her hospital—Great Ormond Street, in London—sat a vial of white
blood cells. The cells had been genetically altered to hunt and destroy
leukemia, but the hospital hadn’t yet sought permission to test them. They were
the most extensively engineered cells ever proposed as a therapy, with a total
of four genetic changes, two of them introduced by the new technique of genome
editing.
Where the technology stands, it's a pretty radical treatment.
Soon a doctor from
Great Ormond was on the phone to Cellectis, a biotechnology company with French
roots that is now located on the East Side of Manhattan. The company owned the
cancer treatment, which it had devised using a gene-editing method called
TALENs, a way of making cuts and fixes to DNA in living cells. “We got a call.
The doctors said, ‘We’ve got a girl who is out of T cells and out of options,’”
André Choulika, the CEO of Cellectis, remembers. “They wanted one of the vials
made during quality-control testing.”
The doctors hoped to
make Layla a “special,” a patient who got the drug outside a clinical trial. It
was a gamble, since the treatment had been tried only in mice. If it failed,
the company’s stock and reputation could tank, and even if it succeeded, the
company might get in trouble with regulators. “It was saving a life versus the
chance of bad news,” Choulika says.
Cellectis began
developing the treatment in 2011 after doctors in New York and Philadelphia
reported that they’d found a way to gain control over T cells, the so-called
killer cells of the immune system. They had shown that they could take T cells
from a person’s bloodstream and, using a virus, add new DNA instructions to aim
them at the type of blood cell that goes awry in leukemia. The technique has
now been tested in more than 300 patients, with spectacular results, often
resulting in complete remission. A dozen drug firms and biotechnology companies
are now working to bring such a treatment to market.
The T cells created by
Cellectis could have even broader applications. The previous treatments use a
person’s own cells. But some patients, especially small children like Layla,
don’t have enough T cells.
Foreseeing this problem,
Cellectis had set out to use gene editing to create a more highly engineered
but ultimately simpler “universal” supply of T cells made from the blood of
donors. The company would still add the new DNA, but it would also use gene
editing to delete the receptor that T cells normally use to sniff out
foreign-looking molecules.
“The T cell has a huge
potential for killing. But the thing you can’t do is inject T cells from Mr. X
into Mr. Y,” Choulika says. “They’d recognize Mr. Y as ‘non-self’ and start
firing off at everything, and the patient will melt down.” But if the T cells
are stripped down with gene editing, like the ones that were sitting in Great
Ormond’s freezer, that risk is mostly eliminated. Or so everyone hoped.
In November, Great
Ormond announced that Layla was cured. The British press jumped on the
heartwarming story of a brave kid and daring doctors. Accounts splashed on
front pages sent Cellectis’s stock price shooting upward. Two weeks later, the
drug companies Pfizer and Servier announced they would ante up $40 million to
purchase rights to the treatment.
Although many of the details of Layla’s case
have yet to be disclosed, and some cancer experts say the role of the
engineered T cells in her cure remains murky, her recovery pointed a spotlight
on “immune engineering,” and on the way that advances in controlling and
manipulating the immune system are leading to unexpected breakthroughs in
cancer treatment. They also could lead to new treatments for HIV and autoimmune
diseases like arthritis and multiple sclerosis.
So we can actually, breathe a sigh of relief - help may be around the corner, if nothing else, it beats a Zombie around the corner...
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We would like to thank our sponsors, for without them - our fine content wouldn't be deliverable!
Source(s)
- Resource: MIT Technology Review (March/April 2016 Issue)
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So “Once more unto the breach, dear friends, once more;”
So “Once more unto the breach, dear friends, once more;”
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About Rick Ricker
An IT professional with over 23 years experience in Information Security, wireless broadband, network and Infrastructure design, development, and support.
About Rick Ricker
For more information, contact Rick at (800) 399-6085 x502


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