Embryonic stem cells have been dubbed "the sleeper issue" of the 2012 election, but stem-cell research (taking cells from human embryos to create new cells that can treat disease) has long been a hot-button topic. The problem is that embryos traditionally are destroyed to extract the cells--something that plenty of people are uncomfortable with. But if there was a way to extract human embyronic stem cells without destroying anything, well, that shouldnt create any ethical quandaries. Advanced Cell Technology, a biotechnology company specializing in cellular therapies, thinks it has the solution.
ACT uses an embryonic stem-cell-removal technique that doesnt destroy anything: It removes a single cell from embryos that are in the eight-cell stage--in other words, extremely early on. Its identical to whats done in in-vitro fertilization clinic for genetic testing of diseases like Tay-Sachs and Huntingtons Disease. "Its a non-destructive, non-harmful method of extracting these cells and creating embryonic stem cells. There are thousands of babies born every year having this exact kind of genetic testing done," says ACT CEO Gary Rabin.
The cells propagate infinitely, so once you have what you need, you never have to go back to an in-vitro fertilization clinic to get more. ACT hasnt taken cells from a clinic since 2005.
The technique is just part of the battle, of course; creating viable medical treatments is also necessary to prove ACTs worth. Despite a history of financial mismanagement--when Rabin joined the company in 2010, it had less than $1 million in the bank (now it has over $10 million)--ACT has some exciting developments coming down the pike.
Most of them have to with the eye, which is an ideal place to start for embryonic stem cell treatment: The subretinal space in the eye is immune-privileged, meaning there shouldnt be any issues with immune system rejection; everything you do in the eye can be observed down to the cellular level thanks to advanced scanning techniques; and there are 15 million patients in the U.S. with age-related macular degeneration (AMD)--a number that is expected to double over the next 20 years as the population ages. There are no real cures or therapies for AMD, and most drugs used in the eye were developed in the 1960s. Its a space thats ripe for change.
ACT is running three phase 1 clinical trials: a U.S. trial of an AMD treatment, and two trials (one in the U.S. and one in the U.K.) with a treatment for Stargardts Macular Dystrophy (SMD), a juvenile disease that causes progressive vision loss, ultimately leading to blindness. The trials have been promising so far.
"All of the [11] patients [in the three trials] treated long enough to have any effect have had subjective improvements in visual acuity, and nearly all have had measurable improvement in visual acuity," says Rabin. "We didnt expect that in this patient population. As this is a phase 1 study, were treating very late stage patients." The three trials are still ongoing, but ACT is on to thinking about how to design phase 2. "Its clear now that we dont have any safety issues with these cells," explains Rabin.
How do the stem cells get implanted in the first place? You start with an embryonic stem-cell line, and through culturing media and differentiation techniques turn them into retinal pigment epithelium (RPE)--cells that are critical for visual function. When RPE cells die because of old age or other causes, theres a corresponding decline in vision. So ACTs technique is to inject RPE cells into the back of the eyes retinal space. "The cells are injected in a suspension of a proprietary media thats more or less like a saline," says Rabin.
ACTs main focus is on its eye treatments, but the company is also looking at the potential to use mesenchymal stem cells (MSCs), a kind of cell that can turn into a variety of cell types, to treat autoimmune disorders like multiple sclerosis and lupus. There are hundreds of clinical trials involving MSCs that are going on right now, but "the usefulness in earlier-stage cells give us a very significant advantage in terms of treating these kinds of diseases," says Rabin.
Right now, at least, ACT says it hasnt experienced too much pushback for its methods. "The problem is in this political climate its a hot button issue. If you raise it with any Republican candidate, its 'Oh, you destroy embyronic stem cells, youre killing babies.' Its just a convenient headline," says Rabin. "Theres a lot of education we have to do to make people aware of how this [works]."
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