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Vision Improves Modestly In Two Patients After Transplant of Human Embryonic Stem Cells

Cautious optimism for the remainder of the macular degeneration clinical trials

January 26, 2012
Source: The Lancet

Findings: This preliminary report provides the first detailed description of the method used to inject human embryonic stem cells (hESC) into the eyes of two patients—one with dry age-related macular degeneration and the other with juvenile Stargardt's macular dystrophy. Study sponsor, Advanced Cell Technology, and the University of California Los Angeles investigators associated with the clinical trials (registered with ClinicalTrials.gov as NCT01345006 and NCT01344993) report that the hESC transplants appear safe and that both patients seem to have experienced some improvement in their vision.

Relevance: Currently, there are no treatments for dry age-related macular degeneration and Stargardt's macular dystrophy. This stem cell treatment was designed to replace the retinal pigment epithelium lost to these diseases. The treated patients didn't seem to reject the cells or have signs of inflammation or cancer after four months; however, continued follow-up is needed. If these trials for safety and effectiveness are successfully completed, future clinical trials will be designed to treat patients earlier in the disease processes, before so much vision is lost.

Study Limitations: The investigators caution that there are a number of limitations to this preliminary report, including:

  • Their conclusions are based upon the treatment of only two individuals.
  • There is little agreement between investigators on how to measure improvement in people with low vision, but it is encouraging that during the four- month observation period neither patient lost vision.
  • Four months is a short amount of time to determine whether the treatment has led to cancer, a safety concern for embryonic stem cell transplants; the two patients will be further monitored.
  • The patient with dry age-related macular degeneration did not take her immunosuppression drugs for the first week after transplantation (to prevent the body from rejecting the cells), and it has been difficult to confirm that the stem cells actually stayed in the retina.
  • They are uncertain whether any of the visual improvements were due to the transplanted cells, the use of immunosuppressive drugs, or a placebo effect (which means a person feels better even though the treatment didn't work).

For more information, please see the UCLA press release below and the original publication from The Lancet with commentary.

Amyloid Fibril Formations

Stem Cell Trials
UCLA's Steven Schwartz
performs stem cell transplant.

(Photo credit: Reed Hutchinson/UCLA)

Researchers at UCLA's Jules Stein Eye Institute and colleagues who successfully transplanted specialized retinal cells derived from human embryonic stem cells into the eyes of two legally blind patients report that the transplants appear safe and that both patients have experienced modest improvement in their vision.

The preliminary findings, published online Jan. 23 in the journal The Lancet, represent a milestone in the therapeutic use of stem cells and may pave the way for a new therapy to treat eye diseases, the researchers said. Because this is the first time physicians have applied the power of regenerative medicine to eye disease, the clinical trials are being watched closely by scientists, stem-cell therapy advocates and the public.

The patients—a woman in her 50s with Stargardt's macular dystrophy and a woman in her 70s with dry age-related macular degeneration—underwent outpatient transplantation surgeries last July, said principal investigator Dr. Steven Schwartz, chief of the retinal division at the Jules Stein Institute and the Ahmanson Professor of Ophthalmology at the David Geffen School of Medicine at UCLA.

Both patients received relatively low doses of stem cell–derived retinal pigment epithelial (RPE) cells, which were transplanted into the space under the retina. The patients then received low-dose immunosuppression therapy over a number of weeks. The researchers monitored the patients' progress over four months and found no safety concerns, no signs of rejection and no abnormal cell growth.

In the Lancet, Schwartz and a team of doctors from UCLA and Advanced Cell Technology Inc., which manufactured the stem cells used in the surgery, report that standard vision tests suggested some improvement in the vision of both patients. The woman with Stargardt's disease, for example, went from only being able to discern hand movements to seeing a single finger move, according to the Lancet article. On a visual acuity letter-chart, she went from being unable to read any letters prior to treatment to reading five letters.

The patient with macular degeneration also showed some improvement after the therapy. Where once she was only able to make out 21 letters on the chart, her reading level stabilized at 28 letters — after peaking at 33 letters just a couple of weeks after the transplantation.

"The ultimate therapeutic goal will be to treat patients earlier in the disease processes, potentially increasing the likelihood of photoreceptor and central visual rescue," the authors of the paper wrote.

The patients are part of two separate clinical trials, each of which will eventually include 12 patients, Schwartz said. The trials will aim to determine the safety of this particular use of stem cell therapy, as well as the patients' ability to tolerate the treatment.

No standard treatments exist for either of these eye diseases. The dry form of macular degeneration, the most common form of the disease and the leading cause of blindness in the developed world, affects as many as 30 million people in the United States and Europe, especially those over age 55; the number of people affected is expected to double over the next 20 years as the population ages. Stargardt's disease causes progressive vision loss, usually starting when patients are between 10 to 20 years old.

In both conditions, the layer of retinal pigment epithelial cells located beneath the retina deteriorates and atrophies. These cells support, protect and provide nutrition for light-sensitive photoreceptors in the eye. Over time, the death of these cells and the eventual loss of the photoreceptors can lead to blindness as central vision is gradually destroyed.

Adapted from UCLA

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