Regulators OK Clinical Trials Using Donor Stem Cells

Japanese health officials approve human experiments to treat macular degeneration with a cell therapy derived from induced pluripotent stem cells.

By | February 6, 2017

WIKIPEDIA, TMHLEE

Update (March 28): Today, doctors administered the first donor-derived iPSC transplant that Takahashi developed, Nature News reported. A man in his 60s received the therapy, aimed at treating macular degeneration. Earlier this year, Takahashi's team reported success using a patient's own iPSCs that were reprogrammed into retinal cells.

Researchers in Japan who have been developing a cell therapy for macular degeneration received support from health authorities this week (February 1) to begin a clinical trial using donor-derived induced pluripotent stem cells (IPSCs) converted to retinal cells. This will be the first trial in which the team’s physicians administer donor cells, an approach expected to lower costs and preparation time.

Previously, this same group of scientists, led by the Riken Center for Developmental Biology’s Masayo Takahashi, tested an iPSC-based therapy for macular degeneration using the patients’ own cells.

“The procedure was expensive and time-consuming, costing about 100 million yen ($930,000) to cultivate and test the iPS cells and about 11 months for the transplant to take place,” The Asahi Shinbum reported in June 2016. “But with the use of the iPS cell stock [from donors], the time frame could be reduced to as short as a month and costs could be significantly reduced.”

In September, Takahashi and her colleagues reported that iPSC-derived retinal pigment epithelial (RPE) cells from monkeys implanted in immune-matched monkeys’ eyes were not rejected. And in a second paper published simultaneously, they demonstrated that human-donor RPE cells made from iPSCs did not spark an immune response from lymphocytes in culture.

“The papers together make a strong case that allogeneic iPSC-derived RPE cells can effectively be used for transplantation into immune matched recipients without eliciting a major immune response,” stem cell biologist Paul Knoepfler of the University of California, Davis, told The Scientist at the time. “What this means is that iPSC-based treatments for macular degeneration, for instance, likely will not have to rely on autologous transplants if matching is done.”

Nikkei Asian Review reported that about five patients will enter the donor-cell trial, which is slated to begin in the first half of 2017.

 

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