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Progress on Stem Cell Therapy to Restore Sight

Published: 2022-08-02
Author: University of Pennsylvania | Contact: upenn.edu
Peer-Reviewed Publication: Yes | DOI: https://dx.doi.org/10.1016/j.stemcr.2022.06.009
Additional References: Regenerative Medicine News Publications

Synopsis: A multi-institutional effort is taking steps to develop an effective technique to regenerate photoreceptors cells and restore sight in people with vision disorders. Beltran and Gustavo Aguirre at Penn Vet have long been interested in addressing blinding retinal disorders. They have had great successes in producing corrective gene therapies for conditions with known causative genes to date. In this study, we wanted to know if we could, one, improve the surgical delivery of these cells to the subretinal space; two, image the cells in vivo; three, improve their survival; and four, see them migrate to the layer of the retina where they should be and start integrating.

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Definition

Stem Cell Therapy

Stem cell therapy is a form of regenerative medicine designed to repair damaged cells within the body by reducing inflammation and modulating the immune system. Stem cell therapies have been used to treat autoimmune, inflammatory, neurological, orthopedic conditions, and traumatic injuries with studies conducted on use for Crohn's disease, Multiple Sclerosis, Lupus, COPD, Parkinson's, ALS, Stroke recovery, and more. Stem-cell therapy has become controversial following developments such as the ability of scientists to isolate and culture embryonic stem cells, to create stem cells using somatic cell nuclear transfer, and their use of techniques to create induced pluripotent stem cells. Research is underway to develop various sources for stem cells and apply stem-cell treatments for neurodegenerative diseases and conditions such as diabetes and heart disease.

Main Digest

What if, in people with blinding retinal disorders, one could introduce into the retina healthy photoreceptor cells derived in a dish from stem cells and restore sight? It's a tantalizingly straightforward strategy for curing blindness. Yet, the approach has been met with several scientific roadblocks, including introduced cells dying rapidly or failing to integrate with the retina.

Related Publications:

A new study, published in Stem Cell Reports, overcomes these challenges and marks significant progress toward a cell-based therapy. The work, led by a team at the University of Pennsylvania School of Veterinary Medicine, in collaboration with researchers at the University of Wisconsin-Madison, Children's Hospital of Philadelphia, and the National Institutes of Health's National Eye Institute (NEI), introduced precursors of human photoreceptor cells into the retinas of dogs. A cocktail of immunosuppressive drugs enabled the cells to survive in the recipients' retinas for months, where they began forming connections with existing retinal cells.

"In this study, we wanted to know if we could, one, improve the surgical delivery of these cells to the subretinal space; two, image the cells in vivo; three, improve their survival; and four, see them migrate to the layer of the retina where they should be and start integrating," says William Beltran, a professor of ophthalmology at Penn Vet and senior author on the study. "The answer to all those questions was yes."

Beltran and Gustavo Aguirre at Penn Vet have long been interested in addressing blinding retinal disorders. They have had great successes in producing corrective gene therapies for conditions with known causative genes to date. But a gene has not been identified for many cases of inherited retinal degeneration. In other patients, the disease has progressed so far that no photoreceptor cells remain intact enough for gene therapy. In either scenario, a regenerative medicine approach would be extremely valuable in which photoreceptors could be regrown outright.

To develop a cell therapy, Beltran's team joined with groups led by John Wolfe of CHOP and Penn Vet; David Gamm at the University of Wisconsin-Madison; and Kapil Bharti at the NEI, in a consortium supported by the NEI's Audacious Goals Initiative for Regenerative Medicine. The partnership combined Beltran's team's expertise in canine models of retinal degeneration and vast experience in cell-based therapy approaches from the Wolfe, Gamm, and Bharti labs.

Photoreceptor cells made up of rods and cones constitute a layer of the outer retina critical to initiating the vision process, whereby the energy of light transforms into an electrical signal. To function properly, they must form a connection, or synapse, with cells of the inner retina to pass along the visual information. Thus, the goal of this cell therapy is to recreate this layer and enable it to integrate with the retina's other cell types to relay signals from one layer to the next.

Human photoreceptor precursor cells labeled red migrated and integrated into a degenerated canine retina following a transplantation procedure. The green label is a synaptic maker, suggesting the transplanted cells began forming a connection with second-order neurons in the retina - Image Credit: Beltran lab/Stem Cell Reports.Human photoreceptor precursor cells labeled red migrated and integrated into a degenerated canine retina following a transplantation procedure. The green label is a synaptic maker, suggesting the transplanted cells began forming a connection with second-order neurons in the retina - Image Credit: Beltran lab/Stem Cell Reports.

In the current work, the team used stem cell-derived precursors of human photoreceptor cells developed in the Gamm lab to serve as the basis of cell therapy. In collaboration with the Bharti lab, they developed a new surgical approach to inject the cells, which were labeled with fluorescent markers, into the retinas of seven dogs with normal vision and three with a form of inherited retinal degeneration, then used a variety of non-invasive imaging techniques to track the cells over time.

"The use of a large animal model that undergoes a naturally occurring form of retinal degeneration and has a human-size eye was instrumental in optimizing a safe and efficient surgical procedure to deliver doses of cells that could be used in patients," says Gamm.

The researchers observed that cell uptake was significantly better in the animals with retinal degeneration than in normal retinas.

"What we showed was that, if you inject the cells into a normal retina that has its photoreceptor cells, the retina is pretty much intact and serves as a physical barrier, so the introduced cells don't connect with the second-order neurons in the retina, the bipolar cells," Beltran says. "But in three dogs at an advanced stage of retinal degeneration, the retinal barrier was more permeable. In that environment, cells had a better ability to start moving into the correct layer of the retina."

Because the dogs' immune system could interpret the transplanted human cells as foreign entities, the researchers did what would be done in other tissue transplant procedures: They gave the dogs immunosuppressive drugs. The trio of medications had been tested previously by Oliver Garden, a veterinary immunologist with Penn Vet at the time of the study, who is now dean of Louisiana State University School of Veterinary Medicine.

Indeed, while the injected cell populations declined substantially in dogs that did not receive the immune-suppressing drugs, the cell numbers dipped but then sustained in the dogs that received the cocktail.

Further characterization of the introduced cells revealed evidence of potential synapses.

"We saw that yes, some are appearing to 'shake hands with those second-order neurons," Beltran says. "There appeared to be contact."

The next stage for this project will be to continue optimizing the therapy and then test whether there is a functional response - in other words, improved vision - in its recipients.

Author and Coauthors

William Beltran is a professor of ophthalmology and director of the Division of Experimental Retinal Therapies at the University of Pennsylvania School of Veterinary Medicine.

Beltran's coauthors on the work were Penn Vet's Ana Ripolles-Garcia, Natalia Dolgova, Svetlana Savina, John H. Wolfe, Oliver A. Garden, and Gustavo D. Aguirre; the University of Wisconsin-Madison's M. Joseph Phillips, Allison L. Ludwig, Sara A. Stuedemann, Uchenna Nlebedum, and David M. Gamm; and the National Eye Institute's Arvydas Maminishkis, Juan Amaral, and Kapil Bharti.

Study Information

This study was supported by the National Institutes of Health (grants EY029890, EY06855, and EY031230), Fighting Blindness Canada, Foundation Fighting Blindness, Research to Prevent Blindness, the Van Sloun Fund for Canine Genetic Research, Retina Research Foundation, Emmett A. Humble Distinguished Directorship of the McPherson Eye Research Institute, the Sanford and Susan Greenberg End Blindness Outstanding Achievement Prize, and the Sandra Lemke Trout Chair in Eye Research.

Reference Source(s):

Progress on Stem Cell Therapy to Restore Sight | University of Pennsylvania (upenn.edu). Disabled World makes no warranties or representations in connection therewith. Content may have been edited for style, clarity or length.

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