Over 2 million people worldwide are suffering from , inherited or acquired, and over 270 genes have been identified which are found to be responsible for these conditions.
, and tight blood-retinal barriers, limiting systemic side effects of the drug.
In recent years, advances in gene therapy in retinal conditions have increasing significantly, with progress in cell-specific targeting and transduction efficiency of gene products through the use of , suggesting that even greater success in future clinical trials is possible.
Gene therapy in mouse models showed promise in preventing vision loss or blindness from serious retinal injury including , and from retinal disease including and , Mount Sinai researchers report.
Their study, published in the July 22 online publication of Cell, could transform treatment for those at risk of major vision loss from retinal degenerative diseases, which currently have no cure. The researchers focused on retinal ganglion cells, which process visual information by sending images to the brain.
These cells can degenerate as a result of retinal injury and retinal disease. The team of researchers demonstrated how reactivation of a and its downstream signaling in through a gene therapy approach provided robust protection against further vision loss or impairment in multiple disease and injury models.
“Neuroprotective strategies to save vulnerable retinal ganglion cells are desperately needed for vision preservation,” said senior author
“We uncovered evidence for the fi rst time that CaMKII is a key regulator of the survival of retinal ganglion cells in both normal and diseased retinas, and could be a desirable therapeutic target for vision preservation in conditions that damage the .”
, the leading cause of irreversible visual impairment worldwide, affects 76 million people, some of whom will progress to blindness despite aggressive treatment to reduce the pressure in their eyes.
The major barrier to restoring vision loss from glaucoma and other retinal diseases and injuries is that the , which allow retinal ganglion cells to process visual information by converting light that enters the eye into a signal transmitted to the brain, do not regenerate.
For that reason, neuroprotective strategies to preserve the RGC’s axons and somas (the main body of the nerve cell from which axons branch off along the optic nerve to the brain) and thereby prevent further vision loss are urgently needed. Mount Sinai researchers investigated whether CaMKII could play such a therapeutic role.
They tested the enzyme across a wide range of injury and disease animal models, including optic nerve damage, excitotoxicity (where nerve cells are destroyed by the overactivation of that result in damage to the cell structure), and two glaucoma models that mimicked the pathophysiology of human disease with both high and normal
The team learned that CaMKII regulated the survival of retinal ganglion cells across many of these pathologies, and that in the small-animal excitotoxicity model, insults to the retinal ganglion cell’s somas or optic nerve injury to its axons led to inactivation of CaMKII and its downstream signaling target CREB (or cAMP response element binding protein).
“Intriguingly, we found that reactivation of CaMKII and CREB provided robust protection for retinal ganglion cells, and that CaMKII-mediated protection slowed down the disease progression in both glaucoma models,” noted Dr. Chen, who is also the
That reactivation was made possible by a gene therapy approach deployed by the researchers to introduce a more active type of CaMKII into the original retinal ganglion cells to boost their activity.
The modifi ed version of CaMKII, with a mutated amino acid, was transferred to the targeted cells through an adeno-associated viral vector, a Food and Drug Administration-approved gene delivery system common to the growing fi eld of gene therapy.
“Our research showed that CaMKII could indeed be a valuable therapeutic target to save retinal ganglion cells and preserve vision in treating potentially blinding diseases like glaucoma,” said Dr. Chen, a winner of the Pew Scholars in the Biomedical Sciences award given to young investigators showing outstanding promise.
“The fact that manipulation of CaMKII would involve a one-time transfer of a single-gene adds to its vast potential to treat serious retinal conditions in humans. The next step is testing this in larger animal models, which may pave the way for starting clinical trials.”
Mount Sinai has fi led patent applications for this technology through , the commercialization arm of the health system. MSIP is in active discussions with multiple companies to help advance this treatment to the clinic.
, along with the Research to Prevent Blindness and The Harold W. McGraw, Jr. Family Foundation.