Restoring Retinal Function in a Mouse Model of Hereditary Blindness

Moore discusses a new study showing rescue of photoreceptor function using gene and drug therapies in a mouse model of Leber congenital amaurosis.

L eber congenital amaurosis (LCA) is a generic term used to describe a heterogeneous group of inherited disorders that result in severe loss of rod and cone photoreceptor function in infancy and early childhood.Although each individual disorder is rare, LCA accounts for 3%-5% of childhood blindness [1].
To date, ten different genes have been implicated in such early onset retinal dystrophies.The genes are expressed in the photoreceptors or the underlying retinal pigment epithelium (RPE), and encode a variety of proteins, including structural proteins, transcription factors, and key components of the phototransduction cascade and the visual cycle.

The Visual Cycle
Light perception in vertebrates is mediated by a group of G proteincoupled receptors called opsins, which are bound to a chromophore (lightabsorbing compound), 11-cis-retinal, derived from vitamin A. Absorption of light induces an 11-cis to all-trans isomerisation of the chromophore, and the ensuing conformational change initiates the visual transduction cascade.In order for the activated opsin to participate again in the visual process, the all-trans-retinal must be isomerised back to the 11-cis form via an enzymatic pathway, the visual cycle (Figure 1).This occurs mainly within the RPE.
Genes encoding a number of enzymes within the visual pathway have been implicated in LCA, namely, RPE65 (retinoid isomerase), retinal dehydrogenase 12, and lecithin:retinol acyl transferase (LRAT).The genetic mutations lead to a lack of 11-cisretinal, resulting in severe loss of photoreceptor function and ultimately in cell death.Therapeutic approaches aimed at restoring levels of 11-cis-retinal by either improving enzyme function or using other biochemical strategies hold promise for restoring visual function.The development of good animal models of LCA is an essential fi rst step in developing effective therapies.

Promising Treatments in a Mouse Model
Batten et al., in this issue of PLoS Medicine, report very encouraging results of two different therapeutic approaches in the Lrat knockout (Lrat -/-) mouse [2].The mutant mice show an early onset rod-cone dystrophy and, as in the human disorder, have disease confi ned to the eye.The mouse model appears to faithfully reproduce the phenotype seen in humans with Lrat defi ciency.In the fi rst approach, the authors used gene therapy with subretinal injection of a recombinant adeno-associated virus carrying the Lrat gene.Treated animals showed high expression of Lrat in the RPE adjacent to the injection site, markedly increased levels of visual pigment, and improvement of rod photoreceptor function measured electrophysiologically.The rescue of retinal function peaked at six weeks and then slowly declined.The reasons for the lack of sustained rescue are unclear.
A second approach was to use the orally administered pro-drugs 9-cis-retinyl acetate and 9-cis-retinyl succinate to bypass the Lrat stage of the visual cycle.(9-cis-retinoids were chosen as they are easier to synthesise and are more stable than 11-cis-forms.)Again, rescue of photoreceptor function could be unequivocally demonstrated.Furthermore, treatment with both gene therapy and synthetic retinoids was more effective than treatment with either alone.

Clinical Implications
What is the relevance of these results for patients with early onset retinal dystrophies and their clinicians?Clearly, there is cause for optimism in that treatment may become available within the next few years.Gene therapy is perhaps the most promising approach.Photoreceptor rescue has now been demonstrated in a number of animal models of inherited retinal disease, including mice and dogs that lack RPE65 [3].The fi rst gene therapy trial in humans with early onset retinal dystrophies as a result of mutations in RPE65 is due to start within the next two years, and if this is successful, treatment of other disorders such as Lrat defi ciency will follow.

Open access, freely available online
The Perspectives section is for experts to discuss the clinical practice or public health implications of a published article that is freely available online.However, unlike RPE65, there is no large animal model of Lrat defi ciency, and patients with Lrat defi ciency are extremely rare; these two problems may limit the development of a treatment trial in humans.To date, only three patients with Lrat defi ciency have been described, and there is very limited information about the clinical phenotype and natural history.

Restoring Retinal Function in a Mouse Model of Hereditary Blindness
What about dietary treatment?This has been used with limited success in other rare retinal dystrophies in humans, for example, Refsum disease and gyrate atrophy, where the biochemistry of the disorder is understood.The results of Batten and colleagues' study suggest that Lrat defi ciency may also respond to dietary treatment [2].It is very interesting that 9-cis-retinoids can replace 11-cis-retinal, and partially restore photoreceptor function.However, as the authors caution, there is much more work that needs to be done before such compounds can be used in humans.We will need to know whether 9-cisretinoids are well tolerated in humans, whether there is any retinal or systemic toxicity, and whether retinal function is improved long term with prevention of cell death.Will the treatment be effective relatively late in the disease process when most patients tend to be diagnosed, or is early treatment essential?

The Next Steps
Batten and colleagues' excellent study highlights the improvements that are being made in our understanding of the disease mechanisms in inherited retinal disease [2].This knowledge will lead to the development of novel therapies for specifi c forms of disease.The challenge for clinicians is to be prepared for treatment trials.We need to identify the genetic mutations causing retinal degeneration in our patients, carefully characterise the phenotype and natural history of disease, and identify those patients who may benefi t from the new therapeutic approaches.