RPE65 is specifically expressed in the retinal pigment epithelium and is essential for the recycling of 11-cis-retinal, the chromophore of rod and cone opsins. In humans, mutations in RPE65 lead to Leber congenital amaurosis or early-onset retinal dystrophy, a severe form of retinitis pigmentosa. The proof of feasibility of gene therapy for RPE65 deficiency has already been established in a dog model of Leber congenital amaurosis, but rescue of the cone function, although crucial for human high-acuity vision, has never been strictly proven. In Rpe65 knockout mice, photoreceptors show a drastically reduced light sensitivity and are subject to degeneration, the cone photoreceptors being lost at early stages of the disease. In the present study, we address the question of whether application of a lentiviral vector expressing the Rpe65 mouse cDNA prevents cone degeneration and restores cone function in Rpe65 knockout mice.
Methods and Findings
Subretinal injection of the vector in Rpe65-deficient mice led to sustained expression of Rpe65 in the retinal pigment epithelium. Electroretinogram recordings showed that Rpe65 gene transfer restored retinal function to a near-normal pattern. We performed histological analyses using cone-specific markers and demonstrated that Rpe65 gene transfer completely prevented cone degeneration until at least four months, an age at which almost all cones have degenerated in the untreated Rpe65-deficient mouse. We established an algorithm that allows prediction of the cone-rescue area as a function of transgene expression, which should be a useful tool for future clinical trials. Finally, in mice deficient for both RPE65 and rod transducin, Rpe65 gene transfer restored cone function when applied at an early stage of the disease.
By demonstrating that lentivirus-mediated Rpe65 gene transfer protects and restores the function of cones in the Rpe65−/− mouse, this study reinforces the therapeutic value of gene therapy for RPE65 deficiencies, suggests a cone-preserving treatment for the retina, and evaluates a potentially effective viral vector for this purpose.
Citation: Bemelmans A-P, Kostic C, Crippa SV, Hauswirth WW, Lem J, Munier FL, et al. (2006) Lentiviral Gene Transfer of Rpe65 Rescues Survival and Function of Cones in a Mouse Model of Leber Congenital Amaurosis. PLoS Med 3(10): e347. https://doi.org/10.1371/journal.pmed.0030347
Academic Editor: Susan Lightman, Moorfields Eye Hospital, United Kingdom
Received: November 28, 2005; Accepted: June 20, 2006; Published: October 10, 2006
Copyright: © 2006 Bemelmans et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported by Fondation Provisu and the Swiss Telethon. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Abbreviations: cd, candela(s); PNA, peanut agglutinin lectin; rAAV, recombinant adeno-associated virus; RPE, retinal pigment epithelium; P[number], postnatal day [number]; SEM, standard error of the mean
Leber congenital amaurosis (LCA) is the name of a group of hereditary diseases that cause blindness in infants and children. Changes in any one of a number of different genes can cause the blindness, which affects vision starting at birth or soon after. The condition was first described by a German doctor, Theodore Leber, in the 19th century, hence the first part of the name; “amaurosis” is another word for blindness. Mutations in one gene called retinal pigment epithelium-specific protein, 65 kDa (RPE65)—so called because it is expressed in the pigment epithelium, a cell layer adjacent to the light-sensitive cells, and is 65 kilodaltons in size—cause about 10% of cases of LCA. The product of this gene is essential for the recycling of a substance called 11-cis-retinal, which is necessary for the light-sensitive rods and cones of the retina to capture light. If the gene is abnormal, the sensitivity of the retina to light is drastically reduced, but it also leads to damage to the light-sensitive cells themselves.
Why Was This Study Done?
Potentially, eyes diseases such as this one could be treated by gene therapy, which works by replacing a defective gene with a normal functional one, usually by putting a copy of the normal gene into a harmless virus and injecting it into the affected tissue—in this case, the eye. The researchers here wanted to see whether expressing wild-type RPE65 using a particular type of gene vector that can carry large pieces of DNA transcript—a lentiviral vector—could prevent degeneration of cone cells and restore cone function in a mouse model of this type of LCA—mice who had had this Rpe65 gene genetically removed.
What Did the Researchers Do and Find?
Injection of the normal gene into the retina of Rpe65-deficient mice led to sustained expression of the protein RPE65 in the retinal pigment epithelium. Electrical recordings of the activity of the eyes in these mice showed that Rpe65 gene transfer restored retinal function to a near-normal level. In addition, Rpe65 gene transfer completely prevented cone degeneration until at least four months, an age at which almost all cones have degenerated in the untreated Rpe65-deficient mice.
What Do These Findings Mean?
These findings suggest that it is theoretically possible to treat this type of blindness by gene therapy. However, because this study was done in mice, many other steps need to be taken before it will be clear whether the treatment could work in humans. These steps include a demonstration that the virus is safe in humans, and experiments to determine what dose of virus would be needed and how long the effects of the treatment would last. Another question is whether it would be necessary (or even possible) to treat affected children during early childhood or when children start losing vision.
Please access these Web sites via the online version of this summary at http://dx.doi.org/10.1371/journal.pmed.0030347.
- The Foundation for Retinal Research has detailed information on Leber's congenital amaurosis
- Contact a Family is a UK organization that aims to put families of children with illnesses in touch with each other
- The Foundation for Fighting Blindness funds research into, and provides information about many types of blindness, including Leber's congenital amaurosis
- This Web site provides information on gene therapy clinical trials, including those dedicated to cure eye diseases
- This foundation provides information on diseases leading to blindness, including Leber's congenital amaurosis
The neuroretina is composed of several cell layers in which light stimuli are converted into an electric signal by the photoreceptors. This conversion process takes place in the visual pigment of the photoreceptors, which is composed of opsin, a protein component, and 11-cis-retinal, a vitamin A chromophore. Absorption of light triggers isomerisation of the chromophore into all-trans-retinal and conformational change of the opsin. Upon this activation, the phototransduction cascade is initiated, which finally results in the generation of the electric signal. To regain light sensitivity, all-trans-retinal must be re-isomerised to 11-cis-retinal. This regeneration requires transport of the all-trans-retinal to the adjacent retinal pigment epithelium (RPE), where a number of enzymatic reactions are involved in the re-isomerisation to 11-cis-retinal, before transport of the chromophore back to the photoreceptors . The pigment epithelial protein RPE65 is essential for this process  because it catalyses the re-isomerisation of the all-trans-retinoid into the 11-cis form [3–5]. In agreement with this essential function, mice deficient for RPE65 have strongly reduced retinal function [2,6]. In humans, RPE65 mutations cause a form of early-onset retinal dystrophy termed Leber congenital amaurosis [7–9], which leads to early blindness.
The ability to efficiently target RPE cells with viral vectors has led to the proposal that RPE65 deficiencies are good candidates for gene therapy protocols [10,11]. In 2001, a study by Acland et al.  revealed the clinical potential of Rpe65 gene transfer. In this study, the treatment of RPE65-deficient dogs by intraocular delivery of a recombinant adeno-associated virus (rAAV) encoding canine Rpe65 partially rescued retinal function and restored vision. Furthermore, long-term follow-up of the treated dogs showed that the visual recovery was stable for more than three years without adverse effects . A second study, by Narfström et al. in 2003 , using the same animal model treated with a rAAV-encoding canine Rpe65 also demonstrated a long-term improvement of the visual function up to three years postinjection, associated with a clear improvement in a behavioural tests conducted in both day and night vision [14,15]. As a consequence of these results, two clinical trials involving rAAV-mediated RPE65 gene transfer were proposed in 2004 in the US, the first being accepted while the second is still under review (NIH GeMCRIS, http://www.gemcris.od.nih.gov/ protocol numbers 0410–677 and 0510–740).
It is important, however, to continue to document the effectiveness of RPE65 gene transfer in animal models, especially in light of the results obtained recently after rAAV-mediated gene transfer of RPE65 in the Rpe65 knockout mouse (Rpe65−/−): Gene transfer was effective when administered in utero, but treatment of adult mice led to only limited improvement of retinal function [16,17]. Therefore, the timing of gene therapy seems to be crucial for the outcome. This is particularly true when aiming at cone vision rescue, which is of prime importance for human patients. Interestingly, cone function is lost in Rpe65−/− mice  due to early-onset degeneration of these cells [18,19], and Chen et al.  demonstrated recently that adenoviral delivery of Rpe65 in Rpe65−−/− mice restores isomerohydrolase activity and prevents, to a certain extent, early cone loss, although this latter study did not examine the cone function. rAAV-mediated Rpe65 gene transfer can also moderately increase cone cell survival, but its effect on the function of these cells remains unclear . Thus, RPE65 seems essential for cones, but the effect of Rpe65 gene transfer on their survival and function remains to be elucidated.
Most of the work published to date in the field of RPE65 gene transfer involved the use of rAAV vectors. These vectors efficiently target retinal cells, and in particular RPE and photoreceptors when they are injected in the subretinal space [21–23]. Moreover, the use of different viral serotypes allows the targeting of both types of cells or the RPE alone . The cloning capacity of rAAV vectors is, however, limited to 4 kb, which hampers the use of large transgenes—for instance ABCA4, the gene mutated in Stargardt disease. In contrast, lentiviral vectors appear as an attractive alternative to rAAV for gene therapy protocols targeting RPE cells: The lentiviral vector has a cloning capacity of up to 10 kb, causes a weak or absent inflammatory response, and expresses transgenes rapidly. Most importantly, the lentiviral vector transduces RPE cells with high efficiency [10,24–27], making of it an ideal candidate for Rpe65 gene transfer.
For the present study, we used Rpe65−/− mice to analyze the therapeutic effect of lentivirus-mediated gene transfer on survival and function of the affected retinal cells. As cone impairment and degeneration progress rapidly in Rpe65−/− mice, we performed a detailed analysis of the therapeutic effect on this photoreceptor subtype. We also used a double-knockout mouse strain modelling RPE65 deficiency on a pure cone function background to study the effect of gene transfer on cone function.
Construction and Production of Lentiviral Vectors
The lentiviral plasmids used in his study were derived from the pLOX-GFP plasmid , which contains the central polypurine tract and central termination sequence (cPPT/CTS ) and the woodchuck hepatitis virus post-transcriptional regulatory element (WPRE ) downstream of the transgene. To construct the control vector encoding GFP, the PGK-GFP expression cassette was excised from the pLOX-GFP plasmid using ClaI (blunted) and BamHI sites, and replaced by the R0.8-GFP cassette previously extracted by KpnI (blunted) and BamHI digestion from the pRPE0.8-GFP plasmid [13,31]. The plasmid encoding Rpe65 was then generated by insertion of RPE65 mouse cDNA in place of the GFP ORF in the control plasmid using BamHI and XhoI sites.
Recombinant lentiviral particles were produced by transient transfection of 293T cells as previously described [27,28]. Viral supernatants were concentrated by ultracentrifugation at 70,000 g for 90 min at 4 °C. Finally, to achieve a 1,000-fold concentration of the initial supernatant, viral pellets were resuspended in a minimal of volume of PBS containing 10 mg/ml BSA. Aliquots of 5–10 μl were then stored at −70 °C until further use. Total particle concentration of the viral stocks was estimated by quantification of the p24 capsid protein using RETRO-TEK HIV-1 p24 Antigen ELISA kit (ZeptoMetrix, Buffalo, New York, United States) according to the manufacturer's instructions. In addition, infectious titres of the Hlox-R0.8-GFP vector were quantified by infection of 293T cells, in which the R0.8 promoter is active. Briefly, 293T cells were seeded on 12-well plates and infected by serial dilutions of the vector stocks. On day 4 postinfection, cells were harvested, dissociated, and fixed for 15 min in 4% paraformaldehyde in PBS. The infectious titres were deduced from the percentage of GFP-expressing cells estimated by flow cytometry on a FACSCalibur (Becton Dickinson, Franklin Lakes, New Jersey, United States). Infectious titres were always in the range of 3 transducing units per pg of p24 protein.
Animals and Surgical Procedures
Animals were handled in accordance with the statement of the “Animals in Research Committee” of the Association for Research in Vision and Ophthalmology (Rockville, Maryland, United States), and protocols were approved by the local institutional committee (Service vétérinaire du canton de Vaud, Lausanne, Switzerland). Mice were kept at 22 °C under a 12 h light–12 h dark cycle with lights on at 7 a.m., and were fed ad libitum. Rpe65−/− mice were obtained from Dr. T. M. Redmond , and Rpe65−/−/Gnat1a−/− double knockout mice were described previously .
Before administration of lentiviral vectors, mice were transferred to a level 2 confinement room. For intravitreal injection at postnatal day 5 (P5), mouse pups were anaesthetized by volatile anaesthesia (2%–3% isoflurane with O2 at a rate of 800 ml/min). A horizontal incision was made on the superior eyelid to access the eye. A 34-gauge bevelled needle mounted on a 5 μl syringe (Hamilton, Bonaduz, Switzerland) was introduced in the vitreal cavity through the dorsal pole of the sclera, without touching the lens. 1 μl of viral suspension diluted in PBS containing 1% BSA was injected into the vitreous, and the needle was left in place for additional 30 s. Mouse pups were then returned to their mothers after they regained consciousness. For subretinal injection during adulthood, the mice were anesthetized by volatile anaesthesia (1.5%–3% isoflurane with O2 at a rate of 800 ml/min). The superior eyelid was maintained open by traction using a suture wire. The eye globe was then immobilized by two suture wires inserted respectively in nasal and temporal positions in the conjunctiva at the proximity of the limb. Using fine ophthalmic scissors, the conjunctiva of the dorsal pole was dissected, and the sclera/choroid layers were punctured with an ophthalmic lancet. A 34-gauge bevelled needle mounted on a 5 μl syringe was then tangentially inserted into this hole to reach the posterior temporal part of the subretinal space. 1.5 μl of viral suspension was injected to create a subretinal bleb, and the needle was left in place 30 s before withdrawal.
ERG recordings were performed on site at Jules Gonin Eye Hospital (Lausanne, Switzerland). For scotopic conditions, mice were dark-adapted overnight. Subsequent procedures were undertaken under dim red light unless otherwise specified. Mice were anaesthetized with a mixture of ketamine (100 mg/kg) and xylazine (15 mg/kg), and pupils were dilated by topical administration of 0.5% tropicamid (Novartis Pharma, Bern, Switzerland). Mice were then positioned on a heated platform to prevent a drop in body temperature. A reference electrode and a ground electrode adapted from 30-gauge needles were inserted below the skin of, respectively, the scalp and the back of the mouse. Recording electrodes made of thin silver wires were put in contact with the surface of the cornea, which was then covered with a carboxymethylcellulose sodium solution (Celluvisc, Allergan, Irvine, California, United States) to prevent drying of the cornea and to ensure maximal contact with the electrodes. The mouse was placed in the centre of a Ganzfeld stimulator from a Multiliner Vision apparatus (Jaeger/Toennies, Höchberg, Germany) adapted for examination of rodents, and placement of the electrodes was corrected until the impedance level dropped below 10 kOhm. The corneal ERG was then recorded in scotopic conditions in response to single flashes of white light of the following intensities: 1 × 10−4, 1 × 10−3, 1 × 10−2, 3 × 10−2, 1 × 10−1, 3 × 10−1, 1, 3, 10, and 25 candelas (cd) s/m2, generated by a stroboscopic light located in the upper part of the Ganzfeld stimulator. For the photopic ERG, the mice were left in the Ganzfeld stimulator where they were adapted for 10 min to a white light of 30 cd/m2. Photopic responses were then recorded in response to single flashes ranging from 10−2 to 25 cd s/m2, in the same illumination conditions. For each stimulus intensity, ten to 15 traces were averaged. Amplitude of the a-wave was defined as the difference between the baseline level at the time of stimulation and the peak of the a-wave. Amplitude of the b-wave was defined as the difference between the peak of the b-wave and the peak of the a-wave (or the baseline level when the a-wave was not detectable). Amplitudes are expressed in μV. At the end of the examination, the eyes were covered with Viscotears (Novartis Pharma), and the mice were kept under surveillance until they regained consciousness.
After mice were sacrificed, the eyes were enucleated, a hole was created through the cornea, and the eyes were fixed for 1 h in 4% paraformaldehyde in PBS. After overnight incubation in 25% sucrose, the eyes were embedded in albumin from hen egg white (Fluka, Buchs, Switzerland) and cut in 14 μm sections using a cryostat. Sections were collected on six serial slides for each eye allowing multiple labelling throughout the entire eye for each slide.
For immunohistological analysis, the slides were blocked for at least 1 h at room temperature in PBS with 10% normal goat serum (Dako, Zug, Switzerland) and 0.2% Triton X-100. Most of the time the primary and secondary antibodies were incubated in PBS with 2% normal goat serum and 0.2% Triton. Mouse monoclonal anti-RPE65 (Abcam, Cambridge, United Kingdom) was incubated overnight at room temperature at 1:1,000, while rabbit polyclonal anti-RPE65 (pin5 ) was incubated overnight at 4 °C at 1:500. Rabbit polyclonal anti-GFP (Abcam) was incubated overnight at room temperature at 1:2,000. Peanut agglutinin lectin (PNA) labelling was performed using PNA linked to TRITC (Sigma, Buchs, Switzerland) diluted at 1:1,000 and incubated overnight at 4 °C. Rabbit polyclonal anti-GNAT2 (Santa Cruz Biochemicals, Santa Cruz, California, United States) was incubated overnight at room temperature at 1:100, anti-S-opsin (Santa Cruz Biochemicals) and anti-MWL (Chemicon, Temecula, California, United States) overnight at 4 °C at 1:1,000. Secondary antibodies were goat anti-rabbit linked to FITC (1:100, Jackson Immunoresearch, Westgrove, Pennsylvania, United States) or Cy3 (1:500, Jackson Immunoresearch) or goat anti-mouse linked to AF488 (1:500, Molecular Probes, Eugene, Oregon, United States) were incubated 1 h at room temperature. For immunolabelling using the anti-S-opsin, horse serum (Jackson Immunoresearch) and anti-goat-Cy3 (1:1,000; Jackson Immunoresearch) were used. Before examination, sections were counterstained with DAPI (Molecular Probes) and mounted under coverslips with Mowiol 4–88 Reagent (VWR International AG, Lucerne, Switzerland).
Sections were analyzed on a BX60 microscope equipped for epifluorescence (Olympus Suisse SA, Aigle, Switzerland) and coupled to the analySIS 3.0 software (Soft Imaging System, Munster, Germany). For quantification of the transduced area, images of the whole area expressing the transgenes were digitized on serial sections separated by 84 μm, the length of the transduced part of the RPE was calculated with the analySIS software, and the area between each section was deduced by multiplication of this length by the intersection distance. To quantify the number of cells positive for PNA, GNAT2, and M/L- and S-opsin, we chose for each eye the section that cut the optic nerve in the middle and was thus the most central. We then counted throughout the retina of this section the number of outer segments that stained positive.
LV-RPE65 Allows Efficient and Specific RPE65 Protein Expression in the Retinal Pigment Epithelium of Rpe65−/− Mice
A major concern in gene therapy protocols is to avoid expression of the therapeutic transgene to nontarget organs and cells. The Rpe65 gene is expressed mainly in the RPE. To limit expression of the transgene to this site, we constructed an HIV-1-derived lentiviral vector known to transduce the RPE with high efficiency when delivered in the subretinal space and with limited diffusion toward the other retinal layers [10,24–27]. Furthermore, we used a 0.8 kbp proximal fragment of the human RPE65 gene (R0.8) with the aim of driving transgene expression specifically in RPE cells.
In a first series of experiments we characterized the pattern of transgene expression from the R0.8 promoter in the lentiviral context (Figure 1). We treated Rpe65−/− mice by intravitreal injection at P5 or subretinal injection at 1 mo with HIV-1-derived lentiviral vectors encoding either the GFP reporter gene (LV-GFP) or the Rpe65 cDNA (LV-RPE65), under the control of the R0.8 promoter. In both cases, immunofluorescence labelling performed 1 wk after gene transfer revealed GFP (Figure 1A–1D) or RPE65 protein expression (Figure 1F and 1G) in a large area of the RPE. In addition, immunolabelling of GFP led to detection of other cell types in the retina. In some cases, a few photoreceptors were transduced after intravitreal injection of neonates only (Figure 1D), as well as occasionally some Müller cells in subretinal injection of adults (Figure 1C). In the latter case, the transduction of Müller cells seemed to be limited to a lesion of the retina due to the surgical procedure. These ectopic expressions always accounted for a very low percentage of the transduced cells. After LV-RPE65 injections, the presence of RPE65 protein in the RPE was confirmed by the use of two different antibodies (see Materials and Methods). Nevertheless, contrary to what we observed after GFP gene transfer, we did not detect RPE65 protein in either photoreceptors or Müller cells. This most probably reflects the difference in detection sensitivity between the GFP and the RPE65 antibodies. These results demonstrate the usefulness of the lentiviral vector and the R0.8 promoter to re-express the RPE65 protein in the RPE of RPE65-deficient mice.
Rpe65−/− mice received the LV-GFP vector (A–D) or the LV-RPE65 vector (F and G) as an intravitreal injection at P5 (A, D–G) or a subretinal injection at 1 mo of age (B and C). 1 wk later GFP expression in the RPE was detected spanning a large proportion of the retina (A and B). Although to a lesser extent, transduced cells were also evident in the photoreceptor layer after injection at P5 (D). GFP expression was detected in the ONL (arrowheads in D) as well as in the outer segments (arrows in D). (E) DAPI counterstaining of the sample in (D). GFP was also detected occasionally in Müller cells after injection in the subretinal space at the age of 1 mo (C). After injection of the LV-RPE65 vector, immunolabelling showed RPE65 expression in the RPE (F and G). (H and I) Control RPE65 immunolabelling on noninjected Rpe65−/− retina (G) and wild-type retina (H). Scale bar in (I): 100 μm in A, B, and G–I; 25 μm in C–F.
Next we undertook a quantitative study to characterize transgene expression in the RPE at a later time point. Rpe65−/− mice at age 5 d received a bilateral injection in the vitreous of LV-GFP (n = 5) or LV-RPE65 (n = 5) at a dose of 20 ng of p24 (corresponding to 6 × 104 transducing units for the GFP vector), and transgenes expression was analyzed at the age of 4 mo. Cryostat serial sections were immunolabelled, and the extent of RPE stained for either GFP or RPE65 was determined. We used the intersection distance to deduce the total area of the RPE expressing the respective transgenes. This quantification revealed long-lasting transgene expression. We determined a transduced area of 0.93 ± 0.33 mm2 in the LV-GFP-treated group and of 0.32 ± 0.2 mm2 in the LV-RPE65-treated group. We also observed significant heterogeneity in the extent of the transduced area within each group. Some eyes displayed transgene expression spanning a large area of the retina, whereas others showed only little or no expression. This heterogeneity was most probably due to the surgical procedure, which, in our hands, remains highly variable. In summary, the histological analysis demonstrated long-term (4 mo) expression of the transgenes in areas of variable size.
Rpe65 Gene Transfer at P5 Restores Retinal Function of Rpe65−/− Mice
To reveal whether Rpe65 transgene expression results in an improvement of retinal function, we recorded the ERG response in Rpe65−/− animals 2 mo following vector injection at P5. In uninjected Rpe65−/− mice, the ERG recorded in scotopic conditions was characterized by an increase of the response threshold (i.e., the retina is less sensitive to light), when compared to wild-type animals. In line with previous studies , a 3.5 log unit (about 3,000-fold) lower stimulus was indeed sufficient to elicit in wild-type animals a b-wave of similar amplitude to the one observed for a stimulus of 3 cd s/m2 in Rpe65−/− mice. Furthermore, in uninjected Rpe65−/− mice, we never detected an a-wave (unpublished data). Similarly, in the LV-GFP treated group, the threshold of the b-wave appeared for the most intense stimuli, i.e., 3–10 cd s/m2, and the a-wave was never detected (Figure 2A, left tracings). In contrast, the LV-RPE65 treatment improved to a great extent the b-wave threshold of the Rpe65−/− mice (Figure 2A, right tracings). In this group, the threshold was improved for 6/10 eyes and, in the best cases (n = 2), the b-wave response appeared for stimuli as low as 10−2 cd s/m2 (i.e., 10-fold less sensitivity than wild type, compared to the 3,000-fold less sensitivity of the LV-GFP group) and could reach an amplitude equivalent to 34.6% of the mean of wild-type controls (333 ± 32.6 μV; n = 12) at the highest stimulus intensity (25 cd s/m2). As did the b-wave, an a-wave was clearly evidenced in the animals showing the best responses, which reached 23.1% of the wild type mean (128.9 ± 15.3 μV; n = 12) for the 25 cd s/m2 stimulus. Although the restoration of retinal function after LV-RPE65 treatment was variable, the statistical analysis of the b-wave amplitude showed a significant difference between LV-GFP and LV-RPE65 treatments (Figure 2B, p = 0.023 determined by ANOVA for repeated measures). It is important to note that we have included in this statistical analysis all the treated animals without discrimination, i.e., even those for which transgene expression was low or undetectable (see quantification below).
Rpe65−/− mice were treated P5 by an intravitreal injection of 20 ng of lentiviral vector.
(A) ERG response to single flashes was recorded in scotopic condition at 2 mo of age. After LV-GFP treatment, the mice showed a response typical for Rpe65−/− mice, with the a-wave absent and the b-wave elicited only for the highest stimuli (i.e., 10 and 25 cd s/m2; left tracings). After LV-RPE65 treatment, a stimulus of 10−2 cd s/m2 was sufficient to trigger the b-wave, and the a-wave appeared for a stimulus of 0.3 cd s/m2 (right tracings). Vertical bars indicate occurrence of the stimuli; x-axis: 40 ms/div; y-axis: 100 μV/div.
(B) Summary of the ERG recordings performed 2 mo after vector delivery at P5 in Rpe65−/− mice. Amplitude of b-wave (expressed in μV) is represented for each stimulus intensity. In the LV-RPE65-treated group (squares), the b-wave rose with a stimulus as low as 10−2 cd s/m2, whereas in the LV-GFP-treated group (triangles) 3 cd s/m2 were necessary to elicit the b-wave. ANOVA for repeated measures showed significant stimulus intensity effect (p < 0.0001), group effect (p = 0.023), and group versus stimulus intensity interaction (p = 0.002). Data are presented as mean ± standard error of the mean (SEM).
(C) Improvement of the ERG response after LV-RPE65 treatment is correlated with the level of RPE65 expression. The area of the retina expressing GFP (triangles) or RPE65 (squares) was quantified for each eye at age 4 mo after gene transfer at P5, and plotted against the b-wave threshold (defined as the intensity of the lowest stimulus capable of eliciting the b-wave, expressed in log mcd s/m2).
To assess whether the degree of ERG restoration was correlated with the size of the RPE area expressing Rpe65 after gene transfer, we attributed a functional score to each eye. This score was defined as the lowest stimulus intensity (expressed in log mcd s/m2) for which a rise of the b-wave was evident (response threshold), and was plotted as a function of the area of RPE expressing the transgene (GFP or Rpe65; Figure 2C). In the LV-GFP group, no b-wave was triggered by stimuli below 3.5 log mcd s/m2 regardless of the size of the transduced area (Figure 2C). In contrast, a b-wave was elicited in some mice of the LV-RPE65 group by stimuli as low as 1 log mcd s/m2, the mice displaying the better sensitivity being also those with the largest transduced area (Figure 2C). This confirmed that LV-RPE65 treatment restores retinal function and that the degree of restoration depends on the size of the transduced area.
LV-RPE65 Treatment Delays Cone Degeneration in Rpe65−/− Mice
Previous studies have described cone loss of function and degeneration in Rpe65−/− mice as early as at 2 wk of age [6,17,19,34]. However, cone survival after Rpe65 gene transfer has not been extensively investigated so far [16,17]. We therefore analyzed in detail cone morphology and the expression of cone-specific markers by quantifying the expression of different markers at 4 mo of age on sections adjacent to the one used for quantification of GFP and Rpe65 expression (after gene transfer at P5, see above). We first labelled the retinas with PNA, which binds the interphotoreceptor matrix sheath surrounding cone outer segments (Figure 3A and 3B). For each eye, PNA-positive structures were counted across the entire span of the retina in sections that cut through the optic nerve head. The optic nerve was used here as a reference to select a central section on which to quantify the different markers. This retinal area does not necessarily correspond to the site of maximal transgene expression, but, considering that cone markers are subjected to regional variability, it has the advantage of delimiting a reproducible area for cell counting. We observed a significantly higher number of PNA-labelled structures after LV-RPE65 treatment (258 ± 24, n = 9) compared to LV-GFP treatment (141 ± 10, n = 7, p = 0.007) or untreated mice (172 ± 10, n = 4, p = 0.018). Moreover, the best scores were obtained in eyes that most widely expressed the Rpe65 transgene as evaluated by the total area of RPE expressing RPE65 protein (unpublished data) and reached up to 50% (mean 37% ± 4%, n = 9) of the amount of PNA present in the wild-type control (Figure 3C). This quantification demonstrated that LV-RPE65 treatment at P5 conserves the interphotoreceptor matrix sheath of cones for an extended period of time.
(A and B) PNA linked to TRITC labels cone outer segments in red in a LV-RPE65-treated eye (A). (B) Merged picture representing RPE65 (green), PNA labelling (red), and cell nuclei (blue) in the same section used in (A).
(C) PNA labelling was quantified by counting the number of PNA-positive outer segments in the sagittal section that bisected the optic nerve for each eye of LV-RPE65 (n = 9) or LV-GFP (n = 7) treated groups as well as of Rpe65−/− (KO; n = 4) and wild-type control groups (n = 4). Values represent percentage of wild type (set to 100%). A significant increase of PNA labelling was seen for LV-RPE65 treated group compared to the LV-GFP (n = 7, p = 0.007) or untreated (n = 4, p = 0.018) groups (*p < 0.05). Data are presented as a mean percentage of the wild-type value ± SEM.
(D) GNAT2 (revealed in green by a secondary antibody linked to FITC) in a wild-type retina.
(E) The GNAT2 staining is extremely weak in Rpe65−/− mice at age 4 mo. *Example of remaining outer segment staining counted in the Rpe65−/− and LV-GFP treated groups.
(F) Quantification of GNAT2 labelling was performed (as described for PNA labelling) and showed a significant increase of GNAT2 expression in the LV-RPE65 group (n = 6) compared to the LV-GFP (n = 8, p = 0.017) or untreated (n = 4, p = 0.03) groups (*p < 0.05). The discrepancy in cone loss between PNA and GNAT2 markers in Rpe65−/− (compare control groups in C and F) is most probably due to the persistence of the cone interphotoreceptor matrix sheath, which can still be present after other cone markers have disappeared . Data are presented as a mean percentage of the wild-type value ± SEM.
(G and H) A GNAT2 pattern similar to that observed in wild-type mice is recovered after LV-RPE65 treatment in Rpe65−/− mice (G). Double labelling shows GNAT2 stained in red, RPE65 in green (H). Example of outer segment positive for GNAT2 is pointed by an arrowhead.
(I) LV-GFP treatment does not improve GNAT2 expression in Rpe65−/−. Example of weak residual labelling for GNAT2 in a control eye treated with LV-GFP (arrow).
(J) After LV-RPE65 treatment, a transitional area with spared GNAT2-positive cones but devoid of RPE65 expression was observed (dashed line).
(K and L) In (K) the diagram depicts a transitional area in a ring (red) surrounding the transduced area (green). The radius of the transduced area is indicated by x; the width of the transitional area is indicated by y. The relation of x to y is graphed in (L); the radius of the transduced area is linearly correlated with the transitional area.
Scale bar in (I): 50 μm in A, B, E, and G–I; 100 μm in D and J. KO, Rpe65−/− mice; LV-GFP, LV-GFP-treated mice; LV-RPE65, LV-RPE65-treated mice; WT, Rpe65+/+ mice.
To assess cone survival more specifically, we used immunofluorescence labelling of the cone-specific protein transducin (GNAT2), the mRNA level of which is drastically reduced at 2 mo of age in Rpe65−/− mice . In wild-type animals, GNAT2 immunolabelling revealed numerous cone outer segments (Figure 3D), while almost no GNAT2 immunoreactivity was detectable in the whole retina of Rpe65−/− mice at 4 mo of age (Figure 3E, asterisk). Treatment of Rpe65−/− mice with LV-RPE65, but not with LV-GFP, significantly increased the number of outer segment labelled with GNAT2 (Figure 3F–3I). Similar to the results obtained for PNA affinity, the best rescue of GNAT2 labelling was observed in eyes with widespread Rpe65 expression (unpublished data) and reached up to 50% (mean 26% ± 9%, n = 6) of the amount of GNAT2 present in the wild-type control. This protective effect of Rpe65 gene transfer corresponds to a 5-fold increase in correctly localized GNAT2 labelling compared to untreated mice (Figure 3F).
All these results represent a mean for the entire section cutting the optic nerve in the middle, but do not accurately show regional rescue at the site of transgene expression. To address this point, we counted the number of GNAT2-positive outer segments in the RPE region expressing the Rpe65 transgene on sections double-labelled for GNAT2 and RPE65 (Figure 3H), and thus established a cone density expressed as cell number per millimeter of epithelium. We found similar numbers of cones labelled for GNAT2 per millimeter for both LV-RPE65 (154 ± 29 cells/mm, n = 4) and wild-type controls (143 ± 12 cells/mm, n = 4). Finally, we noted that the area of GNAT2 staining (i.e., cone rescue) was larger than the area with detectable RPE65 expression. We measured the length of the transitional area (the area with GNAT2-positive cells but without RPE65 expression, Figure 3J, dashed line). Assuming that the transduced area is circular (Figure 3K), we determined its radius (“x” in Figure 3K) and found a linear correlation (Figure 3L) with the width of transitional area (“y” in Figure 3K). In summary, injection of the LV-RPE65 vector at P5 leads to correct GNAT2 expression in Rpe65−/− mice even 4 mo after the treatment not only at the site of transgene expression but in the surrounding area as well.
Two other cone markers that are important for cone function are S- and M/L-opsin. Both of these opsins are thought to be expressed in different proportions in the same cell, thus determining the precise photoreceptor type of the cell, i.e., blue cone (predominant S-opsin expression) or red/green cone (predominant M/L-opsin expression) . It has been shown that expression of these opsins is reduced and that the remaining proteins are mislocalized in Rpe65−/−/Rho−/− double knockout mice as early as P25, identifying 11-cis-retinal as a key partner for correct cone opsin trafficking . In light of this information, we analysed the effect of LV-RPE65 treatment on the amount and distribution of the two cone opsins (Figure 4). In the wild-type retina, the S-opsin and M/L-opsin antibodies strongly labelled the outer segments of different or common subsets of cones with a gradient of expression leading to a predominantly dorsal expression of the M/L-opsin and a predominantly ventral expression of the S-opsin (Figure 4A). In Rpe65−/− mice, a marked decrease in both the M/L-opsin and the S-opsin was noticed with rare labelling showing mostly mislocalized proteins (unpublished data). Similarly, in LV-GFP-treated mice, the rare and weak staining present at this age was mostly mislocalized in the cellular body (Figure 4E and 4F). After LV-RPE65 treatment, we observed an increase in expression of both opsins, which had adopted the correct cellular localization in the outer segments (Figure 4B and 4D). We compared the three eyes showing maximal transgene expression for each group (as determined by the RPE layer area expressing GFP or RPE65) and obtained a significant improvement of both S- and M/L-opsin expression in LV-RPE65-treated animals (respectively, on average 39% ± 5% and 38% ± 9% of the wild-type amount) compared to LV-GFP treated (respectively, on average 3% ± 1.5% and 9% ± 2.3% of the wild-type amount) or untreated knockout (respectively, on average 4% ± 1% and 18% ± 1.4% of the wild-type amount) (Figure 4G). Using the same methodology as for GNAT2 staining, we also quantified the extent of the transitional area on sections double labelled for RPE65 and S-opsin (n = 5). Similar to the quantification of GNAT2 transitional area depicted in Figure 3L, we found a strong correlation between the radius of the transduced area and the extent of the transitional area quantified on S-opsin-stained sections (y = 0.736x + 16.77; r2 = 0.988).
(A) Double immunostaining of wild-type retina with antibodies directed against S-opsin (red) and M/L-opsin (green) localized in the outer segment. Note that some cones express both opsins while others are mainly labelled for only one of these opsins.
(B–D) LV-RPE65 treatment allows similar expression of both S- and M/L-opsin to the wild-type retina in the region expressing the Rpe65 transgene. Arrows indicate double labelling of cone opsins; arrowheads indicate cone stained only for S-opsin.
(E and F) LV-GFP treatment does not rescue S- or M/L-opsin expression and shows a pattern of staining similar to untreated Rpe65−/− (unpublished data). *Mislocalized and reduced S- and M/L-opsin expression.
(G) Quantification of the three eyes with the highest transgene expression for LV-RPE65 and LV-GFP groups shows a significant increase in both S- and M/L-opsin expression after LV-RPE65 treatment compared to the LV-GFP (p = 0.005 for M/L-opsin and p < 0.0001 for S-opsin) or untreated (n = 4, p = 0.024 for M/L-opsin and p < 0.0001 for S-opsin) groups (*p < 0.05). No statistical difference was noted between LV-GFP and untreated knockout animals.
Data are presented as mean ± SEM. Scale bar in (F): 500 μm in A; 50 μm in B–F. KO, Rpe65−/− mice; LV-GFP, LV-GFP-treated mice; LV-RPE65, LV-RPE65-treated mice; WT, Rpe65+/+ mice.
In summary, we show that 4 mo after LV-RPE65 treatment at P5 there is a significant increase in cone sheath labelling by PNA and an increased expression of the three cone-specific markers GNAT2 and S- and M/L-opsin. These results indicate prolonged cone survival due to the restoration of RPE65 activity. Moreover, analysis of cone density in terms of RPE65 expression shows a transitional area where the therapeutic transgene is not detectable but cones are still spared.
Therapeutic Window and Importance of the Vector Dose for Rpe65 Gene Transfer
In utero rAAV-mediated Rpe65 gene transfer in Rpe65−/− mice led to an improvement of the ERG , but the same type of vector failed to substantially restore retinal function when administered at 3 wk of age . These studies indicate that there might be a small therapeutic window during which treatment outcome is optimal. To determine the ideal time point for lentivirus-mediated Rpe65 gene transfer in Rpe65−/− mice, we injected lentiviral vectors in an additional group of mice at 1 mo of age. ERG responses were recorded 1 mo after injection (i.e., at 2 mo, the same age as for P5-treated animals). LV-RPE65 treatment at 1 mo increased retinal sensitivity (b-wave threshold) by 2 log units in comparison to LV-GFP-treated or untreated Rpe65−/− animals (Figure 5A). To identify whether this functional rescue reflects an improved cone survival, we studied cone rescue using PNA labelling and GNAT2 immunofluorescence after sacrifice of these mice at 3 mo of age. For both markers, we observed no improvement related to LV-RPE65 treatment (Figure 5B). In fact, the level of GNAT2-positive cells after LV-RPE65 treatment was 3% ± 1% of the wild-type GNAT2 amount, in the same range as for LV-GFP treated or untreated Rpe65−/− mice (Figure 5B). Thus, despite successful transduction of the RPE and improvement in the overall retinal sensitivity, cones were not rescued when mice were treated at 1 mo of age. These results clearly indicate that early cone loss [18,19] is irreversible and can be prevented only by early treatment (e.g., at P5, as described above).
Rpe65−/− mice were treated by subretinal injection at age 1 mo with 20 ng of lentiviral vector. Treatment at this age with the LV-RPE65 vector restored ERG response with a threshold response of 3 × 10−2 cd s/m2 for the b-wave (A), whereas no improvement was observed in the LV-GFP treated group (unpublished data). (B) Counting of PNA-positive and GNAT2-positive cells revealed that Rpe65 gene transfer performed at age 1 mo was unable to protect the cones from degeneration. Data are presented as mean ± SEM.
The vector dose is a second issue that is critical in view of a clinical application. To explore the importance of this parameter, we treated Rpe65−/− mice at P5 with a 9-fold higher dose of LV-RPE65 vector than in the previous experiments, i.e., 180 ng of p24 (corresponding to 5.5 × 105 transducing units for the LV-GFP vector). In this case, we recorded the ERG after 1 mo, and we again observed heterogeneity in the improvement of the response after Rpe65 gene transfer, but we also found animals with a “near-normal” ERG response characterized by a threshold of 10−3 cd s/m2, similar to wild-type animals (n = 3 eyes). In these animals, a-wave and b-wave amplitudes reached, respectively, 43.8% and 70% of the wild-type control means for the highest stimulus intensity (25 cd s/m2; Figure 6A, left tracings). Moreover, for the stimulus at which the ERG response reached a plateau (10 cd s/m2), we observed a higher b-wave amplitude after treatment with a high dose of the LV-RPE65 vector (119.2 ± 23 μV, n = 6) than after treatment with a low dose (69.6 ± 12.9 μV, n = 8, p = 0.032 determined by Student's t-test). ERG responses in animals treated with a high dose of LV-GFP vector (n = 6, unpublished data) were indistinguishable from untreated knockouts or animals treated with the low dose of LV-GFP vector (Figure 2A). This experiment suggests that the level of functional rescue in Rpe65−/− mice is improved by a higher dose of lentiviral vector.
(A) Scotopic ERG recorded at age 1 mo of a Rpe65−/− mouse treated at P5 with 180 ng of LV-RPE65 (left tracings) and of a Rpe65+/+ untreated mouse (WT, right tracings). At this dose, LV-RPE65 treatment restored an ERG response similar to a wild-type response. For Rpe65−/− eyes showing the best restoration (n = 3), thresholds of both the a-wave and the b-wave reached normal levels with, respectively, 10−1 and 10−3 cd s/m2.
(B and C) At P5 Rpe65−/−/Gnat1a−/− mice received a bilateral intravitreal injection of the vector (LV-RPE65 or LV-GFP) at a dose of 180 ng of p24 capsid protein. 1 mo later, the ERG was recorded in scotopic (B) and in photopic conditions (C). Vertical bars indicate occurrence of the stimuli; x-axis: 40 ms/div; y-axis: 100 μV/div (left tracings), except right tracings in (A) (200 μV/div).
LV-RPE65 Treatment Restores Cone Function in RPE65-Deficient Mice
As rod and cone activity in Rpe65−/− mice cannot be readily distinguished with ERG recordings , we used an additional transgenic mouse line to prove that LV-RPE65 treatment rescues cone function. Mice lacking the rod transducin alpha subunit (Gnat1a−/−)  were crossed with Rpe65−/− mice to obtain Rpe65−/−/Gnat1a−/− double knockout mice. In these mice, any retinal response to light after 11-cis-retinal supplied through Rpe65 gene transfer cannot be derived from the rod transduction cascade, which is disrupted . Similar to the previous experiment, we treated double knockout mice at P5 by intravitreal injection of LV-RPE65 (n = 5) or LV-GFP (n = 5) with 180 ng of p24 capsid protein, and we measured the ERG response after 1 mo. In the LV-GFP-treated group, we were not able to detect an ERG response to any stimulus intensity (Figure 6B, left tracings), similar to what is observed in untreated mice (unpublished data). In contrast, LV-RPE65 treatment of Rpe65−/−/Gnat1a−/− mice restored an ERG response typical of cones, rising for the high-intensity stimuli and showing a bell-shaped curve (Figure 6B, right tracings). Furthermore, a response was also clearly detected when the ERG was recorded in photopic conditions (Figure 6C, right tracings). This, together with the fact that the rods of these mice are unable to function, demonstrates that lentivirus-mediated transfer of the Rpe65 gene is able to rescue a functional response originating from the cones in a model of complete chromophore deprivation, the Rpe65−/− mouse.
We report a successful restoration of retinal function by lentivirus-mediated Rpe65 gene transfer in an animal model of LCA. Furthermore, the rescue of the retinal function assessed by ERG is the best ever reported in the Rpe65−/− mouse model of LCA in terms of cone protection and visual sensitivity restoration [16,17], demonstrating the potential of this vector for a clinical application. In addition, we demonstrated that the use of the R0.8 promoter allows long-lasting expression of the Rpe65 transgene mostly restricted to RPE cells. From a clinical perspective, preservation of cone vision is a critical endpoint—indeed is the final goal for human therapies. We demonstrate, using different markers specific for cones, that Rpe65 gene transfer led to preservation of cone morphology and, in a transgenic line deficient for both RPE65 and the rod phototransduction cascade (Gnat1a−/−), to restoration of cone function. The absence of ERG response in untreated or LV-GFP-treated Rpe65−/−/Gnat1a−/− mice (Figure 6B and 6C), together with the fact that the residual response in Rpe65 knockout animals originates from rods , indicate that the rod response is abolished in this mouse strain due to the knockout of the Gnat1a gene. The ERG response restoration after LV-RPE65 treatment of the double-knockout animals thus demonstrates that Rpe65 gene transfer elicits a functional response from cone photoreceptors in the Rpe65−/− genetic background (Figure 6B and 6C).
As gene therapy trials for RPE65 deficiencies are on the verge of starting, it is important to accumulate data on different preclinical models using various vectors. The value of our results is reinforced by the fact that cone degeneration in Rpe65−/− mice starts just 2 wk after birth [18,19]. As a result, cone function is almost not recordable at P25  and is completely lost by 4–5 wk of age . Accordingly, we show here that LV-RPE65 prolongs cone survival for a protracted period (at least 4 mo, the latest time point studied) when administered at P5, but not at all when applied at 4–5 wk of age. These results are consistent with previous studies using rAAV in Rpe65−/− mice. Dejneka et al. found in utero treatment to be more efficient than treatment of adult mice (1 or 2.5 mo), but cone function and survival were not determined in this report . In another study, by Lai et al., in mice injected at age 3 wk only 50% of the density of S-opsin labelling was restored at the site of injection at 8 mo —consistent with our results showing that gene therapy given at 1 mo does not protect cones compared to that given at P5. Thus, the degeneration of cones beginning at age 2 wk  is irreversible, but can be prevented by early restoration of RPE65 activity (present study) or exogenous 11-cis-retinal . Lentivirus-mediated gene transfer at P5 seems indeed optimal for cone protection in Rpe65−/− mice.
Consistent with the ability of lentiviral vectors to provide long-lasting expression in various cells and tissues in vitro as well as in vivo, and in the eye in particular [10,11], we observed long-term restoration of RPE function and preservation of cone photoreceptors, lasting at least 4 mo after gene transfer, the latest time point studied. Furthermore, phenotypic classification of LCA cases in humans placed RPE65 deficiencies in the rod-cone dystrophies group [8,37,38]. This classification suggests that, to act on cone function, which is the main therapeutic target to restore high-acuity vision for the patient, the intervention window will be proportionally even longer in human patients than in Rpe65−/− mice. Our results thus support a potential clinical application of RPE65 gene transfer in humans.
For clinical trials it is also important to define accurately the vector dose that elicits a satisfactory therapeutic effect without triggering side effects. In the present study we show that a low virus dose restores a “near-normal” retinal sensitivity (Figure 2B) and completely blocks cone degeneration in the area expressing the therapeutic transgene, as well as in the vicinity of the treated area. Our study suggests that increasing the vector dose leads to an improvement of the ERG rescue (Figure 6A), but surgical limitations in mice resulted in the suggestion that increasing the vector dose leads to a higher level of expression in the transduced area rather to an expansion of the transduced area. The area of transgene expression might also be a critical parameter for effective ERG rescue: Above a certain threshold, retinal sensitivity is greatly enhanced (Figure 2C). Furthermore, the size of the transduced area is linearly correlated with the extent of cone survival area (Figure 3L), which exceeds the area of therapeutic transgene expression (Figure 3J). One explanation of this phenomenon could be heterogeneity in transduction efficiency within the injected area, the centre being highly transduced while the periphery expresses the transgene at a lower level (undetectable, but functionally relevant). Nevertheless, we never observed such heterogeneity after GFP or Rpe65 gene transfer, and it has, to our knowledge, never been reported after subretinal injection of a gene transfer vector. Another possible explanation is that lateral diffusion of 11-cis-retinal promotes cone survival also around the actually transduced area. Local concentration (and thus diffusion) of the chromophore should increase with the size of the transduced area, explaining the linear relationship between the sizes of respectively transduced area and cone survival area (Figure 3L). This would imply that, in Rpe65−/− mice, cone survival depends more on the availability of a certain amount of the chromophore than on a restoration of the RPE65 function in the adjacent RPE cell. This hypothesis is reinforced by the observation that exogenously supplied chromophore protects cones until at least P25 in RPE65-deficient mice . However, the exact mechanism underlying cone rescue following Rpe65 gene transfer is still unknown, and we cannot exclude an indirect effect resulting, for example, from the participation of the Müller cells in the regeneration of cone pigments.
The strong correlation between the size of the actually transduced area and the size of the cone survival area is a critical point with regard to the treatment of patients. It may help to determine precisely the retinal region to be treated to reach a therapeutic level of 11-cis-retinal at the site of the fovea. To rescue high-acuity vision in human patients, it might thus be sufficient to target the vicinity of the fovea with a limited dose of vector. Such treatment would be achieved most efficiently by subretinal injection, a procedure already used for conventional drug delivery , and proposed for gene therapy clinical trials (US clinical trials 0410–677 and 0510–740; available at: http://www.gemcris.od.nih.gov/). Furthermore, from a clinical perspective, the existence of a transitional area where cones are rescued but transgene not expressed in RPE cells, is of prime importance to increase the safety of the procedure and optimize the restoration of the biological function. This could indeed allow for a therapeutic effect at the fovea without direct treatment of this zone, a crucial advantage in terms of surgical risk.
Using a rodent model of LCA, we show the potential of lentiviral vectors to efficiently restore a deficient function by specific gene transfer to the RPE. A recent study published by Yanez-Munoz et al. (2006) demonstrates that an integration-deficient lentiviral vector is as efficient as an integration-proficient vector for delivery of Rpe65 in another model of LCA, the Rpe65rd12/rd12 mouse . These new in vivo data obtained with a vector minimizing mutagenesis risks by avoiding integration into the host genome reinforce our results that propose the lentiviral vector as an alternative for patient treatment. Moreover, it is important to note that stable and efficient retinal gene transfer by lentiviral vectors has already been documented in a nonhuman primate model , rendering this family of vectors very attractive for retinal applications targeting the retina. The next step toward a clinical application is to validate the use of classical lentiviral vectors, or of their integration-deficient version, using larger models such as RPE65-deficient dogs, and to analyze precisely the long-term efficiency of lentivirus-mediated RPE65 gene transfer in an eye similar in size to the human one. These studies should determine if the lentiviral vector could represent an alternative to rAAV for gene transfer into the RPE.
The GenBank (http://www.ncbi.nlm.nih.gov/) accession numbers of the genes discussed in this paper are: enhanced green fluorescent protein (egfp) (U55761); human retinal pigment epithelium-specific 61 kDa protein (RPE65), promoter (AH006060); Mus musculus guanine nucleotide binding protein, alpha transducing 1 (Gnat1), mRNA (NM_008140); M. musculus retinal pigment epithelium 65 (Rpe65), mRNA (NM_029987); and woodchuck post-transcriptional regulatory element (WPRE, nucleotides 1093–1684) (J04514).
The authors are particularly grateful to Dana Hornfeld, Muriel Jaquet, and Meriem Tekaya for constant technical support, to Dana Hornfeld for editing of the manuscript, to Drs Didier Trono and Patrick Salmon and the Lentiviral Production Unit (LVPU, Centre Médical Universitaire, Genève, Switzerland) for technical advice on lentiviral vector production, and to Professor Daniel Schorderet for fruitful scientific discussions.
APB, CK, AW, and YA designed the study. APB, CK, SVC, FLM, MWS, AW, and YA analyzed the data. APB, CK, FLM, AW, and YA contributed to writing the paper. WWH provided the R0.8 promoter used. JL created the Gnat1−/− transgenic mouse models used in the study.
- 1. Lamb TD, Pugh EN Jr. (2004) Dark adaptation and the retinoid cycle of vision. Prog Retin Eye Res 23: 307–380.
- 2. Redmond TM, Yu S, Lee E, Bok D, Hamasaki D, et al. (1998) Rpe65 is necessary for production of 11-cis-vitamin A in the retinal visual cycle. Nat Genet 20: 344–351.
- 3. Jin M, Li S, Moghrabi WN, Sun H, Travis GH (2005) Rpe65 is the retinoid isomerase in bovine retinal pigment epithelium. Cell 122: 449–459.
- 4. Moiseyev G, Chen Y, Takahashi Y, Wu BX, Ma JX (2005) RPE65 is the isomerohydrolase in the retinoid visual cycle. Proc Natl Acad Sci U S A 102: 12413–12418.
- 5. Redmond TM, Poliakov E, Yu S, Tsai JY, Lu Z, et al. (2005) Mutation of key residues of RPE65 abolishes its enzymatic role as isomerohydrolase in the visual cycle. Proc Natl Acad Sci U S A 102: 13658–13663.
- 6. Seeliger MW, Grimm C, Stahlberg F, Friedburg C, Jaissle G, et al. (2001) New views on RPE65 deficiency: The rod system is the source of vision in a mouse model of Leber congenital amaurosis. Nat Genet 29: 70–74.
- 7. Gu SM, Thompson DA, Srikumari CR, Lorenz B, Finckh U, et al. (1997) Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophy. Nat Genet 17: 194–197.
- 8. Hanein S, Perrault I, Gerber S, Tanguy G, Barbet F, et al. (2004) Leber congenital amaurosis: Comprehensive survey of the genetic heterogeneity, refinement of the clinical definition, and genotype-phenotype correlations as a strategy for molecular diagnosis. Hum Mutat 23: 306–317.
- 9. El Matri L, Ambresin A, Schorderet DF, Kawasaki A, Seeliger MW, et al. (2006) Phenotype of three consanguineous Tunisian families with early-onset retinal degeneration caused by an R91W homozygous mutation in the RPE65 gene. Graefes Arch Clin Exp Ophthalmol. Epub ahead of print.
- 10. Auricchio A, Kobinger G, Anand V, Hildinger M, O'Connor E, et al. (2001) Exchange of surface proteins impacts on viral vector cellular specificity and transduction characteristics: The retina as a model. Hum Mol Genet 10: 3075–3081.
- 11. Tschernutter M, Schlichtenbrede FC, Howe S, Balaggan KS, Munro PM, et al. (2005) Long-term preservation of retinal function in the RCS rat model of retinitis pigmentosa following lentivirus-mediated gene therapy. Gene Ther 12: 694–701.
- 12. Acland GM, Aguirre GD, Ray J, Zhang Q, Aleman TS, et al. (2001) Gene therapy restores vision in a canine model of childhood blindness. Nat Genet 28: 92–95.
- 13. Acland GM, Aguirre GD, Bennett J, Aleman TS, Cideciyan AV, et al. (2005) Long-term restoration of rod and cone vision by single dose rAAV-mediated gene transfer to the retina in a canine model of childhood blindness. Mol Ther 12: 1072–1082.
- 14. Narfstrom K, Katz ML, Bragadottir R, Seeliger M, Boulanger A, et al. (2003) Functional and structural recovery of the retina after gene therapy in the RPE65 null mutation dog. Invest Ophthalmol Vis Sci 44: 1663–1672.
- 15. Narfstrom K, Vaegan , Katz M, Bragadottir R, Rakoczy EP, et al. (2005) Assessment of structure and function over a 3-year period after gene transfer in RPE65−/− dogs. Doc Ophthalmol 111: 39–48.
- 16. Dejneka NS, Surace EM, Aleman TS, Cideciyan AV, Lyubarsky A, et al. (2004) In utero gene therapy rescues vision in a murine model of congenital blindness. Mol Ther 9: 182–188.
- 17. Lai CM, Yu MJ, Brankov M, Barnett NL, Zhou X, et al. (2004) Recombinant adeno-associated virus type 2-mediated gene delivery into the Rpe65−/− knockout mouse eye results in limited rescue. Genet Vaccines Ther 2: 3.
- 18. Rohrer B, Lohr HR, Humphries P, Redmond TM, Seeliger MW, et al. (2005) Cone opsin mislocalization in Rpe65−/− mice: A defect that can be corrected by 11-cis retinal. Invest Ophthalmol Vis Sci 46: 3876–3882.
- 19. Znoiko SL, Rohrer B, Lu K, Lohr HR, Crouch RK, et al. (2005) Downregulation of cone-specific gene expression and degeneration of cone photoreceptors in the Rpe65−/− mouse at early ages. Invest Ophthalmol Vis Sci 46: 1473–1479.
- 20. Chen Y, Moiseyev G, Takahashi Y, Ma JX (2006) RPE65 gene delivery restores isomerohydrolase activity and prevents early cone loss in Rpe65−/− mice. Invest Ophthalmol Vis Sci 47: 1177–1184.
- 21. Ali RR, Reichel MB, Thrasher AJ, Levinsky RJ, Kinnon C, et al. (1996) Gene transfer into the mouse retina mediated by an adeno-associated viral vector. Hum Mol Genet 5: 591–594.
- 22. Bennett J, Duan D, Engelhardt JF, Maguire AM (1997) Real-time, noninvasive in vivo assessment of adeno-associated virus-mediated retinal transduction. Invest Ophthalmol Vis Sci 38: 2857–2863.
- 23. Flannery JG, Zolotukhin S, Vaquero MI, LaVail MM, Muzyczka N, et al. (1997) Efficient photoreceptor-targeted gene expression in vivo by recombinant adeno-associated virus. Proc Natl Acad Sci U S A 94: 6916–6921.
- 24. Miyoshi H, Takahashi M, Gage FH, Verma IM (1997) Stable and efficient gene transfer into the retina using an HIV-based lentiviral vector. Proc Natl Acad Sci U S A 94: 10319–10323.
- 25. Bainbridge JW, Stephens C, Parsley K, Demaison C, Halfyard A, et al. (2001) In vivo gene transfer to the mouse eye using an HIV-based lentiviral vector; efficient long-term transduction of corneal endothelium and retinal pigment epithelium. Gene Ther 8: 1665–1668.
- 26. Duisit G, Conrath H, Saleun S, Folliot S, Provost N, et al. (2002) Five recombinant simian immunodeficiency virus pseudotypes lead to exclusive transduction of retinal pigmented epithelium in rat. Mol Ther 6: 446–454.
- 27. Kostic C, Chiodini F, Salmon P, Wiznerowicz M, Deglon N, et al. (2003) Activity analysis of housekeeping promoters using self-inactivating lentiviral vector delivery into the mouse retina. Gene Ther 10: 818–821.
- 28. Salmon P, Oberholzer J, Occhiodoro T, Morel P, Lou J, et al. (2000) Reversible immortalization of human primary cells by lentivector-mediated transfer of specific genes. Mol Ther 2: 404–414.
- 29. Zennou V, Petit C, Guetard D, Nerhbass U, Montagnier L, et al. (2000) HIV-1 genome nuclear import is mediated by a central DNA flap. Cell 101: 173–185.
- 30. Zufferey R, Donello JE, Trono D, Hope TJ (1999) Woodchuck hepatitis virus posttranscriptional regulatory element enhances expression of transgenes delivered by retroviral vectors. J Virol 73: 2886–2892.
- 31. Dinculescu A, Glushakova L, Min SH, Hauswirth WW (2005) Adeno-associated virus-vectored gene therapy for retinal disease. Hum Gene Ther 16: 649–663.
- 32. Woodruff ML, Wang Z, Chung HY, Redmond TM, Fain GL, et al. (2003) Spontaneous activity of opsin apoprotein is a cause of Leber congenital amaurosis. Nat Genet 35: 158–164.
- 33. Wenzel A, Oberhauser V, Pugh EN Jr, Lamb TD, Grimm C, et al. (2005) The retinal G protein-coupled receptor (RGR) enhances isomerohydrolase activity independent of light. J Biol Chem 280: 29874–29884.
- 34. Ekesten B, Gouras P, Salchow DJ (2001) Ultraviolet and middle wavelength sensitive cone responses in the electroretinogram (ERG) of normal and Rpe65−/− mice. Vision Res 41: 2425–2433.
- 35. Applebury ML, Antoch MP, Baxter LC, Chun LL, Falk JD, et al. (2000) The murine cone photoreceptor: A single cone type expresses both S and M opsins with retinal spatial patterning. Neuron 27: 513–523.
- 36. Calvert PD, Krasnoperova NV, Lyubarsky AL, Isayama T, Nicolo M, et al. (2000) Phototransduction in transgenic mice after targeted deletion of the rod transducin alpha-subunit. Proc Natl Acad Sci U S A 97: 13913–13918.
- 37. Perrault I, Rozet JM, Ghazi I, Leowski C, Bonnemaison M, et al. (1999) Different functional outcome of RetGC1 and RPE65 gene mutations in Leber congenital amaurosis. Am J Hum Genet 64: 1225–1228.
- 38. Lorenz B, Gyurus P, Preising M, Bremser D, Gu S, et al. (2000) Early-onset severe rod-cone dystrophy in young children with RPE65 mutations. Invest Ophthalmol Vis Sci 41: 2735–2742.
- 39. Haupert CL, McCuen BW 2nd, Jaffe GJ, Steuer ER, Cox TA, et al. (2001) Pars plana vitrectomy, subretinal injection of tissue plasminogen activator, and fluid-gas exchange for displacement of thick submacular hemorrhage in age-related macular degeneration. Am J Ophthalmol 131: 208–215.
- 40. Yanez-Munoz RJ, Balaggan KS, Macneil A, Howe SJ, Schmidt M, et al. (2006) Effective gene therapy with nonintegrating lentiviral vectors. Nat Med 12: 348–353.
- 41. Lotery AJ, Derksen TA, Russell SR, Mullins RF, Sauter S, et al. (2002) Gene transfer to the nonhuman primate retina with recombinant feline immunodeficiency virus vectors. Hum Gene Ther 13: 689–696.
- 42. van der Spuy J, Munro PM, Luthert PJ, Preising MN, Bek T, et al. (2005) Predominant rod photoreceptor degeneration in Leber congenital amaurosis. Mol Vis 11: 542–553.