In Vivo Potency Testing of Subretinal rAAV5.hCNGB1 Gene Therapy in the Cngb1 Knockout Mouse Model of Retinitis Pigmentosa

Animals

Cngb1^{− /−} mice ⁵ were used for testing rAAV5.hCNGB1 and wherever appropriate corresponding Cngb1 wild-type mice (Cngb1 ^+/+) as wild-type controls. The mice were bred on a genetically mixed background of the strains 129/SvJ and C57-Bl6/N, without the rd8 (Crb1 ¹¹ ) mutation. Mice received food and water ad libitum and were maintained in a 12 h light/dark cycle following local regulations and legal guidelines. Animal procedures were approved by the local authority (Regierung von Oberbayern) and were in accordance with the ARVO Statement for the Use of Animals in Ophthalmic and Vision Research.

Cloning and production of rAAV vectors

Standard cloning techniques were used for vector assembly. All sequence manipulations were verified by sequencing. The full-length transcript variant 1 of hCNGB1 (NM_001297.4; 3.75 kb) was PCR amplified ¹² and cloned between the inverted terminal repeats (ITRs) of serotype 2 originating from the pSub201 cis-plasmid (131 bp each) ¹³ together with a short hRHO promoter (hRHO194; 194 bp), which was PCR amplified from full-length hRHO promoter ¹⁴ (primer forward 5′-CAT AGC TAG CTT AAG CCT CTC CTC CCT GAC CTC AG-3′ and reverse 5′-TCA TGG ATC CAC TAG TGA TGA CTC TGG GTT CTG ACC-3′). In addition, a previously used short polyadenylation signal (221 bp) ¹⁰ acting as an effective termination and polyadenylation enhancer ¹⁵ was used. The plasmid backbone contained a pUC18 (Clontech Laboratories, Mountain View, CA) origin of replication, a kanamycin resistance gene (KanR), and randomized synthetic DNA fragments (resulting in the pGL2.0 backbone ¹⁴ ). The size of the designed vector construct was 4.66 kb from 5′ITR to 3′ITR and thus did not exceed the packaging capacity of rAAV vectors. AAV serotype 5 (AAV5) was used for packaging of this viral genome. The vector was produced by Sanofi Genzyme (Framingham, MA) and was manufactured using a producer cell line based on HeLaS3 cells (ATCC CCL-2.2) as described elsewhere ¹⁶ and afterward purified by two-column vector purification using an AVB Sepharose HP column (GE Healthcare) followed by anion exchange chromatography. ¹⁷ Virus particle concentration (∼1 × 10¹³ vector genomes (vg) mL⁻¹) was determined by TaqMan PCR assay. ¹⁸ Balance salt solution (BSS) +0.014% Tween-20 was used for formulation and vector dilution.

Subretinal injections

Mice were anesthetized by intraperitoneal injection of ketamine (100 mg/kg; Medistar GmbH, Ascheberg, Germany) and xylazine (10 mg/kg, Xylariem^®; Ecuphar GmbH, Greifswald, Germany) and pupils were dilated by tropicamide eye drops (Mydriaticum Stulln, Pharma Stulln GmbH, Stulln, Germany). One microliter of diluted viral particles at the indicated dose was slowly injected into the subretinal space using a 34-gauge beveled needle manually operated with a NanoFil syringe (World Precision Instruments, Sarasota, Fl). The process was monitored under a surgical microscope (OPMI 1 FR Pro, Zeiss, Oberkochen, Germany). An injection was considered successful if the formation of a bleb was visible indicating a temporal subretinal detachment of the retina. To confirm the observed result, fundus and retinal monitoring was performed by spectral-domain optical coherence tomography (SD-OCT). ¹⁹ After the procedure, all injected eyes were treated with dexamethasone and gentamicin ophthalmic ointment (Dexamytrex^®; Bausch and Lomb, Berlin, Germany) for prevention of infection and for eye moisturization.

Electroretinography

Full-field electroretinography (ERG) measurements were performed using the Celeris Fullfield ERG (Diagnosys LLC, Lowell, MA). ERGs were measured under scotopic (dark-adapted) conditions to assess rod-dominated activity. The animals were dark adapted overnight (>12 h) before the measurements. Before the ERG, animals were sedated, and pupils dilated as describe before. ²⁰ Eyes were prevented from drying using methylcellulose (Methocel^® 2%; OmniVision), which also provides the corneal contact to the electrode of the Celeris Fullfield ERG. Flashes of varying luminance were directed toward the eyes and the responses were recorded by the ERG device. For single-flash measurements, seven different stimuli from 0.01 to 10 cd s m⁻² were used (see hereunder) based on the International Society for Clinical Electrophysiology of Vision (ISCEV) standardized protocol for clinical dark-adapted ERG recordings. ²¹ All eyes received dexpanthenol eye and nose ointment (Bepanthen^®; Bayer) after measurements. Data were analyzed by the Espion software V6.59.9 (Diagnosys LLC).

Spectral-domain optical coherence tomography

SD-OCT measurements were performed using an adapted Spectralis™ HRA+OCT diagnostic imaging platform (Heidelberg Engineering, Dossenheim, Germany) in combination with optic lenses as described previously. ^19,20 After sedation and dilatation of pupils as described previously, mice were placed on a platform. The eye to be measured received one drop of methylcellulose (Methocel 2%; OmniVision) and a corneal contact lens before the measurement. OCT scans were obtained using a 12° circular scan mode. Data were analyzed by Heidelberg Eye explorer software V1.7.0.0 (Heidelberg Engineering). OCT scans of each mouse eye were performed directly after the subretinal injections to obtain information about the location of the injection site. The area of each eye that was within the subretinal bleb was used for OCT analysis. For comparison of treated and sham-injected eyes, only OCT scans that had the same distance from the optical nerve were used.

Visual water maze

A modified Morris water maze was previously implemented as a test for vision-guided behavior. ¹⁰ In brief, mice had to locate a visible floating platform (10 cm in diameter) in a circular swimming pool (120 cm in diameter, 70 cm high, white plastic; TSE systems, Bad Homburg, Germany). The water was made opaque by the addition of nontoxic white dye to increase visibility of the floating platform. No additional environmental cues were provided. The swimming route of each mouse was tracked using the VideoMot2 software by TSE systems. The experiment was performed on two consecutive days under dim light conditions of 0.32 cd m⁻² (red light; luminance was determined using the LS-100 luminance meter by Minolta, Marunouchi, Japan) to observe rod-mediated vision-guided behavior. Each time mice were predark adapted for at least 12 h. To test for mainly cone-mediated daylight vision, mice were then tested for another day under bright light conditions (82.8 cd m⁻²). Each testing day consisted of six trials and starting positions was changed pseudo-randomly on each of the trials. On the different test days, the platform was placed on a new position. One trial ended if the mouse climbed onto the platform or (if the mouse did not find the platform) after 120 s. In the latter case, the mouse was gently placed onto the platform. After each trial, the mouse was allowed to sit undisturbed (for 10 s) on the platform before being removed, placed under a heating lamp, and then transferred to its home cage. The experiment was performed and analyzed blinded to the animal's genotype.

Immunohistochemistry

Immunohistochemical staining was performed after termination of the in-life phase at 9 months postinjection and following previously described procedures. ^20,22,23 All animals used for OCT were analyzed. We used the following primary antibodies: rabbit anti-cone arrestin (1:300) ²⁴ ; sheep anti-cGMP (1:3,000; Dr. HWM Steinbusch, Maastricht University Medical Center ²⁵ ); Cy3-coupled anti-GFAP #C9205 (1:1,000) ²² ; rabbit anti-CNGB1 #HPA039159 (1:2,000; Sigma-Aldrich); and rabbit anti-CNGA1 (1:2,000), custom-made against the 19-mer Cys-RLTKVEKFLKPLIDTEFS-HN2, corresponding to 727–744 of human CNGA1 (NP_001136036.1). Laser scanning confocal micrographs were taken using a Leica SP8 confocal system (Leica, Wetzlar, Germany) equipped with the following lasers: 405, 448, 514, and 552 nm. Images were acquired as confocal z stacks using LAS X software V3.5.1.18803 (Leica) and deconvolved by the Huygens Essential software suite V18.04.0p8 64b (Scientific Volume Imaging B.V., the Netherlands) using a signal-to-noise ratio of 5. Maximum projection (merging of all z stacks) and background subtraction (value of 30) was performed using Fiji ImageJ V2.1.0/1.53c software.

Statistics

Statistical significance was evaluated by GraphPad Prism software (version 8 and 9). As statistical tests, either paired or unpaired two-way analysis of variance tests were performed followed by Sidak's post hoc test for multiple comparison. All values are given as mean ± standard error of the mean. n is the number of independent measurements and measured values of p ≤ 0.05 were considered significant. It is defined precisely as follows: *p ≤ 0.05, **p < 0.01, ***p < 0.001.

Novel short human rhodopsin promoter drives efficient and specific transgene expression in rod photoreceptors

CNGB1 is specifically expressed in rod photoreceptors, which are the primarily affected cell type in CNGB1-RP and, thus, the target cells for gene supplementation therapy. The human rhodopsin promoter (hRHO) is one of the most established promoters for achieving a rod-specific expression and is already used for clinical gene therapy programs. However, because of the size of the full-length hCNGB1 cDNA (>3.7 kb) and the additional space needed for minimally required regulatory (polyA) and viral (ITR) elements, incorporation of the previously characterized full-length (848 bp) hRHO promoter ²⁶ would have resulted in an rAAV genome, which exceeds the packaging limit of AAVs (∼4.7 kb). Therefore, we first aimed to design a shorter but still efficient and specific hRHO promoter version. In preliminary work, we truncated the full length hRHO promoter aiming to conserve binding sites for important transcription factors such as Crx or Nrl. ²⁷ A sufficiently short but still efficient and specific promoter version was a 194 bp sequence (hereafter termed hRHO194) corresponding to nucleotides 4816–5009 of NCBI Reference Sequence NG_009115.1 and comprising three known Crx and one Nrl binding site (Fig. 1A, for full sequence see Supplementary Fig. S1). We generated an AAV genome comprising a gene expression cassette for the full-length human CNGB1 cDNA under control of this hRHO194 promoter together with a short SV40 polyA sequence and AAV2-ITRs (Fig. 1A) and produced the AAV5 serotype vector rAAV5.hCNGB1, which results in solid expression of human CNGB1 (Fig. 1B).

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Figure 1.

rAAV5.hCNGB1 results in a dose-dependent, efficient, rod-specific transgene expression in the Cngb1 ^−/− retina. (A) Cartoon illustrating the gene expression cassette of rAAV5.hCNGB1. The novel human rhodopsin promoter is shown in higher detail and important transcription factor binding sites are marked. (B) Representative overview image of a confocal scan through a treated Cngb1^{− /−} mouse retina covering treated (within the subretinal bleb) and untreated (outside the subretinal bleb) parts. The treatment border is marked with a dashed line. (C–L) Representative confocal images showing expression of CNGB1 (red, the antibody detects mouse and human CNGB1) and CNGA1 protein (green) in retinal cross sections of wild type (C, D), treated (E–J), and sham-injected control Cngb1^{− /−} mouse retinae (K, L) at 10 months of age (9 months postinjection). Cngb1^{− /−} mice were injected at 4 weeks of age with rAAV5.hCNGB1 at low dose (10⁸ vg; E, F), mid-dose (10⁹ vg; G, H) or high dose (10¹⁰ vg; I, J). Dependent on the dose, varying amounts of hCNGB1 protein (red) were found in the OS, the IS, and the ONL of all treated Cngb1^{− /−} mice. Endogenous CNGA1 (green) expression was rescued in a dose-dependent manner and the protein localized to the OS of the treated area. Cell nuclei were stained with DAPI (blue). The edges of the ONL are marked with horizontal bars (C, E, G, I and K). GCL, ganglion cell layer; ONH, optic nerve head; OPL, outer plexiform layer. Scale bar in (B) marks 100 μm. Scale bar for (C–L) are shown in (K) and (L) and mark 25 μm. Cngb1, channel subunit beta 1; IS, inner segments; ONL, outer nuclear layer; OS, outer segments; vg, vector genomes. Color images are available online.

In a dose-ranging study, rAAV5.hCNGB1 was injected at three different doses (low dose, 10⁸; mid-dose, 10⁹; high dose, 10¹⁰ total vg in 1 μL volume, respectively) into the subretinal space of 4-week-old Cngb1^{− /−} mice. The contralateral eyes received 1 μL of vector diluent (BSS +0.014% Tween-20). After an in-life observation period of 9 months postinjection we dissected the retinae and performed immunohistochemical analysis to evaluate rAAV vector-derived human CNGB1 and endogenous mouse CNGA1 protein expression. Figure 1C–L illustrates typical immunosignals for CNGB1 (red) and CNGA1 (green) obtained in wild-type, sham-injected control and rAAV5.hCNGB1-treated Cngb1^{− /−} mouse retina. The anti-CNGB1 antibody used detects both, the vector-derived human and the endogenous mouse CNGB1 protein. The endogenous mouse CNGB1 and CNGA1 proteins localize exclusively to the rod OS (Fig. 1C, D). Treatment with rAAV5.hCNGB1 resulted in a dose-dependent expression of human CNGB1 (red) in the photoreceptor layer (Fig. 1E, G, I), whereas there was no visible CNGB1 signal in the sham control Cngb1^{− /−} retina (Fig. 1K). Of importance, as already shown for the species-matched gene supplementation therapy, ^9,10 expression of human CNGB1 rescued the expression of the endogenous mouse CNGA1 protein (Fig. 1F, H, J), which in Cngb1^{− /−} mice is degraded in the absence of the endogenous mouse CNGB1 protein. ^5,10 Of note, although the rescued endogenous murine CNGA1 protein always localized exclusively to the OS layer, a substantial amount of vector-encoded human CNGB1 protein was found in the inner segments and throughout the photoreceptor layer (Fig. 1E, G, I). The 10⁹ vg (mid-dose) dose of rAAV5.hCNGB1 also resulted in preservation of about eight rows of photoreceptors (Fig. 1G, H), whereas only one to two rows remained in the sham control Cngb1^{− /−} retina (Fig. 1K, L).

These findings confirmed efficient and long-lasting (throughout the 9-month observation period) rAAV5.hCNGB1-driven transgene expression and efficient reactivation/rescue of endogenous CNGA1 expression, and suggested the mid-dose (10⁹ vg) as the optimal dose.

rAAV5.hCNGB1 results in reactivation of rod CNG channels and gain of rod function

To confirm formation of functional chimeric (mouse alpha/human beta subunit) rod CNG channels, we utilized an indirect immunohistochemical readout based on the immunolocalization of the paraformaldehyde-fixed second messenger cGMP, which was shown to accumulate in Cngb1^{− /−} rods owing to a missing Ca²⁺-mediated negative feedback on the cGMP-producing rod guanylate cyclase. ^10,25 As the natural ligand of CNG channels, cGMP binds to and activates the channels in the dark resulting in a mixed Na⁺/Ca²⁺ inward current, which depolarizes the photoreceptor. In Cngb1^{− /−} rods, the missing Ca²⁺ influx prevents deactivation of cGMP production leading to accumulation inside the photoreceptor cell. To test how the rAAV5.hCNGB1 treatment affects the levels of the cGMP, we performed immunolabeling with an anti-cGMP antibody (Fig. 2). The anti-cGMP antibody showed a clearly detectable cGMP signal in rod inner segment and OS in the untreated Cngb1^{− /−} retina (the untreated part of a mid-dose-treated Cngb1^{− /−} retina is given in Fig. 2C), indicating intracellular accumulation of cGMP, which in the wild type is normally efficiently degraded and nondetectable using these staining conditions (Fig. 2A). In the treated part of a mid-dose-treated Cngb1^{− /−} retina, the cGMP signal was decreased (Fig. 2E), demonstrating a normalization of cGMP turnover, and thereby indirectly confirming a rAAV5.hCNGB1-dependent expression of a functional CNG channel in treated rods. Treatment at low dose (10⁸ vg) or high dose (10¹⁰ vg) did not show a similar effect on the cGMP levels (Supplementary Fig. S2).

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Figure 2.

Normalization of cGMP levels suggests formation of functional chimeric rod CNG channels after treatment with rAAV5.hCNGB1. Representative confocal images of retinal cross sections of a wild-type mouse retina (A, B) and the untreated (C, D) and treated parts (E, F) of a mid-dose–treated (10⁹ vg) Cngb1^{− /−} mouse at 10 months of age. The sections were immunolabeled with anti-cGMP (green) and anti-CNGB1 (red). An accumulation of cGMP was observed in the OS of the untreated part of the Cngb1^{− /−} retina, whereas cGMP accumulation was reduced in the treated part. Cell nuclei in (B, D, and F) were stained with DAPI (blue). Scale bar marks 25 μm. cGMP, cyclic guanosine monophosphate; CNG channel, cyclic nucleotide-gated channel. Color images are available online.

To analyze the rod-dependent retinal function in more detail, the study included multiple ERG measurements during the in-life phase. ERG was performed on dark-adapted animals using a series of light stimuli at increasing luminance, including the ISCEV rod-specific standard luminance of 0.01 cd s m⁻². Although signals obtained in Cngb1^{− /−} wild-type mice showed clear positive deflections (b wave) of the ERG amplitude (Supplementary Fig. S2A–C, gray lines), signals obtained in untreated (sham-injected) Cngb1^{− /−} mice were strongly reduced throughout the range of light stimuli (Fig. 3A and Supplementary Fig. S3A, black lines). At the rod-specific luminance (0.01 cd s m⁻²), a response could not be detected. However, mid-dose treatment of rAAV5.hCNGB1 (Fig. 3A, B and Supplementary Fig. S3A, B, middle graphs, magenta lines; Supplementary Fig. S4C, D) demonstrated a clear increase of b-wave amplitudes compared with the sham-injected contralateral eye especially at rod-specific light stimuli ranges of 0.01 and 0.03 cd s m⁻². In addition, a slight recovery of a-wave signals could be seen with the mid-dose treatment starting from 0.1 cd s m⁻² upward. Furthermore, ERG measurements of low-dose-treated Cngb1^{− /−} mice (Fig. 3A, B and Supplementary Fig. S3A, B, left graphs, green lines; Supplementary Fig. S4A, B) also showed increased responses to different light stimuli, whereas high-dose treatment (Fig. 3A, B and Supplementary Fig. S3A, B, right graphs, orange lines; Supplementary Fig. S4E, F) failed to show obvious improvements. Despite a general decline of amplitudes, 9 months follow-up data (Fig. 3C and Supplementary Fig. S3C, middle graph, magenta line; Supplementary Fig. S4C, D) showed a sustained functional benefit with twofold higher b-wave amplitudes for mid-dose treatment compared with the control, confirming a long-term beneficial effect of rAAV5.hCNGB1 treatment on rod function until an advanced stage of the disease. Although less prominent, a long-term beneficial effect was also seen in the low-dose treatment group (Fig. 3C and Supplementary Fig. S3C, left graph, green line; Supplementary Fig. S4A, B), whereas no differences in b-wave amplitudes were seen between the high-dose treatment and the control group (Fig. 3C and Supplementary Fig. S3C, right graph, orange line; Supplementary Fig. S4E, F). Thus, assessment of rod-driven retinal function with ERG confirmed long-term restoration of photoreceptor function after subretinal gene therapy with rAAV5.hCNGB1 and established the mid-dose (10⁹ vg) as optimal dose.

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Figure 3.

rAAV5.hCNGB1 leads to a dose-dependent gain of rod-driven ERG amplitudes in treated Cngb1^{− /−} mice. (A) Overlays of representative ERG signals of 3-month-old–treated Cngb1^{− /−} mice injected with different doses (low dose 10⁸ vg; mid-dose 10⁹ vg; high dose 10¹⁰ vg) of rAAV5.hCNGB1 at 4 weeks. Vertical dotted lines mark the time point of light stimulation. Respective sham-injected contralateral eyes served as controls showing almost no (rod-mediated) response at low light intensities (0.01 and 0.03 cd s m⁻²). Mid-dose treatment (magenta lines) showed highest gain in photoreceptor function compared with the respective sham-injected control (black lines). In this group the b-wave amplitude (positive deflection) obtained under low light intensities was clearly higher in the treated than in the sham-injected control eye. A treatment effect was also evident at higher luminances. In contrast, only a small increase was seen in ERG signals after treatment at low dose (green lines) and no obvious differences observed after high-dose (orange line) treatment compared with sham-injected control eyes. (B, C) Quantification of b-wave amplitudes of treated and sham injected Cngb1^{− /−} eyes at 3 and 9 months of age shows a dose-dependent beneficial effect on retinal function. Mid-dose and to a lesser extent low-dose treatment resulted in significantly increased b-wave amplitudes, whereas treatment at high dose did not cause any difference on the ERG b-wave. Although overall amplitudes declined over time, a significant gain of ERG function was seen at 9 months of age suggesting a long-term benefit of rAAV5.hCNGB1 treatment. For 3 months pn: low dose n = 7, mid-dose n = 6, high dose n = 6; for 9 months pn: low dose n = 7, mid-dose n = 7, high dose n = 10. Values are given as mean ± SEM (unpaired two-way ANOVA with Sidak's post hoc test; **p ≤ 0.01; ***p ≤ 0.001; ns, not significant). ANOVA, analysis of variance; ERG, electroretinography; pn, postnatal; SEM, standard error of the mean. Color images are available online.

rAAV5.hCNGB1 treatment leads to improved vision-guided behavior

Previous studies with species-matched gene supplementation therapy ^9,10 provided evidence for treatment-dependent improvements of vision. To confirm that the chimeric mouse/human rod CNG channel can also have beneficial effects on vision, we assessed vision-guided behavior in treated Cngb1^{− /−} mice. In particular, we observed spatial navigation in a visual water maze task at 9 months scoring the ability and measuring the latency of mid-dose–treated and untreated Cngb1^{− /−} mice and wild-type control mice to locate a visible swimming platform (Fig. 4). Initial testing was performed for two consecutive days under light conditions that require rod function (dark; see details in Materials and Methods section). Representative swimming routes of the three test groups under these dark conditions are given in Fig. 4A. When placed into the water-filled tank, wild-type mice instantly localized and navigated to the visible floating platform and showed a 100% success rate on the second testing day (Fig. 4B, C and Supplementary Fig. S5, gray line). In contrast, untreated Cngb1^{− /−} mice often struggled to locate the visible platform and showed overall six times longer latencies than wild-type mice (Fig. 4B, C and Supplementary Fig. S5, black line). Vision-guided behavior was not assessed in the high-dose treated group given the lack of improvement in the ERG. Low-dose–treated Cngb1^{− /−} mice did not show significant improvement in navigating in the dark (Supplementary Fig. S5, green line). However, confirming the rAAV5.hCNGB1-mediated gain in vision, mid-dose–treated Cngb1^{− /−} mice performed with higher fidelity (close to 90% on day 2) and reached the platform after an averaged latency of ∼45 s on day 1 and further improved by day 2 to a mean latency time of ∼30 s (Fig, 4B, C and Supplementary Fig. S5, magenta line). Thus, mid-dose rAAV5.hCNGB1-treated Cngb1^{− /−} mice navigated significantly faster in this task than the untreated control group. On the final testing day, the mice were tested under bright light conditions to confirm their principal ability to solve the task and exclude confounding factors, such as surgery-related collateral retinal damage. As given in Fig. 4B, C, mice from all test groups were able to find the platform with a latency of <20 s, proving that cone-mediated visual function was still sufficiently preserved to navigate under bright light conditions. Taken together, rAAV5.hCNGB1-treated Cngb1^{− /−} mice showed a gain in spatial navigation at least until 9 months of age supporting the view that treated mice were able to properly process recovered photoreceptor function.

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Figure 4.

rAAV5.hCNGB1 results in improved spatial navigation of treated Cngb1^−/− mice under dim light conditions. (A) Representative swimming tracks of 9-month-old wild-type (n = 4), untreated (n = 9) and mid-dose–treated (treated at 4 weeks with 10⁹ vg of rAAV5.hCNGB1; n = 5) Cngb1^{− /−} mice in a visual water maze task under dim light conditions. (B) Quantification of latency time until a visible swimming platform was reached during two dim light and one bright light testing days. In contrast to untreated Cngb1^{− /−} mice, those treated with rAAV5.hCNGB1 could improve their performance from days 1 to 2 and needed a shorter time to find the platform on the second test day. (C) Quantification of the success score to locate the swimming visible platform within 1 min (percentage of total runs). Untreated Cngb1^{− /−} mice had a chance success rate of ∼50% on both dim light test days. Again, treated Cngb1^{− /−} mice could improve their performance on reaching a success rate of >80% on day 2. (B, C) Mice from all test groups performed well on the third test day under bright light confirming sufficient remaining cone-mediated vision functionality in the untreated Cngb1^{− /−} mice. Values are given as mean ± SEM (unpaired two-way ANOVA with Sidak's post hoc test; *p ≤ 0.05). Color images are available online.

rAAV5.hCNGB1 treatment preserves photoreceptor layer thickness in treated Cngb1^−/− mice

CNGB1-RP is characterized by degeneration and loss of photoreceptors, ^2,3,9 which is also observed in the animal models and can be monitored over time using SD-OCT. ⁹ In Cngb1^{− /−} mice shortening of rod OS is already evident shortly after eye opening at postnatal day 15. ⁵ With progression of rod photoreceptor degeneration, the thickness of outer nuclear layer (ONL) continuously decreases, resulting in an almost absent ONL at the age of 10 months. ⁹ To assess the effect of rAAV5.hCNGB1 treatment on the progression of photoreceptor degeneration in Cngb1^{− /−} mice, we performed in vivo SD-OCT measurements at 3, 5, and 9 months of age during the in-life phase of the dose-ranging study. A representative SD-OCT scan through the retina of a 9-month-old (8 months postinjection) mid-dose–treated Cngb1^{− /−} mouse spanning the treated (previous subretinal bleb area) and untreated part of the retina is given in Fig. 5A. The treatment resulted in a clear preservation of both ONL and photoreceptor OS layer thickness (Fig. 5B), whereas both layers were severely thinned and hardly discernable in the untreated area (Fig. 5C). Nonphotoreceptor retinal structures, such as the inner nuclear layer (INL), ganglion cell layer (GCL) or the retinal pigment epithelium were not visibly affected and treatment with rAAV5.hCNGB1 did not cause any obvious morphological alterations in these structures. Quantification of SD-OCT scans from sham-injected contralateral Cngb1^{− /−} mice eyes (dashed lines in Fig. 5D–F) confirmed a steady decrease of photoreceptor layer thickness over time, whereas for the wild-type control it remained at ∼110 μm (gray lines in Fig. 5D–F). Although rAAV5.hCNGB1 treatment could not arrest the progression of photoreceptor layer thinning, it resulted in a clear deceleration as evident from the significantly preserved photoreceptor layer thicknesses in treated groups (Fig. 5D–F and Supplementary Fig. S6). Morphological preservation was best at mid-dose (10⁹ vg), but also observed in the low-dose (10⁸ vg) group. Despite the lack of functional improvements in the ERG measurements, a small but significant preservation effect could still be seen by SD-OCT in the high-dose (10¹⁰ vg) group. Thus, in addition to the functional gain, gene supplementation therapy with rAAV5.hCNGB1 also led to a long-lasting, dose-dependent preservation of photoreceptor morphology in Cngb1^{− /−} mice.

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Figure 5.

rAAV5.hCNGB1 gene therapy preserves photoreceptor layer thickness. (A–C) Representative SD-OCT images of a mid-dose–treated Cngb1^{− /−} retina (10⁹ vg; rAAV5.hCNGB1) at 9 months of age demonstrating preservation of photoreceptor layer thickness in the treated (B) compared with the untreated (C) area. In the untreated area only a single thin ONL remained. In contrast, the treated part shows characteristic multiple laminae for OS and ONL separated by a darker band representing the IS. (D–F) Quantification of photoreceptor layer thickness (μm) in 3-, 5-, and 9-month-old Cngb1^{− /−} eyes after treatment with 10⁸ vg (D; low dose), 10⁹ vg (E; mid-dose) and 10¹⁰ vg of rAAV5.hCNGB1 (F; high dose) at 4 weeks compared with their respective sham-injected contralateral eyes and wild type. Significant preservation of photoreceptors structure was seen in all dose groups, the treatment effect was strongest at mid-dose. Wild type n = 3; low dose n = 7; mid-dose n = 7; high dose n = 9, owing to technical reasons only n = 8 for 3 months. Values are given as mean ± SEM (two-way ANOVA paired with Sidak's post hoc test; **p ≤ 0.01, ***p ≤ 0.001). SD-OCT, spectral-domain optical coherence tomography. Color images are available online.

rAAV5.hCNGB1 treatment prolongs cone photoreceptor survival and reduces Müller cell gliosis in treated Cngb1^−/− mice

Secondary to rods, cone photoreceptors also degenerate despite not being directly affected by the Cngb1 mutation. Given the importance of cone photoreceptor-mediated daylight vision, the long-term aim of gene supplementation therapy is to prevent the secondary loss of cones in CNGB1-RP patients. In Cngb1^{− /−} mice, cone degeneration usually starts at ∼6 months of age. ^5,9 As cones make up only ∼3% of all photoreceptors in the mouse retina, ^28,29 OCT measurement cannot visualize a potential rescue effect on cone structure and/or cell number. Therefore, we analyzed the effect of the rAAV5.hCNGB1 treatment by immunohistochemistry using the specific marker cone arrestin, which in the wild type labels the entire cone cell including, OS and inner segment, cell body, axon, and synapse (Fig. 6A, A′). In the untreated area of a mid-dose–treated (10⁹ vg; rAAV5.hCNGB1) Cngb1^{− /−} mouse retina the cone arrestin signal was still present; however, the labeled remaining cone structures did not show the characteristic normal cone photoreceptor morphology (Fig. 6B, B′). OS and inner segment were completely degenerated and merely the spherical cell bodies and remnants of synapses were still visible. In contrast, the treated part of the same retina showed intact cones with the characteristic wild-type–like morphology (Fig. 6C, C′). Cone cell body and synapse was still properly positioned and the radial cone cells spanned the entire remaining ONL. Apparently, the cone photoreceptor axons seemed to have adjusted their length to fit into the thinner ONL (Fig. 6C, C′).

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Figure 6.

rAAV5.hCNGB1 treatment prevents secondary degeneration of cone photoreceptors and reduces Müller cell gliosis. (A–C and 1.5 × magnifications in A′–C′) Representative confocal images from retinal cross sections of wild type (A, A′), untreated part (B, B′), and treated part (C, C′) of a mid-dose–treated (10⁹ vg, rAAV5.hCNGB1) Cngb1^−/− retina at 10 months of age (9 months after treatment). Although the cone arrestin marker (red) stained only spherical (presumably) cone cell bodies and cell residues in the untreated part, it revealed a preserved wild-type–like morphology of cones with all characteristic compartments including OS and IS an axon transecting the entire (still remaining) ONL and a cone pedicle at the OPL in the treated part. (D–F) Representative confocal images from retinal cross sections of wild type (D), untreated part (E), and treated part (F) of a mid-dose–treated (10⁹ vg, rAAV5.hCNGB1) Cngb1^−/− retina at 10 months of age immunostained for the Müller glia marker GFAP and for CNGB1 (the antibody detects mouse and human CNGB1). Mid-dose treatment caused a decrease of GFAP expression (F), which is strongly upregulated in the untreated part (E) owing to retinal stress induced Müller cell gliosis. Scale bars mark 50 μm. GFAP, glial fibrillary acidic protein; IPL, inner plexiform layer. Color images are available online.

The Müller glia cells are another cell type of the Cngb1^{− /−} retina, which shows changes secondary to the photoreceptor degeneration. In particular, it was shown that in response to rod degeneration Müller glia cells upregulate glial fibrillary acidic protein (GFAP) expression. ⁵ Reduction of GFAP levels was already demonstrated as a result of murine Cngb1 gene supplementation. ¹⁰ To prove whether supplementation of human CNGB1 can also reduce GFAP levels, cross-sections of mid-dose–treated (10⁹ vg) Cngb1^{− /−} retinas were immunolabeled for GFAP (Fig. 6D–F). In the wild type, GFAP only labels astrocytes and Müller cell end feet at the inner limiting membrane underneath the GCL (Fig. 6D). In contrast, strongly GFAP-immunopositive fibers can be observed in the untreated part of a treated Cngb1^{− /−} retina (Fig. 6E) indicative of a reactive Müller cell gliosis. ³⁰ Upon mid-dose treatment, a strong reduction of Müller cell gliosis was observed in the treated part of the same Cngb1^{− /−} retina (Fig. 6F). In contrast, low- and high-dose treatment did not reduce Müller cell gliosis (Supplementary Fig. S7). In summary, these data demonstrate that treatment with rAAV5.hCNGB1 preserves cone morphology, providing the basis for maintained daylight vision and reduces Müller cell gliosis suggesting a positive effect of the treatment on degeneration-induced retinal stress.