Preclinical assessment of intravitreal ramucirumab: in vitro and in vivo safety profile

Abstract

Background

Anti-angiogenic drugs remain the mainstay therapy for several vascular retinal pathologies. The repurposing of approved anti-angiogenic drugs for use in ophthalmology can increase therapeutic options and reduce costs. The purpose of this study was to investigate the ocular safety profile of intravitreal (IVT) ramucirumab, an approved anti-vascular endothelial growth factor molecule for systemic treatment, using cell culture and animal models.

Methods

The cytotoxicity of ramucirumab at different concentrations was evaluated in human retinal pigment epithelial cells (ARPE-19) using the MTT assay. In addition, 250 or 500 µg of ramucirumab or vehicle was injected in the eye of 16 chinchilla rabbits. The eyes were evaluated by ophthalmoscopy, electroretinography, spectral-domain optical coherence tomography (SD-OCT) and by light and transmission electron microscopy.

Results

Electroretinography or SD-OCT did not detect functional or morphological alterations at 24 h or one week after injection. Light and transmission electron microscopy confirmed the absence of major signs of toxicity, although we found a statistically significant reduction in ganglion cell number between the controls and the eyes that received 500 µg of ramucirumab after 7 days. Compared to lower concentrations, 500 µg of ramucirumab caused reduction in cell viability and changes in morphology in ARPE-19 cells. Compared to the baseline, ocular and serum osmolarity showed no difference after IVT injection at all timepoints.

Conclusion

In conclusion, IVT injection of ramucirumab in rabbits is safe and does not cause functional damage to the retina. At the lower dose tested in vivo (250 µg), the morphology and ultrastructural anatomy were normal at 24 h and 1 week after the injection. However, the 500 µg dose can cause a decrease in ganglion cell number seven days after the injection.

Background

Abnormal angiogenesis is the core pathogenesis of several ocular blindness diseases such as diabetic retinopathy and age-related macular degeneration (AMD) [1]. The interaction between pro-angiogenic factors and their receptors is tightly regulated with several positive and negative feedback circuits [2]. Vascular endothelial growth factor (VEGF) and its receptors (VEGFRs) constitute the main force driving abnormal and persistent angiogenesis [3].

Vascular endothelial growth factor receptor 2 (VEGFR-2) is one of the main regulators of angiogenesis, during which the receptor is overexpressed on the surface of endothelial cells. The main pro-angiogenic factor is VEGFA, but VEGFC and VEGFD can also activate the VEGFR signaling pathway [4, 5]. The mainstay treatment for ocular neovascular diseases consists in blocking different pro-angiogenic ligands. However, since different ligands can act on the same receptor, the direct inhibition of VEGFR-2 over the inhibition of its ligands may be a more suitable therapeutic target [2].

Ramucirumab (Fig. 1a) is a recombinant, human monoclonal antibody, produced in a transfected NS0 mouse myeloma cell line, that binds specifically to VEGFR-2 and blocks VEGF-A, VEGF-C, and VEGF-D binding [6]. The fragment crystallizable (Fc) portion of ramucirumab is not required for its action [7]. Ramucirumab binds to VEGFR-2 with high affinity (Kd = 50 pM), similar to the dissociation coefficient of bevacizumab (Kd = 58 pM) and ranibizumab (Kd = 46 pM). The molecular weight is 146 kDa, which is similar to bevacizumab (149 kDa) and heavier than ranibizumab (48 kDa) and aflibercept (115 kDa) [8].

Fig. 1

Schematic mechanism of ramucirumab. a Ramucirumab active substance. b Target molecules of different anti-VEGF drugs

Preclinical cellular and animal models have demonstrated that the result of ramucirumab binding to its target is the inhibition of VEGF-induced VEGFR-2 activation and inhibition of VEGF-stimulated cell migration and proliferation [6, 9].

This drug is provided as an intravenous solution (Cyramza^®, Eli Lilly, Indianapolis, USA) in two formulations, 100 mg/10 mL and 500 mg/50 mL and was approved by the US Food and Drug Administration in 2014 to treat advanced gastric and gastroesophageal cancer.

Since ramucirumab inhibits angiogenesis by specifically targeting VEGFR-2 (Fig. 1b), its repurposing to treat vascular eye diseases through intravitreal (IVT) injections is tempting and finds a parallel in the use of bevacizumab to treat neovascular AMD nearly 15 years ago. Although the systemic use of ramucirumab has not shown higher toxicity than other anti-angiogenic agents, to our knowledge, the safety of intraocular injection of ramucirumab has not yet been tested. The purpose of this study was to investigate for the first time the intraocular safety of ramucirumab using human retinal pigment epithelial (RPE) cells and IVT injection in an animal model.

Methods

This was an experimental study and all the procedures were performed following the guidelines of the Association of Research in Vision and Ophthalmology (ARVO). Approval was obtained from Institutional Animal Care and Use Committee (IACUC) prior to the initiation of the study, under the number 6610041117.

Cell viability assay

Human RPE cells (ARPE-19; ATCC CRL-2302) were used to assess the in vitro toxicity of ramucirumab using the MTT (thiazolyl blue tetrazolium bromide) colorimetric assay as previously described [10]. Briefly, the cells were grown in DMEM/F12 containing 10 U/mL penicillin and 10 µg/mL streptomycin and supplemented with 10% fetal bovine serum (Gibco/ Thermo Fisher Scientific Inc.—Waltham, MA, USA). Cells were seeded (5 × 10³ cells per well) and incubated for 24 h in a humidified incubator containing 5% CO₂ at 37 °C.

Cells were treated with increasing concentrations of ramucirumab (from 10 to 500 μg/well) for 2 h and dimethyl sulfoxide (DMSO) was used as a positive control. Absorbance at 570 nm was measured and the value obtained with culture medium was used as blank. The experiments were performed in triplicate and repeated three times.

In vivo experiment design

IVT injections of ramucirumab were performed in 16 male chinchilla rabbits weighing from 1.8 to 2.5 kg. The animals were equally divided into two groups (A and B). The right eye of each animal received 0.05 mL of IVT ramucirumab, corresponding to 500 µg of the drug (group A), or 0.025 mL, corresponding to 250 µg of the drug (group B). The left eye (control group) received 0.05 mL or 0.025 mL of balanced saline solution (BSS) (300 mOsm). Fundus photography, electroretinography (ERG), spectral-domain optical coherence tomography (SD-OCT) and serum/aqueous humor analysis were performed at baseline and 24 h (eight rabbits) or seven days (eight rabbits) after the injection. After the follow-up examination the animals were euthanized, and the eyes were collected for histological preparation.

Functional analysis by electroretinography

ERG was performed at baseline and 24 h or seven days after the intravitreal injection. After complete pupil dilation with tropicamide 1% and cornea anesthesia with proparacaine eye drops, unipolar electrodes (ERG jet^®, Universe SA, La Chaux-de-Fons, Switzerland) were properly placed on each cornea together with methylcellulose 2% (Ophthalmos, São Paulo, Brazil).

After 30 min of dark adaptation, the animals were assessed by the RETI-port gamma plus^® (Roland Consult, Brandenburg an der Havel, Germany) according to four types of response: rod response, combined response, cone response and flicker. A 50% decrease in the post-injection response compared to baseline was considered significant. Statistical analyses were performed using Stata/SE Statistical Software, version 14.0, 2015 (StataCorp, College Station, TX, USA). Data are presented as median (range) and the Wilcoxon signed-rank test was used to compare baseline and follow-up measurements. p values ≤ 0.05 were considered statistically significant.

Fundus photography and spectral-domain optical coherence tomography

We performed anterior segment biomicroscopy, fundus photography (Zeiss Visucam 524^®, Carl Zeiss, Jena, Germany) and SD-OCT (Spectralis^®, Heidelberg Engineering, Heidelberg, Germany) at baseline and 24 h or seven days after intravitreal injection.

Serum and aqueous humor osmolarity

Peripheral blood and aqueous humor tap from both eyes were collected using an insulin syringe with a 27-gauge needle. After collection, the samples were frozen at −80 °C and later assessed using an osmometer. The Wilcoxon signed-rank test was used to compare baseline and follow-up measurements of blood and aqueous humor osmolarity.

Light microscopy and transmission electron microscopy

Eyes were processed for light microscopy (LM) and transmission electron microscopy (TEM) as previously described [11]. Briefly, for LM, eyes were fixed in 4% paraformaldehyde at 4 °C. Following embedding in paraffin, the eyes were sectioned, stained with hematoxylin and eosin (H&E) and imaged using an Axioskop 2-Mot Plus Zeiss microscope (Carl Zeiss, Jena, Germany). The ganglion cells were manually quantified using a 20 × objective in three semi-serial sections of retina for each eye. Values are expressed as the mean ± SEM of the number of cells per mm².

For ultrastructural analysis, eyes were fixed in 4% paraformaldehyde and 0.5% glutaraldehyde in 0.1% sodium cacodylate buffer (pH 7.4) for 24 h at 4 °C. After washing and dehydration in methanol, samples were embedded in LR Gold (Sigma-Aldrich, Steinheim, Germany). Imaging was performed using a ZEISS EM900 electron microscope (Carl Zeiss, Jena, Germany).

Results

Cell viability assay

To evaluate the cytotoxic effects of ramucirumab, we initially performed an in vitro cell viability assays using ARPE-19 cells treated with 10, 25, 50, 100, 200, 250 and 500 µg/well of drug for 2 h. Cell viability was assessed by the MTT colorimetric assay and the results indicated that concentrations up to 250 µg/well did not affect the cells. However, at 500 µg/well, cell viability was reduced, and the cells had slight changes in morphology (Fig. 2).

Fig. 2

Effects of ramucirumab on ARPE-19 cells. Cells were incubated in the presence of ramucirumab at 10, 25, 50, 100, 200, 250 and 500 µg/well for 2 h. The MTT assay was performed to evaluate cell viability. The experiments were performed in triplicate and repeated three times

Functional analysis by electroretinography

There was no difference in retinal response between eyes injected with ramucirumab and eyes injected with BSS in all protocols used and at all timepoints of the study (Fig. 3). Table 1 specifies the results of each ERG protocol used for all groups.

Fig. 3

Full-field ERG assessment. a ERG responses prior to drug treatment. b ERG responses after drug treatment. No alteration was seen in ERG before and after treatment (OD injected with ramucirumab; OS injected with BSS). c Electrode placement setup. d RETI-port gamma plus^® (Roland Consult, Germany)

Table 1 Comparative analysis of full-field electroretinography (ERG) responses

Fundus photography and spectral-domain optical coherence tomography

In all eyes studied, fundus images did not show any significant alterations, and SD-OCT displayed normal anatomical architecture of all retinal layers at all assessed times (Fig. 4).

Fig. 4

Morphological assessment after intravitreal injection of ramucirumab. a Fundus color imaging after intravitreal injections. b OCT prior to intravitreal injections. c OCT after intravitreal injections. All images correspond to the 500 µg group

Serum and aqueous humor osmolarity

Table 2 shows osmolarity values (presented as median) from serum and aqueous humor collected before and after IVT injection of ramucirumab or BSS. Compared to the baseline of each eye, there was no difference in the osmolarity of serum and aqueous humor. Due to technical issues the serum samples from day 7 of follow-up from lower dose group (250 µg) were not evaluated.

Table 2 Serum and aqueous humor osmolarity

Light microscopy and transmission electron microscopy

The morphology assessed by H&E demonstrated similar findings between both doses of ramucirumab and the controls. There was no evidence of recruitment of inflammatory cells, and the retinal layers were preserved. Some vacuolization in the superficial layers was present after 24 h and showed less intensity after 7 days in all groups, including the controls. The retinal thickness measured displayed no difference between eyes injected with ramucirumab and BSS (Fig. 5). Furthermore, we determined the number of ganglion cells in each eye. Ramucirumab at 500 µg caused a significant loss in ganglion cells compared with BSS (59.0 ± 5.0 vs 30.0 ± 2.5, p < 0.01 in the t-test [mean ± SEM. of the number of cells/mm²; n = 4/group]) (Fig. 6).

Fig. 5

Retinal findings by histology with hematoxylin and eosin staining seven days after intravitreal injection of ramucirumab. a control eye. b–d IVT injection of 250 µg ramucirumab. e–h IVT injection of 500 µg ramucirumab. Ganglion cells: focal areas of vacuolization (*). Inner plexiform and nuclear layers showing focal vacuolization. Outer plexiform layer: intact. Outer nuclear layer: artifactual findings (red arrows)

Fig. 6

Quantification of ganglion cells in hematoxylin and eosin stained eyes. Data represent mean ± S.E.M. of the number of cells/2 mm² (n = 4/group). **p < 0.01 vs. control (t-test)

TEM confirmed the LM findings. At 24 h and seven days, retinas showed a normal appearance and integrity of the nerve fiber and inner and outer nuclear layers, without signs of apoptosis, while a small number of vacuoles were seen in the inner and outer plexiform layers (Fig. 7).

Fig. 7

Ultrastructural analysis of rabbit retinas treated with 500 µg ramucirumab at 24 h and seven days. a–d Control. e–h 24 h-treated retina. i–l 7 day-treated retina. All experimental conditions showed retinal layers with normal appearance, without signs of apoptosis. GCL ganglion cell layer, INL inner nuclear layer, ONL outer nuclear layer. In the inner photoreceptor segment (IS), notice the presence of mitochondria (Mi), while outer segment (OS) is characterized by the presence of disc membranes (*)

Discussion

Inhibition of VEGFR-2 by ramucirumab in animal models and human trials has demonstrated significant antitumor activity in a variety of malignancies, both as monotherapy and in combination with other drugs [8, 12, 13]. However, no previous study has evaluated the safety or efficacy of intravitreal use of ramucirumab in the treatment of VEGF-driven diseases.

To study the safety of intraocular ramucirumab, we initially conducted a cell viability test in ARPE-19. We found that ramucirumab did not cause a significant decrease in the viability of ARPE-19 cells when exposed to 250 µg/well. But a concentration of 500 µg/well caused changes in cell morphology and reduced cell viability, compared to the lower concentrations. Figure 2 demonstrates a decrease in cell viability without statistical significance.

Luthra et al. [14] studied the cell damage response to two different anti-VEGF drugs, bevacizumab and ranibizumab, and found that even with 5 times the clinically relevant concentration of these drugs, there were no differences in cell viability in ARPE-19 cells and rat neurosensory retina cells. However, Malik et al. [15] showed that mitochondrial toxicity in ARPE-19 cells could be caused by bevacizumab and ziv-aflibercept (intravenous solutions). Using a similar approach, Dias et al. [11] did not find any cytotoxic effect in human RPE cultured cells exposed to ziv-aflibercept. Regarding aflibercept, different authors reported no changes in ARPE-19 cell viability after different concentrations and times of aflibercept exposure [16, 17]. These findings are consistent with our results, which also demonstrated no decrease in cell viability compared with controls, when ramucirumab concentration was below 500 µg/well.

For functional analysis and to minimize some of the known inter-eye variability of ERG assessment, we used an instrument capable of assessing both eyes at the same time [18, 19]. In our analysis, there was no difference in the ERG when comparing baseline and follow-up of each eye (Table 1), which means the procedure did not cause any retinal functional impairments.

The osmolarity study was essential because the ramucirumab formulation is for intravenous use. Intravitreal injections of strong salt solutions may result in retinal detachment associated with vascular abnormalities [19]. However, recent studies did not see much impact of the pH or osmolarity of drugs in the vitreous cavity [20]. According to our data, osmolarity remained similar in all groups, suggesting that intraocular injections of 250 or 500 µg of ramucirumab in rabbits do not alter either serum or the anterior chamber osmolarity.

All eyes were evaluated by H&E staining. In eyes injected with 250 µg ramucirumab, the morphology of the retina did not show any difference between drug-injected and controls. The ultrastructural findings by TEM confirmed the findings of LM. Some degree of ganglion cell layer vacuolization occurred in all samples, including those from the control group, and the density of vacuoles decreased seven days after the injection compared with 24 h after the injection. This finding may indicate that the retina is able to recover in a few days after ramucirumab injection. To overcome the doubts raised by this finding, we counted the density of ganglion cells in the eyes studied. The quantification of ganglion cells showed a slight loss of cellular density in both groups at 24 h. Seven days after the injection, the quantification of ganglion cells indicated a normal density in the 250 µg group, while in the 500 µg group, there was a statistically significant loss of cellular density.

Conclusion

Ramucirumab is an anti-VEGF drug used in the treatment of several types of adenocarcinomas, and its repurposing to treat neovascular eye disease is promising since it binds to VEGFR-2 and not only with its ligands. Our work presents evidence that this drug can be safely injected in the eyes of rabbits at a dose of 250 µg.