A novel oncolytic viral therapy and imaging technique for gastric cancer using a genetically engineered vaccinia virus carrying the human sodium iodide symporter

GLV-1 h153 is a replication-competent, recombinant vaccinia virus derived from its parental strain, GLV-1 h68, via homologous recombination. It contains four inserted cassettes encoding Renilla Aequorea luciferase- green fluorescent protein (RUC-GFP) fusion protein, a reversely inserted human transferrin receptor (rTfr), β-galactosidase, and human sodium iodide symporter (hNIS) into the F14.5, J2R (encoding thymidine kinase), and A56R (encoding hemagglutinin) loci of the viral genome.GLV-1 h153 was provided by Genelux Corporation (R&D facility in San Diego, CA, USA).

4 × 10⁴ cells per well of each cell line were plated in 12-well plates and incubated in a 5% CO₂ humidified incubator at 37°C overnight. GLV-1 h153 was added to each well at varying Multiplicity of Infection (MOIs) of 0.01, 0.1, and 1.0. Viral cytotoxicity was tested using a lactate dehydrogenase (LDH) assay daily. Cells were washed with PBS once, and then lysed with 1.35% Triton X-100 (Sigma, St. Louis, MO). The intracellular LDH release following lysis was subsequently measured with CytoTox 96® (Promega, Madison, WI) on a spectrophotometer (EL321e, Bio- Tek Instruments) at 490 nm. Results are expressed as the percentage of surviving cells, which were calculated as the LDH release of infected samples compared to uninfected control. All conditions were tested in triplicate.

Supernatants from each infected well were collected daily and immediately frozen at −80°C. Serial dilutions of all supernatant samples were made to perform standard viral plaque assays on confluent CV-1 cells. All samples were measured in triplicates.

All animal experiments were performed under approved protocols and in accordance with ethical guidelines of the Institutional Animal Care and Use Committee (IACUC) at Memorial Sloan-Kettering Cancer Center (MSKCC). MKN-74 xenografts were established in 6- to 8-week-old female nude mice (NCI:Hsd:Athymic Nude-nu, Harlan) by subcutaneously injecting 5 × 10⁶ MKN-74 cells into the right flank. Tumor growth was recorded twice a week using a digital caliber and tumor volume was calculated using the equation, a × b² × 0.5, in which a and b are the largest and smallest diameters, respectively. When tumors reached a diameter of approximately 6–8 mm in 10 days, animals were grouped into control and treatment groups with equitable tumor sizes. A single dose of 2 × 10⁶ plaque-forming units (PFUs) of GLV-1 h153 in 100 μL PBS or 100 μL of PBS as control were injected intratumorally to each designated tumor. Animals were observed daily for any signs of toxicity, and sacrificed when their tumors reached a diameter of approximately 15 mm.

Five MKN-74 xenografts were intratumorally injected with 2 × 10⁷ PFUs GLV-1 h153 and 5 with PBS as controls. Two days after infection, 200 μCi of ^99mTc pertechnetate was administered via tail vein injection. ^99mTc pertechnetate images were obtained over 10 min, 3 hours after radiotracer administration. Imaging was performed using the dual-detector gamma camera sub-system of the X-SPECT small-animal SPECT-CT system (Gamma Medica, Northridge, CA). The X-SPECT γ-camera system was calibrated by imaging a mouse-size (30 mL) cylinder filled with a measured concentration (MBq/mL) of ^99mTc using a photopeak energy window of 126 to 154 keV and low-energy high-resolution collimation. The resulting ^99mTc images were exported to Interfile and then imported into the ASIPro (Siemens Pre-clinical Solutions, Knoxville, TN) image processing software environment. By ROI analysis, a system calibration factor (in cpm/pixel per MBq/mL) was derived. Animal images were likewise exported to Interfile and then imported into ASIPro and parameterized in terms of the decay-corrected percentage injected dose per gram (%ID/g) based on the foregoing calibration factor, the administered activity, the time after administration of imaging, and the image duration.

Three MKN-74 xenografts were injected intratumorally with 2 × 10⁷ PFU GLV-1 h153 and two with PBS. Two days after viral injection, 300 μCi of ¹²⁴I was administered via tail vein injection. One hour after radiotracer administration, 3-dimensional list-mode data were acquired using an energy window of 350 to 700 keV, and a coincidence timing window of 6 nanoseconds. Imaging was performed using a Focus 120 microPET dedicated small animal PET scanner (Concorde Microsystems Inc, Knoxville, TN). These data were sorted into 2-dimensional histograms by Fourier rebinning. The count rates in the reconstructed images were converted to activity concentration (%ID/g) using a system calibration factor (MBq/mL per cps/voxel) derived from imaging of a mouse size phantom filled with a uniform aqueous solution of ¹⁸F. Image analysis was performed using ASIPro.

All five human gastric cancer cell lines were susceptible to oncolysis by GLV-1 h153 (Figure 1). The MKN-74, OCUM-2MD3, and AGS cell lines were more sensitive to viral lysis compared to MKN-45 and TMK-1 cells. All cell lines demonstrated a dose-dependent response, with greater and faster cell kill at higher MOIs. In MKN-74, OCUM-2MD3, and AGS cell lines, more than 90% of the cells were killed by day 9 at an MOI of 1. The MKN-74 cell line was particularly susceptible to viral oncolysis, with greater than 77% cell kill by day 9 at the lowest MOI of 0.01.

Standard viral plaque assays demonstrated efficient viral replication of GLV-1 h153 in all gastric cancer cell lines at an MOI of 1 (Figure 2). MKN-74 demonstrated the highest viral titer with a peak titer of 1.06 × 10⁶ PFUs per well, a 26-fold increase from initial dose, by day 7.

To establish the cytolytic effects of GLV-1 h153 in vivo, mice bearing MKN-74 xenografts were treated with a single dose of intratumoral injection of GLV-1 h153 or PBS. Treated tumors demonstrated sustained/continuous tumor regression over a four-week period. By day 28, the mean tumor volume of the treatment group was 221.6 mm³ (Figure 3). One animal demonstrated a complete tumor regression. In contrast, all of the control tumors continued to grow with a mean volume of 1073.2 mm³ by day 28 (t-test, comparing treatment and control group on day 28, p < 0.001). There was no significant change in body weight in either group, and no morbidity or mortality related to GLV-1 h153 treatment was observed.

GFP expression was monitored by fluorescence microscopy 1, 3, 5, 7, and 9 days after viral infection at an MOI of 1.0. Most MKN-74 cells were infected and expressed GFP by day 7 (Figure 4A). In vivo, GFP signal can be detected only at the xenograft injected with GLV-1 h153 (Figure 4B).

All MKN-74 xenografts injected with GLV-1 h153 showed localized accumulation of ^99mTc radioactivity in the flank tumors while no radioactivity cumulation in control tumors (Figure 5A). GLV-1 h153-infected MKN-74 tumors also facilitated ¹²⁴I radioiodine uptake and allowed for imaging via PET (Figure 5B), while PBS-injected tumors could not be visualized.

Gastric cancer is the fourth most common malignancy and the second most frequent cause of cancer-related death world-wide [1, 14]. Recurrence or distant metastasis is one of the most common complications and often the cause of death [15]. While chemotherapy is a useful adjuvant therapy compared to surgical therapy alone, its therapeutic potential is limited [16]. Most gastric cancers are resistant to currently available chemotherapy regimens. Therefore, novel therapeutic agents are needed to improve outcomes for gastric cancer patients who are not responsive to conventional therapies. Oncolytic viral therapy is a promising approach to cancer treatment that depends on the ability of viruses to infect, replicate within, and lyse a host cell [17, 18]. In this study, we described the cytotoxic effects of GLV-1 h153, a novel recombinant VACV carrying the hNIS gene, on gastric cancer cells in vitro. We further demonstrated that GLV-1 h153-infected gastric cancer xenografts expressed functioning hNIS protein that allowed for non-invasive imaging of the tumor and also efficient tumor regression in vivo.

A variety of viruses have shown oncolytic properties including adenovirus, herpes simplex virus, Newcastle disease virus, vesicular stomatitis virus, and reovirus [17]. Among a variety of oncolytic viral agents, vaccinia virus has several advantages. VACV exclusively replicates in the cytoplasm without using the host’s DNA-synthesis machinery, thereby lowering the risk of integration of the viral genome into the host genome [10]. A large amount of foreign DNA (up to 25 kb) can be incorporated without significantly reducing the viral replication efficiency [19]. Moreover, vaccinia has been proven to have a good safety profile as it has been historically given to millions during the smallpox vaccination. It also demonstrates efficient replication and a broad range of host cell tropisms [10]. Several preclinical studies have shown that systemic injection of recombinant VACV into xenografts resulted in high viral titers in tumors only, indicating tumor-specific colonization [11, 20, 21]. There is a small concern that patients who have received smallpox vaccination in the past have neutralizing antibody against the virus. This could potentially result in compromised treatment efficacy. However, in the blood, complement plays a more important role in inactivating VACV than neutralizing antibodies. We therefore predict that the presence of neutralizing antibodies in patients should not hinder VACV treatment; however, a higher treatment dose might be required.

Genetically engineered VACVs have shown efficacy in the treatment of a wide range of human cancers [12]. GLV-1 h168 has already shown to be an effective diagnostic and therapeutic vector in several human tumor models, including breast tumor, mesothelioma, pancreatic cancers, and squamous cell carcinoma [11] The hNIS protein, which is an intrinsic membrane glycoprotein with 13 putative transmembrane domains, actively transports both Na⁺ and I^- ions across the cell membrane [22]. Functioning hNIS protein can uptake several commercially available radio-nucleotides, including ¹²³I, ¹²⁴I, ¹²⁵I, ¹³¹I, ^99mTc and ¹⁸⁸Re [22, 23]. In this study, GLV-1 h153-mediated expression of hNIS protein in infected MKN-74 xenografts resulted in a localized ^99mTc and ¹²⁴I radiotracer uptake. Our results suggest that hNIS gene expression via viral vector can be used as a non-invasive imaging modality to monitor tumor progression and treatment effects.

A single intratumoral injection of GLV-1 h153 in MKN-74 xenografts exhibited localized intratumoral GFP and hNIS expression. Moreover, there was no evidence of viral spread to any other organs based on GFP imaging, ^99mTc scintigraphy, and ¹²⁴I PET, indicating tumor-specific viral infection and activity. We also demonstrated that GLV-1 h153 is effective and safe in treating gastric tumors in a murine xenograft model. The GLV-1 h153-treated group was continuously followed until day 35 and there was no tumor regrowth (data not shown between day 28 and 35). The control group had to be sacrificed in accordance to our approved animal protocol on day 28. Expressing the hNIS gene in an otherwise non-hNIS-expressing tissue is exciting. It could potentially make use of the well-established radioiodine imaging and therapy in other non-thyroid originated cancers. Several studies have shown promising results in a variety of tumors using radioiodine treatment via tumor-specific expression of the hNIS gene, including medullary thyroid carcinoma [24], prostate cancer [25], colon cancer [26], and breast cancer [27]. Tumor-specific hNIS expression using GLV-1 h153 can maximize localized radioiodine accumulation and minimize non-specific uptake in other organs. Based on our promising results, it would be of significant clinical importance to evaluate the effect of combination therapy of GLV-1 h153 and radioiodine.