Targeting CEA in Pancreas Cancer Xenografts with a Mutated scFv-Fc Antibody Fragment
© Girgis et al; licensee Springer. 2011
Received: 17 June 2011
Accepted: 7 November 2011
Published: 7 November 2011
Sensitive antibody-based tumor targeting has the potential not only to image metastatic and micrometastatic disease, but also to be the basis of targeted therapy. The vast majority of pancreas cancers express carcinoembryonic antigen (CEA). Thus, we sought to evaluate the potential of CEA as a pancreatic cancer target utilizing a rapidly clearing engineered anti-CEA scFv-Fc antibody fragment with a mutation in the Fc region [anti-CEA scFv-Fc H310A].
Immunohistochemistry (IHC) with the antibody fragment was used to confirm expression of CEA on human pancreas cancer specimens. In vivo tumor targeting was evaluated by tail vein injection of I124-labeled anti-CEA scFv-Fc(H310A) into mice harboring CEA-positive and -negative xenografts. MicroPET/CT imaging was performed at successive time intervals. Radioactivity in blood and tumor was measured after the last time point. Additionally, unlabeled anti-CEA scFv-Fc(H310A) was injected into CEA-positive tumor bearing mice and ex vivo IHC was performed to identify the presence of the antibody to define the microscopic intratumoral pattern of targeting.
Moderate to strong staining by IHC was noted on 84% of our human pancreatic cancer specimens and was comparable to staining of our xenografts. Pancreas xenograft imaging with the radiolabeled anti-CEA scFv-Fc(H310A) antibody demonstrated average tumor/blood ratios of 4.0. Immunolocalization demonstrated peripheral antibody fragment penetration of one to five cell diameters (0.75 to 1.5 μm).
We characterized a preclinical xenograft model with respect to CEA expression that was comparable to human cases. We demonstrated that the anti-CEA scFv-Fc(H310A) antibody exhibited antigen-specific tumor targeting and shows promise as an imaging and potentially therapeutic agent.
Keywordsimaging pancreas cancer CEA antibody
Pancreatic cancer is one of the most lethal cancers as incidence approximates mortality . Signs and symptoms that suggest pancreatic cancer are usually vague and occur late in the disease process. Because of this, most patients have metastatic disease at diagnosis resulting in an overall survival of 6% at 5 years . Cure for pancreatic cancer currently hinges upon early diagnosis and surgical resection; however, only 10% to 20% of patients are eligible for surgery at diagnosis due to the presence of locally advanced cancer or metastatic disease . Even still, this cohort of patients has poor survival due to the presence small foci of metastatic disease that is not detected by current imaging modalities. Given our current inability to detect the true burden of disease, pancreas cancer patients are routinely understaged and our local therapies are thus misguided. These data indicate the need to develop novel strategies to detect these small foci of disease for more accurate staging of pancreatic cancer so that we may apply our therapies appropriately.
CEA is a 180-kDa GPI-linked glycoprotein expressed on the cell surface of the normal adult colon at very low levels. However, during carcinogenesis, this oncofetal protein becomes much more highly expressed on the cell surface. Additionally, this protein can be shed into the circulation and measured as a serum tumor marker, reflective of the burden of disease . High levels of CEA expression have been noted on a variety of gastrointestinal epithelial tumors. Adenocarcinoma of the pancreas is no exception, where increased CEA expression has been reported [6–9]. Here, we sought to investigate the potential of CEA as a tumor target of pancreas cancer utilizing our anti-CEA scFv-Fc H310A antibody fragment . First, we validated CEA expression in our pancreas cancer xenograft models and in human pancreatic cancer specimens by performing immunohistochemistry (IHC) with our scFv-Fc (H310A) antibody fragment. We then evaluated our anti-CEA scFv-Fc (H310A) antibody fragment for in vivo antigen-specific tumor targeting of our xenograft models with microPET imaging. Lastly, we investigated the microscopic pattern of tumor targeting of the intravenously injected antibody fragment with ex vivo immunolocalization studies to detect the exact location of the fragment within the tumor, which may have important ramifications for development of antibody-based therapeutics.
Materials and methods
Production, purification, and characterization
Production, purification, and characterization of the anti-CEA scFv-Fc (H310A) antibody have previously been reported in detail . Briefly, after gene assembly and site directed mutagenesis, 1 × 107 NS0 murine myeloma cells were transfected by electroporation with 40 μg of the pEE12 vector containing the anti-CEA scFv-Fc(H310A) construct and selected in glutamine-deficient DMEM/high modified media (JRH Biosciences, Lenexa, KS, USA) as previously described [5, 10]. Cell culture supernatants were screened by enzyme-linked immunosorbent assay and Western blot for selection of high expressing clones followed by sequential protein purification with anion exchange and hydroxyapatite columns by fast performance liquid chromatography (FPLC) . The final concentration of protein was determined by A 280 nm using an extinction coefficient of ε = 1.4. Purity and size of the protein was determined by SDS/PAGE, Western blot, and size exclusion chromatography .
NS0 mouse myeloma cells were maintained with DMEM/high modified media supplemented with 10% fetal bovine serum (FBS, Gemini Biosciences, West Sacramento, CA, USA), and 2 mM glutamine (Invitrogen, Carlsbad, CA, USA). The human pancreatic cancer cell lines, BxPC3, Capan-1, HPAF-II, and MiaPaca-2 were obtained from the American Type Culture Collection (ATCC, Manassas, VA, USA). RPMI-1640 medium, Iscove's Modified Dulbecco's medium, Eagle's Minimum Essential medium, and DMEM were used for BxPC3, Capan-1, HPAF-II, and MiaPaca-2 cells, respectively. All media was supplemented with 100 units of penicillin, 100 μg of streptomycin and 10% FBS. Only DMEM used for MiaPaca-2 cells were additionally supplemented with horse serum (2.5%).
The relative expression of CEA was determined for each cell line by flow cytometry. For each cell line, 1 × 106 cells were harvested from culture and resuspended in 250 μl of phosphate-buffered saline/1% fetal bovine serum (PBS/1%FBS). Primary, intact mouse anti-CEA antibody (Abcam, Cambridge, MA, USA) was added in abundance (4 μg) and incubated for 1 h. The samples were centrifuged at 1000 g for 10 minutes, the supernatant was discarded, and the sample was resuspended in 250 μl of PBS/1% FBS. The secondary antibody, fluorescin isothiocyanate (FITC)-conjugated goat anti-mouse IgG (Fc specific) antibody (4 μg), was incubated with each sample for 1 h and was similarly washed and resuspended. Negative controls included samples with cells only and samples with cells and secondary antibody only. Quantitation of antigen expression for each cell line was performed using the DAKO Qifikit according to the manufacturer's instructions (DAKO, Carpinteria, CA, USA). Briefly, control beads coated with known amounts of antibody and mimicking defined antigen densities were incubated with FITC-conjugated goat anti-mouse IgG (Fc specific) antibody (DAKO) and evaluated by flow cytometry. A standard linear regression plot and equation was extrapolated from the mean fluorescence intensity (MFI) of the control beads. Samples of human pancreatic cancer cells were incubated with commercial intact mouse monoclonal anti-CEA antibody (Invitrogen) and FITC-conjugated anti-mouse IgG and detected by flow cytometry. The MFI of these samples were then applied to the extrapolated equation to determine the antibody binding capacity and thus, based on indirect immunofluorescence, the antigen density per cell. All experiments were performed in triplicate and averaged to provide reliable results.
Human tissue specimens were provided by the Department of Pathology at University of California, Los Angeles (UCLA) Medical Center under an approved UCLA Institutional Review Board protocol. These specimens were evaluated by IHC for expression of CEA using the anti-CEA scFv-Fc(H310A) antibody fragment. Each paraffin embedded specimen was deparaffinized and incubated with the primary anti-CEA scFv-Fc (H310A) antibody fragment (1:50) for 1 h. Specimens were washed with PBS/1%Tween. Specimens were then incubated with the secondary mouse anti-human IgG (Fc specific) antibody (1:200) (Jackson Immunoresearch Laboratories, West Grove, PA, USA). After another wash, specimens were incubated with the tertiary horseradish peroxidase (HRP)-conjugated goat anti-mouse IgG (Fc specific) antibody (1:400) (DAKO). Negative control slides were only incubated with the secondary and tertiary antibodies.
Radioiodination with the positron-emitting isotope 124I was done by the Iodo-Gen method as described . Labeling reactions (0.1 to 0.2 ml) typically contained 0.1 to 0.2 mg purified protein and 0.5 to 1 mCi Na124I (IBA Molecular, Dulles, VA, USA). Labeling efficiency was measured by instant thin layer chromatography (TLC) using the Tec-Control kit (Biodex Medical Systems, Shirley, NY, USA). Immunoreactivity was determined by incubating the radioiodinated anti-CEA scFv-Fc (H310A) antibody (≈100,000 cpm) with excess antigen-positive cells such that there was an abundance of antigen. After incubation and centrifugation, supernatant was collected and measured for the presence of radioactivity. The immunoreactive fraction was determined by use of the following equation: 1-(supernatant radioactivity/total radioactivity).
Xenograft imaging and biodistribution studies
All animal handling was done under a protocol approved by the Chancellor's Animal Research Committee of the UCLA. Mouse xenografts were established in 8-week-old female nude mice (Charles River Laboratories, Wilmington, MA, USA). Three tumor models were developed with antigen-positive tumors on the left shoulder and antigen-negative tumors on the right shoulder so that each mouse served as its own control. Approximately 1 × 106 cells of an antigen-positive (BxPC3, HPAF-II, Capan-1) or -negative (MiaPaca-2) cancer cells were injected subcutaneously (s.c.) and allowed to grow for 10 to 14 days before imaging. Lugol's solution (0.5 ml per 100 ml water) was added to the drinking water 24 h prior to injection to block thyroid uptake of radioiodine. Also, gastric lavage with 1.5 mg of potassium perchlorate in 0.2 ml of PBS 30 min prior to tail vein injection was performed to block stomach uptake of radioiodine. Mice were injected with approximately 50 μg of 124I-anti-CEA scFv-Fc (H310A) antibody (specific activity of 2.40 μCi ± 0.005 μCi/μg) in PBS/1%FBS via the tail vein. At 4 and 20 h post-injection, the mice were anesthetized using 1.5% to 2% isoflurane, placed on the micro positron emission tomography (microPET) bed, and imaged with a Focus microPET scanner (Concorde Microsystems Inc., Knoxville, TN, USA). Acquisition time was 10 min. All images were reconstructed using a FBP algorithm and displayed by the AMIDE software package [11, 12]. Selected animals were also imaged by micro computed tomography (microCT) with the resultant images coregistered with the microPET scans for anatomic reference. Following the last scanning time point, animals were euthanized; tumors and blood were harvested and weighed. Radioactive uptake of organs was counted in a gamma counter (Wizard 3″ 1480 Automatic Gamma Counter, Perkin-Elmer, Covina, CA) for biodistribution analysis. After decay correction, radioactive uptake in the tumor and blood was converted to percentage of injected dose per gram of tissue (%ID/g).
IHC staining was also performed on paraffin-embedded sections of HPAF xenografts to evaluate for the presence of the intravenously injected anti-CEA scFv-Fc (H310A) antibody fragment. Mice were injected with 1 × 106 cells s.c. for xenograft creation. Once an appropriate size was achieved (approximately 0.5 cm), the mice were injected with 50 μg of anti-CEA scFv-Fc(H310A) antibody via the tail vein. After 20 h, mice were sacrificed and tumors were harvested, placed in a dry ice/2-butane bath and embedded in optimal cutting temperature solution. Frozen tumors were cut with a cryostat into 4-μm sections, placed on a glass slide, and fixed with 20% acetone for 20 min. After fixation, IHC staining was performed. All tumor specimen slides were incubated for 10 min with 3% hydrogen peroxide in methanol for blocking of endogenous peroxidase. Tumor specimen slides were incubated with the secondary mouse anti-human IgG (Fc specific) antibody (1:200) (Jackson Immunoresearch Laboratories) followed by the tertiary HRP-conjugated goat anti-mouse IgG (Fc specific) antibody (1:400) (DAKO). The positive control slides were incubated with intact mouse anti-CEA antibody (1:50) and HRP-conjugated goat anti-mouse IgG (Fc specific) antibody (1:400) (DAKO). Negative control slides were only incubated with the secondary and tertiary antibodies. Lastly, one slide was used for hematoxylin and eosin staining.
Production, purification, and characterization
The anti-CEA scFv-Fc (H310A) antibody fragment was expressed in murine NS0 myeloma cells. Clones producing the highest amount of antibody by Western blot were selected for expansion. Protein was purified by FPLC from supernatant yielded an approximate purity of 98% by standard SDS-PAGE and Western blot (Figure 1b) . Also, this scFv-Fc fragment had an elution time from a size exclusion chromatography column between that of the intact IgG (150 kDa) and bovine serum albumin (66 kDa) standards confirming its intermediate size of 105 kDa (Figure 1c) .
Radioiodination, xenograft imaging, and biodistribution studies
Targeting cancer with antibodies is a rapidly expanding field seeking to provide new technology for diagnosis and therapy. Considering molecular imaging applications such as immunoPET, intact antibodies are limited due to their extended serum persistence resulting in a high background signal. However, the growing knowledge of antibody interactions with FcRN receptors resulting in prolonged serum persistence have allowed for development of engineered antibody fragments possessing shorter half-lives while providing the same specific binding to their antigen. In such a way, these engineered antibodies can overcome the limitations of intact antibodies. Indeed, many recent studies have demonstrated that smaller size antibody fragments as well as decreased serum persistence are better imaging agents owing to their improved tumor penetration and rapid blood clearance [4, 13–15]. Previously, our group produced and characterized the anti-CEA scFv-Fc (H310A) antibody fragment with a significantly reduced serum half-life (27 h) when compared to the intact antibody (> 10 days) . With this antibody fragment, we sought to demonstrate the potential of CEA as a target in pancreas cancer and to investigate the utility of this fragment in antigen-specific targeting within our pancreas cancer models.
CEA serum levels have been used clinically for many years to diagnose, stage, and follow patients with colorectal cancer. Although CEA serum levels are not widely elevated in pancreatic cancer, this antigen is expressed on the cell surface of the vast majority of pancreatic cancers. Many reports of CEA on pancreas cancer specimens describe expression ranging from 70% to 98% [7, 8, 16]. In addition to showing high CEA expression on pancreatic cancer cell lines, Kaushal et al. demonstrated tumor targeting of a fluorophore-conjugated intact anti-CEA antibody in a xenograft model of pancreas cancer with the aim of developing an intraoperative imaging probe . Given the reported prevalent expression of CEA in pancreas cancers, we attempted to investigate the immunoPET imaging potential of the anti-CEA scFv-Fc (H310A) antibody fragment in pancreas cancer xenograft models. First, we confirmed high levels of expression on Capan-1, HPAF-II, and BxPC3 cancer cell lines and no expression of CEA on the MiaPaca-2 cell line. Additionally, we found that CEA expression was very similar between the positive CEA cell lines ranging from 230,000 to 310,000 antigens per cell. Next, utilizing a tissue microarray we simultaneously evaluated 107 surgically resected human pancreas cancer specimens for CEA expression with IHC to validate previous reports and compare with our xenograft models. We found moderate to strong staining of CEA on 84% of specimens consistent with results described in the literature [7, 8, 16]. Moreover, we demonstrated similar staining intensity between our mouse pancreatic xenografts and strongly stained human pancreas cancer specimens. Based on these results, we were satisfied that CEA is abundantly expressed in the majority of pancreas cancers and thus a suitable target. Furthermore, our xenograft model recapitulates the human condition with respect to CEA expression.
Using our pancreatic cancer mouse xenograft model, we injected mice with 124I-labeled anti-CEA scFv-Fc (H310A) antibody and imaged at 4 and 20 h after injection with microPET/CT. Our microPET images at 4 h demonstrate quick targeting of the antibody fragment to all CEA-positive pancreatic tumors (data not shown). Moreover, microPET images at 20 h show persistence of signal at the site of the tumor with low blood background signal. Accordingly, biodistribution data at 20 h after injection provides objective confirmation of the microPET images. We were able to achieve positive tumor to negative tumor ratios greater than 17 demonstrating antigen-specific tumor targeting of the anti-CEA scFv-Fc (H310A) antibody fragment. Furthermore, a tumor to blood ratio of 4.0 at 20 h is evidence of the imaging benefit afforded by the decreased serum half-life of the fragment. Overall, these data are very supportive regarding the immunoPET imaging potential of the anti-CEA scFv-Fc (H310A) antibody fragment in pancreas cancer.
To assess the potential ability of converting an antibody-based imaging agent into a tumor-targeting therapeutic, we additionally wanted to define the microscopic pattern of tumor targeting of the anti-CEA scFv-Fc (H310A) antibody fragment in mice xenografts by performing "immunolocalization" studies. These studies provided confirmatory evidence of the microPET images demonstrating the physical presence of the anti-CEA scFv-Fc (H310A) antibody protein in the tumor sections. Furthermore, the intratumoral staining pattern demonstrated localization of antibody to the periphery of microscopic tumor nodules comprising the macroscopic tumor xenograft with antibody penetration approximately one- to five-cell-layers deep from the intervening stroma and vessels. Additionally, antibody tumor penetration models describe a number of factors including antigen density, antibody binding affinity, and antibody metabolism along with physical properties of the cancer tissue (e.g. tumor vascularity) as impacting antibody localization [17–21]. Depending on the cytotoxic bystander effect of the therapeutic modality associated with the antibody fragment, extensive tumor penetration may not be necessary [19, 22, 23]. With respect to radioimmunotherapy, radionuclides such as Yttrium-90 possessing a relatively long radiation range (path length > 1 mm) may supply a sufficient dose of cytotoxic radiation to the nuclei of cells in center or cold area of the tumor micronodules which are not directly bound by the antibody fragment-radionuclide conjugate . Additionally, switching to a radiometal with shorter beta particle range might be more appropriate in considering treatment of smaller tumor deposits such as micrometastases. Although utilizing biodistribution data from using a radioiodine labeled antibody fragment to estimate biodistribution of a radiometal labeled fragment was not performed, one can imagine based on the immunohistochemical staining pattern that a radiolabeled engineered antibody with modest tumor penetration, as demonstrated in this study with the anti-CEA scFv-Fc (H310A) antibody, may have applications for radioimmunotherapy. Future studies should be directed at determining the appropriate radionuclide (e.g. alpha-emitter, long- or short-path-length beta-emitter) sufficient to provide the bystander effect without compromising surrounding tissues.
This work demonstrates the utility of the anti-CEA scFv-Fc (H310A) antibody fragment for imaging pancreas cancer with possible applications for therapy. We show the in vivo imaging potential and targeting capability of this antibody fragment in pancreatic cancer xenografts. Although CEA expression appears to be similar between our xenografts and the majority of human pancreas cancer specimens, data from xenograft models are limited secondary to lack of a competent immune system. Historically, the majority of murine monoclonal antibodies have failed to be translated to the clinical setting because of the human anti-mouse antibody (HAMA) response. This resulted in the advent of chimeric antibodies with murine variable regions (VL and Vh) and human constant domains (CH2 and CH3) as well as humanized and fully human antibodies. Of note, the anti-CEA scFv-Fc (H310A) antibody fragment is a chimeric protein, which should decrease the incidence of the HAMA response, although it may still occur with repeated administration of the protein .
In summary, antigen-specific molecular imaging has the potential to provide a more accurate assessment of the tumor burden for pancreatic cancer patients. CEA is strongly expressed in the majority of pancreas cancers and thus is a potential target for antibody-based molecular imaging and therapy. Using the novel mutated anti-CEA scFv-Fc (H310A) antibody fragment with a reduced serum half-life, we demonstrated in vivo antigen-specific molecular imaging. Furthermore, we define the microscopic pattern of tumor targeting which may have implications regarding radioimmunotherapy. The versatility of this antibody construct, based on the presence or absence of an Fc domain mutation, provides for improved pharmacokinetics in both imaging and therapy making it a very attractive fragment for continued study and development.
Funding support was provided by the Veterans Affairs Career Development Award (James S. Tomlinson). We thank Waldemar Ladno for his assistance with the animal studies and Felix Bergara, MS, for his technical assistance. We would also like to acknowledge the UCLA Translation Pathology Core Laboratory for their immunostaining services and the UCLA Small Animal Imaging Resource Program (NIH CA 92865). Flow cytometry was performed in the UCLA Jonsson Comprehensive Cancer Center (JCCC) and Center for AIDS Research Flow Cytometry Core Facility, supported by NIH awards CA-16042 and AI-28697.
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