Introduction
Antibody based molecular imaging provides a non-invasive means of detecting biological processes and molecular events in vivo. By combining the high sensitivity and resolution of e.g. a PET (positron emission tomography)-scanner with the tumor specificity of a tumor targeting molecule, this technique is of increasing importance to visualize and characterize tumor lesions. Additionally, it can be used for dosimetric calculations, to monitor therapy response and to identify patients who may benefit from a particular therapy (1). With advancements in instrumentation and development of novel targeted probes, immuno-PET has firmly established its role in drug development and in clinical assessment.
Although intact monoclonal antibodies (mAbs) have been considered candidates for molecular imaging due to their specificity and high signal delivery to cell surface molecules, their relatively large size (~150 kDa) and Fc-mediated half-life extension tend to cause suboptimal imaging pharmacokinetics, poorer tumor penetration and increased immunogenicity. Smaller targeting moieties such as antibody fragments have emerged as an alternative to mAbs to overcome the aforementioned limitations. Common antibody fragments are smaller molecules that omit the Fc-region and consist of one Fab (~50 kDa) or two F(ab′)2 (100 kDa) antigen binding arms, respectively. Due to their smaller size, antibody fragments are likely to exhibit better extravasation and diffusion in the intra-cellular space and faster blood clearance compared to their parental antibodies (2). Consequently, normal tissue accumulation and immunologic reactions is expected to be lower with a fragment than with the intact antibody, thus enhancing tumor contrast and allowing imaging at earlier time-points. For several targets, antibody fragments have shown promising results as imaging agents in animals (3) and clinical studies (4). Generally, F(ab′)2 fragments are considered advantageous to Fab fragments in molecular imaging due to their bivalent nature, which can result in an increased functional affinity and tumor uptake compared to Fab. Another possible disadvantage of Fab fragments is that their molecular weight subjects them to glomerular filtration. The larger F(ab′)2 format, with a size above the renal threshold, is expected to exhibit a biodistribution shift from kidneys to liver (5).
An alternative to antibody fragments derived from full-length antibodies generated through immunization are recombinant Fabs obtained in vitro by phage display, generated from selections in phage libraries. Recombinant antibody technology is a rapidly evolving field with a number of major benefits over conventional antibody generation and production methods (6). It enables the use of in vitro selection steps that facilitate the isolation of antibodies with desired characteristics, e.g. antibodies that distinguish closely related antigens (7), and candidates can be engineered using readily available DNA sequences. Furthermore, since recombinant monoclonal antibody fragments can be produced in bacteria this allows for an easier, faster, and less expensive production process than using hybridoma or mammalian cell culture techniques. Moreover, antibodies selected from in vitro libraries of human antibody genes do not elicit the same immune responses in patients that are seen with non-human antibodies. Therefore, such antibodies can be used for therapeutic development. Thus, more and more fully human antibodies obtained from antibody libraries are entering clinical development and are reaching the market (8).
We have developed the CD44v6-targeting human bivalent antibody fragment AbD19384, a recombinant human bivalent Fab antibody, engineered from monovalent Fab AbD15179 by subcloning of the Fab gene into an expression vector containing a self-dimerizing helix-turn helix motif (dHLX) (9,10). The Fab-dHLX constructs represent a novel, attractive platform for cancer targeting. The size and format is functionally equivalent to a F(ab′)2 fragment, but there are also important differences besides the origin of the molecule. AbD19384 is a non-covalent homodimer formed via C-terminal fusion of a small homodimerization domain, whereas disulfide bridges are present in F(ab′)2 fragments enzymatically derived from full length antibodies. These non-covalent homodimers are stable under reducing conditions, whereas F(ab′)2 fragments are not. CD44v6 was chosen as a target, since it is a surface antigen found to be overexpressed in >90% of head and neck squamous cell carcinoma (HNSCC), as well as in other cancers such as lung, esophagus and breast, which makes it an attractive target for molecular imaging and targeted therapy (11). To the best of our knowledge, there are no previous studies of tumor targeting abilities of the Fab-dHLX format in vivo, hence it is not known how this construct functions in an in vivo setting. Thus, the present study is not only relevant for CD44v6-targeted molecular imaging, but also as the first study of a tumor targeting Fab-dHLX construct in vivo.
Consequently, the aim of the present study was to evaluate for the first time the in vitro and in vivo binding properties of the Fab-dHLX construct, and to assess the utility of radio-iodinated AbD19384 as a targeting agent for molecular imaging of CD44v6-expressing tumors.
Materials and methods
AbD19384
AbD19384 is a bivalent antibody fragment, engineered from two fully human AbD15179 Fab-fragments. This format is a non-covalent homodimer of AbD15179 formed via C-terminal fusion of a dHLX (synthetic double helix loop helix) dimerization motif (9,10) to the heavy chain segment of AbD15179. This format, Fab-dHLX, also referred to as ‘bivalent mini-antibody’, has a molecular weight of ~110 kDa, and is functionally equivalent to a F(ab′)2 fragment. The dHLX helix-turn-helix motif is a de novo designed self-associating peptide (9,12). The dimerization occurs spontaneously, and thus the construct is in equilibrium with the monomeric form and possibly also a small fraction of tetramers or higher order aggregates, with a majority of the molecules being in the dimeric form (9). The generation of the monovalent form AbD15179 has been previously described (7). AbD19384 was supplied by Bio-Rad AbD Serotec GmbH (Puchheim, Germany) in 3X PBS.
Surface plasmon resonance (SPR) analysis of AbD19384
Recombinant CD44v3-10 (7) and two BSA-conjugated peptides (Elim Biopharmaceuticals, Hayward, CA, USA) derived from human (CGNRWHEGYRQTPREDS) and murine (CQNGWQGKNPPTPSEDS) CD44v6, respectively, were immobilized by standard amine coupling on a ProteOn XPR36 general layer medium sensor chip (Bio-Rad Laboratories, Hercules, CA, USA). A v6-negative isoform of CD44 (CD44v3-10Δv6) was included as a negative control. Channels with immobilization levels of 200 RU (BSA-conjugated peptides), 500 RU (CD44v3-10) and 1000 RU (CD44v3-10 and CD44v3-10Δv6) were used. Dilution series (3–50 nM) of the Fab-fragment AbD15179 and its corresponding bivalent fragment AbD19384 in PBS 0.05% Tween-20 (pH 7.4) were injected at 50 μl/min at 25°C. Real-time signal from a blank channel and a parallel buffer injection were subtracted and binding data fitted to a 1:1 Langmuir isotherm using ProteOn Manager software version 3.1.0.6 (Bio-Rad Laboratories). Data were double referenced by subtraction of simultaneous responses from a blank surface and a buffer injection. Experimental data were plotted together with curves drawn from a fitted 1:1 Langmuir isotherm. Kinetic constants were calculated from five separate injections using two different immobilization levels of CD44v3-10. Surfaces were regenerated with 10 mM HCl between injections.
Cell lines
The human SCC cell line A431 (obtained from the American Type Culture Collection, Manassas, VA, USA), derived from an epidermal carcinoma of the vulva, was cultured in Ham's F10, supplemented with 10% fetal calf serum, 2 mM L-glutamine, and antibiotics (100 IU penicillin and 100 μg/ml streptomycin). A431 has been shown to be a highly CD44v6-expressing cell line with ~3×106 antigens/cell (13). The human SCC cell line H314 (obtained from the European Collection of Cell Cultures), derived from floor of the mouth, was cultured in a one-to-one mixture of Ham's F12 and Dulbecco's modified Eagle's medium (DMEM) with the same supplements. H314 has demonstrated a medium antigen density of ~0.7×106 CD44v6 antigens per cell (14). The human SCC cell line UM-SCC74B derived from base of the tongue (kindly provided by Professor T.E. Carey, University of Michigan, MI, USA) was cultured in DMEM with the same supplements, as well as 1% non-essential amino acids. UM-SCC74B has demonstrated low expression (~0.1×105) of CD44v6. As a negative control, the breast cancer cell line MDA-MB-231 (obtained from the American Type Culture Collection) was used. It was cultured in DMEM with the same supplements as described above for A431. This cell line has demonstrated no detectable CD44v6 expression (14). Cells were incubated at 37°C in an atmosphere containing 5% CO2. For LigandTracer studies, ~1×106 A431 cells, 2×106 H314 cells, 1×106 UM-SCC74B cells, or 2×106 MDA-MB-231 cells were seeded 2–3 days before measurements in a local part on a 10-cm cell dish (#150350; Nunc) and allowed to adhere firmly to the plastics prior to the addition of fresh medium.
Labeling
AbD19384 was labeled with 125I (Perkin-Elmer, Waltham, MA, USA) using direct chloramine T labeling (CAT) (15) (Sigma-Aldrich). CAT and Na2SO5 (NBS) were dissolved in MilliQ-water to 4 mg/ml. AbD19384 (100 μg) in PBS was added to 10 MBq of 125I and mixed before adding 30 μl of CAT. The reaction mixture was incubated for 1 min on ice before ending the reaction by adding 60 μl of NBS. The sample was purified on a NAP5-size exclusion column (GE Healthcare Life Sciences Uppsala, Sweden) equilibrated with PBS.
Labeling of AbD19384 with 124I (Perkin-Elmer) using 1,3,4,6-Tetrachloro-3α,6α-diphenylglycouril (Iodogen) was performed as following; three Iodogen buffers (A, B and C) were prepared; A, 0.5 M sodium phosphate buffer, pH 7.4; B, 0.05 M sodium phosphate and 5 M NaCl, pH 7.4; C, 0.05 M sodium phosphate, 5% potassium iodide and 0.5% BSA (w/v). All buffers were prepared using MilliQ-water. Iodogen was dissolved in dichloromethane to 0.2 mg/ml. 124I was incubated with cold NaI in a 1:1 molar ratio with the added AbD19384 in order to ensure that the nuclide was in iodide form prior to starting the labeling procedure. 124I and AbD19384 (1 mg/ml in PBS) were mixed in a tube previously coated with 50 μg Iodogen. Buffer A was added in an equivalent volume, incubated at room temperature for 7 min and agitated carefully every 30 sec using a vortex. The reaction mixture was transferred to a new tube and buffer B (480 μl) was subsequently added. Following at least 10 min of rest, buffer C (480 μl) was added, and the sample was mixed thoroughly. Labeled F(ab′)2 was separated from non-reacted radionuclide and low-molecular-weight reaction components by using a NAP-5 or PD10 column pre-equilibrated with PBS. Iodination using Iodogen was also performed using 125I in the same way, in order to optimize and compare labelings.
To determine the yield, purity and stability of the labeled conjugates, instant thin-layer chromatography (ITLC) analyses were performed on labeled conjugates. Samples taken immediately as well as 48 h after the labeling procedure were analyzed. Serum stability tests were performed by 1 h incubation at 37°C in 42% murine serum in PBS, pH 7.4. Approximately 1 μl of the conjugate was placed on an ITLC chromatography strip (Biodex) and placed into a ‘running buffer’ (70% acetone), followed by measurements on a Cyclone Storage Phosphor system. Data were analyzed using OptiQuant image analysis software.
In vitro binding measurements on cultured tumor cells
Real-time in vitro binding and retention measurements of the radiolabeled conjugates were performed at room temperature using LigandTracer instruments (Ridgeview Instruments AB, Uppsala, Sweden) on CD44v6-positive A431, H314 and UM-SCC74B cells. In vitro binding specificity measurements were performed on LigandTracer instruments using MDA-MB-231 cells as negative controls. LigandTracer Grey was used for 125I-AbD19384 and LigandTracer White was used for 124I-AbD19384. Binding traces using several subsequent concentrations (0–90 nM) were obtained for at least 1 h per concentration, followed by a dissociation measurement for at least 15 h. The shapes of the real-time binding curves produced in LigandTracer were compared in the evaluation software TraceDrawer 1.6.1 (Ridgeview Instruments AB, Vänge, Sweden). Through kinetic fitting using a 1:1 and 1:2 models, the dissociation equilibrium constant KD (corresponding to the apparent affinity), the association rate constant ka and the dissociation rate kd were obtained.
Small animal studies
Female nu/nu Balb/c mice were housed under standard laboratory conditions and fed ad libitum. All experiments complied with the Swedish law and were performed with permission from the Uppsala Committee of Animal Research Ethics, ethical permission number C 410/12.
In vivo specificity of <sup>125</sup>I-AbD19384
In the first group (n=5), aimed at analyzing in vivo specific binding of 125I-AbD19384 to CD44v6, approximately (8×106) A431 cells (high CD44v6 expression) suspended in 150 μl 1:1 cell medium:Matrigel were injected s.c. into the right posterior leg. In the same mice, ~8×106 MDA-MB-231 cells (no CD44v6 expression) suspended in 150 μl 1:1 cell medium:Matrigel were injected in the left posterior leg. Two weeks after tumor cell injections, experiments were performed. At the time of study, average animal weights were 19.9±0.9 g (SEM), A431 tumor weights 73±20 mg, and MDA-MB-231 tumor weights 169±23 mg. The mice were injected with 125I-AbD19384 (11 μg in 200 μl PBS, 100 kBq) in the tail vein. At 24 h post injection (p.i), animals were euthanized with a mixture of ketamine and xylazine followed by heart puncture. Blood and tumors were collected and weighed, and tracer uptake was measured in a gamma well-counter (1480 Wizard; Wallace Oy, Turku, Finland). Radioactivity uptake in the organ was calculated as percent of injected activity per gram of tissue (%ID/g). Tumor-to-blood ratio was calculated as activity/gtumor divided by activity/gblood.
Ex vivo biodistribution of <sup>125</sup>I-AbD19384
In a second group (n=20), used to analyze in vivo binding of 125I-AbD19384 to xenografts with varying CD44v6 receptor densities, approximately (8×106) A431 cells suspended in 150 μl 1:1 cell medium:Matrigel were injected s.c. into the left posterior leg and 10×106 H314 cells (moderate CD44v6 expression) suspended in 150 μl 1:1 cell medium:Matrigel were injected in the right posterior leg. Three weeks after tumor cell injections, experiments were performed. At the time of study, average animal weights were 20.1±1.3 g, A431 tumor weights 219±54 mg and H314 tumor weights 23±3 mg. Twenty mice bearing dual A431 (high CD44v6 expression) and H314 (moderate CD44v6 expression) xenografts received an intravenous injection via the tail vein with 125I-AbD19384 (100 kBq), totally 11 μg F(ab′)2 in 200 μl PBS per mouse. Animals were sub-divided into four groups with five mice in each. At 6, 24, 48 and 72 h p.i. animals were euthanized with a mixture of ketamine and xylazine followed by heart puncture. Blood was collected, and tumors and organs of interest such as salivary glands, thyroid (en bloc with larynx), tongue, heart, liver, kidneys, spleen, urinary bladder, colon, upper gastrointestinal tract, skin, bone and muscle were excised, weighed and measured in a gamma well-counter. The tail and the rest of the body were also measured. Three injection standards were measured for each group. Radioactivity uptake in the organ was calculated as percent of injected activity per gram of tissue (%ID/g). Thyroid was excised en bloc with larynx, and uptake was calculated as percent of injected activity per organ. Tumor to organ ratio was calculated as activity/gtumor divided by activity/gorgan.
In vivo PET/CT and ex vivo biodistribution studies with <sup>124</sup>I-AbD19384
A third group was used to analyze in vivo biodistribution of 124I-AbD19384 (n=12) or 18F-FDG (n=4) in mice with xenografts with varying CD44v6 receptor densities and for PET/CT imaging. Approximately (8×106) A431 cells suspended in 150 μl 1:1 cell medium:Matrigel were injected s.c. into the left posterior leg and 10×106 UM-SCC74B tumor cells (low CD44v6 expression) suspended in 150 μl 1:1 cell medium:Matrigel were injected in the right posterior leg. Tumors were allowed to grow for three weeks before start of experiments. At the time of study, average animal weights were 16.1±1.5 g. A day before conjugate injections, mice were given potassium iodide (1%) in drinking water to block uptake of free 124I in thyroid. Animals were then injected with 124I-AbD19384 (11 μg, 1.5 MBq, in 200 μl PBS per mouse) in the tail vein as a single bolus. As verified with native gel analysis, 17% of injected 124I-AbD19384 consisted of monomers or smaller fragments.
Whole body PET/CT studies of 124I-AbD19384 were performed under general anesthesia (isoflurane 1.0–2.5% in 50%/50% medical oxygen:air at 450 ml/min) at 24, 48 and 72 h p.i. Four additional mice were imaged using 18F-FDG (2.7 Mbq) at 30 min p.i. under general anesthesia. Sedated xenograft animals with pre-injected tracer were placed in the gantry of the small animal PET/CT scanner (Triumph™ Trimodality System; TriFoil Imaging, Inc., Northridge, CA, USA). Whole body PET scans were performed for 80 min in list mode followed by a CT examination for 3 min (Field of View = 8.0 cm). 18F-FDG PET scan was acquired for 60 min. At indicated times, animals were euthanized, and organs removed and measured as described above. The breathing rate was monitored with a camera under controlled anesthesia. Animals were placed on the heated bed of the PET scanner to prevent hypothermia and fastened to prevent large movements during study. 18F-FDG was kindly provided by the Nuclear Medicine Department (Akademiska Sjukhuset, Uppsala, Sweden).
The PET data were reconstructed into a static image using an ordered subset expectation maximization 3-D algorithm (20 iterations). The CT raw files were reconstructed using Filter Back Projection. PET data were reconstructed for attenuation and scatter corrections with their respective CT data. PET and CT dicom files were analyzed using PMOD v3.508 (PMOD Technologies Ltd., Zurich, Switzerland). Volumes of interest were drawn manually on tumors, muscle and left ventricle. The measurement from left ventricle was accounted for blood. Tracer uptake in these organs from PET images is expressed as tissue-to-reference tissue ratio. Blood was used as reference tissue.
After PET/CT measurements, animals were euthanized; blood, tumors and organs of interest were collected and treated as described above for ex vivo biodistribution measurements. For animals injected with 124I-AbD19384 (n=12), A431 tumor weights were 567±61 mg, and UM-SCC74B tumor weights 483±77 mg. For animals injected with 18F-FDG (n=4) A431 tumor weights were 681±210 mg, and UM-SCC74B tumor weights 409±241 mg at the time of experiments.
Statistical analyses
Statistical analyses were performed using GraphPad Prism version 5.02 for Windows (GraphPad Software Inc., La Jolla, CA, USA). For in vivo studies, the differences in uptake between MDA-MB-231/UM-SCC74B tumors and A431 tumors were assessed using a two-tailed t-test and were considered statistically significant at P<0.05. The biodistribution data are presented as mean ± standard deviation (SD). Significant differences between the groups over time were tested with one-way analysis of variance (ANOVA) with Newman-Keuls multiple comparison test. The differences were considered statistically significant at P<0.05. The differences in uptake of 125I-AbD19384 and 124I-AbD19384 between low/medium CD44v6 expressing tumors and high CD44v6 expressing tumors were evaluated using repeated measures ANOVA with Newman-Keuls multiple comparison test and were considered statistically significant at P<0.05.
Discussion
The objective of the present study was to evaluate for the first time the in vitro and in vivo binding properties of the radio-iodinated human bivalent fragment AbD19384 for targeting of CD44v6-expressing tumors, and to assess the utility of Fab-dHLX constructs as targeting agents for molecular imaging. As CD44v6 is overexpressed in a number of epithelial tumors AbD19384 could prove to be valuable as a targeting molecule for a number of cancers, for example HNSCC. To the best of our knowledge, this is the first time a Fab-dHLX construct has been used for in vivo targeting and molecular imaging. Previous in vivo studies using a dHLX construct have, however, assessed the possibility of antibody-mediated toxicity neutralization in mice using Fab-dHLX (16), or scFv-dHLX (17) by pre-incubation of targeting molecule and target with promising results.
In the present study, antigen specificity, binding properties, and interaction analysis of AbD19384 were first assessed in vitro. In vivo specificity and biodistribution of 125I-AbD19384 was then evaluated in tumor-bearing mice using a dual-tumor setup. Finally, AbD19384 was labeled with 124I, and its imaging properties were assessed in mice bearing tumors of both low and high CD44v6 expression using small animal PET/CT and compared to 18F-FDG.
SPR measurements clearly demonstrated in vitro specificity of AbD19384, and an improved apparent affinity compared to the monovalent AbD15179 fragment (Fig. 1). AbD19384 did not bind to the murine v6-peptide. Binding of iodinated AbD19384 conjugates was also followed in real-time in vitro on cultured tumor cells with different CD44v6-expression (Fig. 2A). Results further confirmed the specific binding of AbD19384 to CD44v6. Binding and retention on CD44v6-positive cells was in agreement with SPR measurements, with a slower off-rate for AbD19384 (Fig. 2A) than previously observed for the monovalent AbD15179 conjugate on cultured tumor cells (7,14,18). The impact of labeling method (using chloramine-T or Iodogen) and radiohalogen (125I or 124I) was also assessed in vitro (Fig. 2B). No significant differences between the binding interactions of the different conjugates could be seen, demonstrating that the in vitro binding of the conjugates was not significantly influenced by labeling method or radionuclide in the present study.
In vivo specificity of 125I-AbD19384 was assessed by comparing uptake of 125I-AbD19384 in mice bearing both MDA-MB-231 tumors (CD44v6 negative) and A431 tumors (high CD44v6 expression). Uptake in A431 tumors was shown to be significantly higher (four times higher) than the negative control tumors, confirming the specific binding of AbD19384 to CD44v6 also in vivo. A full biodistribution study of 125I-AbD19384 was performed in mice bearing H314 tumors (medium CD44v6-expression) and high CD44v6-expressing A431 tumors. Biodistribution data were favorable, with a pronounced clearance and decrease in activity over time for most organs, and tumor to blood ratios around five from 48 h p.i. (Fig. 3). The high uptake in thyroid, and initially high uptake in salivary glands and stomach, where Na/I symporters are abundantly expressed, can probably be attributed to radio-catabolites of 125I (19).
Biodistribution of 125I-AbD19384 was similar to the previously observed biodistribution of the monovalent 125I-AbD15179 fragment (18), with a maximum uptake in organs at the first time-point and fast clearance of the conjugate. As seen in Table I, kidney uptake was reduced with ~50% for the bivalent fragment, whereas uptake in liver was only slightly increased. The reduced kidney uptake was expected, since AbD19384 displays a size above the renal threshold, whereas AbD15179 does not (20). However, since the bivalent Fab-dHLX construct is in equilibrium with a smaller fraction of the monovalent form, some monovalent tracers are expected to contribute to the biodistribution. It has previously been hypothesized that this may be an advantage in a tumor targeting setting, where monomers may penetrate tumors better and create effective dimers once at the target cells, due to the increased local concentration of the dimerization domains at the target site (9). In the present study, uptake in A431 tumors of monovalent 125I-AbD15179 (18) was comparable to that of bivalent 125I-AbD19384 at all time-points with no statistically significant difference (Table I). The bivalent fragment could have been expected to exhibit higher tumor uptake due to slower off-rate (21), as seen in the in vitro measurements (Fig. 2), but this was not confirmed in the in vivo studies. Thus, we conclude that both radio-iodinated AbD15179 and AbD19384 are suitable for CD44v6-specific tumor targeting in vivo, where AbD19384 can provide a lower kidney uptake than AbD15179 at similar tumor uptake levels. It is possible that tumor uptake for AbD19384 could be further increased by using a residualizing radiolabel, since a bivalent fragment may trigger an increased level of internalization, which could counteract a lower off-rate in the case of non-residualizing radioiodine label (22).
Due to the favorable biodistribution properties seen in the 125I-AbD19384 study, 124I was selected for an imaging study and AbD19384 was subsequently labeled with 124I and assessed in PET/CT examinations, complemented with ex vivo biodistribution measurements (Figs. 4 and 5). Biodistribution measurements demonstrated more than two times higher uptake (calculated as %ID/g) in high CD44v6-expressing A431 tumors compared to the low CD44v6-expressing UM-SCC74B tumors at all time-points. This was also shown by PET imaging, yielding higher contrast and higher uptake in A431 tumors at all three time-points. Uptake and elimination of 124I-AbD19384 was similar to 125I-AbD19384, with a maximum uptake in all organs at the first time-point and fast clearance of the conjugate. There was no significant difference in A431 tumor uptake between 124I-AbD19384 and 125I-AbD19384 conjugates. However, activity in blood was approximately two times higher for 124I-AbD19384 than for 125I-AbD19384 at 24 h p.i., resulting in a corresponding increase in the blood rich organs such as liver, spleen and kidneys for 124I-AbD19384. Uptake of 124I in thyroid was successfully blocked by adding potassium iodide in the drinking water one day before measurements. Furthermore, radioactivity uptake in salivary glands and stomach was reduced with ~2/3 at 24 h p.i., most probably also a result of blocking. Even though the higher blood activity of 124I-AbD19384 resulted in lower tumor-to-blood ratios than obtained with 125I-AbD19384, A431 tumors were clearly visualized at all time-points, with the best contrast achieved at 48 h p.i. PET/CT images were in line with the biodistribution measurements, and tumor-to-blood ratios calculated from PET images were in very close agreement with the ex vivo data (Table II), further confirming the reliability of the non-invasive in vivo imaging technique.
In order to compare 124I-AbD19384 with standard imaging methods, 18F-FDG was also employed as an imaging agent in PET/CT scans, and data were confirmed by ex vivo biodistribution measurements. There was no clear visualization of the tumors using 18F-FDG. Furthermore, there was no clear discrimination between high CD44v6 expressing A431 tumors and low CD44v6 expressing UM-SCC74B tumors, since 18F-FDG uptake is generally proportional to the metabolic activity in tissues and is not specific to tumor cells. High uptake of 18F-FDG was observed in brown adipose tissue in the examinations (Fig. 5). This highlights one of the potential imaging pitfalls sometimes found also in clinical 18F-FDG-PET during tumor staging (23) and emphasizes the need to complement this method with a more tumor-specific imaging technique.
In conclusion, our results describe for the first time a recombinant human Fab-dHLX fusion protein targeted to CD44v6, that possess high affinity, target specificity and potential for in vivo imaging of tumor biomarkers. This bivalent Fab antibody, engineered from monovalent Fab AbD15179 by subcloning of the Fab gene in fusion with a self-dimerizing helix-turn helix motif, was successfully produced and radioiodinated for molecular imaging of CD44v6 in vivo. Biodistribution and small-animal PET studies demonstrated that 124I-AbD19384 is a promising PET probe for imaging CD44v6 antigen expression in vivo. Furthermore, this proof-of-concept research established the feasibility of using recombinant Fab-dHLX constructs for in vivo imaging of tumor biomarkers. Additionally, Fab-dHLX constructs could be useful in the theranostic nanoplatform setting as a targeting ligand, and with further development of the other components of a successful theranostic agent it could also prove to be a valuable addition to personalized cancer treatment.