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Experimental Therapeutics |
Department of Chemical Engineering and Division of Biological Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139
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ABSTRACT |
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 Top ABSTRACT INTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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INTRODUCTION |
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TopABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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Tumor targeting by antibodies is a complex process that involves circulation and clearance from the bloodstream, diffusion or convection into bulk tumors or micrometastases, binding and release of antigen, and metabolism of antigen/antibody complexes. Mathematical models of these processes have been constructed previously, illuminating many of the important features. Weinstein and colleagues (4, 5, 6) examined antibody penetration of tumor spheroids and emphasized the existence of what was termed a "binding site barrier," a phenomenon whereby high-affinity antibodies penetrate to a limited depth from the tumor surface. Subsequent experimental studies have confirmed the existence of this phenomenon (7, 8, 9) . The bulk tumor microenvironment can also cause additional unexpected hindrances: whereas blood vessels may be more permeable to solute transfer in the tumor (10 , 11) , the tumor in general may be less vascularized (12) . Baxter and Jain (13, 14, 15, 16) have carefully examined the unusual pressure and convection patterns in bulk tumors both experimentally and by mathematical modeling, and have found surprising phenomena such as temporary reverse flows out of tumor tissue.
The first generation of therapeutic antibodies consists of entire IgG molecules, the format naturally utilized by the mammalian immune system. However, protein engineering technologies have been developed for a wide variety of antibody fragments varying in size and valency (17) . These smaller fragments are more highly diffusible and therefore penetrate tumor tissue more rapidly. Furthermore, directed evolution has enabled the engineering of extremely high-affinity antibody fragments, in some cases with dissociation half-times exceeding several days (18 , 19) .
The capability to engineer extremely high-affinity antibody fragments raises questions regarding the potential therapeutic benefits attainable by such improvements. In some instances, experimental biodistribution data indicate limiting returns in targeting as affinity is progressively improved (8 , 20) . What affinity is necessary for maximal tumor targeting? Does increasing affinity progressively reduce tumor penetration, or is a limiting velocity for the antibody front reached? What kinetic processes determine tumor penetration rate and subsequent retention time? What is the minimum bolus dose required to fully saturate tumors with an antibody fragment? These questions are considered here in a mathematical framework, one that captures the effects of binding, diffusion, and antigen metabolism but does not consider convective flow effects present in bulk vascularized tumors. The overall process is parsed into two kinetic phases: a diffusion-limited loading phase; and a metabolism-limited retention phase. In particular, the relative rates of intratumor diffusion versus systemic clearance during a tumor-loading kinetic phase are compared, and the relative rates of antibody/antigen dissociation versus antigen turnover during a tumor retention kinetic phase are compared. Spatial heterogeneity of antibody tumor penetration depends on the first comparison (diffusion versus clearance), whereas the magnitude of tumor exposure to antibody depends on the second (metabolism versus release).
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MATERIALS AND METHODS |
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TopABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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With the following dependent variables: Ab 
unbound antibody concentration/tumor volume (nM); Ag unbound antigen concentration/tumor volume (nM); and B antibody/antigen complex concentration/tumor volume (nM).
And the following independent variables: r distance from the center of the spheroid (µm); and t time (s).
And the following parameters, the range of values examined in Table 1
, and discussed further below: 
fraction of tumor volume accessible to antibody; D diffusivity of antibody in tumor tissue (µm2/s); kon association rate constant (M-1s-1); koff dissociation rate constant (s-1); ke rate constant for degradation of antigen and complex by endogenous metabolism (s-1); and Rs rate of synthesis of new antigen, set equal to keAgt.
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and ß = fractions of and ß pharmacokinetic phase, respectively; and 
and ß = half lives for and ß pharmacokinetic phases, respectively. The numerical solution was obtained with the Absoft Fortran 77 software package using the method of lines (IMSL MOLCH). Accuracy of the numerical solutions was validated by comparison with the analytical solution in the limit of zero antigen and also by comparison with the analytical solution in the limit of infinite diffusivity. Essentially identical solutions were obtained when integration was performed with time steps or radius increments reduced by a factor of two. All solutions were automatically checked for consistency with an overall material balance on total antigen in the spheroid.
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RESULTS |
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TopABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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To examine the broad features of antibody penetration into the spheroid, simulations were first performed with constant surface antibody concentration, in the absence of antigen degradation, for a range of antibody affinities (Fig. 1)
. As described previously, high-affinity antibodies fill a "shell" at the rim of the sphere, and this shell moves progressively towards the center of the sphere. Such a moving front has been directly observed previously by confocal fluorescence microscopy with labeled antibodies permeating spheroids of human tumor cell lines (24, 25, 26)
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, the shell of bound antibody grows until essentially all antigen within the sphere is bound by tumor. The bound antibody front moves inward for as long as free antibody at the tumor surface is not depleted. Hence, the binding site barrier effect is created by a dynamic interaction of pharmacokinetics with diffusion: if plasma antibody concentration drops to negligible levels before the shell front has moved entirely to the center of the sphere, antibodies appear to become "stuck" at a fixed distance from the surface, although actually this boundary is only a freeze frame of a kinetic process terminated upon antibody clearance from the plasma.
Note that the moving boundary for the lowest affinity antibody represented in Fig. 1
(Kd = 10 nM) is the least sharp, suggesting that perhaps lower affinity antibodies could be utilized to obtain more uniform penetration. This possibility was explored computationally for affinities ranging from 1 pM to 1 µM, and the results are represented in Fig. 2
. The constant surface antibody exposure time required for 95% maximal antigen binding drops with decreasing affinity (Kd > 10 nM). Lower affinity antibodies penetrate the tumor more rapidly, but at an unacceptable cost, from a therapeutic perspective: because the affinity is lower, the antibody does not bind antigen to a significant extent. At Kd > 1 µM, very little antigen is bound by antibody, and yet penetration is quite rapid. This tradeoff is intrinsic to the system: antigen binding slows tumor penetration, but antigen binding is necessary to accomplish therapeutic effects. It is important to note that the movement of the sharp, slowly moving front of bound antibody reaches an asymptotic lower speed limit at approximately Kd = 10 nM, and further decrease of Kd does not slow the movement of the front further. In other words, the binding site barrier penalty is fully paid once affinity is sufficiently high for complete antigen binding, and further affinity increases do not incrementally affect the rate of tumor penetration.
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 | (4) |
 | (5) |
radius outside which all antigen is complexed with antibody; R spheroid radius (µm); Agt antigen concentration/tumor volume (nM); fraction of tumor volume accessible to antibody; D diffusivity of antibody in tumor tissue (µm2/s); and Abo bulk antibody concentration at tumor surface (nM).
This simplified SCM model was compared with the exact numerical simulations represented in Fig. 1
. The predicted location of the bound antibody front rc as a function of time is indicated by the vertical dashed lines. This location agrees closely with the antibody shell fronts numerically simulated for antibodies with affinities of Kd = 1 nM or lower, indicating that the SCM approximation is reasonable for the high affinity limit. The validity of the SCM was more rigorously examined by varying simulation parameters across a very broad range and comparing numerically simulated time to full tumor penetration with the SCM approximated value (Fig. 3)
. The agreement between SCM and numerical simulation is remarkably good for saturation times over an hour. The assumption of the SCM derivation (i.e. that diffusion is much slower than binding) is less accurate for parameter values associated with rapid penetration; nevertheless, the SCM reasonably predicts scFv saturation times (within 2-fold) for times of 0.5–1.0 h, a kinetic regime in which the slowness of tumor penetration is not a practical concern.
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= 0.1 (29)
, and D = 14 µm2/s (30)
, the time to saturation tsat is predicted to be 1.7 h, in good agreement with the observed time scale. Kwok et al. (31)
examined uptake of two antibodies by human melanoma spheroids, and the SCM predicts the reported uptake kinetics well (Fig. 4,A and B)
. In another study, Olabiran et al. (32)
measured antibody uptake kinetics into human small cell lung cancer spheroids, and the kinetics are consistent with the SCM prediction (Fig. 4C)
. Olabiran et al. (32)
also noted that when antibody concentration was increased 100-fold over the value represented in Fig. 4C
, antibody penetrated more deeply and diffusely in the spheroid at 4 h, consistent with the scaling reflected in Eq. 5
. Langmuir et al. (33)
examined the effect of antibody concentration on uptake of antibody into spheroids of a human colon adenocarcinoma cell line, and this relationship is reflected in the SCM prediction for these experiments (Fig. 4D)
. It is particularly noteworthy that this agreement between model and experiment is observed with no adjustable parameters, because all of the system constants in Eq. 4 and 5 are independently reported as described in the legend to Fig. 4
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describe intrinsic features of tumor physiology that are generally not accessible to therapeutic manipulation [although antigen expression can be up-regulated somewhat pharmacologically in some instances (34)
]. The value of tsat increases as the square of tumor spheroid radius, increases proportionally to antigen concentration, and decreases with increasing tumor porosity. Choice of a highly abundant tumor antigen for increased delivery of tumoricidal activity proportionally increases the time required for tumor saturation. The two parameters accessible to engineering manipulations are D and Abo. The diffusivity D is a function of antibody size and is approximately inversely proportional to molecular weight (35
, 36)
, so an scFv antibody would be expected to saturate the spheroid six times faster than the corresponding IgG. Finally, saturation time is predicted to be inversely proportional to surface antibody concentration, such that doubling the antibody concentration halves the time to tumor saturation. It should be noted in particular that the affinity constant Kd appears nowhere in the SCM expression for tsat. For conditions well described by the SCM model, tumor penetration speed is independent of binding affinity [note, however, that as affinity is lowered to Kd > 10 nM, the SCM approximation becomes less valid (Fig. 1)
].
Spheroid surface antibody concentration was held constant in all of the simulations presented to this point, conditions clinically achievable by steady i.v. infusion. However, bolus dosing is often practiced with antibodies, and so the effect of antibody pharmacokinetics in the plasma must be considered. First, to what extent can the tsat formalism of the SCM be applied to bolus dosing? With constant surface antibody concentration, the product Abotsat is equal to the time integral of the surface antibody concentration, or AUC (AUCAb,plasma). For single exponential antibody pharmacokinetics in plasma, the corresponding AUC is given instead by Abo/ln2, where is the plasma half-life for the antibody. We explored whether a critical value of AUCAb,plasma would predict tumor saturation values for bolus dosing, and the results are presented in Fig. 5
. Given the simplicity of the SCM formalism, the required bolus AUCAb,plasma is remarkably well predicted for a very broad range of parameter values. Hence, the SCM makes the following experimentally testable prediction regarding the initial bolus dose required to obtain 95% spheroid saturation 
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), if one assumes AgT = 1.67 µM, = 0.28, R = 300 µm, D = 80 µm2/s, = 15 min, and plasma volume = 2 ml, this relationship predicts that a minimum of 65 µg of scFv is required to achieve tumor saturation. This dosage is above the range used in most scFv biodistribution experiments (0.2–20 µg; Tables 1
and 2
). Hence, one should expect some degree of spatial heterogeneity in these studies, as has been directly observed (8)
. For IgG localization, assuming AgT = 1.67 µM, = 0.1, R = 300 µm, D = 14 µm2/s, = 12 h, and plasma volume = 2 ml, Eq. 6
predicts that a minimum of 130 µg of IgG would be required to achieve tumor saturation. This dosage is consistent with the observation that over 1 mg of antitumor antibody is required to saturate tumor uptake in a human melanoma tumor s.c. xenograft in mice (37)
, although in that model system the quantity of tumor antigen in the animal is sufficiently high that stoichiometric considerations may necessitate higher doses than those required to satisfy the diffusion constraints. An early experimental verification of the binding site barrier effect utilized a metastatic disease model in guinea pigs (9)
. In this study, it was noted that "to circumvent poor penetration due to specific binding (or specific binding followed by metabolism), the dose of Ab can be increased," an observation consistent with the scaling relationship in Eq. 6
. Spatial heterogeneity on a length scale of 400–700 µm was observed at low doses (30 µg) 72 h after injection, but with high doses (1030 µg), greater homogeneity was observed. The following parameter estimates were obtained directly from the reported data for this system: AgT = 590 nM, = 0.1, D = 15 µm2/s, = 20 h, and plasma volume = 35 ml. For a micrometastasis 300 µm in radius, the minimum bolus size required for saturation is calculated from Eq. 6
to be 450 µg, consistent with the improvement in homogeneity of antibody penetration upon increasing dosage from 30 to 1030 µg. By rearranging Eq. 6
, one can alternatively calculate the maximum size of micrometastasis saturable at each dose: 80-µm radius at 30 µg, and 450-µm radius at 1030 µg. These results are also qualitatively consistent with the reported spatial distributions.
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The time course of tumor antibody exposure is divisible into two qualitatively distinct kinetic phases: (a) uptake by passive diffusion and binding, as just described; and (b) retention of bound antibody in the tumor, which will now be considered. Simulations were performed with time-varying antibody surface concentrations according to single exponential clearance pharmacokinetics, and antigen degradation was incorporated into the model (i.e., ke 
0 in Eqs. 2 and 3
). The results are shown in Fig. 6
as a function of antibody affinity. The qualitative shapes of bound antibody profiles within the spheroid are represented above the plot. As the bound antibody front penetrates the sphere, one obtains a heterogeneous SCM-like distribution. However, after tumor saturation, the decrease in bound antibody occurs more uniformly throughout the tumor. Thus, the overall process can be broken into two distinct kinetic phases: (a) tumor uptake, dominated by diffusion and well described by the SCM; and (b) tumor retention, dominated by antigen turnover rate, as demonstrated below.
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. Although one would not necessarily expect a linear relationship between AUCtumor and tumor cell killing, one generally expects a monotonic relationship, such that increased antibody exposure kills more tumor cells. Expansion of this pharmacodynamic relationship for the various different potential payloads (radioisotopes, prodrug-cleaving enzymes, Fc-mediated cell killing, and so forth) is beyond the scope of this paper but is considered further in "Discussion."
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, note that AUCtumor increases markedly when affinity is increased from 10 nM to 1 nM, less so for an increase from 1 nM to 100 pM, and almost negligibly for a 100-fold further improvement of affinity to Kd = 1 pM. Note also that the antibody versus time curves are bounded by the curve for antigen degradation. This correlation is indicative of the limiting process in tumor retention, antigen turnover. Put into words, this kinetic limit states that there is no incremental benefit to binding to an antigen after it has been metabolized, if bound antibody is metabolized with it.
AUCtumor was calculated for antigens demonstrating a broad range of stabilities to demonstrate the limiting role for antigen turnover (Fig. 7)
. Physiologically, target antigens can be internalized or shed at significantly different rates. Growth factor receptors such as EGFR and ErbB2 are constitutively endocytosed with a half-time of approximately 15 min (38
, 39)
. A number of other tumor surface antigens have been shown to turn over with much slower half times of 1–5 days (40)
. CEA is cleared by a shedding mechanism that exhibits half-times of 3–15 days in cell culture (41
, 42)
. AUCtumor was simulated as a function of both the antibody affinity and antigen stability (Fig. 7)
. For an antigen with a half-life of 2.4 h, an affinity improvement from 1 nM to 1 pM (1000-fold) leads to a rather disappointing 2-fold increase in the dose delivered to the tumor. Conversely, an antigen with a half-life of 10 days will result in a 50-fold increase in the therapeutic dose delivered to the tumor for the same 1000-fold affinity improvement. It can be seen that the benefits of engineering high affinity are directly related to the antigen stability, such that targeting an antigen with a fast internalization or shedding rate will show little incremental benefit from large improvements in affinity.
Model Validation with Xenograft Biodistribution Data.
To test the ability of the model to predict results for in vivo testing of antibodies, several published experimental studies were selected for comparison. The purpose of comparing model calculations with experimental data in this instance is to qualitatively confirm the time scales and trends in tumor localization as a function of antibody affinity and antigen turnover. The model follows spheroid uptake only, with surface antibody concentration specified as a boundary condition based on the reported plasma pharmacokinetics. Consequently, no prediction of localization (%ID/g) is possible because a compartmental physiological pharmacokinetics model was not implemented. Fractional tumor antigen saturation with antibody is not easily measured and is therefore most generally not reported; however, this number can be calculated with the model. Because fractional tumor antigen saturation is proportional to %ID/g, these two variables, respectively calculated and measured, will be compared.
The great majority of tumor targeting studies have examined localization to bulk vascularized tumors, rather than micrometastases. However, transport in the extracellular matrix of bulk tumors generally occurs solely by diffusion because convection is negligible in the absence of draining lymphatics (23) . As such, these simulations are intended to capture the characteristic time scales for diffusion across length scales of 50–300 µm, which encompasses the length scales between blood vessels in tumor vasculature. For example, for a human adenocarcinoma grown in the dorsal skinfold of mice, half of the points within tumor tissue are within 20 µm of a capillary, and essentially all points are within 200 µm of a capillary (43) . Experimental data for bulk tumors therefore reflect some averaging across multiple length scales in the range 0–200 µm. Although the geometry and pressure and flow fields of entire tumors can be complex and quite different from these simplified simulations, the particular time scales necessary for diffusion at short length scales should be qualitatively well described by this model.
There is an extensive literature on experimental studies of antibody penetration of tumors. A number of qualitative or semiquantitative analyses of such reports can be performed, as described above. For several studies, however, sufficient in-depth characterization has been performed to enable simulation of the time course of antibody penetration into tumor spheroids without resorting to any adjustable parameters. Four such studies are examined here in Table 2
and Figs. 7
8
9
, for targeting of ErbB2, EGFRvIII, and CEA.
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. For the simulation, the level of antibody retained in the tumor over time increases with increasing affinity up to a Kd = 1 nM (Fig. 8)
. By taking the simulation value at 24 h, this can be compared with experimentally measured %ID/g (Fig. 8)
. There is strong qualitative agreement between the simulated and experimental data. For both cases, tumor localization increases up to a Kd 
1 nM, where the value plateaus with further affinity improvement. This result can be interpreted by examining the biological properties of the targeted antigen. ErbB2 is constitutively internalized at a rate of 6.67 x 10-4 s-1 (1/2 = 17 min; Ref. 38
), such that engineering antibodies to bind with a half-life greater than 17 min would be of no advantage if the antibody dissociates from antigen at endosomal pH and is degraded with subsequent release of iodotyrosine from the tumor. Thus, the two higher affinity antibodies, Kd = 120 pM (1/2 = 3 h) and Kd = 15 pM (1/2 = 15 h), are predicted to localize no better than the antibody with a dissociation constant of 1 nM (1/2 = 15 min). An experimental prediction based on this result is that SK-OV3 cells in culture will internalize the highest affinity scFvs with a half-time of approximately 15 min under growth conditions mimicking those in vivo and that internalized iodinated scFvs will be degraded to small diffusible products that exit the tumor cells. It is also predicted that tumor localization will be 10-fold higher at 30 min after bolus injection than at 24 h. As mentioned above, a bolus of 65 µg of scFv is predicted by the SCM to be required for tumor saturation, whereas the reported experiments utilized 20-µg boluses.
The second paper studied two scFvs with a 15-fold difference in affinity (44)
. These antibodies targeted an epitope on EGFRvIII. Experimental conditions selected from the paper to be used in the simulation are summarized in Table 2
. In this study, %ID/g was measured at five time points for both of the antibodies. Once again, there is good correlation between the simulated results and those measured in the biodistribution study (Fig. 9A)
. Tumor localization of the higher affinity antibody is predicted to be approximately double that for the lower affinity antibody, consistent with the results shown. Note that tumor localization at 1 h is 10-fold higher than that at 24 h, as predicted for the analogous erbB2-targeted scFvs. In this particular study, the antibody was injected directly into the tumor, which likely accounts for the much higher tumor retention (%ID/g) than that attained with the scFvs that targeted erbB2 (8)
. Nevertheless, the model predicts that only 10–25% of available antigen is saturated with scFv at the peak time of 0.5 h, due to the low bolus size (2 µg).
The final two papers investigated several antibody fragments targeting CEA. Wu et al. (45)
studied two scFvs constructed from the same monoclonal antibody (T84.66), but with amino acid linkers of different lengths connecting the variable fragments. T84.66/C28 was connected by a 28-amino acid linker (VH-linker-VL orientation; Kd = 0.45 nM), and T84.66/212 was connected by a 14-amino acid linker (VL-linker-VH orientation; Kd = 0.24 nM). Turnover of CEA is largely by a shedding mechanism rather than endocytic internalization. The rate of shedding can be estimated from published reports on human colorectal (41)
and medullothyroid (42)
tumor cell lines, and calculated shedding half-lives ranged from 3 to 15 days. The fate of shed CEA/antibody complex depends on the location within the tumor: at the surface, release to plasma is likely; whereas shed CEA in the center of the spheroid diffuses very slowly to the spheroid surface. A CEA metabolic half-life of 1 day was simulated, and qualitative agreement between model and simulation was obtained. Peak tumor localization was at 1 h for scFv T84.66/212 and under 1 h for T84.66/C28 comparable to 0.5 h predicted by the model (Fig. 9B)
, and corresponds to only 10% of antigen saturation for the bolus dose of 0.3–0.5 µg of scFv reported.
Cooke et al. (46)
examined the tumor targeting properties of a single chain antibody fragment/tumor necrosis factor fusion protein (46)
. This fusion protein forms a trimeric structure of Mr 144,000, approximately the same size as a full IgG antibody molecule. The fusion protein was radiolabeled with 125I, and %ID/g was measured at 3, 6, 24, and 48 h after injection. Experimental conditions selected from the paper to be used in the simulation are summarized in Table 2
. As compared with the other simulated data sets, the larger antibody fragment in this study reaches maximal saturation at a later time point (
6 h versus 30 min for the scFvs), as expected due to slower diffusion and slower clearance. The model captures this shift in peak antibody localization time (Fig. 9C)
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DISCUSSION |
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TopABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
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The dynamic processes of antibody uptake and retention in tumor spheroids have been analyzed here as two distinct kinetic phases, and tumor localization was predicted by consideration of the pertinent characteristic time scales for the key processes in each phase (see Table 3
). Note that the characteristic time for binding equilibration is always faster than the diffusive timescale tsat, consistent with the central assumption of the SCM. In the tumor loading phase, a front of bound antibody moves toward the center; if the antibody is cleared from circulation before tumor saturation, the spatial heterogeneity previously termed a "binding site barrier" is observed. The existence of such heterogeneity can be predicted by comparison of the plasma clearance characteristic time to the diffusion characteristic time tsat, which can be reduced by increasing antibody bolus dose (Eq. 5)
. Consequently, the binding site barrier phenomenon can be eliminated by increasing antibody levels, as shown previously (9)
. In the second kinetic phase, tumor retention is determined by the relative rates of antigen turnover and antibody/antigen complex dissociation. The importance of turnover kinetics in antigen selection is highlighted in Fig. 7
. For highly stable antigens, engineering high-affinity antibodies could increase AUCtumor over an order of magnitude, which should translate into greater efficacy in radioimmunotherapy and prodrug therapies. By contrast, for rapidly turned over antigens such as ErbB2, substantially diminished returns are attainable by antibody engineering, as has been demonstrated previously (8)
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A key prediction of the SCM is that higher bolus doses of scFvs will overcome tumor uptake spatial heterogeneity (Eq. 6)
. The doses used in the experimental reports examined here ranged from 0.3–20 µg/mouse, yet the SCM predicts that doses >65 µg will be required to achieve tumor saturation. Given the simplifying assumptions of the SCM, this should be considered an underestimate of the required dosage. For example, even if the model assumptions are correct, the SCM overpredicts tumor penetration (Fig. 5)
. Furthermore, no consideration was made in the model for either a capillary extravasation barrier or diffusion through stromal tissue, both of which would increase the scFv bolus size required to penetrate a spheroid. At sufficiently high antibody boluses, collateral toxicity could become limiting, necessitating a pretargeting approach.
Most biodistribution studies utilize 125I-labeled tumor-targeting scFvs and resection and gamma counting of bulk xenografted tumors. Is it reasonable to expect the qualitative consistency observed in Figs. 7
8
9
between these complex experimental systems and a simplified tumor spheroid simulation that neglects convection and geometric irregularities? The observed consistency can be rationalized if two assumptions are satisfied: (a) diffusion in the tumor interstitium between blood vessels is slower than transport across the microvascular wall; and (b) the length scale for diffusion between tumor blood vessels is similar to spheroid length scales. The first assumption is consistent with the general absence of convection within the interstitium and the leakiness of tumor vasculature to macromolecules (12)
. The second assumption is supported by measurements of the distribution of length scales in fractal tumor capillary networks (39)
. Hence, the tumor spheroid simulations can be considered more broadly to represent a description of binding and diffusion processes in tumor tissue at length scales of 50–300 µm. Consequently, qualitative agreement with the reported experimental results (Figs. 8
and 9)
is not unreasonable.
These analyses provide recommendations for development of tumor-targeting agents. The analyses presented here lead to a description of the following attributes of an optimal tumor-targeting molecule for attainment of maximal AUCtumor: (a) minimum molecular weight, so as to increase diffusivity. scFv fragments represent a 6-fold improvement in penetration speed over IgG; (b) a slowly metabolized, highly expressed antigen. This criterion may be at cross purposes with selection of antigens for biological response modification, such as erbB family members, which are rapidly metabolized; (c) antibody/antigen dissociation kinetics slower than antigen turnover kinetics. Directed evolution of extremely high affinity can satisfy this criterion, as can engineering of multivalent constructs that utilize avidity to decrease dissociation rate (20) ; and (d) bolus dosage at the minimum value predicted by Eq. 6 to saturate tumor while minimizing healthy tissue exposure. Slow clearance of IgGs can substantially reduce the bolus dose required for tumor saturation (Eq. 6) but can also reduce therapeutic index by lengthening exposure to vulnerable healthy tissues.
The analyses presented here may aid in the design of improved tumor targeting antibody fragments. Experimental testing of these predictions will help elucidate whether additional processes, other than simple diffusion and binding, exert dominant effects on tumor penetration by antibodies.
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ACKNOWLEDGMENTS |
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FOOTNOTES |
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1 Supported by a Koch cancer seed grant and by NSF Biotechnology Process Engineering Center. 
2 To whom requests for reprints should be addressed, at Department of Chemical Engineering and Division of Biological Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Room 66-552, Cambridge, MA 02139-5766. Phone: (617) 253-4578; Fax: (617) 258-5766; E-mail: wittrup{at}mit.edu
3 The abbreviations used are: SCM, shrinking core model; AUC, area under the curve; EGFR, epidermal growth factor receptor; CEA, carcinoembryonic antigen; %ID/g, percentage injected dose per gram of tumor.
Received 9/26/02. Accepted 1/17/03.
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A. Nguyen, A. E. Reyes II, M. Zhang, P. McDonald, W. L. T. Wong, L. A. Damico, and M. S. Dennis The pharmacokinetics of an albumin-binding Fab (AB.Fab) can be modulated as a function of affinity for albumin Protein Eng. Des. Sel., July 1, 2006; 19(7): 291 - 297. [Abstract] [Full Text] [PDF]
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C. P. Graff, K. Chester, R. Begent, and K.D. Wittrup Directed evolution of an anti-carcinoembryonic antigen scFv with a 4-day monovalent dissociation half-time at 37{degrees}C Protein Eng. Des. Sel., April 1, 2004; 17(4): 293 - 304. [Abstract] [Full Text] [PDF]
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) or 10 nM (
). Agt = 2.5 µM (from estimated 1–2 x 106 binding/sites/cell.) R = 300 µm.
)] and MR1-1 [Kd = 1.5 nM (
)]. C, simulated results were compared to data from Cooke et al.