Patent Application
20130011381
This invention relates to an improved enzyme, β-glucuronidase, having an improved half-life in the circulation of a mammal such that the treatment of mucopolysachamidosis is improved by intravenous infusion of the mammal with said enzyme.
Many mucopolysachamidosis (MPSw) disorders, including MPS VII, show evidence of significant storage of glycosaminoglycans in the lysosomes of different cell types in the brain as well as in the visceral organs (1). The currently accepted treatment for some of these diseases, referred to as enzyme replacement therapy (ERT) relies on intravenous infusion of recombinant enzyme into the patient. This method of treatment has successfully cleared storage material from visceral organs and resulted in clinical improvement in these lysomal storage diseases (LSDs) (2-5). Unfortunately in these cases little to no infused enzyme has been able to cross the blood brain barrier (BBB) so limited or little improvement has been achieved in the central nervous system (CNS) (6).
When enzyme was infused into newborn mice, considerable enzyme was delivered to brain, and CNS storage was reduced (7-9). However, brain storage was resistant to clearance if ERT was begun after 2 weeks of age. Recent studies indicated that this enzyme delivery to the CNS in the newborn period was caused by mannose 6-phosphate receptor (M6PR)-mediated transcytosis (10). Down-regulation of this receptor by age 2 weeks appeared to explain the resistance of brain to ERT in the adult. Recently, efforts were made to improve the delivery of β-glucuronidase to the brain in the MPS VII mouse model (11). These studies have shown that increasing the dose of enzyme, which results in slower clearance from the circulation, slightly enhanced the delivery to the brain (12-14). Also infusing mice deficient in the mannose receptor increased the amount of time the enzyme stayed in the circulatory system (15). To account for enzyme delivery to adult brain, it was speculated that increasing the enzyme dose saturated the clearance receptors and slowed clearance of the enzyme from the circulation, resulting in more delivery to the brain (11, 15), or clearing CNS storage after multiple infusions of large doses of corrective enzyme (12-14).
Whether the high circulating levels of enzyme were required for delivery by receptors that were less abundant in adults than neonates or exposure to high circulating levels of enzyme led to delivery by another route is an important question. To address this question, we analyzed ERT in MPS VII mice that were mannose receptor (MR)-deficient (15). When GUS was infused into MR-deficient MPS VII mice, the enzyme clearance was indeed prolonged, although considerably less than expected, because of efficient clearance by hepatic M6PR (11, 15).
Novel modified lysosomal enzymes and methods of their use in the treatment of mammals afflicted with LSDs have now been discovered. Such modified enzymes have increased half-life in the circulatory system resulting in improved treatment of LSDs. Such modification chemically inactivates the oligosaccharides on the lysosomal enzymes thereby inactivating traditional recognition markers on the enzyme that mediates their rapid clearance from the circulation system as will be further described below.
In order to slow down the clearance of β-glucuronidase after infusion into the circulatory system of a mammal, the oligosaccharides on the glycoprotein are chemically inactivated by treating the β-glucuronidase sequentially with sodium-meta-periodate and sodium borohydride. This treatment inactivates the two traditional recognition markers on the enzyme that mediate its rapid clearance from the circulation by means of the mannose and mannose 6-phosphate receptors. This in effect increases the half-life in the circulation from 11 minutes for the untreated enzyme (GUS) to 18.5 h for the periodate/borohydride treated enzyme (PB-GUS, also known in the art as PerT-GUS). The efficacy of these enzymes was determined in a 12-week ERT experiment in which MPS VII mice were treated with weekly infusions of GUS vs. PB-GUS at doses of 0, 2 mg/kg and 4 mg/kg body weight. A slight improvement was observed in the amount of storage material in the cortical neurons in the brains of mice treated with 4 mg/Kg. There was a remarkable clearance of 95% of storage from the cortical neurons in the brains of mice treated with both 2 mg/kg and 4 mg/kg of PB-GUS. Also, there was observed significant continued clearance of storage material from the visceral organs from mice treated with both types of enzyme at both doses of 2 and 4 mg/kg body weight.
These results seem to indicate that slowing the clearance and maintaining high concentrations of β-glucuronidase in the circulation after infusion facilitates delivery of the enzyme across the BBB by some mechanism. Since the mannose and mannose 6-phosphate delivery systems have been inactivated as a result of the periodate treatment, this delivery must be mediated by some other method. One possible method would be by increased fluid-phase pinocytosis, a mechanism that would be greatly enhanced by maintaining high levels of enzyme present for long periods of time in the circulation. Whatever the mechanism is, use of the periodate-treated enzyme shows great promise for treating the brain in MPS VII and any of the other lysosomal storage diseases where there is brain pathology. This method may also be extended for use for other glycoproteins where rapid clearance from the circulation by the mannose or mannose 6-phosphate delivery systems hinders their therapeutic effect.
Accordingly, in one aspect the invention is directed to a composition useful in enzyme replacement therapy, the composition comprising a lysosomal storage enzyme treated with a chemical to inactivate carbohydrate moieties on the enzyme, such that the lysosomal enzyme is not readily taken up by a target cell by the mannose and mannose 6-phosphate delivery systems. A preferred chemical-to-inactivate is a periodate followed by treatment with a borohydride. A preferred MPS enzyme is β-glucuronidase. It is preferred to employ any suitable alkali metal periodate and alkali metal borohydride. The preferred alkali metal is sodium.
In another embodiment, the invention is directed to a method of treating a patient having a lysosomal storage disease comprising administering to the patient a therapeutically effective amount of a composition comprising a medically suitable excipient and a lysosomal enzyme treated with a chemical to inactivate carbohydrate moieties on the enzyme, such that the enzyme is not readily taken-up by a target cell by the mannose and mannose 6-phosphate delivery systems. A preferred treatment is with a periodate followed by treatment with sodium borohydride. A preferred MPS enzyme is β-glucuronidase which is effective to treat lysosomal storage disease preferably MPS VII (Sly syndrome).
In summary, there has been discovered a means to successfully treat GUS with periodate and borohydride without significantly reducing the enzymatic activity or stability. The treated protein has been shown to have modified carbohydrate that no longer has functional recognition signals for mannose and mannose 6-phosphate receptors. Because of this, the enzyme exhibits a vastly increased half-life in the circulation after intravenous infusion. This increased availability results in the improved delivery of the enzyme across the BBB by some unknown mechanism. Whether it is increased opportunity for fluid phase pinocytosis or some other “leakiness”, the enzyme, once it has crossed the BBB, has increased access to cells in the brain. It is then able to use its enzymatic activity to clear accumulated storage material in the cells and hopefully reverse the progression of the disease MPS VII.
While not wishing to be bound by any particular theory, the use of periodate treated enzyme shows great promise for treating the brain in MPS VII and any of the other lysosomal diseases where there is brain pathology. This method can reasonably be extended for use with other glycoproteins where rapid clearance from the circulation hinders their therapeutic effect. Any number of lysosomal enzymes are included within the scope of this invention. Examples of such enzymes are heparin N-sulfatase for treatment of MPS III (Sanfillipo A), hexosaminidase A for treatment of Tay-Sachs disease, α-L-iduronidase for treatment of MPS I Hurler Syndrome), palmitoyl thiotransferase (PPT1) for Batten's disease (CLN1), α-glucosidase for Pompe disease, N-acetyl-galactosamine-6-sulfatase for MPS IVA and β-galactosidase for MPS IVB (Morquio disease A and B), and N-acetylgalactosamine 4-sulfatase for MPS VI (Maroteaux-Lamy syndrome). Other enzymes can be easily envisioned by those of ordinary skill in view of this disclosure and are included within the scope of this invention. The enzymes disclosed herein when modified in accordance with this invention are therapeutically effective to treat various diseases. The effective amount of such modified enzymes can be easily determined by simple testing. However the term “effective amount” as used herein is intended to mean that amount which will be therapeutically effective to treat the disease. Such amount is generally that which is known in the art for the use of such enzymes to therapeutically treat known diseases.
Using DNA cloning techniques, the cDNA sequence encoding the full length cDNA for human β-glucuronidase was subcloned (Genbank Accession # NM—000181) (
This plasmid was introduced into the Chinese hamster ovary cell line, CHO-K1 (34) by electroporation (30). After selection in growth medium consisting of Minimal Essential Medium+35 μg/ml proline+15% fetal bovine serum (FBS)+400 μg/ml G418, colonies were picked and grown to confluency in 48-well plates. High level expressing clones were identified by measuring GUS activity secreted into the conditioned medium from these clones. The highest-producing clone was scaled up and secreted enzyme was collected in protein-free collection medium PF-CHO. Conditioned medium collected in this way was pooled, centrifuged at 5000×g for 20 min and the supernatant was collected and frozen at 20° F. until sufficient quantities were accumulated for purification.
GUS activity was measured using the 10 mM 4-methyl-umbelliferyl β-D-glucuronide as substrate in 0.1M sodium acetate buffer pH 4.8, 1 mg/ml crystalline BSA as previously described (31).
β-glucuronidase was purified by two different methods. The first method was by a multi-step procedure using conventional column chromatography. The second method utilized an anti-human β-glucuronidase monoclonal antibody affinity resin followed by a desalting step. The complete procedures for both methods are outlined below.
A: Ultrafiltration: YM-100 membrane; Diafiltrate with 20 mM NaPO4+150 mM NaCl+0.025% NaN3 @ pH 5.5; (2×2.25 L).
B: Blue SEPHAROSE™ FF (GE Healthcare—Separation-Pharmacia-Agarose): Equilibrate 10× column volume column with 20 mM NaPO4 @ pH 5.5; Load concentrate from ultrafiltration (don't adjust pH, range: 5.5-5.7); Wash 10× column volume with 20 mM NaPO4+150 mM NaCl @ pH 5.5; Elute column with 10 mM NaPO4+800 mM NaCl @ pH 7.5; Regeneration: Wash with 10× column 20 mM NaPO4 @ pH 5.5+2M NaCl.
C: Phenyl SEPHAROSE™ (High Sub FF—Separation-Pharmacia-Agarose); Equilibrate 30× column volume with 10 mM NaPO4+1000 mM NaCl @ pH 8.0; Load pooled blue elute as is (don't adjust pH, range: 7.2-7.4); Wash 10× column volume with 10 mM NaPO4+1000 mM NaCl @ pH 8.0; Elute column with 10 mM Tris+1 mM Na-β-Glycerophosphate @ pH 8.0; Dialyze elution with 3 changes of 10 mM Tris+1 mM Na-β-glycerophosphate @ pH 8.0; Regeneration: Wash with 0.5 M NaOH, 30 min contact time; Wash with 30 column volumes of ddH2O.
D: DEAF Sephacel: Equilibrate 10× column volume with 10 mM Tris+1 mM Na-β-glycerophosphate @ pH 8.0; Load pooled dialyzed Phenyl elute. Wash 10× column volume with 10 mM Tris+1 mM Na-β-glycerophosphate @ pH 8.0; Elute with 0-0.4M NaCl gradient; Dialyze DEAE pooled eluate in 25 mM Na Acetate+1 mM Na-β-glycerophosphate; +0.025% NaN3 @ pH 5.5; Regeneration: Wash with 20× column volume 10 mM Tris+1 mM Na-β-glycerophosphate @ pH 8.0+2 M NaCl.
E: CM SEPHAROSE™ (Separation-Pharmacia-Agarose): Equilibrate 10× column volume with 25 mM Na Acetate+1 mM Na-β-Glycerophosphate+0.025% NaN3 @ pH 5.5; Load dialyzed DEAE pooled eluate; Elute with 0-0.3M NaCl gradient. Regeneration: Wash with 20× column volume 25 mM Na Acetate+1 mM Na-β-Glycerophosphate+0.025% NaN3 @ pH 5.5+2M NaCl.
Affinity chromatography procedure was performed essentially as follows: Conditioned medium from CHO cells overexpressing the GUS protein was filtered through a 0.22μ. filter. Sodium chloride (crystalline) was added to a final concentration of 0.5M, and sodium azide was added to a final concentration of 0.025% by adding 1/400 volume of a 10% stock solution. The medium was applied to a 5 ml column of anti-human β-glucuronidase-Affigel 10 (pre-equilibrated with Antibody SEPHAROSE™ (Separation-Pharmacia-Agarose) Wash Buffer: 10 mM Tris pH 7.5, 10 mM potassium phosphate, 0.5 M NaCl, 0.025% sodium azide) at a rate of 25 ml/h at 4° C. The column was washed at 36 ml/h with 10-20 column volumes of Antibody SEPHAROSE™ (Separation-Pharmacia-Agarose) Wash Buffer. The column was eluted at 36 ml/hour with 50 ml of 10 mM sodium phosphate pH 5.0+3.5 M MgCl2. Fractions of 4 ml each were collected and assayed for GUS activity. Fractions containing the purified protein were pooled, diluted with an equal volume of P6 buffer (25 mM Tris pH 7.5, 1 mM β-glycerophosphate, 0.15 mM NaCl, 0.025% sodium azide) and desalted over a BioGel P-6 column (pre-equilibrated with P6 buffer) to remove the MgCl2 and to change the buffer to P6 buffer for storage. GUS protein was eluted with P6 buffer, fractions containing GUS activity were pooled and the final pool assayed for GUS activity and protein. Purified GUS was stored frozen at −80° C. in P6 buffer for long-term stability. For mouse infusions, the enzymes were highly concentrated in Centricon YM-30 concentrators and the buffer was changed to P6 Buffer without azide. These concentrates were frozen in small aliquots at −80° C. until use.
GUS is a 300 kDa protein that exists as a homotetramer consisting of four identical monomers of apparent molecular weight of 75 kDa. The purified recombinant GUS used in these experiments was similar to that described (11, 19). The apparent molecular mass of the enzyme monomer was 75 kDa on reducing SDS-PAGE. The tetrameric enzyme had a molecular mass of ≈300 kDa when analyzed by sizing gel filtration chromatography (data not shown). The specific activity of the purified enzyme was 5.0×106 units/mg. The Kuptake was 1.25-2.50 nM, calculated from uptake saturation curves by using human MPS VII fibroblasts in which the uptake is almost entirely M6PR-dependent. To confirm molecular weight, 2 and 4 μg of purified GUS were analyzed by SDS-PAGE under reducing conditions (35). The apparent molecular weight was 75 kDa as expected.
The following examples are presented to illustrate the instant invention and are not meant to limit the scope of the invention to these particular examples. The skilled artisan, in the practice of this invention, will readily and reasonably understand that the methods and compositions are applicable to any and all enzymes and proteins that gain entry into a cell via the mannose and mannose 6-phosphate pathways.
The mannose and manose 6-phosphate recognition sites on GUS are both located in the carbohydrate portion of GUS enzyme. In order to inactivate this carbohydrate moiety, the enzyme was treated by a well established procedure utilizing reaction with sodium meta-periodate followed by sodium borohydride (17, 18). Approximately 10 mg of purified GUS was treated with a final concentration of 20 mM sodium meta-periodate in 20 mM sodium phosphate, 100 mM NaCl pH 6.0 for 6.5 h on ice in the dark. The reaction was quenched by the addition of 200 mM final concentration ethylene glycol and incubated for an additional 15 mM on ice in the dark. Afterwards, this mixture was dialyzed against 2 changes of 20 mM sodium phosphate, 100 mM NaCl pH 6.0 at 4° C. The periodate treated, dialyzed enzyme was then treated with the addition of 100 mM final concentration sodium borohydride overnight on ice in the dark to reduce reactive aldehyde groups. After this treatment, the enzyme was dialyzed against two changes of 20 mM sodium phosphate, 100 mM NaCl, pH 7.5 at 4° C. The final dialyzed enzyme was stored in this buffer at 4° C. where it was stable indefinitely.
Treatment of GUS with periodate and borohydride resulted in only a slight inactivation of the enzymatic activity. The specific activity prior to treatment was 5.0×106 units/mg and following treatment was 4.5×106 units/mg.
To assess the effectiveness of the periodate and borohydride treatment in inactivating the carbohydrate on the enzyme, the ability of the enzyme to be taken up by human β-glucuronidase deficient fibroblasts or by the permanent J774E mouse macrophage line was analyzed. M6PR-mediated uptake was determined by adding 4,000 units of GUS or PB-GUS±2 mM M6P in 1 ml of growth medium to 35-mm dishes of confluent GM-2784 GUS-deficient fibroblasts. After incubation at 37° C. and 5% CO2 for 2 h, the cells were cooled on ice, washed five times with cold PBS, then solubilized in 0.5 ml of 1% sodium deoxycholate. Extracts were assayed for GUS activity and protein. Values were expressed as units of enzyme taken up per mg of cell protein per hour of uptake.
MR-mediated uptake was measured by adding 10,000 units of GUS or PB-GUS±1.7 mg/ml yeast mannan (Sigma-Aldrich) in 1 ml of growth medium to 35-mm dishes of confluent J774E mouse macrophages (33). After incubation at 37° C. and 5% CO2 for 4 h, the cells were washed as above and then solubilized in 1 ml of 1% sodium desoxycholate and assayed for GUS activity.
Table 1 below shows the M6P-receptor mediated uptake of untreated or mock-treated GUS by the human fibroblast cell line. GUS is taken up by this line at the rate of 377 units/mg cell protein/1 h of uptake. Two mM M6P completely inhibits this uptake. In contrast, the uptake of the periodate and borohydride treated GUS (PBGUS) has been completely destroyed. Table 2 below shows that untreated GUS is taken up by the mouse macrophage line at a rate of 316 u/mg cell protein/1 h of uptake and the uptake is inhibited by the presence of 1.69 mg/ml yeast mannan. In contrast, three separate batches of periodate and borohydride treated GUS (PBGUS) have essentially no uptake by this cell line.
Since both mannose 6-phosphate and mannose receptor mediated uptake are dependent on functional mannose 6-phosphate or mannose residues, respectively, these results indicate that the periodate and borohydride treatment of GUS (PB-GUS) has inactivated the carbohydrate structures on the enzyme.
The carbohydrates on glycoproteins often confer enhanced thermal stability, and removal of oligosaccharide chains often destabilizes glycoproteins (21). Human GUS has been shown to be relatively stable to thermal inactivation at 65° C. (22-26). Purified GUS or PB-GUS was diluted in equal volumes of heat inactivation buffer [40 mM Tris-HCl (pH 7.5), 150 mM NaCl, 10 mg/ml BSA], and aliquots were incubated for 0, 0.5, 1, 2, or 3 h at 65° C. After treatment, aliquots were cooled on ice and then assayed for GUS activity. Results were expressed as the percentage of original units of GUS activity remaining at the indicated times. As shown in
To compare the stability of GUS and PB-GUS in lysosomes of living cells at 37° C., a study was conducted to determine their half-life after uptake by MPS VII fibroblasts. The low rate of endocytosis of PB-GUS by fibroblasts required exposure to 100,000 units/ml PB-GUS per plate for 48 h to accumulate sufficient enzyme by fluid phase pinocytosis (28 units per plate) to allow measurement of its half-life. By contrast, fibroblasts exposed to 500 units/ml M6P containing native GUS for 48 h contained 228 units per plate. Tissue culture dishes (35 mm) of confluent GM-2784 GUS-deficient fibroblasts were incubated with 500 units of GUS or 100,000 units of PB-GUS in 1 ml of growth medium at 37° C. and 5% CO2 for 48 h under sterile conditions. The plates were washed twice with sterile growth medium and then fed with 2 ml of the same. Duplicate plates were taken off at 0, 2, 5, 7, 14, and 21 days, washed five times with PBS and frozen at −20° C. Remaining plates were fed twice weekly with 2 ml of growth medium. After all plates had been collected, the cells were solubilized in 0.5 ml of 1% desoxycholate and assayed for GUS activity. Values were expressed as percentage of zero time cell-associated GUS activity remaining at the indicated time points.
As stated previously, the purpose of treating GUS with periodate and borohydride, was to drastically slow its clearance time from the circulation after infusion. To test this, the tail veins of MPS VII mice were infused with GUS or PB-GUS at a dose of 4 mg/kg body weight in a total volume of 125 μl of PBS. After infusion, blood samples were taken by supraorbital puncture at 2, 5, 10, 20, 60, 90, and 120 min for GUS and 4, 240, 1,440, and 2,880 min for PB-GUS into heparinized capillary tubes. Plasma was collected after centrifugation and assayed for GUS activity. Values were expressed as a percentage of GUS activity remaining compared with the first time point.
Previously, the plasma clearance of the enzyme was observed to be slowed when treating MPS VII mice with high-dose GUS and facilitated enzyme delivery to the brain (11). In these experiments, it was not clear whether it was the higher dose of enzyme itself or the delayed plasma clearance of the enzyme that accounted for improved delivery to brain. To address this question, comparative measurements were made of the distribution of GUS and PB-GUS in brain and other tissues 48 h after infusion into MPS VII mice. Mice were perfused with Tris-buffered saline before collection of tissues to ensure that tissue was not contaminated with residual plasma enzyme. MPS VII mice were infused via tail vein with GUS or PB-GUS at a dose of 4 mg/kg in a total volume of 125 μl of PBS. At 48 h after infusion, the mice were perfused with 30 ml of 25 mM Tris (pH 7.2), 140 mM NaCl. Perfused tissues were collected and flash frozen in liquid nitrogen until further processing. Tissues were thawed, weighed, and homogenized for 30 s with a Polytron homogenizer in 10-20 volumes of 25 mM Tris (pH 7.2), 140 mM NaCl, 1 mM phenylmethylsulfonyl fluoride. Total homogenates were frozen at −80° C., thawed, and then sonicated for 20 s to produce a homogeneous extract. Extracts were assayed for GUS activity and protein, and the results were expressed as units/milligrams of tissue protein. The results of these measurements appear in Table 4 below.
As is evident from the data in Table 4, delivery of native GUS to brain at 48 h was minimal. However, native GUS was delivered to other tissues at levels similar to those previously reported. PB-GUS was delivered to heart, kidney, muscle, lung, and eye at levels higher than those seen with native GUS. The levels in liver and spleen were nearly 4-fold lower after PB-GUS infusion than after GUS infusion. This result undoubtedly reflects the curtailment of receptor-mediated uptake by the MPR and M6PR that are highly expressed in these two tissues. By contrast, brain levels were greatly increased (7.8% of wild-type) in PB-GUS-infused animals. This result suggests that the long circulating PB-GUS has an advantage in crossing the BBB. Thus, it was of great interest to study its effectiveness in clearing storage from cells in the CNS.
As stated previously, it was believed that slowing the clearance of GUS from the circulation might facilitate the delivery to the brain. It has been shown above that the periodate and borohydride treatment accomplished this producing an enzyme with a much reduced rate of clearance from the circulation after IV infusion. The effectiveness of the treated enzyme in clearing the storage material from the lysosomes of the MPS VII mouse after a typical ERT regimen was tested. MPS VII mice were treated with 12 weekly infusions, one group with untreated GUS at doses of 2 or 4 mg/kg body weight and a second group with PB-GUS at doses of 2 or 4 mg/kg body weight. Two other groups of MPS VII mice were infused two times daily for 1 week with a total of 48 mg/kg, one group with GUS and one group with PB-GUS. One week after the last infusion, tissues from the group receiving untreated GUS (n=3), 2 mg/kg (n=3) or 4 mg/kg GUS (n=2), and PB-GUS, 2 mg/kg (n=2) or 4 mg/kg (n=3) were obtained at necropsy after Tris-buffered saline perfusion, fixed in 2% paraformaldehyde and 4% glutaraldehyde, post fixed in osmium tetroxide, and embedded in Spurr's resin. For evaluation of lysosomal storage by light microscopy, toluidine blue-stained 0.5-μm-thick sections of liver, spleen, kidney, brain, heart, rib, and bone marrow were assessed blind. To evaluate storage in cortical neurons, 500 contiguous parietal neocortical neurons were scored for the number of lucent cytoplasmic vacuoles, indicating lysosomal storage. A maximum of seven vacuoles were counted per cell, and results were evaluated by ANOVA or Student's t test. Also evaluated were the hippocampal neurons by counting the number of vacuoles in 100 neurons in CA2 sector. Other tissues were examined by using a semiquantitative scale, as described in ref. 11.
As can be seen in
In
Two of the problems associated in the analysis of micrographs for the clearance of storage material in these types of experiments are: 1) that there is some inconsistency from field to field i.e. the clearance varies from one microscopic field to another; and 2) the procedure is somewhat subjective from person to person as to the amount of storage present. To address these problems, a new method was developed to quantify the storage material by counting the number of vacuoles (distended lysosomes filled with storage material) present in a total of 500 cells counted.
GUS at 2 mg/kg is not very effective at reducing the number of vacuoles, though somewhat better at the higher dose of 4 mg/kg. However, PB-GUS appears to be almost completely effective at both 2 and 4 mg/kg. This analysis agrees with the conclusion drawn from the visual analysis of the images in
Table 5 below summarizes the results of assessment of storage in neocortical and hippocampal neurons of untreated GUS and PB-GUS in MPS VII mice. ERT with GUS over 12 weeks with both 2 mg/kg and 4 mg/kg GUS reduced storage in neocortical neurons compared with untreated MPS VII mice (P=0.002 and P=0.003, respectively), although hippocampal neurons failed to show a morphological response to this therapy. PB-GUS at 2 mg/kg also reduced neocortical neuronal storage (P=0.001). At 4 mg/kg, the therapeutic effect of PB-GUS was even more striking (P=0.003 for 2 vs. 4 mg of PB-GUS and P<0.001 compared with untreated). In addition, there was virtually no storage in the hippocampal neurons in the three PB-GUS-treated mice available for quantitation (the CA2 region was not present in the section and was therefore not available for quantitation in two of the five PB-GUS-treated mice). These results indicate that ERT with PB-GUS is remarkably more effective than traditional GUS at clearing storage in the neocortical and especially hippocampal neurons in the MPS VII mouse. As a group, the PB-GUS-treated mice also had slightly less storage in glial and perivascular cells than the GUS-treated mice. However, the dose-dependent reduction in storage in meninges, which was moderate at 4 mg/kg, was equivalent in the PB-GUS- and the GUS-treated animals.
From the above results it is reasonable to expect that treatment of mammalian species in accordance with this invention will provide relief of lysosomal storage disease, particularly in humans particularly in the brain of humans.
The following references are cited throughout this disclosure and are herein incorporated by reference. They are meant to illustrate and support the invention. Applicants reserve the right to challenge the veracity of any statements made therein.
This application is a divisional application of U.S. patent application Ser. No. 12/042,601, filed Mar. 5, 2008, entitled MODIFIED ENZYME AND TREATMENT METHOD, which claims the benefit of and priority to U.S. Provisional Patent Application No. 60/893,334 filed Mar. 6, 2007, and U.S. Provisional Patent Application No. 61/025,196, filed Jan. 31, 2008. The disclosures of each of the foregoing applications are hereby incorporated herein by reference in their entirety.
| Number | Date | Country | |
|---|---|---|---|
| 60893334 | Mar 2007 | US | |
| 61025196 | Jan 2008 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 12042601 | Mar 2008 | US |
| Child | 13455108 | US |
