US20130030040A1 - Methods and compositions for increasing sialic acid production and treating sialic related disease conditions - Google Patents

Methods and compositions for increasing sialic acid production and treating sialic related disease conditions Download PDF

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US20130030040A1
US20130030040A1 US13/364,181 US201213364181A US2013030040A1 US 20130030040 A1 US20130030040 A1 US 20130030040A1 US 201213364181 A US201213364181 A US 201213364181A US 2013030040 A1 US2013030040 A1 US 2013030040A1
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gne
nucleic acid
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Daniel DARVISH
Yadira Valles-Ayoub
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HIBM Research Group Inc
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Priority to US14/285,602 priority patent/US10098969B2/en
Priority to US17/547,031 priority patent/US20220088223A1/en
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K48/00—Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseases; Gene therapy
    • A61K48/005—Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseases; Gene therapy characterised by an aspect of the 'active' part of the composition delivered, i.e. the nucleic acid delivered
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/43—Enzymes; Proenzymes; Derivatives thereof
    • A61K38/52—Isomerases (5)
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K48/00—Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseases; Gene therapy
    • A61K48/0083—Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseases; Gene therapy characterised by an aspect of the administration regime
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/42—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests having means for desensitising skin, for protruding skin to facilitate piercing, or for locating point where body is to be pierced
    • A61M5/425—Protruding skin to facilitate piercing, e.g. vacuum cylinders, vein immobilising means
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P21/00—Drugs for disorders of the muscular or neuromuscular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04—Antibacterial agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P39/00—General protective or antinoxious agents
    • A61P39/06—Free radical scavengers or antioxidants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis

Definitions

  • the present invention is in the field of gene therapy methods and compositions for increasing production of sialic acid in a biological system by delivering the DNA coding region of the key enzyme of Sialic Acid biosynthesis (UDP-N-Acetylglucosamine 2-Epimerase/N-Acetylmannosamine Kinase, GNE)
  • Hereditary Inclusion Body Myopathy is a young-adult onset progressive skeletal muscle wasting disorder, which causes severe physical incapacitation. There is currently no effective therapeutic treatment for HIBM.
  • HIBM is an autosomal recessive disorder caused by mutation in the GNE gene.
  • the GNE gene encodes for the bifunctional enzyme UDP-GlcNAc 2-epimerase/ManNAc kinase (GNE/MNK). This is the key rate-limiting enzyme catalyzing the first two reactions of cellular sialic acid production.
  • HIBM is also known as Distal Myopathy with Rimmed Vacuoles, Nonaka Myopathy, Vacuolar myopathy sparing the quadricepts, or GNE related myopathy.
  • GNE UDP-GlcNAc 2-Epimerase/ManNAc Kinase enzyme
  • Also disclosed are methods of delivering an encoded GNE enzyme comprising: a) creating an intravenous access at a point below a knee or an elbow of a limb of a subject; b) applying a tourniquet at a point proximal to the rest of the body of the subject than the intravenous access point; c) introducing a single dose of an isolated nucleic acid expression construct into the limb through the intravenous access, wherein the single dose is of sufficient volume to increase intravascular pressure for extravasation of the polynucleotide; wherein, the isolated nucleic acid construct comprises a promoter operatively linked to a nucleic acid sequence encoding a GNE peptide or a therapeutically active fragment thereof, wherein the GNE peptide has the amino acid sequence of SEQ ID NO:3.
  • a GNE peptide in a cell comprising infecting the cell with an isolated nucleic acid construct that comprises a promoter operatively linked to a nucleic acid sequence encoding a GNE peptide or a therapeutically active fragment thereof, wherein the GNE peptide has the amino acid sequence of SEQ ID NO:3.
  • FIG. 1 is a diagram of the NTC8685-GNE expression vector described herein.
  • FIG. 2 shows the nucleotide sequence of NTC8685-GNE vector (SEQ ID NO:1).
  • FIG. 3 is a diagram of UMVC3-GNE vector.
  • FIG. 4 shows the nucleotide sequence of UMVC3-GNE vector (SEQ ID NO:2).
  • FIG. 5 shows the amino acid sequence of GNE protein enzyme (SEQ ID NO:3).
  • FIG. 6 shows the amino acid sequence of GNE isoforms and Allosteric domain. Common allosteric domain mutations allowing higher Sialic Acid production are illulstrated (R263Q/W/L, and R266Q/W).
  • FIG. 7 is a bar graph of sialic acid production in GNE-null CHO cells. In comparison to untreated cells (“Media”, “Empty Vector”), sialic acid production was significant greater in cells transfected with GNE plasmids.
  • FIG. 8 is a bar graph of Sialic Acid GNE-null CHO cells, comparison of UMVC3 and NTC8685 Vectors.
  • FIG. 9 is a bar graph of Sialic Acid content cell fractions of GNE-null CHO cells, comparison of UMVC3 and NTC8685 Vectors.
  • FIG. 10 is a bar graph showing the relative in-vitro dose comparison of GNE vecor vs ManNAc
  • Disease conditions that will benefit from increased cellular sialic production, or enhanced GNE functions include, but not limited to, Hereditary Inclusion Body Myopathy (HIBM) or Distal Myopathy with Rimmed Vacuoles (DMRV).
  • the present methods and compositions also relate to reducing or eliminating non-human sialic acids (e.g. N-Glycolylneuraminate, Neu5Gc) from human cells or tissues.
  • non-human sialic acids e.g. N-Glycolylneuraminate, Neu5Gc
  • Non-human sialic acids may contribute to various human diseases, and long term reduction of cellular levels of non-human sialic acid may prove beneficial in preventing and treating those disease processes (WO/2010/030666) (Varki 2009).
  • Increasing cellular production of Acetylneuraminate (Neu5Ac) can reduce cellular content of non-human sialic acids.
  • the pharmacologic products can be polynucleotides encoding the unmodified or modified forms of GNE protein, polypeptides or amino acid sequences and/or or recombinant proteins, polypeptides or amino acid sequences encoded by the unmodified or modified forms of GNE nucleotide.
  • the delivery methods include (1) external or internal occlusion of major vessels (arteries, veins, and/or lymphatic system) to achieve vascular isolation of the target organ systems, group of organs/tissues, or body area, and (2) administration of the therapeutic product using vascular (e.g. intravenous) access.
  • vascular e.g. intravenous
  • the body organs/tissues/area that are isolated (target organs) are exposed to the compound being delivered, while in other embodiments, the body organs/tissues/area are protected from such exposure.
  • GNE Therapeutic Gene
  • the therapeutic products disclosed herein are polynucleotide (DNA) molecules, while in other embodiments, they are polypeptide (protein, protein fragments, amino acid sequences) molecules.
  • the polynucleotide molecule either linear or circular, may contain various elements in addition to the coding sequence that encodes for the GNE protein, or a modified form of the GNE protein, that is or becomes biologically active within a biological system.
  • GNE protein has the sequence ( FIG. 3 ).
  • the therapeutic methods disclosed herein are commonly known as “Gene Therapy”, and comprise the administration of the above polynucleotide molecule.
  • the therapeutic methods disclosed herein are commonly known as “Enzyme Replacement Therapy (ERT)”, and comprise the administration of the GNE protein, or a modified form of the GNE protein, that is or becomes biologically active within a biological system.
  • ERT Enzyme Replacement Therapy
  • GNE encodes for the key enzyme of sialic acid production (UDP-N-Acetylglucosamine 2-epimerase/N-Acetylmannosamine Kinase).
  • UDP-N-Acetylglucosamine 2-epimerase/N-Acetylmannosamine Kinase Several disease conditions can benefit from increased expression of GNE. The most notable being the severely debilitating progressive muscle wasting disorder known as GNE related myopathy, Hereditary Inclusion Body Myopathy (HIBM) and one of its distinct forms known as IBM2, or Distal Myopathy with Rimmed Vacuoles (DMRV)
  • the GNE enzyme components or domains may be recombined to enhance desired functions of the GNE gene and reduce or eliminate undesired functions. For example, if production of high amounts of sialic acid (NeuAc) is desired in biological organisms, for example prokaryotes or eukaryotes, one may optimize the epimerase domain of the GNE gene to eliminate or reduce the allosteric inhibitory domain function.
  • sialic acid NeAAc
  • ManNAc kinase domain In organisms and animals having redundant ManNAc kinase activity, such as other enzymes able to efficiently perform phosphorylation of ManNAc, one may also reduce or eliminate the GNE kinase domain to reduce the size, the minimum effective dose, and/or maximize the maximum tolerable dose in a biological system.
  • GNE enzyme is also known to have cellular functions besides production of sialic acid (Hinderlich, Salama et al. 2004; Broccolini, Gliubizzi et al. 2005; Krause, Hinderlich et al. 2005; Salama, Hinderlich et al. 2005; Penner, Mantey et al. 2006; Wang, Sun et al. 2006; Amsili, Shlomai et al. 2007; Amsili, Zer et al. 2008; Kontou, Weidemann et al. 2008; Kontou, Weidemann et al. 2009; Paccalet, Coulombe et al.
  • hyposialylation of critical cellular molecules play an important role in human disease process (Huizing, Rakocevic et al. 2004; Noguchi, Keira et al. 2004; Saito, Tomimitsu et al. 2004; Tajima, Uyama et al. 2005; Ricci, Broccolini et al. 2006; Galeano, Klootwijk et al. 2007; Sparks, Rakocevic et al. 2007; Nemunaitis, Maples et al. 2010).
  • CMAH CMP-NANA hydroxylase
  • Neu5Ac is the only sialic acid produced by humans and many humans produce antibodies against Neu5Gc (Tangvoranuntakul, Gagneux et al. 2003).
  • the NeuGc found in human tissues and cells are believed to be from food or cell culture media.
  • Humans produce antibodies against NeuGc, potentially contributing to chronic inflammation, and various common disorders in which chronic inflammation is believed to be a significant factor (e.g. cancer, atherosclerosis, autoimmune disorders) (Hedlund, Padler-Karavani et al. 2008; Varki 2009).
  • NeuGc can also promote human diseases, such as hemolytic uremic syndrome (HUS).
  • HUS hemolytic uremic syndrome
  • a major cause of HUS is Shiga toxigenic Escherichia coli (STEC) infection.
  • Shiga toxin subtilase cytotoxin prefers binding to glycan terminating in NeuGc (Lofling, Paton et al. 2009). This information increases our concern that NeuGc may also increase human susceptibility to some infectious agents.
  • CMAH human sialic acid
  • GNE human sialic acid
  • CMAH may be reduced by either of genetic or metabolic technologies, including, but not limited to, genetic modification of animals to produce CMAH knock-out or knock-down animals, reduction of CMAH enzyme expression by polynucleotide technologies (expressed as inhibitory RNA or antisense oligonucleotide), or inhibition of CMAH enzyme by metabolic substrate analogues.
  • NeuGc may also be reduced in biological systems by overexpression of the enzyme that converts NeuGc to NeuAc.
  • GNE and other sialic acid pathway enzymes can be used in plant, vegetable, and fruit crops to increase sialic acid in food.
  • polynucleotide elements e.g. promoters, enhancers, repeat elements
  • promoters, enhancers, repeat elements can be used to enhance expression in various tissues/organs or developmental stages, which may be desired in various fields of biotechnology including, but not limited to, pharmacologic, food, and cosmetic industries.
  • skeletal muscle is an important tissue that is readily accessible and that is highly vascularized, it could be used as a factory to produce proteins with therapeutic values (reviewed in (Lu, Bou-Gharios et al. 2003; Ratanamart and Shaw 2006)). Indeed, it has been demonstrated that functional therapeutic proteins can be synthesized by the skeletal muscle and secreted into the blood circulation in sufficient amount to mitigate the pathology associated with disorders such as hemophilia, Pompe disease, Fabry's disease, anaemia, emphysema, and familial hypercholesterolemia.
  • the ability to express recombinant proteins in skeletal muscle is also an important issue for the treatment of neuromuscular disorders such as Duchenne and limb girdle muscular dystrophy. These disorders are caused by mutations of a gene that produces an essential muscle protein
  • One potential treatment for such disorders is gene transfer, whose objective is to introduce into the muscle a normal and functional copy of the gene that is mutated.
  • disclosed herein are methods to utilize muscle as protein factory to over-produce and secrete sialic acid.
  • the methods disclosed herein result in an increase of Neu5Ac biosynthesis in plasma, and the reduction of Neu5Gc concentration from cells.
  • the therapeutic product is a polynucleotide, while in other embodiments, the therapeutic product is a polypeptide.
  • the polynucleotide is a DNA molecule, which can comprise the full-length coding region for a protein, the coding region for a domain of a protein, or a coding region for a protein fragment, which is shorter than a recognized and identified domain of a protein.
  • the polynucleotides disclosed herein can range from oligomers of at least 15 base pairs in length to DNA molecule comprising the full-length coding region for a protein.
  • the polypeptide is a full-length protein, e.g., an enzyme or a receptor, while in other embodiments, the polypeptide is a protein fragment.
  • the protein fragment corresponds to a recognized and identified domain of a full-length protein, while in other embodiments, the polypeptide is shorter than a recognized and identified domain of a protein.
  • the polypeptides disclosed herein can range from oligomers of at least 5 amino acids in length to full-length proteins.
  • the protein fragment is a therapeutically active protein fragment.
  • therapeutically active protein fragment it is meant that the protein fragment under physiological conditions has the same biochemical activity (e.g., catalyzes the same reaction) as the wild-type GNE protein, although it may perform the function at a different rate.
  • the polynucleotide is a linear DNA molecule whereas in other embodiments, the polynucleotide is a circular DNA molecule.
  • the polynucleotide is a circular DNA (plasmid, miniplasmid, or minicircle) able to express the GNE gene in the desired biological system.
  • the NTC8685 vector described in this application has few benefits, which include reduced size, reduced bacterial sequence content, and antibiotic free selection. Other vectors known to those of skill in the art can also be used with the methods described herein.
  • the polynucleotide therapeutic product is administered as naked DNA, combined with other molecules to produce various cationic or anaionic particles, or co-administered with other pharmacological agents (e.g. exipients, vasodialaters, analgesics, etc,) to maximize efficacy of therapy and minimize patient discomfort.
  • other pharmacological agents e.g. exipients, vasodialaters, analgesics, etc,
  • other pharmacologic products may be administered using the stated delivery method.
  • muscle specific promoters may be used to reduce chance of host immune response against the transgene and enhance the duration of intramuscular expression of the transgene.
  • the backbone plasmid elements can be altered to allow for muscle specific expression.
  • the ability to achieve high-level and long-term recombinant protein expression after gene transfer in skeletal muscle is desired in many disease conditions. This can be achieved using promoters and enhancers specific for muscle.
  • the muscle creatine kinase (MCK) promoter and truncated versions are the most common muscle specific promoters used (Hauser, Robinson et al. 2000; Yuasa, Sakamoto et al. 2002; Sun, Zhang et al. 2005; Sebestyen, Hegge et al. 2007; Wang, Li et al. 2008).
  • the synthetic C5-12 promoter and similar promoters show promise of being muscle specific while driving high expression of transgene (Li, Eastman et al. 1999). This C5-12 promoter drives expression levels similar to the ubiquitous CMV promoters in AAV vectors (Gonin, Arandel et al. 2005).
  • the C5-12 can be further improved by adding the MCK enhancer (E-Syn promoter) (Wang, Li et al. 2008).
  • the hybrid ⁇ -myosin heavy chain enhancer-/MCK enhancer-promoter (MHCK7) promoter also was used for high expression in muscles (Salva, Himeda et al. 2007).
  • the desmin promoter is also recently described as a muscle-specific promoter capable or driving high level expression in muscle cells (Pacak, Sakai et al. 2008; Talbot, Waddington et al. 2010).
  • the upstream enhancer elements (USE, USEx3/AUSEx3) of genes such as the troponin gene is also a promising candidate for developing muscle specific promoters (WO 2008124934 20081023; Blain, Zeng et al. 2010).
  • the GNE-encoding sequences, and/or the associated delivery vehicles used therewith may be targeted towards specific cell types, for example, muscle cells, muscle tissue, and the like.
  • the promoter associated with the GNE coding sequence can be made to express GNE only in specific tissues or developmental stages.
  • the expression cassette can be packaged with other molecules, compounds, or biologic moieties (e.g. protein/carbohydrate/lipid containing molecules, part or whole antibody molecules, part or whole cytokine molecules, viral capsids) to generate a biological mixture or specific biological particles designed to bind to and enter specific cell types. This binding or affinity can facilitate the uptake of the DNA into the cell.
  • these protein, carbohydrate, and/or lipd containing molecules targeting moieties are, but are not limited to, microbial, plant, microbial, or synthetic compounds (e.g. antibodies, cytokines, lectins, other large or small molecules).
  • polynucleotides products described herein comprise the following elements: 1) Bacterial Control Elements, which are active in bacteria for the purpose of selection and growth process, 2) Eukaryotic Control Elements, which are active in eukaryotic or mammalian cells for the purpose of expression of a therapeutic gene product or recombinant protein, and 3) the GNE coding region, which is the therapeutic gene product or recombinant gene.
  • prokaryotic/bacterial selection marker is based on antibiotic resistance (e.g. kanamycin resistance, as present in the UMVC3 vector, FIG. 3 ), or RNA based (e.g. RNA-OUT, present on the NTC8685 vector, FIG. 1 ).
  • NTC8685-GNE vector is set forth in FIG. 2 and in SEQ ID NO:1, while the nucleotide sequence of UMVC3-GNE vector is set forth in FIG. 4 .
  • eukaryotic promoter, enhancer, introns or other elements are used for efficient transcription and translation of the therapeutic protein encoded by the GNE gene
  • prokaryotic selection marker that is not based on antibiotic resistance is preferred by regulatory agencies such as World Heath Organization (WHO), US Food and Drug Administration (FDA), or European Agency for the Evaluation of Medicinal Products (EMEA) (Williams, Carnes et al. 2009).
  • WHO World Heath Organization
  • FDA US Food and Drug Administration
  • EMEA European Agency for the Evaluation of Medicinal Products
  • pDNA naked or plasmid DNA
  • Clinical use of naked or plasmid DNA (pDNA) to express therapeutic genes is a promising approach to treat muscle disease caused by IBM2.
  • Naked DNA as gene therapy vehicle has an excellent safety record and repeat administration in the same subject can achieve higher expression levels.
  • pDNA delivered to skeletal muscle of rodents or primates is retained in myofibers and expresses the encoded gene product for many months (Danko, Fritz et al. 1993; Danko, Williams et al.
  • pDNA does not typically elicit an immune response against the vector (Hagstrom, Hegge et al. 2004; Romero, Braun et al. 2004; Glover, Lipps et al. 2005; Wolff, Budker et al. 2005), which makes it possible to repeat administrations in same subject. Additionally, compared to viral or based vectors, pDNA is relatively inexpensive to produce in large quantities and remains stable for many months (Walther, Stein et al. 2003; Urthaler, Ascher et al. 2007; Voss 2007).
  • an external tourniquet is placed on the limb of a human being or animal, and the therapeutic product is administered using a peripheral intravenous access using a specific volume (typically 30-50% of the limb volume below the tourniquet) in a specific amount of time or volume flow (typically 1-3 ml/second).
  • a specific volume typically 30-50% of the limb volume below the tourniquet
  • a specific amount of time or volume flow typically 1-3 ml/second
  • the delivery method has been improved.
  • Human and animal limbs of same volume may be composed of varying ratios of muscle and non-muscle (e.g. fatty or scar) tissues.
  • Muscle is often more vascular and requires higher blood flow that lipid or scar tissue.
  • administering therapeutic products using a specific volume may not confer optimum distribution of the therapeutic product in limbs of individuals.
  • Limbs with higher muscle/non-muscle tissue may require higher infusion volumes to achieve same therapeutic benefit.
  • Controlling the infusion based on intravascular (or infusion line) pressure and duration of infusion may convey improved distribution of therapeutic product to the target limb.
  • the following alterations of the described method accordingly improve this delivery method:
  • vascular administration distal or proximal to the site of vascular occlusion, one can either expose or protect the target organs, tissues, or body area.
  • IV Intravenous plasmid is cleared rapidly by the liver (Liu, Shollenberger et al. 2007).
  • HBV hydrodynamic limb vein
  • pDNA administered IV can effectively and uniformly transfect skeletal muscle of an entire limb in small and large animals including non-human primates (Hagstrom, Hegge et al. 2004), that results in reversible microvasculature damage (Toumi, Hegge et al. 2006; Vigen, Hegge et al. 2007).
  • a single dose can result in long-term gene expression, and the ease of repeat administration makes HLV suitable for delivering GNE transgene to the limbs of IBM2 patients.
  • Using a tourniquet blood flow in an arm or leg temporarily occluded, and a plasmid DNA solution is rapidly injected intravenously. This elevates the pressure within the occluded region, leading to remarkably efficient migration of the gene vehicle into the adjoining myofibers. Blood flow is restored to normal in 10-20 minutes, with no irreversible or persistent adverse affects.
  • Similar high pressure intravenous approaches are being adopted and adapted for delivery of DNA, and possibly other potential therapeutic molecules, to various organs. (Al-Dosari, Knapp et al. 2005; Arruda, Stedman et al. 2005; Wolff, Lewis et al. 2005; Herweijer and Wolff 2007; Toromanoff, Cherel et al. 2008).
  • IBM2/DMRV is an ideal orphan disorder to be treated by pDNA gene delivery using HLV for the following reasons:
  • GNE gene is relatively small (cDNA size 2,169 bp, coding for 722 amino acids), functioning as a protein enzyme that is expressed at low levels in skeletal muscle. Expression of low amounts of wild-type, or very low amounts of sialuria form of GNE, may prove remarkably effective or even curative. Additionally, it is possible to use the hypermorphic (Sialuria) form of the GNE gene allowing for very low expressions of the GNE gene to translate to significant therapeutic benefit. This is in sharp contrast to other muscle diseases such as Duchenne' or Becker muscular dystrophies where relatively large amounts of dystrophin (or truncated mini-dystrohpin) are needed to realize therapeutic benefit.
  • Other muscle diseases such as Duchenne' or Becker muscular dystrophies where relatively large amounts of dystrophin (or truncated mini-dystrohpin) are needed to realize therapeutic benefit.
  • GNE protein that differs from wild-type by one amino acid (missense mutation). Additionally, GNE is evolutionarily conserved with 98% homology between mice and men at the amino acid level. Thus, the chance of host immune response or producing neutralizing antibodies against the GNE transgene is minimal. Coupling GNE with a muscle specific promoter such as creatine kinase (CK) further reduces chance of host antibody response (Fabre, Bigey et al. 2006).
  • CK creatine kinase
  • ECRL Extensor Carpi Radialis Longus
  • Possibility of distant effect was also suggested following the surprising observation that distant muscle groups (trapezius and quadriceps) improved transiently in correlation with left ECRL rGNE transgene expression and increased sialylation (Nemunaitis, Maples et al. 2010).
  • GNE plasmid is expected to be a very safe vector for use in IBM2 patients.
  • naked DNA as gene therapy vehicle has an excellent safety record and repeat administration in the same subject can achieve higher expression levels.
  • the experiment group received high dose GNE plasmid (0.6 mg suspended in 0.1 ml normal saline) administered via IV tail, and the control group received only 0.1 ml normal saline.
  • the groups were further divided into 3 dose frequency groups of 2 mice (1 female, 1 male) each as follows: 1) every day administration for 14 days, 2) every other day administration, and 3) once per week. All animals survived the experiment. No significant change were observed between the experiment and the control groups with respect to all measured parameters, which included body weights, temperature, food and water intake, CBC blood tests (performed at pre-dose day 1 and at necropsy on day 15).
  • HED human equivalent dose
  • GNE-lipoplex In comparison to naked plasmid GNE, the GNE-lipoplex form is more toxic.
  • the plasmid vector was encapsulated in a cationic liposome composed of 1,2-dioleoyl-3-trimethylammonium-propane (DOTAP) and cholesterol (GNE-lipoplex).
  • DOTAP 1,2-dioleoyl-3-trimethylammonium-propane
  • GNE-lipoplex cholesterol
  • the vector was injected into BALB/c mice, and ingle intravenous (IV) infusion of GNE-lipoplex was lethal in 33% of animals at 100 ⁇ g (0.1 mg) dose, with a small proportion of animals in the 40 ⁇ g cohort demonstrating transient toxicity (Phadke, Jay et al. 2009).
  • HED Human equivalent dose
  • the patient has received several infusions (0.4, 0.4, 1.0 mg) of 1-3 months apart, and transient grade 1, 2 tachycardia and fever were observed within 12 hours of each infusion.
  • Patient's liver function tests were also reported as transiently elevated, but exact numbers were not reported in the abstract (Nemunaitis, Jay et al. 2010).
  • HBV Hydrodynamic Limb Vein
  • the HLV delivery method using pDNA is considered mature technology that has proven effective and safe in non-human primates, and is ready to be tested in clinical therapeutic trials (Wells 2004; Al-Dosari, Knapp et al. 2005; Herweijer and Wolff 2007).
  • the main disadvantage of this approach is the inability to easily transfect diaphragm, heart, and trunk/neck muscles without invasive methods to temporarily clamp the major internal vessels (e.g. surgical, laparoscopic, or transcutaneous balloon-occlusion). Although this disadvantage is significant for many muscular dystrophies, it is not nearly as important in patients affected by IBM2.
  • HLV delivery of pDNA for delivering GNE transgene to limb skeletal muscles is an attractive therapeutic option for IBM2 that may delay loss of physical independence, and offer significant hope for many IBM2 patients.
  • the GNE-encoding sequences and related compositions may contain any conventional non-toxic pharmaceutically-acceptable carriers, adjuvants or vehicles.
  • the pH of the formulation may be adjusted with pharmaceutically acceptable acids, bases or buffers to enhance the stability of the formulated composition or its delivery form.
  • sterile injectable aqueous or oleaginous suspensions may be formulated according to the known art using suitable dispersing or wetting agents and suspending agents.
  • the sterile injectable preparation may also be a sterile injectable solution, suspension or emulsion in a nontoxic parenterally acceptable diluent or solvent.
  • the acceptable vehicles and solvents that may be employed are water, Ringer's solution, U. S. P. and isotonic sodium chloride solution.
  • sterile, fixed oils are conventionally employed as a solvent or suspending medium.
  • any bland fixed oil may be employed, including synthetic mono- or diglycerides.
  • fatty acids such as oleic acid may be used in the preparation of injectables.
  • a Plasma-Lyte® carrier may be employed and used to deliver a GNE-encoding sequence, particularly for parenteral injection.
  • Plasma-Lyte® is a sterile, non-pyrogenic isotonic solution that may be used for intravenous administration.
  • Each 100 mL volume contains 526 mg of Sodium Chloride, USP (NaCl); 502 mg of Sodium Gluconate (C6H11NaO7); 368 mg of Sodium Acetate Trihydrate, USP (C2H3NaO2 ⁇ H2O); 37 mg of Potassium Chloride, USP (KCl); and 30 mg of Magnesium Chloride, USP (MgCI2>>6H2O). It contains no antimicrobial agents.
  • the pH is preferably adjusted with sodium hydroxide to about 7.4 (6.5 to 8.0).
  • the injectable formulations used to deliver GNE-encoding sequences may be sterilized, for example, by filtration through a bacterial-retaining filter, or by incorporating sterilizing agents in the form of sterile solid compositions, which can be dissolved or dispersed in sterile water, Plasma-Lyte® or other sterile injectable medium prior to use.
  • a GNE-encoding sequence within a system (or to prolong the effect thereof), it may be desirable to slow the absorption of the composition from subcutaneous or intramuscular injection. This may be accomplished by the use of a liquid suspension of crystalline or amorphous material with poor water solubility. The rate of absorption of the composition may then depend upon its rate of dissolution, which, in turn, may depend upon crystal size and crystalline form.
  • delayed absorption of a parenterally administered GNE-encoding sequence may be accomplished by dissolving or suspending the composition in an oil vehicle.
  • Injectable depot forms may be prepared by forming microencapsule matrices of the GNE-encoding sequence in biodegradable polymers such as polylactide-polyglycolide. Depending upon the ratio of GNE-encoding sequence material to polymer and the nature of the particular polymer employed, the rate of GNE-encoding sequence release can be controlled. Examples of other biodegradable polymers include poly(orthoesters) and poly(anhydrides).
  • depot injectable formulations may also be prepared by entrapping the GNE-encoding sequence in liposomes (or even microemulsions) that are compatible with the target body tissues, such as muscular tissue.
  • the present invention further encompasses methods for producing wild-type GNE in a system.
  • the system e.g., the muscle cells of a human patient
  • the system may comprise a mutated endogenous GNE-encoding sequence (e.g., the GNE-M712T sequence).
  • the present invention includes providing, for example, a cell or muscular tissue that harbors a mutated (defective) GNE-encoding sequence with a functional wild-type GNE encoding sequence.
  • the wild-type GNE encoding sequence may be delivered to such a system using, for example, the liposomes or lipid nanoparticles described herein, via parenteral injection.
  • methods for treating, preventing, and/or ameliorating the effects of Hereditary Inclusion Body Myopathy generally comprise providing a patient with a therapeutically effective amount of a wild-type GNE-encoding nucleic acid sequence.
  • the wild-type GNE-encoding nucleic acid sequence may, preferably, be delivered to a patient in connection with a lipid nanoparticle and a carrier similar to that of Plasma-Lyte®, via parenteral injection.
  • a wild-type GNE-encoding nucleic acid sequence refers to a sufficient amount of the sequence to express sufficient levels of wild-type GNE, at a reasonable benefit-to-risk ratio, to increase sialic acid production in the targeted cells and/or to otherwise treat, prevent, and/or ameliorate the effects of HIBM2 in a patient. It will be understood, however, that the total daily usage of the wild-type GNE-encoding nucleic acid sequence and related compositions of the present invention will be decided by the attending physician, within the scope of sound medical judgment.
  • One of the advantages of the methods described herein is that, because the polynucleotides are administered to the affected limb directly, as opposed to a systemic administration, the therapeutically effective amount that is administered is less than that in the methods described previously. Therefore, the present methods reduce or eliminate many of the side effects that are associated with the methods described previously.
  • the specific therapeutically effective dose level for any particular patient may depend upon a variety of factors, including the severity of a patient's HIBM2 disorder; the activity of the specific GNE-encoding sequence employed; the delivery vehicle employed; the age, body weight, general health, gender and diet of the patient; the time of administration, route of administration, and rate of excretion of the specific GNE-encoding sequence employed; the duration of the treatment; drugs used in combination or contemporaneously with the specific GNE-encoding sequence employed; and like factors well-known in the medical arts.
  • a maintenance dose of a GNE-encoding sequence may be administered, if necessary. Subsequently, the dosage or frequency of administration, or both, may be reduced, as a function of the symptoms, to a level at which the improved condition is retained when the symptoms have been alleviated to the desired level.
  • novel compositions are provided for expressing wild-type GNE in a system.
  • the compositions preferably include a wild-type GNE-encoding nucleic acid sequence.
  • the GNE-encoding nucleic acid sequence may comprise various transcriptional control elements, such as a promoter, termination sequence, and others.
  • a non-limiting example of a composition encompassed by the present invention includes the pUMVC3-GNE expression vector described herein, shown in FIG. 3 . so as described relative to other embodiments of the present invention, the GNE-encoding nucleic acid sequence may be disposed within or connected to an appropriate vehicle for delivery to a system, such as a liposome or lipid nanoparticle.
  • the delivery vehicle may, optionally, be decorated with agents that are capable of recognizing and binding to target cells or tissues, such as muscle cells or muscle tissues.
  • GNE expression vectors from human cDNA were created.
  • the transfected GNE expressing cell lines produced significantly more sialic acid than untransfected cells.
  • GNE Cloning Parental vectors containing the GNE cDNA were provided by Daniel Darvish (HIBM Research Group, Encino, Calif.) and included pGNE-NB8 (wild type), pGNE-MB18 (M712T mutant), and pGNE-R266Q (R266Q mutant).
  • GNE cDNA inserts wildtype and M712T were produced by reverse transcription of RNA isolated from patient whole blood.
  • cDNA was then amplified using specifically designed primers bearing EcoR1 and BamH1 recognition 5′ tails, and subsequently subcloned into the pUMVC3 expression vector (Aldevron) by T4 ligation (Invitrogen). Competent E. coli cells (Invitrogen) were then transformed with the pUMVC3 expression vector.
  • Positive pUMVC3-GNE clones were grown overnight in 175 mis LB broth+50 ⁇ g/ml Kan and 150 mis culture was used for a Qiagen (Valencia, Calif.) HiSpeed Plasmid Maxi kit according to the manufacturer protocols.
  • DNA DNA.lipid complex.
  • the DNA:lipid complex used in this example was produced by mixing, at room temperature, 1,2-Dioleoyl-3-Trimethylammonium-Propane (DOTAP) with test DNA (pUMVC3-GNE).
  • DOTAP is a commercially-available lipid particle that is offered by Avanti Polar Lipids, Inc. (Alabaster, Ala.).
  • the DOTAP was mixed with the pUMVC3-GNE DNA in a manner to achieve the desired total volume, which exhibited a final ratio of 0.5 ⁇ g DNA:4 mM DOTAP1 in a final volume of 1 ⁇ l.
  • GNE-deficient CHO-Lec3 cells were provided by Albert Einstein College of Medicine. The cells were grown at 37° C. in 5% CO 2 in ⁇ -MEM media supplemented with 4 mM L-glutamine and 10% heat inactivated, Fetal Bovine Serum. Cells for transient transfections were plated at 1 ⁇ 106 cells per well in 6-well plates and grown overnight. Lec3 cells were weaned to reduced serum conditions by reducing the FBS by 2.5% per passage.
  • Lec3 cells were transfected for 6 hours with DNA:lipid complex per well in OptiMEM (Invitrogen, Carlsbad Calif.), then the media was changed to normal ⁇ -MEM growth media and the cells were cultured overnight.
  • DNA:lipid complexes were formed by mixing 4 ⁇ g DNA+10 ⁇ l Lipofectamine 2000 (Invitrogen) according to the manufacturers protocol. Twenty-four hours post-transfection, cells were harvested by trypsin digest and washed once with PBS before subsequent western blot or enzyme/sugar assays.
  • Sialic Acid Quantitation Approximately 4 ⁇ 10 6 cells were used for the quantification of membrane-bound sialic acid by the thiobarbituric acid method. Cells were resuspended in water and lysed by passage through a 25 gauge needle 20 times and centrifuged. The supernatant was used for Bradford protein estimation and the remaining pellet was resuspended in 100 ⁇ l 2M acetic acid and incubated for 1 hour at 800 C to release glycoconjugate-bound sialic acids. 137 ⁇ l of periodic acid solution (2.5 mg/ml in 57 mM H 2 SO 4 ) were added and incubated for 15 minutes at 37° C.
  • Lec3 CHO cells obtained from Dr. Pamela Stanley (Albert Einstein College of Medicine) were initially grown in ⁇ -MEM media containing 10% fetal bovine serum (FBS) (Invitrogen), received subsequent passages of ⁇ -MEM FBS medium by 2.5% decrements until 0% FBS, and trypsinized prior to transfection.
  • FBS fetal bovine serum
  • transfections were prepared in triplicate using 2.0 ⁇ 106 CHO cells, 2.5 mL of Freestyle Media (Invitrogen), 500 ⁇ l of Opti-MEM (Invitrogen), 10 ⁇ l of Lipofectamine (Invitrogen) and 4 ⁇ g of DNA (except for the no vector set) and incubated at 37° C. in 5% CO 2 .
  • Sets prepared included GNE wild-type pUMVC3 vector, GNE M712T pUMVC3 vector, GNE R266Q pUMVC3 vector, empty vector, and no vector media. Cells were collected 48 hours post-transfection, washed with PBS, and resuspended in lysis buffer.
  • Sialic acid content was detected using a modified version of the Leonard Warren method (Warren 1959) and measured with NanoDrop-1000 Spectrophotometer (Thermo Fisher Scientific) at 549 nm using the UBV-Vis module.
  • a standard curve was created with known sialic acid concentrations and denoted a clear linear association between absorbance and sialic acid concentration.
  • GNE clones The GNE cDNA clones that were tested included a human wild type cDNA and two human mutant cDNAs. The mutants included the M712T GNE deficient clone and the R266Q sialuria clone. Sialuria is a human disease caused by point mutations in the CMP-sialic acid binding site of GNE, leading to a loss of feedback inhibition and mass production of sialic acids.
  • GNE cDNAs were subcloned from their original vectors to the expression vector, pUMVC3, by restriction digest cloning. Clones were screened by directional restriction enzyme digest to confirm the GNE insert was in the correct orientation.
  • Positive clones were sequenced in both orientations to confirm that no mutations occurred during the cloning process.
  • the resulting chromatograms were compared against the GNE sequence from GenBank (accession # NM — 005467) and the wild type did not exhibit any mutations, while the M712T and R266Q clones contained only the expected point mutations.
  • Positive pUMVC3-GNE clones were scaled using a maxi prep plasmid purification procedure and sequenced again to confirm that no mutations occurred. These DNA stocks were used for all subsequent experiments.
  • CHO-Lec3 cells were grown in 10% serum and transiently transfected with pUMVC3-GNE-wt DNA for 24 hours to quantitate the amount of recombinant GNE RNA that was expressed.
  • Total RNA was extracted and RT-qPCR was performed to amplify a 230 bp fragment from the GNE transcript.
  • Serial dilutions of pUMVC3-GNE-wt were used to determine that the concentration of GNE-wt expressed in transfected Lec3 cells was equal to 4.1 pg/ ⁇ l.
  • the dynamic range of the qPCR was from 5 ng-5 fg and there was no GNE mRNA product detected in control (untransfected) CHO-Lec3 cells (the cT value for untransfected cells was greater than 42 cycles, which is less than 5 fg). Therefore, recombinant GNE mRNA expression was detected in transfected Lec3 cells, while untransfected cells had undetectable amounts of GNE mRNA.
  • Silic acid production by provision of ManNAc The level of Sialic acid production was measured by supplementing cell culture media with N-Acetylmannosamine (ManNAc). Besides provision of ManNAc, all other cell culture variables were identical to transfection studies ( FIG. 10 ).
  • mice Preliminary high dose plasmid toxicity.
  • MFD maximum feasible dose
  • Limitation was based on solubility of plasmid (6 ⁇ g/ ⁇ l) and total volume per injection (100 ⁇ L).
  • HED human equivalent dose
  • the experiment group received high dose GNE plasmid (0.6 mg suspended in 0.1 ml normal saline) administered via IV by tail vein, and the control group received 0.1 ml normal saline.
  • the groups were further divided into 3 dose frequency groups of 2 mice (lfemale, 1 male) each as follows: 1) Every day administration for 14 days, 2) Every other day administration, and 3) Once per week. All animals survived the experiment. No significant change were observed between the experiment and the control groups with respect to all measured parameters, which included body weights, temperature, food and water intake, CBC blood tests (performed at days 1 and 15).

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