Patent Application
20120295960
The present invention relates to improved methods for dopamine replacement therapy for use in the prevention and/or treatment of Parkinson's disease.
Parkinson's disease (PD) is a progressive neurodegenerative disorder characterized by the loss of the nigrostriatal pathway. Although the cause of Parkinson's disease is not known, it is largely associated with the progressive death of dopaminergic (tyrosine hydroxylase (TH) positive) mesencephalic neurons, inducing motor impairment. The characteristic symptoms of Parkinson's disease appear when up to 70% of TH-positive nigrostriatal neurons have degenerated. Symptoms of PD include hypokinesia (reduction in movement), bradykinesia (slowness of movement), rigidity, postural instability and rest tremors. Although PD is predominantly a movement disorder, other impairments frequently develop, including psychiatric issues such as depression and dementia. Autonomic disturbances and pain can occur in later stages, and as PD progresses, it causes significant disability and impaired quality of life for the affected person.
There is currently no satisfactory cure for Parkinson's disease. Dopaminergic replacement is believed to be the most effective therapeutic strategy currently in use for PD. Symptomatic treatment of the disease-associated motor impairments involves oral administration of the dopamine precursor dihydroxyphenylalanine, also known as levodopa (L-Dopa). In early stage PD, oral L-Dopa is efficacious, but patients progressively lose the ability to convert L-Dopa to dopamine as more and more dopaminergic neurons degenerate. In addition, after long-term L-Dopa therapy (on the order of one to four years), L-Dopa treatment begins to cause severe side effects, including drug-induced dyskinesias. It is believed that these effects are due to the irregular pharmacokinetics and pharmacodynamics of L-Dopa that results from intermittent oral dosing. Continuous delivery of dopamine may prevent dyskinesias by restoring a constant dopaminergic tone in the striatum.
One alternative strategy for the treatment of PD is gene therapy. Viral vector-based approaches are being evaluated for the treatment of various neurological diseases, through the introduction of therapeutic genes by transduction of the viral vector into neuronal and/or support cells. For example, a multicistronic lentiviral vector product, ProSavin®, has been developed to treat Parkinson's disease. ProSavin® mediates intrastriatal dopamine production by transduction of non-dopamine cells and transfer of the genes for aromatic L-amino acid decarboxylase, tyrosine hydroxylase, and GTP cyclohydrolase I (Azzouz et al (2002) J. Neurosci. 22: 10302-10312). Expression of these three genes in the transduced cell converts the cell into one that can manufacture dopamine.
ProSavin® is thought to provide sufficient dopamine to the striatum, by delivering a continual supply of this neurotransmiiter, to restore beneficial movements in the absence of central and peripheral side effects. The continual dopamine replacement is beneficial since it mediates a ‘smoothing out’ of dopamine receptor stimulation and hence reduces the motor function side effects associated with the pulsatile delivery of exogenous L-Dopa.
The present inventors have surprisingly found that the contribution of ProSavin® to the dopamine levels in the striatum is sufficient to allow decrease or maintenance of the L-Dopa dosage in the treatment regimen, which reduces the potential side effects of L-Dopa, especially as the dose is increased during disease progression and when the L-Dopa side-effects become more prominent, as does the ‘ON-OFF’ effect.
In one aspect, the present invention provides a method for reducing the daily dose of L-Dopa required to maintain locomotor activity in a Parkinson's disease subject by administering to the subject a vector system for dopamine replacement gene therapy.
In particular, the invention provides a treatment regimen for Parkinson's Disease (PD) patients comprising administering to a patient having PD: (i.) a lentiviral vector comprising three nucleotides of interest (NOIs), wherein the NOIs encode tyrosine hydroxylase (TH), GTP-cyclohydrolase I (GTP-CH1), and aromatic amino acid dopa decarboxylase (AADC), and wherein the three NOIs are expressed to stimulate dopamine synthesis in the brain; and (ii) a daily dosage of L-Dopa sufficient to improve motor function in the ON state compared to the OFF state, as measured by the Unified Parkinson's Disease Rating Scale (UPDRS), wherein the daily dosage of L-Dopa is reduced or maintained for at least six months following administration of the lentiviral vector. In a preferred embodiment, the lentiviral vector is an EIAV vector. The NOIs can be operably linked by one or more Internal Ribosome Entry Sites (IRES).
The “ON state” is the period where the patients are receiving benefit from a dose of L-Dopa and have satisfactory movement. The “OFF state” is the period where the effects of L-Dopa have worn off and the patients have poor mobility.
Daily administration of L-Dopa can be commenced prior to administration of the lentiviral vector. In one embodiment, the time the patient is in the ON state is increased for at least six months following administration of the lentiviral vector compared to time in the ON state prior to administration of the lentiviral vector. In another embodiment, the time the patient is in the OFF state is decreased for at least six months following administration of the lentiviral vector compared to time in the OFF state prior to administration of the lentiviral vector. In a preferred embodiment, the patient experiences an increase in time in the ON state and a decrease in time in the OFF state for at least six months following administration of the lentiviral vector.
Orally administered L-Dopa is transported across the blood-brain barrier and converted to dopamine, primarily by residual dopaminergic neurons, leading to a substantial improvement of motor function. Initially, patients with PD experience excellent benefits from pharmacological treatment with, which boosts dopamine levels from the remaining nigral neurons. However, as the disease progresses, the further degeneration of these neurons dictates less efficient metabolism of L-Dopa into dopamine in the striatum. Eventually it is impossible to provide sufficient L-Dopa to provide stable motor correction without incurring side effects of severe debilitating motor dysfunction. With chronic L-Dopa intake, most PD patients display fluctuations in motor response to the drug, and develop involuntary abnormal movements called dyskinesias. These fluctuations in motor function are present in approximately 50% of patients after five years and nearly all patients after 10 years of L-Dopa treatment (Verhagen, Amino Acids 23:414-415 (2002); Poewe et al., Neurology 49:S146-152 (1996)). Dyskinesias and motor fluctuations are associated with a hyperactive response to dopamine replacement, coupled with an increased loss of dopaminergic neurons (Widnell, Mov. Disord. 20:S17-S22 (2005)). As the disease advances there is an increased requirement for higher doses of L-Dopa to manage the PD symptoms, but this in turn leads to increased motor fluctuations. This treatment regime often results in the side effects of the treatment becoming as disabling as the disease. Delaying L-Dopa treatment in early PD patients and limiting the dose of L-Dopa to the lowest effective amount are strategies used to reduce the development of motor complications caused by L-Dopa therapy.
Once on L-Dopa therapy, patients cycle between ON-drug periods, during which L-Dopa provides periods of benefit that are complicated by disabling dyskinesias, and OFF-drug periods, characterized by akinesias when the benefit is wearing off prior to the next dose. Such fluctuations are correlated to the highest and lowest plasma concentrations of dopamine, where peak plasma levels produce dyskinesias and the trough between doses results in an akinetic state (see
L-Dopa can be administered as part of the treatment regimen of the present invention by any means known in the art including but not limited to oral (including buccal, sublingual, etc.), enteral, parenteral, mucosal, and transdermal. L-Dopa formulations can have any known release profile, including immediate-release, modified-release, and extended-release. Formulations can be provided in any know form, such as a tablet, capsule, liquid, solution, suspension, or emulsion.
Gene therapy is the prevention and/or treatment of disease by introducing, replacing, altering, or supplementing a prophylactic or therapeutic gene in a subject. Gene therapy is a powerful means to deliver proteins continuously to the central nervous system in a site-specific manner.
The present invention relates to dopamine gene therapy, in which one or more the genes responsible or related to dopamine synthesis is introduced into the subject.
In vivo, dopamine is synthesised from tyrosine by two enzymes, tyrosine hydroxylase (TH) and aromatic amino acid Dopa-decarboxylase (AADC). In the dopamine gene therapy method of the present invention, the vector system is preferably capable of delivering a nucleic acid sequence(s) encoding TH and AADC. The sequences of both genes are available: Accession Nos. X05290 and M76180 respecively.
The vector system used in the invention may comprise a truncated form of the TH gene, lacking the regulatory domain. The truncated TH avoids end-product feed-back inhibition by dopamine (Wu J. et al (1992) 267: 25754-25758).
Functional activity of tyrosine hydroxylase depends on the availability of its cofactor tetrahydrobiopterin (BH4). The level of cofactor may be low in the denervated striatum, and so it may be preferable if the vector system is also capable of delivering GTP cyclohydrolase I (CH1), the enzyme that catalyses the rate limiting step on the pathway of BH4-synthesis, to ensure that sufficient levels of L-Dopa are produced in vivo. The sequence of the CH1 gene is also available: Accession No. U19523.
The vector system may also be capable of delivering a nucleic acid sequence encoding Vesicular Monoamine Transporter 2 (VMAT2—Accession number L23205.1).
Dopamine replacement gene therapy may therefore involve the use of a vector system to deliver genes encoding one or more of the following genes to a subject: TH, AADC, CH1 and/or VMAT2 to the subject. The vector system may, for example deliver genes encoding TH, AADC, and CH1 to the subject. Such a vector system is described in WO 02/29065.
The vector may alternatively or also comprise a gene encoding a growth factor capable of blocking or inhibiting degeneration in the nigrostriatal system. An example of such a growth factor is a neurotrophic factor. For example the gene may encode glial cell-line derived neurotrophic factor (GDNF), brain-derived neurotrophic factor (BDNF), nerve growth factor (NGF), persephin growth factor, artemin growth factor, or neurturin growth factor, cilliary neurotrophic factor (CNTF), neurotrophin-3 (NT-3), neurotrophin-4 (NT-4) and/or pantropic neurotrophin.
The vector may alternatively or also comprise a gene encoding a neuroprotective factor. In particular, the NOI(s) may encode molecules which prevent TH-positive neurons from dying or which stimulate regeneration and functional recovery in the damaged nigrostriatal system.
In the dopamine replacement gene therapy method of the present invention, the genes involved in dopamine synthesis are delivered to the subject by a vector system, such as a viral vector system.
In the context of the present invention, the terms “vector system,” “vector” and “vector particle” are used synonymously to mean an entity capable of transducing a target cell with one or more nucleotides of interest (NOIs).
The concept of using viral vectors for gene therapy is well known (Verma and Somia (1997) Nature 389:239-242). The vector system may be based on a retrovirus, such as murine leukemia virus (MLV), human immunodeficiency virus (HIV), equine infectious anaemia virus (EIAV), mouse mammary tumour virus (MMTV), Rous sarcoma virus (RSV), Fujinami sarcoma virus (FuSV), Moloney murine leukemia virus (Mo-MLV), FBR murine osteosarcoma virus (FBR MSV), Moloney murine sarcoma virus (Mo-MSV), Abelson murine leukemia virus (A-MLV), Avian myelocytomatosis virus-29 (MC29), and Avian erythroblastosis virus (AEV) and all other retroviridiae, including lentiviruses.
Lentiviral vectors are part of a larger group of retroviral vectors. A detailed list of lentiviruses may be found in Coffin et al. (1997) “Retroviruses” Cold Spring Harbor Laboratory Press Eds: J M Coffin, S M Hughes, H E Varmus pp 758-763). In brief, lentiviruses can be divided into primate and non-primate groups. Examples of primate lentiviruses include but are not limited to: the human immunodeficiency virus (HIV), the causative agent of human auto-immunodeficiency syndrome (AIDS), and the simian immunodeficiency virus (SIV). The non-primate lentiviral group includes the prototype “slow virus” visna/maedi virus (VMV), as well as the related caprine arthritis-encephalitis virus (CAEV), equine infectious anaemia virus (EIAV) and the more recently described feline immunodeficiency virus (FIV) and bovine immunodeficiency virus (BIV).
Lentiviruses differ from other members of the retrovirus family in that lentiviruses have the capability to infect both dividing and non-dividing cells (Lewis et al (1992) EMBO J. 11(8):3053-3058) and Lewis and Emerman (1994) J Virol 68 (1):510-516). In contrast, other retroviruses, such as MLV, are unable to infect non-dividing or slowly dividing cells such as those that make up, for example, muscle, brain, lung and liver tissue.
In the provirus, the viral genes are flanked at both ends by regions called long terminal repeats (LTRs). The LTRs are responsible for proviral integration, and transcription. LTRs also serve as enhancer-promoter sequences and can control the expression of the viral genes.
The LTRs themselves are identical sequences that can be divided into three elements, which are called U3, R and U5. U3 is derived from the sequence unique to the 3′ end of the RNA. R is derived from a sequence repeated at both ends of the RNA and U5 is derived from the sequence unique to the 5′ end of the RNA. The sizes of the three elements can vary considerably among different viruses.
The basic structure of retrovirus and lentivirus genomes share many common features such as a 5′ LTR and a 3′ LTR, between or within which are located a packaging signal to enable the genome to be packaged, a primer binding site, integration sites to enable integration into a host cell genome, and gag, pol and env genes encoding the packaging components, which are polypeptides required for the assembly of viral particles. Lentiviruses have additional features, such as rev and (Rev response element) RRE sequences in HIV, which enable the efficient export of RNA transcripts of the integrated provirus from the nucleus to the cytoplasm of an infected target cell.
In a particularly preferred embodiment the viral vector is derived from EIAV. EIAV has the simplest genomic structure of the lentiviruses and is particularly preferred for use in the present invention. In addition to the gag, pol and env genes, EIAV encodes three other genes: tat, rev, and S2. Tat acts as a transcriptional activator of the viral LTR (Derse and Newbold (1993) Virology 194(2):530-536 and Maury et al (1994) Virology 200(2):632-642) and Rev regulates and coordinates the expression of viral genes through rev-response elements (RRE) (Martarano et al. (1994) J Virol 68(5):3102-3111). The mechanisms of action of these two proteins are thought to be broadly similar to the analogous mechanisms in the primate viruses (Martarano et al. (1994) J Virol 68(5):3102-3111). The function of S2 is unknown. In addition, an EIAV protein, Ttm, has been identified that is encoded by the first exon of tat spliced to the env coding sequence at the start of the transmembrane protein.
The gag-pol sequence may be codon optimised for use in the producer cell. The env protein encoded by the nucleotide sequence transfected into the producer cell may be a homologous retroviral or lentiviral env protein. Alternatively, it may be pseudotyped with a heterologous env, or an env from a non-retro or lentivirus. For example, the vector system of the present invention may be pseudotyped with a heterologous env protein, e.g., at least part of the rabies G protein or the vesicular stomatitis virus-G (VSV-G) protein. WO 00/52188 describes the generation of pseudotyped retroviral and lentiviral vectors, from stable producer cell lines, having VSV-G as the membrane-associated viral envelope protein, and provides a gene sequence for the VSV-G protein. Other envelopes which can be used to pseudotype retroviral vectors include the Ross River virus envelope, (Kang et al., J Virol 76(18):9378-9388 (2002)) the baculovirus GP64 protein (Kumar et al., Hum. Gene Ther. 14(1):67-77 (2003)), and the envelopes from Mokola, Ebola, 4070A, and lymphocytic choriomeningitis virus (LCMV).
In a typical lentiviral vector for use in the present invention, at least part of one or more protein coding regions essential for replication may be removed from the virus. This makes the viral vector replication-defective. In a defective lentiviral vector genome, gag, pol and env may be absent or not functional. Portions of the viral genome may also be replaced by an NOI in order to generate a vector comprising an NOI which is capable of transducing a target non-dividing host cell and/or integrating its genome into a host genome.
In one embodiment the lentiviral vectors are non-integrating vectors as described in WO 2007/071994.
In a further embodiment the vectors have the ability to deliver a sequence which is devoid of or lacking viral RNA. In a further embodiment a heterologous binding domain (heterologous to gag) located on the RNA to be delivered and a cognate binding domain on gag or pol can be used to ensure packaging of the RNA to be delivered. Both of these vectors are described in WO 2007/072056.
The vector system used in the methods of the present invention may be a self-inactivating (SIN) vector system. By way of example, self-inactivating retroviral vectors have been constructed by deleting the transcriptional enhancers or the enhancers and promoter in the U3 region of the 3′ LTR. After a round of vector reverse transcription and integration, these changes are copied into both the 5′ and the 3′ LTRs producing a transcriptionally inactive provirus (Yu et al (1986) Proc. Natl. Acad. Sci. 83:3194-3198; Dougherty and Temin et al (1987) Proc. Natl. Acad. Sci. 84:1197-1201; Hawley (1987) Proc. Natl. Acad. Sci. 84:2406-2410 and Yee et al (1987) Proc. Natl. Acad. Sci. 91:9564-9568). However, any promoter(s) internal to the LTRs in such vectors will still be transcriptionally active. This strategy has been employed to eliminate effects of the enhancers and promoters in the viral LTRs on transcription from internally placed genes. Such effects include increased transcription (Jolly et al (1983) Nucleic Acids Res. 11:1855-1872) or suppression of transcription (Emerman and Temin (1984) Cell 39:449-467). This strategy can also be used to eliminate downstream transcription from the 3′ LTR into genomic DNA (Herman and Coffin (1987) Science 236:845-848). This is of particular concern in human gene therapy where it is of critical importance to prevent the adventitious activation of an endogenous oncogene.
A recombinase assisted mechanism may be used which facilitates the production of high titre regulated vectors from producer cells. As used herein, the term “recombinase assisted system” includes but is not limited to a system using the Cre recombinase/loxP recognition sites of bacteriophage P1 or the site-specific FLP recombinase of S. cerevisiae which catalyses recombination events between 34 by FLP recognition targets (FRTs).
The site-specific FLP recombinase of S. cerevisiae which catalyses recombination events between 34 by FLP recognition targets (FRTs) has been configured into DNA constructs in order to generate high level producer cell lines using recombinase-assisted recombination events. A similar system has been developed using the Cre recombinase/loxP recognition sites of bacteriophage P1. This was configured into a lentiviral genome such that high titre lentiviral producer cell lines were generated.
A retroviral vector particle for use in the present invention may be made by a producer cell, for example, one in which the necessary genes have been introduced by a “triple transfection” method. In this approach, the three different DNA sequences that are required to produce a retroviral vector particle i.e. the env coding sequences, the gag-pol coding sequence and the defective retroviral genome containing one or more NOIs (for example, capable of encoding one or more enzymes involved in dopamine synthesis) are introduced into the cell at the same time by transient transfection. WO 94/29438 describes the production of producer cells in vitro using this multiple DNA transient transfection method.
By using producer/packaging cell lines, it is possible to propagate and isolate quantities of retroviral vector particles (e.g. to prepare suitable titres of the retroviral vector particles) for subsequent transduction of, for example, a site of interest (such as adult brain tissue). Producer cell lines are usually better for large scale production or vector particles.
It is desirable to use high-titre virus preparations for transduction in tissues such as the brain. Techniques for increasing viral titre include using a psi plus packaging signal as discussed above and concentration of viral stocks.
A high-titre viral preparation for a producer/packaging cell is usually of the order of 105 to 107 retrovirus particles per ml. For transduction of the brain it is necessary to use very small volumes, so the viral preparation is concentrated by ultracentrifugation. Other methods of concentration such as ultrafiltration or binding to and elution from a matrix may be used.
The presence of a sequence termed the central polypurine tract (cPPT) may improve the efficiency of gene delivery to non-dividing cells. This cis-acting element is located, for example, in the EIAV polymerase coding region element. The genome of the vector system used in the present invention may comprises a cPPT sequence.
In addition, or in the alternative, the viral genome may comprise a translational enhancer.
The plasmid vector used to produce the viral genome within a host cell/packaging cell will also include transcriptional regulatory control sequences. For example, the lentiviral genome or the to direct transcription of the genome in a host cell/packaging cell. These regulatory sequences may be the natural sequences associated with the transcribed lentiviral sequence, i.e. the 5′ U3 region, or they may be a heterologous promoter such as another viral promoter, for example the CMV promoter. Some lentiviral genomes require additional sequences for efficient virus production. For example, in the case of HIV, rev and RRE sequence can be included.
Preferably the recombinant lentiviral vector for use in the present invention has a minimal viral genome. As used herein, the term “minimal viral genome” means that the viral vector has been manipulated so as to remove the non-essential elements and to retain the essential elements in order to provide the required functionality to infect, transduce, and deliver a nucleotide sequence of interest to a target host cell.
It has been demonstrated that a lentivirus minimal system can be constructed from HIV, SIV, FIV, and EIAV viruses. Such a system requires none of the additional genes vif, vpr, vpx, vpu, tat, rev and nef for either vector production or for transduction of dividing and non-dividing cells. It has also been demonstrated that an EIAV minimal vector system can be constructed which does not require S2 for either vector production or for transduction of dividing and non-dividing cells. The deletion of additional genes is highly advantageous. Firstly, it permits vectors to be produced without the genes associated with disease pathology in lentiviral (e.g. HIV) infections, such as tat. Secondly, the deletion of additional genes permits the vector to package more heterologous DNA. Thirdly, genes whose function is unknown, such as S2, may be omitted, thus reducing the risk of causing undesired effects. Examples of minimal lentiviral vectors are disclosed in WO-A-99/32646 and in WO-A-98/17815.
The delivery system used in the invention may therefore be devoid of at least tat and S2 (if it is an EIAV vector system), and possibly also vif, vpr, vpx, vpu and nef. The systems of the present invention may also be devoid of rev and RRE. Rev was previously thought to be essential in some retroviral genomes for efficient virus production. For example, in the case of EIAV, it was thought that rev and RRE sequence should be included. However, it has been found that the requirement for rev and RRE can be reduced or eliminated by codon optimisation. As expression of the codon optimised gag-pol is rev independent, RRE can be removed from the gag-pol expression cassette, thus removing any potential for recombination with any RRE contained on the vector genome.
The requirement for rev and RRE can alternatively be reduced or eliminated by replacement with other functional equivalent systems such as the Mason Pfizer monkey virus (MPMV) system. This is known as the constitutive transport element (CTE) and comprises an RRE-type sequence in the genome which is believed to interact with a factor in the infected cell. The cellular factor can be thought of as a rev analogue. Thus, CTE may be used as an alternative to the rev/RRE system. Any other functional equivalents which are known or become available may be relevant to the invention. For example, it is also known that the Rex protein of HTLV-I can functionally replace the Rev protein of HIV-1. It is also known that Rev and Rex have similar effects to IRE-BP.
The NOIs may be operatively linked to one or more promoter/enhancer elements. Transcription of one or more NOIs may be under the control of viral LTRs, i.e. the 5′ U3 region, or they may be a heterologous promoter. Preferably the promoter is a strong viral promoter such as CMV, or is a cellular constitutive promoter such as PGK, beta-actin or EF1alpha. The promoter may be regulated or tissue-specific. Such promoters may be selected from genes such as neurofilaments, nestin, parkin, dopamine receptors, tyrosine hydroxylase. Such promoters may also contain neurorestrictive suppressor sequences such as that found in the mu-opoid receptor gene. In a preferred embodiment, the promoter may be glial-specific or neuron-specific. The control of expression can also be achieved by using such systems as the tetracycline system that switches gene expression on or off in response to outside agents (in this case tetracycline or its analogues).
A vector system used in the present invention, capable of delivering genes which encode TH, AADC and CH1, may have one or more of the following features, explained in more detail below:
Lentiviral vectors suitable for use in the present invention are also described in U.S. Pat. No. 7,259,015.
Tags, such a polyhistidine tags or a FLAGTM tag are commonly used at the N-terminus of proteins to aid protein purification or detection of the protein using tag-specific antibodies. Tags may be added by inserting the protein-coding DNA into a vector which comprises a sequence encoding the tag, so that it is automatically included within the coding sequence. Alternatively, PCR may be performed with primers which have the tag-encoding sequence adjacent to the start codon.
For dopamine-replacement gene therapy, there is no need for the encoded dopamine synthesis enzymes to have N-terminal tags. The presence of N-terminal tags therefore unnecessarily increases the length of the genome.
Codon optimisation has previously been described in WO99/41397. Different cells differ it their usage of particular codons. This codon bias corresponds to a bias in the relative abundance of particular tRNAs in the cell type. By altering the codons in the sequence so that they are tailored to match with the relative abundance of corresponding tRNAs, it is possible to increase expression. By the same token, it is possible to decrease expression by deliberately choosing codons for which the corresponding tRNAs are known to be rare in the particular cell type. Thus, an additional degree of translational control is available.
The genes delivered by the gene therapy system as well as components of the vector system may be codon optimised.
Many viruses, including HIV and other lentiviruses, use a large number of rare codons and by changing these to correspond to commonly used mammalian codons, increased expression of the packaging components in mammalian producer cells can be achieved. Codon usage tables are known in the art for mammalian cells, as well as for a variety of other organisms.
Codon optimisation has a number of other advantages. By virtue of alterations in their sequences, the nucleotide sequences encoding the packaging components of the viral particles required for assembly of viral particles in the producer cells/packaging cells have RNA instability sequences (INS) eliminated from them. At the same time, the amino acid sequence coding sequence for the packaging components is retained so that the viral components encoded by the sequences remain the same, or at least sufficiently similar that the function of the packaging components is not compromised. Codon optimisation also overcomes the Rev/RRE requirement for export, rendering optimised sequences Rev independent. Codon optimisation also reduces homologous recombination between different constructs within the vector system (for example between the regions of overlap in the gag-pol and env open reading frames). The overall effect of codon optimisation is therefore a notable increase in viral titre and improved safety.
In one embodiment only codons relating to INS are codon optimised. Alternatively sequences may be codon optimised in their entirety, with the exception of the sequence encompassing the frameshift site.
The gag-pol gene comprises two overlapping reading frames encoding gag and pol proteins respectively. The expression of both proteins depends on a frameshift during translation. This frameshift occurs as a result of ribosome “slippage” during translation. This slippage is thought to be caused at least in part by ribosome-stalling RNA secondary structures. Such secondary structures exist downstream of the frameshift site in the gag-pol gene. For HIV, the region of overlap extends from nucleotide 1222 downstream of the beginning of gag (wherein nucleotide 1 is the A of the gag ATG) to the end of gag (nt 1503). Consequently, a 281 by fragment spanning the frameshift site and the overlapping region of the two reading frames is preferably not codon optimised. Retaining this fragment will enable more efficient expression of the gag-pol proteins.
For EIAV the beginning of the overlap has been taken to be nt 1262 (where nucleotide 1 is the A of the gag ATG). The end of the overlap is at 1461 bp. In order to ensure that the frameshift site and the gag-pol overlap are preserved, the wild type sequence has been retained from nt 1156 to 1465.
Derivations from optimal codon usage may be made, for example, in order to accommodate convenient restriction sites, and conservative amino acid changes may be introduced into the gag-pol proteins.
Due to the degenerate nature of the Genetic Code, it will be appreciated that numerous gag-pol sequences can be achieved by a skilled worker. Also there are many retroviral variants described which can be used as a starting point for generating a codon optimised gag-pol sequence. Lentiviral genomes can be quite variable. For example there are many quasi-species of HIV-1 which are still functional. This is also the case for EIAV. These variants may be used to enhance particular parts of the transduction process. Examples of HIV-1 variants may be found at http://hiv-web.lanl.gov. Details of EIAV clones may be found at the NCBI database: http://www.ncbi.nlm.nih.gov.
The strategy for codon optimised gag-pol sequences can be used in relation to any retrovirus. This would apply to all lentiviruses, including EIAV, FIV, BIV, CAEV, VMR, SIV, HIV-1 and HIV-2. In addition this method could be used to increase expression of genes from HTLV-1, HTLV-2, HFV, HSRV and human endogenous retroviruses (HERV), MLV and other retroviruses.
Codon optimisation can render gag-pol expression Rev independent. In order to enable the use of anti-rev or RRE factors in the retroviral vector, however, it would be necessary to render the viral vector generation system totally Rev/RRE independent. Thus, the genome also needs to be modified. This is achieved by optimising vector genome components. Advantageously, these modifications also lead to the production of a safer system absent of all additional proteins both in the producer and in the transduced cell.
As described above, the packaging components for a retroviral vector include expression products of gag, pol and env genes. In addition, efficient packaging depends on a short sequence of 4 stem loops followed by a partial sequence from gag and env (the “packaging signal”). Thus, inclusion of a deleted gag sequence in the retroviral vector genome (in addition to the full gag sequence on the packaging construct) will optimise vector titre. To date efficient packaging has been reported to require from 255 to 360 nucleotides of gag in vectors that still retain env sequences, or about 40 nucleotides of gag in a particular combination of splice donor mutation, gag and env deletions. It has surprisingly been found that a deletion of all but the N-terminal 360 or so nucleotides in gag leads to an increase in vector titre. Thus, preferably, the retroviral vector genome includes a gag sequence which comprises one or more deletions, more preferably the gag sequence comprises about 360 nucleotides derivable from the N-terminus.
To ensure that translation begins from the correct start codon (ATG), upstream start codons in gag may be manipulated. Conveniently, upstream start codons are mutated by substitution e.g. ATG to ACG or insertion ATG to ATTG by techniques known in the art.
This ensures that the first available ORF of the mature mRNA in the target cells will be for the therapeutic gene.
In the context of the present invention, at least one potential start codon, preferably all the potential start codons in gag are mutated.
Insertion of an open reading frame, or part thereof, downstream of a viral LTR and upstream of an internal promoter has been shown to enhance viral titre in the absence of rev (as described in WO 03/064665). Thus in a preferred embodiment, a Neo-expression cassette is inserted downstream of gag.
The viral genome may comprise a post-translational regulatory element. For example, the genome may comprise an element such as the woodchuck hepatitis virus posttranscriptional regulatory element (WPRE), such as that described in U.S. Pat. No. 7,419,829.
The vector system may comprise a plurality of vectors, each capable of delivering a gene encoding an enzyme involved in dopamine synthesis.
An alternative strategy is to deliver all three genes to target cells using a single vector.
WO 02/29065 describes a tricistronic lentiviral vector capable of delivering genes encoding tyrosine hydroxylase (TH), aromatic L-amino acid decarboxylase (AADC), and GTP cyclohydrolase 1 (CH1) to a host cell. It is shown that expression of there enzymes causes production of dopamine, L-Dopa and DOPAC in cells in culture and is therapeutically effective against a rodent model of Parkinson's disease.
Adeno-associated virus vectors (AAVs) have also been used to deliver to the brain, genes associated with dopamine synthesis. The use of separate AAV vectors to transfer two or three critical genes has demonstrated some behavioural benefit in rat and non-human primate (NHP) models of PD (Kirik et al (2002) PNAS 99:4708-4713; Muramatsu et al (2002) Human Gene Therapy 13:345-354).
It was previously thought that delivery of three genes (for example genes encoding AADC, TH and GCH-1) to striatal cells using a single AAV vector would not be achievable due to the packaging restraints of these vectors (Kirik et al (2002) as above; Muruamatsu et al (2002) as above; Shen et al (2000) Human Gene Therapy 11:1509-1519; Sun et al (2004) Human Gene Therapy 15:1177-1196; Carlsson et al (2005) Brain 128:559-569).
However, recent reports have demonstrated that certain AAV vectors can efficiently incorporate large payloads (up to 8.9 kb). The most efficient of these vectors was found to have an AAV5 capsid and an AAV2 ITR (Allocca M. et al J. Clin Invest. (2008) 118: 1955-1964).
The viral genome of the vector system used in the invention comprises two or more NOIs. In order for both of the NOIs to be expressed, there may be two or more transcription units within the vector genome, one for each NOI. Retroviral vectors achieve the highest titres and most potent gene expression properties if they are kept genetically simple, and so it is preferable to use an internal ribosome entry site (IRES) to initiate translation of the second (and subsequent) coding sequence(s) in a poly-cistronic message.
Insertion of IRES elements into retroviral vectors is compatible with the retroviral replication cycle and allows expression of multiple coding regions from a single promoter. IRES elements were first found in the non-translated 5′ ends of picornaviruses where they promote cap-independent translation of viral proteins. When located between open reading frames in an RNA, IRES elements allow efficient translation of the downstream open reading frame by promoting entry of the ribosome at the IRES element followed by downstream initiation of translation.
A number of different IRES sequences are known including those from encephalomyocarditis virus (EMCV); BiP protein; the Antennapedia gene of Drosophila (exons d and e) as well as those in polio virus (PV).
According to WO-A-97/14809, IRES sequences are typically found in the 5′ non-coding region of genes. In addition to those in the literature they can be found empirically by looking for genetic sequences that affect expression and then determining whether that sequence affects the DNA (i.e. acts as a promoter or enhancer) or only the RNA (acts as an IRES sequence).
The term “IRES” includes any sequence or combination of sequences which work as or improve the function of an IRES.
The IRES(s) may be of viral origin (such as EMCV IRES, PV IRES, or FMDV 2A-like sequences) or cellular origin (such as FGF2 IRES, NRF IRES, Notch 2 IRES or EIF4 IRES).
In order for the IRES to be capable of initiating translation of each NOI, it should be located between or prior to NOIs in the vector genome. For example, for a multicistronic sequence containing n NOIs, the genome may be as follows:
For bi and tri-cistronic sequences, the order may be as follows:
Alternative configurations of IRESs and NOIs can also be utilised. For example transcripts containing the IRESs and NOIs need not be driven from the same promoter.
An example of this arrangement may be:
In any construct utilising an internal cassette having more than one IRES and NOI, the IRESs may be of different origins, that is, heterologous to one another. For example, one IRES may be from EMCV and the other IRES may be from polio virus.
IRESs are also suitable for use with AAV and adenoviral vectors.
The vector for dopamine replacement gene therapy used in the present invention may be present in a pharmaceutical composition, wherein the composition comprises a prophylactically or therapeutically effective amount of the vector.
The composition may optionally comprise a pharmaceutically acceptable carrier, diluent, excipient or adjuvant. The choice of pharmaceutical carrier, excipient or diluent can be selected with regard to the intended route of administration and standard pharmaceutical practice. The pharmaceutical compositions may comprise as (or in addition to) the carrier, excipient or diluent, any suitable binder(s), lubricant(s), suspending agent(s), coating agent(s), solubilising agent(s), and other carrier agents that may aid or increase the viral entry into the target site (such as for example a lipid delivery system).
The viral preparation may concentrated by ultracentrifugation. WO 2009/153563 describes methods for the downstream processing of lentiviral vectors. The resulting pharmaceutical composition may have at least 107 T.U./mL, for example from 107 to 109 T.U./mL, or at least 109 T.U./mL. (The titer is expressed in transducing units per mL (T.U./mL) as titred on a standard D17 of HEK293T cell lines).
The dopamine replacement gene therapy methods are used in conjunction with dopamine therapy. As shown in the Examples presented herein, gene therapy using a lentiviral vector expressing TH, AADC and CH1 shows a synergistic effect with L-Dopa treatment.
The vector system may be administered by injection. For example, the composition may be administered by injection into the caudate putamen. The vector may be administered via one, two, three, four, five, six or more tracts per hemisphere. Systems for administering lentiviral vectors are discussed in detail by Jarraya et al., Sci. Transl. Med. 1(2): 2ra4 (2009) and in GB application nos. 1009052.0, 1100502.2, and 1107184.2.
L-Dopa may be administered by any convenient means, such as orally or by intramuscular injection, and may be prior to or contemporaneous with dopamine replacement gene therapy.
Dyskinesia is the impairment of the power of voluntary movement, resulting in fragmentary or incomplete movements. Dyskinesias are a common side-effect of chronic L-Dopa intake. In many cases patients cycle between ON-drug periods, which are complicated with abnormal involuntary movements (dyskinesias), and OFF-drug periods where the patients are akinetic (muscle rigidity). It is thought that dyskinesias are at least partly caused by intermittent oral uptake of L-Dopa and consequent pulsatile stimulation of striatal dopamine receptors. Because the vector system used in the invention replaces dopamine by gene therapy, continuous delivery of dopamine should be achieved which maintains or restores constant dopaminergic tone in the striatum. Dyskinesias associated with aberrations in striatal tone in the subject should therefore be avoided. Dopaminergic tone may be achieved at physiological levels or subphysiological levels.
It has surprisingly been shown that dopamine replacement gene therapy is not only able to avoid dyskinesias associated with L-Dopa treatment, but to provide therapy for patients who have already developed dyskinesias from long-term L-Dopa treatment (see WO 2010/055290). Thus dopamine replacement gene therapy can prevent subsequent occurrences of dyskinesia following oral L-Dopa therapy.
The gene therapy strategy used in the present invention may induce dopamine synthesis in the striatum such that levels of dopamine are achieved which are higher than those associated with the untreated PD striatum, but lower than those associated with the non-PD striatum. The vector system may cause the production of sub-physiological levels of dopamine in the striatum.
Production of sub-physiological levels of dopamine has been shown by the present inventors to be therapeutically effective in a primate model of PD. Production of sub-physiological levels is preferable to the production of super-physiological levels as “over-dosing” with dopamine can be harmful, for example because it may induce dyskinesias. Also, over-production of the dopamine-producing enzymes may be harmful for the host cell.
Production of lower levels of enzymes also necessitates administration of less of the vector system for gene therapy, reducing costs and minimising any adverse effect associated with the treatment.
sIRNA/Micro RNA
The vector system may comprise or encode a siRNA or micro-RNA or shRNA or regulated micro or shRNA (Dickins et al. (2005) Nature Genetics 37: 1289-1295, Silva et al. (2005) Nature Genetics 37:1281-1288).
Post-transcriptional gene silencing (PTGS) mediated by double-stranded RNA (dsRNA) is a conserved cellular defence mechanism for controlling the expression of foreign genes. It is thought that the random integration of elements such as transposons or viruses causes the expression of dsRNA which activates sequence-specific degradation of homologous single-stranded mRNA or viral genomic RNA. The silencing effect is known as RNA interference (RNAi) (Ralph et al. (2005) Nature Medicine 11:429-433). The mechanism of RNAi involves the processing of long dsRNAs into duplexes of about 21-25 nucleotide (nt) RNAs. These products are called small interfering or silencing RNAs (siRNAs) which are the sequence-specific mediators of mRNA degradation. In differentiated mammalian cells dsRNA>30 bp has been found to activate the interferon response leading to shut-down of protein synthesis and non-specific mRNA degradation (Stark et al. (1998)). However this response can be bypassed by using 21nt siRNA duplexes (Elbashir et al. (2001), Hutvagner et al. (2001)) allowing gene function to be analysed in cultured mammalian cells.
Micro-RNAs are a very large group of small RNAs produced naturally in organisms, at least some of which regulate the expression of target genes. Founding members of the micro-RNA family are let-7 and lin-4. The let-7 gene encodes a small, highly conserved RNA species that regulates the expression of endogenous protein-coding genes during worm development. The active RNA species is transcribed initially as an ˜70 nt precursor, which is post-transcriptionally processed into a mature ˜21 nt form. Both let-7 and lin-4 are transcribed as hairpin RNA precursors which are processed to their mature forms by Dicer enzyme.
Oral L-Dopa treatment can be associated with cognitive impairment.
Parkinson's disease is characterised primarily by dopamine depletion in the dorsal striatum. Dopamine function in the ventral or “cognitive” striatum and the prefrontal cortex is usually unaffected. Oral administration of L-Dopa stimulates all the brain dopaminergic systems, meaning that it “over-doses” the cognitive striatum and impairs associated cognitive functions.
It has surprisingly been found that, by using gene therapy to replace dopamine, both local and tonic dopamine levels are restored. In other words, dopamine replacement gene therapy elevates dopamine levels in the dorsal striatum without over-raising dopamine levels in the cognitive striatum.
The methods of the present invention therefore treat and/or prevent Parkinson's disease without causing cognitive impairment.
Motor dysfunction associated with Parkinson's disease is thought to arise from dysfunction of the basal ganglia, the deep brain structures which control movement.
It is thought that abnormal over-activity of output nuclei such as the internal globus pallidus (GPi) is responsible.
Surprisingly it has been found that dopamine replacement gene therapy can normalise neuronal activities in the basal ganglia output nuclei, reducing the abnormal high firing rate of PD GPi neurons and reducing the proportion of spikes per burst and the number of burst events in the neuronal firing pattern.
Dopamine replacement gene therapy also reduces neuronal hyperactivity in the subthalamic nucleus (STN). This is detectable by looking at decreases in metabolic activity of the STN.
The present invention provides a method for normalising neuronal electrical activity in basal ganglia and/or subthalamic nucleus in a Parkinson's disease subject by administration of a vector system for dopamine replacement gene therapy to the subject.
The term “normalising” in this context means that the increase in the mean firing rate of GPi neurons and/or neuronal hyperactivity in the STN associated with PD is reduced. The mean firing rate and/or neuronal activity may be maintained at a normal, non-PD level, reduced to a non-PD level, or reduced such that it is still elevated compared to a non-PD individual, but still less that the level which would be expected in an individual without treatment.
Looking at the pattern of neuronal firing, administration of the vector system reduces the number of spikes per burst and/or the number of burst events in the GPi.
If the patient is treated before onset of symptoms, the vector system may normalise number of spikes per burst and/or the number of burst, such that they are not raised or not raised to the same extent that they would be in the absence of treatment.
The invention will now be further described by way of Examples, which are meant to serve to assist one of ordinary skill in the art in carrying out the invention and are not intended in any way to limit the scope of the invention.
A tricistronic lentiviral vector was designed that encodes the genes for TH, AADC and CH1 (Lenti-TH-AADC-CH1). To improve vector-mediated dopamine production, a number of changes were made to the original EIAV vector genome that expressed the tricistronic cassette called pONY8.1TSIN (Azzouz et al (2002) J. Neurosci. 22:10301-10312). These changes led to at least a 2 log increase in dopamine production per integrated genome as assessed in vitro after transduction of human HEK293T cells (
To model advanced PD in non-human primates, the selective neurotoxin MPTP was systemically administered to adult Macaca fascicularis until they reached a severe and stable bilateral Parkinsonian syndrome, including akinesia, flexed posture, balance impairment and tremor. Before MPTP treatment, all primates scored 0 on the clinical rating scale (CRS). After MPTP, but before any lentiviral injection, macaques displayed a significant increase in the CRS approaching the maximal disability score (max=14) compared to the control pre-MPTP state (Normal state;
The construction and production of lentiviral vectors was performed by Oxford BioMedica. Lentiviral vectors were derived from EIAV, and encoded for either TH-AADC-CH1 in the same polycistronic vector (Lenti-TH-AADC-CH1), or for lacZ as a control (Lenti-lacZ). Twenty-six adult male Macaca fascicularis were used. The synthetic agent 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) is a neurotoxin that is transformed in vivo into MPP+, which has both high-affinity and high-toxicity for dopaminergic neurons. The MPTP macaque is considered as the most predictable among preclinical experimental models of PD. A subchronic protocol for MPTP intoxication was used (0.2 mg/kg/day). Objective behavioural analysis was used to determine when MPTP treatment should be halted. As soon as the primates had reached the behavioural criteria that corresponded to advanced PD model, MPTP treatment was stopped. Special attention was made to feed and nurse the animals, especially following MPTP lesioning. Lentiviral vectors were injected into the motor putamen of MPTP macaques. All surgical procedures used individual MRI based stereotaxy. Behavioural analysis used both automated quantitative video approaches, and qualitative clinical evaluation made in strict blind conditions. Immunohistochemistry and stereology were performed using standard techniques. Dopamine production was assessed by HPLC analysis of in vivo microdialysis samples and post-mortem brain tissue. L-Dopa was administrated orally, except during microdialysis experiments where it was injected i.m. Apomorphine was injected i.m. Single cell electrophysiology recording was performed using standard techniques. Functional imaging was performed by assessment of local cerebral glucose utilization using [14C]-2-Deoxyglucose (2-DG). Data were analysed with Kruskal-Wallis (KW) or Friedman test (the non-parametric equivalent of the repeated measures ANOVA) and then, with Mann-Whitney (MW) post-hoc test at the individual time-points, corrected for multiple comparisons.
All animal studies were conducted in accordance with the European convention for animal care (86-406) and the NIH's Guide for the Care and Use of Laboratory Animals. Twenty-six adult male Macaca fascicularis, weighing 5-7 kg, were included in this study. Animals were housed individually with a 12/12 h light/dark cycle. Following lentiviral vector injections, experiments were performed using level III Biosafety procedures (BSL3).
Neurotoxin MPTP was first administrated to 23 macaques until they developed severe Parkinsonism, these were then divided into experimental groups according to the following experiments:
For all MPTP-treated animals, the complete study involved daily clinical assessment, plus a series of behavioural analyses. One additional normal, non MPTP-treated, animal was included for immunohistochemistry and biochemistry studies. Two MPTP-treated and two unlesioned animals were included in the imaging and electrophysiological studies. Autoradiography imaging studies were performed in the final stage of the experiments, one month after electrophysiological recordings in the GPi.
To improve vector-mediated dopamine production, a number of changes were made to the original EIAV vector genome that expressed the tricistronic cassette called pONY8.1TSIN (
HEK293T cells were seeded in DMEM-HEPES with 10% (v/v) FCS at a density of 4.4×104 cm−2 in a 10 layer cell factory. The next day cells were transfected with the pESYNGP (an EIAV codon optimized gag/pol expression construct), pRV67 (a VSV-G envelope expression plasmid) and EIAV-lacZ (an EIAV vector genome expressing LacZ under the control of the human cytomegalovirus immediate-early enhancer/promoter, or Lenti-TH-AADC-CH1 using Fugene-6 (Roche). Sixteen hours after transfection the cells were treated with 10 mM Sodium Butyrate for 6 hours and then the culture medium was replaced with butyrate-deficient medium. At 40 hours post transfection the culture medium was collected, centrifuged at 1000×g for 5 min and filtered through a 0.45 μm filter unit. The vector was concentrated by low speed centrifugation (6000×g for 16 h at 4° C.) followed by ultracentrifugation (50000×g, for 90 minutes at 4° C.). The vector was resuspended in TSSM buffer consisting of sodium chloride (100 mM), Tris, pH 7.3 (20 mM), sucrose (10 mg·ml) and mannitol (10 mg·ml), aliquoted and stored at −80° C. The vector titre was obtained by carrying out a DNA integration assay. Briefly this involves transducing HEK293T cells with the viral vector and passaging the cells for approximately 10 days. The titre of Lenti-lacZ was 3.5×109 TU/ml and Lenti-TH-AADC-CH1 1.0-2.7×108 TU/ml.
All animals were assessed daily for their general clinical condition with special attention paid to the nutritional status. At the same time, the general neurological state of each macaque was assessed both pre- and post-lentiviral injections. To objectively quantify our neurological observations, animals were video-taped for 30 minutes before MPTP lesioning and at regular intervals following viral injections. The videos were then analyzed off-line by an examiner blinded to the experimental conditions. A clinical rating-scale was adapted from the Papa and Chase MPTP primate Parkinsonian scale (posture 0-2, gait 0-2, tremor 0-2, general mobility 0-4, hand movements 0-2, climbing 0-4; a score of 0 corresponds to a normal monkey). The quantitative analysis of dyskinesia was performed using a motion counting software (The Observer 7, Noldus, Wageningen, The Netherlands) that allowed to count predefined movements (superior and inferior members, trunk, face and neck chorea and dystonia for dyskinetic movements) during the video recording period. Video-movement analysis was performed using a motion tracking software (Ethovision 3, Noldus, Wageningen, The Netherlands) that allowed an objective measurement of total distance moved (traveled distance, cm), maximum velocity (maximal velocity, cm/sec) and rearing behaviour frequency (rearing, number of events) during the video-recording period.
All primates received a daily intramuscular dose of 0.2 mg/kg of MPTP (Sigma Aldrich, St Louis, Mo.) until they reached a severe stable bilateral Parkinsonian syndrome. MPTP administration was halted when animals reached an increase of the clinical rating scale to ≧10 and a decrease of traveled distance ≦500 cm/30 min, maximal velocity ≦5 cm/sec/30 min, rearing ≦5/30 min, as assessed by video-recording session performed 1 week after last MPTP injection. The stability of Parkinsonian syndrome was then checked, using same behavioural criteria, during the 8 weeks following the last MPTP injection.
Under generalized anaesthesia with a mixture of Ketamine and Xylazine (15 mg/kg+1.5 mg/kg, every hour), nine Parkinsonian MPTP macaques received five stereotaxic injections of Lenti-lacZ or Lenti-TH-AADC-CH1 bilaterally (10 μl/injection i.e. 50 μl/putamen and a total of 100 μl per animal) into the commissural (10 μl) and post-commissural putamen (10 μl×4) under sterile conditions. Target coordinates were based upon MRI guidance (1.5-T MR magnet, General Electric medical system, Waukesha, Wis.) using neuronavigation methods. The first injection was aimed at the commissural level of the putamen followed by a group of 2 injections (second and third injection, 1 mm apart) 2 mm caudal from the anterior commissure and by a second group of 2 injections (forth and fifth injection, 1 mm apart) 5 mm caudal from the anterior commissure. All injections were placed in the dorsolateral part of the putamen. Lentiviral vector was injected manually in each of the 10 stereotactical tracks through a 10-μl Hamilton syringe at a rate of 1 μl/min. The needle was left in situ for an additional 2 min. All needle tracks were bilaterally located in the putamen as observed by Niss1 staining and immunohistochemical studies (
Eight weeks after lentiviral vector injections, six macaques were deeply anesthetized with ketamine (15 mg/kg), euthanized by an overdose of pentobarbital (100 mg/kg, intravenously; Sanofi, France) and perfused transcardially with cold saline. Brains were removed immediately, hemisected by a midline sagittal cut and slabbed on a monkey brain slicer. Slabs through the right putamen were punched for HPLC studies, using cylindric brain punchers (internal diameter 1.5 mm). Length of punches was approximately 1 mm. The tissue slabs were then immersed in a cold 4% paraformaldehyde fixative solution for 6 days, washed in a series of cold graded sucrose solutions for 4 days and sectioned in a coronal plane on a freezing microtome (sections 40 μm in thickness). Sections for immunohistochemical labeling were first incubated for 48 h at room temperature or 72 h at 4° C. in phosphate buffer saline containing 0.5% triton-X100, 2% bovine serum albumin, 3.5% normal serum and the appropriate dilution of the first antibody: anti-TH, 1:1000 dilution (Institut Jacques Boy, Reims, France); anti-AADC, 1:250 dilution (Chemicon, CA); anti-dopamine, 1:1000 dilution (AbCam, Cambridge, UK), anti-CH1, 1:3000 (a kind gift from Ernst Werner, University of Innsbruck); anti-β-Gal, dilution 1:2000 (Chemicon, CA), anti-NeuN, dilution 1:5000 (Chemicon, CA), anti-DAT, dilution 1:7500 (Chemicon, CA), anti-GFAP, dilution 1:30000 (DakoCytomation, Glostrup, Denmark), anti-CD68, dilution 1:100 (DakoCytomation, Glostrup, Denmark). After incubation in the primary anti-serum, sections were processed with the avidin-biotin peroxidase method. The TH transgene used in the present lentiviral vector is a truncated form (trunc-TH2) of the human TH isoform 2 (hTH2). To study the expression of striatal transgenic TH, a TH antibody that recognizes both N-terminal regulatory and C-terminal catalytic units of hTH2 was used.
To identify the cell types transduced with EIAV vectors, an indirect immunofluorescence double-label technique was employed. An indirect immunofluorescence double-label technique was employed to label βGal-positive cells in the striatum of EIAV-lacZ injected animals with a neuronal (NeuN) and glial (GFAP) markers. For each experiment, background staining was inhibited with a 1-h incubation in a blocking solution (4.5% normal goat serum and 0.2% Triton X-100 in PBS, pH 7.4) at room temperature. Sections were then incubated in primary rabbit polyclonal antibody to βGal (AbCam, 1:1000) overnight at room temperature. After washes, the sections were incubated in the secondary goat anti-rabbit IgG coupled to the fluorescent marker Alexa 488 (1:200) for 1 h. After washes, sections were incubated in one of the following the primary antibodies: mouse monoclonal anti-NeuN (Chemicon; 1:1000), mouse monoclonal anti-GFAP (Sigma; 1:3000), overnight at RT. After incubation in the secondary antibody (biotinylated goat anti-mouse IgG 1:200) for 1 h at room temperature, the sections were placed in fluorolink Cy 3-labeled streptavidin (1:1000) for 1 h at room temperature. All fluorescence images were analyzed with the Zeiss Confocal Fluoroview microscope equipped with argon and He—Ne lasers.
Stereological analysis was used for cell counts. To evaluate the total number of EIAV-positive cells within the striatum, i.e. number of transduced cells, alternate sections were stained for β-galactosidase immunoreactivity βGal-ir) and positive cells counted throughout the entire striatum of Lenti-lacZ injected animals. To evaluate the total number of remaining dopaminergic cells within the substantia nigra, alternate sections stained for tyrosine hydroxylase immunoreactivity (TH-ir cells) were counted throughout the entire SNpc of unlesioned normal controls, MPTP-Lenti-lacZ and MPTP-Lenti-TH-AADC-CH1 injected animals. Stereological count of cells was processed using Olympus stereology software C.A.S.T.-Grid (Olympus Denmark, Albertslund, Denmark) and a computer-assisted image analysis system (Olympus Pentium II) linked to an Olympus Provis microscope (Olympus France, Rungis, France) equipped with a video camera (HAD Power 3CCD, Sony) and a computer-controlled motorized stage. Stereological analyses used the optical fractionator procedure, a design-based stereological method for estimating total number of structures in a known fraction of a defined reference space without being affected by tissue shrinkage.
For the striatal EIAV-positive cell counting, a coefficient of error of <0.10 due to the estimation was accepted. For the SNpc TH-ir cells, a higher coefficient of error (<0.35) was accepted. This was related to the dramatic decrease in the number of TH-ir cells after the MPTP intoxication, leaving a very few objects to count.
The animals in the L-Dopa group were treated chronically with an average daily oral dose of 20 mg/kg L-Dopa and benserazide (at a 4:1 ratio, Modopar Dispersible®, Roche, France) (termed “L-Dopa” thereafter). During the L-Dopa challenge of MPTP, Lenti-LacZ and Lenti-TH-AADC-CH1 non-primed primates, animals received a single oral dose of 20 mg/kg of L-Dopa and benserazide (at a 4:1 ratio, Modopar Dispersible®, Roche, France). During the microdialysis experiment, primates were challenged with a single dose of 40 mg/kg i.m. of L-Dopa and benserazide (at a 4:1 ratio, methyl-esther-L-Dopa, Sigma Aldrich, St Louis, Mo.).
Short acting D1/D2 Agonist Administration
Apomorphine (Aguettant, Lyon, France), a short acting non selective D1/D2 agonist, was administered systemically at a dose (0.1 mg/kg i.m.) known to induce dyskinesia in MPTP-treated macaques.
Primates were anesthetized with Ketamine and Xylazine (15 mg/kg+1.5 mg/kg, every hour) and placed in a stereotaxic frame. The body temperature was stabilized at 37° C. throughout the experiment with a thermostatic blanket. The microdialysis probes (CMA/12, membrane length 5 mm, cut-off 20 kDa; CMA Microdialysis, North Chelmsford, Mass.) were implanted bilaterally in the striatum. Microdialysis probes were placed into the post-commissural putamen of four normal unlesioned animals, four MPTP animals, three MPTP-Lenti-LacZ animals, and two MPTP-Lenti-TH-AADC-CH1 animals. Probes were perfused with aCSF (in mM: 147 NaCl, 2.7 KCl, 1.2 CaCl2, and 0.85 MgCl2) at a rate of 2 μl/min. Microdialysates were collected every 15 min into a refrigerated fraction collector and frozen at −80° C. until analysis. Following implantation of each probe into the primate brain, microdialysis samples were taken over a 2 hour stabilisation period allowing recovery from any transient increase in neurotransmitter release due to procedural trauma. Baseline samples were then taken over the next hour. Then, following collection of baseline samples, animals were subjected to an acute Dopamine (Dopamine 40 mg/kg i.m.) or L-Dopa challenge (L-Dopa methyl ester, 40 mg/kg i.m.) and additional microdialysis samples were taken continuously over a 2 hour period. By the end of the microdialysis session, additional control samples were generated by performing microdialysis for 30 minutes in a solution of known dopamine concentration (1 μM) following removal of the probe from the putamen. This allows for the calculation of the efficiency of each probe and will enable estimation of the actual dopamine concentration in the putamen. After each experiment, the location of probes was checked using T2*-weighted MRI.
High-performance liquid chromatography (HPLC) with electrochemical detection was used to measure striatal levels of catecholamines in brain punches and microdialysis samples. Briefly, brain punches were homogenized in homogenization buffer (1.2 mM HEPES, 1% Triton X-100, 10% glycerol supplemented with protease inhibitors, pH 7.2). Catecholamines were extracted by mixing the tissue homogenates with one tenth of a volume of extraction buffer (0.4M perchloric acid, 0.1 mM EDTA pH8.0). The supernatants were then centrifuged and filtered. Microdoalysis samples were treated with one sixth of a volume of 0.2M perchloric acid. The supernatants or microdialysis samples were applied to an HPLC system (Agilent 1100) equipped with an ESA Coulochem II electrochemical detector (ESA Analytical). Catecholamines from brain homogenates were separated using a HR-80 column (ESA Analytical) and Cat-A-Phase mobile phase (ESA Analytical) at a flow rate of 1.5 ml/min and then detected electrochemically.
The sensitivity of the HPLC system was validated by running catecholamine standards through the HPLC and detection system and evaluation of output traces. Standard solutions containing L-Dopa, DOPAC, HVA and dopamine in the range of 10-1000 pg/ml were made up in a solution of 1:5 artificial CSF in standard diluent to ensure the same background signal as the microdialysis samples. One hundred microlitres of each standard solution (0.5-100 pg of each catecholamine) was run through the HPLC system and the output for each metabolite analysed. Standard curves for each metabolite were generated from these data and the concentration of catecholamines in microdialysis samples was calculated from these curves.
Microdialysis samples were thawed and 5 μl of 0.2M perchloric acid added to each sample prior to HPLC analysis. Samples were diluted 1 in 5 in standard diluent (ESA) and 100 μl injected for each analysis. Further dilution (1/10) was required for analysis of L-Dopa and HVA levels using the remaining sample. Samples were run on an Agilent 1100 HPLC machine and separated using a MD-150 column (ESA Analytical) and MD-TM mobile phase (ESA Analytical) at a flow rate of 0.6 ml/min and then detected electrochemically using a Coulchem II electrochemical detector (ESA). To improve efficiency of dopamine detection a specialised Microdialysis cell (5014B, ESA) was used in conjunction with the detector to allow detection of low levels (<1 pg) of dopamine.
Under constantly monitored ketamine/xylazine anesthesia (15 mg/1.5 mg/kg), single-unit activities were recorded only during a time period when stable heart rate, respiratory frequency, and CO2 expiratory flow were observed. A glass-coated tungsten microelectrode was stereotactically implanted under MRI guidance into the internal Globus Pallidus. Recording locations were verified by histological reconstruction of the electrode tracks. Signal was amplified and band-pass filtered (300-5000 Hz) using Leadpoint (Medtronic, Minneapolis, Minn.). Single-cell action potentials were first threshold or template extracted, and only well-isolated units were selected for further analysis. Twenty second spike trains were recorded and stored for offline analysis. Neuronal activity was extracted using a threshold or template-matching algorithm (Dataview4.5; W. J. Heitler, University of St. Andrews, Scotland), and mean firing rates were calculated. Bursting discharge was quantified using the Poisson “surprise” method of burst detection with a Poisson surprise value of >10. The proportion of spikes in burst discharges compared with the total number of spikes sampled for each cell was determined.
LCGU was measured in macaques on the day they were sacrificed. Experiments were performed on animals anaesthetized with propofol. Body temperature was monitored rectally and maintained at 37° C. using a thermostatically controlled heating pad. Polyethylene catheters were inserted into a femoral vein and artery for subsequent i.v. administration of 2-DG and sampling of arterial blood. The procedure was initiated by the infusion of an intravenous pulse of 100 μCi/kg 2-deoxy-D-[14C]glucose (PerkinElmer Life Sciences, Boston, Mass.; specific activity 50-55 mCi/mmol). Timed arterial blood samples (0.25, 0.5, 0.75, 1, 2, 5, 7.5, 10, 15, 25, 35, and 45 min) were drawn thereafter at a schedule sufficient to define the time course of the arterial 2-[14C]deoxyglucose and glucose concentrations. Arterial blood samples were centrifuged immediately. Plasma 14C concentrations were determined by liquid scintillation counting (Beckman Instruments, Fullerton, Calif.), and plasma glucose concentrations assessed using a glucometer (OneTouch® Ultra® Blood Glucose Monitoring System, Lifescan, Johnson&Johnson, Issy-les-Moulineaux, France). Forty-five min after tracer injection, the animals were sacrificed by an intravenous overdose of sodium pentobarbital (150 mg/kg i.v.). The brain was rapidly removed and frozen in isopentane (−45° C.), and stored at −80° C. for later autoradiography processing. Coronal brain sections (20 μm thick) covering the entire striatum, premotor and pre-frontal cortex (50 sections) were obtained at −20° C. with a cryomicrotome, mounted on superfrost slides, quickly dried and exposed onto an autoradiographic film (Kodak BioMax MR) for 7-10 days, with calibrated [14C]-standards (American Radiochemical Company, St. Louis, Mo., USA). The same brain sections were then stained with Cresyl Violet, and optical images from these sections were reconstructed in a 3D volume space. Autoradiograms were digitized and analyzed using a computer-based image analysis system (MCID Analysis, St. Catharines, Ontario, Canada). Then optical images from autoradiograms were co-aligned with the co-registered 3D anatomical space to provide anatomic and functional volumes. Optical densities determined in the STN on the autoradiograms (10-13 sections per STN) were converted to radioactivity and then to glucose consumption values using the [14C] standards and the modified operational equation of Sokoloff.
Values are mean±s.e.m. Data were analysed with Kruskal-Wallis (KW) or Friedman test (the non-parametric equivalent of the repeated measures ANOVA) and then, with Mann-Whitney (MW) post-hoc test at the individual time-points, corrected for multiple comparisons, using SPSS software (SPSS Inc., Chicago, Ill.).
To investigate the potential of gene transfer of TH, AADC and CH1 to correct Parkinsonism, a long term study was performed in the MPTP primate model of PD. A tricistronic lentiviral vector was designed that encodes the genes for TH, AADC and CH1 (Lenti-TH-AADC-CH1). One to eight weeks after the cessation of MPTP intoxication, 18 MPTP treated macaques were assigned into three behaviourally equivalent groups. The first group (MPTP-Lenti-TH-AADC-CH1, n=6) received bilateral injections of Lenti-TH-AADC-CH1 into each motor putamen. The second group (MPTP-Lenti-lacZ, n=6) received a control EIAV vector encoding the LacZ reporter gene. The third group (MPTP-long term, n=6) did not receive any surgical intervention but were included as an additional control to evaluate the stability of the MPTP model. All animals were maintained throughout the study without treatment using L-Dopa or dopaminergic drugs.
Animals treated with Lenti-TH-AADC-CH1 demonstrated significant improvements in akinesia and posture as early as the second week post-vector injection compared with controls (Friedman P<0.001, Post-hoc MW MPTP-long term, p<0.05, MPTP-LacZ p<0.05) (
To investigate in vivo gene transfer and lentiviral mediated dopamine production, histological analysis of transgene expression was performed and local dopamine levels were measured in the striatum of study animals. Animals treated with Lenti-LacZ were demonstrated to have an average of 54 947 transduced cells per injected putamen, which were mostly neurons (NeuN-ir positive >90%,
To quantitatively measure lentiviral mediated dopamine production in the putamen, two indices were applied: (1) whole tissue dopamine levels [DA]wt, measured by post-mortem analysis of striatal punches: this index quantifies both intracellular dopamine (presynaptic nigral dopaminergic terminals) and extracellular dopamine contents; (2) extracellular dopamine levels [DA]wt, measured by in vivo microdialysis: this index specifically quantifies the released dopamine within the extracellular milieu. To measure [DA]wt, fresh brain punches were taken from each animal at the time of sacrifice. Lenti-TH-AADC-CH1 significantly increased [DA]wt in dorsal putamen (
To assess dopaminergic tone within the striatum, [DA]ec levels were measured in Normal (unlesioned n=6), MPTP-long term (n=7), MPTP-Lenti-LacZ (n=5) and MPTP-Lenti-TH-AADC-CH1 (n=3) primates. Microdialysis probes were placed in the post-commissural putamen for each animal (see methods section,
The behavioural efficacy observed in MPTP-Lenti-TH-AADC-CH1 animals was not a consequence of less efficient nigro-striatal lesioning. Stereology counts of dopaminergic neurons in the substantia nigra pars compacta (SNpc) showed a dramatic decrease in the number of TH-ir neurons of both MPTP-Lenti-TH-AADC-CH1 and MPTP-LacZ groups compared to normal animals (KW p<0.001; Post-hoc MW p<0.001,
To determine the mechanism by which Lenti-TH-AADC-CH1 corrected motor dysfunction, neuronal activity was investigated within the basal ganglia system. The current model of basal ganglia dysfunction in PD suggests that abnormal over-activity of output nuclei such as the internal globus pallidus (GPi) account for the motor symptoms observed in this disorder. To determine if Lenti-TH-AAADC-CH1 could normalize neuronal electrical activities in basal ganglia output nuclei, normal and MPTP-treated macaques underwent unitary recordings in the GPi. In agreement with previous reports, a significant increase (52%, MW; p<0.01) in the mean firing rate of GPi neurons was found in drug naïve untreated MPTP macaques compared to controls (
The pattern of neuronal firing in the GPi is also important in the pathophysiology of PD, and so the burst activity of recorded GPi neurons was also analyzed. Pattern analysis revealed that the proportion of spikes per burst and the number of burst events significantly increased in MPTP primates (15.9% and 9.7 events/cell/min respectively) compared to controls animals (3.8% and 1.7 events/cell/min respectively; MW, p<0.05). Treatment with Lenti-TH-AAADC-CH1 significantly decreased the proportion of spikes per burst and the number of burst events in GPi neurons to levels that were very similar to those observed in normal unlesioned animals (5.3% and 1.6 events/cell/min respectively; p<0.05) (
Neuronal hyperactivity in the subthalamic nucleus (STN) is another key pathophysiological feature of PD, and its electrical neuromodulation has been therapeutically successful both in MPTP macaques and PD patients. Metabolic studies of basal ganglia both in PD patients and primate models of nigrostriatal degeneration have demonstrated alterations in the cortico-basal loops. Using [14C] 2-deoxyglucose (2-DG) (150 μm spatial resolution) functional imaging, it was found that the STN in an MPTP control macaque showed an increase in metabolic activity compared to a normal macaque (
A major challenge in PD is to restore dopaminergic function without inducing any dyskinetic movement. Because striatal histological abnormalities can induce dyskinesia, the morphological alterations following gene transfer were investigated. Whereas all needle tracks were located in the putamen (
One critical issue for the clinical application of Lenti-TH-AADC-CH1 is the potential of the vector to induce dyskinesias in PD patients. Evaluation of dyskinesias was performed in the efficacy studies describe above using a novel method for dyskinesia quantification based on video dyskinesia analysis (VDA) that assesses the whole range of dyskinetic movement continuously during the observed video sequence, using a standardized protocol. Lenti-TH-AADC-CH1 did not induce any dyskinetic movements in MPTP primates up to 30 months, in contrast to oral L-Dopa intake in control MPTP animals (n=5) (
To mimic clinical conditions, these drug-naive animals were further challenged with acute systemic administration of L-Dopa then with a pro-dyskinetic short-acting D1/D2 dopaminergic agonist (apomorphine). Oral L-Dopa intake and apomorphine injection both improved the locomotor activity of MPTP-long term and MPTP-LacZ primates to levels similar to that of normal primates (MW, p<0.05) (
Having demonstrated the capability of dopamine gene therapy to prevent dyskinesia, the approach was subsequently tested in a primate model of L-Dopa induced dyskinesia (LID) to see if ProSavin® treatment could reverse dyskinesias that were already established in the animal model.
A group of six MPTP-treated primates were treated with repeated, daily oral L-Dopa, from 20 mg/kg/d to 100 mg/kg/d, adjusted for each individual, until animals developed sustained and severe LID (LID-MPTP animals) (n=6). The animals then received bilateral injections into the motor striatum (as performed in the MPTP-treated drug-naïve primates) of either Lenti-TH-AADC-CH1 (n=3) or Lenti-lacZ (n=3). To closely mimic the clinical trial situation in LID PD patients, we then adjusted the daily dose of L-Dopa treatment for each individual animal (in the MPTP-LacZ and MPTP-Lenti-TH-AADC-CH1 group) to maintain the daily locomotor activity at its pre-MPTP-lesioning value. Thus changes in the dose of the daily L-Dopa treatment were based only on the “OFF” drug motor state (as evaluated with VMA). This approach is currently used to find optimal L-Dopa doses in patients implanted with deep brain stimulation electrodes (Bejjani et al (2000) Ann Neurol 47:655-658). Following striatal injections of Lenti-TH-AADC-CH1, LID-MPTP animals progressively recovered from their parkinsonism in the OFF L-Dopa state. Accordingly the treatment management protocol led to a progressive decrease of average L-Dopa intake in the LID-MPTP-Lenti-TH-AADC-CH1 animals from 70 mg/kg/day to 30 mg/kg/day at 6 months after vector injection, whereas daily L-Dopa treatment was stable at 67 mg/kg/day in LID-MPTP-Lenti-LacZ since no behavioural recovery was observed. (See Jarraya et al., Sci. Transl. Med. 1(2): 2ra4 (2009).)
In the ON L-Dopa state (periodic challenge with a set dose of 40 mg/kg of L-Dopa), the level of dyskinesia in Lenti-TH-AADC-CH1 treated animals was decreased and reached less than 25% of their initial levels (
These results indicate that treatment with Lenti-TH-AADC-CH1 has the potential to not only provide therapeutic efficacy in a PD patient that has already developed dyskinesias from long term L-Dopa treatment but also to reverse the physiological mechanism of dyskinesias and thus prevent subsequent occurrences following L-Dopa therapy.
A phase I/II clinical trial is ongoing to evaluate the safety and efficacy of ProSavin® for the treatment of PD. As part of the trial, the therapeutic potential of ProSavin® to correct symptoms of Parkinson's disease was evaluated. A total volume of 50 μL or 125 μL of vector was administered to each putamen through 5 needle tracts using a Hamilton syringe and 23-gauge needle at an administration rate of 1 μL/min, or a total volume of 125 μL of vector was administered through 3 needle tracts using a Hamilton syringe and a 28-gauge needle at an administration rate of 3 μL/min.
All patients were injected with ProSavin intrastriatally under general anaesthesia using bilateral stereotaxic injections. A cranial MRI scan was performed prior to the administration to provide precise injection coordinates for targeting the sensorimotor putamen region of the putamen.
For each injection a guide tube of 130 mm in length with a bore diameter of 1.2 mm was inserted into the correct position within the brain, using the MRI-derived coordinates, without entering the putamen. ProSavin® was loaded into a Hamilton syringe attached to a 23 gauge or 28 gauge point two style bevelled non coring needle, 150 mm in length. The needle was lowered into the brain through the guide tube and penetrated the motor putamen. The guide tube was then withdrawn approximately 10 mm prior to infusion of ProSavin®. A new guide tube, Hamilton syringe and needle were used for each hemisphere of the brain.
ProSavin® (50 or 125 μL) was administered to each of three or five separate tracts in both brain hemispheres. Administration was performed manually in each of the injection tracts at a rate of 1 μL per minute or using continuous infusion (controlled by the use of a pump) at a constant delivery rate of 3 μL/min.
The surgical procedures were safe and well tolerated in all patients, and there were no serious adverse events reported in any patients relating to either ProSavin®.
The primary efficacy endpoint of the study was improvement in the motor part (part III) of the Unified Parkinson's Disease Rating Scale (UPDRS) at 6 months post treatment, compared with baseline scores.
A summary of improvements in motor function to date, is shown in Table 1 (motor function is assessed according to the Unified Parkinson's Disease Rating Scale [UPDRS] in patients' “OFF” state). Assessments in the “OFF” state are defined as before the first morning dose of L-Dopa and at least 12 hours after the last administration of L-Dopa the previous day.
A mean improvement in UPDRS part III scores of 30-43% was observed at 6 months post treatment. Improvement was sustained in the two cohorts tested at one year post-treatment, and beneficial effects were also observed at two years post-treatment in one cohort.
The patients discussed in Example 6 were also evaluated in the ON state. Assessments in the “ON” state are defined as a minimum of one hour after a dose of L-Dopa. These patients showed an average improvement of 26% in UPDRS part III “ON” score at 6 months post-treatment.
Following treatment with ProSavin® the mean daily L-Dopa equivalent dosages (LEDD) remained stable or were reduced for up to 24 months post treatment for the three cohorts of Parkinson's patients treated with ProSavin in the Phase I/II clinical trial (
Patients completed self reporting diaries detailing their motor function so that a percentage of time in ON and OFF L-Dopa states could be evaluated. Cohorts 1 and 2a kept diaries for seven routine days and patients in cohort 2b kept diaries for two routine days in the week preceding baseline assessments and assessments performed at days 1, 14, 21, 28 and 42, and months 2, 3, 6, 9 and 12 (where applicable). “Routine days” are days during which the patient undertakes normal daily activities, and excludes days such as holidays or days when the patient is carrying out tasks that they would not ordinarily do or if they are ill. Diaries were not completed on a day the patient was administered to hospital as PD medication is stopped in the evening to allow for measurements in the “OFF” state to be captured the follow day.
ProSavin®-treated patients in cohorts 1 and 2a recorded time spent in each of four conditions: “ON” and dyskinetic, completely “ON,” partially “OFF” and completely “OFF.” ProSavin®-treated patients in cohort 2b recorded time spent in five conditions: asleep, “OFF,” “ON” without dyskinesia, “ON” with non-troublesome dyskinesia and “ON” with troublesome dyskinesia. The ON state corresponds to the period where the patients are receiving benefit from L-DOPA therapy and have satisfactory movement. The OFF state refers to the period where the effects of L-DOPA have worn off and the patients have poor mobility. ON with dyskinesias indicate the presence of dyskinetic movement in response to L-DOPA treatment and are separated into troublesome and non-troublesome depending on their severity. Patient diary data (
The data demonstrate that treatment with ProSavin® results in an overall increase in the time spent in the ON state for cohorts 1 and 2 (
This result is surprising since it would not be expected that the duration of the ON/OFF times in response to L-DOPA would be altered by ProSavin®. The result indicates a combinatorial effect of treatment of patients with ProSavin® and L-DOPA. It appears that treatment with ProSavin® unexpectedly increases the effects of L-DOPA by extending the window of therapeutic benefit. This is achieved without an increase in the dose of L-DOPA since the LEDD doses are either reduced or stabilized in these patients. The increase in non-troublesome dyskinesias in the ON state provides further evidence of an enhanced effect of ProSavin® and L-DOPA since these probably reflect an increase in dopamine from the combination of the two therapies. The non-troublesome dyskinesias were subsequently resolved by a reduction in the LEDD.
All publications mentioned in the above specification are herein incorporated by reference. Various modifications and variations of the described methods and system of the invention will be apparent to those skilled in the art without departing from the scope and spirit of the invention. Although the invention has been described in connection with specific preferred embodiments, it should be understood that the invention as claimed should not be unduly limited to such specific embodiments. Indeed, various modifications of the described modes for carrying out the invention which are obvious to those skilled in cellular studies using flow cytometry or related fields are intended to be within the scope of the following claims.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 13112582 | May 2011 | US |
| Child | 13346297 | US |
