1.1. Choice of vector
Successful gene therapy requires an adequate level of long-term transgene expression in the target tissues. While various viral vectors have been considered for the delivery of genes in vivo, an adeno-associated virus (AAV)-based vector is emerging as the gene transfer vehicle with the most potential for use in the neuromuscular gene therapies. The advantages of the AAV vector include the lack of disease associated with a wild-type virus, the ability to transduce non-dividing cells, and the long-term expression of the delivered transgenes. Some serotypes of recombinant AAV (rAAV) exhibit a potent tropism for striated muscles. Therefore, a supplementation of secretory protein can be achieved with this vector to use intramuscular injection. Since a 5-kb genome is considered to be the upper limit for a single AAV virion, various truncated genes could be provided to meet size capacity, if nessessarry.
Due to ingenious cloning and preparation techniques, adenovirus vectors are efficient delivery systems of episomal DNA into eukaryotic cell nuclei. The utility of adenovirus vectors has been increased by capsid modifications that alter tropism, and by the generation of hybrid vectors that promote chromosomal insertion. Also, gutted adenovirus vectors devoid of all adenoviral genes allow for the insertion of large transgenes, and trigger fewer cytotoxic and immunogenic effects than do those only deleted in the E1 regions of the adenovirus early genes. Human artificial chromosomes (HACs) have the capacity to deliver genes in any size into host cells without integrating the gene into the host genome, thereby preventing the possibility of insertional mutagenesis and genomic instability.
Long-term correction of genetic diseases requires permanent integration of therapeutic genes into chromosomes of the affected cells. However, retrovirus vector integration can trigger deregulated premalignant cell proliferation with unexpected frequency, most likely driven by retrovirus enhancer activity on the LMO2 gene promoter.  A goal in clinical gene therapy is to develop gene transfer vehicles that can integrate exogenous therapeutic genes at specific chromosomal loci as a safe harbor, so that insertional oncogenesis is prevented. AAV can insert its genome into a specific locus, designated AAVS1, on chromosome 19 of the human genome. The AAV Rep78/68 proteins and the Rep78/68-binding sequences are the trans- and cis-acting elements needed for this reaction. A dual high-capacity adenovirus-AAV hybrid vector with full-length human dystrophin-coding sequences flanked by AAV integration-enhancing elements was tested for targeted integration.
1.2. AAV biology
AAV is a small (20-26nm) non-enveloped dependent parvovirus with a single-stranded linear genome that contains two open reading frames (rep and cap). The viral genome is characterized by the inverted terminal repeats (ITRs) to flank these open reading frames (Figure 1A). The genome encodes four replication proteins (Rep78, Rep68, Rep52, and Rep40) and three capsid proteins (Cap: VP1, VP2, and VP3). The large Rep (Rep78 and Rep68) proteins regulate AAV gene expression and hold nicking activity at the terminal resolution site as well as binding activity at Rep binding elements to process AAV replication (Figure 1B). The small Rep proteins (Rep52 and Rep40) are used for the accumulation of single-stranded viral genome followed by packaging within AAV capsids.
The minimum sets of regions in helper adenovirus that mediate AAV vector replication are the E1, E2A, E4, and VA. A human embryonic kidney cell line 293 encodes the E1 region of the Ad5 genome. The helper plasmid assembling E2A, E4, and VA regions (Ad-helper plasmid) is cotransfected into the 293 cells, along with plasmids encoding the AAV vector genome (vector plasmid) as well as rep and cap genes (AAV-helper plasmid). AAV vector is produced as efficiently as when adenovirus infection is employed as a helper virus. Furthermore, contamination of most adenovirus proteins can be avoided in AAV vector stock made by this helper virus-free method.
1.3. Vector application using various serotypes
The preparation of AAV vector for gene therapy study of neuromuscular diseases is greatly facilitated. Although AAV2 has been the serotype most extensively studied in preclinical and clinical trials, recently we have focused on the use of AAV vectors pseudotyped with capsid protein of alternative serotypes. A number of primate AAV serotypes have been characterized in the literature and are designated. There is divergence in homology and tropism for various AAV serotypes. For instance, the homology with capsid protein is only about 60% between AAV2 and AAV5, therefore the capsid structure could be responsible for the improved transduction efficiency.
We found that choice of AAV serotypes and promoters could be quite useful for targeted transgene expression. For instance, the transgene expression of rAAV5 with the Rous sarcoma virus (RSV) promoter was preferentially found in the granular cells of the gerbil hippocampus, whereas transgene expression of rAAV2 with the RSV promoter was found in the pyramidal and granular cells. Since AAV3 vector can specifically transduce cochlear inner hair cells with high efficiency in vivo, rAAV-mediated transduction might be promising for gene replacement strategies to correct recessive genetic hearing loss due to monogenic mutation. Also, there is a significant difference in transgene expression by various AAV serotypes transduced into muscle. We observed that intramuscular injection of AAV5-IL-10 promoted a much higher serum level of secreted transgene product, as compared to AAV2-mediated transfer. We further demonstrated that AAV1 could more efficiently transduce the muscle than AAV5. Intramuscular single injection of modest doses of rAAV1 expressing IL-10 (6x1010 g.c. per rat) introduced therapeutic levels of the transgene expression over the long-term to treat pulmonary arterial hypertension. rAAV1-mediated sustained IL-10 expression also significantly ameliorated hypertensive organ damage to improve survival rate of Dahl salt-sensitive rats. Furthermore, this protein supplementation therapy by rAAV1-mediated muscle transduction was quite effective to prevent vascular remodeling and end-organ damage in the stroke-prone spontaneously hypertensive rat. Interestingly, alpha-sarcoglycan expression with single intramuscular injection of rAAV8 was widely distributed in the hind limb muscle as well as cardiac muscle, and persisted for 7 months with a reversal of the muscle pathology and improvement in the contractile force in the alpha-sarcoglycan-deficient mice. Intravenous administration of rAAV8 into the hind limb in dogs resulted in improved transgene expression in the skeletal muscles lasting over a period of 8 weeks. Moreover, rAAV9 would be administered systemically with excellent cardiac tropism. Further strategies have been attempted to discover novel AAV capsid sequences from primate tissue, which can be used to develop newer-generation rAAVs with a greater diversity of tissue tropism for clinical gene therapy.
Clinical gene therapy often requires rapid transduction with reasonable efficiency. In the case of AAV, second strand synthesis of the vector genome in the nucleus is the rate-limiting step for efficient transduction. Therefore, self-complementary AAV (scAAV) vector would be quite promising to promote efficient transduction regardless of DNA synthesis or annealing. The scAAV vectors can bypass the inter-molecular annealing or second-strand synthesis by using intra-molecular annealing to immediately form transcriptionally active double-stranded DNA (Figure 2). Although immediate and efficient transduction could be observed with scAAV, the maximal insert size of the transgene cassette is reduced to 3.3 kb.
2. Effective production strategies of rAAV
2.1. Principle of production
To gain acceptance as a medical treatment with a dose of over 1x1013 genome copies (g.c.)/kg body weight, therapeutic strategies with AAV vectors require a scalable and provident production method. However, the production and purification of recombinant virus stocks with conventional techniques entails cumbersome procedures not suited to the clinical setting. Therefore, development of effective large-scale culture and purification steps are required to meet end-product specifications.
A production protocol of AAV vectors in the absence of a helper virus is widely employed for triple plasmid transduction of human embryonic kidney 293 cells. The adenovirus regions that mediate AAV vector replication (namely, the VA, E2A and E4 regions) were assembled into a helper plasmid. When this helper plasmid is co-transfected into 293 cells along with plasmids encoding the AAV vector genome and rep-cap genes, the AAV vector is produced as efficiently as when using adenovirus infection. Importantly, contamination of most adenovirus proteins can be avoided in AAV vector stock made by this helper virus-free method.
Although various subtypes of the 293 cells harbor the E1 region of the adenovirus type 5 genome, to utilize a 293 cell stably expressing Bcl-xL (293B) has great advantage to support E1B19K function and protect cells from apoptosis. Despite improvements in vector production, including the development of packaging cell lines expressing Rep/Cap or methods to regulate Rep/Cap, maintaining such cell lines remains difficult, as the early expression of Rep proteins is toxic to cells.
We developed a large-scale transfection method of producing AAV vectors with an active gassing system that uses large culture vessels to process labor-effective transfection in a closed system. This vector production system achieved reasonable production efficiency by improving gas exchange to prevent pH drop in the culture medium. Also, vector purification with the dual ion-exchange membrane adsorbers was effective and allowed higher levels of gene transfer in vivo. Furthermore, the membrane adsorbers enabled the effective recovery of the AAV vector in the supernatant exosomes of the transduced cells culture. This rapid and scalable viral purification protocol is particularly promising for considerable in vivo experimentation and clinical investigations (Figure 3).
Recent developments also suggest that AAV vector production in insect cells would be compatible with current good manufacturing practice production on an industrial scale.
2.2. Large-scale production with active gassing
Our protocol utilizes the transfection of 293B cells in one 10-Tray flask (CF10; Nalge Nunc International, Rochester, NY) with a surface area of 6320 cm2 by using an active gassing at 500 ml/min. Typical transduction procedure is conducted with one or two CF10 to meet downstream purification protocol. Although previous protocols for recombinant virus production in a large culture vessel had the problem of insufficient transduction efficiency because of inadequate gas exchange, this method to use active gassing significantly improves productivity of the vectors and is linearly scalable from the small 225-cm2 flask.
The 293B cells are cultured in Dulbecco’s modified Eagle’s medium and Nutrient Mixture F-12 (D-MEM/F-12, Invitrogen, Grand Island, NY) with 10% fetal bovine serum (SIGMA-ALDRICH, St Louis, MO), 100 units/ml penicillin, and 100 µg/ml streptomycin at 37 oC in a 5% CO2 incubator. Cells are initially plated at 8 x 107 cells per CF10 to achieve a monolayer of 20 to 40% confluency when cells attached to surface of the flask. The volume of medium utilized per flask is 1120 ml. Subsequently, cells are grown for 48-72 h until reaching 70-90% confluence and are consequently transfected with appropriate triple plasmids. An aquarium pump (Nisso, Tokyo, Japan) should be used to circulate the gas through the CF10 with 5% CO2 and humidity in an incubator.
Half of the medium in the CF10 tissue culture flask are exchanged with fresh D-MEM/F-12 containing 10% FBS, 1 h before transfection of the 293 cells. Subsequently, the cells are co-transfected with 650 µg of each plasmid: a proviral vector plasmid, an AAV helper plasmid, as well as an adenoviral helper plasmid, using calcium phosphate co-precipitation. Each plasmid was added to 112 ml of 300 mM CaCl2. This solution was gently added to the same volume of 2 x HBS (290 mM NaCl, 50 mM HEPES buffer, 1.5 mM Na2HPO4, pH 7.0) and gently inverted 3 times to form a uniform solution. This solution was immediately mixed with fresh D-MEM/F-12 containing 10% FBS to produce a homogeneous plasmid solution mixture. Subsequently, the medium in the culture flask was replaced with this plasmid solution mixture. At the end of a 6-12 h incubation, the plasmid solution mixture in the culture flask was replaced with pre-warmed fresh D-MEM/F-12 containing 2% FBS.
2.3. Purification phase
The culture supernatant sample for the ion-exchange procedure is processed by centrifugation and filtration. The culture supernatant fluid 72-96 h after the transduction is sampled and then clarified with an appropriate amount of the activated charcoal (Wako Pure Chemical Industries, Osaka, Japan). Insoluble debris is removed by a centrifugation at 3,000 g for 15 min and filtration. The elucidated culture supernatant is enriched with a hollow fiber cross flow membrane (100,000 NMWC, GE Healthcare, Pittsburgh, PA). For the material obtained from a CF10, 5 mM MgCl2 (final concentration) with 2,500-5,000 units of Benzonase nuclease is added to incubate for 30 min at 37 oC. Sequentially, 5 mM EDTA (final concentration) is added to terminate the reaction. Place 38 ml of the sample solution in a semi-sterile ultracentrifuge tube (Ultrabottle #3430-3870; Nalge Nunc, Rochester, NY) and remove the cell debris by centrifugation at 10,000g for 15 minutes at 4 oC to achieve cleared lysates. The sample is quickly concentrated by the brief two-tier CsCl (1.25 and 1.60 g/cm3) step gradient centrifugation for 3 h and then the vector fraction is dialyzed in the MHA buffer (3.3 mM MES 3.3 mM HEPES [pH 8.0], 3.3 mM NaOAc).
Chromatography can be performed using an appropriate FPLC system, such as AKTA explorer 10S (Amersham Biosciences, Piscataway, NJ, USA) equipped with a 50 ml Superloop. The sample which passed through the MustangTM S membrane (optional treatment, PALL corporation, NY) is dialyzed against MHA buffer and further loaded onto an anion-exchange membrane (acrodisc unit with MustangTM Q membrane, PALL corporation, equilibrated with MHA buffer) at a rate of 3 ml/min. The membrane is then washed with 10 column volumes of MHA buffer. Bound virus on the MustangTM Q membrane is eluted over a 50 column volume span with a 0-2 M linear NaCl gradient in MHA buffer and 0.5-1 ml fractions are collected. Recombinant rAAV particle number is determined by quantitative PCR of DNase I-treated stocks with plasmid standards. The final titer of the purified vectors from a CF10 usually ranges around 5 x 1013 genome copies (g.c.), although it depends on the vector constructs and transgene.
3. AAV-mediated therapeutic approach to neuromuscular disease
3.1. DMD gene replacement therapy
Duchenne muscular dystrophy (DMD) is the most common form of childhood muscular dystrophy and is an X-linked recessive disorder with an incidence of one in 3500 live male births. DMD causes progressive degeneration and regeneration of skeletal and cardiac muscles due to mutations in the dystrophin gene, which encodes a 427-kDa subsarcolemmal cytoskeletal protein. DMD is associated with severe, progressive muscle weakness and typically leads to death between the ages of 20 and 35 years. Due to recent advances in respiratory care, much attention is now focused on treating the cardiac conditions suffered by DMD patients. The approximately 2.5-megabase dystrophin gene is the largest gene identified to date, and because of its size, it is susceptible to a high sporadic mutation rate. Absence of dystrophin and the dystrophin-glycoprotein complex (DGC) from the sarcolemma leads to severe muscle wasting. Whereas DMD is characterized by the absence of functional protein, Becker muscular dystrophy, which is commonly caused by in-frame deletions of the dystrophin gene, results in the synthesis of an incompletely functional protein.
Successful therapy for DMD requires the restoration of dystrophin protein in skeletal and cardiac muscles. While various viral vectors have been considered for the delivery of genes to muscle fibers, the AAV-based vector is emerging as an appropriate gene transfer vehicle with the most potential for use in DMD gene therapies. As for another candidate vehicle, the gutted adenovirus vector can package 14-kb of full-length dystrophin cDNA due to the large deletion in virus genome. Multiple proximal muscles of seven-day-old utrophin/dystrophin double knockout mice (dko mice), which typically show symptoms similar to human DMD, were effectively transduced with the gutted adenovirus bearing full-length murine dystrophin cDNA. However, further improvements are needed to regulate the virus-associated host immune response before clinical trials can be performed.
A series of truncated dystrophin cDNAs containing rod repeats with hinge 1, 2, and 4 were constructed (Figure 4A). Although AAV vectors are too small to package the full-length dystrophin cDNA, AAV vector-mediated gene therapy using a rod-truncated dystrophin gene provides a promising appraoch. The structure and, particularly, the length of the rod are crucial for the function of micro-dystrophin. An AAV type 2 vector expressing micro-dystrophin (DeltaCS1) under the control of a muscle-specific MCK promoter was injected into the tibialis anterior (TA) muscles of dystrophin-deficient mdx mice, and resulted in extensive and long-term expression of micro-dystrophin that exhibited improved force generation. Likewise, AAV6 vector-mediated systemic micro-dystrophin gene transfer was effective in treating dko mice. The potential for ameliorating the pathology of advanced-stage muscular dystrophy by systemic administration of AAV6 vectors encoding a micro-dystrophin expression construct was also demonstrated. Furthermore, AAV9 vector-mediated micro-dystrophin transduction of mdx mice accomplished prevention of cardiac fibrosis as well as heart failure. The transduction efficiency achieved with rAAV9 was nearly complete, with persistent expression for 74 weeks after transduction (Figure 4BC). Both the strong affinity of the rAAV9 for cardiac tissue and the therapeutic effect of the expressed micro-dystrophin might be involved in the prevention of the degeneration of the cardiomyocytes and cardiac fibrosis.
The impact of codon usage optimization on micro-dystrophin expression and function in the mdx mouse was demonstrated to compare the function of two different configurations of codon-optimized micro-dystrophin genes under the control of a muscle-restrictive promoter (Spc5-12). Codon optimization of micro-dystrophin significantly increased micro-dystrophin mRNA and protein levels after intramuscular and systemic administration of plasmid DNA or rAAV8. By randomly assembling myogenic regulatory elements into synthetic promoter recombinant libraries, several artificial promoters were isolated whose transcriptional potencies greatly exceed those of natural myogenic and viral gene promoters.
3.2. Intravascular vector administration by limb perfusion
Although recent studies suggest that vectors based on AAV are capable of body-wide transduction in rodents, translating the characteristics into large animals with advanced immune system remains a lot of challenges. Intravascular delivery can be performed as a form of limb perfusion, which might bypass the immune activation of DCs in the injected muscle. We performed limb perfusion-assisted intravenous administration of rAAV8-lacZ into the hind limb of Beagle dogs (Figure 5A). Administration of rAAV8 by limb perfusion demonstrated extensive transgene expression in the distal limb muscles of canine X-linked muscular dystrophy in Japan (CXMDJ) dogs without obvious immune responses for the duration of the experiment over four weeks after injection.
3.3. Systemic transduction and immunological issues
In comparison with fully dystrophin-deficient animals, targeted transgenic repair of skeletal muscle, but not cardiac muscle, paradoxically elicits a five-fold increase in cardiac injury and dilated cardiomyopathy. Because the dystrophin-deficient heart is highly sensitive to increased stress, increased activity by the repaired skeletal muscle provides the stimulus for heightened cardiac injury and heart remodeling. In contrast, a single intravenous injection of AAV9 vector expressing micro-dystrophin efficiently transduces the entire heart in neonatal mdx mice, thereby ameliorating cardiomyopathy.
Since a number of muscular dystrophy patients can be identified through newborn screening in future, neonatal transduction may lead to an effective early intervention in DMD patients. After a single intravenous injection, robust skeletal muscle transduction with AAV9 vector throughout the body was observed in neonatal dogs. Systemic transduction was achieved in the absence of pharmacological intervention or immune suppression and lasted for at least six months, whereas rAAV9 was barely transduced into the cardiac muscle of dogs. Likewise, in utero gene delivery of full-length murine dystrophin to mdx mice using a high-capacity adenoviral vector resulted in effective protection from cycles of degeneration and regeneration.
Neo-antigens introduced by AAV vectors evoke significant immune reactions in DMD muscle, since increased permeability of the DMD muscle allows leakage of the transgene products from the dystrophin-deficient sarcolemma of muscle fibers. rAAV2 transfer into skeletal muscles of normal dogs resulted in low levels of transient expression, together with intense cellular infiltration, and the marked activation of cellular and humoral immune responses. Furthermore, an in vitro interferon-gamma release assay showed that canine splenocytes respond to immunogens or mitogens more strongly than do murine splenocytes. Therefore, co-administration of immunosuppressants, cyclosporine (CSP) and mycophenolate mofetil (MMF) was attempted to improve rAAV2-mediated transduction. The AAV2 capsids can induce a cellular immune response via MHC class I antigen presentation with a cross-presentation pathway, and rAAV2 could also stimulate human dendritic cells (DCs). Whereas the non-immunogenic nature of AAV6 in murine studies, rAAV6 also elicited robust cellular immune responses in dogs. In contrast, other serotypes, such as rAAV8, induce T-cell activation to a lesser degree. The rAAV8-injected muscles showed lowed rates of infiltration of CD4+ and CD8+ T lymphocytes in the endomysium than the rAAV2-injected muscles.
Resident antigen-presenting cells, such as DCs, myoblasts, myotubes and regenerating immature myofibers, should play a substantial role in the immune response against rAAV. Our study also showed that MyD88 and co-stimulating factors, such as CD80, CD86 and type I interferon, are up-regulated in both rAAV2- and rAAV8-transduced dog DCs (Figure 5B).
4. Safety and potential impact of clinical trials
4.1. Clinical trials for muscle transduction
While low immunogenicity was considered a major strength supporting the use of rAAV in clinical trials, a number of observations have recently provided a more balanced view of this procedure. An obvious barrier to AAV transduction is the presence of circulating neutralizing antibodies that prevent the virion from binding to its cellular receptor. This potential threat can be reduced by prescreening patients for AAV serotype-specific neutralizing antibodies or by performing therapeutic procedures such as plasmapheresis before gene transfer. Another challenge recently revealed is the development of a cell-mediated cytotoxic T-cell (CTL) response to AAV capsid peptides. In the human factor IX gene therapy trial in which rAAV was delivered to the liver, only short-term transgene expression was achieved and levels of therapeutic protein declined to baseline levels 10 weeks after vector infusion. This was accompanied by elevation of serum transaminase levels and a CTL response toward specific AAV capsid peptides. To overcome this response, transient immunosuppression may be required until AAV capsids are completely cleared. Additional findings suggest that T-cell activation requires AAV2 capsid binding to the heparan sulfate proteoglycan (HSPG) receptor, which would permit virion shuttling into a DC pathway, as cross-presentation. Exposure to vectors from other AAV clades, such as AAV8, did not activate capsid-specific T-cells.
The initial clinical studies lay the foundation for future studies, providing important information about vector dose, viral serotype selection, and immunogenicity in humans. The first virus-mediated gene transfer for muscle disease was carried out for limb-girdle muscular dystrophy type 2D using rAAV1. The study, consisting of intramuscular injection of virus into a single muscle, was limited in scope and the main conclusion was to establish the safety of this procedure in phase I clinical trials. The first clinical gene therapy trial for DMD began in March 2006. This was a Phase I/IIa study in which an AAV vector was used to deliver micro-dystrophin to the biceps of boys with DMD. The study was conducted on six boys with DMD, each of whom received an injection of mini-dystrophin-expressing rAAV2.5 in a muscle of one arm and a placebo in the other arm. Dystrophin-specific T cells were detected after treatment, providing evidence of transgene expression even when the functional protein was not visualized in skeletal muscle. The potential for T-cell immunity to self and non-self dystrophin epitopes should be considered in designing and monitoring experimental therapies for this disease. Basically, this issue is in common with the treatment of genetic diseases. Although concerns regarding risk of an immune response to the transgene product limited the ability to achieve therapeutic efficacy, rAAV2-mediated gene transfer to human skeletal muscle can persist for up to a decade.
4.2. Gene therapy medicine
After more than two decades of expectations, the field of gene therapy appears close to reaching a regulatory approval by proposing rAAV-mediated muscle transduction. European medicine agency eventually recommends first gene therapy medicine for approval. (http://www.ema.europa.eu/ema) The European Medicines Agency’s Committee for Medicinal Products for Human Use has recommended the authorization of Glybera (rAAV1-expressing LPL S447X variant) for marketing in the European Union. It is intended to treat lipoprotein lipase deficiency in patients with severe or multiple pancreatitis attacks, despite dietary fat restrictions.
5. Challenges and future perspectives
5.1. Immunomodulation to augment clinical benefits
To regulate host immune response against vectors and transgene products, treatments involving immunosuppressants and other strategies have been attempted in the animal models. A brief course of immunosuppression with a combination of anti-thymocyte globulin (ATG), CSP and MMF was effective in permitting AAV6-mediated, long-term and robust expression of a canine micro-dystrophin in the skeletal muscle of a dog DMD model. To establish the feasibility of multiple AAV1 injections for extending the treatment to whole body muscles, the dystrophic mdx mouse was repeatedly transduced with AAV1 vector, and the immune response was characterized. By blocking the T-B crosstalk with anti-CD40 Abs and CTLA4/Fc fusion protein, a five-day-long immunomodulation treatment was found to be sufficient for totally abrogating the formation of anti-AAV1 antibodies.
There have been numerous reports to develop the therapeutic potential of mesenchymal stem cells (or mesenchymal multipotent stromal cells MSCs). Because of their immunomodulatory properties, increasing experimental and early clinical observations indicate that allogeneic, and even xenogeneic, MSCs may be useful for tissue transplantation. In fact, the immune tolerance with MSCs is well investigated in various animal studies. Infusion of syngeneic MSCs into a sensitized mouse model of kidney transplantation resulted in the expansion of donor-specific T- regulatory cells into lymphoid organs, prolonged allograft survival and promoted the development of tolerance.
5.2. Pharmacological intervention
The use of a histone deacetylase (HDAC) inhibitor depsipeptide effectively enhances the utility of rAAV-mediated gene therapy. In contrast to adenovirus-mediated transduction, the improved transduction with rAAV induced by the depsipeptide is due to enhanced transgene expression rather than to increased viral entry. The enhanced transduction is related to the histone-associated chromatin form of the rAAV concatemer in the transduced cells. Since various HDAC inhibitors are approved in clinical usage for many diseases to achieve therapeutic benefits, the application of such inhibitors to the rAAV-mediated gene therapy is theoretically and practically reasonable.
5.3. In situ gene therapy
Transplantation of genetically modified vector-producing cells is a possible future treatment for genetic diseases as an in situ gene therapy. MSCs are known to accumulate at the site of inflammation or tumors, and therefore can be utilized as a platform for the targeted delivery of therapeutic agents. The MSCs-based targeted gene therapy should enhance the therapeutic efficacy, since MSCs would deliver therapeutic molecules in a concentrated fashion. This targeted therapy can also reduce systemic adverse side effects, because the reagents act locally without elevating their systemic concentrations. We developed the genetically-modified MSCs that produce viral vectors to augment therapeutic efficacy of systemic gene therapy. MSCs isolated from the SD rats bone marrow were transfected with retroviral vector components by nucleofection. As a result, the injection of luciferase-expressing vector-producing MSCs caused significantly stronger signal of bioluminescence at the site of subcutaneous tumors in mice compared with luciferease-expressing non-vector-producing MSCs. Furthermore, tumor-bearing nude mice were treated with the vector-producing MSCs combined with HSV-tk/GCV system to demonstrate improved anti-tumor effects. This study suggests the effectiveness of vector-producing MSCs in systemic gene therapy. The therapeutic benefit of this strategy should be further examined by using rAAV-producing MSCs in the various animal models of inflammatory diseases including neuromuscular disorders.
5.4. Capsid modification
A DNA shuffling-based approach for developing cell type-specific vectors is an intriguing possibility to achieve altered tropism. Capsid genomes of AAV serotypes 1-9 were randomly reassembled using PCR to generate a chimeric capsid library. A single infectious clone (chimeric-1829) containing genome fragments from AAV1, 2, 8, and 9 was isolated from an integrin minus hamster melanoma cell line previously shown to have low permissiveness to AAV. Molecular modeling studies suggest that AAV2 contributes to surface loops at the icosahedral threefold axis of symmetry, while AAV1 and 9 contribute to two-fold and five-fold symmetry interactions, respectively.
A versatile rAAV targeting system to redirect rAAV-mediated transduction to specific cell surface receptors would be useful. Insertion of an IgG binding domain of protein A into the AAV2 capsid at amino acid position 587 could permit antibody-mediated vector retargeting, although producing mosaic particles is required to avoid low particle yields. Alternatively, a targeting system using the genetic fusion of short biotin acceptor peptide along with the metabolic biotinylation via a biotin ligase was developed for the purification and targeting of multiple AAV serotypes.
6. Conclusions and outlook
Although an increasing number of scalable methods for purification of rAAV have been described, in order to generate sufficient clinical-grade vector to support clinical trials we need to further improve a large-scale GMP-compatible system for production and purification. To translate gene transduction technologies into clinical practice, development of an effective delivery system with improved vector constructs as well as efficient immunological modulation must be established. A novel protocol that considers all of these issues would help improve the therapeutic benefits of clinical gene therapy.
This work was supported by the Grant for Research on Nervous and Mental Disorders, Health Science Research Grants for Research on the Human Genome and Gene Therapy; and the Grant for Research on Brain Science from the Ministry of Health, Labor and Welfare of Japan. This work was also supported by Grants-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology (MEXT). We would like to thank Dr. James M. Wilson for providing p5E18-VD2/8 and pAAV2/9.