Current Pediatrics Reports

, Volume 2, Issue 2, pp 102–112

Therapy of Genetic Disorders: Novel Therapies for Duchenne Muscular Dystrophy

  • Jane T. Seto
  • Niclas E. Bengtsson
  • Jeffrey S. Chamberlain
Genetics (BR Pober, Section Editor)

DOI: 10.1007/s40124-014-0044-x

Cite this article as:
Seto, J.T., Bengtsson, N.E. & Chamberlain, J.S. Curr Pediatr Rep (2014) 2: 102. doi:10.1007/s40124-014-0044-x


Duchenne muscular dystrophy is an inherited, progressive muscle-wasting disorder caused by mutations in the dystrophin gene. An increasing variety of approaches are moving towards clinical testing that all aim to restore dystrophin production and to enhance or preserve muscle mass. Gene therapy methods are being developed to replace the defective dystrophin gene or induce dystrophin production from mutant genes. Stem cell approaches are being developed to replace lost muscle cells while also bringing in new dystrophin genes. This review summarizes recent progress in the field with an emphasis on clinical applications.


Duchenne muscular dystrophy Dystrophin Gene therapy Adeno-associated viral vectors Antisense oligonucleotide Inducible pluripotent stem cell Mesoangioblast Myoblast Satellite cell 


Duchenne muscular dystrophy (DMD) is the most common and severe form of childhood muscular dystrophy, affecting approximately 1 in 5,000 boys [1]. The disease is characterized by progressive muscle weakness with delayed motor and speech milestones and elevated serum creatine kinase levels. Patients demonstrate reduced motor skills by age 3–5 and typically lose ambulation by 12 years of age. Glucocorticoids (prednisone or deflazacort) are prescribed to slow disease progression, but to date there is no cure for this disease. Despite intensive clinical attention to respiratory support and management of cardiac complications [2], most patients do not live beyond age 30.

DMD is caused by loss of function mutations in the X-linked DMD gene (commonly called ‘dystrophin’) resulting in near complete deficiency of dystrophin in cardiac, skeletal and smooth muscles. The types of mutations that lead to DMD include: point mutations that can encode premature termination codons (nonsense mutations, or “stop codons”); deletions or exon–intron splice site mutations that disrupt the normal protein or open reading frame (ORF) of the dystrophin messenger RNA (mRNA); partial gene duplications that disrupt the normal ORF; and, rarely, point mutations or deletions that disrupt critical functional domains of dystrophin. Mutations that enable expression of partially functional dystrophin lead to the milder Becker muscular dystrophy (BMD). Clinical observations of a BMD patient who remained ambulatory past age 70 despite absence of 46 % of the dystrophin gene [3] lent proof of principle that restoring some functional dystrophin expression can ameliorate the disease severity of DMD. Expression of 20–30 % of normal dystrophin levels is sufficient to avoid muscular dystrophy in mice and humans, while lower levels can lead to various severities of BMD [4, 5].

A major challenge for therapy of DMD and other muscular dystrophies is the need to devise a treatment strategy that targets all the major muscles in the body. These include limb muscles, respiratory muscles (intercostal and diaphragm muscles), cardiac muscle and smooth muscles of the gastroesophageal tract. Often emerging therapies are tested by direct intramuscular injection into a single site or into several sites of one muscle. While such an approach is useful for measuring local effects, it is difficult to envision ways to extend intramuscular injection strategies to achieve global muscle targeting. Instead, therapeutic interventions require whole-body targeting of the musculature, an approach generally referred to as systemic delivery. Multiple methods can be used for systemic delivery, depending on the drug or compound being tested, but most current approaches rely on oral or intravascular delivery. This review summarizes the current therapeutic strategies to restore dystrophin expression in DMD animal models and patients, with particular emphasis on the outcomes and discussions arising from the most recent clinical trials, as well as promising new therapies from current pre-clinical studies (Fig. 1).
Fig. 1

Functional dystrophin can be restored through rAAV-mediated gene replacement, exon skipping, mutation suppression (not shown) or cell therapies (not shown). For gene replacement, minimally essential regions of dystrophin are removed to fit the limited carrying capacity of rAAV vectors and generate short dystrophin constructs (microdystrophins). Despite the truncation, microdystrophins restored dystrophin protein production and ~90 % of strength in dystrophic mice. Larger dystrophin constructs (minidystrophins) that incorporate additional regions necessary for recruiting important dystrophin binding partners (e.g., nNOS) result in even greater physiological improvements. Minidystrophins are delivered in pieces using multiple rAAV vectors and reassembled in muscle cells by various methods such as homologous recombination. In exon-skipping, synthetic antisense oligonucleotides (AON) are specifically designed to anneal to precursor mRNA (pre-mRNA) and alter RNA splicing to restore normal open-reading frames, resulting in the production of a smaller, but functional dystrophin. These techniques can be used in combination with cell therapies to correct genetic mutations prior to transplantation back into the patient in ex vivo therapies

Small Molecule Therapies

Approximately 10 % of DMD mutations are single-base “point” mutations that introduce premature stop codons into the dystrophin mRNA. One strategy to restore dystrophin expression in patients with such nonsense mutations is mutation suppression, specifically, of premature termination codon (PTC) mutations. Nonsense mutations signal an end to protein translation and result in production of a shortened, non-functional protein that is usually unstable and degraded in the cell. These ‘PTC’ mutations account for ~10 % of DMD cases [6] (see also Certain antibiotics such as gentamicin can induce translational read-through of PTC mutations. At high concentrations, the binding of gentamycin to the protein production machinery in cells induces read-through of PTCs in mRNA, inserting a new amino acid to continue translation of the complete protein [7]. However, serious dose-limiting toxicities preclude the use of gentamicin in patients for this purpose. Drug discovery programs led to the identification of PTC124 (also known as ataluren), a compound shown to be more potent in PTC read-through than gentamicin [8], although recent in vitro studies have raised questions regarding the genuine read-through ability of ataluren [9, 10, 11]. Regardless of the mechanism, ataluren was somewhat effective in restoring functional dystrophin expression in mdx mice, resulting in improved strength and decreased injury in response to exercise-induced damage [8]. A phase I study in healthy volunteers established safety and tolerability at doses exceeding pre-clinical efficacy [12]. Phase 2b studies over 48 weeks involving DMD and BMD patients aged 5–20 years showed that patients receiving a low-dose treatment (20 mg/kg) experienced a significantly slower disease progression, demonstrating a 29-m improvement in a 6-min walk test (6MWT) compared to patients who received placebo (; Intriguingly, patients who received a higher dose (40 mg/kg) showed a similar decline as the placebo group, suggesting that ataluren may have an inverted bell-shaped dose–response curve. As of March 2013, a phase 3 study of ataluren was initiated, with recruitment restricted to DMD patients with PTC (stop codon) mutations. This will be a randomized, double-blind, placebo-controlled study with higher power to determine the potential efficacy and safety of low-dose ataluren (

The majority of DMD cases arise from partial dystrophin gene deletions or duplications or from mutations that affect the normal splicing of the dystrophin RNA transcript into mRNA. Each of these types of gene mutations is a problem when it disrupts the normal dystrophin mRNA open reading frame such that a functional dystrophin protein can not be produced in muscle cells. An approach to restore the normal mRNA reading frame involves exon skipping. This can be induced by short, synthetic fragments of nucleic acids known as “antisense oligonucleotides” (AONs), which are designed to bind (anneal) with RNA sequences that regulate how a gene’s initial RNA transcript is spliced into a functional mRNA. By altering RNA splicing near the mutation on the precursor mRNA (pre-mRNA), the cell can be tricked into making a slightly shorter than normal mRNA that lacks a mutation and that carries an otherwise normal open reading frame (Fig. 1). This strategy is theoretically applicable to ~80 % of all DMD patients [13]. Recent drug development for exon skipping has targeted exon 51 of the DMD gene, as this could be applied to ~13 % of boys with DMD. Two types of AONs have been taken into clinical trials, each made using different nucleic acid chemistries. Drisapersen (previously known as PRO051, GSK-2402968) was developed by Prosensa and GSK. The other was eteplirsen (AVI-4658) developed by Sarepta Therapeutics. Therapeutic efficacy of these AONs has been demonstrated in several mouse models for DMD (mdx) and the dystrophic cxmd dog [14, 15, 16, 17]. Both compounds demonstrated safety and efficacy by direct intramuscular injections in patients, with restoration of dystrophin expression in the majority of muscle fibers near the injection site without severe treatment-related adverse effects [18, 19].

Initial phase 1/2A studies for both drisapersen and eteplirsen appeared promising, but disappointingly, neither compound succeeded in demonstrating significant improvements in the primary outcome measure, the 6MWT, in larger cohorts. In early phase 1/2A drisapersen trials involving 12 patients, a subset of patients who received the higher doses (4.0 and 6.0 mg/kg/week) showed some variable de novo dystrophin expression and demonstrated a mean improvement of 35 m in the 6MWT after 12 weeks of treatment [20••]. However, phase 3 trials where 125 patients (aged 5–16 years) were administered 6 mg/kg/week over 48 weeks did not result in statistically significant improvements in the 6MWD or in secondary measures of motor function when all patients were analyzed. However, Prosensa recently announced that when the analysis was confined to patients younger than 7, a 49-m difference was observed in the 6MWT in patients on a 96-week extension trial. Some of these studies also revealed kidney toxicity and low platelet counts in a few patients at high drug doses. To date, these latest results have only been discussed at conferences and in press releases (;; GSK recently announced that it would not continue studies of drisapersen and is returning rights to the drug to Prosensa, which will continue its development (

Similarly, early phase 2 studies for eteplirsen showed low and variable increases in dystrophin expression in 7 out of 19 patients (all but one who received the highest dose of 10 or 20 mg/kg over 12 weeks). There was a post-treatment increase in dystrophin protein expression from 9 to 16 % of normal controls; three patients showed between 15 and 55 % dystrophin-positive myofibers. Notably, restored dystrophin was shown to be functional and restored β-dystroglycan, α-sarcoglycan and nNOS expression in patients with exon 49–50 deletions, in keeping with the nNOS binding domain being encoded in exons 42–45. Inflammatory cell infiltrate was also reduced in the 10–20 mg/kg cohorts, suggesting that restored dystrophin is tolerated by the immune system [21, 22••]. In a second, more recent phase 2 study, increased dosage of eteplirsen was further assessed in a double-blind placebo-controlled test in 12 DMD boys aged 7–13 years [23]. Patients were administered with placebo, 30 mg/kg/week or 50 mg/kg/week of eteplirsen for 24 weeks, followed by an open-label extension study at the two doses through week 48. Results showed that at least 12 weeks of treatment was required to produce significant increases in dystrophin. At 48 weeks, the mean increase in dystrophin-positive fibers was 47 %, and the four patients in the placebo/delayed group (after 12 weeks of treatment) showed a significant increase of 38 %. Similarly, functional assessment by the 6MWT shows a divergence between the placebo and the eteplirsen groups at week 12, after which the treated group no longer showed a significant decline and stabilized. The placebo/delayed cohort likewise appeared to stabilize by 36 weeks (12 weeks after treatment). Comparison of the 48-week-treated group to the delayed group showed a significant difference of 67 m by week 48 in the 6MWT. Recent natural history data have shown that patients who could walk >350 m at baseline tend to stabilize over 1 year [24], and mean baseline 6MWT for all patients in the eteplirsen study was >350 m [23]. In a very recent press release, Sarepta announced continued stabilization of the 6MWT test in the phase 2b study where patients were continued on high-dose drug (30–60 mg/kg) for 120 weeks (

Despite these modest gains, the FDA declined to grant accelerated approval for eteplirsen, citing concerns about the study design ( Moreover, there was growing concern over the disconnect between increased expression of dystrophin and clinical efficacy, at least in these relatively short trials, raising doubt about the quantification methods used to reliably assay dystrophin expression and the use of dystrophin as a biomarker to reasonably predict clinical benefit over 1 year. Another concern is the use of the 6MWT as the primary clinical endpoint. Although the 6MWT is to date the most reliable and sensitive global measure of lower extremity strength, biochemical inefficiencies, endurance and cardiorespiratory function [24, 25], the 6MWT excludes younger boys who cannot perform such a demanding test and older boys who are no longer ambulatory [26]. Therefore, it was suggested that future studies be designed to mathematically combine findings from a series of tests that measure a broader array of function in a larger range of patients. Redesign of this confirmatory study is currently underway, with dosing expected to initiate mid-2014.

Gene Replacement

Replacement of the defective DMD gene with a synthetic substitute using delivery vehicles such as recombinant adeno-associated virus (rAAV)-based vectors is another promising approach for safe, long-term therapy (Fig. 1). A significant advantage of gene replacement technologies is that they should be applicable to all patients, regardless of their underlying genetic mutation. Wild-type AAV is a small, non-pathogenic parvovirus that contains a 4.7-kb single-stranded DNA genome. Generation of rAAV delivery vectors involves removing all viral genes and replacing them with a therapeutic gene. Advantages of using rAAV-based vectors are that they can be produced at high titers on an industrial scale [27] and can stably persist for years in muscle cells. Of the many known serotypes, AAV6, 8 and 9 exhibit a high tropism for striated muscles, which is ideal for lessening off-target events in the treatment of muscular dystrophies [28, 29].

A significant limitation of rAAV vectors is that they can carry only a limited amount of DNA, i.e., they cannot deliver large genes. To accommodate this minimal carrying capacity of rAAV vectors, a common strategy is to insert miniaturized but highly functional copies of the dystrophin gene into the vector. These microdystrophin genes are deleted for sequences that code for several minimally essential regions in the dystrophin protein [30]. While there are numerous ways to generate a microdystrophin protein, and improved versions are still being developed, all share the feature of retaining only the most crucial functional domains, while taking care to retain structural flexibility and stability of the final protein [31]. Effective treatment of severely dystrophic mice was achieved by intravascular administration of rAAV6 vectors carrying microdystrophin, which restored dystrophin production in the respiratory, cardiac and limb muscles, improving muscle function and extending the lifespan [32, 33, 34, 35, 36].

Another strategy to overcome the limited carrying capacity of rAAV vectors is to co-deliver two or more rAAVs that have the gene of interest split between them, with reconstitution of the larger gene occurring inside the muscle cell. Reconstitution can be induced in various ways by specific design. One method is trans-splicing, where reconstruction of the larger gene occurs following a process where the various AAV vectors bind together and form large concatemers. A modification of this method involves splicing together of smaller protein pieces to produce a complete protein [37]. Still another modification involves co-infection of AAV vectors carrying overlapping portions of the desired gene, which reconstitutes the larger gene inside muscle cells by an exchange of DNA pieces known as “homologous recombination” [38••, 39, 40]. These ‘two vector’ methods have been used to deliver larger and more functional “minidystrophins” to dystrophic mice, resulting in somewhat greater physiological improvements compared to microdystrophin delivery [31, 38••, 40]. Recently, delivery of the entire dystrophin gene has been achieved using a triple-AAV vector system, although the efficiency is quite low [41].

Despite efficient gene transfer in mouse models of muscular dystrophy, a major obstacle in the field of AAV-mediated gene transfer is the host immune response. Unlike rodents, large animal models such as dogs and non-human primates, as well as humans, are born with a fully developed immune system, and immune responses against both the viral vector and the delivered therapeutic protein have been observed [42, 43, 44, 45, 46, 47••]. This highlights the need for pre-clinical testing in large animals before trialling in humans. In the only human trial to date of rAAV-mediated dystrophin gene transfer, intramuscular injections of a rAAV-minidystrophin into the biceps of six patients induced a minidystrophin-specific T cell immune response from as early as day 15 post-vector treatment in at least one patient, with none of the six patients displaying significant levels of vector-delivered dystrophin [45, 46]. Some of the patients also displayed elevated T-cell immune responses against the AAV vector [42]. Priming of the dystrophin T-cell activity was thought to have occurred through low levels of dystrophin that are produced naturally in rare, so-called ‘revertant fibers’ found in most DMD patients [45]. Recently, it was shown in a study of 70 DMD patients that ~28 % have anti-dystrophin T-cell immunity, with increasing age correlating with increased risk of anti-dystrophin immunity [47••]. Transient immunosuppression has been shown to be effective in preventing activation of T-cell-mediated immune responses and maintains production of vector-delivered microdystrophin in dog DMD models [48, 49], suggesting a need to incorporate an immunosuppressive regimen in future clinical trials.

In addition to cell-mediated responses to the AAV and therapeutic proteins, there have also been reports of pre-existing antibody (humoral) immunity against AAV (including AAV6) in some large animal models, especially in non-human primates and dogs [50, 51•, 52]. However, other groups have found no [53] or low titers of anti-AAV6 pre-existing neutralizing antibodies (NAbs) in dogs [54], suggesting that the source of the animals can skew results. NAbs against AAV2 have also been reported in many patients [46], and cross-reacting antibodies can cause sero-positivity against other serotypes [46, 53, 54, 55]. Proper patient screening and careful NAb titering are thus critical prior to future trials, which can also aid in selecting the AAV serotype with the best chance of success for particular patients.

A number of novel methods are being developed to overcome NAb inhibition and enhance gene transfer. Recently, it was found that empty AAV vehicles (i.e., carrying no genes) could act as “decoys” for NAbs when co-delivered with AAV vectors carrying a therapeutic gene [56]. Removal of NAbs by plasmapheresis can also enhance gene transfer [57•]. Directed evolution of AAV vectors is another strategy to enhance muscle tropism, overcome pre-existing neutralizing antibodies and allow for readministration with variants of the original vectors as required [46]. Other methods to reduce immune rejection include the use of muscle-specific gene regulatory switches to prevent protein production in non-muscle cells [58, 59, 60], sequence-optimization of the therapeutic gene to be delivered to reduce vector dosage [61], and thorough purification from contaminating viral gene products during vector preparation [27].

An increasing focus is being devoted to developing methods to deliver genes to dispersed muscle groups by using vector perfusion into the vasculature of isolated limbs. This approach includes the use of vascular ligatures, compression bandages or recirculation in the limb to increase gene transfer [48, 62, 63], simultaneous perfusion with agents that promote vector exit from capillaries to underlying muscles, such as histamine [64] and vascular endothelial growth factor [65], or delivering vector using high pressure injections [66, 67]. Importantly, efficient cardiac gene transfer, which is critical for DMD therapies, was achieved by direct “transendocardial injections” of rAAV vectors, with rAAV6 demonstrating the greatest cardiac targeting compared to rAAV8 and rAAV9 vectors in canine and non-human primate models [54, 68•]. In this method, vector is injected directly into cardiac muscle using catheters inserted into the cardiac vasculature. Direct infusion of vector via the jugular vein using rAAV6 and rAAV8 also resulted in good transgene delivery to canine heart and diaphragm [48, 69], with homogeneous gene expression being obtained in the heart 2.5 months after infusion [69]. Widespread gene delivery to the canine skeletal musculature was also achieved with rAAV9, though with relatively poor delivery to the heart [70, 71].

AAV vectors are also being used as a vehicle to deliver antisense oligonucleotides (AONs), since AONs by themselves have not worked well in the heart [72]. Embedding the antisense DNA sequence into an AAV vector carrying a small nuclear RNA (snRNA) particle protects it from degradation and improves the efficiency of pre-mRNA splice site modulation. A single administration of a rAAV expressing an ASO gene restored dystrophin expression and ameliorated pathology in muscles of dystrophic mice [73, 74]. Although the level of dystrophin restoration will decline over time as AAV vectors are lost, thus requiring repeat injections, recent studies in mice showed sustained exon skipping in the heart after 1 year [75]. Based on these promising results, AAV-mediated exon skipping is currently in preclinical stages to treat DMD patients (

Surrogate Genes

Delivery of surrogate genes, such as utrophin, could also potentially circumvent an immune response against dystrophin in DMD patients. Utrophin is a close evolutionary relative (paralog) of dystrophin, sharing 80 % amino acid sequence identity, and is normally produced in muscle at the neuromuscular and myotendinous junctions. Utrophin has also been found to partially compensate for the loss of dystrophin in DMD patients and animal models. rAAV-mediated delivery of microutrophin performed favorably relative to microdystrophin in dystrophic mdx:utrophin−/− (double knock out, dko) mice [76]. Upregulation of utrophin by treatment with SMT C1100, an orally bioavailable small molecule utrophin modulator, partially reversed dystrophic pathology in mdx mice [77•]. A phase 1B clinical trial of SMT C1100 commenced in December 2013 and is being carried out by Summit, a UK-based drug discovery company. In addition to utrophin, rAAV-mediated transfer of follistatin, a muscle-building gene, improved histology and increased muscle mass and strength in mdx mice and non-human primates [78]. It is in the phase 1 clinical trial for patients with BMD and Sporadic Inclusion Body Myositis ( Recently, rAAV-mediated co-delivery of microdystrophin and follistatin was shown to fully restore force and resistance to eccentric contraction-induced injury in aged mdx mice, thus presenting a viable treatment option for DMD patients with advanced pathology [79•].

Cell Therapies

One caveat for dystrophin replacement therapies is that effectiveness in patients is dependent on both the number of remaining myofibers and the degree to which fibrotic connective tissue might limit the accessibility of myofibers to AAV vectors or small molecules. For patients in advanced stages of the disease, the use of gene replacement/correction in conjunction with cell therapies would likely have the greatest potential for an effective therapy.

While gene replacement therapies typically aim to stop the progression of muscle degeneration, cell therapies carry possibilities of both halting disease progression and restoring lost muscle mass. Resident muscle stem cells, termed satellite cells [80], are responsible for normal muscle maintenance and essential for muscle regeneration following injury [81, 82, 83]. Upon injury, satellite cells are activated to both self-renew and give rise to pools of proliferating myogenic progenitor cells (myoblasts), which fuse to repair damaged myofibers [83]. Throughout constant bouts of injury and repair in DMD patients, the capacity of resident satellite cells to self-renew and replenish injured muscle eventually diminishes, contributing to significant loss of muscle mass and function. A major feature of DMD is therefore a loss of regenerative capacity, and hence it could be amenable to stem cell therapy.

Based on promising results in animal models [84], cell therapies for DMD initially focused on local intramuscular injections of myoblasts derived from healthy donors to re-introduce dystrophin expression in muscles of DMD patients [85, 86, 87]. Unfortunately myoblast transfer strategies have thus far failed to produce adequate therapeutic effects, in part because of issues of poor survivability, limited migration from the injection site and immune rejection of transplanted cells [85, 88, 89, 90]. Expectations have been further tempered by challenges in expanding sufficient numbers of myogenic stem/progenitor cells in culture while preserving their ability to self-renew and efficiently engraft in vivo [91]. However, these early observations helped identify hurdles that needed to be overcome to improve treatment outcomes.

These findings led to the exploration of alternative cell sources with myogenic potential that could be more easily grown in culture while also being able to distribute to a wider range of affected muscles following systemic, intravascular delivery. Bone marrow-derived stem cells as well as muscle blood vessel-associated cells such as pericytes and mesoangioblasts (MABs) were shown capable of contributing to muscle regeneration, albeit with lesser efficiency than traditional myogenic stem/progenitor cells [92, 93]. Promising cell candidates eventually emerged, including MABs for which phase 1/2 clinical trials relying on transplantations of MABs derived from healthy HLA-matched donors are in progress (EudraCT no. 2011-000176-33). The next goal was to generate MABs from a dystrophic patient, correct the genetic mutation during cell expansion in culture, then transplant the corrected cells back into the patient (an approach known as ex vivo gene therapy). However, a recent report showed a drastic reduction of MABs in dystrophic patients, thereby limiting the ability to obtain sufficient number of cells for transplantation [94].

Induced pluripotent stem (iPS) cells have recently gained attention in re-programming strategies aimed at “manufacturing” ideal cell candidates that fulfill many of the identified needs for successful stem cell therapies of DMD. These iPS cells can be “induced” to a pluripotent, stem cell state by addition of several combinations of transcription factors important during early embryonic development [94]. iPS cells harbor virtually limitless expansion potential during which dystrophin vectors can be re-introduced to correct or bypass the genetic mutation [95, 96]. Corrected iPS cells can be subsequently directed toward adopting myogenic fates using various techniques, such as gene transfer of myogenic determination factors, and serve as a patient-specific cell source for autologous transplantation. Successful re-programming of iPS cells into stem/progenitor cells capable myogenic differentiation has been reported following gene-transfer of the regulatory genes encoding MyoD, Pax7 and Pax3 [97, 98••, 99].

MyoD is an extremely important regulator of gene transcription in muscle, which plays a key role during muscle regeneration where its expression in muscle stem (satellite) cells precedes myogenic differentiation [100]. The potency of MyoD for inducing myogenic fates in both muscle and non-muscle cell types has been well documented [101, 102]. A recent study aimed at stimulating muscle differentiation in human iPS cells modified with a MyoD gene that could be turned on or off reported up to 90 % myogenic reprogramming efficiency in vitro with the ability of reprogrammed cells to engraft into dystrophic muscles [97]. A possible drawback of using MyoD is that its expression leads to irreversible muscle differentiation, potentially reducing the chance for transplanted cells to become muscle stem cells (rather than myofibers) within transplanted muscles. However, recent data have indicated that subsets of iPS cell-derived MyoD-expressing cells are capable of forming muscle stem cells and engrafting into regenerating myofibers [103].

Other transcription factors that control the decision of stem cells to become myogenic cells are also attractive gene-transfer candidates to generate new muscle stem cells. Pax7 plays a key part in the function of satellite cells and is indispensible for adult skeletal muscle regeneration following injury [82]. The transcription factor Pax7 has also been used to convert human iPS cells into a muscle fate, and those cells were also able to partially restore dystrophin expression, generate new satellite (stem) cells and improve muscle function following transplantation into dystrophic mice [104]. Pax3, like Pax7, is expressed during myogenesis as well as embryonic development of non-muscle lineages such as those giving rise to the peripheral nervous system and melanocytes [105]. This necessitates careful sorting of cells derived via forced Pax3/7 gene expression in order to separate non-myogenic and possibly tumorigenic cells from myogenic cells prior to transplantation. Similarly, a version of the Pax3 transcription factor was used to generate myogenic stem cells from iPS cells genetically corrected with a micro-utrophin gene [98••]. Following activation of the Pax3 gene, cells were allowed to differentiate in culture prior to cell sorting for markers normally found on mesodermal cells destined to form muscle. The resulting stem/progenitor cells exhibited typical myogenic differentiation characteristics in culture and were able to generate functional microutrophin-expressing myofibers, migrate to stem cell harboring sites in muscle and improve muscle function following intramuscular injection into dystrophic mice [98••]. Importantly, these cells were also able to disseminate to several affected muscle groups following intravenous delivery.

iPS cells could potentially also solve the issue of obtaining sufficient MABs from dystrophic patients for autologous cell transplantation therapies. In two recent reports, iPS cells derived from both mice and humans with limb-girdle muscular dystrophy (LGMD) or DMD were used to generate α-sarcoglycan- or microdystrophin-corrected MABs for transplantation studies in immunodeficient mouse models of each condition [94, 103]. Following intramuscular and intraarterial administration, gene-corrected MABs were stimulated to adopt myogenic fates using an inducible version of MyoD [102]. Induced MABs engrafted a majority of affected muscles where they both fused with myofibers and formed new satellite/stem cells. Engrafted muscles exhibited a restoration of up to 25 % of normal expression levels of the mutant gene as well as significant morphological and physiological improvements. While promising, further studies are warranted to determine the safety and efficacy of these cell therapy approaches before translation into patients.


Development of therapeutics for the muscular dystrophies had progressed from basic studies in mice to ongoing early phase human clinical trials. While none of the methods being tested has yet risen to the level of a cure or major therapy, multiple approaches are showing significant promise, and it is becoming clear that treatments can and will be developed. It will be important to continue refining current approaches in animal models while expanding testing in patients. Recent clinical results also serve as a reminder that early encouraging success is no guarantee of long-term benefit, and it will be important to seek alternative strategies while refining those approaches already in advanced stages of testing.


We thank John Hall for critical reading of the manuscript. Supported by NIH grants R37AR40864 and R01AG033610 (to JSC). JTS was supported by an Early Career Fellowship from the NHMRC of Australia (Grant No. 1036656).

Copyright information

© Springer Science + Business Media New York 2014

Authors and Affiliations

  • Jane T. Seto
    • 1
  • Niclas E. Bengtsson
    • 1
  • Jeffrey S. Chamberlain
    • 1
  1. 1.Department of NeurologyUniversity of WashingtonSeattleUSA

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