What this is
- () leads to severe muscle degeneration and currently lacks a cure.
- This study evaluates the long-term effects of -expressing chimeric (DEC) cell therapy in a mouse model of .
- Human demonstrated significant improvements in cardiac, respiratory, and skeletal muscle function over 180 days.
Essence
- Human improves muscle function and reduces pathology in cardiac, respiratory, and skeletal muscles in a mouse model over 180 days. This therapy has potential as a universal treatment for .
Key takeaways
- Human resulted in a significant increase in expression in muscle tissues, with levels reaching 5.34%±0.36% and 7.29%±0.52% in the diaphragm for the lower and higher doses, respectively, compared to 2.68%±0.36% in controls.
- Significant reductions in muscle fibrosis were observed, with fibrosis levels at 3.81%±0.53% and 2.77%±0.21% for the lower and higher DEC doses, respectively, compared to 6.98%±0.48% in vehicle controls.
- Ejection fraction improved significantly in the higher DEC dose group, reaching 66.86%±3.13% at day 90 and 64.40%±3.81% at day 180, while vehicle controls dropped to 52.86%±0.88%.
Caveats
- The study used an immunocompromised mouse model, limiting the assessment of potential immune responses to .
- Findings are based on preclinical data; clinical relevance in human patients remains to be established.
Definitions
- Duchenne Muscular Dystrophy (DMD): A severe genetic disorder causing progressive muscle degeneration due to lack of dystrophin.
- Dystrophin: A protein essential for muscle fiber stability, its absence leads to muscle degeneration in DMD.
- DEC therapy: Dystrophin Expressing Chimeric therapy, a cell-based treatment aimed at restoring dystrophin expression in muscle tissues.
Simplified
Background
Duchenne Muscular Dystrophy is an X-linked recessive neuromuscular disorder caused by mutations in the dystrophin gene with the incidence of approximately 1 in 3,500–5,000 newborn boys [1].
Due to the lack of dystrophin, a large structural protein that stabilizes the plasma membrane in muscle fibers, progressive weakness of skeletal, cardiac, and respiratory muscles is observed. First symptoms of abnormal gait and walking are observed in the affected boys between 3 and 5 years of age and by age 12, most boys are wheelchair-dependent [2]. Due to continuous degradation and asynchronous regeneration of the myofibers, the normal muscle tissue is replaced by fat deposits and scarring, as a result of chronic inflammation and fibrosis [3, 4]. Over time, the majority of DMD patients develop dilated cardiomyopathy, which is accompanied by deterioration of respiratory function leading to significant morbidity and premature death around the age of 20 due to the cardiac and respiratory failure. Despite significant scientific efforts, there is no cure for DMD patients. Currently, the available treatment options addressing cardiac and pulmonary problems include corticosteroids, vasodilators, antioxidants and supportive measures such as respiratory muscle training and non-invasive respiratory support [4–8]. Since the supportive measures and clinical management of DMD have not improved or halted progression of the disease, new therapeutic approaches are needed in order to restore the cardiac, respiratory, and skeletal muscles function to clinically relevant levels [9–11]. Different approaches targeting the genetic defect have been investigated including exon skipping therapy [4, 12], gene editing via viral vectors [13–16] and genome editing using CRISPR technology [14, 16]. Since gene therapies are usually targeting very specific mutations, they are not applicable to all DMD patients [17, 18]. Although the preliminary results for genetic correction are encouraging, the clinical efficacy is still debatable due to the safety concerns for the “off-target mutations”, tumorigenicity and sensitization [15, 19, 20]. Recent reports on the microdystrophin AVV-based therapy are promising, however side effects related to the dose-dependent immune response are of concern [21]. Cell-based therapies including myoblasts or mesoangioblasts transplantation, aiming for regeneration of the damaged muscles, have shown early promising results [22–25]. However, the reported limitations included the short-term cell engraftment, allogeneic immune response, and the side effects of the supportive immunosuppressive therapy [3, 26, 27]. Therefore, the optimal cell-based therapy should be characterized by low immunogenic phenotype, accessibility, proper expansion, and high transplanted cell survival rate which is crucial for the maintenance of the long-term engraftment without the need for immunosuppression [17, 22, 28–34]. We have addressed these specific unmet needs for cell-based therapies using a new chimerism-based tolerance inducing strategy for bone marrow and vascularized composite allotransplantation (VCA) and generated new chimeric cell lines of hematopoietic, mesenchymal and myoblast lineage origin for DMD therapy [35–39].
Moreover, we have applied the chimeric cell therapy concept to muscular dystrophy and created Dystrophin Expressing Chimeric (DEC) Human cells by fusion of human myoblasts (MB) derived from normal and DMD-affected donors (MBN/MBDMD). Administration of DEC therapy to the mdx mouse models of DMD resulted in restoration of dystrophin expression which correlated with significant improvement of cardiac, respiratory and skeletal muscle function [39, 40].
Furthermore, we have investigated the systemic effect of DEC therapy and confirmed restoration of dystrophin expression and reduced mdx muscle pathology which correlated with improvement of cardiac, pulmonary and skeletal muscle function at 90 days after systemic-intraosseous DEC administration [41]. Currently, the major challenge, precluding routine application of cell-based therapies in DMD is the lack of maintenance of long-term engraftment and function.
Therefore, considering the dynamic progression of DMD and to bring DEC technology closer to the clinical application, in the current study we have assessed a long-term (180 days) efficacy of human DEC therapy after systemic-intraosseous administration. Our goal was to assess the protective effect of DEC therapy in the most affected by the DMD organs before severe progression of the disease and before development of the overt DMD -related cardiomyopathy or pulmonary failure, to make it more clinically relevant, since once organ failure occurs, treatment with stem-cell based therapies would not reverse damage created by DMD disease.
Thus, in this study, the maintenance of long-term engraftment of DEC correlating with restoration of function was confirmed by normalized muscle morphology, reduced pathology, and improved function in the most severely affected by DMD organs including heart, diaphragm, and long skeletal muscles. This encouraging preclinical data introduces human DEC as a novel Advanced Therapy Medicinal Product (ATMP) with the potential to improve or halt progression of the disease and enhance quality of life of DMD patients.
Materials and Methods
Mice and Animal Care
This study was approved by the Institutional Animal Care and Use Committee (IACUC) of University of Illinois at Chicago, which is approved by the American Association for the Accreditation of Laboratory Animal Care (AAALAC). All animals received humane care in compliance with the ‘Principles of Laboratory Animal Care’ formulated by the National Society for Medical Research and the ‘Guide for the Care and Use of Laboratory Animal Resources’. Six- to eight-week-old male mdx/scid mice—the animal model for Duchenne Muscular Dystrophy (B10ScSn.Cg-Prkdcscid Dmdmdx/J, stock number 018018) with respective background wild type mice (C57BL/10ScSnJ, stock number 000476) were purchased from Jackson Laboratories. Animals were kept in a pathogen-free environment on a light/dark cycle. Prior to study initiation, aged matched male mdx/scid mice were ear tagged and randomized into following experimental groups: vehicle control injected with 60 µl phosphate-buffered saline, PBS (n = 4), DEC therapy group injected with 1 × 106 DEC cells suspended in 60 µl PBS (n = 5), and DEC therapy group injected with 5 × 106 DEC cells suspended in 60 µl PBS (n = 5).
Cell Culture
Normal human myoblasts (MB) were purchased from Lonza Bioscience (Mapleton, IL, USA), and DMD-affected myoblasts were purchased from Creative Bioarray Ltd. (Shirley, NY, USA). Myoblasts (MB) were cultured in Skeletal Muscle Cell Growth Medium-2 (Lonza Clonetics, Mapleton, IL, USA) supplemented with the human Epidermal Growth Factor (hEGF); Fetal Bovine Serum (FBS); Dexamethasone; Gentamicin/Amphotericin B (GA) (Lonza Clonetics, Mapleton, IL, USA). Upon reaching 60–70% confluence, myoblasts were harvested using 0.25% trypsin/EDTA (Sigma-Aldrich, MO, USA). Enzymatic activity was inhibited with 10% serum-supplemented culture media. Human MBs were harvested between passages 3–7, which is optimal for the ex vivo cell fusion procedure.
Cell Fusion Procedure
After harvesting, staining and viability assessment with 0.4% Trypan Blue (Gibco-ThermoFischer, Waltham, MA, USA), parent myoblasts (MBN and MBDMD) were washed in serum-free media supplemented with antibiotics (1% Antibiotic–Antimycotic solution, Gibco-ThermoFischer, Waltham, MA, USA). Next cell fusion procedure was performed. As previously described [38–40] parent myoblasts (MBN and MBDMD) were fluorescently labeled using PKH26 or PKH67 (Sigma-Aldrich, St. Louis, MO) membrane dyes respectively, according to manufacturer’s instructions. Parent cells were mixed, washed and fusion was performed using 1.46 g/mL PEG solution (PEG 4000, EMD) containing 16% DMSO (Sigma, St. Louis, MO) [42–44]. Fused cells were transferred to fluorescently activated cells sorting (FACS) buffers containing 5% HEPES, 1% EDTA and 5% FBS. Finally, cells presenting double (PKH26/PKH67) staining were selected via FACS (MoFlow Astrios, Beckman Coulter, San Jose, CA, USA) sorter and were used for intraosseous administration to the mdx/scid mice.
Systemic–Intraosseous DEC Administration
Mice were anesthetized with 2% isoflurane inhalation along with 1 mL/kg buprenorphine subcutaneous injection. DEC intraosseous administration was performed as previously reported [39, 41]. Briefly, a 5 mm incision was made at the lateral-mid thigh level and muscles were separated to expose femoral bone. DEC cells were transferred in a 60 µl volume of sterile PBS to a tuberculin syringe (cat. ThermoFischer, Waltham, MA, USA). A 25G needle was used to aspirate 60 µl of bone marrow followed by DEC cells injection directly into the femur. Bone wax was applied to the injection site. Next, muscles were approximated, and the wound was closed with 5–0 nylon sutures. Animals recovered in a heated environment with post-operative monitoring and returned to the colony.
Immunofluorescence for Dystrophin Expression Assessment
For immunofluorescence the optimal cutting temperature (OCT) frozen sections of the heart, diaphragm and gastrocnemius muscle were fixed with ice-cold acetone for 10 min and blocked for the unspecific binding with 10% normal goat serum for 60 min in 4 °C. Next, specimens were incubated with mouse monoclonal anti-human dystrophin (1:50, cat. ab15277, Abcam, Cambridge, UK) and mouse monoclonal anti-human spectrin (Leica, Clone RBC2/3D5, Biosystems, NCL-SPEC1) primary antibodies, followed by incubation with a goat anti-mouse conjugated AlexaFluor-647 secondary antibody for dystrophin (1:400, cat. A-21241, ThermoFischer, Waltham, MA, USA) and goat anti-mouse secondary antibody for spectrin (IgG) Alexa Fluor® 647 (1:400, ab150115, Abcam, Cambridge, UK). Appropriate positive and negative controls were used. Nuclear counter-staining was performed using 4′,6-diamidino-2-phenylindole (DAPI) (cat. ab104139, Abcam, Cambridge, UK). A Zeiss Meta confocal microscope with ZEN software (Carl Zeiss, Oberkochen, Germany) and Leica DM4000B microscope were used for fluorescence signal detection and analysis.
Histology for Muscle Pathology Assessment
For histological analysis, the heart, diaphragm and gastrocnemius muscles were harvested, fixed in 10% neutral buffered formalin and embedded in paraffin. Next, the paraffin blocks were cut into 5 µm non-consecutive transverse cross-sections. Samples were deparaffinized and subsequently stained with appropriate staining kits, then mounted (Poly-Mount, PolySciences Inc. Warrington, PA, USA) to analyze overall muscle morphology, to assess infiltration of inflammatory cells, and to quantify the centrally nucleated fibers (CNF), fibers minimal Feret’s diameter size, and finally to assess the level of fibrosis. All histological assessments were done on 12 ROI (region of interest) acquired from three non-serial cross sections from n = 3 mice (12 ROI/organ/mouse or 36 ROI/organ/group) using ImageJ NIH software. The digital images were acquired (BX51/IX70 Olympus, Japan) and processed using ImageJ.
H&E-stained sections of target organs of heart, diaphragm and gastrocnemius muscle of DEC injected mdx/scid mice were assessed and compared with the vehicle-injected controls and Wild Type (WT) mice. Inflammation was assessed by counting the total number of small (5–9 inflammatory cells) and large (groups of 10 or more inflammatory cells) foci in the representative images. The numbers of foci counts were normalized to the area unit (number of foci/mm2).
For analysis of centrally nucleated fibers, H&E-stained sections of diaphragm and gastrocnemius muscle were assessed by counting the number of fibers with centrally located nuclei, which represent pathological changes in the muscle tissue. The number of CNF was compared to the total number of fibers and expressed as a percentage.
Fiber diameters were assessed by minimal Feret’s diameter on H&E-stained sections of heart, diaphragm, and gastrocnemius using ImageJ measurement plug-ins. Average number of fibers falling into 5 µm increments was normalized to the total number of fibers and expressed as a percentage.
For analysis of cardiac muscle fibrosis, cross sections of heart samples were stained with Picro-Sirius Red kit specific for cardiac muscle (Abcam, cat. 245,887, Cambridge, MA, USA). Fibrosis of the diaphragm and gastrocnemius muscle was analyzed in the sections, which were stained with Trichrome Stain kit (Abcam, cat. ab150686, Cambridge, MA, USA) for visualization of collagenous fibrotic tissue.
Pixels corresponding to the area stained in red (for Picro-Sirius), or blue (for Trichrome) or indicating collagenous areas reflecting fibrosis, were normalized to the total pixel area of the tissue in the assessed image. Results were expressed as a percentage of collagenous area versus total tissue area in the region of interest.
Echocardiography for Cardiac Function Assessment
Echocardiography was performed as previously described [39, 41]. Briefly, mice were anesthetized with isoflurane (1–3%) and placed on the ultrasound stage. Paws were taped to the electrocardiograph (ECG) electrodes to monitor heart rate (maintained at 350–450 bmp). Assessments were made at the baseline—before administration of DEC and at 30 days, 90 days, and at 180 days endpoint after intraosseous DEC administration. M-mode echocardiographic images were obtained from the parasternal long axis view through the center of the left ventricle (FujiFilm, VisualSonics, Vevo 2100, Toronto, Canada) [45, 46]. Recordings were analyzed using VevoLab (ver. 3.2.0).
Plethysmography for Pulmonary Function Assessment
Whole body plethysmography was applied for assessment of respiratory function as described elsewhere [41, 47]. Small animal plethysmography set-up (Buxco/DSI, St. Paul MN, USA) using FinePointe (Buxco/DSI) was applied. The assessment was performed at the study endpoint of 180 days post-DEC administration. The following parameters were calculated: Enhanced pause (Penh) and Expiration time (Te).
Aurora Test for ex vivo Muscle Force Assessment
After animal euthanasia at the study endpoint of 180 days post-DEC administration, the contractile and passive properties of the gastrocnemius muscle (GM) were measured ex vivo using Aurora Scientific test system as described previously [38]. After dissection of the whole left and right GM, the Achilles tendon and proximal pole of muscle were attached to the force transducer. Muscle force was measured after establishing optimal length through a standardized stimuli pattern until reaching the maximal wave and maximal strain. Results were averaged for the right and left gastrocnemius muscles and reported as the force/muscle weight (g/g).
Grip Strength Assessment
The assessment of mdx/scid mice motor function after systemic-intraosseous administration of DEC cells was tested by the right hindlimb grip strength test. The function was monitored up to a 180-day endpoint. The tests were performed weekly, for 26 weeks of follow-up. The order of animals for test performance was randomly assigned. A grip meter (Digital Force Gauge, HL-50) was used to measure the GM-specific force. This test allows forelimb force measurements, providing information on the muscle strength. The hook of a grip meter was placed touching the animal’s toes. Once gripped, it was repeatedly pulled 10 times, and the average maximum peak was used for further analysis.
Statistical Analysis
Data are expressed as mean ± SEM (standard error of the mean). GraphPad Prism (ver. 9.2.1) software was used to perform statistical analysis. Two-tailed Student t-test for group comparisons was used to define statistical significance. Results were considered statistically significant for p < 0.05. The graphs represent mean values with standard error of mean (SEM), statistical significance is marked with asterisks: *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001.
Results
I. The Long-Term Amelioration of the mdx Pathology in Cardiac, Respiratory and Skeletal Muscles at 180 days after Systemic-Intraosseous Administration of Human DEC Therapy to the mdx/scid Mouse Model of DMD.
This study assessed the long-term (180 days) effect of DEC therapy after systemic-intraosseous administration to the mdx/scid mice. At the study baseline, the six to eight-weeks old mdx/scid mice were randomly assigned to two therapy groups of 1 × 106 and 5 × 106 dose of human DEC cells in the respective groups. Following intraosseous administration of DEC, animals were monitored up to the study endpoint of 180 days, when they were assessed for muscle pathology and by the ex vivo and in vivo functional tests.
All animals tolerated well the intraosseous administration of both dosages of human DEC therapy into the femoral bone. The injections were performed under surgical microscope magnification of 20X and the PBS-based DEC cell solution was injected without any spill or leakage. There was no presence of hematoma, inflammation, or infection observed at the surgical site after injection and no side effects were observed during the entire follow-up period up to 180 days.
Human DEC Therapy Increases Dystrophin Expression in Cardiac, Respiratory and Skeletal Muscles at 180 Days after Systemic Administration
The diaphragm IF sections (Fig. 1C) confirmed significant increase in dystrophin expression in both DEC-injected groups of 1 × 106 (5.34% ± 0.36%) and 5 × 106 (7.29% ± 0.52%) DEC cells when compared to the vehicle-injected controls (2.68% ± 0.36%). Moreover, a significant increase in dystrophin positive fibers was observed in 5 × 106 dose when compared to 1 × 106 DEC indicating a dose-dependent effect of DEC therapy on restoration of dystrophin in the diaphragm of mdx/scid mice (Fig. 1D).
Assessment of gastrocnemius muscle IF sections (Fig. 1E) revealed increase of dystrophin expression in both DEC-injected groups of 1 × 106 (7.09% ± 0.46%) and 5 × 106 (8.67% ± 0.50%) DEC cells when compared to the vehicle-injected controls (2.57% ± 0.24%) (Fig. 1F). In addition, co-localization of dystrophin expression with expression of the human-specific spectrin (red) in the heart, diaphragm and GM samples of the mdx/scid hosts injected with both doses (1 × 106 and 5 × 106) of human DEC cells confirms the long-term engraftment of DEC and human origin of the dystrophin positive muscle fibers (Fig. 1G).
Systemic-intraosseous administration of human DEC (1 × 10and 5 × 10) cells confirms long-term DEC engraftment and increased dystrophin expression in the heart, diaphragm and gastrocnemius muscle at 180 days after DEC transplant to themice. Immunofluorescence images of dystrophin expression in the heart, diaphragmand gastrocnemius muscle (after systemic DEC transplant compared to vehicle and WT controls. White arrows indicate positive fibers, showing differences between the therapy groups and the vehicle control; Magnification 25X, scale bar = 50 μm; for merge: dystrophin (green), human spectrin (red), DAPI nuclei counterstaining (blue).Representative immunofluorescence images of human spectrin (red) expression in the heart, diaphragm and gastrocnemius muscle samples of thehosts injected with human DEC (1 × 10and 5 × 10), dystrophin (green), nuclei counterstained with DAPI (blue); Magnification 140X, scale bar 20 μm (ZEISS 710 META, Oberkochen, Germany).Significant increase of dystrophin expression in target organs of: heart, diaphragm—dose-dependent effect, and gastrocnemius muscleof DEC-injected compared to vehicle injectedmice, n = 3/group, 10 ROI/organ/mouse. Dystrophin-positive fibers were counted and normalized to the total number of fibers. All data presented as mean ± SEM. One-way ANOVA with post-hoc Tukey’s test. **< 0.01, ***< 0.001 6 6 6 6 mdx/scid mdx/scid mdx/scid p p (A) (C) E) (G) (B, D, F) (B) (D) (F)
DEC Therapy Reduces Inflammation in the DMD-Targeted Organs of Heart, Diaphragm, and GM at 180 days after Intraosseous Administration
We have previously confirmed short-term reduction of the inflammatory response at 90 days after systemic DEC administration [41]. Since inflammation is the hallmark of DMD progression, thus in this study, we assessed the long-term effect of DEC therapy on amelioration of inflammation in the DMD affected organs of heart, diaphragm and skeletal muscle.
Administration of human DEC therapy (1 × 10and 5 × 10) results in reduced inflammation in the heart, diaphragm and gastrocnemius muscle at 180 days following DEC administration. Representative images of Hematoxylin and Eosin (H&E) stained cross-sections of heart, diaphragm, and gastrocnemius muscleconfirmed reduced muscle inflammation in both DEC groups compared to vehicle-injected controls. Magnification 40x (heart panel) 20x (diaphragm and gastrocnemius muscle), scale bar 50 μm, n = 3/group, 12 ROI/organ/mouse.In heart H&E sections the number of small and large foci was significantly reduced in both DEC groups and was dose-dependent. No large foci were seen in the 5 × 10group.Dose-dependent reduction of total number of inflammatory foci was observed in cardiac muscle in both DEC groups but not in vehicle-injected group and was dose-dependent.In diaphragm, significant dose-dependent reduction of small and large inflammatory foci was observed in DEC-injected compared to vehicle-injected mice.Total number of inflammatory foci in diaphragm was significantly reduced in both DEC groups when compared to vehicle-injected controls and was dose-dependent.In gastrocnemius muscle significant reduction of the total number of inflammatory foci was observed in both DEC-injected mice when compared to vehicle-injected controls.Total number of inflammatory foci in GM was reduced in DEC-injected compared to vehicle-injected groups. Data presented as mean ± SEM. One-way ANOVA with post-hoc Tukey’s test *p < 0.05, **p < 0.01, *** p < 0.001, **** p < 0.0001 6 6 6 (A) (D) (G) (B) (C) (E) (F) (H) (I)
DEC Therapy Reduces Percentage of Centrally Nucleated Fibers in the Diaphragm and Gastrocnemius Muscle at 180 days after Systemic -Intraosseous Administration
Systemic-intraosseous transplantation of human DEC (1 × 10and 5 × 10) improves muscle pathology via reduced number of Centrally Nucleated Fibers (CNF) at 180 days after administration tomice. Representative images of Hematoxylin and EosinH&E) stained transverse sections of diaphragmand gastrocnemius muscleconfirmed reduced number of centrally nucleated fibers (CNF) in DEC-injected groups compared to vehicle controls. Magnification 20x, scale bar 50 μm,= 3/group, 12 ROI/organ/mouse. Significant dose-dependent reduction of CNF in diaphragmand gastrocnemius musclein both DEC-injected, but not vehicle-injected mice. Number of CNF was normalized to the total number of fibers. CNF were marked with black arrows. Data presented as mean ± SEM. One-way ANOVA with post-hoc Tukey’s test. ***< 0.001, ****< 0.0001 6 6 mdx/scid n p p ( (A) (C) (B) (D)
Intraosseous Administration of Human DEC Therapy Normalizes Muscle Fiber Diameters in the DMD-Targeted Organs of mdx/scid mice at 180 days after DEC Transplant
Presence of variations in the muscle fiber diameter size represents characteristic features of muscles affected by DMD. We reported short term normalization of fiber size after DEC therapy [41]. Thus, in this study to further assess clinical applicability of DEC, we used Feret’s method to measure both, the overall change and the maintenance of normalization of fiber size diameters at the long-term (180 days) follow-up after systemic DEC administration.
Human DEC (1 × 10and 5 × 10) administration improves muscle morphology via normalized fiber size and homogeneity in the heart, diaphragm and gastrocnemius muscle at 180 days after systemic DEC administration. Representative histology images of Hematoxylin and Eosin (H&E) stained cross-sections of the cardiacdiaphragmand gastrocnemius muscleofmice at 180 days after systemic-intraosseous administration of DEC therapy compared with vehicle-injected and WT controls. Magnification 40x, scale bar 50 μm (heart); magnification 20x, scale bar 100 μm (diaphragm and gastrocnemius muscle), n = 3/group, 12 ROI/organ/mouseFeret’s diameter measurements in the heart revealed a right-ward shift in fiber size distribution towards larger fibers in both DEC injected groups, bars represent means ± SEM.Fiber size in the diaphragm was increased after DEC therapy when compared to vehicle controls, bars represent mean ± SEM.In the gastrocnemius muscle there was a significant increase in the fiber size of DEC-injected compared to vehicle injected mice specifically in the fiber size increment between 30-35 µm. Fibers diameters were marked with black arrows. Data presented as mean ± SEM. Two sample t-test assuming unequal variances. *< 0.05, **< 0.01, ***< 0.001, ****< 0.0001 6 6 (A), (C) (E) (B) (D) (F) mdx/scid p p p p
Systemic Administration of Human DEC Therapy Reduces Fibrosis in Cardiac, Respiratory and Skeletal Muscles at 180 days after DEC Transplant
Muscle fibrosis is the hallmark of muscular dystrophies and is progressing over the course of the disease. We have previously confirmed reduction of cardiac fibrosis in the mdx and mdx/scid mice models of DMD as well as amelioration of fibrosis in the diaphragm and gastrocnemius muscle at 90 days after systemic human DEC administration [39, 41]. In this study, the goal was to assess the long-term effect of DEC therapy on reduction of muscle fibrosis in the most severely DMD- affected organs of heart, diaphragm and gastrocnemius muscle.
Moreover, this effect was dose-dependent showing lower percentage of fibrosis in the mice injected with higher dose of 5 × 106 DEC cells (Fig. 5D). Furthermore, protective effect of DEC therapy was confirmed by reduction of fibrosis on the Trichrome stained gastrocnemius muscle samples (Fig. 5E) of mice injected with both DEC doses of 1 × 106 DEC cells (3.81% ± 0.53%) and 5 × 106 DEC cells (2.77% ± 0.21%) when compared to vehicle-injected mdx/scid mice (6.98% ± 0.48%) (Fig. 5F), thus, confirming amelioration of fibrosis at 180 days after systemic DEC administration.
Intraosseous DEC (1 × 10and 5 × 10) administration results in reduced fibrosis in the heart, diaphragm, and gastrocnemius muscle at 180 days after transplant.Picro-Sirius staining of heart cross-sections assessing fibrosis after DEC therapy compared to vehicle and WT controls; fibrotic collagenous tissue (red), muscle fibers (yellow). Magnification 20x, scale bar = 50 µm, n = 3/group, 12 ROI/organ/mouse.In the cardiac muscle, significant reduction of fibrosis was observed in both DEC-injected groups compared to vehicle-injected controls. Trichrome stained cross-sections of diaphragmand gastrocnemius muscleconfirmed significantly reduced fibrosis in both DEC-injected mice compared to vehicle-injected controls. Blue-stained areas represent collagenous tissue (fibrosis) and red-stained areas represent muscle fibers. Magnification 20x, scale bars = 100 µm.In the diaphragm sections, significant, dose-dependent reduction of fibrosis was observed in both DEC-injected but not vehicle- injected mice.In gastrocnemius muscle, significant decrease of fibrosis was observed in both DEC-injected groups compared to vehicle-injected controls. Fibrosis was measured and normalized to total tissue area. Data presented as mean ± SEM. Two sample t-test assuming unequal variances. Abbreviations: *< 0.05, **< 0.01, ***< 0.001, ****< 0.0001 6 6 (A) (B) (C) (E) (D) (F) p p p p
II. Long-term Functional Improvement of Cardiac, Respiratory and Skeletal Muscles at 180 Days after Systemic—Intraosseous Administration of Human DEC Therapy to the mdx/scid mouse model of DMD.
Echocardiography Reveals Improvement of Cardiac Functional Parameters at 180 days after Human DEC Administration
Since progressive cardiomyopathy is responsible for premature death of DMD patients, evaluation of cardiac function is essential for assessment of disease severity and prognosis. We have reported the protective effect of DEC therapy on cardiac function in mdx and mdx/scid mouse models of DMD at 90 days after systemic DEC administration [39, 41]. In the current study, to check the potential clinical value of the systemic application of DEC therapy, we have assessed the dose-dependent effect of human DEC cells (1 × 106 and 5 × 106 dose) on cardiac function monitored by echocardiography over the entire follow-up period from the baseline over and at day 30, day 90 and day 180 after systemic-intraosseous injection of DEC.
Assessment of Ejection Fraction (EF) in mice injected with 1 × 106 DEC cells revealed an increase over the vehicle control EF and revealed maintenance of the EF values at baseline levels up to 180 days after DEC administration. Administration of higher DEC dose of 5 × 106 resulted in significantly higher EF (66.86% ± 3.13%) at day 90 and at day 180 (64.40% ± 3.81%) compared with vehicle-injected controls (54.41% ± 2.82% and 52.86% ± 0.88%, respectively) (Fig. 6B). In addition, a gradual drop in ejection fraction which was observed in the vehicle-injected mdx mice, when compared to baseline (baseline – 64.29% ± 4.25%; day 30 – 56.16% ± 5.48%), and at day 180 a significant EF drop was observed (day 180 – 52.86% ± 0.88%) in the treated mice (Fig. 6C). This confirms a gradual progression of the DMD disease and decline of cardiac function over the 26-weeks follow-up period in the non-injected control mice.
Similarly, echocardiographic evaluation of Fractional Shortening (FS) confirmed maintenance of FS values at baseline levels for 1 × 106 DEC dose over the entire 180 days follow-up, whereas administration of 5 × 106 DEC resulted in a continuous increase in the FS values observed from the baseline until day 90 (baseline – 33.20% ± 2.79%; day 30—37.55 ± 4.32%; day 90 – 39.14 ± 1.47%). Additionally, at 90 days, mice injected with 5 × 106 DEC dose demonstrated increased FS compared to the vehicle injected controls (28.05% ± 1.70%). The 1 × 106 DEC dose revealed similar trends (Fig. 6D). At day 180, the FS values increased in 5 × 106 DEC dose (34.83% ± 2.80%) compared with the vehicle-injected controls (26.57% ± 0.52%). In contrast, a gradual FS drop was only observed in the vehicle-injected controls over the entire follow-up period and at 180 days, revealed significant decrease when compared with baseline values (baseline – 35.13% ± 3.02%; day 180 – 26.57% ± 0.52) confirming progression of the DMD disease (Fig. 6E).
Assessment of Stroke Volume (SV) for 1 × 106 DEC dose revealed maintenance of SV at the baseline levels (baseline – 29.27 ± 2.38; day 180 – 30.39 ± 5.16 µl) over the entire 180 days follow-up period. Administration of higher DEC dose (5 × 106 cells) resulted in continuous increase in the SV values from day 30 up to day 180 (baseline – 23.42 ± 4.19 µl; day 30 – 18.23 ± 2.75 µl; day 90 – 35.94 ± 1.93 µl; day 180 – 43.69 ± 4.96) (Fig. 6F) and at 180 days, SV was significantly increased when compared to the vehicle-injected controls (28.15 ± 2.37 µl) and 1 × 106 DEC dose (30.39 ± 5.16 µl) confirming the long-term dose-dependent protective effect of DEC therapy on cardiac function (Fig. 6G).
Evaluation of Cardiac Output (CO) after administration of 1 × 106 DEC cells demonstrated maintenance of CO values at baseline levels over the entire 180 days period (Fig. 6H). Administration of higher DEC dose of 5 × 106 revealed continuous increase of CO values from day 30 to day 180 (baseline – 9.05 ± 2.34 ml/min; day 30 – 7.07 ± 2.66 ml/min; day 90 – 13.43 ± 2.65 ml/min; day 180 – 17.46 ± 3.92) and at day 180, was significantly increased compared to vehicle-injected controls (10.38 ± 1.07 ml/min) and 1 × 106 DEC dose (10.38 ± 2.15 ml/min) confirming the long-term, dose-dependent protective effect of DEC therapy on cardiac function (Fig. 6I).
Administration of human DEC (1 × 10and 5 × 10) results in long-term maintenance of cardiac function up to 180 days after systemic DEC transplant to themice.M-mode of the left ventricular (LV) parasternal long axis and LV tracing measurement after DEC administration compared to vehicle control. Vehicle-injected mice demonstrated gross thickening of the posterior LV wall and reduced size of the LV compared to DEC-injectedmice. VEVO 2100 system (VisualSonics) and a 30-MHz cardiac probe (RMV707B), VEVO Lab ver. 3.2.0.Echocardiography at 180 days post-transplant revealed maintenance of Ejection fraction (EF) after 1 × 10DEC dose and significant dose-dependent increase of EF after administration of 5 × 10DEC dose. In contrast, vehicle-injected mice revealed a significant drop in EF indicating progressive impairment of cardiac function.At day 180 post-transplant, significant dose-dependent increased EF values were observed in the 5 × 10DEC group compared to vehicle-injected controls, confirming long-term protective effect of DEC therapy.Fractional shortening (FS) in the 1 × 10DEC group was maintained at baseline values throughout 180 days follow-up, whereas significant dose-dependent increase in FS values was observed after administration of 5 × 10DEC dose. In contrast, vehicle-injected mice revealed a significant drop in FS.At day 180 post-transplant significant, dose-dependent increase of FS was observed in the 5 × 10DEC injected mice confirming long-term protective effect of DEC therapy.Stroke volume (SV) in the 1 × 10DEC group was maintained at baseline values throughout 180 days, whereas administration of higher DEC dose of 5 × 10DEC cells revealed continuous and significant increase in SV values from day 30 up to day 180.At day 180 SV in the 5 × 10DEC-injected mice was significantly increased, confirming long-term and dose-dependent protective effect.Cardiac output (CO) in the 1 × 10DEC group was maintained at the baseline values throughout 180 days follow-up whereas administration of higher DEC dose of 5 × 10DEC cells revealed continuous and significant increase in SV values from day 30 up to day 180.At day 180 the CO in the 5 × 10DEC injected mice was significantly increased compared to vehicle-injected controls confirming long-term and dose-dependent protective effect. Data presented as mean ± SEM. Mann–Whitney test,= 4. *< 0.05 6 6 6 6 6 6 6 6 6 6 6 6 6 6 mdx/scid mdx/scid n p (A) (B) (C) (D) (E) (F) (G) (H) (I)
| Morphometric parameters | ||||
|---|---|---|---|---|
| Experimental group/ Timepoint | LVESD (mm) | LVEDD (mm) | LVESV (μl) | LVEDV (μl) |
| Baseline | ||||
| Vehicle (= 4)n | 2.30 ± 0.54 | 3.36 ± 0.29 | 17.71 ± 7.33 | 46.80 ± 9.26 |
| MBN/MBDMD1 × 106 (= 4)n | 2.50 ± 0.3 | 3.53 ± 0.39 | 23.99 ± 8.47 | 53.27 ± 12.49 |
| MBN/MBDMD5 × 106 (= 4)n | 2.01 ± 0.38 | 3.03 ± 0.39 | 18.91 ± 10.55 | 42.33 ± 6.67 |
| Day 30 | ||||
| Vehicle (= 4)n | 2.25 ± 0.43 | 3.13 ± 0.47 | 18.88 ± 7.31 | 41.00 ± 12.60 |
| MBN/MBDMD1 × 106 (= 4)n | 2.62 ± 0.32 | 3.63 ± 0.37 | 25.84 ± 8.21 | 56.50 ± 13.65 |
| MBN/MBDMD5 × 106 (= 4)n | 2.66 ± 1.71 | 3.54 ± 2.69 | 10.84 ± 11.20 | 29.08 ± 16.71 |
| Day 90 | ||||
| Vehicle (= 4)n | 2.79 ± 0.27 | 3.86 ± 0.14 | 30.86 ± 6.96 | 65.26 ± 5.89 |
| MBN/MBDMD1 × 106 (= 4)n | 2.83 ± 0.17 | 3.93 ± 0.13 | 31.17 ± 4.29 | 67.95 + 5.49 |
| MBN/MBDMD5 × 106 (= 4)n | 2.30 ± 0.34 | 3.60 ± 0.27 | 19.39 ± 7.06 | 55.33 ± 10.11 |
| Day 180 | ||||
| Vehicle (= 4)n | 2.16 ± 0.28 | 3.36 ± 0.29 | 25.53 ± 6.04 | 53.69 ± 10.68 |
| MBN/MBDMD1 × 106 (= 4)n | 2.50 ± 0.34 | 3.53 ± 0.53 | 23.06 ± 6.85 | 53.45 ± 16.63 |
| MBN/MBDMD5 × 106 (= 4)n | 2.65 ± 0.28 | 3.92 ± 0.19 | 25.92 ± 7.00 | 69.61 ± 9.42 |
Human DEC Therapy Improves Respiratory Function at 180 days after Systemic-Intraosseous Administration
Since pulmonary fibrosis and respiratory failure is significantly contributing to the premature death of DMD patients, we evaluated pulmonary function via plethysmography at the baseline and at 180 days after systemic administration of two doses (1 × 106 and 5 × 106) of DEC cells.
In addition, at 180 days, the time of expiration (Te) was reduced in DEC-injected mice in both: 1 × 106 DEC (109.59 s ± 2.51) dose and was significant in 5 × 106 DEC dose (95.31 s ± 0.63) due to reduced diaphragm pathology leading to amelioration of passive exhalation after DEC therapy when compared to the vehicle-injected controls (113.33 s ± 3.96). A significantly lower Te value was observed in 5 × 106 DEC dose compared to 1 × 106 DEC dose confirming a dose-dependent protective effect of DEC therapy on pulmonary function (Fig. 7B).
Systemic-intraosseous administration of human DEC results in reduced-mediated respiratory disease at 180 days after transplant. Assessment of respiratory function by whole body plethysmography revealed:significant decrease in enhanced pause (PENH) in 5 × 10DEC-injected mice when compared to the vehicle-injected control at 180 days after DEC transplantSignificant decrease in expiration time (Te) was observed in both DEC-injected groups compared to the vehicle-injected controls and was dose dependent, confirming protective effect of DEC therapy on pulmonary function. Data were normalized to individual animals' Penh and Te values at baseline (starting at 100% at a baseline for all of the groups, as indicated by the white bars). Data presented as mean ± SEM; Two sample t-test assuming unequal variances. Buxco Instrument. Abbreviations:< 0.05 mdx p (A) (B) 6
Administration of Human DEC Therapy Improves Skeletal Muscle Function at 180 days after Systemic DEC Administration
Deterioration of the skeletal muscle function affects significantly daily activities and overall quality of life of DMD patients; thus, evaluation of muscle function is essential for assessment of disease progression. We have previously reported amelioration of gastrocnemius muscle function at 90 days after DEC therapy [41]. Here, we aimed to assess the long-term effect and dose response of human DEC on the grip strength and gastrocnemius muscle function assessed at 180-days after systemic-intraosseous administration of two doses of DEC cells (1 × 106 and 5 × 106) to the mdx/scid mice.
Human DEC therapy (1 × 10and 5 × 10) improves skeletal muscle strength at 180 days after systemic-intraosseous administration to themice.At 180 days after DEC transplant the ex vivo Aurora muscle test identified a significant increase of maximum stretch-induced contraction of the gastrocnemius muscle in both DEC-injected groups compared to the vehicle-injected controls. Data presented as mean ± SEM; Aurora Scientific in vitro Muscle Test System. *< 0.05.Grip strength analysis at 180 days after systemic-intraosseous administration of DEC therapy revealed improved grip strength between 5–10 weeks follow-up period in both DEC-injected groups compared to the vehicle-injected controls, and significant grip strength improvement at 9-weeks in 1 × 10DEC-injected group when compared to the vehicle- injected control. **< 0.01. Data presented as mean ± SEM 6 6 6 mdx/scid p p (A) (B)
DEC Therapy Improves Grip Strength at 180 days after Systemic-Intraosseous Administration
Deterioration of the skeletal muscle function in DMD patients represent the early signs of the disease, thus we assessed muscle strength in the mdx/scid mice by in vivo grip strength test which revealed improved performance after treatment with both doses of DEC cells when compared with the vehicle-injected controls and at weeks 5–10 and for 1 × 106 DEC dose revealed: (week 5- 17.25 ± 1.36, week 6- 18.70 ± 2.57, week 7- 17.35 ± 2.62, week 8- 18.08 ± 7.00, week 9- 24.23 ± 3.44, week 10- 18.32 ± 3.86; and for 5 × 106 DEC dose revealed: week 5- 15.86 ± 5.59, week 6- 18.06 ± 4.89, week 7- 16.65 ± 3.98, week 8- 15.79 ± 4.14, week 9- 19.46 ± 8.02, week 10- 16.72 ± 3.36 when compared to the vehicle-injected controls (week 5—14.02 ± 2.16, week 6—16.30 ± 3.56, week 7—16.05 ± 3.68, week 8—17.19 ± 6.29, week 9—15.66 ± 3.94, week 10—15.94 ± 6.10). Additionally, mice injected with 1 × 106 DEC dose significantly improved grip strength of the right limb at 9-weeks (24.23 ± 3.44) when compared with the vehicle-injected controls (15.66% ± 3.94%) (Fig. 8B).
Discussion
Duchenne Muscular Dystrophy is a severe, genetic disease, caused by the lack of functional dystrophin in the affected muscles. DMD is characterized by progressive course and premature death, usually due to cardiopulmonary complications [48, 49]. Despite promising outcomes of the preclinical studies and recent reports on new approaches targeting the genetic defect, there is still no cure for DMD [3, 50–52].
Current approaches to treat DMD focus on dystrophin restoration by replacing and/or repairing the mutated dystrophin genes or by application of cell-based therapies [1, 2]. Although some of the gene therapies based on the exon skipping such as eteplirsen and ataluren have been approved for clinical use and were successfully introduced to the market, they are only applicable to the limited number of patients with the specific gene mutations [53, 54]. Another drug, drisapersen was not approved by the FDA due to the poor treatment benefits and the uncertain safety profile [2, 55, 56]. The efficacy of AAV-based microdystrophin administration [19, 20] in DMD is still understudied, although a recent clinical trial proved safety and functional improvement after intravenous delivery (www.clinicaltrials.gov/ct2/show/NCT03375164↗) [57, 58]. However, there are current reports on the immune response against the viral vectors, which is of a significant safety concern and limits repeated dosing of microdystrophin therapy [24, 58]. The CRISPR/Cas9 approach was aimed to restore dystrophin defect and revealed a broad range of dystrophin gene corrections in the experimental studies [14], however, this approach is not yet clinically applicable [13, 17, 50, 59]. Moreover, therapies involving genetic modification and viral vector application require a thorough preclinical testing, since low efficacy, tumorigenesis, sensitization and “off-target” mutations are still of a significant concern.
In the light of the limitations of gene therapies, the stem cell-based therapies are considered as the most promising therapeutic method for DMD patients. This approach aims for the restoration of dystrophin by distribution of normal, dystrophin expressing cells to the DMD affected muscles. Initial studies confirmed safety of human myoblast and stem cells transplantation, however, a major drawback was the immune response resulting in low efficacy of engraftment and the need for immunosuppressive therapy, to prevent myoblasts rejection [23, 26, 60, 61].
Only a few cell populations with myogenic properties and regenerative potential were investigated as a source for cell-based therapies in DMD and the satellite cells, muscle-derived stem cells and mesenchymal stem cells were found to be the most promising [62–66]. Initial studies testing satellite cells (SCs) confirmed dystrophin expression and improvement of muscle function in dystrophic mice, however, autologous transplantation of SCs was not clinically efficient due to insufficient engraftment and low myogenic potential [26]. Autologous transplantation of mesoangioblasts with PiggyBac transposon vector, enabled persistent full-length dystrophin expression by stable integration of DNA cargo into the cell genome in mdx/scid mouse model, however, the level of dystrophin expression was low, and amelioration of dystrophic muscle function has not been proven in the in vivo studies [60].
One of the most important factors determining efficacy of myoblast-based therapy is the route of cell administration and long-term engraftment. Previous studies testing systemic, therapeutic effect of mesoangioblasts, cardiomyocytes, MSC and iPS, investigated the intravenous, intramuscular, intracardiac and intraarterial routes of delivery with different efficacy results [23, 25, 34, 67–69].
Interestingly, the intraarterial and intravenous delivery of cardiomyocytes representing the striated muscles and cardiosphere-derived cells confirmed improvement of cardiac function as well as elicited the off-cardiac effects confirmed by improvement of the upper limb function, thus supporting the rationale for systemic delivery of cells of muscle tissue origin [69, 70].
We previously confirmed higher engraftment rates and better efficacy of chimeric cells following the systemic-intraosseous cells administration when compared with intravenous route of cell delivery [35, 71].
Moreover, we reported better engraftment of our Dystrophin Expressing Chimeric (DEC) therapy, after systemic intraosseous administration, when compared to the local intramuscular DEC delivery [39–41] and intravenous delivery (unpublished data). Similar findings of higher engraftment rate and amelioration of multi-organ function were confirmed by other investigators following intraosseous administration of bone marrow, cord-blood cells and MSC tested in clinical trials and treatment of blood disorders in both, the adult and pediatric patients’ population [72–76]. Recent Phase I clinical trial confirmed better efficacy of engraftment and safety after intra-bone co-administration of cord blood cells and MSC [77].
Until now, problems of limited engraftment, low dystrophin expression, limited cell survival and the need for immunosuppression remain unsolved and limit the routine clinical application of cell-based therapies. Thus, we have developed more effective approaches including systemic-intraosseous route of cell delivery for enhancement and maintenance of cell engraftment [37].
Furthermore, to improve engraftment without the need for immunosuppressive therapy, we have created chimeric cells of hematopoietic, mesenchymal and myoblast stem cell lineages of murine and human origin [35, 38, 39, 41]. We developed human Dystrophin Expressing Chimeric (DEC) cell lines via ex vivo fusion of human myoblasts (MB) derived from normal and DMD affected donors (MBN/MBDMD). Intramuscular administration of human DEC tested in preclinical studies in the mdx and mdx/scid mice models confirmed high myogenic potential which correlated with increased dystrophin expression and improved function [40]. Thus, to make this therapeutic approach more clinically relevant, we assessed the effect of systemic-intraosseous administration of human DEC and demonstrated long-term engraftment which correlated with increased dystrophin expression, reduced muscle pathology and improved function of cardiac, pulmonary and skeletal muscles at 90 days after systemic DEC transplant [41].
In the current study, considering the dynamic progression of DMD, our goal was to assess the long-term systemic effect of human DEC therapy for potential clinical applications. Moreover, considering the fact that clinical reports on assessment of current DMD therapies are tested in children of age 4–7-12 years old [78, 79] before development of severe cardiac or pulmonary problems, thus our goal in current study was to assess the protective effect of DEC therapy before severe progression of the disease and before development of the overt DMD -related cardiomyopathy or pulmonary failure, since it would be difficult to expect that either steroids, gene or cell-based therapies will reverse the organs failure and progression of the DMD disease Thus, the current preclinical study was performed on 6–8-weeks old mdx/scid mice which were observed up to 26 weeks after intraosseous DEC transplant. When considering the correlation of the age of tested animals and the length of the preclinical study with the future clinical trials in humans, it is estimated that based on this study the conversion of the age of mice to humans corresponds to the human age span from children to adults (7–20 years of age) and covers the age of DMD patients which will be considered in the future clinical trials [80, 81]. Thus, the reported here findings are encouraging since they may be relevant to the outcomes of future clinical studies in the DMD patients.
Since restoration of dystrophin is the major goal of all current therapies tested for DMD, in this report we have confirmed increased dystrophin expression in the heart, diaphragm and gastrocnemius muscle at 180 days after systemic administration of DEC to the mdx/scid mice. The increase in dystrophin expression was accompanied by amelioration of muscle pathology revealed by reduced fibrosis and inflammation in the assessed target organs of the DEC-injected mice. Specifically, at the histological level assessment of heart samples confirmed significantly reduced fibrosis, improved midventricular myocardium morphology, less prominent necrosis and decreased number of inflammatory cell infiltrates. Furthermore, amelioration of inflammation and fibrosis as well as normalization of muscle fiber size was observed in the diaphragm, and gastrocnemius muscle further confirming the multiorgan effect of DEC therapy. Moreover, DEC cell migration and long-term engraftment to the heart, diaphragm and gastrocnemius muscle of the mdx host was confirmed by expression of spectrin—the human-specific membrane protein marker, further confirming human origin of the engrafted cells at 180 days after systemic intraosseous DEC administration.
These findings are of clinical importance, since reports on histopathological assessments reveled that the fibro-fatty replacement of cardiomyocytes is a significant pathophysiological mechanism in the development of cardiomyopathy in the mdx mice [7]. Currently only few DMD clinical studies including assessment of givinostat therapy, reported a positive effect on muscle fiber regeneration, reduced fibrosis, and decreased muscle necrosis, however that study has not confirmed functional efficacy of the therapy [7].
In the current study, we confirmed a complimentary, multi-level effect of DEC therapy which was observed at both, the tissue level and the functional level, as confirmed by improvement of cardiac, respiratory and skeletal muscle pathology and function maintained up to 180 days after systemic DEC administration. It should be emphasized that the reported here long-term protective effect was maintained after a single dose of DEC therapy. These observations are clinically relevant, since studies assessing cardiomyopathy linked to DMD in humans, revealed that functional decline in progressive cardiopulmonary is characterized by the thinned wall thickness of the left ventricular (LV) and a progressive decrease in the ejection fraction and fractional shortening [81]. Thus, to assess the long-term efficacy of DEC therapy on cardiac function, we monitored echocardiographic changes over the entire study follow-up and confirmed both, the maintenance of the LV function at the baseline level up to 180 days post-transplant, as well as the dose dependent long-term improvement of the ejection fraction and fractional shortening recorded at 180-days after DEC administration.
In contrast, the vehicle-injected controls showed gradual decline of the left ventricular (LV) function leading to the significant drop in the ejection fraction and fractional shortening at 180-days after DEC transplant. Furthermore, there was a dose-dependent increase of the values of LV functional parameters of the stroke volume and cardiac output between the baseline and 180-day endpoint observed after administration of the higher DEC dose of 5 × 106 cells, further confirming long-term protective effect of DEC therapy, since these parameters normally decline with age in the mdx mouse model [80]. In addition, the functional improvements recorded by echocardiography correlated with the reduced cardiac muscle pathology evidenced by reduced fibrosis and inflammation which are considered the leading mechanism of development of cardiomyopathy [82–84].
Interestingly, the dose-dependent increase of ejection fraction was observed also at 90 days after DEC administration, which highlights differences between the current study and our previous report [41], where the lower DEC doses (0.5 × 106 and 1 × 106) did not show dose dependent effect on cardiac function.
Importantly, the long-term improvement in cardiac function correlated with the improvement of respiratory function represented by the reduction of the enhanced pause (Penh) and time of expiration (Te) confirmed by plethysmography at 180-days after DEC transplant.
Finally, the analysis of long-term effect of human DEC therapy on the functional outcomes of skeletal muscle revealed increase in the maximum stretch induced contraction of the gastrocnemius muscle at 180-day study endpoint further confirming long-term multi-organ protective effect of DEC therapy after systemic-intraosseous administration.
There are several limitations of the study which should be addressed. We have based our study on the literature review of cardiac assessments by echocardiography [46, 85, 86] and MRI [87] and plethysmography [88, 89] reported by other investigators, where the number of evaluated animals (4–5) was similar to our study. Moreover, echocardiography and plethysmography assessments in mdx mice models were established in the independent laboratories by experienced investigators [39, 41] and were comparable with echocardiography [90] and plethysmography reports of other investigators [82, 88, 89, 91].
It should be noted that we have tested DEC therapy in the immunocompromised animal model since it allows for assessment of engraftment and efficacy of cells of human origin, but limits evaluation of the potential immune response. However, we have addressed this limitation in our previous work and have proven in the immunocompetent mdx mouse model that increased dystrophin expression correlated with significant improvement of skeletal and cardiac muscle function after intramuscular as well as intraosseous DEC administration, without evidence of side effects and without the need for immunosuppression [38–41]. Furthermore, the mdx/scid mouse model of DMD provides opportunity to test human DEC therapy created from normal and DMD affected donors according to the same manufacturing protocol which will be tested in the clinical trials. This fulfills regulatory requirements for the ex-vivo engineered DEC therapy as the novel, Advanced Therapy Medicinal Product (ATMP) [41]. Other investigators used immunocompromised NOD-scid mice model in the preclinical studies validating new ATMP of human skin-derived ABCB5 -positive mesenchymal stromal cells for clinical application (https://clinicaltrials.gov/ct2/show/NCT04971161↗) [67].
It is important to highlight, that functional improvements assessed in heart, diaphragm, and gastrocnemius muscle by standard functional tests of echocardiography, plethysmography and muscle strength tests, correlated with reduced muscle pathology parameters showing evidence of reduced interstitial fibrosis and inflammation, a trend towards normalization of the muscle fiber size, and decreased percentage of the centrally nucleated fibers in diaphragm and GM suggesting normalization of mdx muscle pathology in the selected DMD-affected organs at 180 days after systemic DEC transplant.
It should be emphasized, that despite the natural progression of DMD disease in the aging mdx mouse, the proven efficacy and the protective effect of DEC therapy over the long-term follow-up period of this study ranging between 6 and 26 weeks after DEC administration, represents valuable and clinically relevant findings, confirming both, the maintenance of the selected morphological and functional parameters at the baseline levels over the entire study follow-up, indicating the hold on the progression of the DMD disease, as well as the improvement of the important parameters of cardiac, respiratory and skeletal muscle function, confirming the long-term therapeutic effect of DEC therapy on the mdx pathology.
Conclusions
In this study we have tested the long-term efficacy of DEC therapy by assessment of morphological, pathological and functional changes in the selected DMD-affected organs of heart, diaphragm and skeletal muscles. We confirmed that systemic-intraosseous administration of human DEC therapy restored dystrophin expression, which correlated with improved muscle morphology and pathology and long-term amelioration of function of the heart, respiratory and skeletal muscles as confirmed by standard echocardiography, plethysmography and muscle strength tests. DEC therapy does not require immunosuppression, is not limited to the specific gene mutation, does not cause sensitization and as such is universal for all DMD patients. These attributes make DEC therapy unique among other therapeutic approaches for DMD. Moreover, the long-term (180 days) protective effect of DEC on functional and morphological outcomes assessed in the most severely affected by DMD organs of heart, diaphragm and limb skeletal muscles, supports future clinical application of DEC as a safer and potentially more efficacious therapeutic approach applicable to all DMD patients regardless of gene mutation.
To the best of our knowledge, this is the first report assessing the long-term, multi-organ improvement after systemic administration of human DEC therapy.
This encouraging preclinical data introduces human DEC as a novel and universal therapeutic modality of the Advanced Therapy Medicinal Product (ATMP) with the potential to improve or halt progression of the disease and enhance quality of life of DMD patients.
Supplementary Information
Below is the link to the electronic supplementary material. Suppl Fig. 1 (3.57 MB) High resolution image (TIF 836 KB)