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Stem cell technology may be useful in the treatment of tendon and ligament injuries
Strain induced tendon or ligament injuries are an all too common consequence of athletic endeavour in both horses1 and humans,2–4 resulting in high morbidity and often compromising a return to the same level of activity.
In the horse, the most commonly injured structures are the weight bearing digital flexor tendons which lie on the palmar aspect of the metacarpus (fig 1). There are many similarities between the weight bearing tendons of the horse and the human athlete—for example, Achilles tendon—in function, matrix composition, and the nature of the injuries sustained. In contrast with positional tendons, such as the hand tendons, all weight bearing tendons function as springs, storing energy under weight bearing load for efficient locomotion.5 The horse has maximised this potential, resulting in efficiency of locomotion in excess of 100% at the gallop.6
Whereas immature tendon shows an ability to adapt to the loads placed on it, this appears to be lost, or dramatically reduced, in the adult.7,8 Thus over-strain injuries, although they occur spontaneously during exercise, are preceded by progressive degeneration of the tendon matrix brought about by cumulative loading cycles, accelerated by competitive sport. It is not surprising therefore that weight bearing tendons, which operate close to their functional limit, commonly fail in both horses and humans.
Clinical injury results in a variable disruption of the tendon matrix, which induces an inflammatory response. This response is often short lived. Very soon after the injury, fibroplasia is initiated resulting in the formation of scar tissue within the tendon. In the later stages of repair, inflammation is no longer an obvious clinical feature, giving rise to a debate whether the disease is a tendinitis or a tendinopathy. The latter logically encompasses all stages, but the absence of inflammation does not indicate that it was not present at the outset even though it is often missed clinically in cases of mild repetitive injury. Over a number of months, the immature scar tissue remodels, increasing not only in strength but also in stiffness, which reduces the efficiency of the tendon as a spring, compromising the performance of the horse (or human) and putting the tendon at risk of reinjury.
A multitude of treatments have been advocated for the management of tendon over-strain injuries, but there is little evidence in any species that any is more effective than a prolonged period of rehabilitation with carefully controlled exercise. Indeed, current clinical data for the horse shows that the greatest influence on prognosis is the severity of the initial injury. However, there is a lesser influence on the prognosis by the ultrasonographic longitudinal fibre pattern when the animal returns to full exercise, suggesting that the quality of the repair tissue has a lesser, but nevertheless, significant effect on prognosis.
“…new treatments should aim at regenerating the tendon tissue…”
Because of the poor functionality of scar tissue, new treatments should aim, ideally, at regenerating the tendon tissue if we are going to be able to return equine and human athletes to full function.
AUTOLOGOUS TRANSPLANTATION OF MESENCHYMAL STEM CELLS INTO INJURED TENDONS: THE HOPE FOR THE FUTURE?
At present, no treatment is successful at promoting the formation of tendon matrix. We have hypothesised that the best hope for engineering new tendon tissue that has compositional and functional similarities to non-degenerate weight bearing tendon will require a cell based approach with the delivery of mesenchymal stem cells, in far greater numbers than are present normally, into the damaged tendon.
Embryonic stem cells are truly pluripotential but have the disadvantages of being allogenic (although with immunological tolerance) and associated with a risk of teratoma formation. Postnatally derived stem cells are thought to be multipotential, having a restricted number of cell lineages into which they can differentiate. They are subdivided into haemopoietic (blood cell lines) and mesenchymal stem cells which can give rise to osteoblasts (bone), chondrocytes (cartilage), tenocytes (tendon and ligament), fibroblasts (scar tissue), adipocytes (fat), and myofibroblasts (myotubes). Furthermore, these stem cells can be recovered from adult tissue, and hence there is the possibility of autologous reimplantation.
“…the transplantation of mesenchymal stem cells into injured tendons has been shown to promote tendon healing in laboratory animal models.”
Little work has been carried out into the tenocytic potential of mesenchymal stem cells and the growth factors and mediators required to elicit tenocyte differentiation, although a combination of mechanical stimuli and proximity to tenocytes and tendon matrix (as provided by direct implantation of cells into the tendon) are believed to be important. In spite of these unanswered questions, the transplantation of mesenchymal stem cells into injured tendons has been shown to promote tendon healing in laboratory animal models. Young et al9 seeded mesenchymal stem cells (so-called bone marrow derived stromal cells) on to a biodegradable scaffold in a 1 cm defect in a rabbit Achilles tendon. The results after 12 weeks showed the regeneration of new tendon-like tissue in the defect. Awad et al10 used a similar rabbit model, but investigated injury to the patellar tendon where mesenchymal stem cell mediated repair improved the biomechanical characteristics.
These experimental studies used laceration injuries, where maintaining the cells within the laceration site required a scaffold, which can also exert an influence, positively or negatively. However, equine digital flexor tendon strain injuries invariably provide a central core lesion which can retain implanted mesenchymal stem cells (fig 1). To take advantage of these experimental and clinical observations, we, in conjunction with VetCell Bioscience Ltd, have developed a stem cell based treatment for the management of acute tendon injuries in horses using autologous bone marrow derived stromal cells11 (summarised in fig 2).
Bone marrow is harvested from the sternum of the horse under standing sedation and shipped immediately to the laboratory, where the bone marrow stromal cells (or mesenchymal stem cells) are recovered and expanded in vitro until in excess of 4 × 106 cells are present. These cells are then suspended in citrated bone marrow supernatant for implantation under ultrasonographic guidance into the core lesion of the damaged tendon, again under standing sedation. The bone marrow supernatant is used to resuspend the stem cells to utilise its stimulatory effects (J Smith, unpublished data), and citrate is the anticoagulant of choice as the injected solution clots after injection (because of diffusion of the citrate), thereby immobilising the implanted cells and reducing the risk of leakage from the needle injection sites.
Clinical experience has suggested that the optimal time for bone marrow aspiration is within the first month after injury so that implantation is performed one to two months after injury. This allows the initial inflammatory debridement phase to subside and a suitable granulation bed to form, which would support the survival of the implanted stem cells, but before substantial fibrosis had occurred. Mesenchymal stem cells can also be harvested before injury and/or stored for subsequent use if the animal suffers a reinjury or a different tendon/ligament injury. We have indeed been able to show the successful reculture and implantation of frozen, stored mesenchymal stem cells, without the need for recovery of further bone marrow.
In cases where the lesion is present within a tendon sheath, the implantation is performed under tenoscopic guidance under general anaesthesia to ensure no surface defects are present from which the implanted cells could leak into the tendon sheath. If no defect is present, the cells are then implanted accurately into the lesion under a combination of tenoscopic and ultrasonographic control. Direct tenoscopic visualisation of the injected area after withdrawal of the needle has also enabled us to show that there is no leakage of the implanted solution from the needle tract, confirming that the implanted solution stays within the tendon.
After implantation, the horses enter a controlled ascending exercise regimen with regular ultrasonographic examinations every two to three months, so that they are back in full training after 48 weeks. To date, more than 100 horses from the United Kingdom and across Europe have been treated using this technique. Ultrasonographic evaluation after implantation has revealed no deleterious effects to the healing tendon by the implantation, and shown evidence of rapid infilling of the defect (fig 3). Six cases were also evaluated radiographically and scintigraphically after three months and there was no evidence of any bone formation within the treated tendon.
At this stage it is not possible to show significantly improved healing over conventionally treated animals because of limited case numbers with sufficient follow up time. Furthermore equine superficial digital flexor tendon injuries are highly variable, and controlled studies are almost impossible to perform in an environment in which treatment is essentially private and dominated by owner/trainer preference. So far, a limited number of racehorses has been followed for over 12 months and have shown rates of return to racing that are better than those published in a previous study of racehorses with similar severity of injuries.12 Reinjuries have occurred, although these horses were implanted later when fibrosis was already advanced, suggesting that early implantation is important.
The technique has proved highly practical within the clinic environment. To avoid misuse of this technology, VetCell Bioscience Ltd runs training courses, and more than 200 veterinarians Europe-wide have attended. Bone marrow aspirates are submitted for stem cell recovery and cultured cells returned to the veterinarians for implantation in special couriered containers.
In summary, this technology has shown encouraging, but not yet proven, efficacy for treating acute tendon lesions in horses. A truly valid comparison between stem cell treated and conventionally managed cases will require a large clinical trial, but we believe that the technique at least deserves further evaluation for its use in a variety of tendon and ligament injuries. Should this technique be proven effective, it is hoped that our experience with horses will pave the way for this technology to be used successfully in human tendon and ligament injuries.
Stem cell technology may be useful in the treatment of tendon and ligament injuries
Competing interests: RKWS is a director of VetCell Bioscience Ltd.
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