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Spinal cord injury (SCI) is a devastating neurological disorder that has a substantial detrimental impact on a person’s quality of life. The estimated global incidence of SCI is 40 to 80 cases per million people and around 90% of cases are traumatic. Various etiologies can be recognized for SCI, and post-traumatic SCI represents the most common of these. Patients worldwide with SCI suffer from a persistent loss of motor and sensory function, which affects every aspect of their personal and social lives. Given the lack of effective treatments, many efforts have been made to seek a cure for this condition.
- spinal cord injury
- stem cells
- stem cell therapy
1. Ongoing Clinical Trials of Stem Cell Therapy for Spinal Cord Injuries (SCI)
The number of clinical trials based on stem cells has increased in recent years. There are already thousands of registered studies worldwide that claim to use “stem cells” in experimental treatments [16]. Several clinical trials are ongoing throughout the world to investigate the safety and efficacy of stem cell treatment for SCI, and they use a range of stem cell sources and delivery modalities. The cell preparation and transplantation technique in clinical trial research should follow or correspond to the norms and guidelines. Clinical study results will aid in determining the best type of stem cell to use, as well as the most successful method of administration, and prospective, multicenter, double-blind or observing-blind, placebo-control, randomized control trials need to be conducted to firmly prove the neurorestorative effects or obtain greater benefits. With continued biotechnological and nanomaterial advances, stem cell therapy for the treatment of SCI can become a real therapeutic option over the next few years, and focus on the molecular mechanisms related to both the injury and the processes of functional recovery and regeneration of nerve tissue can bring a paradigm shift in the management of SCI [17].
2. Advances and Prospects of Stem Cell Therapy for SCI
Recent advancements in stem cell research have boosted the prospect of novel SCI therapeutics. Stem cells are a type of cell in the body that can differentiate into numerous types of cells. Given their ability to heal injured nervous tissue, they are a prospective candidate for SCI treatment. Generally speaking, they can be classified into two main categories: embryonic stem cells (ESCs) and adult stem cells. ESCs can develop into any form of cell in the body. Adult stem cells, on the other hand, can specialize into specific types of cells and are found in a variety of organs throughout the body, including bone marrow. Stem cells have been found in animal models of SCI to improve motor and sensory function and have also been shown to enhance axon regeneration, reduce inflammation, and increase tissue repair. According to a recent meta-analysis, the ASIA impairment scale score can improve at least in one grade in 48.9% of individuals with SCI; furthermore, it can improve urinary and gastrointestinal system function by 42.1 and 52.0 percent, respectively [17].
Despite the fact that ESCs have the ability to differentiate into any type of cell, their usage is controversial due to ethical considerations. Recent studies have concentrated on induced pluripotent stem cells (iPSCs), which are adult cells that have been reprogrammed to act like ESCs. iPSCs can differentiate into any type of cell and can be created from the patient’s own cells, lowering the chance of rejection. The generation methods of iPSCs vary in the vehicles of genes, combinations of reprogramming factors, and cell types. Yamanaka factors (combination of OCT3/4, SOX2, KLF4, and C-MYC) are common techniques; however, the quality would be improved by introducing Zscan4 through forced expression. Furthermore, it has been documented how stem cells produce a variety of growth factors, cytokines, and chemokines that aid in tissue repair and regeneration, reducing the pro-inflammatory environment related to SCI and decreasing scar production. This paracrine impact has been proven in preclinical models of SCI to increase functional recovery and may also contribute to the favorable benefits of stem cell therapy in clinical studies [18,19,20].
Mesenchymal stromal cells have more clinical research reported in SCI treatment than other types of cells. Their advantages include abundant sources, as well as easy culture and preparation procedures. A retrospective study observed some functional improvements in one third of patients with acute complete SCI and also in nearly half of patients with chronic complete SCI after a two-to-five-year follow-up. Repeated subarachnoid administrations of umbilical cord MSCs in 41 patients with SCI led to a significant improvement in assessing neurological dysfunction and the quality of life in a phase 1/2 pilot study [18,21]. Vaquero et al. reported autologous bone marrow MSC transplantation in 12 patients with chronic complete paraplegia; all patients experienced functional improvement, including sensitivity, sphincter control, motor activity, decreases in spasms and spasticity, and improved sexual function, significantly improving their overall quality of life. Also, this kind of cell therapy could relieve neuropathic pain due to SCI, reduce syrinx, and show clinical improvements for post-traumatic syringomyelia [22,23,24,25].
Zhao et al. [21] implanted scaffolds with umbilical cord MSCs following scar resection with chronic complete SCI; some functional improvements were observed in some patients during 1 year of follow-up. Larocca et al. [26] reported that the image-guided percutaneous intralesional administration of MSCs showed some functional improvement. Santamaría et al. [27] reported that intrathecal injections of bone marrow stromal cells in a patient with C2 tetraplegia were associated with clinical and neurophysiological improvement [26,27,28]. A study conducted by Park et al. [29] observed negligible improvements in the motor power of the upper extremities and in activities after directly injecting autologous bone marrow MSCs into both the spinal cord and the intradural space with SCI. Oraee-Yazdani et al. reported that the transplantation of an autologous MSC and SC combination directly into the injury site showed negligible sensory improvement [30,31,32].
Some research also found no motor improvement in patients with chronic SCI who received an intrathecal transplantation of umbilical cord MSCs. Chotivichit et al. [33] used MRI to track autologous bone MSC transplantation in a patient with persistent SCI; however, this showed no functional improvements. According to Satti et al. [34], the intrathecal injection of autologous MSC transplantation is safe in individuals with full SCI [35].
Basic research has also shown that hematopoietic stem cells can help with SCI. HSCs are advantageous due to their ability to be autologously-derived and have a record of safety in humans, but they are rare and pose major risks with graft rejection. In a retrospective investigation, Al-Zoubi et al. [36] implanted purified autologous leukapheresis-derived CD34+ and CD133+ stem cells into 19 patients with chronic full SCI; over half of the patients showed segmental sensory or motor improvement after long-term follow-up. Ammar et al. [37] revealed in a pilot trial, using a biological scaffold containing autologous HSCs and platelet-rich protein for four individuals with SCI, a patient who demonstrated motor and objective sensory improvement.
Some prior research found a slight neurological improvement from transplanting neural stem/progenitor cells into people with chronic SCI. NSCs are multipotent and can replace damaged neural tissue and have the capacity for neuronal differentiation and functional improvement. In a phase I trial, perilesional intramedullary injections of human central nervous system stem cells (HuCNS-SC) from a fetal brain proved safe and viable; however, a few patients demonstrated small motor benefits in phase II single-blind, randomized research. Transplanting HuCNS-SCs into chronic SCI patients’ injured thoracic cords revealed safety, and follow-up studies indicated consistent sensory improvements without motor improvement [29,38,39,40,41].
3. Drawbacks of Stem Cell Therapy for SCI
One of the most complex challenges in the realm of stem cell therapy for SCI is the careful selection of the most suitable type of stem cells. A substantial hurdle is the lack of viable stem cell sources. Though it is possible to generate induced pluripotent stem cells (iPSCs) from adult cells, this approach comes with an elevated risk of cancer development. Furthermore, the delivery of stem cells to the injured area is an obstacle that should not be underestimated. Stem cells must be introduced in a manner that ensures their survival and integration with the host tissue. This is particularly difficult due to the harsh environment present at the injury site, characterized by inflammation and the presence of inhibitory chemicals that can interfere with cell survival and differentiation. Allogeneic stem cells, such as embryonic stem cells (ESCs) or iPSCs, when transplanted into a recipient, can elicit an immunological response. To mitigate this, strategies like immunosuppressive medications and the utilization of autologous stem cells are employed to reduce the risk of immunological rejection. Previous research has documented 28 distinct adverse effects associated with stem cell transplantation. These include neuropathic pain, unusual sensations, muscle spasms, vomiting, and urinary tract infections. However, it is worth underlining that major side effects such as cancer may not have been observed due to relatively short follow-up periods [17]. Assessing the effectiveness of stem cells through head-to-head comparisons in meta-analyses is challenging. Variations in factors such as cell types, sources, culture conditions, patient demographics, and SCI severity contribute to the complexity of research in this field [30,42].
Existing research has unfortunately only demonstrated minor improvements in sensory and motor function, which do not meet the criteria necessary for walking or performing daily activities. Moreover, the recovery of bowel and bladder function, which many SCI patients consider vital, has shown limited improvement in current studies. Enrolling an adequate number of SCI patients in clinical trials is hindered by criteria such as injury severity, patient age, and overall physical condition. The accuracy of subjective outcome measurements, including the ASIA scale, can be compromised, leading to imprecise assessments of stem cell efficacy [21,28,43,44].
The potential for spontaneous recovery and the lack of a control group in most trials make it difficult to conclusively determine whether the observed therapeutic effects are solely attributable to stem cell transplantation [17,45,46]. Further research is imperative to delve deeper into the actual therapeutic effects of stem cells through standardized controlled trials. The implementation of blinding techniques is crucial to ensure the reliability of clinical trial outcomes. Many prior studies have failed to report adverse events comprehensively, potentially resulting in an overstatement of stem cell safety and efficacy [21,36,37]. Consequently, extending the follow-up period is essential to comprehensively investigate the safety profile of stem cell therapy.
Additional limitations in stem cell research encompass issues like inadequately estimating patient enrollment numbers for trials and, consequently, therapeutic efficacy being lower than in animal models; inconsistent criteria for patient inclusion and exclusion; variability in stem cell sources and transplantation methods which are different from animal studies; and the lack of standardized risk assessment methods for tumorigenicity and oncogenicity [37,39,47,48,49,50].
4. Future Research and Directions
For designs in the context of stem cell therapy for SCI, more stringent testing requirements must be established. The lack of suitable control groups makes it difficult to reach a conclusive determination in most trials; therefore, the incorporation of an appropriate control group in trials will be helpful to reach a conclusion. Future research should prioritize elucidating the specific mechanisms by which stem cells facilitate tissue repair and regeneration; however, studies should follow standardized research methodology to enhance the quality of findings [13,17,51].
Improvements in delivery systems are a critical area for future research. The use of iPSCs, which can be derived from a patient’s own cells, holds promise in addressing the scarcity of autologous stem cells. Additionally, more efficient delivery methods, including microscale and nanoscale delivery systems, should be explored to enhance stem cell survival and integration. Techniques such as injection, implantation, and scaffolding all have their respective advantages and disadvantages, necessitating further research to determine the most effective mode of delivery [52,53,54,55].
Optimizing stem cell differentiation and integration into host tissue is another pressing area for future investigation. The application of gene editing technology has the potential to precisely modulate stem cell differentiation and integration. Moreover, tissue engineering technologies, such as organoid production or the creation of bioengineered spinal cord tissue, could provide a more physiologically realistic environment for stem cell differentiation and integration. Interdisciplinary approaches are also important, involving bioengineering and neurology for more precise outcomes [56,57,58].
To address concerns about the safety of stem cell therapy, particularly regarding tumor growth and immunological rejection, ongoing research efforts should focus on developing techniques to mitigate these risks and improve transplantation efficacy. This entails accurate sample size calculations, the inclusion of well-diagnosed SCI patients, and ensuring a sufficiently long follow-up duration to comprehensively assess potential adverse events. The genome has been popular to improve the safety of cell transplantation therapies. Orthogonol systems have also been developed to selectively kill cell products if necessary [59,60].
Exploring combinations of stem cell therapy with other treatments, such as physical therapy, electrical stimulation, or medication therapy, is a promising avenue for future research. Research focusing on the combination of genetic engineering technology with nanobiotechnology, combinational therapy with neuroprotective agents, cell coupling, and rehabilitation may help to improve the effectiveness of stem cells. Rigorous clinical trials and long-term follow-up studies are paramount for advancing stem cell therapy for SCI and, ultimately, enhancing patient outcomes [61,62,63]. There are guidelines from the International Society for Stem Cell Research for “ethical, scientifically, medically and socially responsible” stem cell research. There is also a series of guidelines and standards for clinical trial design from the International Campaign for Cures of Spinal Cord Injury Paralysis (ICCP). However, proper guidelines focused on the correct management of SCI using stem cells, including the identification of the most suitable stem cells, delivery site, and timing of intervention, are required to be established. Effective collaboration among policymakers, researchers, and clinicians is vital for developing appropriate guidelines [17,64].
To overcome the obstacles regarding safety, therapeutic efficacy, and immunocompatibility, extensive research on gene-editing technologies (i.e., CRISPR/Cas9) should be evolved. Advanced research on tissue engineering techniques would be able to identify more effective therapies, growth factors, and bio-active molecules, which could result in a breakthrough in this area. A conductive environment for the survival, differentiation, and integration of stem cells is a challenge, and 3D-printed biometric spinal cords have shown some efficacy; thus, more research is required in this area to design advanced scaffolds and biomaterials. Moreover, research should be conducted to identify new sources of stem cells, which would have better efficacy and safety. Continuous efforts should also be given toward the combination of stem cell therapy with electrical stimulation and personalized therapeutic interventions [17,22,64].
This entry is adapted from the peer-reviewed paper 10.3390/brainsci13121697
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