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Stem Cells International
Volume 2018, Article ID 5373294, 9 pages
https://doi.org/10.1155/2018/5373294
Review Article

New Approaches to Treat Osteoarthritis with Mesenchymal Stem Cells

1Australian Veterinary Stem Cells and Magellan Stem Cells P/L, 116-118 Thames St, Box Hill VIC 3129, Australia
2Department of Chemistry and Biotechnology, Faculty of Science, Engineering and Technology, Swinburne University of Technology, John St, Hawthorn VIC 3122, Australia

Correspondence should be addressed to Huseyin Sumer; ua.ude.niws@remush

Received 25 January 2018; Revised 21 July 2018; Accepted 29 July 2018; Published 16 September 2018

Academic Editor: Alain Chapel

Copyright © 2018 Kiran Shah et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Osteoarthritis is one of the most common chronic health problems in the world that causes disability and chronic pain with reduced mobility and is a progressive degenerative disease in weight-bearing joints such as the knee. The pathology of the joint resulting from OA includes loss of cartilage volume and cartilage lesions leading to inflammation of the articular joint structures; its incidence and progression are associated with a variety of risk factors. Most of the current treatments focus on symptom management such as physical and occupational therapies, pharmacological intervention for pain management, and surgical intervention with limited success and do not address nor halt the progression of the disease. In this review, we will describe the current treatment options for OA and the exciting new translational medical research currently underway utilising mesenchymal stem cells for OA therapy.

1. Osteoarthritis

Osteoarthritis is the pathology of articular joints most commonly associated with defects in cartilage such as osteochondral defects and is one of the most common chronic disabling diseases affecting people worldwide. It can cause severe limitation of daily activities that can seriously affect the quality of life. Approximately, 9.6% of men and 18% of women who are over 60 years old have symptomatic osteoarthritis worldwide [1, 2]. The musculoskeletal condition is characterized by degenerative articular cartilage that leads to thinning of cartilage (Figure 1) resulting in bone contact, eventually leading to symptoms of stiffness, pain, and limitation of movement. The major risk factors for OA are older age, obesity, previous injury, sports-related injury, occupational overuse, and genetic background [3, 4]. As the elderly population and obesity increase around the world, OA has become more widely spread causing a substantial health and economic burden globally [5]. It is estimated that associated costs of OA have a socioeconomic burden between 1.0 and 2.5% of gross domestic product in developed countries [6].

Figure 1: Diagram of the synovial knee joint in (a) a healthy individual and (b) an individual with mild osteoarthritis.

OA is usually associated with synovial joints (diarthroses), also known as the freely moveable joints [7]. The normal synovial joint (Figure 1) is formed by two bones’ ends covered with a thin layer of smooth, firm articular cartilage, a capsule filled with the synovial fluid, ligaments, tendons, muscles, blood vessels, and nerves [8]. Those structural components form a functional unit with their mechanical interaction. The changes in any component lead to the anabolic or catabolic responses in other components [9]. The abnormality in the synovial joint tissues such as articular cartilage, subchondral bone, ligaments, menisci, synovium, peripheral nerves, and muscles can cause stress in the joint and eventually result in degeneration of articular cartilage resulting in OA [7, 10].

Articular cartilage is a special type of connective tissue which is nonneural, nonlymphatic, nonvascular, and therefore restricted in self-repair. Articular cartilage is a metabolically active tissue, and its architecture and biochemical composition are regulated, developed, and repaired by chondrocytes. Chondrocytes are the only cell type in the articular cartilage [9]. Nutrition is supported by the synovial fluid and subchondral bone by diffusion through regular joint movement. The movement of the synovial joint forces the synovial fluid in and out of the articular cartilage to deliver nutrients and dispose of waste products for cartilage [11]. The proximal subchondral bone provides nutrients such as glucose, oxygen, and water to cartilage by perfusion from their dense vessels in the subchondral region [12]. Therefore, cartilage, subchondral bone, and synovium interact with each other and play key roles in pathogenesis of OA when there are abnormal mechanics involving the entire articular joint [13, 14].

OA is also associated with the physiological imbalance of degradation and synthesis by chondrocytes resulting in alterations in the composition of the cartilage matrix [15]. In the early stages of OA, the quiescent chondrocytes become activated to remodel the contents of the cartilage matrix [16], the water content increases, and loss of glycosaminoglycan in the cartilage leads to the changes in cartilage mechanical properties at this hypertrophic anabolic phase [17, 18]. After failure of these early compensating attempts, chondrocytes become catabolic and undergo senescence and apoptosis and ultimately result in the progressive degeneration of articular cartilage [19] which is considered as an irreversible state of OA [18, 20]. Furthermore, fibrillations (microscopic cracks) in the superficial zone are formed, as well as deep fissures, bone marrow lesions, and delamination in the cartilage [21]. In addition to the progressive degraded articular cartilage, subchondral bone interacts with cartilage through various signaling mechanisms that are presented and associated with the increased pain and dysfunction [18], due to peripheral and central pain sensitization [16].

2. Current Pharmacological Treatment of Osteoarthritis and Its Limitations

As mentioned above, the degeneration of the articular cartilage remains the most significant structural change seen in OA, resulting in severe pain and reduced mobility [16, 22]. The innate ability to heal the degenerated cartilage is limited by the avascular nature of cartilage, posing a significant challenge in the treatment of OA. Currently, there is no cure for this debilitating condition and most of the treatments focus on the symptom management including 3 main modalities as outlined in Figure 2 [23]. These are, firstly, physical and occupational therapies such as weight loss or assistive devices for load-bearing joints; secondly, pharmacological intervention for pain management by nonsteroidal anti-inflammatory drugs (NSAIDs), opioids, viscosupplements, or corticosteroid injection; and thirdly, surgical intervention such as arthroscopy, microfracture, or total joint replacement.

Figure 2: Current recommended treatment modalities for osteoarthritis (source: Arden et al. 2014).

The Arthritis Foundation (www.arthitis.org) recommends that OA patients undertake self-education in managing the condition and encourages losing weight for overweight and obese patients. This entails diet and exercise to reduce and manage healthy weight; however, due to pain and physical limitation resulting from OA, exercise is hard to implement and sustain. Joint targeted physical therapy has shown to improve the pain and function; however, there is no long-term improvement. An assistive device is designed to provide mechanical support to the joint structure in the patients with OA causing instabilities in the joint and also to distribute the load bearing for relief in pain and improve function, but these only have limited success.

Currently, the primary strategy of OA pharmacological management is mainly to relieve pain, improve function, and manage the OA process [22, 23]. Pharmacological treatment is used for patients with mild to moderate pain, and medications such as NSAID, opioids, and corticosteroid are used routinely to alleviate the pain; however, there is no long-term relief and these pharmacological agents have unwanted side effects [24].

Acetaminophen (paracetamol) used to be the first-line pharmacologic management to treat mild to moderate OA pain. However, it became an inconclusive recommendation due to lack of compelling evidence [15]. Furthermore, using acetaminophen was associated with risks such as gastrointestinal (GI) adverse events and multiorgan failure [17] with minimal short-term benefit [21]. Despite it being less effective than NSAIDs and since some patients have adverse effects with NSAIDs, it is still used by some patients but is recommended with conservative doses and treatment duration [15].

Nonsteroidal anti-inflammatory drugs (NSAIDs) are a big family of drugs including oral NSAIDs such as ibuprofen, aspirin, naproxen, COX-2 inhibitors, and topical NSAIDs such as diclofenac formed as cream, patches, gels, or solution. Issues with oral NSAIDs include adverse gastrointestinal (GI) effects and need to be taken in conjunction with the GI protectant [25]. Furthermore, they are associated with potential toxicity especially in elderly patients [22]. The oral COX-2 inhibitors can reduce GI side effects but can cause other adverse effects such as the risk of cardiovascular events. The use of topical NSAIDs eliminates the GI side effects of the oral NSAIDs but can be less effective [26] and has been associated with dermatological adverse events [27].

Opioids can be used for pain relief when patients cannot use NSAIDs and acetaminophen due to their associated side effects. However, they have limited long-term efficacy [27] and are associated with adverse effects such as respiratory depression, opioid use disorder, and overdose [28]. In meta-analysis of trials, patients who received opioid therapy were four times more likely to drop out due to adverse effects as compared to patients receiving placebo, and their long-term use is not recommended [27]. There is a wide range of medicines aimed at pain relief and improvement of quality of life for patients with OA. However, currently there are no pharmacological agents that can prevent, halt, or reverse the onset of OA. These studies highlight lack of effective pharmacological solutions for OA sufferers.

3. Surgical Intervention to Treat OA

Surgical interventions are recommended when the progression of OA has resulted in severe damage to the joint, severity in pain, and function deterioration that cannot be managed with any other options. The initial surgical option to restore the structural stability such as joint debridement by arthrotomy or arthroscopy to remove loose cartilage, fragments of meniscus, shaving of the cartilage, and removing osteophytes has shown to result in limited pain and function relief [29]. Arthroscopy remains the most performed surgery in the developed world by orthopedic surgeons to help with the mechanical movement of the affected stiff knee. A blinded controlled clinical trial on the arthroscopy for the debridement and lavage with a placebo showed that there is no pain relief achieved after the surgery when compared with the placebo [30].

Joint replacement is considered the final option provided to OA patients when the condition progresses to the most severe. Surgical procedures for the replacement of the hip and the knees are extremely painful and require a long period of time for rehabilitation. Furthermore, total knee replacement has shown adverse outcomes such as pulmonary embolism, infections, and surgery-related deaths in some cases [31].

4. Cellular Therapy and Regenerative Medicine for OA

In more recent times, many regenerative techniques have been used such as autologous chondrocyte transplantation (ACT) for focal damage of cartilage, microfracture, and mosaicplasty. The ACT technique in addressing confined cartilage damage involves the transplantation of chondrocytes that are harvested from non-weight-bearing cartilage from the patient [32] but does not address generalized OA. This method has some concerns since it causes not only donor site morbidity but also chondrocyte dedifferentiation in the transplanted site leading to the expression of type I collagen rather than type II collagen that may result in fibrocartilage rather than the desired hyaline-like cartilage [33]. Another common surgical technique is the microfracture, which triggers the migration of bone marrow cells to the articular surface through stimulation of inflammatory response by drilling holes in the subchondral plate at the chondral defect site. The purpose of this technique is to provide an enriched environment for tissue regeneration [34]. However, the resultant tissue is again fibrocartilage containing type I collagen or hybrid repair cartilage tissue, not the normal hyaline cartilage (type II collagen). Furthermore, the observed subchondral bone overgrowth (25%–49%) might limit durability and the long-term outcome of the microfracture [35]. Finally, the mosaicplasty procedure is similar to the ACT technique and involves the use of autologous osteochondral grafts; however, the results are disappointingly minimal and only offer short-term benefits [19].

The above demonstrates that the current treatment for OA is only focused on symptom management and none of these options addresses or halts the progression of the disease or offers long-term benefits. Hence, there is an unmet medical demand for the treatment for OA suffers that can halt the progression of the disease and to provide long-term relief from the symptoms of OA. Cellular therapy has provided a real promise to combat this debilitating degenerative condition and can provide disease-modifying long-term benefit. Tremendous efforts have been made in the preclinical studies and now in the clinical trials evaluating the regenerative potential of the adult stem cells, especially mesenchymal stem cells (MSCs), to repair the structural damages of the joint space, cartilage degeneration, and inflammation.

5. Mesenchymal Stem Cell Therapy for OA: A New Therapeutic Paradigm for OA

Modern medicine is exploring the regenerative potential of cellular therapy to address the currently unmet medical needs of various degenerative conditions such as OA. Cellular therapy has been extensively invested in exploring a new paradigm for the treatment of many degenerative conditions including degenerative disc disease (DDD) and osteoarthritis of the joints, among many other conditions. For this reason, this review will focus on the therapeutic properties of MSCs to treat OA. The disease-modifying potential of cellular therapy such as the use of adult stem cells for regeneration of the damaged tissues has been hailed as a breakthrough in the 21st century and provides an exciting promise to chronic degenerative conditions. Currently, there are over 500 clinical trials registered on ClinicalTrials.gov, exploring the safety and efficacy of adult stem cells, e.g., pluripotent stem cells, umbilical cord-derived stem cells, placental stem cells, and mesenchymal stem cells, to treat OA. Of these, mesenchymal stem cells have been a leading choice for many medical researchers around the world with over 352 registered clinical trials [36]. In the clinical studies, MSCs are isolated from the patient either from the bone marrow or from adipose tissues, purified, and administered as intra-articular injection in the affected joint under ultrasound guidance (Figure 3). MSCs are described to exert their therapeutic effects by homing to the injured site when injected locally to the joint for a short period of time and then disappearing and are believed to be secreting a myriad of growth factors and cytokines to initiate the repair process, as discussed below.

Figure 3: Model of regeneration of a knee joint before and after treatment with MSCs.

In 1974, Friedenstein and colleagues first described stromal precursors derived from the bone marrow that were able to form plastic-adherent fibroblast colonies in the monolayer culture and their differentiation characteristics [37]. The term mesenchymal stem cell has been in use since it was firstly coined by Caplan in 1991 [38]. MSCs are ubiquitous throughout the musculoskeletal system in the human body and are classified as self-renewing, postnatal, multipotent stem cells that can be differentiated into all tissue types of skeletal system and connective tissues such as bone, fat, cartilage, and muscle [39]. MSCs produce a vast array of cytokines, growth factors, and anti-inflammatory bioactive molecules [40]. MSCs are heterogeneous, clonogenic, and relatively easily isolated from various tissues and can be cultured expended in vitro due to their plastic adherence property and have a fibroblast-like morphology under the microscope [41]. Multipotent MSCs are originally derived from the embryonic tissue-mesenchyme which is developed from the mesoderm and can be isolated from various sources including bone marrow, periosteum, trabecular bone, adipose tissue, synovium, skeletal tissues, and deciduous teeth [39]. In vivo, the main role of MSCs is believed to be for self-repair and for maintaining tissue homeostasis [42]. The resident MSCs are distributed into the tissues at various stages of maturation and are involved in tissue regeneration [43].

Originally, MSCs were isolated from bone marrow, but more recently they have been successfully isolated from various other tissues such as adipose tissue [44], brain, muscle tissue [45], skin [46], and teeth [47]. Moreover, MSCs can also be derived from different organs and tissues including the spleen, liver, kidney, lung, thymus, pancreas, and blood vessels and could readily be proliferated in vitro [48].

Since human MSCs are heterogeneous and can be obtained from many sources, different methods of isolation and expansion, and different approaches to characterize the cells have been described in the literature, this has caused the difficulty of comparing study outcomes. The Mesenchymal Stem Cell Committee of the International Society for Cellular Therapy (ISCT) has provided three minimal criteria to define MSCs for laboratory-based investigation and preclinical studies in 2006. First, MSCs must be plastic-adherent in the tissue culture flasks. Second, more than 95% of the MSC population must express CD105, CD73, and CD90 and lack expression (less than 2% population) of CD45, CD34, CD14 or CD11b, CD79a or CD19, and HLA class II. Third, MSCs must be able to differentiate into osteoblasts, adipocytes, and chondroblasts in vitro with standard differentiation conditions [49].

The “stemness” of MSCs is maintained by the leukemia inhibitory factor (LIF), fibroblast growth factors (FGFs), and mammalian homologues of Drosophila wingless (Wnts), among other growth factors and cytokines [50]. The intrapopulations of MSCs are functionally heterogeneous regarding their multilineage differentiation potentials. The tripotent clones of MSCs (able to be differentiated into three cell types, e.g., osteoblasts, adipocytes, and chondroblasts) display the highest rate of proliferation and a lower rate of apoptosis compared with the bipotent (only two cell types) and unipotent (only one cell type) clones [51, 52]. The proliferation capacity of MSCs is both affected by the cell seeding density [53] and decreases as cells progress toward terminal differentiations [54]. The long-term expansion of MSCs might impact the composition, function, and therapeutic potency of MSC populations [55]. Furthermore, culture conditions such as culture media and oxygen tension have a major impact on gene expression and proteome and cellular organization [56, 57].

The differentiation process of MSCs is tightly controlled and involves the activities of various transcription factors, cytokines, growth factors, and extracellular matrix molecules [54]. The differentiation efficiency is also correlated with patients’ age, whereby isolated cells from younger patients showed higher differentiation capacity in culture [58]. A number of biomarkers are used to determine differentiation towards adipogenic, chondrogenic, and osteogenic lineages. The biomarkers for adipogenic differentiation are adiponectin, C/EBPα, FABP4, leptin, and peroxisome proliferate receptor gamma (PPARγ); the biomarkers for chondrogenic differentiation are aggrecan collagen type II and Sox9; and alkaline phosphatase, bone sialoprotein, osteocalcin, osterix, and runx2 are biomarkers for osteogenic differentiation [5962].

MSCs have shown disease-modifying effects in bone and cartilage defects, as discussed previously. Because of the multipotent properties of MSCs, they have also generated significant clinical interest in cardiovascular, neural, and orthopedic therapeutic applications. Moreover, the anti-inflammatory and antifibrotic properties of MSCs make them the ideal candidate for regenerative medicine. These cells are able to suppress the growth of activated T-cells and help regulate the production of regulatory T-cells (Treg) [36, 63]. The investigation of the anti-inflammatory properties of MSCs is well advanced, and there are a number of advanced-phase clinical trials for the treatment of graft versus host diseases (GVHD) and Crohn’s disease [36]. Furthermore, the therapeutic effects of MSCs have been studied extensively focusing on the immunomodulatory properties and the paracrine activity by secreting a wide variety of cytokines and growth factors that are attributed to the angiogenic and regenerative potential in the damaged tissues [36]. More recently, studies have shown that MSC paracrine effects are mediated by secretion of extracellular vesicles such as exosomes [64, 65]. The use of MSC exosomes might serve as an alternative therapy over MSC transplantation for tissue regeneration [66]. A recent study reported the efficacy of MSC exosomes secreted from the synovial membrane and induced pluripotent stem cell-derived MSCs to treat mouse osteoarthritis whereby both source exosomes demonstrated exosome-attenuated OA [67].

MSC-based treatment of OA has a lower risk to the patient and a variety of sources such as adipose tissue, bone marrow, and synovium [68]. These autologous cells can be harvested from patients by either liposuction or aspirated from bone marrow. The adipose-derived MSCs are preferred by patients as compared to MSCs aspirated from the bone marrow because comparatively MSCs are more abundant in adipose tissues than in the bone marrow aspirate. However, bone marrow-derived MSCs may have higher chondrogenic potential than adipose-derived MSCs [69]. Furthermore, synovial tissues obtained from the surgical removal of subsynovial tissue, a noncartilaginous area of the medial condyle of the femur, have also become an attractive source of MSCs in treatment of OA [9, 68].

6. Current Clinical Trials and Case Series Investigating MSCs to Treat OA

A proof-of-concept clinical trial conducted in Korea showed promising safety and efficacy results of adipose-derived MSCs to treat OA. Patients showed reduced pain, improved function of the joint and in the high-dose patient cohort, and regeneration of hyaline-like cartilage suggesting the disease-modifying effects of MSCs when injected into the affected joint [70]. Another pilot study by Orozco et al. demonstrated significant improvement in the pain and functional improvement of up to 65% to 78% in chronic OA patients when treated with bone marrow-derived MSCs, as compared with the conventional treatment methods [71]. Cartilage mapping by T2 MRI showed evidence of improvement in the good cartilage quality, i.e., hyaline-like cartilage, and significant decrease in the poor cartilage quality, i.e., fibrocartilage. The same group conducted a pilot clinical trial examining the safety and efficacy of MSC as a novel treatment of intervertebral disc disorder [72]. After a 1-year follow-up, the primary end point of pain and functional improvement was met in approximately 85% of the cases and no adverse event was observed; the water content was significantly improved in the treated disc and patient-reported significant improvement in the quality of life index [72]. Furthermore, the phase I dose-escalation trial to treat severe OA of the knee by using adipose-derived MSCs to treat patients with symptomatic and severe OA of the knee with single-articular injection of autologous adipose-derived MSCs also showed significant improvement in patients after six months of follow-up [73]. These results showed that the treatment was safe and well tolerated by all patients.

Adipose-derived MSCs to treat patients with joint disease also act as a precursor to treat degenerative OA. Osteochondritis dissecans is a joint disorder pertaining to articular cartilage and chondral defects resulting in damage to the articular cartilage and underlying bone. Adipose-derived MSCs have been reported to have disease-modifying effects in a clinical case series published recently [74]. This study showed regeneration of the lost cartilage and significant reduction of pain and improvement in mobility (Figure 4) [74].

Figure 4: (a) Pretreatment proton density- (PD-) weighted coronal and sagittal MRI images of the knee showing the isolated chondral defect involving the central weight-bearing area of the medial femoral condyle. (b) Posttreatment PD-weighted coronal and sagittal MRI imaging at 18 months indicating articular cartilage regeneration at the site of the osteochondral defect [74].

These evidence-based clinical outcomes strengthen the model for treatment of OA with MSCs (Figures 4 and 5). The results of these trials provide an exciting and promising long-term relief for OA patients and herald a new paradigm for the treatment of chronic and debilitating OA and other degenerative conditions. Intriguingly, several hundred clinical trials globally have been registered in the past 10 years, but only a handful of results from these trials are published. Therefore, there is a need for more clinical trial data to be released from the completed trials to further support and develop this novel model of treatment.

Figure 5: (a) Pretreatment proton density fat-suppressed axial MRI of the knee showing the isolated chondral defect involving the medial facet of the patella. (b) Posttreatment proton density axial MRI indicating articular cartilage regeneration at the site of the chondral defect with smooth integration with the surrounding joint surface [75].

7. Autologous versus Allogeneic MSCs for Therapy

The choice between autologous and allogeneic MSC treatment is another aspect that will need further supportive data. Due to the immune-privileged aspect of MSCs [63], allogeneic stem cell treatment shows more promise and is likely to attract more attention as an “off the shelf” product. However, long-term safety and efficacy data are warranted. The mechanism involved in modulating the host immune system is believed to be facilitated by the ability of MSCs to influence immune cells’ cytokine secretion. MSCs influence mature dendritic type 1 cells to decrease secretion of tissue necrosis factor-alpha (TNF-α) and instruct mature type 2 dendritic cells to increase the anti-inflammatory cytokine IL-10. MSCs can direct T helper cells to decrease secretion of interferon gamma (IFN-γ), and T helper cell 2 to increase IL-4 production and help reduce production of IFN-γ from natural killer (NK) cells [7678]. When cocultured with immune cells, MSCs also enhanced the production of prostaglandin E2 (PGE2); therefore, MSCs are able to modulate the immune system by alteration of cytokine production in the host [7678]. In a comparative study with autologous and allogeneic MSCs, in which 5 patients each received MSCs, the results revealed a similar level of favourable benefits to the quality-of-life improvement in patients with ischemic cardiomyopathy and no immune rejection in the allogeneic group [79]. In a canine study, when autologous and allogeneic MSC transplants were compared in spinal cord injury, both types of cells exhibited therapeutic benefits and transplanted cells were observed in the injured tissue for up to 4 weeks and no immune reactions or adverse effects were reported [80]. Given the safety reports of allogeneic MSC therapy and the surgery-related complications involved in autologous treatment, MSCs derived from a donor for allogeneic therapy provide a better and more affordable treatment option.

8. Future Direction

With the approval of Prochymal, an adult stem cell therapy to treat graft versus host disease (GVHD) in children, in Canada and New Zealand, it heralds a new era for cellular therapy to address the unmet medical conditions of previously untreatable diseases. The translational medical research currently underway targeting MSCs for OA therapy in the clinical trial database is promising; however, they need careful evaluation of the outcome data. The results require focus primarily on the safety and then on the efficacy. Furthermore, the various stages of clinical trials currently registered need their outcome data published for the wider scientific community to consider and to evaluate the robustness of the therapy. The large number of MSCs trials indicates the promise of these cells; however, there is considerable paucity of the published clinical trial data and therefore it is early to envisage the extent of their therapeutic application.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Acknowledgments

We would like to thank Associate Professor Julien Freitag for the help with the MRI images.

References

  1. Chronic rheumatic conditions, “Chronic diseases and health promotion,” 2016, 2016-11-17 16:03:27, Go to WoS://WOS:000333776900001. View at Google Scholar
  2. “Arthritis Information,” 2017, http://www.arthritisaustralia.com.au/index.php/arthritis-information.html.
  3. V. Silverwood, M. Blagojevic-Bucknall, C. Jinks, J. L. Jordan, J. Protheroe, and K. P. Jordan, “Current evidence on risk factors for knee osteoarthritis in older adults: a systematic review and meta-analysis,” Osteoarthritis and Cartilage, vol. 23, no. 4, pp. 507–515, 2015. View at Publisher · View at Google Scholar · View at Scopus
  4. M. Blagojevic, C. Jinks, A. Jeffery, and K. P. Jordan, “Risk factors for onset of osteoarthritis of the knee in older adults: a systematic review and meta-analysis,” Osteoarthritis and Cartilage, vol. 18, no. 1, pp. 24–33, 2010. View at Publisher · View at Google Scholar · View at Scopus
  5. I. J. Wallace, S. Worthington, D. T. Felson et al., “Knee osteoarthritis has doubled in prevalence since the mid-20th century,” Proceedings of the National Academy of Sciences of the United States of America, vol. 114, no. 35, pp. 9332–9336, 2017. View at Publisher · View at Google Scholar · View at Scopus
  6. M. Hiligsmann, C. Cooper, N. Arden et al., “Health economics in the field of osteoarthritis: an expert’s consensus paper from the European Society for Clinical and Economic Aspects of Osteoporosis and Osteoarthritis (ESCEO),” Seminars in Arthritis and Rheumatism, vol. 43, no. 3, pp. 303–313, 2013. View at Publisher · View at Google Scholar · View at Scopus
  7. N. E. Lane, K. Brandt, G. Hawker et al., “OARSI-FDA initiative: defining the disease state of osteoarthritis,” Osteoarthritis and Cartilage, vol. 19, no. 5, pp. 478–482, 2011. View at Publisher · View at Google Scholar · View at Scopus
  8. E. Arden, D. Hunter, and N. Arden, Osteoarthritis, Oxford University Press, Oxford, NY, USA, 2008.
  9. A. M. Säämänen, J. P. A. Arokoski, J. S. Jurvelin, and I. Kiviranta, The Structure and Regenerative Capacity of Synovial Joint Tissues-1, Elsevier Ltd., 2010. View at Publisher · View at Google Scholar · View at Scopus
  10. F. Eckstein, D. Burstein, and T. M. Link, “Quantitative MRI of cartilage and bone: degenerative changes in osteoarthritis,” NMR in Biomedicine, vol. 19, no. 7, pp. 822–854, 2006. View at Publisher · View at Google Scholar · View at Scopus
  11. A. J. Sophia Fox, A. Bedi, and S. A. Rodeo, “The basic science of articular cartilage: structure, composition, and function,” Sports Health, vol. 1, no. 6, pp. 461–468, 2009. View at Publisher · View at Google Scholar · View at Scopus
  12. H. Imhof, I. Sulzbacher, S. Grampp, C. Czerny, S. Youssefzadeh, and F. Kainberger, “Subchondral bone and cartilage disease - a rediscovered functional unit,” Investigative Radiology, vol. 35, no. 10, pp. 581–588, 2000. View at Publisher · View at Google Scholar · View at Scopus
  13. S. Glyn-Jones, A. J. R. Palmer, R. Agricola et al., “Osteoarthritis,” Lancet, vol. 386, no. 9991, pp. 376–387, 2015. View at Publisher · View at Google Scholar · View at Scopus
  14. D. T. Felson, “Osteoarthritis as a disease of mechanics,” Osteoarthritis and Cartilage, vol. 21, no. 1, pp. 10–15, 2013. View at Publisher · View at Google Scholar · View at Scopus
  15. A. E. Nelson, K. D. Allen, Y. M. Golightly, A. P. Goode, and J. M. Jordan, “A systematic review of recommendations and guidelines for the management of osteoarthritis: the Chronic Osteoarthritis Management Initiative of the U.S. Bone and Joint Initiative,” Seminars in Arthritis and Rheumatism, vol. 43, no. 6, pp. 701–712, 2014. View at Publisher · View at Google Scholar · View at Scopus
  16. P. A. Dieppe and L. S. Lohmander, “Pathogenesis and management of pain in osteoarthritis,” Lancet, vol. 365, no. 9463, pp. 965–973, 2005. View at Publisher · View at Google Scholar · View at Scopus
  17. D. G. N. Craig, C. M. Bates, J. S. Davidson, K. G. Martin, P. C. Hayes, and K. J. Simpson, “Staggered overdose pattern and delay to hospital presentation are associated with adverse outcomes following paracetamol-induced hepatotoxicity,” British Journal of Clinical Pharmacology, vol. 73, no. 2, pp. 285–294, 2012. View at Publisher · View at Google Scholar · View at Scopus
  18. C. R. Scanzello, B. McKeon, B. H. Swaim et al., “Synovial inflammation in patients undergoing arthroscopic meniscectomy molecular characterization and relationship to symptoms,” Arthritis and Rheumatism, vol. 63, no. 2, pp. 391–400, 2011. View at Publisher · View at Google Scholar · View at Scopus
  19. E. B. Hunziker, “Articular cartilage repair: basic science and clinical progress. A review of the current status and prospects,” Osteoarthritis and Cartilage, vol. 10, no. 6, pp. 432–463, 2002. View at Publisher · View at Google Scholar · View at Scopus
  20. R. F. Loeser, S. R. Goldring, C. R. Scanzello, and M. B. Goldring, “Osteoarthritis: a disease of the joint as an organ,” Arthritis and Rheumatism, vol. 64, no. 6, pp. 1697–1707, 2012. View at Publisher · View at Google Scholar · View at Scopus
  21. G. C. Machado, C. G. Maher, P. H. Ferreira et al., “Efficacy and safety of paracetamol for spinal pain and osteoarthritis: systematic review and meta-analysis of randomised placebo controlled trials,” BMJ, vol. 350, article h1225, 2015. View at Publisher · View at Google Scholar · View at Scopus
  22. D. J. Hunter and D. T. Felson, “Osteoarthritis,” British Medical Journal, vol. 332, no. 7542, pp. 639–642, 2006. View at Publisher · View at Google Scholar
  23. N. Arden, F. Blanco, C. Cooper et al., Atlas of Osteoarthritis, Springer Healthcare Limited, 2014. View at Publisher · View at Google Scholar
  24. C. M. Balmaceda, “Evolving guidelines in the use of topical nonsteroidal anti-inflammatory drugs in the treatment of osteoarthritis,” BMC Musculoskeletal Disorders, vol. 15, no. 1, 2014. View at Publisher · View at Google Scholar · View at Scopus
  25. E. Manheimer, K. Cheng, K. Linde et al., “Acupuncture for peripheral joint osteoarthritis,” Cochrane Database of Systematic Reviews, no. 1, 2010. View at Publisher · View at Google Scholar
  26. S. Derry, R. A. Moore, and R. Rabbie, “Topical NSAIDs for chronic musculoskeletal pain in adults,” Cochrane Database of Systematic Reviews, no. 9, 2012. View at Publisher · View at Google Scholar · View at Scopus
  27. T. E. McAlindon, R. R. Bannuru, M. C. Sullivan et al., “OARSI guidelines for the non-surgical management of knee osteoarthritis,” Osteoarthritis and Cartilage, vol. 22, no. 3, pp. 363–388, 2014. View at Publisher · View at Google Scholar · View at Scopus
  28. D. Dowell, T. M. Haegerich, and R. Chou, “CDC guideline for prescribing opioids for chronic pain-United States, 2016,” JAMA, vol. 315, no. 15, pp. 1624–1645, 2016. View at Publisher · View at Google Scholar · View at Scopus
  29. J. L. Cook and J. T. Payne, “Surgical treatment of osteoarthritis,” Veterinary Clinics of North America-Small Animal Practice, vol. 27, no. 4, pp. 931–944, 1997. View at Publisher · View at Google Scholar · View at Scopus
  30. J. B. Moseley, K. O'Malley, N. J. Petersen et al., “A controlled trial of arthroscopic surgery for osteoarthritis of the knee,” New England Journal of Medicine, vol. 347, no. 2, pp. 81–88, 2002. View at Publisher · View at Google Scholar · View at Scopus
  31. W. Zhang, R. W. Moskowitz, G. Nuki et al., “OARSI recommendations for the management of hip and knee osteoarthritis, part II: OARSI evidence-based, expert consensus guidelines,” Osteoarthritis and Cartilage, vol. 16, no. 2, pp. 137–162, 2008. View at Publisher · View at Google Scholar · View at Scopus
  32. M. Brittberg, “Autologous chondrocyte implantation-technique and long-term follow-up,” Injury, vol. 39, no. 1, pp. 40–49, 2008. View at Publisher · View at Google Scholar · View at Scopus
  33. R. B. Jakobsen, L. Engebretsen, and J. R. Slauterbeck, “An analysis of the quality of cartilage repair studies,” Journal of Bone and Joint Surgery-American Volume, vol. 87, no. 10, pp. 2232–2239, 2005. View at Publisher · View at Google Scholar · View at Scopus
  34. J. R. Steadman, W. G. Rodkey, K. K. Briggs, and J. J. Rodrigo, “The microfracture technique to treat full thickness articular cartilage defects of the knee,” Der Orthopäde, vol. 28, no. 1, pp. 26–32, 1999. View at Publisher · View at Google Scholar · View at Scopus
  35. K. Mithoefer, T. McAdams, R. J. Williams, P. C. Kreuz, and B. R. Mandelbaum, “Clinical efficacy of the microfracture technique for articular cartilage repair in the knee an evidence-based systematic analysis,” American Journal of Sports Medicine, vol. 37, no. 10, pp. 2053–2063, 2009. View at Publisher · View at Google Scholar · View at Scopus
  36. A. Trounson and C. McDonald, “Stem cell therapies in clinical trials: progress and challenges,” Cell Stem Cell, vol. 17, no. 1, pp. 11–22, 2015. View at Publisher · View at Google Scholar · View at Scopus
  37. A. J. Friedenstein, R. K. Chailakhyan, N. V. Latsinik, A. F. Panasyuk, and I. V. Keiliss-Borok, “Stromal cells responsible for transferring the microenvironment of the hemopoietic tissues: cloning in vitro and retransplantation in vivo,” Transplantation, vol. 17, no. 4, pp. 331–340, 1974. View at Publisher · View at Google Scholar · View at Scopus
  38. A. I. Caplan, “Mesenchymal stem cells,” Journal of Orthopaedic Research, vol. 9, no. 5, pp. 641–650, 1991. View at Publisher · View at Google Scholar · View at Scopus
  39. P. Bianco, ““Mesenchymal” stem cells,” Annual Review of Cell and Developmental Biology, vol. 30, no. 1, pp. 677–704, 2014. View at Publisher · View at Google Scholar · View at Scopus
  40. D. Drago, C. Cossetti, N. Iraci et al., “The stem cell secretome and its role in brain repair,” Biochimie, vol. 95, no. 12, pp. 2271–2285, 2013. View at Publisher · View at Google Scholar · View at Scopus
  41. G. Steinhoff, Regenerative Medicine - from Protocol to Patient 2. Stem Cell Science and Technology, Springer International Publishing, Cham, 3rd edition, 2016.
  42. D. McGonagle, T. G. Baboolal, and E. Jones, “Native joint-resident mesenchymal stem cells for cartilage repair in osteoarthritis,” Nature Reviews Rheumatology, vol. 13, no. 12, pp. 719–730, 2017. View at Publisher · View at Google Scholar · View at Scopus
  43. A. Klimczak and U. Kozlowska, “Mesenchymal stromal cells and tissue-specific progenitor cells: their role in tissue homeostasis,” Stem Cells International, vol. 2016, Article ID 4285215, 11 pages, 2016. View at Publisher · View at Google Scholar · View at Scopus
  44. P. A. Zuk, M. Zhu, H. Mizuno et al., “Multilineage cells from human adipose tissue: implications for cell-based therapies,” Tissue Engineering, vol. 7, no. 2, pp. 211–228, 2001. View at Publisher · View at Google Scholar · View at Scopus
  45. Y. Jiang, B. Vaessen, T. Lenvik, M. Blackstad, M. Reyes, and C. M. Verfaillie, “Multipotent progenitor cells can be isolated from postnatal murine bone marrow, muscle, and brain,” Experimental Hematology, vol. 30, no. 8, pp. 896–904, 2002. View at Publisher · View at Google Scholar · View at Scopus
  46. J. G. Toma, I. A. McKenzie, D. Bagli, and F. D. Miller, “Isolation and characterization of multipotent skin-derived precursors from human skin,” Stem Cells, vol. 23, no. 6, pp. 727–737, 2005. View at Publisher · View at Google Scholar · View at Scopus
  47. B. C. Perry, D. Zhou, X. Wu et al., “Collection, cryopreservation, and characterization of human dental pulp-derived mesenchymal stem cells for banking and clinical use,” Tissue Engineering Part C-Methods, vol. 14, no. 2, pp. 149–156, 2008. View at Publisher · View at Google Scholar · View at Scopus
  48. L. da Silva Meirelles, P. C. Chagastelles, and N. B. Nardi, “Mesenchymal stem cells reside in virtually all post-natal organs and tissues,” Journal of Cell Science, vol. 119, no. 11, pp. 2204–2213, 2006. View at Publisher · View at Google Scholar · View at Scopus
  49. M. Dominici, K. le Blanc, I. Mueller et al., “Minimal criteria for defining multipotent mesenchymal stromal cells. The International Society for Cellular Therapy position statement,” Cytotherapy, vol. 8, no. 4, pp. 315–317, 2006. View at Publisher · View at Google Scholar · View at Scopus
  50. C. M. Kolf, E. Cho, and R. S. Tuan, “Mesenchymal stromal cells. Biology of adult mesenchymal stem cells: Regulation of niche, self-renewal and differentiation,” Arthritis Research and Therapy, vol. 9, no. 1, p. 204, 2007. View at Publisher · View at Google Scholar · View at Scopus
  51. A. Muraglia, R. Cancedda, and R. Quarto, “Clonal mesenchymal progenitors from human bone marrow differentiate in vitro according to a hierarchical model,” Journal of Cell Science, vol. 113, no. 7, pp. 1161–1166, 2000. View at Google Scholar
  52. K. C. Russell, M. R. Lacey, J. K. Gilliam, H. A. Tucker, D. G. Phinney, and K. C. O'Connor, “Clonal analysis of the proliferation potential of human bone marrow mesenchymal stem cells as a function of potency,” Biotechnology and Bioengineering, vol. 108, no. 11, pp. 2716–2726, 2011. View at Publisher · View at Google Scholar · View at Scopus
  53. D. C. Colter, R. Class, C. M. DiGirolamo, and D. J. Prockop, “Rapid expansion of recycling stem cells in cultures of plastic-adherent cells from human bone marrow,” Proceedings of the National Academy of Sciences of the United States of America, vol. 97, no. 7, pp. 3213–3218, 2000. View at Publisher · View at Google Scholar · View at Scopus
  54. D. Baksh, L. Song, and R. S. Tuan, “Adult mesenchymal stem cells: characterization, differentiation, and application in cell and gene therapy,” Journal of Cellular and Molecular Medicine, vol. 8, no. 3, pp. 301–316, 2004. View at Publisher · View at Google Scholar · View at Scopus
  55. D. G. Phinney, “Functional heterogeneity of mesenchymal stem cells: implications for cell therapy,” Journal of Cellular Biochemistry, vol. 113, no. 9, pp. 2806–2812, 2012. View at Publisher · View at Google Scholar · View at Scopus
  56. J. M. Gimble, A. J. Katz, and B. A. Bunnell, “Adipose-derived stem cells for regenerative medicine,” Circulation Research, vol. 100, no. 9, pp. 1249–1260, 2007. View at Publisher · View at Google Scholar · View at Scopus
  57. M. E. Bernardo, A. M. Cometa, D. Pagliara et al., “Ex vivo expansion of mesenchymal stromal cells,” Best Practice and Research: Clinical Haematology, vol. 24, no. 1, pp. 73–81, 2011. View at Publisher · View at Google Scholar · View at Scopus
  58. B. Bunnell, M. Flaat, C. Gagliardi, B. Patel, and C. Ripoll, “Adipose-derived stem cells: isolation, expansion and differentiation,” Methods, vol. 45, no. 2, pp. 115–120, 2008. View at Publisher · View at Google Scholar · View at Scopus
  59. P. Bourin, B. A. Bunnell, L. Casteilla et al., “Stromal cells from the adipose tissue-derived stromal vascular fraction and culture expanded adipose tissue-derived stromal/stem cells: a joint statement of the International Federation for Adipose Therapeutics and Science (IFATS) and the International Society for Cellular Therapy (ISCT),” Cytotherapy, vol. 15, no. 6, pp. 641–648, 2013. View at Publisher · View at Google Scholar · View at Scopus
  60. P. A. Zuk, M. Zhu, P. Ashjian et al., “Human adipose tissue is a source of multipotent stem cells,” Molecular Biology of the Cell, vol. 13, no. 12, pp. 4279–4295, 2002. View at Publisher · View at Google Scholar · View at Scopus
  61. G. R. Erickson, J. M. Gimble, D. M. Franklin, H. E. Rice, H. Awad, and F. Guilak, “Chondrogenic potential of adipose tissue-derived stromal cells in vitro and in vivo,” Biochemical and Biophysical Research Communications, vol. 290, no. 2, pp. 763–769, 2002. View at Publisher · View at Google Scholar · View at Scopus
  62. G. Yu, X. Wu, M. A. Dietrich et al., “Yield and characterization of subcutaneous human adipose-derived stem cells by flow cytometric and adipogenic mRNA analyzes,” Cytotherapy, vol. 12, no. 4, pp. 538–546, 2010. View at Publisher · View at Google Scholar · View at Scopus
  63. J. D. Glenn and K. A. Whartenby, “Mesenchymal stem cells: emerging mechanisms of immunomodulation and therapy,” World Journal of Stem Cells, vol. 6, no. 5, pp. 526–539, 2014. View at Publisher · View at Google Scholar
  64. S. Bruno, M. Tapparo, F. Collino et al., “Renal regenerative potential of different extracellular vesicle populations derived from bone marrow mesenchymal stromal cells,” Tissue Engineering Part A, vol. 23, no. 21-22, pp. 1262–1273, 2017. View at Publisher · View at Google Scholar · View at Scopus
  65. R. C. Lai, R. W. Y. Yeo, S. S. Tan et al., “Mesenchymal stem cell exosomes: the future MSC-based therapy?” in Mesenchymal Stem Cell Therapy, L. G. Chase and M. C. Vemuri, Eds., no. article 10.1007/978-1-62703-200-1_3, pp. 39–61, Humana Press, Totowa, NJ, USA, 2013. View at Google Scholar
  66. H. S. Kim, D. Y. Choi, S. J. Yun et al., “Proteomic analysis of microvesicles derived from human mesenchymal stem cells,” Journal of Proteome Research, vol. 11, no. 2, pp. 839–849, 2012. View at Publisher · View at Google Scholar · View at Scopus
  67. A. Eirin, X. Y. Zhu, A. S. Puranik et al., “Comparative proteomic analysis of extracellular vesicles isolated from porcine adipose tissue-derived mesenchymal stem/stromal cells,” Scientific Reports, vol. 6, no. 1, 2016. View at Publisher · View at Google Scholar · View at Scopus
  68. J. Burke, M. Hunter, R. Kolhe, C. Isales, M. Hamrick, and S. Fulzele, “Therapeutic potential of mesenchymal stem cell based therapy for osteoarthritis,” Clinical and Translational Medicine, vol. 5, no. 1, p. 27, 2016. View at Publisher · View at Google Scholar
  69. H. Afizah, Z. Yang, J. H. P. Hui, H. W. Ouyang, and E. H. Lee, “A comparison between the chondrogenic potential of human bone marrow stem cells (BMSCs) and adipose-derived stem cells (ADSCs) taken from the same donors,” Tissue Engineering, vol. 13, no. 4, pp. 659–666, 2007. View at Publisher · View at Google Scholar · View at Scopus
  70. C. H. Jo, Y. G. Lee, W. H. Shin et al., “Intra-articular injection of mesenchymal stem cells for the treatment of osteoarthritis of the knee: a proof-of-concept clinical trial,” Stem Cells, vol. 32, no. 5, pp. 1254–1266, 2014. View at Publisher · View at Google Scholar · View at Scopus
  71. L. Orozco, A. Munar, R. Soler et al., “Treatment of knee osteoarthritis with autologous mesenchymal stem cells: a pilot study,” Transplantation, vol. 95, no. 12, pp. 1535–1541, 2013. View at Publisher · View at Google Scholar · View at Scopus
  72. L. Orozco, R. Soler, C. Morera, M. Alberca, A. Sánchez, and J. García-Sancho, “Intervertebral disc repair by autologous mesenchymal bone marrow cells: a pilot study,” Transplantation, vol. 92, no. 7, pp. 822–828, 2011. View at Publisher · View at Google Scholar · View at Scopus
  73. Y. M. Pers, L. Rackwitz, R. Ferreira et al., “Adipose mesenchymal stromal cell-based therapy for severe osteoarthritis of the knee: a phase I dose-escalation trial,” Stem Cells Translational Medicine, vol. 5, no. 7, pp. 847–856, 2016. View at Publisher · View at Google Scholar · View at Scopus
  74. J. Freitag, K. Shah, J. Wickham, R. Boyd, and A. Tenen, “The effect of autologous adipose derived mesenchymal stem cell therapy in the treatment of a large osteochondral defect of the knee following unsuccessful surgical intervention of osteochondritis dissecans - a case study,” BMC Musculoskeletal Disorders, vol. 18, no. 1, p. 298, 2017. View at Publisher · View at Google Scholar · View at Scopus
  75. J. Freitag, D. Li, J. Wickham, K. Shah, and A. Tenen, “Effect of autologous adipose-derived mesenchymal stem cell therapy in the treatment of a post-traumatic chondral defect of the knee,” BMJ Case Reports, vol. 2017, 2017. View at Publisher · View at Google Scholar · View at Scopus
  76. S. Aggarwal and M. F. Pittenger, “Human mesenchymal stem cells modulate allogeneic immune cell responses,” Blood, vol. 105, no. 4, pp. 1815–1822, 2005. View at Publisher · View at Google Scholar · View at Scopus
  77. C. G. Williams, T. K. Kim, A. Taboas, A. Malik, P. Manson, and J. Elisseeff, “In vitro chondrogenesis of bone marrow-derived mesenchymal stem cells in a photopolymerizing hydrogel,” Tissue Engineering, vol. 9, no. 4, pp. 679–688, 2003. View at Publisher · View at Google Scholar · View at Scopus
  78. W. Zhang, W. Ge, C. Li et al., “Effects of mesenchymal stem cells on differentiation, maturation, and function of human monocyte-derived dendritic cells,” Stem Cells and Development, vol. 13, no. 3, pp. 263–271, 2004. View at Publisher · View at Google Scholar · View at Scopus
  79. J. M. Hare, J. E. Fishman, G. Gerstenblith et al., “Comparison of allogeneic vs autologous bone marrow-derived mesenchymal stem cells delivered by transendocardial injection in patients with ischemic cardiomyopathy the POSEIDON randomized trial,” JAMA, vol. 308, no. 22, pp. 2369–2379, 2012. View at Publisher · View at Google Scholar · View at Scopus
  80. D. I. Jung, J. Ha, B. T. Kang et al., “A comparison of autologous and allogenic bone marrow-derived mesenchymal stem cell transplantation in canine spinal cord injury,” Journal of the Neurological Sciences, vol. 285, no. 1-2, pp. 67–77, 2009. View at Publisher · View at Google Scholar · View at Scopus