Therapeutic potential of periodontal ligament stem cells

Aline Queiroz, Emmanuel Albuquerque-Souza, Leticia Miquelitto Gasparoni, Bruno Nunes de Fran?a, Cibele Pelissari, Marília Trierveiler, Marinella Holzhausen

Aline Queiroz, Cibele Pelissari, Marília Trierveiler, Laboratory of Stem Cell Biology in Dentistry-LABITRON, Department of Oral and Maxillofacial Pathology, School of Dentistry, University of S?o Paulo, S?o Paulo 05508-000, Brazil

Emmanuel Albuquerque-Souza, Leticia Miquelitto Gasparoni, Bruno Nunes de Fran?a, Marinella Holzhausen, Department of Stomatology, Division of Periodontics, School of Dentistry,University of S?o Paulo, S?o Paulo 05508-000, Brazil

Abstract Inflammatory periodontal disease known as periodontitis is one of the most common conditions that affect human teeth and often leads to tooth loss.Due to the complexity of the periodontium, which is composed of several tissues, its regeneration and subsequent return to a homeostatic state is challenging with the therapies currently available.Cellular therapy is increasingly becoming an alternative in regenerative medicine/dentistry, especially therapies using mesenchymal stem cells, as they can be isolated from a myriad of tissues.Periodontal ligament stem cells (PDLSCs) are probably the most adequate to be used as a cell source with the aim of regenerating the periodontium.Biological insights have also highlighted PDLSCs as promising immunomodulator agents.In this review, we explore the state of knowledge regarding the properties of PDLSCs, as well as their therapeutic potential, describing current and future clinical applications based on tissue engineering techniques.

Key Words: Periodontal ligament stem cell; Mesenchymal stem cell; Regenerative dentistry; Therapeutics; Immunology; Cellular

INTRODUCTION

Mesenchymal stem cells (MSCs) can be isolated from different tissues and, in culture, show characteristics such as: fibroblast-like morphology, plastic adherent properties, and the ability to form colonies and to differentiate into osteogenic, adipogenic, and chondrogenic lineages[1].Other known features of MSCs include their migratory activity, immunomodulatory capacity, and paracrine effects on other cell types[2-4].Despite these common aspects, different sources of MSCs present peculiarities related to the tissue from which they are isolated.By considering these source-dependent characteristics, dental stem cells are likely to be more suitable for regeneration in dentistry.It is also important to take into account that dental tissues samples are easily obtained during procedures of relative low invasiveness.

The first dental MSCs to be isolated and well-characterized were dental pulp stem cells (DPSCs)[5].Subsequently, other tissue sources were discovered, including the pulp of deciduous teeth[6], periodontal ligament[7], apical papilla[8], dental follicle[9], alveolar bone[10], dental germ[11], and gingiva[12].

Periodontal ligament stem cells (PDLSCs), also known as periodontal ligament mesenchymal cells, are a unique cell population that are easily obtained and exhibit important characteristics of MSCs, such as self-renewal, multipotency, and immunomo-dulation[13].For these reasons, PDLSCs have been extensively studied over the years and have shown potential in the regeneration of not only the periodontal complex but also other dental and non-dental tissues[7,14].

Pre-clinical studies, carried out using differentin vivomodels, as well as pilot studies and clinical trials published so far, show promising results regarding the effectiveness of PDLSCs in regeneration of the periodontal complex and the safety of their use in humans[15-17].In this review, we address the current knowledge regarding the properties of PDLSCs as well as their therapeutic potential, describing current and future clinical applications based on tissue engineering techniques.

PERIODONTAL LIGAMENT GENERAL FEATURES AND PDLSCS MARKERS

The periodontium is a complex set of tissues composed of the gingiva, periodontal ligament, cementum, and alveolar bone.The periodontal ligament is a unique specialized connective tissue responsible for anchoring the teeth to the alveolar bone, providing them with the necessary fixation and protection against the forces of the masticatory system.Thus, it guarantees homeostasis and the other functions performed by this system[18,19].By considering this complexity, the regeneration of lost or damaged periodontal tissues due to periodontitis remains a challenge for the currently available therapeutics.To date, periodontitis is a complex chronic inflammatory disease that is the result of a dysregulated immune response to a dysbiotic biofilm with the presence of pathogens such asPorphyromonas gingivalis (P.gingivalis).This causes destruction of the supporting periodontal tissues (i.e., periodontal ligament, cementum, and alveolar bone) and eventually loss of the tooth.

PDLSCs seem to have a fundamental role as progenitor cells and coordinate the events related to regeneration of the periodontal tissues[20].They are heterogeneous, clonogenic, highly proliferative, and multipotent cells capable of differentiating into osteoblasts, cementoblasts, chondrocytes, and adipocytes[7,21,22].Not surprisingly, they promote neoformation of periodontal tissues, including periodontal ligament fibers similar to Sharpey’s fibers, bone and cementum[13,23,24].Osteoblasts, cementoblasts and fibroblasts are the main cell types responsible for tissue homeostasis of the alveolar bone, cementum, and periodontal ligament, respectively.From this comes the importance of evaluating the role of PDLSCs as a source of differentiation for these cells[25].

Currently, there is no specific cell surface marker that can discriminate PDLSCs from other constitutive periodontal cells.Instead, a combination of markers can be used to identify and isolate them, as they correspond to a small fraction of cells in the heterogeneous cell population of the periodontal ligament[7].The minimum criteria for isolating PDLSCs include positivity for MSCs surface markers, such as CD90/Thy-1, CD73, CD105 and CD166/VCAM-1[24].Other markers known to be expressed by MSCs are also positive on PDLSCs, including CD44[26-28], CD10[29], CD13[27,29], CD29[26,27], CD26[30], STRO-3[28], and STRO-4/HSP90[26].In addition, PDLSCs are negative for endothelial (CD31) and hematopoietic markers (CD45, CD34, CD14, CD11b, CD79α, CD19), as well as for molecules related to antigen presentation (HLADR, CD40, CD54, CD80, CD86)[27-29].

In one of the first studies that characterized PDLSCs, it was observed that they express the pericyte markers STRO-1 and CD146, and the typical tendon antigen Scleraxis[7].It was further observed that PDLSCs express other markers shared by pericytes and stem cells as well, including NG2 and CD140b/platelet-derived growth factor receptor β[31].Pericytes are cells that surround endothelial cells in the microvasculature, and MSCs are believed to reside in these perivascular niches[32].

PDLSCs also express the following neural crest derived cell markers: Nestin[33,34], β-tubulin III[35], CD271/p75NTR[33,34], SLUG[33] and SOX10[33,34].Due to these features, the induction of the neural phenotype in PDLSCs can be an interesting and effective method for future neuroregenerative therapies.In fact, a combination of surface markers for CD51/CD140α, CD271/STRO-1, and CD271/CD146 could help to isolate populations of PDLSCs with a large range of potential for cell differentiation[36].

The pluripotent embryonic stem cells markers NANOG[30,34,37], OCT-4[30,34,37,38], SOX2[34,37,38], SSEA-1[30,37], SSEA-3[37], SSEA-4[30,37], TRA-1-60, and TRA-1-81[37] were also reported to be expressed by PDLSCs, which may indicate an even more undifferentiated state of these cells.In a recent study, we reported that about 10% of PDLSCs could present double positivity for SOX2 and OCT-4[38], two transcription factors important for the pluripotency of embryonic stem cells, but which are also detected in somatic stem cells, such as those derived from the periodontal ligament[39].

PROLIFERATION AND DIFFERENTIATION POTENTIAL OF PDLSCS

By isolating stem cells from the periodontal ligament for the first time, Seoet al[7] demonstrated a population of multipotent MSCs that could perform adipogenic differentiation and acquire an osteoblast-cementoblast-like phenotype.Subsequently, it was actually proved that PDLSCs could differentiate into osteoblasts, chondrocytes, and adipocytes under appropriate culture conditions[21].

The fibroblastic activity of PDLSCs has been demonstrated.When stimulated with appropriate growth factors, these cells express fibrogenic-like genes [e.g., Collagen-1 (COL1), COL3, fibroblast-specific protein 1, Periodontal-ligament-associated protein 1], and Elastin and exhibit a strong immunofluorescence label for fibronectin.In fact, the stimulus with connective tissue growth factor increases the synthesis of collagen by PDLSCs, which points to their potential to differentiate into periodontal ligament fiber-forming cells[40].

Primary cultures containing fibroblasts derived from periodontal ligament fibers with a phenotype of undifferentiated mesenchymal cells also expressed endothelial cell markers when cultured in medium containing fibroblast growth factor (FGF) and heparin.This single cell-derived culture was able to form structures similar to blood vessels by using a three dimensional (3D) type 1 collagen scaffold.This angiogenic potential was associated with activation of the PI3K signaling cascade[41].The angiogenic differentiation of CD105+-enriched PDLSCs can be reached using endothelial growth medium-2, and down-regulation of neuropilin-2 is observed in this process, which further indicates the role of this molecule for the angiogenic differentiation of PDLSCs[42].

Since cells isolated from the periodontal ligament also express neural crest markers, it was proposed that they could differentiate into neural lineages[33,34].Under cultivation in a neurogenic induction medium, cells derived from the periodontal ligament underwent morphological changes similar to neurons.PDLSCs transplanted into the brains of adult mice were able to survive, migrate, and differentiate into cells with a neural-like phenotype[43].Recently, PDLSCs grown in appropriate media exhibited cellular and nuclear morphology similar to rodent brain cells.They were able to develop domains similar to axon branches and dendrites, which was further confirmed by positive staining for β-tubulin III and F-actin.In addition, morphological analysis demonstrated that these cells could connect to each other through synapticlike interactions and expressed related proteins, such as synaptophysin and synapsin-1[44].

With a view to the future use of these cells in neuroregenerative medicine, Fortinoet al[35] differentiated PDLSCs to glial and neuron-like cells by treating them with specific growth factors (EGF and βFGF).In addition, the transdifferentiation of PDLSCs in retinal ganglia cells was followed by the regulation of microRNAs argued to control neural differentiation, especially miR-132[45,46].However, the exact mechanisms involved in the neural differentiation of PDLSCs are still unknown, and neuroinduction protocols still need to be improved.

Populations of PDLCs positive for well-known markers of embryonic stem cells and neural crest markers also expressed genes related to cardiomyogenesis after treatment with low concentrations of hydrogen peroxide[33].Upon discovering this potential, neural crest stem cells residing in the periodontal ligament were able to express cardiomyocyte markers, and their contraction activity was observed after induction by pulsed infrared radiation[47].The potential for differentiating PDLSCs into pancreatic islet-like cells has also been reported.These cells could release insulin in response to glucose stimulus[48].

Regarding the factors that can affect the differentiation potential of PDLSCs, a lower osteogenic capacity was observed in PDLSCs grown in medium containingP.gingivalis-derived lipopolysaccharide (LPS), an important pathogen associated with the etiopathogenesis of periodontal diseases.A reduced activity of alkaline phosphatase and in the number of calcified deposits, as well as down-regulation of COL1 and Osteocalcin genes were observed[49].Similar results were found underEscherichia coli-LPS stimulus[50], which was further argued to be associated with the activation of Toll-like receptor 4 (TLR-4) and its downstream NF-κB cascade[51].

On this basis, we recently showed that inflammatory conditions in periodontal tissues also alter the expression of typical pluripotent embryonic stem cell markers in PDLSCs, as well as their proliferative activity, ability to differentiate into osteoblasts and cementoblasts, and their expression of periodontal ligament related markers (periostin, tenomodulin, and α-SMA).If a typical pro-inflammatory environment with the presence of cytokines such as interleukin (IL)-1β and tumor necrosis factor-α would reduce these properties, the induction of a pro-resolving environment with the synthesis of specialized lipid mediators such as maresin and resolvin would act by improving these properties on PDLSCs[38].Thus, although future studies are necessary, it is known that periodontal disease conditions can have the potential to affect the regenerative capacity of PDLSCs.

The different methods for culturing and isolating PDLSCs were also analyzed for their ability to affect the differentiation potential of these cells.The use of the outgrowth instead the enzymatic digestion method to isolate PDLSCs was shown to be more suitable for inducing cementogenesis.Better results for this method were observed in terms of the formation of mineralized deposits similar to cementum in bothin vitroandin vivoexperiments, and the expression of cementoblast-like genes[52].Additionally, thein vitroexpansion of PDLSCs cultures also induces morphological changes, by bursting their myofibroblastic phenotype, which up-regulates their contractile activity and reduces the expression of NANOG, SOX2 and OCT-4, factors associated with pluripotency of embryonic stem cells, but that are also expressed in MSCs[53].

There is still insufficient evidence of differences in the potential for differentiating PDLSCs due to donor populations related characteristics.To date, PDLSCs isolated from deciduous teeth exhibited a greater expression of genes related to adipogenic differentiation compared to those from permanent teeth[54].In a later study, PDLSCs from either deciduous or permanent dentitions presented similarin vitroadipogenic and osteogenic differentiation[55].By analyzing the donor-age impact, it was observed that PDLSCs from elderly populations exhibited less osteogenic activity, and a relationship between age and expression of osteogenesis-related genes (i.e.Osteocalcin, COL1, and Runx2) was established[56].

POTENTIAL OF PDLSCS IN IMMUNOMODULATORY THERAPY

Over the years, immunomodulation has been presented as a typical characteristic of mesenchymal stem cell-like populations.The absence of the expression of costimulatory factors such as major histocompatibility complex class II antigen, CD40, and CD80, have been highlighted as responsible for the low immunogenicity of MSCs[4,57].Further evidence demonstrated the mechanisms activated by mesenchymal cells from periodontal tissues that could result in modulation of the host response[28,58-60].Therefore, in addition to their low immunogenicity/compatibility, MSCs perform their function by suppressing the function of a range of immune response cells and by improving immune regulatory functions.As a result of these activities, MSCs became a prominent alternative for the immune therapy of chronic inflammatory disorders, such as periodontitis.

Overall, MSCs reveal their potential by inducing phenotypic changes in several cell types, including dendritic cells (DCs), T and B lymphocytes, monocytes/macrophages, and natural killer cells[61-64].Although the ability of periodontal ligament cells to perform such functions remains under review, recent findings point to promising correlated activities of MSCs from this tissue.How MSCs exert their immuneregulatory properties is still a matter of debate, albeit both soluble factors/secretome and cell-cell contact were described as mechanisms implicated to mediate such functions.To date, living, apoptotic, and dead MSCs, as well as their secretome consisting of a diverse range of cytokines, chemokines, growth factors, and extracellular vesicles may mediate regulatory activity[61,65,66].

Supporting a cell-cell interaction effect, PDLSCs co-cultured with human monocytederived DCs under stimulation withP.gingivalis-derived LPS, a keystone pathogen in the etiopathogenesis of periodontitis, down-regulated the expression of non-classical major histocompatibility complex glycoprotein CD1b on DCs.This, in turn, resulted in defective proliferation of T lymphocytes[60].Indeed, the proliferative index of CD4+ T cells can be considerably reduced in the presence of PDLSCs, as well as a decrease in the ratio of CD4 + CD25 high/CD4 + CD25 low T cells within mitogen-stimulated peripheral blood mononuclear cells (PBMNCs) can be observed.Alongside these effects, PDLSCs when co-stimulated with LPS up-regulated COX-2 and IL-6 through downstream activation of extracellular signal-regulated kinase 1/2, and reduced the frequency of CD14+ cells within PBMNCs[50].However, the supernatant of CD105-enriched PDLSCs challenged withP.gingivalistotal protein extract increased neutrophil recruitmentin vitro, suggesting secretome-mediated signaling as importantviaparacrine immune regulation[67].Similarly, PDLSCs exhibited non-cell contact or secretome dependent suppression activity on the rate of monocyte proliferation in coculture experimentsviasecretion of metabolites such as indoleamine 2, 3-dioxygenase, hepatocyte, and transforming growth factors (TGF-β)[28].

Indoleamine 2, 3-dioxygenase has been identified as an important molecule for the immunomodulation process triggered by MSCs in the typical microenvironment of chronic inflammatory diseases, particularly periodontitis[4,28,63,68].When PDLSCs were co-stimulated with (interferon) INF-γ and TLRs agonists, an increase in the expression of this enzyme as well as IL-6, CXCL8, and MCP-1 was observed[69].Nevertheless, the effect of these cells is not only dependent on cytokines and chemokines release.Recently, it was demonstrated that PDLSCs reduced apoptosis and stimulated the microbicidal activity of human neutrophils,viaboth cell-cell interactions and paracrine mechanisms.This effect could be related to the synthesis of specialized pro-resolving lipid mediators,e.g., resolvins, protectins, maresins, and lipoxins, which are major molecules responsible for orchestrating the resolution phase of inflammation and the return to tissue homeostasis[59].

However, the immunomodulatory capacity of MSCs seems to be dependent on the conditions of the source tissue.MSCs have been reported as important regulators of the T cell phenotype by inducing an increase in the proportion of T regulatory (Treg) populations (FOXP3+ lymphocytes) over typical pro-inflammatory Th17 subsets (RORγT+ lymphocytes)[70].Notwithstanding, compared to healthy cells, PDLSCs collected from inflamed periodontal sites present less regulatory properties, reducing Treg differentiation as well as its signature cytokine IL-10.The suppressive effect on Th17 differentiation and its signature cytokine IL-17 was also reduced in PDLSCs collected from periodontally healthy individuals compared to those from periodontitis affected patients[58].Thus, it is also important to keep in mind such biological differences in the future therapeutic application of these cell types.

MSCs present tissue-specific functional differences[71,72] that may be related to the composition of the secretome of these cells, which as reported above plays an important role in their regulatory properties.Not surprisingly, mass-spectrometry analysis of PDLSCs metabolites showed differences in the endogenous level of 5-lysophosphatidylcholines and 3-lysophosphatidylethanolamines, which can discriminate these cells from MSCs from other sources, such as adipose tissue and salivary glands[73].These differences are also age-dependent as PDLSCs from deciduous teeth have a higher expression of cytokines that regulate the host immunity (e.g., interleukins I, II, and IV) and secreted proteinse.g., matrix metalloproteinases and cullins) responsible for tissue degradation and catalytic activities when compared to those from permanent teeth[74].In fact, the lack of clear-cut assays that help to clarify the heterogeneity of MSCs populations is a further challenge within a translational therapeutic perspective.

Alongside the natural potential of PDLSCs to be used in regulating the host response in periodontitis, more recently MSCs of dental origin have also been mentioned as possible sources for cell therapy in other cases of inflammatory imbalance-related disorders, such as those affecting the brain (e.g., Alzheimer's disease, Parkinson's disease) and gut (e.g., Crohn’s disease, colitis)[75].Recently, PDLSCs were used to control colitis in anin vivomodel, and the authors concluded that their immunomodulatory activity was mediated by a group of deoxyribonucleic acid demethylases of the ten-eleven translocation family (Tet1 and Tet 2)[76].

Cell therapy with MSCs, taking immunomodulation as the perspective, is still in its infancy, especially with respect to those from periodontal origin, and further studies need to be delineated so that the mechanisms by which these cells exert such activity are unraveled.Doubts still exist as to whether these cells would actually need to be injected into patients, or whether it is their products that may exert more appropriate host response regulation, which could overcome common risks associated with this therapy such as ectopic differentiation and tumor growth promotion.It is necessary to overcome discrepancies between studies that apply different isolation methods, cell culture, expansion conditions and cryopreservation of PDLSCs.In addition, it appears that preconditioning these cells prior to treatment may improve their immunoregulatory functions, as suggested in a previous study with PDLSCs under INF-γ stimuli[69].Of note, MSCs are thought to be immunoprivileged, but repeated infusion of mismatched MSCs may also induce alloimmunization[77].Hence, more mechanistic investigations and more caution still need to be taken into account before the clinical application of this therapy, which despite the challenges, seems promising for immunomodulation.

POTENTIAL OF PDLSCS IN REGENERATIVE THERAPY

Current approaches to treatment of periodontitis limit disease progression, but periodontal regeneration of the dental supporting tissues (alveolar bone, cementum and periodontal ligament) cannot be predictably achieved[78,79].In the early 1990s, Tissue Engineering was proposed as a field that would apply the principles of human biology and engineering to the development of functional substitutes for damaged tissues.This strategy should be based on three strategies: (1) cells; (2) scaffolds; and (3) signaling molecules[80].

In 2004, Seoet al[7] investigated the ability of PDLSCs during tissue regeneration and found that PDLSCs were able to generate structures similar to the cementum/ periodontal ligamentin vivo.This study suggested the important role of PDLSCs in periodontal regeneration[7].Since then, many studies have evaluated the regeneration of periodontal tissue by combining PDLSCs in scaffolds and signaling molecules.PDLSCs exhibit a multipotent differentiation capacity and are good candidates for use in tissue engineering due to their potential to promote regeneration of dental and nondental tissues.

Scaffolds have a key role in periodontal regeneration.The ideal scaffold has the following properties: (1) Ability to recruit or retain cells; (2) Biocompatibility; and (3) Biodegradation.In this sense, countless attempts have been made to find an ideal scaffold, that is, a material engineered to support desirable cellular interactions and contribute to the formation of new functional tissues.In such structures, specific mediators are responsible for mediating signaling transduction between cells.Such molecules include growth factors which bind to surface receptors that modulate target cells and accordingly improve the regenerative potential of PDLSCs sheet engineering[81].Parallel experiments demonstrated that PDLSC sheets were able to generate structures similar to cementum and periodontal ligament-connective tissue when transplanted in a hydroxyapatite/tricalcium phosphate matrix to immunocompromised mice[82].The potential of a nanohydroxyapatite-chitosan scaffold combined with PDLSCs in bone regeneration was also demonstrated in a calvarial bone repair model[83].

Within the molecules artificially used to mimic biological processes, FGF is a mediator that promotes regeneration of the periodontium.The application of TGFβ1 subsequent to growth under FGF stimulus for the differentiation of PDLSCs into fibroblastic cells was reported to accelerate the generation of a functional periodontium[84].Furthermore, a combination of platelet-rich plasma and PDLSCs sheets suggested that this stimulus could increase the production of extracellular matrix and affect cellular behavior[85].Another study evaluated the effects of human PDLSCs sheets potentiated by an enamel matrix derivative and showed that they had better mineralization capacityin vitro[86].Our group has also been working on the incorporation of specific molecules for transmembrane receptors, as we have shown that the activation of the protease-activated receptor type 1 enhances the osteogenic activity of PDLSCs[87].

New scaffold technologies have also emerged.A better understanding of the mechanisms related to growth factors and the advent of these new technologies that can be combined with the cells highlight the potential of PDLSCs to be applied for future periodontal regeneration[81].

Tissue engineering using PDLSCs can also assist in the neoformation of periodontal tissues on the titanium surface of dental implants, facilitating their fixation and providing better mechanical and immunological properties in patients with a previous history of tooth loss treated by implant replacement therapy.Studies have reported that the use of PDLSCs sheets on the surface of titanium implants stimulate the formation of cementum-like and periodontal ligament-like tissues, both in xenogenic and autologous models[53,88].

In addition, the properties of PDLSCs,e.g., immunomodulation, homeostasis, and remodeling of the periodontal ligament, allow these cells to play an important role in tooth movement during orthodontic treatments.PDLSCs are involved in the control of compression and tension forces caused by the orthodontic movement, as well as in the periodontal ligament recovery process when such forces are removed[89-91].PDLSCs isolated from healthy individuals and those from periodontitis responded differently to static mechanical stress, indicating that the microenvironment of periodontitis directly influences the activity of these cells, making them more susceptible to greater mechanical loads[90,92].

Besides the use of PDLSCs in dental therapies, studies have proposed their use as a source of autologous cells in patients with non-odontogenic conditions, especially considering that their isolation is easier compared to other MSCs[92].Aimed at their use in patients with multiple sclerosis, human PDLSCs obtained from both, healthy and multiple sclerosis patients, were evaluated and showed similar immunophenotypic, proliferative and differentiating properties, which suggests that they may be effective in personalized therapies for such conditions[93].Also, PDLSCs have the potential to be used in corneal regenerative therapy.It was demonstrated that they are able to differentiate into corneal stromal keratocyte-like cells.To date, dental MSCs and the corneal stromal keratocytes share a common embryological origin, which is the cranial neural crest[94].

CLINICAL TRIALS AND TRANSLATIONAL STUDIES WITH PDLSCS

Hematopoietic stem cells have been widely used in humans for several decades, mainly for the treatment of neoplasms and other hematolymphoid disorders.These were the first stem cells described and characterized, and the efficacy and safety of these populations have already been shown by countlessin vitroandin vivostudies[95].In contrast, the description of MSCs is more recent albeit in preclinical studies and clinical trials involving these cells.Clinical studies using dental MSCs are at a less advanced stage than those involving several other stem cells, which can be explained by the lack of well described methods to obtain these cells, and efficient and safe protocols for their use in humans[96].

A search on the ClinicalTrials.gov portal website for registered clinical trials using PDLSCs transplantation for regenerative therapies in humans resulted in only two studies that fit these criteria.A phase I and already concluded trial (NIH Clinical Trial Registration Number: NCT01357785), evaluated 35 patients with periodontitis over a 12-mo follow-up period.Autologous PDLSCs sheets were transplanted into intraosseous defects in association with lyophilized bone, and it was concluded that, despite the good results regarding the absence of adverse effects on patients, there was no statistical difference in relation to the reduction of probing depth (PD)[15].To date, PD is one of the main outcomes evaluated in regenerative therapy for periodontitis.The second study, a phase I and II clinical trial, was registered in 2010 and remains with unknown status so far.Its objective was to transplant PDLSCs from healthy patients into 80 adults (40-50 years) with periodontitis (NCT01082822).

Figure 1 Immunomodulatory periodontology/medicine.

Of note, a pilot clinical study evaluated three patients with periodontitis treated with autologous PDLSCs.A significant reduction in PD and improvement in clinical attachment level were observed in the patients who underwent cell therapy.No adverse effects of this therapy were found[16].

In another study registered with the UMIN Clinical Trials Registry, autologous transplantation of PDLSCs in 10 patients resulted in improvement of PD, clinical attachment level, and radiographic bone height (alveolar bone regeneration).PDLSCs sheets were transplanted in association with β-tricalcium phosphate granules into severe alveolar bone defects.During the 3 and 6-mo follow-up, no adverse effects were noted[97].

Furthermore, it is worth mentioning that there are also ongoing and finalized clinical trials aiming to regenerate periodontal tissues with stem cells from other sources, such as DPSCs (NCT02523651; NCT0338687), bone marrow MSCs (NCT00221130; NCT02449005), and adipose-derived stem cells (NCT04270006).Gingival MSCs are the cell source in two clinical trials that aimed to treat periodontal defects using these cells in collagen (NCT03137979) and β-tricalcium phosphate (NCT03638154) scaffolds.

CONCLUSION

In summary, the regenerative and therapeutic potential of PDLSCs seems to be auspicious from a biological perspective.Clinical studies with these cells are already a reality in regenerative periodontology.No clinical evidence of their application with specific use for immunomodulatory periodontology/medicine has been reported so far.Despite some promising clinical results and biological insights herein discussed (summarized Figure 1), several gaps need to be filled before adopting a protocol for their clinical use in patients with periodontitis or other inflammatory conditions.In this sense, we draw attention to the fact that most studies associate PDLSCs with osteoinductive/osteoconductive materials.These materials, especially those synthetic and xenogenic, can affect therapeutic efficacy and safety by reducing mechanical properties, impairing bone remodeling, and inducing an immunological reaction[98].Standardization of the bone defects in periodontitis affected patients, as well as a larger number of individuals allocation and multicenter trials are also necessary.

In addition, tissue-dependent factors are critical to successful cell therapy with PDLSCs, as the effectiveness of their autologous transplantation also depends on variables such as the number of isolated cells, the microenvironment from which they were collected (the presence of inflammation is a known limitation), the general health status of the patient, and the differentiation pathway after transplantation[99].Basic research in this field still has a long way to go.Defining better protocols for cultivating, storing, expanding, and differentiating PDLSCs is the challenge to ensure safety, reproducibility, and cost-effectiveness of clinical applications.