The oral cavity contains distinct mucosal surfaces, each with its own unique distribution of dendritic cell (DC) subsets. In addition to tissue-specific properties, such organization might confer differential immune outcomes guided by tissue-resident DCs, which translate in the lymph node into an overall immune response. This process is further complicated by continual exposure and colonization of the oral cavity with enormous numbers of diverse microbes, some of which might induce destructive immunity. As a central cell type constantly monitoring changes in oral microbiota and orchestrating T-cell function, oral DCs are of major importance in deciding whether to induce immunity or tolerance. In this review, an overview of the phenotype and distribution of DCs in the oral mucosa is provided. In addition, the role of the various oral DC subsets in inducing immunity vs. tolerance, as well as their involvement in several oral pathologies is discussed.
The term oral mucosa refers to the tissue that lines the oral cavity and is composed of the masticatory and lining mucosa. The masticatory mucosa forms the attached gingiva and hard palate, and its structure allows it to resist the abrasion of rough food particles. The lining mucosa represents the largest part of the oral mucosa, consisting of the buccal, sublingual, and vestibular mucosae. The two major layers of the oral mucosa, namely the epithelium and the underlying connective tissue (termed lamina propria), are equivalent to the epidermis and dermis of the skin. In most oral tissues, a submucosa layer can be found just beneath the lamina propria and is not easily discriminated from it. Similar to the epidermis, the oral epithelium maintains its structural integrity by a process of continuous cell renewal and migration from the deepest layers to the surface in order to replace those cells that were shed. The oral epithelium is a stratified (multi) layer of squamous cells that may be either keratinized or non-keratinized, with the latter being thicker and more permeable. Nonetheless, unlike the intestinal lining, the oral epithelium does not have an adsorptive capacity, although differences in permeability exist in direct correlation to the thickness of the epithelial barrier.1, 2
The oral mucosa exploits various mechanisms to protect the host against invading pathogens. The tough but yet resilient lamina propria provides resistance to tear and compression forces, thus maintaining tissue integrity that is crucial in such an active site that is constantly exposed to microorganisms. Protection from microorganisms is also afforded by cell shedding from the surface layer, therefore minimizing colonization. Furthermore, salivary secretion aids in keeping the oral mucosa moist and limiting excessive bacterial accumulation. In addition to the aforementioned tissue-integral mechanisms, the oral mucosa contains an elaborate immune system. This system is thought to be pro-tolerogenic in nature as the oral mucosa remains in a relative state of health despite the heavy microbial load.3 Still, an inflammatory infiltrate composed mainly of lymphocytes and neutrophils can be regularly detected in the gingiva, even in those considered clinically healthy.4 This emphasizes the complicated mechanisms exerted by the oral immune system in order to maintain immunological homeostasis.
As the most potent cells activating and polarizing naive T cells, oral dendritic cells (DCs) are of major importance in induction of immunity and tolerance. DCs are a heterogeneous population of antigen-presenting cells (APCs) that are widely distributed in lymphoid and non-lymphoid tissues in the steady state.5, 6, 7 These cells can be generally categorized into two classes: conventional DCs and plasmacytoid DCs (pDCs). In their immature state, conventional DCs constantly patrol tissue microenvironments, whereas upon encountering a foreign antigen they efficiently sample it via various pathways. The DCs then migrate to the draining lymph nodes (LNs) while undergoing a maturation process that enables the presentation of pathogen-derived peptides to CD4+ and CD8+ T cells.8 To induce accurate and efficient pathogen-specific immunity, DCs adjust their immune response to the type of pathogen. In contrast to conventional DCs, pDCs are difficult to detect in peripheral tissues; they circulate in the blood and can be found in peripheral lymphoid organs.9, 10 Upon infection, pDCs can enter inflamed tissues, produce type I interferon, and activate T cells in the LNs.11 In recent years, advanced immunological techniques and new mouse models have facilitated in vivo studies that have provided new insights into the developmental and functional aspects of DCs. This progress has also enriched our knowledge regarding the phenotype and function of oral DCs.
DC phenotypes in the murine oral mucosa
Among the various distinct oral mucosal tissues, the buccal, gingival, and sublingual mucosa are the most studied with regard to their DC composition. This may be attributed to the accessibility of the tissue, similarity to a well-characterized non-oral tissue (buccal mucosa and skin), relevance to oral diseases (gingiva), and due to therapeutic interests (sublingual). Nevertheless, these tissues mirror adequately the DC heterogeneity of the oral mucosa, which is discussed below.
Several mouse studies have demonstrated a high resemblance between the buccal mucosa and the skin immune system. At least four different DC subsets can be identified in the buccal tissue based on their expression of CD11c, CD103, Ep-CAM (epithelial cell adhesion molecule), and langerin (CD207): (1) Langerhans cells (LCs) located in the mucosal epithelium, (2) interstitial (or lamina propria) DCs (iDCs), which are the equivalent of dermal DCs, (3) langerin-expressing iDCs that also express the CD103 molecule (Ln+iDCs), and (4) langerin− CD103+iDCs12 (Figure 1). The latter DC population was identified in mice expressing the human diphtheria toxin receptor (DTR) under transcriptional control of the endogenous langerin/CD207 promoter (langerin-DTR). In these mice, a single administration of diphtheria toxin (DT) eliminates langerin-expressing cells (i.e., LCs and Ln+iDCs). Whereas Ln+iDCs return as soon as 3–5 days post-DT injection, repopulation of LCs occurs only after 2 weeks. This allows discrimination between these two DC subsets in vivo by employing a single vs. repeated injections of DT. The CD103+iDC subset was present in mice repeatedly administered with DT, suggesting that these cells do not express langerin like their counterpart Ln+iDCs. The presence of langerin-expressing iDCs in the buccal mucosa was also recently confirmed by another study.13 Of note, an additional population of APCs (presumably macrophages) expressing CD11b but not CD11c (CD11b+CD11c−) exists in the buccal lamina propria in lower numbers than iDCs that express both markers.
The epithelium of the sublingual mucosa is particularly thin and thus provides a useful route of entry for antigens, allergens, and drugs. APCs in the sublingual mucosa have been analyzed by immunohistochemistry and flow cytometry.14, 15 These techniques showed that the frequency of LCs in the sublingual epithelium is much lower than in that of the buccal mucosa.14 CD11c+ CD11b+ cells (iDCs) and a large population of CD11b+CD11c− cells is located in the lamina propria/submucosa interface. Interestingly, pDCs expressing B220+120G8+ are also found, predominantly in the submucosa/muscular area. Another study reported that most APCs in this tissue (CD11b+CD11c− cells) are F4/80+ macrophages, whereas most CD11c+ myeloid DCs also express CD11b (iDCs).15
The gingiva does not contain submucosa and the lamina propria is bound directly to the membrane that lines the outer surface of the alveolar bone. Low percentages of LCs (CD11c+ major histocompatibility complex (MHC) class II+ langerin+ and Ep-CAM+) are located in the gingival epithelium in comparison to buccal and skin tissues.16 Most of the APCs express CD11c+ CD11b+ (iDCs), whereas CD11b+CD11c− cells are also present but in lower frequencies (A-H. Hovav, unpublished). A minor population of iDCs (about 5%) also expresses the CD103 integrin.16 CD103+iDCs that also express langerin are rarely found, thus doubting the presence of Ln+DCs in the gingiva (Table 1).
The phenotypes of DCs described above indicate that, despite constituting an entrance of the aerodigestive pathways, the oral mucosa contains distinct subsets of DCs in comparison to the lung and gut mucosa.17, 18 This probably reflects histological and functional differences such as the type of the epithelium, a multi-layer in the mouth vs. a single layer in the gut and lung, resulting in the presence of LCs only in the oral mucosa. Still, the oral lamina propria contains CD11c+CD11b+ DCs, which are also present in the lamina propria of the lung and small intestine.17, 18 This is also true for CD103+ DCs that are present in the lamina propria of the small intestine but seem to differ from those in the lung, which also express langerin and are located in the epithelial layer.
DC phenotypes in the human oral mucosa
In contrast to mice, characterization of DCs in human oral tissues is limited, and it is generally focused on LCs. This could be related to the abundant presence of human oral LCs in the mucosa in comparison to other myeloid DCs and pDCs.19 Analysis of the gingiva identified langerin-expressing DCs (LCs) in the mucosal epithelium and CD209-positive DCs in the lamina propria, which are considered the equivalent of dermal DCs (Table 2).20 The majority of lamina propria-resident DCs also expressed the mannose receptor (CD206). Gingival LCs can be also identified in the epithelium based on the expression of the CD1a molecules.21 Nevertheless, although both langerin and CD1a can be used to classify LCs, langerin was reported to be a more specific marker.22 Three-dimensional analysis of gingival LCs demonstrated that these cells distribute their dendritic processes toward the gingival surface, reflecting their ability to monitor external stimuli.23 In a recent study, the distribution of LCs in various human oral tissues was examined based on the expression of CD1a.19 The highest numbers of LCs were found in the vestibulum, buccal, palate, and lingual tissues, while lower numbers were observed in the sublingual area and gingiva. Interestingly, these frequencies of LCs are similar to those observed in the mouse (buccal>gingival>sublingual), suggesting high resemblance in this regard between humans and mice. LCs from all human oral tissues expressed also langerin, albeit in a lower intensity than epidermal LCs. Furthermore, these LCs express similar levels of MHC class II and the CD83 maturation marker, suggesting that oral LCs from all tissues are in a similar maturation stage in steady state.19 With regard to pDCs, these cells are present in low frequencies in healthy oral tissues, whereas under inflammatory conditions, significant infiltration of CD123+BDCA-2+ pDCs to the epithelium and lamina propria can be seen.24
Antigen capture and migrational capabilities of oral mucosal DCs
Because of the relatively non-adsorptive nature of the oral mucosa, it is thought that the antigen has to activate or penetrate the epithelium in order to elicit potent immune responses. This could be achieved by mechanical means (i.e., needle, microneedle, and mucoadhesive nanoparticles) or by the intrinsic invasion capability of the immunological insult. The sublingual mucosa is an exception, as the antigen can be easily adsorbed and reach DCs.25 Once capturing antigen, migration of DCs into the draining LNs is critical for the induction of protective immunity as well as for immunological tolerance.26, 27 Following exposure to a pathogen, DCs mature en route to the LNs where they encounter T cells and present the antigen. Although the murine oral mucosa drains directly to the cervical LNs, in humans, distinct LNs drain different areas of the oral cavity that then reach the superficial and deep cervical LNs. Several studies have examined the ability of DCs from various oral mucosal tissues to travel to the draining LNs. In concurrence with the similarity between buccal and skin DCs, migration kinetics of buccal mucosa DCs to the LN is quite comparable with that of skin DCs, albeit in lower numbers.28 By applying fluorescein isothiocyanate (FITC) and the hapten dibutyl phthalate (DBP) to the mouse buccal tissue, it was shown that whereas iDCs rapidly migrate to the LNs, LCs are much slower, peaking at 96 h after hapten application. A more thorough examination demonstrated that buccal LCs migrated to the LNs at a slower rate than epidermal LCs.13 Moreover, in this experimental setting, buccal LCs were found to express lower levels of the co-stimulatory molecules CD40, CD86, CD273 (B7-DC/PD-L2), and CD274 (B7-H1/PD-L1) as compared with other buccal-derived DCs. Aside from these two subsets, a third population of DCs expressing CD11cintermeidate/low also migrated from the buccal mucosa, representing a newly recruited DC subset arriving after FITC application. These cells migrated continuously to the LNs and maintained the highest ratio of all the three subsets.28 Rapid recruitment (within 2–6 h) of inflammatory cells to the buccal mucosa was also observed following topical delivery of DNFB (1-fluoro-2,4-dinitrobenzene) hapten or immunization with measles virus nucleoprotein.29, 30, 31 This recruitment was mediated by the chemokine receptor 6 (C-C motif chemokine receptor 6 (CCR6))/chemokine ligand 20 (C-C motif chemokine ligand 20 (CCL20)) pathway and could be enhanced by FMS-like tyrosine kinase 3 treatment.30, 31 Similar migration of DCs from the buccal and skin tissues was reported after immunization with plasmid DNA.12, 32 Although not verified, it is likely that buccal DCs employ the CCR7-CCL19/CCL21 axis to migrate to the LN, like skin DCs.33, 34 Expression of CCR7 in activated buccal mucosa is in line with this assumption.35 The CCR7-CCL19/CCL21 axis has also been shown to mediate DC migration from the sublingual mucosa.15 Following sublingual application of an antigen, antigen-bearing DCs can be detected in the cervical LNs as soon as 6 h later, with maximal trafficking observed 12 h after the application.36 Finally, migration of gingival DCs to the draining cervical LNs was observed following application of FITC/DBP solution or infection with the oral pathogen Porphyromonas gingivalis.16 Although the precise migration kinetics of each DC subset was not reported, antigen-experienced iDCs, LCs, and CD103+iDCs were found in the LNs 3 days post exposure to P. gingivalis.
Antigen presentation and T-cell induction by oral DCs
Despite being considered a tolerogenic environment, T cells can be efficiently induced by DCs in the oral mucosal immune system. Numerous studies have shown the induction of antigen-specific T-cell responses by buccal DCs following topical or penetrable administration of hapten, protein antigen, and plasmid DNA.12, 29, 30, 37, 38 The sublingual mucosa has also been shown to initiate broad systemic and mucosal antigen-specific protective immune responses (reviewed by Czerkinsky and Holmgren39). Moreover, immune responses induced by sublingual immunization have been reported to surpass those achieved by intramuscular, traditional intranasal, or other oral mucosal immunizations.40 Sublingual administration of adenoviral vectors was able to prime potent protective pathogen-specific T cells and even overcome pre-existing immunity.40, 41 Taken together, these studies provide compelling evidence for T-cell activation by oral DCs upon migration to the LNs.
Nevertheless, migration of tissue-derived DCs to the LNs following infection/immunization does not always indicate that these migratory DCs will directly activate T cells. For example, skin-derived DCs efficiently prime T cells following immunization with lentivirus but fail to do so after infection with herpes simplex virus type 1 (HSV-1).42, 43, 44 The reason for this discrepancy is that HSV-1, but not lentivirus, interferes with the capability of infected DCs to present antigen.45 With regard to HSV-1, it was also suggested that the route of delivery greatly impacts the type of DCs presenting viral antigens. Whereas mucosal infection with HSV-1 triggered direct presentation by mucosal-resident DCs, administration of the virus by needle injection resulted in presentation by LN-resident DCs.46 These findings suggest that the type of immunological insult, as well as the route of entry, have a major impact on the antigen-presenting abilities of oral DCs.
In a recent study examining the mechanisms of immune induction by buccal DCs following DNA vaccination, delayed antigen-presenting activity was observed in mice.12 Presentation of the antigen to CD8+ T cells was mediated mainly by buccal-derived iDCs, while Ln+ iDCs showed limited presentation. This activity is similar to the antigen-presenting activity observed following intradermal immunization with plasmid DNA.32 The skin and buccal tissues also presented similar kinetics of antigen expression, exhibiting maximal expression of the plasmid-encoded antigen 24–48 h post immunization. However, despite the high similarity among these tissues, major differences were found as well. First, restricting antigen expression to CD11c+ cells (i.e., DCs) abrogated CD8+ T-cell responses in the buccal tissues but not in the skin. This suggests that following plasmid DNA immunization, buccal DCs rely on cross-presentation to prime CD8+ T cells. Cross-presentation refers to the ability of certain DC subsets to transfer exogenously derived antigen to the MHC class I, instead of MHC class II pathway, in order to present it to CD8+ T cells.47 It can thus be proposed that some buccal DCs have cross-presenting capabilities. Second, in the absence of LCs, CD8+ T-cell responses induced by buccal immunization with plasmid DNA were considerably reduced, whereas no effect was observed in intradermal immunization.12, 32 Collectively, these observations suggest that DCs of the buccal mucosa engage unique mechanisms for immune induction; therefore, care should be taken when comparing DC function between skin and buccal tissues.
Antigen presentation was also examined following sublingual vaccination using the ovalbumin antigen and cholera toxin as an adjuvant.15 In this system, robust proliferation of CD4+ T cells, and to a lesser extent CD8+ T cells, was observed primarily in the cervical LNs. Sublingual iDCs were shown to transfer the antigen to the LNs, and presentation of the antigen to CD4+ T cells was mediated by both sublingual migratory DCs and LN-resident DCs. Ablation of langerin-expressing cells (i.e., LCs) in this model had no effect on antigen presentation. Interestingly, in a recent study sublingual iDCs were shown to be dispensable in eliciting tolerance against ovalbumin, a function that was mediated by oral macrophage-like (CD11b+CD11c−) cells.36 It is thus likely that in a mouse model sublingual iDCs primarily induce immunity, whereas CD11b+CD11c− cells are involved in mediating tolerance.
The ability of gingival DCs to present antigen and prime T cells was examined almost solely in the setting of experimental periodontal diseases. In this model, mice are infected several times with the oral pathogen P. gingivalis by oral gavage, resulting in local inflammation and CD4+ T-cell-mediated bone loss.16 P. gingivalis–derived peptides were presented mainly by iDCs to both CD4+ and CD8+ T cells. These findings suggest that iDCs located in the lamina propria can take up oral pathogen administered by gavage. This may be explained by the invasiveness of P. gingivalis.48 LCs were not able to present antigen and activate T cells. However, in their absence, activation of CD4+ T cells was increased, suggesting a regulatory role for LCs in experimental periodontitis.16 LN-resident DCs also presented antigens to T cells, albeit at a lower magnitude. As live bacteria were not found in the draining LNs, it is likely that LN-resident DCs acquired antigens arriving via the lymph or from migrating oral DCs. CD103+iDCs were able to present antigen only to CD8+ T cells, albeit to some extent.
Induction of tolerance by oral DCs
Despite continuous exposure to large amounts of antigens derived from food and microbes, the latter could be either commensal or pathogenic, severe inflammatory responses in the oral cavity are relatively rare.3 This is attributed to the tolerogenic properties of the oral mucosa that are critical for maintaining immunological homeostasis. Whereas the mechanisms involved in this process are a subject of extensive investigation, the oral cavity is an attractive site for inducing tolerance against allergens. Particular attention was given to the sublingual mucosa as a site of allergen application.
Studies employing human oral LCs demonstrated higher expression of Toll-like receptors 2 and 4 (TLR2 and TLR4) on oral LCs in comparison to epidermal LCs in steady state.49 In a response to TLR triggering with lipopolysaccharide, oral LCs upregulate expression of the co-inhibitory molecules B7-H1 and B7-H3, whereas expression of the co-stimulatory molecule CD86 (B7-2) is decreased. This resulted in a polarized development of T regulatory (Treg) cells and secretion of interleukin (IL)-10 and transforming growth factor-β by stimulated T cells.50 This suggests that human oral LCs, which are located in the mucosal epithelium and thus exposed constantly to microbial stimuli, act in a tolerogenic fashion to maintain immune homeostasis. An additional support for the repeated exposure of human oral LCs to microbes could be reflected by their higher activation state in the tissue as compared with epidermal LCs. Oral LCs express higher levels of MHC class II, CD86(B7-2), CD80(B7-1), and CD40 molecules and are more effective in stimulating allogeneic T cells than epidermal LCs.51, 52, 53 Of note, expression of the CD83 maturation marker was similar in oral and epidermal LCs, suggesting a state of partial maturation in oral DCs, which may facilitate tolerance as previously proposed.7, 54 Interestingly, partial maturation of oral LCs with tolerogenic properties was observed recently in an ex vivo model of allergen application, a phenomenon that was not detected in epidermal DCs under similar conditions.49
In contrast to the important role of human sublingual LCs in tolerance induction, mouse studies suggested that these cells are dispensable in this process. Instead, macrophage-like F4/80+CD11b+CD11c− cells were shown to polarize T cells into Treg expressing both interferon (IFN)-γ and IL-10 cytokines.36 Furthermore, similar to the tolerogenic macrophages found in the lamina propria of the small intestine, the sublingual CD11b+CD11c− cells express mannose receptor (CD206) and class-2 retinaldehyde dehydrogenase. This dissimilarity could be explained by the relatively lower numbers of LCs in the sublingual mucosa of mice in comparison to human.14, 50 Nonetheless, studies in both human and mice point out that the sublingual mucosa is an attractive immunological site to induce tolerance.
Balancing between tolerance and immunity
The ability of oral DCs to mediate either immunity or tolerance highlights the question of how these cells discriminate between commensals and pathogens. Similar to oral pathogens, oral commensals can induce maturation and activation of monocyte-derived human DCs.55 Thus, it is likely that additional mechanisms other than just a direct recognition of pathogen-specific molecules might be involved. It has been proposed that in the intestine, tissue-resident DCs are educated by epithelial cells to be tolerogenic, whereas newly infiltrating DCs induce inflammatory responses.56 In such a scenario, DCs can tolerate commensals, whereas pathogens capable of invading or activating epithelial cells will trigger the recruitment of pro-inflammatory DCs that will elicit immunity. This could also be the case in the oral cavity, and it might also explain the enhanced tolerogenic properties of the sublingual tissue, which contains a thin epithelium that might be more vulnerable for invasion. Still, in contrast to the intestine, the oral epithelium is a multi-layer tissue that harbors LCs, and thus pathogen recognition might involve additional mechanisms. One possibility is the ability of microbes to cross the epithelium and reach the lamina propria, where iDCs can sample it and activate T cells.57 We recently showed that iDCs prime P. gingivalis–specific T cells following oral gavage, suggesting that P. gingivalis might traverse the gingival epithelium, as previously suggested.16, 57 A recent study proposed that oral pathogen can alter the balance of the oral commensals, which subsequently facilitate local destructive immune responses.58 It is thus possible that under certain conditions commensals can also act as pathogens and activate the immune system. Such a situation might happen when immune regulatory cells such as oral LCs are impaired by constant activation or due to aging. Collectively, it is likely that the decision to react against a certain microorganism depends on its potential to invade the oral mucosa or alter its microbial homeostasis, as well as by the integrity of the oral immune system.
Do oral lymphoid foci exist?
In contrast to other mucosal tissues, which generally contain mucosa-associated lymphoid tissue (MALT) for local immune induction, the oral mucosa lacks such immunological structure. The MALT resembles a lymphoid organ as it contains T cells, B cells, plasma cells, and APCs such as DCs and macrophages, which are well situated to encounter antigens passing through the mucosal epithelium. In the case of Payer’s patches of the intestine, the antigen is sampled by specialized M cells that transfer it from the lumen to the lymphoid tissue.
Studies analyzing human gingiva during periodontitis have noticed an accumulation of mature CD83+ DCs in the T-cell-rich area of the lamina propria.59 In that study, the authors also assumed that LCs migrating from the epithelium contributed to the pool of mature DCs in the lamina propria that interact with T cells. Similar co-localization of DCs and lymphocytes in the lamina propria was also observed by another study.60 Based on these findings, the concept of oral lymphoid foci was established, suggesting that inflamed gingiva might serve as a site for immune induction rather than just an effector site during periodontitis. Interestingly, the notion of oral lymphoid foci was also recently proposed in the context of tolerance induction. It was shown that besides exhibiting a partial maturation state, allergen-experienced LCs migrating from oral tissue explant expressed lower CCR7 levels compared with other migratory LCs.49 As CCR7 mediate migration to the LNs, the authors speculated that low expression of this chemokine receptor might imply migration of LCs to the lamina propria rather than to the draining LNs. Nevertheless, in both cases, there are no direct evidences for the migration and accumulation of mature LCs in the lamina propria. It was demonstrated that LCs alter the expression of matrix metalloproteinases 2 and 9 and their tissue inhibitors during periodontitis, suggesting migration of these cells towards the connective tissue, thus supporting their accumulation in the lamina propria.61 Still, such movement might represent migration to lymphatic vessels that directs LCs to the draining LNs. Another caveat in the concept of oral lymphoid foci is the absence of B cells.59 As abovementioned, in addition to T cells and APCs, the MALT contains also B cells. It is possible that B cells were overlooked during the immunohistochemical analysis of the inflamed gingiva, as another study employing flow cytometry analysis demonstrated that the majority of CD83+ cells in the diseased gingiva were, in fact, B cells.62 Indeed, the presence of CD83+ B cells in the lamina propria was confirmed shortly also by immunohistochemistry, although the relative contribution of DCs and B cells to this mature APC pool is not clear.20 In this regard, B cells were reported to promote expansion of Treg cells in tolerance induced by allergen application via the oral mucosa.63 Also, IL-10-producing B cells were found to restrain inflammation by promoting differentiation of immunoregulatory over pro-inflammatory T cells.64 It is thus possible that the oral lymphoid foci are, in fact, sites in which antigen-experienced mature B cells interact with T cells. Such interaction could facilitate the generation of Treg cells either for tolerance induction or in order to control inflammation during periodontitis. Further investigation is required to verify whether lymphoid foci exist in oral mucosa and what their roles are in immune induction.
The impact of aging and smoking on oral DCs
Accumulating data from non-oral tissues suggested that DC’s function is hampered with age. Although there is no considerable impact on the number and phenotype of myeloid DCs in the blood of healthy aged human,65, 66, 67 their capability to sample antigen, migrate to the LNs, and prime T cells is diminished.65, 68, 69, 70 Aging appears to compromise the ability of DCs to accurately direct immunity vs. tolerance. This could be attributed, in part, to the basic tendency of aged DCs to produce pro-inflammatory cytokines,71 which decreases their stimulation upon exposure to foreign antigen while increasing response against self antigens.71, 72, 73, 74, 75 Interestingly, in contrast to the above observations in the blood, the density of LCs in healthy gingival epithelium was shown to be reduced in aged subjects as compared with young.76 Such age-related differences in the density of LCs were not observed in other healthy human oral tissues,77 while existing in murine oral samples.78 With regard to their morphology, LCs showed fewer dendritic-branching processes and had a rounded shape in the older age group. Reduced numbers of LCs in the gingival epithelium of older individuals was also found during chronic periodontitis.79, 80 In the latter case, LCs of older subjects were located in the upper epithelium and their dendritic processes were shorter and less numerous. The obvious differences between the gingiva and other oral tissues might be related to the presence of a chronic low-grade inflammatory state in the gingiva.81, 82, 83 This might lead to gradual decline in the integrity of the local immune cells, particularly LCs being crucial for maintaining tolerance.16, 84, 85 Of note, an age-dependent decrease in the number of LCs was also observed in the epidermis.68, 86 Similar to the gingival epithelium, this might be partly due to the result of constant exposure to sunlight, which was shown to reduce epidermal LCs numbers.87
Smoking is a significant risk factor for various oral pathologies.88 Although the precise mechanisms remain to be elucidated, there are observations that tobacco smoking can affect oral DCs. Nicotine, a constituent of cigarette smoke, was recently shown to modulate the immunoregulatory function of DCs that were exposed to lipopolysaccharide of P. gingivalis.89 Nicotine-experienced DCs preferentially induced T helper type 2 (Th2) responses and decreased Th1 responses, an activity that was partially mediated by upregulation of the peroxisome proliferator-activated receptors-γ, which has immunomodulatory properties.90 In agreement with the ability of smoking to modulate DC function in vitro, it was shown that smoking reduces the ability to mount and maintain an effective defense reaction to plaque accumulation.91 This could be attributed to a decrease in the quantitative distribution of oral LCs and DCs during chronic gingivitis in smokers.92 A decrease in the density of oral LCs was observed in the context of smokeless tobacco as well.93 Taken together, it is likely that smoking alters oral DC function in a manner that might facilitate the development of oral diseases.
The involvement of DCs in oral pathologies
As DCs are essential for initiating immune responses, they also have a central role in the generation and perpetuation of immune-mediated diseases. Indeed, DCs of the oral mucosa were demonstrated to be directly involved in various oral diseases. Furthermore, a very recent study even proposed the involvement of DCs harboring oral pathogens during chronic periodontitis with coronary artery disease.94 This suggests that besides of being involved in oral diseases, oral DCs might also have a systemic impact on the host.
It is well established that whereas bacterial plaque is essential for the initiation and progression of chronic periodontitis, tissue damage is mediated primarily by the host immune response developed against the accumulating bacteria.95 In a murine model of periodontitis, CD4+ T cells were found to have a critical role in the destruction of alveolar bone, the hallmark of this disease.96 Particularly, expression of receptor activator of NF-κB ligand (RANKL), a molecule involved in the regulation of bone remodeling by CD4+ T cells, was proposed to have a critical influence on bone resorption.97, 98 As the key cells activating and regulating T cells, DCs and LCs were suggested to have an important role in the transition of human periodontitis-associated immune responses from protective to destructive. LCs seems to be of major importance in this aspect due to their localization in the gingival sulcular epithelium, thus putting them in a perfect position to survey the development of bacterial plaque.19, 23, 99 In agreement, the number of LCs in the gingiva increases as dental plaque accumulates, whereas its removal results in their decrease.100, 101, 102 These observations suggest that oral LCs respond to changes in the oral microbiota and local inflammatory status. Further verifications to this hypothesis were obtained from analysis of individuals with chronic periodontitis in which lower numbers of LCs were found in the oral epithelium as compared with gingivitis or health.103, 104 Moreover, it was demonstrated that the numbers of LCs are significantly reduced as periodontal disease progressed.105, 106 It should also be noted that aging and smoking increase the prevalence of periodontitis,107, 108 two conditions by which epithelial LCs network is damaged.76, 77, 92 Based on these observations, a recent study was set up to directly address the role of LCs in experimental periodontitis.16 Using Langerin-DTR mice to ablate LCs in vivo, it was shown that the absence of LCs during experimental periodontitis increased alveolar bone loss. LCs were shown to downregulate the generation of destructive RANKL-expressing CD4+ T cells by inducing higher numbers of Treg cells. These results proposed a protective role for oral LCs during periodontitis.
Oral lichen planus
Oral lichen planus (OLP) is a chronic oral inflammatory disease of unknown etiology. The disease is characterized by a massive infiltration of lymphocytes, mainly T cells, which chronically destructs the epithelium basal layer resulting in an abnormal epithelial keratinization cycle. Early studies demonstrated the presence of activated LCs/DCs in the OLP infiltrate, suggesting their involvement in disease progression.109, 110 Although discrepancies exist regarding the numbers of LCs in OLP tissues24, 110, 111, 112, 113 (probably due to the differences in tissue sampling and techniques), it suggests that LCs might have a role in the disease. More recent studies identified accumulation of mature LCs and DCs in the submucosa of OLP biopsies, and these cells were co-localized with lymphocytes.111, 113 Such cellular organization was proposed to allow ongoing presentation of self antigen to T cells that facilitate tissue destruction. Interestingly, such contact between mature DCs and T cells in the oral mucosa, which was observed also by other studies,114, 115 supports the concept of the oral lymphoid foci discussed above. Beside myeloid DCs, pDCs were also observed in OLP and were found adjacent to mature DCs.24 These pDCs were shown to secrete IFN-α and to contain granzyme B, thus proposed to facilitate DC maturation and to synergize lymphocytes in tissue destruction.
Sjögren’s syndrome is a chronic systemic inflammatory and lymphoproliferative autoimmune disease of unknown etiology. It is characterized by dryness of the mouth and eyes due to progressive infiltration of immune cells into the salivary and lacrimal glands, which decreases their glandular secretion. CD4+ T cells with cytotoxic capability were shown to be the predominant cells mediating infiltration into the glands; still, CD8+ T cells, B cells, and plasma cells are also present.116, 117 As activation of the type I IFN system has been described in the salivary gland of Sjögren’s syndrome patients, pDCs were proposed to have a role in the disease.118, 119 pDCs are considered to be the main type I IFN-producing cells,120, 121 and analysis of diseased salivary glands identified IFN-α-producing cells while no pDCs were observed in healthy glands. Interestingly, the increase in pDC numbers in the salivary gland was accompanied by a reduction of their numbers in the blood.122 In addition to pDCs, myeloid DCs also seem to have a role in the pathogenesis of Sjögren’s syndrome. It was shown that the levels of blood myeloid DCs decrease in the peripheral blood of Sjögren’s syndrome patients, while preferential trafficking of these cells to salivary glands was observed in the early stage of the disease.123, 124 Following entry to the glands, myeloid DCs were proposed to activate Th1 cells.123 A contribution of infiltrating monocytes to the pool of mature DCs in the salivary gland was also suggested.125
The complexity of the oral immune system might reflect the diverse immunological challenges constantly faced by this tissue. DCs have a critical role in linking innate and adaptive immunity, as well as in mediating immunity or tolerance. Thus, oral DCs should be thoroughly studied in our attempt to understand oral immunity. Unfortunately, we know very little about the function of oral DCs, and as indicated in this review, it is not always possible to extrapolate their function from their counterparts in non-oral tissues. Future works should investigate how DCs in different oral immunological niches respond to a given immunological insult, and how simultaneous activation of these sites is integrated in the LNs for an overall immune response. In addition, it is important to characterize the type of monocytes entering the oral mucosa during inflammation. Some of these infiltrating cells could differentiate into DCs and may be involved in immune induction. Answering such questions will increase our knowledge of the mechanisms engaged by the oral immune system, facilitating their translation into novel therapeutic approaches.
This work was supported by the Israel Science Foundation (grant no. 1418/11 to A-HH), the German Israeli Foundation for young investigators (GIF Young), and the Dr. I. Cabakoff Research Endowment Fund at the Hebrew University-Hadassah School of Dental Medicine, Jerusalem, Israel.
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