Regulation of lung immunity by dendritic cells: Implications for asthma,chronic obstructive pulmonary disease and infectious disease

Abstract

Since the first description of dendritic cells by Steinman and Cohn in 1973, this important cell type has gained increasing attention. Over 4000 papers have been published on this topic annually during the last few years. At the beginning, dendritic cells were recognized for their immune stimulatory properties and their importance in initiating an adaptive immune response. Later, it was found that dendritic cells do not only initiate but also regulate immune responses. This attribute makes the so-called regulatory dendritic cells highly important for the prevention of exaggerated immune responses. Immune cells make contact with different Ags every day and must be tightly controlled to prevent excessive inflammation and subsequent organ destruction, particularly in organs such as the gut and lungs. Here, we give a brief overview of our current knowledge on how immune responses are controlled by dendritic cells, highlighting how they are involved in the induction of peripheral tolerance. We focus on what is known about these processes in the lung, with a closer look at their role in the induction and control of diseases such as bronchial asthma, chronic obstructive pulmonary disease and lung infections. Finally, we summarize some current approaches to modulate the behavior of dendritic cells that may hopefully lead to future therapeutics to control exaggerated immune responses.

Keywords

Asthma COPD tolerogenic dendritic cell anergy

The role of dendritic cells in innate and adaptive immunity

Dendritic cells (DCs) were first described by Steinman and Cohn in 1973 as a distinct population of immune cells in the spleen of mice.¹^,² This cell type was subsequently identified in all lymphoid tissues and many other organs, and is particularly detectable in the epithelium.³ DCs are a highly specialized cell population able to present peptides bound to the proteins of the MHC on their surface.⁴ Proteins from the cytosolic compartment are cleaved via the proteasome, transported to the lumen of the endoplasmic reticulum and bound to MHC class I molecules, the MHC I peptide complex is then transported to the cell surface. Proteins from the environment surrounding the cell are continuously engulfed by pinocytosis or when opsonized by Abs, or complement can be taken up by receptor-mediated endocytosis later being cleaved to generate peptides in the endosomal compartment.⁵ Subsequently, these peptides are loaded on MHC class II molecules and transported to the cell surface. Although peptides from exogenous proteins are predominantly displayed on MHC II, they can also be presented on MHC I via cross-presentation.⁶ Similarly, proteins from the extracellular compartment can enter the endoplasmic reticulum to be presented on MHC I molecules. Therefore, a portion of the proteins engulfed are transported from the phagosomes to the cytosol via retro-translocation. In contrast, proteins from the cytosol can be brought to the endosomal compartment via autophagy and, in this way, introduced into the MHC II presentation pathway. Cross-presentation is important not only for the induction of antiviral and antitumor immunity, but also in peripheral tolerance.⁷

In their role as professional APCs, DCs are the most important immune cells for the activation of T lymphocytes.⁸ This is particularly clear due to the recent advances in immunological tools such as transgenic mice.⁹ However, in their bridging role between innate and adaptive immunity, DCs do not only play a role in the protection against pathogens, but also in the induction and the perpetuation of diseases such as asthma.¹⁰ The activation status of DCs decides the activation or inhibition of a T cell. Activated DCs differ from resting cells in their shape and the expression of specific membrane receptors. The expression, for instance, of CD40, CD80, CD83, CD86 and CD252 (OX40 ligand), the so-called costimulatory molecules, were all shown to have an impact on the activation of T lymphocytes.⁴^,^11–13 All these membrane receptors are expressed at low-density under steady state conditions but become up-regulated after DC activation. This gives the DCs the license to activate naive T lymphocytes, given that the MHC-presented peptides are recognized by the specific T-cell receptor.¹⁴

Different exogenous signals can trigger the productive activation of DCs after binding to their PRRs. The large group of molecules belonging to the PAMPs provide the ligands for the PRRs.¹⁵ The PRRs can be divided into the Toll-, NOD- and retinoic acid (RA)-inducible gene I-like receptors predominantly recognizing bacterial and viral PAMPs and the C-type lectin receptors (CLR) detecting glycostructures from fungi and from bacteria. In addition to these pathogen-derived signals, endogenous ‘danger signals’ coming from dying cells and necrotic tissues can further lead to the activation of DCs.¹⁶^,¹⁷ Later, these danger signals were called a damage-associated molecular pattern and shown to activate the inflammasome leading to maturation of strong pro-inflammatory signals such as IL-1β and IL-18.¹⁸ The production of cytokines plays an important role not only in the regulation of the induced T-cell response regarding T-cell polarization into subpopulations, but also in preventing exaggerated T-cell responses.

The phenotype of different DC subsets of the lung

Conventional DCs (cDCs), plasmacytoid DCs (pDCs) and macrophages of the tissues are derived from Lin⁻cKit^intCD115⁺Flt3⁺ common progenitors.¹⁹ These cells are generated in the bone marrow, from where they start to populate the lymphatic tissues and different organs. Mouse cDCs are characterized by their high expression of CD11c, whereas mouse pDCs only express low levels of CD11c but do express additional characteristic markers, such as CD45R (B220) and CD317 (PDCA1). Many cDCs are found in the mucosa of the conducting airways.²⁰ They protrude their pseudopodia between the epithelial cells to capture Ag from the airway lumen. In addition to CD11c, these cDCs partially express the integrin CD103, which is a specific marker for a subset of lung cDCs (cDC1). The other subset of cDCs express CD11b in addition to the CD11c marker (cDC2). When a trigger of airway inflammation is encountered, another population of cells comes into play, the inflammatory DCs. They are generated from Ly6C⁺ blood monocytes under the influence of a granulocyte macrophage colony stimulating factor. These inflammatory CD11c⁺ and CD11b⁺ DCs retain the monocytic marker Ly6c.²¹ This cell type shows many similarities to the widely used DCs generated in vitro that can be utilized, for instance, to sensitize mice via their airways.²² The pDCs can also be detected in the conducting airways, although in a lower density, and they have also been described as present in lung parenchyma.²³ Human DCs can generally be divided in similar subgroups to their murine counterparts.²⁴ However, there are additional markers used for the characterization of human DCs in addition to markers such as CD11c, also common for human DCs. The different subsets of human lung cDCs express CD141 (BDCA3) on cDC1 cells and CD1c (BDCA1) on cDC2 cells, respectively.²⁵ Human lung pDCs express CD303 (BDCA2) and CD304 (BDCA4).

Induction of peripheral tolerance by DCs

There are distinct immunological mechanisms responsible for the induction of tolerance of T lymphocytes to harmless Ags. Central tolerance is induced in the thymus during the interaction of maturing T cells with specialized thymic epithelial cells and DCs presenting a huge repertoire of self-Ags. Even tissue-restricted Ags are produced under the influence of the transcription factor, Auto Immune Regulator. However, it is known that some potentially autoreactive T lymphocytes leave the thymus, because not every possible auto-Ag is presented.²⁶ Induction of peripheral tolerance comes into play to prevent the activation of these potentially autoreactive T lymphocytes. Three distinct mechanisms of peripheral tolerance induction by DCs are known: activation of regulatory T cells (T_reg), induction of anergy in Ag-specific T cells and negative feedback regulation.²⁷

Negative feedback regulation

Negative feedback regulation in DCs means extracellular stimulation addressed to DCs, which leads to a tolerogenic DC phenotype (Figure 1a). An example of this feedback regulation is the action of IL-10 on DCs. The source of this anti-inflammatory cytokine could be, for example T_reg, known to be good producers of IL-10, which may act in a paracrine manner on the DCs, arresting the latter in an immature state with low expression of costimulatory molecules. Another possibility is that the IL-10 released acts in an autocrine manner after being induced, for instance, by activation of the CLR, for example, DC-specific ICAM3-grabbing non-integrin (DC-SIGN).²⁸ This mechanism is thought to be involved in the dormancy of mycobacteria infection, since polysaccharides of the cell envelope of, for example, Mycobacterium tuberculosis, are known to activate DC-SIGN and, therefore lead possibly to anergy induction in T-helper cells. Another example of such a negative feedback is the direct cell contact-dependent interaction of DCs with T_reg. This interaction was shown to be extraordinarily strong and may lead to down-regulation of costimulatory molecules on DCs.²⁹^,³⁰ This negative feedback given by T_reg can lead to enhanced anergy induction by DCs after interaction with an Ag-specific T cell. It has been shown more recently that DCs also respond to the cytokines of the WNT family. Canonical signaling via β-catenin is able to down-regulate the NFκB pathway and may, therefore, block DC activation by PAMPs or cytokines, leaving the DC in a tolerogenic state.³¹ Similarly, signaling through DC receptors with intracellular immunoreceptor tyrosine-based inhibitory motif domains (results in the inhibition of the NFκB pathway and results, therefore, in negative feedback regulation.³²

Figure 1.

Negative feedback regulation (a): IL-10 is secreted in a paracrine manner by regulatory T cell (T_reg) and by dendritic cells (DCs) in an autocrine manner upon activation of DC-specific ICAM3-grabbing non-integrin (DC-SIGN), which is a carbohydrate receptor containing an immunoreceptor tyrosine-based inhibitory motif domain. The T_reg can adhere very strongly to DCs via LFA-1 and ICAM-1. These mechanisms result in the down-regulation of costimulatory molecules on DCs. Induction of anergy (b): the longest known way to induce anergy is via Ag presentation in the absence of costimulation. This way is known in T-helper cells and via cross-presentation in cytotoxic T cells. Anergy induction is enhanced by the interaction of cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) with B7 molecules on DCs or the binding of PD1 to PD-L1. Induction of T_reg (c): CD103-positive DCs secrete TGFβ1 and retinoic acid (RA), which leads to the induction of T_reg in the absence of IL-6. Activity of indoleamine 2,3-dioxygenase (IDO) in DC catalysis the production of kynurenine, which may bind to the aryl hydrocarbon receptor (AHR) in T cells. Without a ligand, the AHR transcription factor is localized in the cytoplasm in complex with other proteins. Upon ligand binding, its conformation changes and a translocation into the nucleus takes place, where AHR can activate gene transcription and the activation of T_reg. The amino acid sensors mammalian target of rapamycin (mTOR) and general control nonderepressible 2 (GCN2) kinase are influenced by tryptophan deficiency as a result of IDO activity. This contributes, on the one hand, to anergy and suppression of effector cells and, on the other hand, to a hyperactivation of T_reg.

Induction of anergy

Induction of anergy or clonal deletion of specific T cells is a second mechanism by which DCs can establish peripheral tolerance (Figure 1b). One well-known pathway to induce anergy in specific T cells is the presentation of Ag in the absence of costimulation; this was shown for T-helper cells³³ and for cytotoxic T cells.³⁴ The constant uptake of auto-Ags from the surrounding tissues by DCs is important for anergy induction. This mechanism has already been exploited by delivering Ag via targeting endocytic receptors, such as CD205 (Dec205).³⁵ Cross-presentation of engulfed Ags via MHC I is an essential mechanism for tolerizing cytotoxic T cells.³⁶ As has already been mentioned, anergy induction is observed when Ag is presented in the absence of costimulation, i.e. the lack of expression of CD80/86 and cytokines. Anergy induction by DCs can also be facilitated when DCs express certain molecules, such as IL-10, discussed above, or the membrane receptor PD-L1, which interacts with PD1 on the T cell.³⁷ The interaction between PD1 and its ligand on DCs is such an important mechanism in anergy induction that there have already been several clinical studies showing promising results in the reactivation of the immune response against tumor cells in cancer patients by blocking this interaction and, therefore, preventing the anergy of tumor-Ag-specific T cells.³⁸ Another example of such a negative regulation is the interaction of DCs with T cells expressing cytotoxic T-lymphocyte-associated protein 4 (CTLA-4).³⁹ CTLA-4 binds to CD80/86 with a greater affinity than CD28, leading to the down-regulation of T-cell activity. CTLA-4 can capture its ligands, CD80 or CD86, from cells presenting Ag by a process of trans-endocytosis. The costimulatory molecules are degraded in the CTLA-4-expressing cells. By this depletion, CTLA-4 acts as an effector molecule to inhibit CD28 costimulation.⁴⁰ Additionally, CTLA-4 induces the production of indoleamine 2,3-dioxygenase (IDO) in DCs. The role of IDO in tolerance induction is discussed in the following chapter.

Induction of T_reg

The T_reg are a highly important group of lymphocytes that protect the body from autoimmune responses. The essential role of these cells becomes clear in mouse models where T_reg were depleted. Fatal autoimmunity was observed in this model even when the cells were depleted later in life.⁴¹ In addition to naturally occurring T_reg that are already preformed in the thymus, inducible T_reg are induced by DCs with TGFβ1 in the absence of IL-6, leading to the expression of the transcription factor Foxp3 (Figure 1c). Interestingly, the activation of inducible T_reg also relies on conventional signals for T-cell activation, such as MHC II molecules and costimulation via CD80/86.⁴²^,⁴³ The cDCs expressing CD103 are a source of TGFβ1 and known to be potent inducers of T_reg in models of oral tolerance induction.⁴⁴ The RA produced by the enzyme retinaldehyde dehydrogenases expressed by these cDCs stabilizes the T_reg lineage. However, it seems to be important that RA signaling is in context with TGFβ signaling, otherwise RA can also have pro-inflammatory roles.⁴⁵ Human CD1c⁺ DCs were also shown to be capable of producing RA under the influence of vitamin D3.⁴⁶ Another molecule involved in the peripheral tolerance induction by DCs is the enzyme IDO. The importance of IDO for peripheral tolerance was first identified due to its important role in the protection of the fetus against attacks from the immune system.⁴⁷ IDO acts through its enzymatic activity; it catalyzes the production of kynurenine from tryptophan. Kynurenine is a natural ligand of the aryl hydrocarbon receptor (AHR) and the consumption of tryptophan by IDO activates the amino acid sensors general control nonderepressible 2 and mammalian target of rapamycin. IDO activity facilitates the suppression and anergy of effector cells, on the one hand, and boosts the activity of T_reg cells existing already, on the other hand.⁴⁸

Regulation of inflammation by DCs in asthma

The DCs play an essential role in the induction and regulation of the asthmatic response. After the first contact with the allergen, they transport these to the bronchial lymph nodes and activate allergen-specific T cells. When DCs are eliminated by in vivo depletion of all CD11c-expressing cells during the sensitization phase in a mouse model of asthma, the characteristic features of asthma are abrogated.⁴⁹ Meanwhile, the cells and processes involved in allergic sensitization via the airways are understood in more detail. After contact with allergen, the airway epithelium is exposed to adjuvants, such as proteases, PAMP and pollen-associated lipid mediators, leading to the release of chemokines and the alarmins IL-25, IL-33 and Thymic stromal lymphopoietin, resulting in the recruitment of innate lymphoid cells and DCs, such as cDC2 cells expressing CD11b.⁵⁰ This highly migratory DC population transports the allergens to the lymph nodes to induce an allergen-specific Th2 response. Although the precise phenotype these migratory cells must achieve to elicit Th2 immunity in the secondary lymphatics has yet to be described, some parameters have already been revealed to be relevant. The expression, for instance, of OX40L on the surface of DCs due to the contact with TSLP was shown to be relevant.⁵¹ Moreover, it was believed that the expression of Jagged-2 on DCs is important in delivering signals via Notch receptors on T cells resulting in Th2 differentiation. However, this model has been challenged recently, because it was shown that the expression of Jagged-1/2 is dispensable for the induction of a Th2 response.⁵² IL-6 was shown to be significant regarding soluble factors that are important for Th2 induction and are released by DCs.⁵³^,⁵⁴

The skin, gut and lungs are the most important contact zones between environmental Ags, such as allergens, and the immune system. Therefore, it is thought the healthy human contact with harmless Ags does not lead to an allergic sensitization. Indeed, it was shown that contact with a foreign Ag via the airways without an adjuvant leads to tolerance induction.⁵⁵ This peripheral tolerance induction is mediated by transient production of IL-10 by DCs, leading to the generation of IL-10-producing Ag-specific T_reg. The regulatory DCs described in the study of Akbari et al. were likely to be cDCs, because of their high expression of MHC II and Dec205. Newer studies have shown that induction of T_reg to inhaled Ags is attributable to CD103⁺ cDCs. These cDCs up-regulate RALDH upon contact with the Ags and start to produce RA, which, in turn, leads to the generation of T_reg-expressing Foxp3.⁵⁶ Interestingly, the transcription factor Foxp3, known for its importance in determining the fate of T_reg, has also been shown to be expressed by tolerogenic DCs of the lung.⁵⁷ Because Foxp3 is known to bind to the promotor of TGFβ, these cells are good TGFβ producers, thereby inhibiting T-cell activation.

In addition to these reports indicating that cDCs may induce tolerance under certain conditions, pDCs were also shown to play an important role in the induction of tolerance against harmless Ags by transporting them to the regional lymph nodes.⁵⁸ In the case of oral tolerance induction towards gastrointestinal Ags, they play a pivotal role by the induction of T_reg.⁵⁹ The pDCs were also shown to be essential in the induction of tolerance to harmless Ags in the lungs under steady-state conditions and to be of merit in suppressing ongoing allergic sensitization when transferred adoptively.⁶⁰ This discovery reveals pDCs are a highly relevant target to be exploited for the control of allergic inflammation. There are first reports showing that the attraction of pDCs by treating mice with Flt3L resulted in down-regulation of the allergic immune response.⁶¹ However, one must be very careful when manipulating the Janus-faced DC network, because there have been recent reports showing that pDCs may also be involved in the exacerbation of allergic asthma.⁶²

Regulation of inflammation by DCs in chronic obstructive pulmonary disease

The role of DCs in chronic obstructive pulmonary disease (COPD) pathogenesis is more obscure than their role in asthma. One reason for this might be the undefined nature of Ags involved in COPD immune response. By contrast, the Ags (allergens) playing a role in asthma are well defined and can be used as a tool to study the interaction of DCs with specific T cells. Interestingly, newer studies have shown that autoimmunity consisting of both autoreactive T cells and B cells are involved in the pathogenesis of COPD.⁶³^,⁶⁴ Although the precise contribution of this maladaptive autoimmune response in COPD has yet to be revealed, it shows that at some time during disease development, auto-Ags have to be presented by DCs to activate autoreactive T cells. Nevertheless, it is known that cigarette smoke, the leading cause for the development of COPD, attracts cDCs into the human lung.⁶⁵ The infiltrating DCs have an activated phenotype with the expression of costimulatory molecules, such as CD83.⁶⁶

Because cigarette smoke is a source of high amounts of ligands for the AHR,⁶⁷ one would think there must be a continuous stimulation of the AHR due to smoking leading to the induction of tolerogenic DCs.⁶⁸ Indeed, there are reports showing that deletion of the AHR in mice resulted in enhanced inflammation upon smoke exposure.⁶⁹ However, it is still unclear whether the increased inflammation depends on a dysfunction of regulatory DCs. Intriguingly, a subset of human lung cDCs, the cDC2 expressing CD1c, was demonstrated to exhibit enhanced tolerogenic activity in COPD patients.⁷⁰ These cDC2 expressed tolerogenic surface molecules, such as PD-L1, and were potent inducers of T_reg cells exerting their immune regulating activity via production of IL-10 and TGFβ1. From this study, the question arose of whether this regulatory activity may predispose COPD patients to respiratory infections leading to exacerbation of the disease. However, pDCs were also discussed as having an immune suppressive role due to smoking.⁷¹ In this report, Sorrentino et al. showed that murine cDCs exposed to cigarette smoke attract pDCs to the lung that subsequently suppress the immune response to Chlamydophila pneumoniae, presumably involving an IDO-mediated mechanism. A similar accumulation of pDCs was found in lung bronchial-associated lymphoid tissue in COPD patients.⁷² In contrast to the report in the murine model system, it was not investigated whether the accumulating pDCs have immune-suppressive properties. However, treatment of human pDCs with cigarette smoke extract renders the cells reluctant to activation with agonists of TLR7 or TLR9, suggesting they become unresponsive to the virus. Such a state of enhanced susceptibility to virus infection with influenza and respiratory syncytial virus is known to be one of the major problems in advanced COPD, often leading to the exacerbation of the disease.

Regulation of the immune response by DCs during respiratory infection

The most obvious and important role of DCs in the lungs is protection against respiratory infections by bridging innate and adaptive immunity to mount a robust adaptive immune response towards pathogens. Following influenza infection, cDC1 migrate from their intraepithelial origin to the draining mediastinal lymph nodes, where they can activate cytotoxic T lymphocytes.⁷³ The cDC2 are attracted and activated by alarmins secreted by airway epithelial cells that were stimulated with PAMPs. These cells are also involved in the activation of T cells, but they are thought to activate predominantly T-helper cells via the presentation of virus Ag on MHC II.⁷⁴ The pDCs are important cells particularly in defense against a virus. They are known for their high capacity to produce type 1 IFN, but they are also able to activate T lymphocytes via Ag presentation. It was shown recently that pDCs must be directly infected by influenza A to induce highly effective cytotoxic T-cell response.⁷⁵ By contrast, pDCs stimulated with respiratory syncytial virus (RSV) do not directly activate T cells.⁷⁶ They seem to support the immune response against RSV predominantly by producing type 1 IFN. The importance of this for the control of the RSV infection was shown in mice by in vivo depletion of pDCs. In pDC-depleted mice, there was reduced viral clearance and enhanced RSV-mediated pathology.⁷⁷ The most severe RSV infections causing a bronchiolitis often requiring hospitalization are found in neonates. One reason for this might be that their immune system is still developing and the pDC compartment was shown to be immature. It was shown in neonatal mice that RSV infection leads to inefficient pDC activation, with an inadequate type 1 IFN response leading to problems in the control of virus infection. By contrast, the pDCs of adult mice were infected efficiently, consequently releasing IFN-α.⁷⁸ As discussed earlier, pDCs may be involved in protection against de novo sensitization to allergens. Because sensitization is thought to occur predominantly during early infancy, it is interesting to speculate that this is due to the immature state of the pDCs. Intriguingly, Tsuchida et al. showed that the RSV infection of adult mice subverts pDCs allergy-protective activity, leading to aggravated asthma, as shown earlier.⁷⁹ Similar to the RSV, mouse, pneumovirus (PVM) belongs to the group of Paramyxoviridae. Infection of mice with pneumovirus once more reveals the importance of pDCs in prevention of severe bronchiolitis.⁸⁰ Although they are not directly anticipating virus elimination, they prevent excessive inflammation by T_reg induction via semaphorin 4a. What was shown to be beneficial in the prevention of exaggerated inflammation due to infection with virus was also found to contribute to the pathogenesis of the fungal infection mediated by Paracoccidioides brasiliensis.⁸¹ In this report, the authors demonstrated that elimination of pDCs resulted in decreased T_reg numbers and an enhanced immune response against the fungus, leading to a reduced microbial burden. Later, the same authors showed the activation of IDO leading to the formation of AHR ligands is involved in the activation of T_reg that suppresses the anti-fungal Th17 immune response.⁸² Similarly, it was shown in tuberculosis that the activity of T_reg contributes to the persistence of M. tuberculosis in the host lung of patients who are extensively drug resistant.⁸³ The exact pathways leading to activation of these T_reg are still unknown, although there are some reports showing that cell wall compounds of mycobacteria may modulate the behavior of DCs in favor of T_reg induction. Geitjenbeek et al. showed that mannosylated lipoarabinomannans from the cell envelope of mycobacteria bind to the CLR DC-SIGN on monocyte-derived DCs leading to enhanced IL-10 production by the DCs.⁸⁴ The authors provide further evidence that this leads to negative feedback inhibition preventing the activation of DCs. In contrast, it is conceivable that the DCs producing IL-10 will contribute to T_reg differentiation, because it is known that IL-10 is able to potentiate T_reg formation.⁸⁵ Later, it was shown that DC-SIGN-modulated IL-10 production may be involved in the down-regulation of the immune response against several different pathogens.⁸⁶

‘Therapeutic’ induction of tolerogenic DCs

The first efforts to exploit DCs for clinical purposes came from trials to induce a tumor-specific immune response. However, the predominant proportion (> 90%) of clinical trials applying DCs is made to enhance the anti-tumor response. Due to the awareness that DCs not only induce but also suppress T-cell responses, new efforts were made to manipulate DCs in such a way that they induce tolerance. Tolerogenic DCs are already in use in some clinical trials to treat autoimmune disease, such as multiple sclerosis, type 1 diabetes, rheumatoid arthritis or to prevent organ rejection after transplantation. Several substances were shown to have the property to induce DCs with a tolerogenic behavior. For instance, dexamethasone, a drug that has been used for many years to control inflammation, was shown to activate tolerogenic DCs.⁸⁷ Treatment of human DCs with this anti-inflammatory drug leads to cells in a semi-mature state that express high levels of PD-L1. Cultivation of DCs treated with dexamethasone alongside T cells leads to the activation of T cells producing IL-10. Similarly, DCs that were treated with rapamycin are able to induce T_reg responses.⁸⁸ Here, the authors showed that rapamycin-treated DCs that were loaded with allo-Ags led to the longtime survival of skin allografts in rats. In addition to small-molecule drugs that were used for the induction of tolerogenic DCs, there are studies revealing a pronounced activity of distinct cytokines in the induction of tolerogenic DCs. Both IL-10 and TGFβ1 in particular are under extensive investigation. Different protocols were described to differentiate tolerogenic DCs under the influence of IL-10 with or without TGFβ1.⁸⁹ The DCs treated with IL-10 have shown their immune regulatory behavior in several animal models and it is believed they can also be of benefit for the treatment of patients.⁹⁰ However, the stimulation of DCs with PRR or CLR ligands to generate cells that produce IL-10 on their own could be even more efficient in generating tolerogenic DCs to regulate immune responses. The advantage of this would be that these cells, on the one hand, lead to the activation of T_reg and, on the other hand, arrest themselves in an immature state via negative feedback regulation. Some substances have already been shown to act in that way via activation of TLRs or CLR.^91–94 The stimulation particularly of DCs via CLR seems to be effective in generating tolerogenic DCs.⁸⁴^,⁹⁵^,⁹⁶ Treatment with substances aiming to induce tolerogenic DCs do not necessarily occur ex vivo and in vivo induction of tolerogenic DCs is possible, for example, by the targeting of Ag to DC receptors such as DEC205.⁹⁷ Several examples for the manipulation of DCs to induce tolerance are given in Table 1.

Table 1.

Examples of substances known from the literature to induce tolerogenic DCs and their mode of action. Most experiments are performed in mouse models of allergic disease.

Substances for stimulation of DCs	Disease	Mode of action	Reference
Arabinogalactan	Murine asthma model	IL-10 production by DCs	⁹⁸
Cowshed dust extract	Murine asthma model	IL-10 production by DCs	⁹²
Bacterial lipopeptides	Murine asthma model	IL-10 production by DCs, IRAK-M induction, arrest in immature state	⁹¹
Immune complexes Ag and sialylated IgG	Delayed type hypersensitivity (mouse model)	Arrest in immature state, inhibition of IL-12/23 and IL-6 release	⁹⁹
Lactobacillus reuteri and Lactobacillus casei	In vitro studies with human cells	DC-SIGN ligation activation of IL-10 producing T_reg	¹⁰⁰
Lactococcus lactis	Murine asthma model	TLR13 activation	⁹⁴
Complement (C5a)	Murine asthma model	Attraction of pDCs?	¹⁰¹ ^, ¹⁰²
Staphylococcal enterotoxin B	Intestinal allergic inflammation	Foxp3 induction in DCs release of TGFβ	⁵⁷
Fungal β-glucan	Autoimmune diabetes	Dectin-1 ligation, induction of T_reg	⁹⁵
IL-10	Allergic sensitization (house dust mite)	In vitro induction of T_reg	¹⁰³
Flagellin	Allergic sensitization (birch pollen)	IL-10 production of DCs via a mTOR pathway	⁹³
Cisplatin	In vitro studies with murine cells	IL-10 production of DCs via MAPK pathway	¹⁰⁴

DC: dendritic cell; pDC: plasmacytoid DC; mTOR: mammalian target of rapamycin; DC-SIGN: DC-specific ICAM3-grabbing non-integrin; T_reg: regulatory T cell.

Conclusions

Our knowledge about the circumstances under which tolerogenic DCs differentiate have increased continuously over the last 15 yr. This is an important development because DCs are already in use in clinical studies for the treatment of cancer. Knowing the precise parameters involved in the differentiation of tolerogenic DCs will avoid trials under risk of inducing T_reg against tumor Ags. Exemplarily, DCs treated with the Dectin-1 ligand β-glucan were successfully used to induce tolerance against auto-Ags.⁹⁵ Confusingly, DCs treated with β-glucan were also shown to initiate an anti-tumor immune response.¹⁰⁵ Thus, much more research is needed to delineate all the parameters distinguishing between activating versus tolerogenic DCs. Once the best way to induce stable tolerogenic DCs is deciphered, the ground is prepared for the development of new treatment opportunities for asthma bronchiale and other chronic inflammatory airway disorders. Moreover, the extended knowledge will enable us to perform meaningful trials to modulate the tolerogenic behavior of DCs in vivo, aiming to break the tolerance against pathogens hiding in the cells of infected patients.

Footnotes

Acknowledgements

We would like to thank Philip Saunders (Language Support Services, Berlin, Germany) for proofreading the manuscript.

Declaration of conflicting interests

The authors declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Funding

The authors received no financial support for the research, authorship, and/or publication of this article.

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