Targeting Antigen-Presenting Cells in Multiple Sclerosis Treatment

: Multiple sclerosis (MS) is common neurological disease of the central nervous system (CNS) affecting mostly young adults. Despite decades of studies, its etiology and pathogenesis are not fully unraveled and treatment is still insufﬁcient. The vast majority of studies suggest that the immune system plays a major role in MS development. This is also supported by the effectiveness of currently available MS treatments that target immunocompetent cells. In this review, the role of antigen-presenting cells (APC) in MS development as well as the novel therapeutic options targeting those cells in MS are presented. It is known that in MS, peripheral self-antigen-speciﬁc immune cells are activated during antigen presentation process and they enter the CNS through the disrupted blood–brain barrier (BBB). Myelin-reactive CD4+ T-cells can be activated by dendritic cells, inﬁltrating macrophages, microglia cells, or B-cells, which all express MHC class II molecules. There are also suggestions that brain endothelial cells may act as non-professional APCs and present myelin-speciﬁc antigens with MHC class II. Similarly, astrocytes, the major glial cells in the CNS, were shown to act as non-professional APCs presenting myelin antigens to autoreactive T-cells. Several currently available MS drugs such as natalizumab, ﬁngolimod, alemtuzumab, and ocrelizumab may modulate antigen presentation in MS. Another way to use this mechanism in MS treatment may be the usage of speciﬁc tolerogenic dendritic cells or the induction of tolerance to myelin antigens by peptide vaccines.


Introduction
Multiple sclerosis (MS) is an autoimmune, inflammatory, and demyelinating disease of the central nervous system (CNS). Its etiology is still unknown, despite the fact that the new concepts appear with more in-depth studies. The pathogenesis is clearer, and we know that pathological processes such as inflammation, demyelination, astrogliosis, and neurodegeneration play an important role in this complex mechanism [1]. For many years, autoimmune inflammation was considered to be the initial step in MS pathogenesis. It is suggested that the major target of autoimmune attack is protein autoantigens localized in the CNS myelin sheaths. This concept was confirmed in animal models of the disease [2]. The complex clinical and pathological picture of MS is not reflected by single animal models. Rather, various animal models are utilized for studies on different aspects of this disease. One of the most frequently used model, especially in the context of autoimmunity, is EAE (experimental autoimmune encephalomyelitis). There are two main types of EAE-active and passive-depending on the selected method of induction [3]. Moreover, this model can be induced in various animals, such as mice, rats, guinea pigs, and primates. EAE resembles MS in pathological changes observed in the CNS (inflammation, demyelination, neurodegeneration) and in some aspects of clinical signs [4]. However, the etiology has varied greatly, as EAE is induced by animal immunization with selected myelin peptides, whereas in patients with MS, the autoantigen responsible for disease induction is not known.
The clinical picture of MS is also complex. Four different clinical courses of MS can be distinguished. The most common (85%) is the remitting-relapsing type of the disease cessful antigen presentation during T-cell priming and re-activation, other co-stimulatory molecules such as CD40, CD80, CD86, and integrins are required [16,17].
Myelin-reactive CD4+ T-cells are activated by dendritic cells, microglia cells, infiltrating macrophages, and B-cells-all expressing MHC class II molecules. CD8+ T-cells, which are highly present in the acute lesions of MS, mediate inflammation and demyelination after their activation by myelin peptide presentation with APCs expressing MHC class I molecules. All nucleated cells, including oligodendrocytes, astrocytes, and neurons, expressed MHC I [18][19][20].
The antigen-priming of T-cells is an important process in chronic and acute inflammation. In animal models of MS, infiltrating auto-reactive CD4+ T-cells are re-activated within CNS by APCs, which results in monocyte recruitment into the CNS, as well as in naïve CD4+ T-cells priming through epitope spreading, which boosts disease inflammatory reaction.
In autoimmune diseases, epitope spreading contributes to chronicity of inflammation and to diversification of the ongoing immune response. Epitope spreading is a process in which immune responses are directed to epitopes that vary from the initial ones [9]. In EAE, it has been shown that initial immune response is focused on a certain epitope and, then, during disease progression, spreads to others [21,22]. Spreading of epitopes may be intramolecular-within one molecule, e.g., various epitopes of MBP, or intermolecular, e.g., from PLP to MOG [21,23,24]. Various EAE models suggested that this process may begin within CNS, and that it was associated with clinical relapses [24,25]. Both intramolecular and intermolecular epitope spreading has also been observed in patients with MS [26][27][28]. However, what is the exact role of such process on disease course requires further analyses, as some studies were not able to detect any associations with disease exacerbations [26,29].
Numerous studies emphasize the importance of microglia and infiltrated dendritic cells/macrophages as an antigen-presenting cells in the CNS. Recently, it was speculated that B-cells may also act as professional APCs.

Dendritic Cells
A lot has been said about the pathogenesis of MS and the role of T-cells in inflammation and demyelination of the CNS. Considering MS as an autoimmune disorder, it could be assumed that initiation of immune reaction is linked with an interplay between the elements of innate and adoptive immunity. As the disease is characterized by a specific immune response toward the CNS myelin antigens, its induction depends on the activation of naive T-cells recognizing processed myelin antigens. Various cell types are able to present antigens for T-lymphocytes; however, only dendritic cells are called the professional antigen-presenting cells-it means that only these cells are capable of priming naive T-cells to differentiation. Since their first description by Steinman [30][31][32][33], dendritic cells became considered one of the most important players in the induction of antigen-specific immune responses. Actually, dendritic cells are the aim of newly designed therapeutic strategies in every field where the specific immune response matters (i.e., allergic disorders, cancer therapies, autoimmune disorders) [34].
Because of their biological properties, DCs are thought to be a key players in the initiation of MS, its development, maintenance, and progression. Dendritic cells are heterogeneous group of cells localized in various tissues, where they act as sentinels-filtrating extracellular tissue environment for antigens. In this functional state, dendritic cells possess immature phenotype due to their low ability for antigen presentation, but high endocytic activity and high expression of molecules that facilitates antigen recognition and uptake, for example C-type lectin mannose receptor MR (CD206) or DC-SIGN (CD209). Ingested antigens are processed and presented on the MHC molecules class II (but also class I) on the cell surface. For efficient antigen presentation, antigen uptake must be associated with dendritic cell maturation-which is triggered by danger signals provided with foreign (bacterial or viral) antigens and recognized by DCs via the set of pattern recognition receptors recognizing pathogen-associated molecular patterns [35]. Danger signals may also be provided by tissue destruction and inflammatory cytokines released from other cells. De- pending on the recognized signal, located in tissue, immature DCs undergo maturation and their phenotype changes: the expression of antigen uptake receptors as the pinocytic and endocytic activity decreases, whereas the expression of MHC class II and co-stimulatory molecules (CD86, CD83, CD80, CD40) increases. During the maturation, DCs migrate from the tissue via lymph vessels to the draining lymph nodes. Migration to the lymph nodes is regulated by the chemokine milieu. The expression of CCR7 molecules on the surface of maturing DCs regulates their trafficking to the lymph nodes in response to CCL19 and CC21 chemokines [36,37]. This chemotactic process is also regulated by CXCR4-a receptor for chemokine CXCL12 [38]. In lymph nodes, mature DCs present processed antigens for T-cells, prime their activation, and shape the development of antigen-specific immune response. If the migrated DCs are not activated enough, then the possible result of antigen presentation for T-cells will be the anergy of antigen-specific T-cells or induction of Treg cells, resulting in the induction of peripheral tolerance to antigens. Recent findings suggest that the ability of DCs to prime immune tolerance to presented antigen is linked rather with a specific activation state developed after antigen recognition (tolerogenic phenotype) than the lack of maturation. The maturation process occurs, however, into the different phenotype.
In MS, the uptake and transport of brain antigens by DCs or another APC cells has been contentious, due to the alleged independence of CNS from the immune system and the presence of BBB, which was believed to block immune cells trafficking into the brain. Recent findings have finally shown that dendritic cells may also be present in the central nervous system not only during inflammation, but also at steady-state conditions. It is discussible whether DCs may home the brain parenchyma; however, it is already confirmed that these cells are present in choroid plexus, perivascular spaces of BBB, meninges, and in cerebrospinal fluid. Their presence seems to be the effect of migration of bone marrow precursors from blood [39]. It was also found that microglia cells-brain-specific macrophages-may differentiate into immature dendritic cells after GM-CSF stimulation [40]; however, the comparative microarray analysis of gene expression profile suggests the close resemblance of the brain DCs to the dendritic cells of spleen, but not to the microglia [41]. Localization of DCs in close proximity to neurons gives a chance for myelin antigens uptake and initiation disease-specific immune response. The myelin antigens uptake and the source of danger signals are still open and unsolved questions. It seems rather unbelievable that myelin antigens alone may provide the efficient signal for DCs' activation and maturation; however, coexisting viral infections as well as local physical injuries may strengthen the danger signal.
Another aspect of specific immune response is the place of naive T-cells priming by antigen-loaded mature DCs. On periphery, antigen-processing DCs migrate to the draining lymph nodes via lymphatic vessels. However, there is no typical lymphatic drainage of the brain and the exact path for dendritic cells' migration is not yet fully identified. However, observations on animal models describe the presence of labeled OVA antigens in cervical lymph nodes after its intracerebral injection into the brain [42]. Accumulation of myelin-loaded CD11c-positive dendritic cells in cranial lymph nodes was also reported [43]. Studies on dendritic cells loaded with antigens and injected into the cerebellum or CSF also reported their movement to the cervical lymph nodes and localized their antigen presentation [44,45]. The exact route for cells migration from brain to draining lymph nodes is not fully identified. Recent studies describe the role of meningeal lymphatic vessels as a route for antigen-loaded cells from the brain to the cranial lymph nodes [46][47][48]. Another route for antigen-presenting cells from the brain to the peripheral lymph nodes was reported by Hochmeister et al., where injection of monocyte-derived DCs into the striatum resulted in their perivascular accumulation and migration across the endothelium into the vessel lumen [49]. The third possible route for CD11c-positive DCs was reported by Mohammad et al. and utilizes olfactory bulb and rostral migratory stream [50].
The separate issue is the possible role of microglia cells as potential professional APCs and their possible role in initiation of antigen-specific immune response in MS. Microglia are cells that are located in the brain parenchyma in the close proximity to myelin. The recent findings of Schiefenhövel et al. suggest the possible ability of microglia cells to migrate from the brain parenchyma to cervical lymph nodes for antigen presentation [51].
Microglia represents a subset of CNS resident cells with macrophage-like morphology, derived from early post-embryonic precursors. In resting state, ramified microglia continually surveys the microenvironment for threats. The activated amoeboid microglia have round or oval shape, process antigens, and clear them from the vicinity. Microglia may be divided into two subgroups: M1, which promote inflammation and oligodendrocyte damage, and M2, which regulate immune function, clear cellular debris, and promote repair in inflammatory diseases of the CNS [52,53]. However, now, it is assumed that microglia may differentiate into various subtypes with diverse functions, which is affected by a variety of environmental stimuli [54][55][56][57][58].
Microglia express MHC class I and II molecules and secrete many pro-and antiinflammatory cytokines, as well as co-stimulatory molecules, such as intercellular adhesion molecule-1 (ICAM-1), CD80, and CD86 [59,60]. As APCs, microglia interact with other immune cells, which leads to the activation of various T-cell subsets during demyelination and remyelination [59,61]. Microglia can interact with CD28 or CTLA4 expressed on Tcells, which results in different outcomes. Microglial co-stimulatory molecules CD80 and CD86 bind CD28 to stimulate T-cells proliferation, differentiation, and cytokine production. Conversely, binding to CTLA4 leads to T-cell anergy or apoptosis [62].
Results from a number of studies indicated that microglia are not effective as APCs, DCs, or macrophages [8,63,64]. However, contradictory results exist. Wlodarczyk et al. have shown that DC and microglia sorted from CNS of mice with EAE have similar expression levels of MHC class I and II, CD80, and CD86. Moreover, it was shown that both cell populations were able to induce an antigen-specific proliferative response in primed T-cells. However, CD11c+ microglia were weak inducers of Th1 and Th17 differentiation, due to the lack of expression of necessary cytokines, conversely to infiltrating CD11c+ cells that strongly induced such cytokines [65]. Interestingly, CD11c− microglia have been shown to be poor inducers of T-cells proliferation, but this subset has the capability to produce Th1-and Th17-inducing cytokines, pointing to the synergized mode of action of both microglia subpopulations [65]. Thus, it is speculated that CD11c + and CD11c− microglia may function as CNS-resident APCs being as effective as infiltrating CD11c + cells.
B-cells, despite their function in antibodies production, may also act as antigenpresenting cells. It has been demonstrated that in the subset of MS patients, B-cells supported proliferation and/or IFN-γ production by autologous T-cells in response to neuroantigens, such as MOG and MBP [66]. Additionally, B-cells from MS patients, but not from healthy donors (HD), were able to induce proliferation and IL-17 production by Th17 cells in response to neuroantigens [67]. Similar results were obtained in the EAE model, where B-cells also promoted MOG-specific Th1 and Th17 cell differentiation [68]. Additionally, animals with MHC class II molecules deficiencies were resistant to disease induction and have attenuated Th1 and Th17 responses [69].
Several studies have shown that CD40-activated B-cells from HD and MS patients induce T-cell responses specific to myelin antigens [70,71]. However, Ireland et al. have indicated that B-cells from MS patients may support myelin antigen-specific T-cell priming without previous in vitro activation [67]. Thus, B-cells are efficient APCs, capturing antigens through a membrane-bound B-cell receptor, processing them, and presenting via MHC class II molecules [72]. Moreover, it has been reported that B-cells from the peripheral blood of MS patients have increased the expression of co-stimulatory CD40 and CD80 molecules compared to HD [73]. Immunomodulatory treatment decreased B-cell co-stimulatory molecules expression, resulting in reduced T-cell responses induced by B-cells [74,75]. The increased expression level of co-stimulatory molecules CD80, CD86, and HLA-A/B/C was also observed on B-cells isolated from CSF [73].
Clonal expansion of B-cells allows them to activate many T-cells, thus leading to an exacerbation of inflammation. In an animal model of MS depending on B-and T-cells, it Appl. Sci. 2021, 11, 8557 6 of 19 was shown that B-cell function as APCs is necessary for disease induction, instead of their ability to produce antibodies [69,72].
The vascular endothelial cells separating the blood stream from the brain parenchyma are referred to as a blood-brain barrier. This barrier regulates the entry of various substances and myeloid cells into the CNS, thus providing anatomical and physiological protection. Migration of myelin-specific CD4+ T-cells across the BBB, a crucial step in the pathogenesis of MS, is suggested to be an antigen-specific process. It has been proposed that this process is mediated by brain endothelium. Lopes et al. reported that in inflammatory conditions, brain endothelial cells (BECs) act as a non-professional APCs able to process and present myelin-derived antigens complexed with MHC class II. Such complexes stimulated myelin-reactive Th1 and Th17 2D2 cells to transmigration through endothelium. Blocking of interactions between myelin/MHC II complexes and reactive T-cells abrogated the trafficking of the latter across the BBB [11]. It has been reported that BECs express MHC class I, but the MHC class II is present in very low levels in physiological conditions. Induction of the inflammatory process activates BECs and results in increased expression of MHC II, CD40, and ICOSL and, subsequently, enhances their ability to induce T-cells proliferation in vitro [76]. Additionally, it was shown that myelin enters the endosomal/lysosomal pathway after internalization by BECs, which was autonomous from their activation status [77]. This is opposite to what is observed for professional APCs such as DCs, where internalization of antigens takes place in an immature state of these cells [78,79]. Overall, these results pointed out that brain endothelium is an active and important contributor to the pathogenesis of MS.
Astrocytes are the most abundant cells in the CNS and they can act as a non-professional APCs modulating the activity of autoreactive T-cells by myelin antigen presentation and secretion of pro-or anti-inflammatory cytokines.
The role of astrocytes as APCs has remained controversial. There are reports that have shown that astrocytes express low levels of MHC class II molecules constitutively, and their expression may be upregulated during inflammatory reactions [80,81]. The expression of co-stimulatory molecules, such as CD40, CD80, and CD86, is also upregulated during astrocytes activation [81][82][83]. However, studies utilizing human fetal astrocytes in vitro failed to detect the expression of co-stimulatory molecules, even after stimulation [84]. Functional studies have shown that stimulated murine astrocytes moderately activate CD4+ and CD8+ T-cells, whereas cytokine-treated human astrocytes did not induce proliferation of encephalitogenic T-cells [80]. These may reflect differences between species or artifacts associated with astrocytic cell cultures, which may be contaminated by microglia. It has also been reported that activated astrocytes efficiently presented MBP, PLP, and MOG epitopes [85][86][87]. Yet, they were incapable of processing and presenting native myelin peptides. Thus, the astrocytes potential for antigen presentation needs more detailed studies to elucidate its role for the development and progression of MS.

MS-Approved Drugs Targeting Immunocompetent Cells
Currently, several drugs used in MS therapy target inflammatory cell subpopulations, which play a significant role in MS pathogenesis (Table 1) [88]. Natalizumab and fingolimod are anti-migratory drugs and influence inflammatory T-cell migration to the CNS of MS patients. Natalizumab is a humanized monoclonal antibody targeting adhesion molecule α4-integrin on effector T-cells in the blood, which leads to the blockade of inflammatory cell migration to the CNS. This mechanism is very efficient leading to lowering of the annual relapse rate by 68% and diminishing the number of demyelinating lesions in MRI of the CNS by 92% [89]. Natalizumab is delivered by intravenous infusions every month. A very serious side effect of this treatment is the possibility of developing progressive multifocal leukoencephalopathy (PML), which may be limited by controlling the level of anti-JC antibody in candidate MS patients [90,91]. Fingolimod is the second anti-migratory drug used in MS and the first effective oral drug for this disease. It targets sphingosine S1P receptors. The major effect of this action is inhibition of migration of T-cells out of the lymphatic nodes. In consequence, effector T-cells cannot invade the CNS and initiate the development of MS pathology. This treatment effectively reduces annual relapse rate and slows down clinical and radiological disease progression. There are also solid data confirming positive influence of this treatment on brain atrophy in MS patients [92].
Alemtuzumab is recombinant humanized monoclonal antibody targeting glycoprotein CD52 on T and B-cells. It is delivered once a year, because drug infusions lead to the depletion of both types of lymphocytes, with their slow repopulation from non-affected progenitor cells. The mechanism of action of this drug is very complex. Besides T-and B-cell lymphopenia, another effect is an increased number of Tregs, upregulation of several inflammatory cytokines, and the induction of neurotrophin-producing lymphocytes. Alemtuzumab significantly inhibits the progression of MS symptoms and diminishes the annual relapse rate and number of new lesions in the CNS of MS patients [93,94].
The clinical trials on anti-CD20 mAbs therapeutic efficacy in MS revealed their significant potential in reducing the clinical and MRI activity in patients. Four currently studied mAbs-rituximab, ocrelizumab, ofatumumab, and ublituximab-differ from each other by their structure, immunogenicity (chimeric, humanized, fully human, or glycoengineered), the type of cytotoxicity they induce (antibody-dependent cellular cytotoxicity and complement-dependent cytotoxicity), and also by the CD20 epitope they recognize [95]. Studies on their mode of action in RR-MS patients suggested that the main mechanism is not related to a reduction in the Abs level, but it is rather the modulation of APC function of B-cells. B-cells, as was mentioned in the previous section, are able to process and present antigens to T-cells. They recognize myelin antigens in MS via their surface receptors, and they efficiently capture antigens presented at low concentration [96]. Moreover, CD20 is not expressed on plasmablasts or plasma cells, the B-cell subtypes responsible for antibody secretion. Thus, after CD20 mAbs treatment, there was no reduction observed in antibody titers [74,97]. It is worth mentioning that ocrelizumab is also the first diseasemodifying therapy approved for primary progressive MS, but is also registered for patients with remitting-relapsing MS [98]. In multi-center randomized clinical trials, it demonstrated higher efficacy in both forms of MS, when compared to patients in the placebo group and group treated with interferon beta [99]. It reduces number of disease relapses, slows the progression of disability, and reduces number of MRI lesions in the CNS of MS patients [100].
Another example of surface receptor with therapeutical potential is CD83, especially its soluble form (sCD83). Recombinant soluble CD83 (rsCD83) have demonstrated its potential via immunosuppressive properties observed in animal models of autoimmune diseases, including MS [101]. All of the studies indicate that this receptor is able to suppress immune responses, via inhibition of human monocyte differentiation into DCs, changing the DC cytoskeleton, preventing DC maturation, and reducing DC-mediated Tcell proliferation [102][103][104][105][106][107]. Results obtained from EAE studies indicate that administration of rsCD83 prevents EAE development and also reduces the level of T-cell cytokines, such as IFN-γ, IL-2, IL-4 and IL-10 [101].
Dimethyl fumarate (DMF) is the first-line oral drug approved for RR-MS patients, with moderate to high efficacy [108]. The main mechanism of action of DMF is an alteration of Th-cells differentiation and total number, induction of regulatory B-cells, and its antioxidative potential [109]. The naïve and regulatory T-cell subpopulations are elevated, whereas there is a reduction in memory T-cells, as well as in Th1 and Th17 cells [110,111]. However, it was also shown that DMF may alter activity of APCs, such as monocytes and dendritic cells [108]. Moreover, it has been shown that DMF has ameliorated a B-cellaccentuated EAE by diminishing the capacity of B-cells to act as APCs for T-cells [112]. In the studies conducted on blood obtained from MS patients, it was reported that the total number of B-cells was reduced after DMF treatment, with the emphasis on differentiated cells [113][114][115][116]. The level of mature and memory B-cells, together with plasmablasts, was reduced, whereas the frequency of immature, transitional B-cells increased [112].
One of the therapeutic goals in MS treatment is the induction of long-term, durable, antigen-specific T-cell tolerance. Antigen-specific immunotherapies are emerging to suppress targeted immune responses without altering the global immune system [117,118].

Dendritic Cells in MS Therapy
As a key player in the initiation and maintenance of antigen-specific immune response, dendritic cells are considered not only as a target for drug-based treatment. The use of specific tolerogenic dendritic cells is also considered a therapeutic option. The idea of using tolerance-inducing dendritic cells depends on the use of antigen-loaded DCs primed to tolerogenic phenotype, which are able to polarize the immune response against presented antigens towards the induction of immune tolerance, which results in the expansion of antigen-specific regulatory T-cells. Phenotype of tolerance-inducing DCs is traditionally characterized as semi-mature with weak expression of MHC class II molecules and costimulatory receptors (CD86, CD83, CD80, CD40), high level of surface inhibitory molecules (PDL1/2, ILT3, ILT4), and specific secretory activity with evident IL-10 or TGF-β production and weak release of proinflammatory cytokines [122]. Induction of tolerance to antigens depends mainly on the ability of DCs to promote differentiation of naive T-cells to Treg during antigen presentation in lymph nodes. Moreover, tolerance-inducing DCs were also reported to be able to inhibit the proliferation of T-cells, induce T-cells hyporesponsiveness, and T-cells anergy [123][124][125]. The level of conventional DCs in circulating blood is quiet low; thus, in numerous studies, DCs are derived from blood monocytes. Standard protocol utilizes moDCs differentiation from monocytes in the presence of IL-4 and GM-CSF to immature DCs [126,127]. Tolerogenic phenotypes may be obtained in numerous ways; the most popular utilizes vitamin D3 or IL-10; however, the use of corticosteroids, rapamycin, or specific NF-κB inhibitors were also described as possible strategies [128].
Up to date, the most interesting and well-studied are tolerogenic DCs induced by vitamin D3 or glycocortycosteroid dexamethasone. In vitro and animal studies with vitD3-tolDC confirmed their ability to induce hyporesponsiveness of T-cells toward presented antigens, as well as the stability of promoted tolerogenic phenotype, which was not abol-ished by cryopreservation [129,130]. Animal studies conducted using an EAE model revealed the potential of myelin antigen-loaded tolDC administration to suppress immune response and enhance the proliferation of regulatory B-cells and T-cells. Recently, Mansilla et al. identified CD115 (CSF1R) as a biomarker for tolerogenic properties of DCs, which is also involved in the vitamin D-mediated induction of tolerogenic phenotypes. What is more, authors reported CSF1R-CSF1 signaling to be important for metabolic reprogramming of vitamin D-modulated DCs, related with elevated glucose uptake and lactate production [131]. Release of lactic acid is a novel, recently identified mechanism utilized by tolerogenic DCs to suppress T lymphocytes proliferation [132]. These findings improve further tolDC studies and improve time-consuming identification of tolerogenic phenotype of DCs induced with vitamin D. It should be checked if regulatory properties of another already described tolerance-inducing DCs, obtained on different priming protocols (dexamethasone, IL-10, TGF-β, synthetic NF-κB inhibitors), are also lactate and CSF1R-CSF1 signaling dependent. It is worth to consider CSF1R as a target for improvement of regulatory activity of antigen loaded DCs derived from monocytes, as well as circulating conventional DCs in the body.
A major disadvantage of this form of therapy is the necessity to use tolerogenic DCs loaded with multiple myelin antigens as the immune response among the patients is heterogeneous, and the antigen spreading must always be considered. Although experimental tolDC therapy was effective in early stages of EAE, there was no beneficial effect of its use for chronic EAE [129,[133][134][135][136]. Similar results should be expected in accordance with MS in humans. In the early stage of inflammation, when the autoimmune reaction targets major myelin antigens, the tolDC-based therapy should be the most effective [136].

Tolerogenic DCs in Clinical Trials
Actually, two independent phase I clinical trials utilizing tolDC are taking place, and one has already finished [136,137]. A phase Ib clinical trial with dexamethasoneinduced tolerogenic DC loaded with myelin antigens or Aquaporin 4 that finished in 2019 confirmed safety of the therapy and provided the proof of concept for use of tolerance inducing DCs in future. Within 12 weeks after intervention, a significant increase in IL-10 release by PBMC cells exposed to myelin antigens and elevated Treg frequency have been observed in study participants, which suggests the induction of immune tolerance to used antigens. What is important is that there was no serious side effects and during the 24-week follow-up, researchers noticed only non-severe episodes, not related with the study [138]. Such a form of therapy depending on restoring immune tolerance without general immune suppression is needed. Actually, two phase I studies are recruiting MSaffected participants to evaluate safety and tolerability of the treatment, as well as to determine the most suitable administration option of vitamin D-induced tolerogenic DC loaded with myelin immunopeptides (Figure 1). It seems necessary to evaluate the most effective route for tolDC administration, as well as the development of a fast and reliable method for the induction of tolerance-inducing DCs and assessment of the tolerogenic potential of DCs [138]. Future trials for testing the efficiency of tolDC-based therapies on the clinical level, involving a higher number of participants, should be carried out, as well as the frequency of side effects being evaluated. [138]. Future trials for testing the efficiency of tolDC-based therapies on the clinical level, involving a higher number of participants, should be carried out, as well as the frequency of side effects being evaluated.

Targeting the APC Activity by Peptide Vaccines
Induction of tolerance to myelin antigens may be also obtained by administration of the antigen by non-conventional route. Numerous trials investigated the effect of myelin antigens administered orally, intravenously, subcutaneously, or intranodally. Therapy with myelin peptides depends on their uptake without strong activation of APCs, which induce tolerance to the antigen. Trials utilizing the immune peptides administration were

Targeting the APC Activity by Peptide Vaccines
Induction of tolerance to myelin antigens may be also obtained by administration of the antigen by non-conventional route. Numerous trials investigated the effect of myelin antigens administered orally, intravenously, subcutaneously, or intranodally. Therapy with myelin peptides depends on their uptake without strong activation of APCs, which induce tolerance to the antigen. Trials utilizing the immune peptides administration were summarized in Table 2. Common disadvantages of peptide administration are the necessity of repetitive administration in high doses and the fast clearance of injected peptide [122,[139][140][141].  Expansion of autoreactive T-cells [122,150] This process may be facilitated by the incorporation of selected peptides into the liposomes modified to elevate their uptake by DCs via specific surface receptors. For example, immunodominant MBP peptides are incorporated into mannosylated liposomes, which increase their uptake by APCs via the CD206 receptor. This approach enhances immune tolerance for the CNS antigens [151,152].
Another option is nanoparticles loaded with self-antigen, with or without a bioactive payload, which have been developed to induce immune tolerance [153][154][155][156][157]. It has been shown that biodegradable particles loaded with myelin-specific antigen, either alone or with immunomodulators, ameliorate EAE [158,159]. Particles around 500 nm in size are phagocytosed by APCs [160][161][162]. Poly (lactide-co-glycolide) (PLG) and poly (DL-lactide) (PLA) particles have been mostly investigated in antigen-specific treatment for MS and have shown the capability to modulate immune cells for EAE disease amelioration [157,159,163].

Conclusions
Several currently available experimental data suggest that targeting antigen presentation may be a promising way to develop the new, more effective methods of MS treatment.