Background
Multiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system (CNS) that is mediated mainly by activated pro-inflammatory CD4+ T helper (Th) cells and cytotoxic CD8+ T cells [
1,
2]. Growing evidence is available that suggest a role for antigen-presenting cells (APC) in the pathogenesis of MS via their extraordinary capacity for inducing and expanding pro-inflammatory T cell populations [
3,
4]. In particular, dendritic cells (DC) play a crucial role in regulating the balance between encephalitogenic and tolerogenic immunity in MS [
5]. We recently demonstrated the presence of 6-sulfo LacNAc+ (slan) DCs, which are the major pro-inflammatory and most potent T cell-activating DC populations, in active inflammatory MS lesions. SlanDCs represent a new potential link between innate and adaptive immunity in MS and are specifically modulated by different MS therapies [
6,
7]. As such, future treatments should include targeted modulation of selective DC and APC functions [
8,
9].
Fingolimod (FTY) is the first approved oral therapy for highly active relapsing remitting (RR) MS. Fingolimod exerts its effect via modulation of the sphingosine-1-phosphate (S1P)-receptor (S1PR) [
10,
11]. Extensive data on the mechanism of action of fingolimod demonstrate its principal effects on T and B cell trafficking via impairment of S1PR1-mediated recirculation, which results in significantly reduced lymphocyte egress from lymphoid tissues into the general circulation [
12]. In addition to the effects on T and B cells, modulation of the innate immune system, including actions on DCs, have been proposed [
13‐
17]. Sphingolipids and their G-protein-coupled receptors appear to play an important role in the modulation of the innate immune system. Additionally, all of the known sphingolipid receptor-subtypes (S1PR1-S1PR5) are apparently involved in the modulation of function and metabolism of APCs [
13,
18,
19]. Although the circulation of APCs is not primarily regulated by the S1P-system, FTY and its active metabolite FTY-phosphate (FTYP) appear to affect APC migration into lymph nodes and tissues possibly via modulation of inflammatory chemokines [
18,
20‐
22]. However, human data on effects of FTY on APC subsets in MS patients are rare, and the detailed impact on pro-inflammatory potential and DC-dependent T cell regulation lack detailed understanding.
To gain novel insights into immunomodulatory effects of FTY on innate immunity beyond the established effects on lymphocyte recirculation, we investigated the FTY-stimulated ex vivo and in vitro modulation of frequency and function of slanDC (the most potent pro-inflammatory DC population) to evaluate the impact of FTY on inflammatory and T cell regulatory properties. Here, we present data on the impact of FTY on the inflammatory properties of slanDCs and classical APCs via in vitro and ex vivo analyses of FTY-treated MS patients.
Methods
Patients and controls
Blood samples of 35 RRMS patients diagnosed according to the McDonald criteria were used to evaluate immunomodulatory effects on APC during FTY treatment (Table
1). Blood samples were drawn prior to and during FTY treatment up to 24 months. Further blood samples were collected of ten untreated RRMS patients with stable disease course compared to ten RRMS patients with stable disease after 12 months of FTY therapy to perform additional ex vivo analyses. Blood of healthy donors was collected for in vitro analyses.
Table 1
Patient characteristics
1 | F | 23 | 3 | Interferon-beta | 1.5 | Yes |
2 | F | 54 | 9 | None | 2 | Yes |
3 | M | 28 | 4 | Interferon-beta | 1.5 | Yes |
4 | M | 33 | 14 | Natalizumab | 4 | Yes |
5 | F | 42 | 14 | Glatiramer acetate | 3 | Yes |
6 | F | 53 | 16 | Interferon-beta | 3.5 | Yes |
7 | F | 47 | 3 | Interferon-beta | 3 | Yes |
8 | F | 47 | 7 | Interferon-beta | 2 | Yes |
9 | F | 41 | 11 | Interferon-beta | 6 | Yes |
10 | F | 46 | 15 | Natalizumab | 4 | Yes |
11 | F | 42 | 2 | None | 1 | Yes |
12 | F | 19 | 2 | None | 1.5 | Yes |
13 | F | 30 | 11 | Natalizumab | 2 | Yes |
14 | M | 35 | 3 | Glatiramer acetate | 2 | Yes |
15 | M | 27 | 3 | Glatiramer acetate | 2 | Yes |
16 | F | 44 | 4 | Interferon-beta | 2.5 | Yes |
17 | F | 27 | 11 | Natalizumab | 2 | No |
18 | F | 29 | 15 | Natalizumab | 6 | Yes |
19 | F | 24 | 11 | None | 1 | Yes |
20 | F | 47 | 6 | Glatiramer acetate | 3 | Yes |
21 | F | 45 | 11 | Glatiramer acetate | 1.5 | Yes |
22 | M | 42 | 3 | Glatiramer acetate | 4 | Yes |
23 | F | 44 | 10 | Interferon-beta | 1.5 | Yes |
24 | M | 38 | 3 | Glatiramer acetate | 1.5 | Yes |
25 | M | 26 | 4 | Interferon-beta | 1.5 | No |
26 | F | 42 | 4 | Glatiramer acetate | 2 | Yes |
27 | M | 29 | 2 | Glatiramer acetate | 2 | Yes |
28 | F | 35 | 2 | Glatiramer acetate | 3 | Yes |
29 | M | 41 | 1 | None | 2 | Yes |
30 | M | 30 | 6 | Interferon-beta | 1.5 | Yes |
31 | M | 28 | 1 | None | 1.5 | Yes |
32 | M | 44 | 10 | Interferon-beta | 4 | Yes |
33 | F | 45 | 10 | Interferon-beta | 4 | Yes |
34 | M | 41 | 19 | Natalizumab | 3 | Yes |
35 | F | 33 | 8 | Glatiramer acetate | 2.5 | Yes |
All experiments were approved by the institutional review board of the University Hospital of Dresden. All donors gave their written informed consent.
Flow cytometric analysis
Preparation of blood cells and analysis by fluorescence-activated cell sorting (FACS) have been performed by a previously validated protocol defined by standard operating procedures (SOPs): Peripheral blood mononuclear cells (PBMCs) were prepared by Ficoll–Hypaque (Biochrom, Berlin, Germany) density centrifugation. Cell surface staining was performed by using fluorescence-labeled anti-CD3, anti-CD4, anti-CD8, anti-CD14, anti-CD19, anti-CD40, anti-CD80, anti-CD83, anti-CD86, anti-CD150, anti-HLADR (BD Biosciences, Heidelberg, Germany), anti-BDCA1, anti-slan, or anti-CD39 (Miltenyi Biotec, Bergisch Gladbach, Germany) according to the manufacturer’s instructions. Negative controls included directly labeled or unlabeled isotype-matched irrelevant antibodies (BD Biosciences). For further characterization of intracellular markers, PBMCs were suspended in culture medium consisting of RPMI 1640 (Biochrom), 5% human AB serum (CC pro, Neustadt, Germany), 2 mM l-glutamine, 100 U/ml penicillin, and 100 μg/ml streptomycin (Biochrom). Analysis of T regulatory cells (Treg cells) was performed directly, whereas Th17 cells were stimulated with 10 ng/ml phorbol myristate acetate (PMA, Sigma-Aldrich, Steinheim Germany) and 1 μg/ml ionomycin (Sigma-Aldrich) in the presence of 0.2 μM Monensin (Biomol, Hamburg, Germany) for 6 h prior to analysis. For intracellular characterization of IL-17, CD154, and FoxP3, cells were fixed with fresh prepared fixation concentrate and permeabilized with wash-permeabilization concentrate (Fixation/Permeabilization Buffer Set, eBioscience). Subsequently, cells were stained using fluorescence labeled anti-IL-17 (BioLegend, London, UK), anti-CD154 and anti-FoxP3 antibody (both Miltenyi Biotec), or isotype-matched irrelevant antibody (BD Biosciences). After the staining procedure, cells were evaluated on a FACScan Calibur (BD Bioscience). Exact preparation of the cells, staining protocol, and procedure as well as adjustment and compensation of the FACScan was established prior to first analysis of samples. Complete blood cell count was performed additionally to FACS analysis. No patients with lymphopenia <0.2 GPt/l or lower medical drug possession rate >95% during fingolimod treatment were included to guarantee reliable data.
Immunomagnetic cell sorting
Isolation of slanDCs was performed as described previously [
6]. PBMCs were incubated with M-DC8 hybridoma supernatant containing 10 μg/ml of antibody and additional rat anti-mouse IgM paramagnetic microbeads (Miltenyi Biotec). Cells were sorted on two columns via the autoMACS device (Miltenyi Biotec, Bergisch Gladbach, Germany). CD1 + DC were sorted by depletion of CD19+ cells first, followed by positive selection of BDCA1+ using immunomagnetic separation according to the manufacturer’s instructions (Miltenyi Biotec, Bergisch Gladbach, Germany). CD14+ monocytes were isolated by positive selection, and CD4+ T cells, CD8+ T cells, and naive CD45RA + CD4+ T cells were isolated by depletion using immunomagnetic separation (Miltenyi Biotec, Bergisch Gladbach, Germany). The purity of the isolated cell populations was >95% as always assessed by flow cytometry afterwards.
Cytokine assay
Sorted slanDCs, CD1 + DCs, and monocytes of untreated or FTY-treated patients were cultured for 24 h. For the last 18 h, lipopolysaccharide (LPS, Sigma Aldrich) was added to stimulate cytokine release by TLR4 activation; unstimulated cells served as control. Additionally, cells of healthy controls and FTY-treated patients were maintained in the presence or absence of 30 ng/ml FTY, 30 ng/ml FTYP (Caltag, Buckingham, UK), or 20 or 200 nM S1P (Sigma Aldrich) in culture before LPS was added. Supernatants were collected, and the concentration of tumor necrosis factor alpha (TNF-alpha), IL-1beta, IL-6, IL-12, and IL-23 was determined using a commercial ELISA kit (BD Biosciences) according to the manufacturer’s instructions.
Maturation and activation profile
Sorted slanDCs, CD1+ DCs, and monocytes of healthy controls or FTY-treated patients were cultured in the presence or absence of 30 ng/ml FTY or 30 ng/ml FTY-phosphate or 20 or 200 nM S1P in vitro. Cells were collected and characterized with regard to surface activation and maturation markers by staining with fluorescence labeled anti-CD40, anti-CD80, anti-CD83, anti-CD86, anti-CD150, and anti-HLA-DR (BD Biosciences). Cells were evaluated on a FACScan Calibur.
DC-depending T cell proliferation and programming
SlanDCs or CD1 + DCs of healthy controls were cultured with or without 3 or 30 ng/ml FTY or FTYP for 6 h and washed with phosphate-buffered saline (PBS, Sigma Aldrich). To evaluate T cell proliferation, allogeneic CD4+ T cells or CD8+ T cells were labeled with carboxyfluorescein-di-acetate-N-succinimidylester (CFSE, Molecular Probes, Eugene, USA) at a final concentration of 0.3 μM. Treated and untreated DCs (1 × 104 cells/well) were co-cultured with CFSE-labeled allogeneic CD4+ T cells or CD8+ T cells (1 × 105 cells/well) for 4 days. Cells were harvested, and proliferation was calculated by CFSE-incorporation by flow cytometry and quantified by cell division index (CDI). For ex vivo analyses, slanDCs of FTY-treated patients compared to healthy controls were co-cultured with CFSE-labeled allogeneic CD4+ or CD8+ T cells of the same healthy donor to compare different potentials to induce T cell proliferation. To assess direct effects of FTY or FTYP on T cells, sorted CFSE-labeled CD4+ T cells or CD8+ T cells of healthy donors or FTY-treated patients were cultured in the presence of 5 μg/ml human anti-CD3 and 1 μg/ml human anti-CD28 (both BD Bioscience) without or with FTY or FTYP for 4 days. CFSE-incorporation was evaluated and counted as described above.
To evaluate DC-dependent T cell programming, FTY or FTYP pretreated and untreated slanDCs or CD1 + DC (1 × 104 cells/well) of healthy controls were co-cultured with allogeneic naïve CD45RA + CD4+ T cells (1 × 105 cells/well) in the presence of LPS for 8 days. Thereafter, T cells were stimulated with 10 ng/ml PMA and 1 μg/ml ionomycin in the presence of 0.2 μM monensin for 4 h. For intracellular characterization of IFN-gamma, IL-17 and IL-4 production, cells were fixed with freshly prepared ice-cold 4% paraformaldehyde (Merck) and permeabilized with 0.1% saponin (Merck) in PBS containing 1% fetal calf serum (FCS, Biochrom). Subsequently, cells were stained using fluorescence-labeled anti-IFN-gamma, anti-IL-17, and anti-IL-4 antibody or isotype-matched irrelevant antibody (BD Biosciences). After the staining procedure, cells were evaluated on a LSR Fortessa (BD Bioscience). For ex vivo analyses, slanDCs of FTY-treated patients compared to healthy controls were co-cultured with naïve CD45RA+ CD4+ T cells of the same healthy donor to compare different potential in T cell programming. To compare impact of FTY or FTYP on potential of polarization directly on T cells, naïve CD45RA+ CD4+ T cells stimulated with 5 μg/ml human anti-CD3 and 1 μg/ml human anti-CD28 treated without or with FTY or FTYP served as control. Differentiation into Th1 T cells was induced by adding 10 ng/ml human IL-12 and 10 μg/ml human anti-IL4, whereas Th2 differentiation was ensured by adding 10 ng/ml human IL-4 and 10 μg/ml human anti-IFN-gamma (all R&D Systems). After 8 days of cell culture, T cells were prepared and analyzed as described above.
Phagocytosis assay
Sorted slanDCs, CD1+ DCs, and CD14+ monocytes of healthy donors were maintained for 12 h in the presence or absence of 3 ng/ml or 30 ng/ml of FTY or FTYP in culture. To analyze, phagocytotic ability cells were treated with 1 μm carboxylate-modified yellow–green fluorescent FluoSpheres beads (Thermo Fisher Scientific, MA, USA) for 60 min at 37 °C. After cells were washed with PBS, incorporation of beads was evaluated by FACScan Calibur.
Apoptosis assay
Sorted slanDCs, CD1 + DCs, and CD14+ monocytes of healthy donors were cultured for 24 or 48 h in the presence or absence of different concentrations of FTY or FTYP (3 ng/ml; 30 ng/ml). Annexin was measured using a FITC-labeled antibody (BD Bioscience) to determine apoptosis at early stage, and APC-labeled fixable viability dye staining (BD Bioscience) was used to evaluate apoptosis at late stage characterized by DNA fragmentation. After, staining cells were analyzed by FACScan Calibur.
Statistical analysis
For repeated measure testing, repeated measure analysis of variance (ANOVA) with Bonferroni’s correction for compared pairs was used. Analyses with multiple comparisons but not repeated testing were evaluated by ANOVA with Bonferroni’s correction. Analyses without multiple testing were assessed by Student’s t test. Values of *p < 0.05, **p < 0.01, and ***p < 0.001 were considered significant.
Discussion
A growing number of studies highlight the relevance of sphingolipids and their related pathways that regulate innate immunity [
13,
17,
18]. Due to their characteristic properties of antigen uptake and antigen presentation to T cells, DCs are particular key players in balancing tolerogenic and immunogenic immune responses [
5]. Many studies hint at the importance of APCs, and particularly DCs, in the pathogenesis of MS by virtue of the initiation and perpetuation of T cell responses in periphery as well as in the CNS [
3,
6‐
9]. Growing evidence supports the concept of distinct modulation of innate immune cells in S1PR-focused therapies beyond their effects on lymphocyte recirculation [
14,
17,
18].
During long-term follow-up, the relative number of peripheral slanDCs, CD1+ DCs, and monocytes increased in FTY-treated patients. These effects are in line with the redistribution of peripheral lymphocytes during FTY treatment. But the absolute number of slanDCs also increased. Expression of S1PR1-S1PR4 on monocyte-derived DC surfaces has been investigated, and S1PR4 appears to be one of the dominant receptors subtypes in that environment [
19]. The impact of FTY and S1PR agonists on APC migration are contradictory and seem to depend on maturation and differentiation [
18,
22,
23]. Some reports have shown an increase in peripheral DC numbers in mice, combined with a decrease in the number of DCs in lymph nodes, thereby suggesting a downregulation of CCR7—but not S1PR1—during FTY treatment [
18,
20,
22‐
24]. Additionally, reduced migration of DCs in the presence of certain chemokines after FTY has been shown, and this indicates the possibility of inhibited DC migration into the CNS in inflammatory conditions such as those seen in active MS [
20,
24]. Different studies demonstrated significant expression of S1PR1-4 on human and murine DC subtypes [
16,
23,
25]. Systemic FTY administration leads to a decrease in expression of surface adhesion molecules and chemokine receptors including CCR7, which are essential for a variety of migratory processes [
20,
23]. S1PR agonism impaired DCs in activation and differentiation, which is important to upregulate adhesion molecules and chemokine receptors as well [
16,
23]. Reduced expression of these markers contributes to a decreased homing of DCs into lymphoid organs, but into inflamed tissues. These findings indicate that DC migration is additionally controlled by S1PRs and affected by S1PR-targeted therapies that account for increase in peripheral absolute DC count in our and recent study [
20,
23]. Further studies are needed to investigate the exact effect of FTY and its homologues on migration of slanDCs or other dendritic cells.
Due to the established effects of FTY on lymphocyte recirculation, CD4+ T cell counts decreased in our FTY-treated patients. But among CD4+ T cells exposed to FTY, the proportion of Th17 cells was reduced, while Treg cell numbers increased, thereby increasing the Treg/Th17 cell ratio of cells. These data are in line with previous reports of FTY use in patients that demonstrated a re-balanced distribution of T cells by virtue of decreased levels of effector T cells and increased levels of Treg cells [
26‐
28]. However, a direct or DC-independent impact of FTY on T cell polarization or proliferation in vitro could not be demonstrated [
29]. As APCs, and particularly DCs, are the most potent inducers and regulators of T cell responses, the potential modulation of DC function by FTY could be very powerful.
Upon activation and antigen uptake, DCs maturate, differentiate, and upregulate expression of surface markers such as CD83 or CD150 and co-stimulatory molecules including HLA-DR, CD86, CD80, or CD40. During FTY treatment in our patients, chiefly slanDCs, but also CD1 + DCs and monocytes, failed to maturate and express the co-stimulatory marker HLA-DR. This is in line with previous data [
16,
21].
APCs that fail to differentiate or increase expression of their co-stimulatory markers have impaired antigen presentation and T cell activation properties, which may lead to decreased induction of pro-inflammatory Th1/Th17 cell responses. CD86 is upregulated during the differentiation process on APCs, and there are some reports suggesting its relevance for induction of tolerance mechanisms in a range of immunological diseases [
30]. In our analysis, the expression of CD86 was increased in slanDCs and CD1+ DCs. These data are in concordance with those previously presented for other DC subsets [
14].
Our data suggest distinct but straightforward modulation of APC function by FTY treatment. In the literature, data on DC surface markers during FTY treatment have provided mixed results. Some studies did not find any impact on surface expression, particularly in in vitro studies [
15,
16]. Other findings are in line with our results [
14,
24,
31]. Certainly, in our analyses, impact of FTY and FTYP on expression of co-stimulatory and maturation markers was more pronounced in ex vivo analyses compared to in vitro investigations. These differences may be explained by the relatively shorter exposure time for in vitro FTY and FTYP compared with in vivo experiments. Human DCs present a pattern of selective expression of S1PR1-4 with highest levels of S1PR4 on immature DCs [
16,
25]. Upon maturation, especially S1PR1 is upregulated whereas S1PR4 is slightly decreased and S1PR2-3 are almost unaffected [
16,
32]. After FTY exposure, expression of S1PR1 and S1PR4 is reduced already after a short time period in human DCs [
16]. Further reports demonstrated direct modulation of inflammatory and T cell stimulatory characteristics via S1PR4 [
33,
34]. FTY acts as unselective S1PR agonist affecting S1PR1-5. Interestingly, compared to FTY, findings on S1PR expression differ after treatment with selective S1PR agonists in human DCs [
20]. These results indicate that impact of FTY on DCs is mediated by regulation of specific receptor expression profiles as well as direct intracellular signaling after S1PR agonism.
Interestingly, addition of S1P decreased surface expression of co-stimulatory molecules in slanDCs of healthy donors, leaving other APS subtypes unaffected. However, in FTY-treated patients, S1P-dependent modulation of surface markers on slanDCs was abrogated. These data further highlight slanDCs as distinct targets in modulation of S1P pathways via S1PR, and distinct from other APCs.
In addition to modulation of surface markers, further FTY-stimulated inhibition of pro-inflammatory cytokines was detected in slanDCs, CD1+ DCs, and monocytes both in vitro and ex vivo. Previous reports have shown a similar pattern of decrease of pro-inflammatory cytokines by fingolimod in murine bone marrow-derived DCs and induction of anti-inflammatory macrophages [
14,
15,
19,
24]. Furthermore and comparable to other reports in mice, phagocytic capacity was inhibited in FTY-treated slanDCs and monocytes in our study [
15]. These results suggest that FTY impairs important DCs capabilities, which are important for antigen uptake and processing as well as the pro-inflammatory destructive demyelinating process of the CNS in MS pathology [
15,
35‐
38].
IL-12 and IL-23 are known as essential regulators in DC-depending Th1 and Th17 differentiation and programming. The relevance of sphingolipids in IL-12 and IL-23 secretion in DCs and decreased expression of IL-12 in bone marrow-derived DCs and monocytes-derived DCs after FTY has been already reported [
15,
16,
18,
39‐
41]. However, slanDCs are one of the most potent inducers of Th17 and Th1 cells [
42,
43]. Our data demonstrate significant inhibition of IL-12 and IL-23 secretion after FTY exposure in vitro and ex vivo in slanDCs, but not in other DCs. In addition, we were able to demonstrate that FTY- or FTYP-treated slanDCs had reduced capacity to induce Th17 and Th1 cells as well as T cell proliferation in vitro. For the first time, these results could be confirmed in ex vivo experiments using slanDCs of FTY-treated patients. Th17 cells are known to be reduced in peripheral blood and CNS during FTY treatment [
26‐
28]. Previous studies presented that S1PR4 on DCs is critically involved in promotion of Th17 cells [
33].
We suggest that modulation of slanDCs by FTY treatment promotes the reduction of pro-inflammatory T cell activation and proliferation in MS. Effects on CD1+ DCs were less pronounced. Other studies have demonstrated a decrease in polarization of Th1 cells, but promotion of Th2 cells by FTY-treated monocytes-derived DCs [
16,
18,
19,
44]. Nevertheless, we could not identify increased activation of IL-4-producing Th2 cells by FTY-treated slanDCs or CD1+ DCs in vitro or ex vivo.
Acknowledgements
We thank M. Marggraf, N. Kretschmann, and S. Dartsch for the excellent technical assistance. Editorial support was provided by Nigel Eastmond of Eastmond Medicomm Ltd.