The JI
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
QUICK SEARCH:   [advanced]


     
 

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Penna, G.
Right arrow Articles by Adorini, L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Penna, G.
Right arrow Articles by Adorini, L.
The Journal of Immunology, 2007, 178: 145-153.
Copyright © 2007 by The American Association of Immunologists, Inc.

1,25-Dihydroxyvitamin D3 Selectively Modulates Tolerogenic Properties in Myeloid but Not Plasmacytoid Dendritic Cells1

Giuseppe Penna*, Susana Amuchastegui*, Nadia Giarratana*, Kenn C. Daniel*, Marisa Vulcano{dagger}, Silvano Sozzani{dagger} and Luciano Adorini2,*

* BioXell, Milan, Italy; and {dagger} Section of Immunology, Università degli Studi Brescia, Brescia, Italy


   Abstract
Top
 Abstract
Introduction
 Materials and Methods
 Results
 Discussion
 Disclosures
 References
 
1,25-Dihydroxyvitamin D3 (1,25(OH)2D3) is an immunomodulatory agent inducing dendritic cells (DCs) to become tolerogenic. To further understand its mechanisms of action, we have examined the effects of 1,25(OH)2D3 on tolerogenic properties of blood myeloid (M-DCs) and plasmacytoid (P-DCs) human DC subsets. Exposure of M-DCs to 1,25(OH)2D3 up-regulated production of CCL22, a chemokine attracting regulatory T cells, whereas production of CCL17, the other CCR4 ligand, was reduced. 1,25(OH)2D3 also decreased IL-12p75 production by M-DCs, as expected, and inhibited CCR7 expression. 1,25(OH)2D3 treatment markedly increased CD4+ suppressor T cell activity while decreasing the capacity of M-DCs to induce Th1 cell development. Surprisingly, 1,25(OH)2D3 did not exert any discernible effect on tolerogenic properties of P-DCs, and even their high production of IFN-{alpha} was not modulated. In particular, the intrinsically high capacity of P-DCs to induce CD4+ suppressor T cells was unaffected by 1,25(OH)2D3. Both DC subsets expressed similar levels of the vitamin D receptor, and its ligation by 1,25(OH)2D3 similarly activated the primary response gene cyp24. Interestingly, 1,25(OH)2D3 inhibited NF-{kappa}B p65 phosphorylation and nuclear translocation in M-DCs but not P-DCs, suggesting a mechanism for the inability of 1,25(OH)2D3 to modulate tolerogenic properties in P-DCs.


   Introduction
Top
 Abstract
 Introduction
Materials and Methods
 Results
 Discussion
 Disclosures
 References
 
The activated form of vitamin D, 1,25-dihydroxyvitamin D3 (1,25(OH)2D3),3 is a secosteroid hormone that has, in addition to its central function in calcium and bone metabolism, important effects on the growth and differentiation of many cell types and pronounced immunoregulatory properties (1, 2, 3, 4). The biological effects of 1,25(OH)2D3 are mediated by the vitamin D receptor (VDR), a member of the superfamily of nuclear hormone receptors functioning as a agonist-activated transcription factor that binds to specific DNA sequence elements, vitamin D responsive elements, in vitamin D responsive genes and ultimately influences their rate of RNA polymerase II-mediated transcription (5).

APCs, and notably dendritic cells (DCs), express the VDR and are key targets of VDR agonists, both in vitro and in vivo. A number of studies has clearly demonstrated that 1,25(OH)2D3 and its analogs markedly modulate DC phenotype and function (6, 7, 8, 9, 10, 11). These studies, performed either on monocyte-derived DCs from human peripheral blood or on bone marrow-derived mouse DCs, have consistently shown that in vitro treatment of DCs with 1,25(OH)2D3 and its analogs leads to down-regulated expression of the costimulatory molecules CD40, CD80, CD86, and to decreased IL-12 and enhanced IL-10 production, resulting in decreased T cell activation. The block of maturation, coupled with abrogation of IL-12 and strongly enhanced production of IL-10, highlight the important functional effects of 1,25(OH)2D3 and its analogs on DCs and are, at least in part, responsible for the induction of DCs with tolerogenic properties (12).

DCs are heterogeneous in terms of origin, morphology, phenotype, and function. Two distinct DC subsets, defined as myeloid DCs (M-DCs) and plasmacytoid DCs (P-DCs), have been identified in human and mouse blood (13, 14, 15). Human and mouse DCs of lymphoid and myeloid origin express a different repertoire of pattern recognition receptors and are characterized by a different cytokine production profile. P-DCs produce large amounts of type I IFNs in response to viruses and other pathogens, whereas M-DCs are the main IL-12 producers (16). Likewise, P-DCs and M-DCs produce a different pattern of chemokines (17) and exhibit a different migratory response upon exposure to a variety of ligands (18). The different properties of DC subsets highlight their complementary roles in the induction and regulation of innate and adaptive immune responses. M-DCs are the most efficient APCs directly able to prime naive T cells and can become, under different conditions, immunogenic or tolerogenic (19). P-DCs, under steady-state conditions, appear to play a key role in maintaining peripheral immune tolerance, and may be considered naturally occurring tolerogenic DCs (16).

Although the immunomodulatory effects of 1,25(OH)2D3 on DCs are well established, the capacity of this hormone to modulate DC subsets has not yet been addressed. In the present study, we have analyzed the immunomodulatory effects of 1,25(OH)2D3 on human blood M-DCs and P-DCs. The results demonstrate a differential capacity of 1,25(OH)2D3 to modulate cytokine and chemokine production in DC subsets, showing marked effects in M-DCs and negligible ones in P-DCs. Also inhibition of Th1 development and enhancement of CD4+ suppressor T cell activity are selectively induced by 1,25(OH)2D3 in M-DCs but not P-DCs. This different capacity of DC subsets to respond to 1,25(OH)2D3 is not due to a diverse VDR expression or to VDR-dependent signal transduction, but is associated with differential effects of this hormone on NF-{kappa}B p65 phosphorylation and nuclear translocation in DC subsets. The selective modulation of tolerogenic properties in DC subsets has important implications for understanding the immunoregulatory role of 1,25(OH)2D3.


   Materials and Methods
Top
 Abstract
 Introduction
 Materials and Methods
Results
 Discussion
 Disclosures
 References
 
Peripheral blood DC purification and culture

PBMCs were isolated from buffy coats by Ficoll gradient (Pharmacia Biotech), and peripheral blood M-DCs and P-DCs were magnetically sorted with blood DC Ag (BDCA)-1 and BDCA-4 cell isolation kits (Miltenyi Biotec), respectively, as described (20), to a purity of 95–98% in both cases. Blood M-DCs and P-DCs (2 x 104 cells/well) were cultured as described (18) in RPMI 1640 culture medium supplemented with 10% FCS (HyClone), 2 mM L-glutamine, 50 µg/ml gentamicin, 1 mM sodium pyruvate, and 1% nonessential amino acids (complete medium) containing 10 ng/ml recombinant human GM-CSF (BD Pharmingen) or 20 ng/ml IL-3 (BD Pharmingen), respectively. DC subset cells were stimulated with 1 µg/ml LPS (Escherichia coli O111:B4; Sigma-Aldrich), 6 µg/ml CpG oligonucleotide 2006 (MWG Biotec), CD40L (CD154)-transfected J558L cells at a ratio of 4:1, or PMA (100 ng/ml) plus ionomycin (1 µg/ml), both from Sigma-Aldrich. Crystalline 1,25(OH)2D3 was a gift of M. Uskokovic (BioXell), dexamethasone was purchased from Sigma-Aldrich, and recombinant human IL-10 from BD Pharmingen.

CD4+ T cell purification and culture

CD4+ T cells were purified from PBMC by negative selection with CD4 T cell isolation kit (Miltenyi Biotec), and CD4+CD45RA+ T cells were subsequently negative selected with CD4CD45RO beads (Miltenyi Biotec). CD4+ T cell were cocultured with allogenic ex vivo purified blood M-DC or P-DC in complete medium with or without 10 nM 1,25(OH)2D3. After 6 days of culture, CD4+ T cells were stained for the detection of intracellular IFN-{gamma}, IL-4, and IL-2 as previously described (21).

Assay for suppressive activity

Peripheral blood naive CD4+ T cells, purified as previously described from donor C, were cultured in the presence of purified DC subsets from donor D (ratio 1:10) with or without 10 nM 1,25(OH)2D3. At 7–10 days after primary stimulation, cells were restimulated under the same conditions. After two rounds of restimulation, CD4+ T cells were tested for suppressive activity. The read-out system was composed of CD4+CD25– cells from donor A PBMCs cultured in the presence of 1:10 LPS-matured monocyte-derived DCs from donor B. To evaluate the induction of regulatory T cells, graded amounts of CD4+ T cells from donor C, generated by three rounds of restimulation with allogeneic DC subsets from donor D, were added to the MLR read-out culture system. The suppression assay was performed in the presence of 1 µg/ml anti-human CD3 mAb. After 72 h of culture, IFN-{gamma} production in culture supernatants was quantified by two-site ELISA.

Chemokine and cytokine quantification

Concentrations of CCL17/TARC (R&D Systems), CCL22/MDC (R&D Systems), IL-12p75 (BD Pharmingen), IFN-{alpha} (Bender MedSystem) in DC subset culture supernatants were evaluated by sandwich ELISA according to the manufacturer’s instructions. IFN-{gamma} concentration was determined using paired mAb, as described previously (6). Detection limits were 5–15 pg/ml.

Flow cytometric analysis

Flow cytometric analysis was performed as previously described (17), in the presence of 200 µg/ml mouse IgG, using the mAbs anti-CD1c (BDCA-1) FITC or PE, anti-BDCA-2 FITC, or PE (Miltenyi Biotec), anti-HLA-DR (BD Pharmingen), and anti-CCR7 PE (BD Pharmingen). Analysis of NF-{kappa}B p65 phosphorylation was performed using the K10-895.12.50 PE mAb recognizing the phosphorylated S529 in the transactivation domain of NF-{kappa}B p65 (BD Biosciences), according to the manufacturer’s protocol. Cells were analyzed with a LSR flow cytometer (BD Biosciences) using CellQuest software.

Real-time quantitative RT-PCR

RNA was extracted using TRIzol (Invitrogen Life Technologies) according to the manufacturer’s instruction, followed by a cleanup with the RNeasy kit (Qiagen). Reverse transcription was performed, and real-time quantitative RT-PCR of total cDNA using specific primers was conducted using an ABI PRISM 7000 Sequence Detection System (Applied Biosystems) and TaqMan chemistry. The primers used are commercially available from Applied Biosystems as assays-on-demand. Relative quantification of target cDNA was determined by arbitrarily setting the control value to 1 and changes in cDNA content of a sample were expressed as a multiple thereof. Differences in cDNA input were corrected by normalizing to beta-actin or GAPDH signals. To exclude amplification of genomic DNA, RNA samples were treated with DNase (Sigma-Aldrich).

NF-{kappa}B nuclear translocation

Cells placed on poly-L-lysine-coated glass slides were permeabilized with 0.1% Triton X-100 for 4 min at 4°C and stained with rabbit anti-NF-{kappa}B p65 Ab (Santa Cruz Biotechnology), followed by polyclonal anti-rabbit FITC (Sigma-Aldrich). After washing, cells were stained with 2.5 µg/ml propidium iodide. Negative controls were performed by incubation with appropriate isotype-matched primary Abs. The slides were then washed again and mounted with 90% glycerol/PBS. Slides were analyzed with an MRC-1024 confocal microscope (Bio-Rad). Images were acquired and processed with Laser Sharp 3.2 software (Bio-Rad).


   Results
Top
 Abstract
 Introduction
 Materials and Methods
 Results
Discussion
 Disclosures
 References
 
1,25(OH)2D3 differentially modulates CCR4 ligand production in M-DCs without affecting it in P-DCs

We have previously shown that production of the homeostatic chemokines CCL17 and CCL22 is strictly compartmentalized in human DC subsets, and is a prerogative of M-DCs (17). Data in Fig. 1 confirm the selective capacity of M-DCs but not P-DCs to constitutively produce CCL17 and CCL22. In addition, they clearly show an opposite effect of 1,25(OH)2D3 on the production of these CCR4 ligands by M-DCs. CCL17 production is inhibited dose-dependently by 1,25(OH)2D3 in culture supernatants of unstimulated M-DCs after both 24 and 48 h of culture, whereas a marked up-regulation of CCL22 production is observed in the same culture supernatants. Conversely, neither CCL22 nor CCL17 production was induced in P-DCs by 1,25(OH)2D3.


Figure 1
View larger version (11K):
[in this window]
[in a new window]

  		FIGURE 1. 1,25(OH)2D3 modulates constitutive production of CCR4 ligands in M-DCs but not in P-DCs. Magnetically purified blood M-DCs and P-DCs (2 x 104 cells/well) were cultured in GM-CSF or IL-3, respectively, in the presence of the indicated concentrations of 1,25(OH)2D3. Secreted chemokines (ng/ml) were detected 24 h ({blacktriangleup}) and 48 h later (•) by two-site ELISA. The data are from one representative experiment of five performed.

 
Next, the effect of 1,25(OH)2D3 on CCR4 ligand production by DC subsets unstimulated or stimulated via CD40 ligation was compared (Fig. 2). CD40 ligation up-regulated CCL17 production in M-DCs, but failed to induce it in P-DCs (Fig. 2, see graphs), as previously reported (17). 1,25(OH)2D3 inhibited constitutive and induced CCL17 production by M-DCs equally well, with negligible effects on its production by P-DCs (Fig. 2). Two other anti-inflammatory agents targeting DCs, the glucocorticoid dexamethasone and IL-10, were also tested. Opposite to 1,25(OH)2D3, dexamethasone markedly up-regulated CCL17 production by M-DCs, whereas this production was inhibited by IL-10 similarly to 1,25(OH)2D3. A strong dose-dependent up-regulation of CCL17 was also induced by dexamethasone in unstimulated and CD40L-stimulated P-DCs, whereas no effect was induced by IL-10 (Fig. 2).


Figure 2
View larger version (16K):
[in this window]
[in a new window]

  		FIGURE 2. 1,25(OH)2D3, dexamethasone, and IL-10 modulate basal and CD40L-induced CCL17 and CCL22 production by M-DCs and P-DCs. Magnetically purified M-DCs and P-DCs (2 x 104 cells/well) were cultured in GM-CSF or IL-3, respectively, with or without CD40L-transfected J558 cells (CD40L). The indicated concentrations of 1,25(OH)2D3, dexamethasone, or IL-10 were added at culture initiation. Mean and SE of secreted chemokines (ng/ml) detected by two-site ELISA from 7 to 10 experiments are indicated. Data are representative of absolute values of chemokine production after 48 h of culture in basal conditions and following CD40 ligation. The effects of immunomodulatory agents tested are expressed as a percentage of the chemokine production in unstimulated control cultures.

 
CCL22 production was up-regulated by CD40 ligation both in M-DCs and P-DCs, as expected (17), and was further enhanced in unstimulated but not stimulated M-DCs by 1,25(OH)2D3, whereas a profound inhibition was induced by dexamethasone and IL-10 in both unstimulated and stimulated M-DCs. In CD40L-stimulated P-DCs, CCL22 production was again not substantially modulated by 1,25(OH)2D3, but was decreased markedly by dexamethasone and only slightly by IL-10.

1,25(OH)2D3 inhibits the Th1 cell-inducing capacity of M-DCs but not P-DCs

1,25(OH)2D3 selectively affects DC subsets also in their capacity to direct T cell development. Results in Fig. 3A show that both M-DC and P-DC induce naive alloreactive CD4+ T cells to differentiate mainly into Th1 cells, as defined by intracytoplasmic staining for IFN-{gamma} and IL-4. M-DCs compared with P-DCs activate a larger proportion of CD4+ T cells characterized by production of both IFN-{gamma} and IL-2. Incubation with 1,25(OH)2D3 inhibits the Th1-inducing capacity of M-DCs, as indicated by the selective inhibition of IFN-{gamma}-producing CD4+ T cells, with a modest effect on IL-2-producing CD4+ T cells (Fig. 3A). Conversely, no effect on the Th1-inducing capacity of P-DCs is exerted by 1,25(OH)2D3 (Fig. 3A). No observable skewing to the Th2 phenotype was induced by 1,25(OH)2D3 treatment in cultures containing either M-DCs or P-DCs. To analyze mechanisms potentially accounting for these differential effects, we have determined the capacity of 1,25(OH)2D3 to modulate IL-12p75 and IFN-{alpha} signature Th1-inducing cytokines selectively produced by M-DCs and P-DCs, respectively (16). 1,25(OH)2D3 reduces IL-12p75 production by CD40L-stimulated M-DCs, whereas IFN-{alpha} production by P-DC is not affected, thus suggesting an explanation for the selectivity of this agent in the inhibition of Th1 cell development (Fig. 3B). In contrast to 1,25(OH)2D3, other DC-targeting immunomodulatory agents, as dexamethasone and IL-10, inhibit constitutive and CD40L-induced IFN-{alpha} production by P-DCs (Fig. 3C).


Figure 3
View larger version (18K):
[in this window]
[in a new window]

  		FIGURE 3. 1,25(OH)2D3 inhibits the Th1 cell-inducing capacity of M-DCs but not P-DCs. Magnetically purified blood DC subsets were cocultured with allogeneic blood naive CD4+ cells for 7 days with or without 10 nM 1,25(OH)2D3. A, Percentage of positive cells evaluated by cytofluorimetry following intracellular staining for IFN-{gamma}, IL-2, and IL-4. A representative experiment of three performed is shown. B, IL-12p75 and IFN-{alpha} production by magnetically purified blood DC subsets cultured in GM-CSF or IL-3, respectively. After 48 h of culture, DC subsets were stimulated with CD40L-transfected J558 cells (CD40L) for additional 24 h with or without 10 nM 1,25(OH)2D3. Secreted IL-12p75 and IFN-{alpha} (ng/ml) were detected by two-site ELISA. C, 1,25(OH)2D3, unlike dexamethasone or IL-10, fails to inhibit IFN-{alpha} production by P-DCs. Magnetically purified M-DCs and P-DCs (2 x 104 cells/well) were cultured for 24 h in GM-CSF or IL-3, respectively, with medium alone or containing CD40L-transfected J558 cells (CD40L). The indicated concentrations of 1,25(OH)2D3, dexamethasone, or IL-10 were added at culture initiation. Mean and SE of secreted IFN-{alpha} detected by two-site ELISA from three independent experiments are indicated.

 
1,25(OH)2D3 enhances the capacity of M-DCs but not P-DCs to induce CD4+ suppressor T cell activity

To evaluate the capacity of 1,25(OH)2D3 to modulate tolerogenic properties of DC subsets, purified M-DCs and P-DCs were cultured with allogenic naive CD4+ cells for three rounds of restimulation in the presence or absence of 1,25(OH)2D3. The marked IFN-{gamma} production of CD4+CD25– cells (5853 pg/ml) is completely inhibited by addition of blood CD4+CD25+ cells (Fig. 4A). M-DCs give rise to CD4+ cells with suppressive activity, which at a 1:1 cell ratio reduces IFN-{gamma} production by ~60% from 5853 to 2418 pg/ml. This suppressive activity is greatly enhanced by addition of 1,25(OH)2D3, leading to near abrogation of IFN-{gamma} production at 1:1 suppressor to target cell ratio (Fig. 4B). P-DCs also induce CD4+ cells with suppressive activity, which appears to be slightly more potent compared with M-DCs, inducing 84% suppression at 1:1 cell ratio, but in this case no effect of 1,25(OH)2D3 can be observed (Fig. 4C).


Figure 4
View larger version (12K):
[in this window]
[in a new window]

  		FIGURE 4. 1,25(OH)2D3 enhances the capacity of M-DCs but not P-DCs to induce CD4+ suppressor T cell activity. The read-out system to test for suppressive activity was composed of CD4+CD25– cells from donor A PBMCs cultured with 1:10 DC subset cells from donor B in the presence of 1 µg/ml anti-human CD3 mAb. To evaluate the induction of T cells with suppressive activity, CD4+ T cells from donor C were generated by three rounds of restimulation with allogeneic DC subsets from donor D cultured with or without 10 nM 1,25(OH)2D3. IFN-{gamma} production was quantified in culture supernatants by two-site ELISA. A, IFN-{gamma} production by CD4+CD25– cells (5 x 104/well) cultured alone or with the indicated number of purified blood CD4+CD25+ T cells. B, Suppressive activity of CD4+ cells induced by allogenic M-DCs cultured with (circles) or without (triangles) 10 nM 1,25(OH)2D3. C, Suppressive activity of CD4+ cells induced by allogenic P-DCs cultured with (circles) or without (triangles) 10 nM 1,25(OH)2D3.

 
1,25(OH)2D3 modulates MHC class II, Ig-like transcript (ILT)3, and costimulatory molecule expression selectively in M-DCs

The selective capacity of 1,25(OH)2D3 to modulate cytokine and chemokine production in M-DCs but not P-DCs, prompted us to examine whether surface molecules crucial for DC activity were differentially affected in DC subsets. To this end, we analyzed the effects of 1,25(OH)2D3 on MHC class II and CD40 molecules, key players in CD4+ T cell responses, and expression of ILT3, an inhibitory receptor expressed by tolerogenic DCs (11, 22). Incubation with 1,25(OH)2D3 inhibited basal levels of MHC class II and CD40 molecule expression in M-DCs but not P-DCs (Fig. 5A). ILT3 expression was selectively up-regulated in M-DCs, while it remained unaffected in P-DCs, following treatment with 1,25(OH)2D3 (Fig. 5A). In addition, no modulation of CD80 and CD86 expression was induced by 1,25(OH)2D3 in P-DCs unstimulated or stimulated with CD40L-transfected cells. In contrast, a marked inhibition of CD80 and CD86 expression was induced by 1,25(OH)2D3 in M-DCs, either unstimulated or stimulated with CD40L-transfected cells (Fig. 5B). CD40 ligation enhanced expression of costimulatory molecules in both DC subsets, up-regulating CD80 mean fluorescence intensity from 438 to 1647 in M-DCs and from 673 to 2981 in P-DCs, whereas CD86 mean fluorescence intensity increased from 1352 to 6051 in M-DCs and from 426 to 3922 in P-DCs.


Figure 5
View larger version (20K):
[in this window]
[in a new window]

  		FIGURE 5. 1,25(OH)2D3 modulates MHC class II, ILT3, and costimulatory molecule expression selectively in M-DCs. Magnetically purified blood M-DCs and P-DCs (2 x 104 cells/well) were cultured in GM-CSF or IL-3, respectively. A, Surface expression of HLA-DR, CD40, and ILT3 in unstimulated DC subpopulations from a representative donor cultured for 48 h in medium alone or containing the indicated concentrations of 1,25(OH)2D3. B, Surface expression of CD80 and CD86 in DC subsets unstimulated or stimulated with CD40L-transfected J558 cells (CD40L) cultured for 48 h in medium alone or containing the indicated concentrations of 1,25(OH)2D3. Mean data from two individual donors are shown. The geometric mean fluorescence intensity (MFI) data represent the percentage variation compared with the marker expression in M-DCs ({circ}) or P-DCs (•) cultured without 1,25(OH)2D3.

 
Gene modulation induced by 1,25(OH)2D3 in M-DCs and P-DCs

Given the apparent lack of P-DC responsiveness to 1,25(OH)2D3, we investigated VDR expression and response to 1,25(OH)2D3 in DC subsets. A comparably high VDR expression was observed in ex vivo purified M-DCs and P-DCs (Fig. 6), which was similar to VDR expression detected in immature monocyte-derived DC and monocytes (data not shown). VDR signal transduction was also comparable in both DC subsets, as shown (Fig. 6) by the marked up-regulation of cyp24, a primary VDR response gene encoding the 24-hydroxylase enzyme catalyzing 1,25(OH)2D3 metabolism, which is rapidly induced following exposure to 1,25(OH)2D3 (5). Thus, both M-DCs and P-DCs express similar VDR levels, and respond equally well to VDR ligation by up-regulating primary response genes.


Figure 6
View larger version (4K):
[in this window]
[in a new window]

  		FIGURE 6. Gene modulation induced by 1,25(OH)2D3 in M-DCs and P-DCs. M-DCs and P-DCs express similar levels of VDR and up-regulate equally well primary VDR response genes following stimulation with 1,25(OH)2D3. Magnetically purified blood M-DCs and P-DCs (2 x 104 cells/well) were cultured with or without 10 nM 1,25(OH)2D3. After 2 h, RNA was extracted and expression of VDR and cyp24 transcripts evaluated by real-time RT-PCR. Data are representative of arbitrary units normalized to GAPDH signals and are from one representative experiment of five conducted.

 
1,25(OH)2D3 inhibits NF-{kappa}B phosphorylation and nuclear translocation in M-DCs but not P-DCs

The transcription factor NF-{kappa}B regulates in DCs expression of genes encoding several cytokines and chemokines. NF-{kappa}B family proteins, c-Rel, RelA (p65), RelB, NF-{kappa}B1 (p50), and NF-{kappa}B2 (p52) are present in the cytoplasm in an inactive form as a result of their association with the inhibitory proteins I{kappa}B{alpha}, I{kappa}Bbeta, and I{kappa}B{epsilon}, and must be phosphorylated and translated to the nucleus to become activated (23). To test whether 1,25(OH)2D3 could reduce phosphorylation of NF-{kappa}B p65, untreated and 1,25(OH)2D3-treated M-DCs and P-DCs were stimulated with PMA with ionomycin, a nonspecific stimulus activating both subsets, and stained with a mAb recognizing the phosphorylated S529 in the transactivation domain of NF-{kappa}B p65. Results in Fig. 7A show that phosphorylation of NF-{kappa}B p65, detected by cytofluorimetry, was reduced by 1,25(OH)2D3 in M-DCs but not in P-DCs, whereas dexamethasone was able to inhibit it in both DC subsets. Inhibition of NF-{kappa}B p65 phosphorylation in P-DCs by dexamethasone but not by 1,25(OH)2D3 was confirmed in a time-course experiment (Fig. 7B). In this experiment, the area under the curve for control P-DCs was 34,913, which was reduced by ~40% in dexamethasone-treated cells (area under the curve was 22,065), but was unaffected following treatment of P-DCs with 1,25(OH)2D3 (area under the curve was 36,270). Supporting these data, 1,25(OH)2D3 could reduce translocation of NF-{kappa}B p65 to the nucleus in M-DCs but not P-DCs. M-DCs and P-DCs were cultured for 18 h with or without 1,25(OH)2D3 followed by stimulation for 45 min with LPS or CpG, respectively, before staining with anti-NF-{kappa}B p65 mAb and propidium iodide (Fig. 7, C and D). Individual and merged staining obtained by confocal microscopic analysis clearly show translocation of NF-{kappa}B p65 to the nucleus in stimulated M-DCs, whereas NF-{kappa}B p65 is mostly retained in the cytoplasm in cells treated with 1,25(OH)2D3 (Fig. 7C). Conversely, the nuclear translocation induced in P-DCs by CpG stimulation is not affected by 1,25(OH)2D3 treatment (Fig. 7D).


Figure 7
View larger version (37K):
[in this window]
[in a new window]

  		FIGURE 7. 1,25(OH)2D3 inhibits NF-{kappa}B p65 phosphorylation and traps it into the cytoplasm in M-DCs but not P-DCs. Magnetically purified M-DCs and P-DCs were cultured in GM-CSF or IL-3, respectively, with medium alone or containing 100 nM 1,25(OH)2D3 or 100 nM dexamethasone (Dex). After an 18-h culture, M-DCs and P-DCs were incubated with medium only (unstimulated), or containing 100 ng/ml PMA plus 1 µg/ml ionomycin (A and B), 1 µg/ml LPS (C), or 6 µg/ml CpG 2006 (D), respectively, for 45 min or as indicated. NF-{kappa}B p65 phosphorylation was determined by cytofluorimetry. A, The percentage of cells positive for phosphorylated S529 in the transactivation domain of NF-{kappa}B p65, relative to controls, for 60 min after stimulation. B, The geometric mean fluorescence intensity (MFI) of P-DCs positive for phosphorylated NF-{kappa}B p65 at the indicated times after PMA-ionomycin stimulation. Histogram analysis of positive cells is shown (right) 15 min after stimulation. C and D, Cells were fixed and stained with anti-NF-{kappa}B p65 mAb and propidium iodide (PI). Individual and merged stainings are shown. Original magnifications is x63.

 

   Discussion
Top
 Abstract
 Introduction
 Materials and Methods
 Results
 Discussion
Disclosures
 References
 
VDR agonists share with other immunomodulatory agents, and in particular with immunosuppressive and anti-inflammatory drugs, the capacity to target DCs, rendering them tolerogenic and fostering the induction of regulatory rather than effector T cells (12, 24). Multiple mechanisms contribute to induction of DC tolerogenicity by VDR agonists, from down-regulation of costimulatory molecules, both membrane-bound as CD40, CD80, CD86 and secreted as IL-12, to up-regulation of anti-inflammatory molecules like IL-10 (4, 25). Additional mechanisms involve modulation of chemokine secretion, enhancing the production of chemokines able to recruit regulatory/suppressor T cells, and inhibiting chemokine production by target organs in autoimmune diseases (26, 27). These effects are not limited to in vitro activity: 1,25(OH)2D3 and its analogs can also induce DCs with tolerogenic properties in vivo, as demonstrated in models of allograft rejection (28, 29). Tolerogenic DCs induced by a short treatment with 1,25(OH)2D3 are probably responsible for the capacity of this hormone to induce CD4+CD25+ regulatory T cells that are able to mediate transplantation tolerance (28) and arrest the development of type 1 diabetes (30).

CCL22 and CCL17 are chemokines able to recruit activated T cells, and in particular Th2 cells, via CCR4 (31, 32). In addition, these chemokines can recruit CD4+CD25+ regulatory T cells (33). CCL22, a chemokine mostly produced by DCs (34), has been found to selectively recruit, in ovarian carcinoma patients, Foxp3+CCR4+CD4+CD25+ regulatory T cells able to suppress antitumor responses, leading to reduced patient survival (35). Similarly, CCL22 secreted by lymphoma B cells attracts Foxp3+ CCR4+CD4+CD25+ regulatory T cells able to suppress proliferation and cytokine production by tumor-infiltrating CD4+CD25– T cells (36). We have found that, in contrast to the high production by circulating M-DCs, the CCR4 agonists CCL17 and CCL22 are very poorly produced by unstimulated P-DCs and only CCL22 is secreted at high levels by this DC subset following CD40 ligation, as previously reported (17). Blood-borne M-DCs, in contrast to P-DCs, constitutively produce high levels of CCL17 and CCL22 ex vivo, which are further enhanced by CD40 stimulation, confirming previous data (17). This high constitutive and inducible production of CCR4 agonists by immature M-DCs could lead to the preferential attraction of CD4+CD25+ regulatory T cells. Intriguingly, the production of CCL22 is markedly enhanced by 1,25(OH)2D3 in blood M-DCs, indicating that VDR agonists may favor the recruitment of regulatory T cells by this DC subset. 1,25(OH)2D3 not only regulates in M-DCs production of chemokines potentially able to recruit regulatory T cells, but also enhances their induction, a novel finding consistent with previous in vivo data (28, 30). Conversely, neither CCL22 nor CCL17 are modulated by 1,25(OH)2D3 in P-DCs, and although this DC subset induces regulatory T cells, consistent with previous reports (37, 38), this property is not modified by 1,25(OH)2D3. However, other chemokines may be involved in regulatory T cell recruitment by P-DCs, which produce large quantities of the CCR5 agonist CCL4 (17). Thus, in analogy with the proposed role for CCL4 in CD4+CD25+ regulatory T cell attraction by activated B cells (39), P-DCs could recruit them via secretion of this chemokine.

In addition to CCL22 and CCL17, neither IFN-{alpha}, the signature cytokine produced by P-DCs (16), nor expression of MHC class II molecules, CD40, CD80, CD86 costimulatory molecules, or ILT3 inhibitory molecule are affected in P-DCs by 1,25(OH)2D3 treatment. Conversely, production of IL-12, the M-DC signature cytokine (16), as well as MHC class II and costimulatory molecule expression are markedly inhibited by 1,25(OH)2D3 in M-DCs, while the inhibitory molecule ILT3 is strongly up-regulated. Interestingly, these novel findings confirm in blood M-DCs the capacity of 1,25(OH)2D3, previously observed in monocyte-derived DCs (6, 11), to inhibit MHC class II and costimulatory molecule expression while up-regulating the inhibitory molecule ILT3. All these molecules are controlled by NF-{kappa}B, a signal transduction pathway crucially involved in the inflammatory response (23). In particular, production of IL-12 (40, 41), type I IFNs (42), CCL17 (43, 44), CCL22 (44, 45, 46), and expression of MHC class II molecules (47), CD40 (48), CD80 (49), CD86 (50), and ILT3 (22) have been shown to be regulated by NF-{kappa}B activity. Our data showing inhibition of NF-{kappa}B p65 phosphorylation and nuclear translocation by 1,25(OH)2D3 in M-DCs but not P-DCs demonstrate a mechanism of action selectively targeting NF-{kappa}B in DC subpopulations. The selective targeting of NF-{kappa}B components by VDR agonists in M-DCs could thus contribute to explain the lack of activity of these agents on cytokine and chemokine production by P-DCs, which nevertheless respond to 1,25(OH)2D3, as shown by cyp24 up-regulation.

NF-{kappa}B is a target for many anti-inflammatory and immunosuppressive agents (12), including glucocorticoids, anti-inflammatory drugs that bind to a nuclear receptor in the same superfamily as the VDR, as shown by the observation that dexamethasone up-regulates the transcription of Nfkbia, resulting in increased rate of I{kappa}B{alpha} synthesis and in reduced NF-{kappa}B p65 phosphorylation and translocation to the nucleus (51, 52). Our results show that 1,25(OH)2D3 and dexamethasone exert opposite effects on CCL17 and CCL22 regulation in both M-DCs and P-DCs. Strikingly, dexamethasone markedly enhances constitutive and inducible CCL17 production in M-DCs, and induces it in P-DCs. Differential effects of these anti-inflammatory agents on chemokine production by bone marrow-derived DCs have been reported, possibly due to differential regulation of NF-{kappa}B family members by the two steroid pathways (53, 54). Additional levels of NF-{kappa}B regulation by 1,25(OH)2D3 and dexamethasone have also been reported in other immune and nonimmune cell types, including up-regulation of I{kappa}B{alpha}, direct intranuclear binding of NF-{kappa}B proteins, and direct negative regulation of NF-{kappa}B-induced genes (26, 40, 51, 52, 55, 56). This complex regulation could also explain the increased CCL22 and decreased CCL17 production induced by 1,25(OH)2D3 in M-DCs.

DCs are able to synthesize 1,25(OH)2D3 in vitro as a consequence of increased 1{alpha}-hydroxylase expression (57), and this could also contribute to promote regulatory T cell induction and recruitment. It is also possible that 1,25(OH)2D3 may contribute to the physiological control of immune responses, and possibly be also involved in maintaining tolerance to self Ags, as suggested by the enlarged lymph nodes containing a higher frequency of mature DCs in VDR-deficient mice (29). Our results showing increased induction of suppressor CD4+ T cell activity by M-DCs in the presence of 1,25(OH)2D3 support this possibility. Conversely, 1,25(OH)2D3 does not modulate the intrinsic tolerogenic capacity of P-DCs, consistent with earlier observations showing selective up-regulation of the inhibitory receptor ILT3 on M-DCs, without affecting its high expression on P-DC (11). Because P-DCs are key cells linking innate and adaptive immunity (16), the lack of up-regulation by 1,25(OH)2D3 of their constitutive tolerogenic function may contribute to explain the intact host resistance against infectious agents following 1,25(OH)2D3 administration (58).

In conclusion, 1,25(OH)2D3 appears to up-regulate tolerogenic properties in M-DCs, down-regulating IL-12 and Th1 cell development, while promoting CD4+ suppressor T cell activity and enhancing the production of CCL22, a chemokine able to recruit regulatory T cells. In contrast, no immunomodulatory effects induced by 1,25(OH)2D3 are observed in P-DCs, a DC subset prone to favor tolerance under steady-state conditions (16) or during an immune response (59). Indeed, P-DCs, characterized by an intrinsic ability to prime naive CD4+ T cells to differentiate into IL-10-producing T cells (60, 61, 62, 63) and CD4+CD25+ regulatory T cells (38), and to suppress immune responses (64, 65), may represent naturally occurring regulatory DCs (16). The lack of immunoregulatory feature modulation by 1,25(OH)2D3 in P-DCs would thus leave their tolerogenic potential unmodified.


   Disclosures
Top
 Abstract
 Introduction
 Materials and Methods
 Results
 Discussion
 Disclosures
References
 
G. Penna, S. Amuchastegui, and L. Adorini own stock or equity interests in BioXell.


   Footnotes
 
The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked advertisement in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

1 This work was supported in part by the European Community grant INNOCHEM (to L.A.), and by grants from Associazione Italiana Ricerca Cancro and Ministero dell’Università e della Ricerca scientifica (to S.S.). Back

2 Address correspondence and reprint requests to Dr. Luciano Adorini, BioXell, Via Olgettina 58, I-20132 Milan, Italy. E-mail address: Luciano.Adorini{at}bioxell.com Back

3 Abbreviations used in this paper: 1,25(OH)2D3, 1,25-dihydroxyvitamin D3; DC, dendritic cell; M-DC, myeloid DC; P-DC, plasmacytoid DC; VDR, vitamin D receptor; BDCA, blood DC Ag; ILT, Ig-like transcript. Back

Received for publication July 10, 2006. Accepted for publication October 18, 2006.


   References
Top
 Abstract
 Introduction
 Materials and Methods
 Results
 Discussion
 Disclosures
 References
 

  1. Deluca, H. F., M. T. Cantorna. 2001. Vitamin D: its role and uses in immunology. FASEB J. 15: 2579-2585. [Abstract/Free Full Text]
  2. Mathieu, C., L. Adorini. 2002. The coming of age of 1,25-dihydroxyvitamin D3 analogs as immunomodulatory agents. Trends Mol. Med. 8: 174-179. [Medline]
  3. Adorini, L.. 2002. 1,25-Dihydroxyvitamin D3 analogs as potential therapies in transplantation. Curr. Opin. Investig. Drugs 3: 1458-1463. [Medline]
  4. Dong, X., T. A. Craig, N. Xing, L. A. Bachman, C. V. Paya, F. Weih, D. J. McKean, R. Kumar, M. D. Griffin. 2003. Direct transcriptional regulation of RelB by 1{alpha},25-dihydroxyvitamin D3 and its analogs: physiologic and therapeutic implications for dendritic cell function. J. Biol. Chem. 278: 49378-49385. [Abstract/Free Full Text]
  5. Carlberg, C., P. Polly. 1998. Gene regulation by vitamin D3. Crit. Rev. Eukaryot. Gene Expr. 8: 19-42. [Medline]
  6. Penna, G., L. Adorini. 2000. 1,25-Dihydroxyvitamin D3 inhibits differentiation, maturation, activation and survival of dendritic cells leading to impaired alloreactive T cell activation. J. Immunol. 164: 2405-2411. [Abstract/Free Full Text]
  7. Piemonti, L., P. Monti, M. Sironi, P. Fraticelli, B. E. Leone, E. Dal Cin, P. Allavena, V. Di Carlo. 2000. Vitamin D3 affects differentiation, maturation, and function of human monocyte-derived dendritic cells. J. Immunol. 164: 4443-4451. [Abstract/Free Full Text]
  8. Griffin, M. D., W. H. Lutz, V. A. Phan, L. A. Bachman, D. J. McKean, R. Kumar. 2000. Potent inhibition of dendritic cell differentiation and maturation by vitamin D analogs. Biochem. Biophys. Res. Commun. 270: 701-708. [Medline]
  9. van Halteren, A. G., E. van Etten, E. C. de Jong, R. Bouillon, B. O. Roep, C. Mathieu. 2002. Redirection of human autoreactive T-cells upon interaction with dendritic cells modulated by TX527, an analog of 1,25 dihydroxyvitamin D3. Diabetes 51: 2119-2125. [Abstract/Free Full Text]
  10. Gauzzi, M. C., C. Purificato, K. Donato, Y. Jin, L. Wang, K. C. Daniel, A. A. Maghazachi, F. Belardelli, L. Adorini, S. Gessani. 2005. Suppressive effect of 1{alpha},25-dihydroxyvitamin D3 on type I IFN-mediated monocyte differentiation into dendritic cells: impairment of functional activities and chemotaxis. J. Immunol. 174: 270-276. [Abstract/Free Full Text]
  11. Penna, G., A. Roncari, S. Amuchastegui, K. C. Daniel, E. Berti, M. Colonna, L. Adorini. 2005. Expression of the inhibitory receptor ILT3 on dendritic cells is dispensable for induction of CD4+Foxp3+ regulatory T cells by 1,25-dihydroxyvitamin D3. Blood 106: 3490-3497. [Abstract/Free Full Text]
  12. Adorini, L., N. Giarratana, G. Penna. 2004. Pharmacological induction of tolerogenic dendritic cells and regulatory T cells. Semin. Immunol. 16: 127-134. [Medline]
  13. Shortman, K., Y. J. Liu. 2002. Mouse and human dendritic cell subtypes. Nat. Rev. Immunol. 2: 151-161. [Medline]
  14. Colonna, M., G. Trinchieri, Y. J. Liu. 2004. Plasmacytoid dendritic cells in immunity. Nat. Immunol. 5: 1219-1226. [Medline]
  15. Asselin-Paturel, C., G. Trinchieri. 2005. Production of type I interferons: plasmacytoid dendritic cells and beyond. J. Exp. Med. 202: 461-465. [Abstract/Free Full Text]
  16. Liu, Y. J.. 2005. IPC: professional type 1 interferon-producing cells and plasmacytoid dendritic cell precursors. Annu. Rev. Immunol. 23: 275-306. [Medline]
  17. Penna, G., M. Vulcano, A. Roncari, F. Facchetti, S. Sozzani, L. Adorini. 2002. Differential chemokine production by myeloid and plasmacytoid dendritic cells. J. Immunol. 169: 6673-6676. [Abstract/Free Full Text]
  18. Penna, G., S. Sozzani, L. Adorini. 2001. Cutting edge: selective usage of chemokine receptors by plasmacytoid dendritic cells. J. Immunol. 167: 1862-1866. [Abstract/Free Full Text]
  19. Steinman, R. M., D. Hawiger, M. C. Nussenzweig. 2003. Tolerogenic dendritic cells. Annu. Rev. Immunol. 21: 685-711. [Medline]
  20. Dzionek, A., A. Fuchs, P. Schmidt, S. Cremer, M. Zysk, S. Miltenyi, D. W. Buck, J. Schmitz. 2000. BDCA-2, BDCA-3, and BDCA-4: three markers for distinct subsets of dendritic cells in human peripheral blood. J. Immunol. 165: 6037-6046. [Abstract/Free Full Text]
  21. Rogge, L., D. D’Ambrosio, M. Biffi, G. Penna, L. J. Minetti, D. H. Presky, L. Adorini, F. Sinigaglia. 1998. The role of Stat4 in species-specific regulation of Th cell development by type I IFNs. J. Immunol. 161: 6567-6574. [Abstract/Free Full Text]
  22. Chang, C. C., R. Ciubotariu, J. S. Manavalan, J. Yuan, A. I. Colovai, F. Piazza, S. Lederman, M. Colonna, R. Cortesini, R. Dalla-Favera, N. Suciu-Foca. 2002. Tolerization of dendritic cells by TS cells: the crucial role of inhibitory receptors ILT3 and ILT4. Nat. Immunol. 3: 237-243. [Medline]
  23. Li, Q., I. M. Verma. 2002. NF-{kappa}B regulation in the immune system. Nat. Rev. Immunol. 2: 725-734. [Medline]
  24. Hackstein, H., A. W. Thomson. 2004. Dendritic cells: emerging pharmacological targets of immunosuppressive drugs. Nat. Rev. Immunol. 4: 24-34. [Medline]
  25. Adorini, L., G. Penna, N. Giarratana, A. Roncari, S. Amuchastegui, K. C. Daniel, M. Uskokovic. 2004. Dendritic cells as key targets for immunomodulation by vitamin D receptor ligands. J. Steroid Biochem. Mol. Biol. 89–90: 437-441.
  26. Giarratana, N., G. Penna, S. Amuchastegui, R. Mariani, K. C. Daniel, L. Adorini. 2004. A vitamin D analog downregulates proinflammatory chemokine production by pancreatic islets inhibiting T cell recruitment and type 1 diabetes development. J. Immunol. 173: 2280-2287. [Abstract/Free Full Text]
  27. Gysemans, C. A., A. K. Cardozo, H. Callewaert, A. Giulietti, L. Hulshagen, R. Bouillon, D. L. Eizirik, C. Mathieu. 2005. 1,25-Dihydroxyvitamin D3 modulates expression of chemokines and cytokines in pancreatic islets: implications for prevention of diabetes in nonobese diabetic mice. Endocrinology 146: 1956-1964. [Abstract/Free Full Text]
  28. Gregori, S., M. Casorati, S. Amuchastegui, S. Smiroldo, A. M. Davalli, L. Adorini. 2001. Regulatory T cells induced by 1{alpha},25-dihydroxyvitamin D3 and mycophenolate mofetil treatment mediate transplantation tolerance. J. Immunol. 167: 1945-1953. [Abstract/Free Full Text]
  29. Griffin, M. D., W. Lutz, V. A. Phan, L. A. Bachman, D. J. McKean, R. Kumar. 2001. Dendritic cell modulation by 1{alpha},25 dihydroxyvitamin D3 and its analogs: a vitamin D receptor-dependent pathway that promotes a persistent state of immaturity in vitro and in vivo. Proc. Natl. Acad. Sci. USA 98: 6800-6805. [Abstract/Free Full Text]
  30. Gregori, G., N. Giarratana, S. Smiroldo, M. Uskokovic, L. Adorini. 2002. A 1{alpha},25-dihydroxyvitamin D3 analog enhances regulatory T cells and arrests autoimmune diabetes in NOD mice. Diabetes 51: 1367-1374. [Abstract/Free Full Text]
  31. Andrew, D. P., M. S. Chang, J. McNinch, S. T. Wathen, M. Rihanek, J. Tseng, J. P. Spellberg, C. G. Elias, III. 1998. STCP-1 (MDC) CC chemokine acts specifically on chronically activated Th2 lymphocytes and is produced by monocytes on stimulation with Th2 cytokines IL-4 and IL-13. J. Immunol. 161: 5027-5038. [Abstract/Free Full Text]
  32. Imai, T., M. Nagira, S. Takagi, M. Kakizaki, M. Nishimura, J. Wang, P. W. Gray, K. Matsushima, O. Yoshie. 1999. Selective recruitment of CCR4-bearing Th2 cells toward antigen-presenting cells by the CC chemokines thymus and activation-regulated chemokine and macrophage-derived chemokine. Int. Immunol. 11: 81-88. [Abstract/Free Full Text]
  33. Iellem, A., M. Mariani, R. Lang, H. Recalde, P. Panina-Bordignon, F. Sinigaglia, D. D’Ambrosio. 2001. Unique chemotactic response profile and specific expression of chemokine receptors CCR4 and CCR8 by CD4+CD25+ regulatory T cells. J. Exp. Med. 194: 847-853. [Abstract/Free Full Text]
  34. Vulcano, M., C. Albanesi, A. Stoppacciaro, R. Bagnati, G. D’Amico, S. Struyf, P. Transidico, R. Bonecchi, A. Del Prete, P. Allavena, et al 2001. Dendritic cells as a major source of macrophage-derived chemokine/CCL22 in vitro and in vivo. Eur. J. Immunol. 31: 812-822. [Medline]
  35. Curiel, T. J., G. Coukos, L. Zou, X. Alvarez, P. Cheng, P. Mottram, M. Evdemon-Hogan, J. R. Conejo-Garcia, L. Zhang, M. Burow, et al 2004. Specific recruitment of regulatory T cells in ovarian carcinoma fosters immune privilege and predicts reduced survival. Nat. Med. 10: 942-949. [Medline]
  36. Yang, Z. Z., A. J. Novak, M. J. Stenson, T. E. Witzig, S. M. Ansell. 2006. Intratumoral CD4+CD25+ regulatory T-cell-mediated suppression of infiltrating CD4+ T-cells in B-cell non-Hodgkin lymphoma. Blood 107: 3639-3646. [Abstract/Free Full Text]
  37. Gilliet, M., Y. J. Liu. 2002. Generation of human CD8 T regulatory cells by CD40 ligand-activated plasmacytoid dendritic cells. J. Exp. Med. 195: 695-704. [Abstract/Free Full Text]
  38. Moseman, E. A., X. Liang, A. J. Dawson, A. Panoskaltsis-Mortari, A. M. Krieg, Y. J. Liu, B. R. Blazar, W. Chen. 2004. Human plasmacytoid dendritic cells activated by CpG oligodeoxynucleotides induce the generation of CD4+CD25+ regulatory T cells. J. Immunol. 173: 4433-4442. [Abstract/Free Full Text]
  39. Bystry, R. S., V. Aluvihare, K. A. Welch, M. Kallikourdis, A. G. Betz. 2001. B cells and professional APCs recruit regulatory T cells via CCL4. Nat. Immunol. 2: 1126-1132. [Medline]
  40. D’Ambrosio, D., M. Cippitelli, M. G. Cocciolo, D. Mazzeo, P. Di Lucia, R. Lang, F. Sinigaglia, P. Panina-Bordignon. 1998. Inhibition of IL-12 production by 1,25-dihydroxyvitamin D3: involvement of NF-{kappa}B downregulation in transcriptional repression of the p40 gene. J. Clin. Invest. 101: 252-262. [Medline]
  41. Lyakh, L. A., M. Sanford, S. Chekol, H. A. Young, A. B. Roberts. 2005. TGF-beta and vitamin D3 utilize distinct pathways to suppress IL-12 production and modulate rapid differentiation of human monocytes into CD83+ dendritic cells. J. Immunol. 174: 2061-2070. [Abstract/Free Full Text]
  42. Remoli, M. E., E. Giacomini, G. Lutfalla, E. Dondi, G. Orefici, A. Battistini, G. Uze, S. Pellegrini, E. M. Coccia. 2002. Selective expression of type I IFN genes in human dendritic cells infected with Mycobacterium tuberculosis. J. Immunol. 169: 366-374. [Abstract/Free Full Text]
  43. Komine, M., T. Kakinuma, S. Kagami, Y. Hanakawa, K. Hashimoto, K. Tamaki. 2005. Mechanism of thymus- and activation-regulated chemokine (TARC)/CCL17 production and its modulation by roxithromycin. J. Invest. Dermatol. 125: 491-498. [Medline]
  44. Nakayama, T., K. Hieshima, D. Nagakubo, E. Sato, M. Nakayama, K. Kawa, O. Yoshie. 2004. Selective induction of Th2-attracting chemokines CCL17 and CCL22 in human B cells by latent membrane protein 1 of Epstein-Barr virus. J. Virol. 78: 1665-1674. [Abstract/Free Full Text]
  45. Berin, M. C., M. B. Dwinell, L. Eckmann, M. F. Kagnoff. 2001. Production of MDC/CCL22 by human intestinal epithelial cells. Am. J. Physiol. 280: G1217-G1226.
  46. Ghadially, H., X. L. Ross, C. Kerst, J. Dong, A. B. Reske-Kunz, R. Ross. 2005. Differential regulation of CCL22 gene expression in murine dendritic cells and B cells. J. Immunol. 174: 5620-5629. [Abstract/Free Full Text]
  47. Blanar, M. A., L. C. Burkly, R. A. Flavell. 1989. NF-{kappa}B binds within a region required for B-cell-specific expression of major histocompatibility complex class II gene E{alpha}d. Mol. Cell. Biol. 9: 844-846. [Abstract/Free Full Text]
  48. Hinz, M., P. Loser, S. Mathas, D. Krappmann, B. Dorken, C. Scheidereit. 2001. Constitutive NF-{kappa}B maintains high expression of a characteristic gene network, including CD40, CD86, and a set of antiapoptotic genes in Hodgkin/Reed-Sternberg cells. Blood 97: 2798-2807. [Abstract/Free Full Text]
  49. Zhao, J., G. J. Freeman, G. S. Gray, L. M. Nadler, L. H. Glimcher. 1996. A cell type-specific enhancer in the human B7.1 gene regulated by NF-{kappa}B. J. Exp. Med. 183: 777-789. [Abstract/Free Full Text]
  50. Li, J., Z. Liu, S. Jiang, R. Cortesini, S. Lederman, N. Suciu-Foca. 1999. T suppressor lymphocytes inhibit NF-{kappa}B-mediated transcription of CD86 gene in APC. J. Immunol. 163: 6386-6392. [Abstract/Free Full Text]
  51. Scheinman, R. I., P. C. Cogswell, A. K. Lofquist, A. S. Baldwin, Jr. 1995. Role of transcriptional activation of I{kappa}{alpha} in mediation of immunosuppression by glucocorticoids. Science 270: 283-286. [Abstract/Free Full Text]
  52. Auphan, N., J. A. DiDonato, C. Rosette, A. Helmberg, M. Karin. 1995. Immunosuppression by glucocorticoids: inhibition of NF-{kappa}B activity through induction of I{kappa}B synthesis. Science 270: 286-290. [Abstract/Free Full Text]
  53. Xing, N., L. M. ML, L. A. Bachman, D. J. McKean, R. Kumar, M. D. Griffin. 2002. Distinctive dendritic cell modulation by vitamin D3 and glucocorticoid pathways. Biochem. Biophys. Res. Commun. 297: 645-652. [Medline]
  54. Griffin, M. D., N. Xing, R. Kumar. 2004. Gene expression profiles in dendritic cells conditioned by 1{alpha},25-dihydroxyvitamin D3 analog. J. Steroid Biochem. Mol. Biol. 89–90: 443-448.
  55. Yu, X. P., T. Bellido, S. C. Manolagas. 1995. Down-regulation of NF-{kappa}B protein levels in activated human lymphocytes by 1,25-dihydroxyvitamin D3. Proc. Natl. Acad. Sci. USA 92: 10990-10994. [Abstract/Free Full Text]
  56. De Bosscher, K., W. Vanden Berghe, L. Vermeulen, S. Plaisance, E. Boone, G. Haegeman. 2000. Glucocorticoids repress NF-{kappa}B-driven genes by disturbing the interaction of p65 with the basal transcription machinery, irrespective of coactivator levels in the cell. Proc. Natl. Acad. Sci. USA 97: 3919-3924. [Abstract/Free Full Text]
  57. Hewison, M., L. Freeman, S. V. Hughes, K. N. Evans, R. Bland, A. G. Eliopoulos, M. D. Kilby, P. A. Moss, R. Chakraverty. 2003. Differential regulation of vitamin D receptor and its ligand in human monocyte-derived dendritic cells. J. Immunol. 170: 5382-5390. [Abstract/Free Full Text]
  58. Cantorna, M. T., D. A. Hullett, C. Redaelli, C. R. Brandt, J. Humpal-Winter, H. W. Sollinger, H. F. Deluca. 1998. 1,25-Dihydroxyvitamin D3 prolongs graft survival without compromising host resistance to infection or bone mineral density. Transplantation 66: 828-831. [Medline]
  59. Ochando, J. C., C. Homma, Y. Yang, A. Hidalgo, A. Garin, F. Tacke, V. Angeli, Y. Li, P. Boros, Y. Ding, et al 2006. Alloantigen-presenting plasmacytoid dendritic cells mediate tolerance to vascularized grafts. Nat. Immunol. 7: 652-662. [Medline]
  60. Kuwana, M., J. Kaburaki, T. M. Wright, Y. Kawakami, Y. Ikeda. 2001. Induction of antigen-specific human CD4+ T cell anergy by peripheral blood DC2 precursors. Eur. J. Immunol. 31: 2547-2557. [Medline]
  61. Martín, P., G. M. del Hoyo, F. Anjuère, C. F. Arias, H. H. Vargas, A. Fernández-L, V. Parrillas, C. Ardavin. 2002. Characterization of a new subpopulation of mouse CD8{alpha}+B220+ dendritic cells endowed with type 1 interferon production capacity and tolerogenic potential. Blood 100: 383-390. [Abstract/Free Full Text]
  62. Wakkach, A., N. Fournier, V. Brun, J. P. Breittmayer, F. Cottrez, H. Groux. 2003. Characterization of dendritic cells that induce tolerance and T regulatory 1 cell differentiation in vivo. Immunity 18: 605-617. [Medline]
  63. Bilsborough, J., T. C. George, A. Norment, J. L. Viney. 2003. Mucosal CD8{alpha}+ DC, with a plasmacytoid phenotype, induce differentiation and support function of T cells with regulatory properties. Immunology 108: 481-492. [Medline]
  64. de Heer, H. J., H. Hammad, T. Soullie, D. Hijdra, N. Vos, M. A. Willart, H. C. Hoogsteden, B. N. Lambrecht. 2004. Essential role of lung plasmacytoid dendritic cells in preventing asthmatic reactions to harmless inhaled antigen. J. Exp. Med. 200: 89-98. [Abstract/Free Full Text]
  65. Baldwin, T., S. Henri, J. Curtis, M. O’Keeffe, D. Vremec, K. Shortman, E. Handman. 2004. Dendritic cell populations in Leishmania major-infected skin and draining lymph nodes. Infect. Immun. 72: 1991-2001. [Abstract/Free Full Text]



This article has been cited by other articles:


Home page
 J. Immunol.Home page
Y. A. Taher, B. C. A. M. van Esch, G. A. Hofman, P. A. J. Henricks, and A. J. M. van Oosterhout
1{alpha},25-Dihydroxyvitamin D3 Potentiates the Beneficial Effects of Allergen Immunotherapy in a Mouse Model of Allergic Asthma: Role for IL-10 and TGF-{beta}
J. Immunol., April 15, 2008; 180(8): 5211 - 5221.
[Abstract] [Full Text] [PDF]

Home page
 Ann. N. Y. Acad. Sci.Home page
J. S. ADAMS, P. T. LIU, R. CHUN, R. L. MODLIN, and M. HEWISON
Vitamin D in Defense of the Human Immune Response
Ann. N.Y. Acad. Sci., November 1, 2007; 1117(1): 94 - 105.
[Abstract] [Full Text] [PDF]

Home page
 J. Immunol.Home page
S. Gorman, L. A. Kuritzky, M. A. Judge, K. M. Dixon, J. P. McGlade, R. S. Mason, J. J. Finlay-Jones, and P. H. Hart
Topically Applied 1,25-Dihydroxyvitamin D3 Enhances the Suppressive Activity of CD4+CD25+ Cells in the Draining Lymph Nodes
J. Immunol., November 1, 2007; 179(9): 6273 - 6283.
[Abstract] [Full Text] [PDF]

Home page
 Ann. N. Y. Acad. Sci.Home page
J. F. CARVALHO, M. BLANK, E. KISS, T. TARR, H. AMITAL, and Y. SHOENFELD
Anti-Vitamin D, Vitamin D in SLE: Preliminary Results
Ann. N.Y. Acad. Sci., August 1, 2007; 1109(1): 550 - 557.
[Abstract] [Full Text] [PDF]

Home page
 J. Immunol.Home page
S. F. Yates, A. M. Paterson, K. F. Nolan, S. P. Cobbold, N. J. Saunders, H. Waldmann, and P. J. Fairchild
Induction of Regulatory T Cells and Dominant Tolerance by Dendritic Cells Incapable of Full Activation
J. Immunol., July 15, 2007; 179(2): 967 - 976.
[Abstract] [Full Text] [PDF]

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow