1α,25-Dihydroxyvitamin D3 Has a Direct Effect on Naive CD4+ T Cells to Enhance the Development of Th2 Cells

André Boonstra, Franck J. Barrat, Chad Crain, Victoria L. Heath, Huub F. J. Savelkoul and Anne O’Garra
J Immunol November 1, 2001, 167 (9) 4974-4980; DOI: https://doi.org/10.4049/jimmunol.167.9.4974

Abstract

1α,25-Dihydroxyvitamin D3 (vitD3) is an immunoregulatory hormone with beneficial effects on Th1 mediated autoimmune diseases. Although the inhibitory effects of vitD3 on macrophages and dendritic cells are well documented, any direct effects of vitD3 on Th cell development are not clearly defined. Using CD4+Mel14+ T cells derived from mice on a BALB/c and a C57BL/6 genetic background we examined the effect of vitD3 on Th cell development. We demonstrated that vitD3 affects Th cell polarization by inhibiting Th1 (IFN-γ production) and augmenting Th2 cell development (IL-4, IL-5, and IL-10 production). These effects were observed in cultures driven with splenic APC and Ag, as well as with anti-CD3 and anti-CD28 alone, indicating that CD4+ cells can also be direct targets for vitD3. The enhanced Th2 development by vitD3 was found in both BALB/c and C57BL/6 mice. An increased expression of the Th2-specific transcription factors GATA-3 and c-maf correlated with the increased production of Th2 cytokines after vitD3 treatment. The vitD3-induced effects were largely mediated via IL-4, because neutralization of IL-4 almost completely abrogated the augmented Th2 cell development after vitD3 treatment. These findings suggest that vitD3 acts directly on Th cells and can, in the absence of APC, enhance the development of a Th2 phenotype and augment the expression of the transcription factors c-maf and GATA-3. Our findings suggest that the beneficial effects of vitD3 in autoimmune diseases and transplantation operate through prevention of strong Th1 responses via the action on the APC, while simultaneously directly acting on the T cell to enhance Th2 cell development.

The CD4+ Th cells can be divided into Th1 and Th2 cells based on their cytokine profile upon antigenic stimulation (1, 2). The Th1 subset produces IFN-γ and lymphotoxin and is important for protection against intracellular pathogens and has also been associated with autoimmune pathologies (3). The Th2 subset produces IL-4, IL-5, and IL-13 and is implicated in eradicating helminth and other extracellular parasites, as well as being involved in allergic manifestations. The development of CD4+ T cells into either Th1 or Th2 cells determines the outcome of an immune response, and is primarily directed by cytokines; Th1 cells develop in response to IL-12, whereas IL-4 induces the development of Th2 cells (4, 5, 6, 7). Studies on the molecular mechanisms of Th development have demonstrated the importance of Th1 (T-bet) and Th2 (c-maf and GATA-3) specific transcription factors in the regulation of the Th1/Th2 balance. c-maf increases the expression of IL-4 (8), whereas GATA-3 can induce the expression of a wide range of Th2-specific cytokines (9, 10). Furthermore, forced expression of GATA-3 can elicit the production of Th2-specific cytokines in developing and committed Th1 cells, and inhibit IFN-γ production (11, 12, 13). The Th1-specific transcription factor T-bet induces the expression of IFN-γ, and represses IL-4 and IL-5 production in developing and committed Th2 cells (14).

Beside the dominant role of cytokines in Th development, additional factors have been described which affect the Th1-Th2 balance, e.g., the Ag dose, the strength of TCR signaling, and costimulatory signals (7). Furthermore, a number of nonprotein compounds have been reported to influence Th cell development, such as glucocorticoids, eicosanoids, and vitamins (15, 16, 17, 18, 19).

1α,25-Dihydroxyvitamin D3 (vitD3)3 is a seco-steroid hormone that is not only involved in mineral and skeletal homeostasis, but also regulates the differentiation, growth, and function of a broad range of cells, including cells of the immune system (20). VitD3 acts through its receptor, the nuclear vitD3 receptor, which in turn acts as a transcription factor by binding to distinct vitD3 receptor responsive elements that are present in the promoter regions of target genes. VitD3 also modulates gene transcription by affecting the activity of transcription factors, such as the NF-AT, NF-κB, and SMAD families of transcription factors (21, 22, 23). Activated macrophages possess the enzyme 1-α-hydroxylase that allows for the production of vitD3, which suggests a role for this endogenously produced steroid hormone in regulation of immune responses (24). Furthermore, vitD3 has been demonstrated to prevent Th1-mediated autoimmune diseases in animal models for experimental allergic encephalomyelitis, systemic lupus erythematosus, and type I diabetes (25, 26, 27). A number of studies have demonstrated that vitD3 modulates the activity of monocytes/macrophages and dendritic cells (16, 28, 29, 30, 31, 32). It was found that vitD3 inhibits the differentiation and maturation of DC; reduces the expression of MHC class II, CD40, CD80, and CD86; and inhibits the secretion of IL-1, IL-6, TNF-α, and IL-12 (30, 31, 32). In vitro stimulation in the presence of APC, showed a vitD3-induced reduction of IFN-γ production, whereas the Th2 compartment was not affected (26, 33, 34). In vivo administration of vitD3 resulted in an increase in IL-4 expression (35) and production (36), with a concomitant reduction of IFN-γ levels. The inhibition of Th1 development by vitD3 is thought to be primarily mediated via its action on the APC as a consequence of reduced IL-12 production after vitD3 treatment (31).

These studies suggest that the vitD3-induced switch from Th1 to Th2 may be attributable to its ability to modulate the APC. However, it is unclear to date whether the effects of vitD3 on Th cell development are mediated solely via effects on the APC (e.g., reduced IL-12) or whether CD4+ cells are also direct targets. It has been shown that vitD3 can act directly on T cells by inhibiting T cell proliferation (37). However, no studies have yet addressed whether vitD3 has any direct effects on CD4+ T cells to affect their subsequent development into Th1 and Th2 cells. In this study we describe that vitD3 has a direct effect on CD4+ T cells to enhance the development of Th2 cells in the absence of APC, producing IL-4, IL-5, and IL-10, and to augment the expression of GATA-3 and c-maf.

Materials and Methods

Mice

DO.11.10 mice transgenic for an OVA323–339-specific αβTCR were used as a source of Ag-specific T cells (38). BALB/cAnN (Taconic Farms, Germantown, NY) and C57BL/6J (The Jackson Laboratory, Bar Harbor, ME) mice were used to provide splenic APCs or T cells. All mice were housed under specific pathogen-free conditions and were used between 8 and 12 wk of age.

Reagents

mAb used in culture were anti-IL-4 (11B11) (39), anti-IL-12 (clone C17.8.20, a kind gift of G. Trinchieri, Ref. 40), and anti-IFN-γ (XMG 1.2, J. Abrams, DNAX, Palo Alto, CA). IL-2 and IL-4 were obtained from DNAX. IL-12 was purchased from R&D Systems (Minneapolis, MN). Anti-mouse CD3 (145-2C11) and anti-CD28 (37.51) mAb used for T cell stimulation were purchased from BD PharMingen (San Diego, CA). mAb used for T cell preparation were anti-B220, anti-CD8α, anti-Mac-1, anti-CD4-FITC, and anti-L-selectin-PE (all mouse specific, BD PharMingen). mAb used for intracellular staining were anti-IFN-γ (clone XMG1.2), anti-IL-4 (11B11), anti-IL-10 (JES5-16E3), anti-IL-5 (TRFK-5) and isotype controls (all from BD PharMingen).

Tissue culture medium used was RPMI 1640 (J.R. Scientific, Woodland, CA) supplemented with 10% FCS (heat inactivated for 30 min at 56°C, J.R. Scientific), 0.05 mM 2-ME (Sigma, St. Louis, MO), 10 mM HEPES buffer (Life Technologies, Grand Island, NY), 100 U/ml penicillin (Life Technologies) and 100 μg/ml streptomycin (Life Technologies), 2 mM l-glutamine (BioWhittaker, Walkersville, MD), and 1 mM sodium pyruvate (BioWhittaker). 1,25(OH)2-vitamin D3 was purchased from Biomol (Plymouth Meeting, PA). OVA peptide was used as a synthetic peptide encoding chicken OVA323–339 (Biosynthesis, Lewisville, TX).

Preparation of T cells and APC

CD4+ T cells were enriched by negative depletion using a mixture of anti-CD8α, anti-B220, and anti-Mac-1 mAb, followed by goat-anti-rat Ig coated beads (Biomag; Polysciences, Warrington, PA) as described previously (13). Enriched CD4+ T cells were then further purified using a FACStarPlus flow cytometer (BD Biosciences, San Jose, CA) to achieve >99% naive CD4+ T cells on the basis of bright Mel-14, CD4 staining (41). Staining did not alter the function of the T cells (data not shown).

Stimulation of transgenic CD4+ T cells for cytokine production

Primary stimulations of CD4+ T cells (2.5 × 105/well) were conducted using OVA peptide (0.6 μM) and RBC-lysed spleen cells (5 × 106/well, 3000 rad) as APC in a total volume of 2 ml in 24-well plates. In some cases, Ag and APC were replaced by cross-linked anti-CD3 (10 μg/ml) and soluble anti-CD28 (1 μg/ml) mAb, and 1.5 × 106 cells were used per 2-ml well in 24-well plates. Cultures received only medium (i.e., neutral) or vitD3 (4 × 10−8 M). In addition, some cultures were supplemented with anti-IL-4, anti-IL-12, or anti-IFN-γ mAb (10 μg/ml) to block endogenously produced cytokines. The dose of vitD3 is in the range of that used in other studies (18, 30, 31) and did not induce apoptosis or strong inhibition of Th cell proliferation. Cells were split on day 3, and harvested on day 7, washed twice, counted, and restimulated as described for the primary stimulation with the addition of 10 ng/ml IL-2. Restimulation of the cells in the APC-free system was with 2 μg/ml anti-CD3, 2 μg/ml anti-CD28 mAb, and 10 ng/ml IL-2.

Cytokine assays

IL-4 and IFN-γ sandwich ELISA assays were performed as previously described (42). The method for intracellular cytokine staining was as reported (43). Briefly, cultured CD4+ cells were stimulated with 10 ng/ml IL-2, 1 μg/ml PMA (Sigma), and 2 μg/ml ionomycin (Sigma) at 106 cells/ml for 2 h at 37°C. After 2 h, 10 μg/ml brefeldin A (Epicentre Technologies, Madison, WI) was added and the cells were incubated for another 2 h. The cells were then fixed with 2% formaldehyde, permeabilized with 0.5% saponin, and stained as described before (43). Samples were analyzed on a FACScan flow cytometer (BD Biosciences) and analyzed using CellQuest software (BD Biosciences).

RNase protection assay

RNA was prepared using the Rnazol B method (Cinna/Biotecx Laboratories, Houston, TX) according to the manufacturer’s instructions, and 7 μg RNA was used to perform the RNase protection assay. Riboprobes of GATA-3, T-bet, and 18S inserted in the pGEM vector were prepared by linearization with HindIII. c-maf, inserted in the pBSK vector, was linearized using BglII before use in the RNase protection assay. The expected band size was as follows. GATA-3, 418 bp; c-maf, 329 bp; T-bet, 290 bp; and 18S, 187 bp. The probes (0.1 μg each) were labeled with 32P using an in vitro transcription kit (BD PharMingen). Samples were run on a 5% acrylamide gel and were visualized using phosphorimaging (Molecular Dynamics, Sunnyvale, CA). Transcript levels were quantified using ImageQuant software (Molecular Dynamics).

Results

VitD3 enhances Th2 cell development in the presence of APC

To address the effect of vitD3 on Th cell development we cultured naive TCR-transgenic CD4+ DO11.10 T cells with splenic APC and OVA peptide under neutral conditions (medium alone, no additions) or medium supplemented with vitD3. After two rounds of stimulation, the cytokine profile for intracellular cytokine production was determined by flow cytometry upon restimulation. As depicted in Fig. 1⇓A, vitD3-driven Th cells showed an increased frequency of IL-4-producing cells and a reduction in the number of IFN-γ-producing cells as compared with cells grown under neutral conditions. Consistent with augmented Th2 development after culture with vitD3, an increase in IL-10- and IL-5-producing Th cells was also detected. Culture of Th cells under Th2 (IL-4/anti-IL-12) polarizing conditions resulted in a more pronounced Th2 phenotype (55% IL-4-producing cells) as compared with cells cultured with vitD3 (41% IL-4-producing cells). As shown in Fig. 1⇓B, the effect of vitD3 on the cytokine production reflects augmented Th2 development with reduced IFN-γ and increased IL-4 production, which is in accordance with the cytokine profile as determined by flow cytometry. Although the effects of vitD3 on Th development were more pronounced after repeated stimulation, a single stimulation was sufficient to demonstrate enhanced development of Th2 cells by vitD3 (Fig. 1⇓C).

FIGURE 1.
FIGURE 1.

VitD3 enhances Th2 cell development in the presence of APC. CD4+Mel14+ DO11.10 T cells were activated with OVA323–339 peptide and γ-irradiated splenic APC. The cells were stimulated with or without (neutral) the addition of vitD3, or with IL-12/anti-IL-4 (Th1 control), or IL-4/anti-IL-12 (Th2 control). After two rounds of stimulation, cells were harvested and restimulated with PMA/ionomycin for cytokine production by intracellular cytokine staining for 4 h (A) or immunoassay for 48 h (B). C, The cytokine profile after one and two rounds of stimulation.

VitD3-induced Th2 development is dependent on IL-4

Because IL-4 is the major cytokine that directs the development of Th2 cells, we determined whether IL-4 played a role in the observed augmented development of Th2 cells after in vitro culture in the presence of vitD3. To examine this we included cultures in which IL-4 was neutralized during the entire culture period. Fig. 2⇓ shows that addition of anti-IL-4 mAb to the cultures containing vitD3 completely abrogated the development of Th2 cells producing IL-4. In fact, when IL-4 was neutralized, the frequency of IL-4-producing cells cultured with vitD3 was similar to that observed when cells were cultured under neutral conditions in the presence of anti-IL-4 mAb (Fig. 2⇓). These data indicate that IL-4 is required for the vitD3-induced effects on Th cells development. Addition of anti-IL-4 mAb resulted in a significant increase in the frequency of IFN-γ-producing cells.

FIGURE 2.
FIGURE 2.

IL-4 dependence of vitD3 induced Th2 development when cultured in the presence of APC. CD4+Mel14+ DO11.10 T cells were activated with OVA323–339 peptide and γ-irradiated splenic APC. Cultures were performed with and without the addition of vitD3, as well as with or without the addition of anti-IL-4 mAb. After three rounds of stimulation the cells were restimulated with PMA/ionomycin and the cytokine profile was determined by flow cytometry. A, The staining for IFN-γ and IL-4; B, IFN-γ and IL-10 staining.

VitD3 has a direct effect on Th cells resulting in strong polarization toward a Th2 profile

A number of studies have reported vitD3-induced reduction of IL-2 and IFN-γ production, but only in some cases a subsequent enhancement of Th2-type cytokines by T cells in the presence of APC (18, 33, 44). To determine whether vitD3 also has a direct effect on Th cell development independently of APC related effects we activated naive CD4+ Mel14+ T cells with plate bound anti-CD3 and soluble anti-CD28 mAb in the presence or absence of vitD3. The cells were repeatedly stimulated, and their cytokine profile was assessed after 3 wk in culture. Fig. 3⇓A shows that purified naive CD4+ Mel14+ T cells obtained from BALB/c mice stimulated in the absence of APC develop into a highly polarized Th2 population when cultured with vitD3, similarly to APC-driven cultures. The frequency of IL-4-producing cells was enhanced from 8.0 to 55.8%. In accordance with this, the frequency of IL-10- and IL-5-producing cells was also dramatically increased, whereas the frequency of IFN-γ-producing cells was reduced. The frequency of IL-4-producing cells after culture with vitD3 was similar to cultures with Th cells under Th2 (IL-4/anti-IL-12) polarizing conditions (55.8 and 58.6%, respectively). To examine whether the effects of vitD3 are limited to the BALB/c genetic background or more generalized, we stimulated CD4+Mel14+ T cells from C57BL/6 mice with anti-CD3/anti-CD28 in the presence of vitD3. As shown in Fig. 3⇓B Th cells from C57BL/6 mice also develop into highly polarized Th2 cells after single or multiple rounds of stimulation. These findings clearly indicate that Th cells can be direct targets for the effects of vitD3 on Th development as demonstrated by significant induction of Th2 polarization in both BALB/c and C57BL/6 mice.

FIGURE 3.
FIGURE 3.

Enhanced vitD3-induced Th2 development occurs in the absence of APC. CD4+ Mel14+ T cells from BALB/c mice were activated with plate-bound anti-CD3 mAb and soluble anti-CD28 mAb in the presence or absence of vitD3, or with IL-12/anti-IL-4 (Th1 control), or IL-4/anti-IL-12/anti-IFN-γ (Th2 control). Cells were restimulated three times and the cytokine profile was determined after restimulation with PMA/ionomycin and assessed by flow cytometry (A). Identical experiments were performed with CD4+Mel14+ T cells obtained from C57BL/6 mice, and their cytokine profile was determined after one, two, and three rounds of stimulation (B).

Neutralization of IL-4 abrogates vitD3-induced Th2 polarization independently of IFN-γ

The enhanced vitD3-driven Th2 development was also abolished in these APC-free cultures by neutralization of IL-4 (Fig. 4⇓). However, neutralization of IL-4 also led to an increase in the percentage of IFN-γ-producing cells. Thus it was possible that overproduction of IFN-γ, which can inhibit Th2 development (45), could be responsible for reduced numbers of IL-4-producing cells, rather than a requirement for IL-4 in vitD3-driven Th2 development. To exclude this possibility we simultaneously neutralized both IL-4 and IFN-γ and assessed the cytokine profile of naive CD4+ cells after culture in the presence or absence of vitD3. Cells were repeatedly stimulated with cross-linked anti-CD3 and soluble anti-CD28 mAb. As depicted in Fig. 4⇓, when anti-IL-4 and anti-IFN-γ mAb were added throughout the culture period of vitD3-driven cultures, the cytokine profile of these vitD3 cultured cells resembled that of cells cultured under neutral conditions (with no blocking mAb) with a low frequency of IL-4-producing cells in vitD3-driven cultures when IL-4 and IFN-γ were absent. Taken together, these data clearly demonstrate that the effects of vitD3 on the development of CD4+ T cells are largely dependent on IL-4, although small numbers of IL-4-producing cells can develop in the complete absence of IL-4.

FIGURE 4.
FIGURE 4.

Neutralization of IFN-γ and IL-4 simultaneously compensates for the vitD3 induced effects on Th cell development. CD4+Mel14+ T cells from BALB/c mice were activated as described in Fig. 3⇑. Additionally, cultures were included containing anti-IL-4 alone, or a mixture of anti-IL-4, anti-IFN-γ mAb, and anti-IL-12 mAb.

VitD3 up-regulates the expression of GATA-3 and c-maf in developing Th cells

In recent years considerable progress has been made in the knowledge of transcription factors involved in Th1 and Th2 cell differentiation. The transcription factor T-bet has been described to direct the differentiation and commitment of Th1 cells, and to induce IFN-γ expression (14). c-maf and GATA-3 are Th2-specific transcription factors that regulate the Th2 cytokine genes (8, 9, 10, 11, 12, 13). We examined whether vitD3 cultured Th cells showed a transcription factor pattern reflecting the augmented Th2 development as indicate by their cytokine profile. As shown in Fig. 5⇓ and in accordance with previously published findings, highly polarized Th1 cells obtained after repeated stimulation expressed T-bet, but low to undetectable levels of c-maf and GATA-3. Conversely, Th2 cells expressed GATA-3 and c-maf, but not T-bet. Naive CD4+Mel14+ T cells stimulated with anti-CD3 and anti-CD28 mAb in the presence of vitD3 showed enhanced levels of GATA-3 and c-maf expression as compared with cells grown under neutral conditions. No T-bet expression was detected in cells cultured under neutral or vitD3-driven conditions. These findings are representative of two independent experiments. Therefore, the transcription factor profile correlates with the increased Th2 cytokine production of CD4+ cells cultured in the presence of vitD3.

FIGURE 5.
FIGURE 5.

VitD3 up-regulates the expression of GATA-3 and c-maf in developing Th cells. A, RNase protection assay for GATA-3, c-maf, T-bet, and 18s transcripts was performed using total cellular RNA of CD4+Mel14+ cells stimulated in the presence or absence of vitD3. RNA from cells cultured at Th1 (IL-12, anti-IL-4) or Th2 (IL-4, anti-IL-12, anti-IFN-γ) priming conditions are included as positive controls. B, Expression of GATA-3 and c-maf as determined by densitometry. Values are expressed in arbitrary units relative to the 18s signal. Values are representative of two independent experiments.

Discussion

In the present study we demonstrated that vitD3 affects the Th1-Th2 balance in that it inhibits Th1 and augments Th2 cell development. These effects were observed when T cells were stimulated with anti-CD3/anti-CD28 alone, as well as when stimulated with APC and Ag, indicating that CD4+ cells themselves can be direct targets for vitD3 resulting in enhanced Th2 development. The increased production of Th2 cytokines correlated with increased expression of the Th2-specific transcription factors GATA-3 and c-maf after vitD3 treatment in vitro. Furthermore, we determined IL-4 to be a major mediator of the enhanced vitD3 induced Th2 development, although small numbers of IL-4-producing cells were induced in the absence of IL-4 and IFN-γ.

It has been suggested that the immunomodulatory effects of vitD3 are mainly mediated via modulation of the activity of macrophages and dendritic cells, via inhibition of their differentiation, maturation, and T cell-stimulatory activity (30, 31, 46). More specifically, reduced expression of costimulatory molecules (CD80, CD86, CD58, and CD40) and inhibition of the production of cytokines, like TNF-α, IL-6, and IL-12, were shown to result in impaired T cell activation (30). The inhibitory effect of vitD3 on IL-12p70 production by DC via inhibition of NF-κB activation and transcriptional repression of the IL-12p40 gene (31) is likely to play a dominant role in the observed reduction of Th1 cell development after treatment with vitD3.

Although APC can be direct targets for the immunomodulatory activities of vitD3, we clearly show that vitD3 also has a direct effect on the differentiation of naive CD4+Mel14+ T cells upon TCR stimulation, resulting in inhibition of Th1 and augmented Th2 development. The vitD3 induced skewing toward a Th2 phenotype was much more pronounced when CD4+Mel14+ T cells were activated with anti-CD3/anti-CD28 mAb as compared with cells activated in the presence of APC and Ag. It is possible that APC may deliver signals to inhibit Th2 development, such as via IL-12 (31) or ICAM-1 (47, 48) which counteract the effects of vitD3. Additionally by its effect on downstream signaling pathways known to be triggered by TCR ligation, it is possible that vitD3 may modify the strength of the signal delivered to the T cell which has been shown to affect the development of Th1 and Th2 responses (49).

It has been reported that the transactivation of the IFN-γ promoter is down-regulated by vitD3 in transfected Jurkat cells (50). Thus, in our system, it is possible that transcriptional suppression of the IFN-γ gene takes place, thereby providing a possible explanation for the suppression of IFN-γ production. This can be augmented by up-regulation of GATA-3 seen in the presence of vitD3, because GATA-3 has been shown to inhibit the development of IFN-γ-producing cells early during Th cell differentiation (11, 13). To date no vitD3 receptor responsive elements in the IL-4 promoter have been described, but the ability of vitD3 to up-regulate c-maf expression could account for increased transactivation of the IL-4 promoter.

The vitD3 induced effects on Th development were largely mediated via IL-4. However, a small population of IL-4-producing cells was detected after culture in the presence of vitD3 in the presence of neutralizing mAb to IFN-γ and IL-4. This IL-4-independent Th2 cell development may be reminiscent of the findings by Ouyang et al. (51), who showed STAT6-independent Th2 development.

We showed that Ag-specific stimulation of CD4+ T cells in the presence of vitD3 inhibits the development of Th1 cells. Conversely, we demonstrated the development of highly Th2 skewed populations after in vitro culture with vitD3 with increased IL-4, IL-5, and IL-10 production as determined by the intracellular cytokine profile and immunoassay. The presence of vitD3 is required during each phase of stimulation, because the developing Th2 cells are still unstable until they are committed. Even Th cells cultured with IL-12/anti-IL-4 mAb or IL-4/anti-IL-12 require these additives until they are committed to the Th1 or Th2 phenotype, respectively (7). Additionally, we provide data that vitD3 induced Th2 development can also be seen not only on the BALB/c but also on the C57BL/6 genetic background. The vitD3 induced inhibition of Th1 development in APC/Ag stimulated cultures has been described before (18, 33); therefore, our data confirm these findings. However, the vitD3 induced increase of Th2 development has not been demonstrated in vitro, and appears in apparent conflict with previous studies where effects on Th2 development were minimal. In contrast to other studies (18, 33), we used naive CD4+ T cells and assessed the role of vitD3 in the well-defined OVA-TCR transgenic system. Mattner et al. (33) showed the effect of vitD3 on human cord blood CD4+CD45RA+ T cells after stimulation autologous adherent cells and PHA. After 10 days in culture they found a reduction of IFN-γ production but only a mild increase of IL-4. Differences may thus be explained by the different source of naive T cells, and it is also possible that there is donor variation in humans.

The physiological role of vitD3 in immune responses is still not defined. Macrophages have been shown to synthesize vitD3 when activated with LPS and IFN-γ (52) (data not shown). This implies that upon triggering of APC by microbial factors vitD3 is synthesized by these cells and thus may down-regulate the production of inflammatory mediators, such as IL-12. This could initiate a cascade of events resulting in reduced APC function and polarization of Th cells toward Th2 dominated responses. The suppression of IFN-γ production might prevent a sustained synthesis of vitD3, thereby providing a negative feedback mechanism. Therefore, it is likely that vitD3 functions to dampen cell-mediated immune responses through prevention of strong Th1 responses via the action on the APC, while simultaneously directly acting on the T cell to enhance Th2 cell development. VitD3 is also synthesized by keratinocytes after exposure of the skin to ultraviolet B irradiation. Little is known about the role of locally produced vitD3 in the skin. However, it is tempting to speculate that vitD3 contributes to the immunomodulatory effects of ultraviolet B by affecting the activity of APC and Th cells.

The dose of vitD3 used in our study was in the range of that used by others and did not induce apoptosis or strong inhibition of Th proliferation. Because macrophages, dendritic cells, and keratinocytes can produce vitD3 it is likely that at the localized level in vivo, high vitD3 can be found which may exert its effect on neighboring Th cells. For these reasons, however, it may be difficult to extrapolate from physiologically relevant concentrations of vitD3 in vivo to the in vitro system we are using.

In this study we have provided insight into the effect of vitD3 on Th polarization by showing for the first time that vitD3 is able to enhance Th2 development in the absence of APC. The potent direct effect of vitD3 on Th cells may, at least in part, explain its beneficial effects in the treatment of psoriatic lesions as well as a number of other autoimmune diseases. Augmented immune deviation into strong Th2 mediated responses by combined effects on APC and Th cells are likely to underlie the immunosuppressive activity of vitD3.

Acknowledgments

We thank Dr. J. Cupp, the members of the FACS facility at DNAX, and H. de Wit (Erasmus University) for their excellent assistance in obtaining sorted T cells, and Dr. M. Andonian for graphics.

Footnotes

  • ↵1 DNAX Research Institute of Molecular and Cellular Biology is supported by Schering-Plough Corporation.

  • ↵2 Address correspondence and reprint requests to Dr. André Boonstra, Department of Immunology, DNAX Research Institute, 901 California Avenue, Palo Alto, CA 94304. E-mail address: andre.boonstra{at}dnax.org

  • ↵3 Abbreviation used in this paper: vitD3, 1α,25-dihydroxyvitamin D3.

  • Received April 23, 2001.
  • Accepted August 31, 2001.

References

  1. ↵
    Mosmann, T. R., H. Cherwinski, M. W. Bond, M. A. Giedlin, R. L. Coffman. 1986. Two types of murine helper T cell clone. I. Definition according to profiles of lymphokine activities and secreted proteins. J. Immunol. 136: 2348
    OpenUrlAbstract
  2. ↵
    Sher, A., R. T. Gazzinelli, I. P. Oswald, M. Clerici, M. Kullberg, E. J. Pearce, J. A. Berzofsky, T. R. Mosmann, S. L. James, H. C. Morse. 1992. Role of T-cell derived cytokines in the down-regulation of immune responses in parasitic and retroviral infection. Immunol. Rev. 127: 183
    OpenUrlCrossRefPubMed
  3. ↵
    Abbas, A. K., K. M. Murphy, A. Sher. 1996. Functional diversity of helper T lymphocytes. Nature 383: 787
    OpenUrlCrossRefPubMed
  4. ↵
    Seder, R. A., W. E. Paul. 1994. Acquisition of lymphokine-producing phenotype by CD4+ T cells. Annu. Rev. Immunol. 12: 635
    OpenUrlCrossRefPubMed
  5. ↵
    Murphy, K. M., W. Ouyang, J. D. Farrar, J. Yang, S. Ranganath, H. Asnagli, M. Afkarian, T. L. Murphy. 2000. Signaling and transcription in T helper development. Annu. Rev. Immunol. 18: 451
    OpenUrlCrossRefPubMed
  6. ↵
    Trinchieri, G.. 1995. Interleukin-12: a proinflammatory cytokine with immunoregulatory functions that bridge innate resistance and antigen-specific adaptive immunity. Annu. Rev. Immunol. 13: 251
    OpenUrlCrossRefPubMed
  7. ↵
    O’Garra, A.. 1998. Cytokines induce the development of functionally heterogeneous T helper cell subsets. Immunity 8: 275
    OpenUrlCrossRefPubMed
  8. ↵
    Ho, I. C., M. R. Hodge, J. W. Rooney, L. H. Glimcher. 1996. The proto-oncogene c-maf is responsible for tissue-specific expression of interleukin-4. Cell 85: 973
    OpenUrlCrossRefPubMed
  9. ↵
    Zhang, D. H., L. Yang, A. Ray. 1998. Differential responsiveness of the IL-5 and IL-4 genes to transcription factor GATA-3. J. Immunol. 161: 3817
    OpenUrlAbstract/FREE Full Text
  10. ↵
    Zheng, W., R. A. Flavell. 1997. The transcription factor GATA-3 is necessary and sufficient for Th2 cytokine gene expression in CD4 T cells. Cell 89: 587
    OpenUrlCrossRefPubMed
  11. ↵
    Ouyang, W., S. H. Ranganath, K. Weindel, D. Bhattacharya, T. L. Murphy, W. C. Sha, K. M. Murphy. 1998. Inhibition of Th1 development mediated by GATA-3 through an IL-4-independent mechanism. Immunity 9: 745
    OpenUrlCrossRefPubMed
  12. ↵
    Lee, H. J., N. Takemoto, H. Kurata, Y. Kamogawa, S. Miyatake, A. O’Garra, N. Arai. 2000. GATA-3 induces T helper cell type 2 (Th2) cytokine expression and chromatin remodeling in committed Th1 cells. J. Exp. Med. 192: 105
    OpenUrlAbstract/FREE Full Text
  13. ↵
    Ferber, I. A., H. J. Lee, F. Zonin, V. Heath, A. Mui, N. Arai, A. O’Garra. 1999. GATA-3 significantly downregulates IFN-γ production from developing Th1 cells in addition to inducing IL-4 and IL-5 levels. Clin. Immunol. 91: 134
    OpenUrlCrossRefPubMed
  14. ↵
    Szabo, S. J., S. T. Kim, G. L. Costa, X. Zhang, C. G. Fathman, L. H. Glimcher. 2000. A novel transcription factor, T-bet, directs Th1 lineage commitment. Cell 100: 655
    OpenUrlCrossRefPubMed
  15. ↵
    Blotta, M. H., R. H. DeKruyff, D. T. Umetsu. 1997. Corticosteroids inhibit IL-12 production in human monocytes and enhance their capacity to induce IL-4 synthesis in CD4+ lymphocytes. J. Immunol. 158: 5589
    OpenUrlAbstract
  16. ↵
    Vieira, P. L., P. Kalinski, E. A. Wierenga, M. L. Kapsenberg, E. C. de Jong. 1998. Glucocorticoids inhibit bioactive IL-12p70 production by in vitro-generated human dendritic cells without affecting their T cell stimulatory potential. J. Immunol. 161: 5245
    OpenUrlAbstract/FREE Full Text
  17. ↵
    Snijdewint, F. G., P. Kalinski, E. A. Wierenga, J. D. Bos, M. L. Kapsenberg. 1993. Prostaglandin E2 differentially modulates cytokine secretion profiles of human T helper lymphocytes. J. Immunol. 150: 5321
    OpenUrlAbstract
  18. ↵
    Lemire, J. M., D. C. Archer, L. Beck, H. L. Spiegelberg. 1995. Immunosuppressive actions of 1,25-dihydroxyvitamin D3: preferential inhibition of Th1 functions. J. Nutr. 125: 1704S
    OpenUrlAbstract/FREE Full Text
  19. ↵
    Racke, M. K., D. Burnett, S. H. Pak, P. S. Albert, B. Cannella, C. S. Raine, D. E. McFarlin, D. E. Scott. 1995. Retinoid treatment of experimental allergic encephalomyelitis: IL-4 production correlates with improved disease course. J. Immunol. 154: 450
    OpenUrlAbstract
  20. ↵
    Lemire, J. M.. 1995. Immunomodulatory actions of 1,25-dihydroxyvitamin D3. J. Steroid Biochem. Mol. Biol. 53: 599
    OpenUrlCrossRefPubMed
  21. ↵
    Alroy, I., T. L. Towers, L. P. Freedman. 1995. Transcriptional repression of the interleukin-2 gene by vitamin D3: direct inhibition of NFATp/AP-1 complex formation by a nuclear hormone receptor. Mol. Cell. Biol. 15: 5789
    OpenUrlAbstract/FREE Full Text
  22. ↵
    Yu, X. P., T. Bellido, S. C. Manolagas. 1995. Down-regulation of NF-κB protein levels in activated human lymphocytes by 1,25-dihydroxyvitamin D3. Proc. Natl. Acad. Sci. USA 92: 10990
    OpenUrlAbstract/FREE Full Text
  23. ↵
    Yanagisawa, J., Y. Yanagi, Y. Masuhiro, M. Suzawa, M. Watanabe, K. Kashiwagi, T. Toriyabe, M. Kawabata, K. Miyazono, S. Kato. 1999. Convergence of transforming growth factor-β and vitamin D signaling pathways on SMAD transcriptional coactivators. Science 283: 1317
    OpenUrlAbstract/FREE Full Text
  24. ↵
    Reichel, H., H. P. Koeffler, J. E. Bishop, A. W. Norman. 1987. 25-Hydroxyvitamin D3 metabolism by lipopolysaccharide-stimulated normal human macrophages. J. Clin. Endocrinol. Metab. 64: 1
    OpenUrlCrossRefPubMed
  25. ↵
    Lemire, J. M., A. Ince, M. Takashima. 1992. 1,25-Dihydroxyvitamin D3 attenuates the expression of experimental murine lupus of MRL/l mice. Autoimmunity 12: 143
    OpenUrlCrossRefPubMed
  26. ↵
    Lemire, J. M., D. C. Archer. 1991. 1,25-dihydroxyvitamin D3 prevents the in vivo induction of murine experimental autoimmune encephalomyelitis. J. Clin. Invest. 87: 1103
    OpenUrlCrossRefPubMed
  27. ↵
    Mathieu, C., M. Waer, J. Laureys, O. Rutgeerts, R. Bouillon. 1994. Prevention of autoimmune diabetes in NOD mice by 1,25-dihydroxyvitamin D3. Diabetologia 37: 552
    OpenUrlCrossRefPubMed
  28. ↵
    Tsoukas, C. D., D. M. Provvedini, S. C. Manolagas. 1984. 1,25-dihydroxyvitamin D3: a novel immunoregulatory hormone. Science 224: 1438
    OpenUrlAbstract/FREE Full Text
  29. ↵
    Walters, M. R.. 1992. Newly identified actions of the vitamin D endocrine system. Endocr. Rev. 13: 719
    OpenUrlCrossRefPubMed
  30. ↵
    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
    OpenUrlAbstract/FREE Full Text
  31. ↵
    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-κB downregulation in transcriptional repression of the p40 gene. J. Clin. Invest. 101: 252
    OpenUrlCrossRefPubMed
  32. ↵
    Penna, G., L. Adorini. 2000. 1α,25-Dihydroxyvitamin D3 inhibits differentiation, maturation, activation, and survival of dendritic cells leading to impaired alloreactive T cell activation. J. Immunol. 164: 2405
    OpenUrlAbstract/FREE Full Text
  33. ↵
    Mattner, F., S. Smiroldo, F. Galbiati, M. Muller, P. Di Lucia, P. L. Poliani, G. Martino, P. Panina-Bordignon, L. Adorini. 2000. Inhibition of Th1 development and treatment of chronic-relapsing experimental allergic encephalomyelitis by a non-hypercalcemic analogue of 1,25-dihydroxyvitamin D(3). Eur. J. Immunol. 30: 498
    OpenUrlCrossRefPubMed
  34. ↵
    Muller, K., N. Odum, K. Bendtzen. 1993. 1,25-Dihydroxyvitamin D3 selectively reduces interleukin-2 levels and proliferation of human T cell lines in vitro. Immunol. Lett. 35: 177
    OpenUrlCrossRefPubMed
  35. ↵
    Cantorna, M. T., W. D. Woodward, C. E. Hayes, H. F. DeLuca. 1998. 1,25-Dihydroxyvitamin D3 is a positive regulator for the two anti-encephalitogenic cytokines TGF-β1 and IL-4. J. Immunol. 160: 5314
    OpenUrlAbstract/FREE Full Text
  36. ↵
    Overbergh, L., B. Decallonne, M. Waer, O. Rutgeerts, D. Valckx, K. M. Casteels, J. Laureys, R. Bouillon, C. Mathieu. 2000. 1α,25-Dihydroxyvitamin D3 induces an autoantigen-specific T-helper 1/T-helper 2 immune shift in NOD mice immunized with GAD65 (p524–543). Diabetes 49: 1301
    OpenUrlAbstract
  37. ↵
    Rigby, W. F., R. J. Noelle, K. Krause, M. W. Fanger. 1985. The effects of 1,25-dihydroxyvitamin D3 on human T lymphocyte activation and proliferation: a cell cycle analysis. J. Immunol. 135: 2279
    OpenUrlAbstract
  38. ↵
    Murphy, K. M., A. B. Heimberger, D. Y. Loh. 1990. Induction by antigen of intrathymic apoptosis of CD4+CD8+TCRlo thymocytes in vivo. Science 250: 1720
    OpenUrlAbstract/FREE Full Text
  39. ↵
    Ohara, J., W. E. Paul. 1985. Production of a monoclonal antibody to and molecular characterization of B-cell stimulatory factor-1. Nature 315: 333
    OpenUrlCrossRefPubMed
  40. ↵
    Ozmen, L., M. Pericin, J. Hakimi, R. A. Chizzonite, M. Wysocka, G. Trinchieri, M. Gately, G. Garotta. 1994. Interleukin 12, interferon γ, and tumor necrosis factor α are the key cytokines of the generalized Shwartzman reaction. J. Exp. Med. 180: 907
    OpenUrlAbstract/FREE Full Text
  41. ↵
    Bradley, L. M., D. D. Duncan, S. Tonkonogy, S. L. Swain. 1991. Characterization of antigen-specific CD4+ effector T cells in vivo: immunization results in a transient population of MEL-14-, CD45RB-helper cells that secretes interleukin 2 (IL-2), IL-3, IL-4, and interferon γ. J. Exp. Med. 174: 547
    OpenUrlAbstract/FREE Full Text
  42. ↵
    Macatonia, S. E., N. A. Hosken, M. Litton, P. Vieira, C. S. Hsieh, J. A. Culpepper, M. Wysocka, G. Trinchieri, K. M. Murphy, A. O’Garra. 1995. Dendritic cells produce IL-12 and direct the development of Th1 cells from naive CD4+ T cells. J. Immunol. 154: 5071
    OpenUrlAbstract
  43. ↵
    Openshaw, P., E. E. Murphy, N. A. Hosken, V. Maino, K. Davis, K. Murphy, A. O’Garra. 1995. Heterogeneity of intracellular cytokine synthesis at the single-cell level in polarized T helper 1 and T helper 2 populations. J. Exp. Med. 182: 1357
    OpenUrlAbstract/FREE Full Text
  44. ↵
    Rigby, W. F., S. Denome, M. W. Fanger. 1987. Regulation of lymphokine production and human T lymphocyte activation by 1,25-dihydroxyvitamin D3. Specific inhibition at the level of messenger RNA. J. Clin. Invest. 79: 1659
    OpenUrlCrossRefPubMed
  45. ↵
    Gajewski, T. F., F. W. Fitch. 1988. Anti-proliferative effect of IFN-γ in immune regulation. I. IFN-γ inhibits the proliferation of Th2 but not Th1 murine helper T lymphocyte clones. J. Immunol. 140: 4245
    OpenUrlAbstract/FREE Full Text
  46. ↵
    Muller, K., K. Bendtzen. 1996. 1,25-Dihydroxyvitamin D3 as a natural regulator of human immune functions. J. Invest. Dermatol. Symp. Proc. 1: 68
    OpenUrlCrossRef
  47. ↵
    Luksch, C. R., O. Winqvist, M. E. Ozaki, L. Karlsson, M. R. Jackson, P. A. Peterson, S. R. Webb. 1999. Intercellular adhesion molecule-1 inhibits interleukin 4 production by naive T cells. Proc. Natl. Acad. Sci. USA 96: 3023
    OpenUrlAbstract/FREE Full Text
  48. ↵
    Salomon, B., J. A. Bluestone. 1998. LFA-1 interaction with ICAM-1 and ICAM-2 regulates Th2 cytokine production. J. Immunol. 161: 5138
    OpenUrlAbstract/FREE Full Text
  49. ↵
    Constant, S. L., K. Bottomly. 1997. Induction of Th1 and Th2 CD4+ T cell responses: the alternative approaches. Annu. Rev. Immunol. 15: 297
    OpenUrlCrossRefPubMed
  50. ↵
    Cippitelli, M., A. Santoni. 1998. Vitamin D3: a transcriptional modulator of the interferon-γ gene. Eur. J. Immunol. 28: 3017
    OpenUrlCrossRefPubMed
  51. ↵
    Ouyang, W., M. Lohning, Z. Gao, M. Assenmacher, S. Ranganath, A. Radbruch, K. M. Murphy. 2000. Stat6-independent GATA-3 autoactivation directs IL-4-independent Th2 development and commitment. Immunity 12: 27
    OpenUrlCrossRefPubMed
  52. ↵
    Hewison, M.. 1992. Vitamin D and the immune system. J. Endocrinol. 132: 173
    OpenUrlAbstract/FREE Full Text
Back to top

In this issue

Print
Download PDF
Article Alerts
Email Article
Citation Tools

Jump to section