Loss of T Regulatory Cell Suppression following Signaling through Glucocorticoid-induced Tumor Necrosis Receptor (GITR) Is Dependent on c-Jun N-terminal Kinase Activation*

Background: Ligation of the glucocorticoid-induced tumor necrosis (TNF) receptor (GITR) regulates T suppressor cell activity. Results: Regulation of JNK phosphorylation following GITR ligation plays a central role in the suppressive activity of T regulatory cells. Conclusion: Inhibition of JNK phosphorylation modulates T regulatory effector cell function in vitro and in vivo. Significance: Identification of JNK phosphorylation as a regulator of T suppressor cell function. Naturally occurring Foxp3+CD4+CD25+ T regulatory cell (nTreg)-mediated suppression of lung allergic responses is abrogated following ligation of glucocorticoid-induced tumor necrosis receptor (GITR) family-related protein. In vitro stimulation of nTregs with GITR ligand increased phosphorylation of c-Jun N-terminal kinase (JNK) but not extracellular signal-regulated protein kinase (ERK) or p38 MAPK. SP600125, a known JNK inhibitor, prevented GITR-mediated phosphorylation of JNK. Activation of JNK was associated with increases in the upstream mitogen-activated protein kinase kinase 7 (MKK7) and the downstream transcription factor NF-κβ. Phosphorylated c-Jun (p-c-Jun), indicative of the activation of JNK, was detected in the immunoprecipitates of nTregs from wild-type but not JNK- or GITR-deficient mice. Treatment with an inhibitor of JNK phosphorylation resulted in complete reversal of all GITR-induced changes in nTreg phenotype and function, with full restoration of suppression of in vivo lung allergic responses and in vitro proliferation of activated CD4+CD25− T cells. Thus, regulation of JNK phosphorylation plays a central role in T regulatory cell function with therapeutic implications for the treatment of asthma and autoimmune diseases.

Glucocorticoid-induced tumor necrosis factor receptor (GITR) 2 family-related protein, also know as TNFRSF18, was first described in mice as a dexamethasone-inducible molecule in T cells (1), and subsequently the human equivalent was defined (2). GITR is a type 1 transmembrane protein with an extracellular N terminus and cytoplasmic C terminus, and it shares significant homology in the C-terminal domain with other members of the TNF receptor family, including 4-1BB, CD27, CD40, and OX40 (1,2). Signaling cascades triggered through members of the TNF receptor superfamily influence many physiologic and pathologic immune responses by differentially regulating proliferation, differentiation, survival, and functions of cells in both the innate and adaptive immune systems (3). Specifically in the lung, GITR was shown to play a role in acute inflammation (4) and airway hyper-responsiveness (AHR) (5). Constitutive expression and function of GITR in CD4 ϩ CD25 ϩ T regulatory cells (Tregs) have been described (6,7). Stimulation of GITR on T regulatory cells (nTregs) by either GITR ligand (GITRL) or an agonistic antibody (DTA-1) abolished suppression of allergen-induced lung allergic responses (8), in contrast to rendering effector cells resistant to the suppressive activities of Tregs (9 -11).
In both humans and experimental animal models, allergic asthma is an inflammatory disease of the airways characterized by an increase in AHR, airway inflammation, Th2 cytokine skewing, goblet cell metaplasia, excessive mucus production, elevated antigen-specific IgE, and structural remodeling of the airways. Increasingly, nTregs have been shown to be important in modifying the development and outcome of lung allergic diseases (12,13) through both antigen-specific (14) and antigen-nonspecific mechanisms (15). However, the phenotypic and functional stability of nTregs has been shown to depend on a number of factors, including the expression of the key transcription factor, Foxp3 (16). Mutations of Foxp3 are associated with multiorgan autoimmune disease in Scurfy mice (17) and immune dysregulation, polyendocrinopathy, enteropathy, and X-linked syndrome in humans (18). Cytokines such as IL-6 (19) and the expression of CD8 have also been shown to alter nTreg function (13,15). Importantly, in the absence and/or interference with MHC-I/CD8 interactions, regulatory functions were subverted, resulting in the loss of suppression. Indeed, under these conditions nTregs were converted into pathogenic effector cells, enhancing lung allergic responses in sensitized and challenged mice (8). Furthermore, the maintenance of suppressive activities in peripheral tissues and the regulation of endog-enous IL-6 production by nTregs were shown to be dependent on the presence of CD8 ϩ T cells (19). Conversion of Tregs to pathogenic effector cells has now been described in other animal models (20,21).
In contrast to earlier studies (6,7), host GITRL was demonstrated to effectively abrogate suppression in vivo, associated with the pathogenic conversion of nTregs (8). Moreover, enhancement of lung allergic responses was prevented by in vivo administration of anti-GITRL antibody prior to the transfer of nTregs, identifying the importance of GITRL-GITR signaling in controlling the phenotype of these cells (8). Although various signaling cascades through GITR have been described in T cells (22)(23)(24) and macrophages (25), there are little or no data linking GITR signal transduction pathways to the loss of suppression and phenotypic conversion of nTregs.
In this study, we defined the signaling pathways activated through GITR in nTregs in vitro and in vivo and determined the impact of interfering with activation on the expression of surface receptors, production of immunosuppressive cytokines, suppression of proliferation of activated T cells, and the consequences in the airways of allergen-sensitized and challenged mice.

EXPERIMENTAL PROCEDURES
Animals-Pathogen-free, 6 -8-week-old female C57BL/6 and JNK Ϫ/Ϫ mice were obtained from The Jackson Laboratory (Bar Harbor, ME). GITR Ϫ/Ϫ mice were kindly provided by Dr. Carlo Riccardi (Perugia, Italy). All mice were maintained on an OVA-free diet, and all protocols were approved by the Institutional Animal Care and Use Committee of National Jewish Health.
Sensitization and Challenge-Sensitization was carried out by intraperitoneal injection of 20 g of OVA (Sigma) emulsified in 2.25 mg of alum hydroxide (AlumImject; Pierce) in a total volume of 100 l on days 1 and 14. Sensitized and challenged mice, denoted OVA/OVA, and nonsensitized but challenged littermates (PBS/OVA) received aerosol challenges for 20 min each day on 3 consecutive days (days 26, 27, and 28) with 1% OVA in PBS using an ultrasonic nebulizer (Omron, Vernon Hills, IL) (10).
Measurement of Airway Responsiveness-Airway responsiveness was assessed 48 h following the last challenge as a change in airway function to increasing concentrations of aerosolized methacholine administered for 10 s (60 breaths/min, 500 l of tidal volume). Lung resistance was continuously computed (Labview, National Instruments, TX) by fitting flow, volume, and pressure to an equation of motion. Maximum values of lung resistance were taken and expressed as the percent change from base line following PBS aerosol.
Bronchoalveolar Lavage-Immediately following measurement of AHR, lungs were lavaged. Total leukocyte numbers were counted (Coulter Counter, Coulter Corp., Hialeah, FL), and differential cell counts were performed in a blinded manner under light microscopy by counting at least 200 cells on cytocentrifuged preparations (Cytospin 2; Cytospin, Shandon Ltd., Runcorn, Cheshire, UK) stained with Leukostat (Fisher Diagnostics, Middletown, VA) and differentiated by standard hematological procedures.
In Vitro Treatment and Adoptive Transfer-Isolated CD4 ϩ CD25 ϩ T cells were pretreated with JNKi (SP600125) or inactive JNKi alone (50 M, all from Calbiochem) and prior to stimulation with GITRL (1 g/ml, R&D Systems, Minneapolis, MN) in complete medium for assessing the in vitro production of cytokines in the supernatants, protein extraction for quantifying kinase phosphorylation by Western blotting, and intratracheal adoptive transfer of 5 ϫ 10 5 nTregs in 50 l of PBS into sensitized recipients prior to allergen challenge.
Real Time PCR-Total RNA was isolated using the Qiagen RNeasy mini kit (Valencia, CA) according to the manufacturer's instructions. Total RNA was reverse-transcribed using Bio-Rad iScript cDNA synthesis kit. TaqMan primers and probes for mouse Foxp3 and GAPDH were obtained from Applied Bio-systems (Carlsbad, CA). Real time PCR was performed using ABI Prism 7000 sequence detection system. Relative amounts of cDNA were normalized by subtracting the threshold cycle (Ct) of internal GAPDH reference gene to target gene generating a ⌬Ct value. Relative mRNA expression of specific gene was obtained by using the formula 2ˆ(Ϫ⌬Ct).
JNK Activation-The assay for JNK activity was performed according to the manufacturer's directions (SAPK/JNK kinase assay, Cell Signaling, Danvers, MA). Briefly, similar amounts of cell lysate from the different cell groups were incubated with the recommended amount of immobilized c-Jun fusion protein overnight. Mixtures were washed extensively with 1ϫ cell lysis buffer and the kinase buffer. SAPK phosphorylation of c-Jun substrate was carried out for 30 min at 30°C by adding the same volume of 1ϫ kinase buffer supplemented with 200 M ATP. The reaction was terminated with 25 l of 3ϫ SDS. The supernatants were then prepared for standard Western immunoblotting probing for p-c-Jun.
Histochemistry-Lungs were fixed by inflation (1 ml) and immersion in 10% formalin. Cells containing eosinophilic major basic protein were identified by immunohistochemical staining as described previously using rabbit anti-mouse major basic protein (kindly provided by Dr. J. J. Lee, Mayo Clinic, Scottsdale, AZ). The slides were examined in a blinded fashion with a Nikon light microscope. Numbers of eosinophils in the tissues were evaluated with ImageJ counting 6 -8 different fields per animal. For detection of mucus-containing cells in formalin-fixed airway tissue, sections were stained with periodic acid-Schiff.
Statistical Analysis-Analysis of variance was used to determine statistical significance. Comparisons for all pairs were performed by the Tukey-Kramer highest significant difference test. The p values for significance were set to 0.05. Values for all measurements were expressed as the means Ϯ S.E.

RESULTS
GITR Stimulation Activates c-Jun N-terminal Kinase-In mammalian cells, three main families of the MAPKs, including extracellular signal-regulated kinase (ERK), c-Jun N-terminal kinase (JNK), and p38, have been implicated in developing immune responses, and individual MAPKs are activated by different stimuli (26). Although p38 (27), ERK (28), and TAK1 (29) have been implicated in the development and function of Tregs, the involvement of MAPK in GITR-mediated loss of suppression and phenotypic conversion has not been described. We investigated the activation of the MAPK pathways in nTregs following GITR stimulation with different concentrations of GITRL ( Fig. 1, A-C). Compared with nonstimulated cells, GITRL significantly increased the phosphorylation of JNK without evidence for activation of ERK or p38, as determined by densitometric quantification of immunoreactive bands on autoradiographs. Total JNK, ERK, and p38 were unchanged under all conditions. In contrast to CD4 ϩ CD25 ϩ T cells, CD4 ϩ CD25 Ϫ T cells, which express lower levels of GITR (8), demonstrated no increases in GITRL-stimulated increases in p-JNK (Fig. 1D).
Similar to other MAPKs, full activation of JNK requires dual phosphorylation on Thr-183 and Tyr-184 of the tripeptide motif (Thr-Xaa-Tyr) (30), and specific activity of JNK can be blocked by SP600125, an anthrapyrazolone inhibitor (31). In an animal model, treatment with SP600125 was shown to reduce airway inflammation and levels of OVA-IgE in the serum of sensitized and challenged mice (32). The effect of treatment with SP600125 on the phosphorylation of JNK following GITR stimulation was investigated. Pretreatment of nTregs with the active but not inactive JNK inhibitor (JNKi) decreased GITRLinduced phosphorylation of JNK ( Fig. 2A).
The specificity of activation of JNK following GITR ligation was confirmed by comparing nTregs from wild-type (WT) with nTregs from JNK Ϫ/Ϫ or GITR Ϫ/Ϫ mice. JNK activity detected as phosphorylation of c-Jun (p-c-Jun) was only detected in the immunoprecipitates from WT but not the deficient (JNK Ϫ/Ϫ or GITR Ϫ/Ϫ ) or JNKi-treated nTregs (Fig. 2B).
We next investigated which of the upstream MAPK kinases (MKK) were involved in GITR-mediated activation of JNK at the time point associated with changes in levels of cytokines in the supernatants of in vitro cultured cells. To date, only MKK4 (SEK1) and MKK7 have been implicated in the activation of JNK (26,33,34). Following the in vitro addition of GITRL, increases in protein levels of MKK7 but not MKK4 were detected (Fig. 3).
Upon activation, JNK phosphorylates a number of downstream targets, including c-Jun, which heterodimerizes with Fos to form the transcription factor activator protein 1 (35). To further define the role of JNK in the signaling cascade through GITR, total protein and phosphorylation of c-Jun were determined. Both total protein and phosphorylation of c-Jun increased following GITR stimulation, consistent with the results detected in immunoprecipitates. Correspondingly, increased c-Jun was detected in the nuclear extracts of stimulated compared with nonstimulated nTregs.
Consistent with a previous report (9), increases in activation of subunits of NF-B, including c-Rel, p65, and to a lesser degree p50, were detected following GITR stimulation, indicated by the increases in nuclear translocation of these subunit proteins (Fig. 3). Activation of NF-B can also be determined by assessing the levels of the protein inhibitor of NF-B (I␤) (22).
In contrast to nonstimulated cells, GITR-stimulated cells had less I␤ protein in the cytoplasm.
GITRL Stimulation Induces Changes in the Phenotype, Function, and Cytokine Production of nTregs and Are Prevented by Inhibition of JNK Activation-Naturally occurring CD4 ϩ CD25 ϩ nTregs have been characterized by the expression of CD25, CTLA-4, and GITR (6,7,12,36), and under certain experimental conditions, decreased expression of these receptors was shown to associate with loss or attenuation of suppressive activity (19 -21, 36). The effects of GITR ligation on the expression of surface markers were assessed by flow cytometry in the presence or absence of the JNKi. Compared with nonstimulated cells, nTregs treated with GITRL expressed lower  Previously, nTregs isolated from naive BALB/c and C57BL/6 mice were shown to produce the immunosuppressive cytokines IL-10 and TGF-␤ (12,13,15). We determined the consequences of sustained GITR ligation over 72 h on cytokine production and the impact of adding the JNKi. Despite the phenotypic changes induced following the shorter incubation, intracellular staining of Foxp3 and immunocytokines (Fig. 4A), similar to levels detected in the supernatants of in vitro cultures (Fig. 4B), did not change to any appreciable degree. In contrast, significant changes in cytokine profile were detected following the longer stimulation. Compared with nonstimulated nTregs, GITRL-stimulated nTregs released lower amounts of IL-10 and TGF-␤ in the culture supernatants (Fig. 4C), similar to GITRLtreated cells in the presence of the inactive inhibitor (data not shown). In contrast, treatment with the active JNKi prevented these decreases, maintaining the levels seen in untreated cells. In parallel, similar to previous results showing increased IL-13 production when nTregs were shown to have reduced IL-10 and TGF-␤ production (8), levels of IL-13 were increased in cultures of GITRL-treated nTregs but not those that included the active JNKi. Furthermore, decreases in Foxp3 protein (Fig.  4D) and mRNA (Fig. 4E) expression were associated with the changes in cytokine production (Fig. 4C).
Consistent with others (6, 7), we reported that the proliferation of CD4 ϩ CD25 Ϫ T cells activated with anti-CD3 and anti-CD28 was inhibited by nTregs (19) and that treatment of nTregs with either the GITRL or agonistic anti-GITR antibody (DTA-1) abolished their suppressive activity. Here, we confirmed that in vitro stimulation of nTregs with GITRL abolished the suppression of CD4 ϩ CD25 Ϫ T cell proliferation triggered by anti-CD3/anti-CD28 (Fig. 5A). The loss of suppression, in contrast to a previous report (40), was not associated with GITR-induced proliferation of nTregs (Fig. 5B). However, suppression was maintained in the presence of the active, but not inactive, JNKi. This was not due to any toxic effects of the inhibitor, as washing out of the inhibitor after a similar incubation period was associated with full proliferative activity of the cells (data not shown).
Taken together, these in vitro studies demonstrated that ligation of GITR had profound effects on kinase phosphorylation, surface receptor expression, suppressive activity, and cytokine production, and all of these effects were reversed in the presence of the active JNKi.
Prevention of JNK Activation in Vivo Is Associated with Maintenance of Suppression in an Experimental Model of Asthma-Following adoptive transfer, nTregs suppressed the development of allergen-induced lung allergic responses in sensitized and challenged mice (8,12,13,15,19). This suppression mediated by nTregs was abolished by the in vitro treatment of nTregs with GITRL or agonistic antibody when transferred after sensitization but prior to challenge (8). We determined whether prevention of JNK activation affected the activity of nTregs in sensitized and challenged mice. Prior to transfer, cell viability of GITRL-and JNK-treated cells exceeded 85-90%. Transfer of nTregs treated with GITRL, as compared with nontreated cells, failed to suppress AHR (Fig. 6A). In contrast, treatment of nTregs with the active but not inactive JNKi restored the suppression of AHR. Associated with the increases in AHR, the numbers of airway eosinophils were significantly increased in sensitized and challenged mice as shown in Fig. 6B. Airway eosinophilia was significantly reduced in recipients of nonstimulated nTregs and GITRL-stimulated nTregs treated with the active inhibitor but was maintained in the GITRL-stimulated nTregs treated with the inactive inhibitor. Similar effects of treatment with the JNKi were also observed in BALB/c mice (data not shown).
Following sensitization and challenge with allergen, Th2 cytokine levels were increased in BAL fluid. Significant increases in levels of IL-4, IL-5, and IL-13 were detected, and levels of IL-10 and IFN-␥ were decreased; levels of TGF-␤ were modestly increased (Fig. 6C). Intratracheal transfer of nonligated nTregs decreased the levels of IL-5 and IL-13, whereas IL-10 and TGF-␤ levels were increased. Little change was seen in levels of IL-4 and IFN-␥. Transfer of GITRL-stimulated nTregs, untreated or treated with the inactive JNKi, failed to significantly reduce the levels of IL-5 and IL-13, and the levels of IL-4, IL-10, TGF-␤, and IFN-␥ were similar to the levels in sensitized and challenged mice that did not receive transferred cells (Fig. 6C). In contrast, treatment of GITRL-stimulated nTregs with the active JNKi reversed the effects of GITR stimulation, with restoration of levels of IL-10 and TGF-␤ and decreased levels of IL-5 and IL-13.
Lung histopathology paralleled the changes in inflammatory cell composition and numbers and levels of cytokines in BAL fluid. The lung tissue from sensitized and challenged mice that received GITRL-stimulated nTregs, untreated or treated with inactive JNKi, similar to mice given PBS, showed a significant accumulation of eosinophils, mucus hyperproduction, and goblet cell metaplasia (Fig. 6D). In contrast, mice that received non-GITRL-stimulated or nTregs that were GITRL-stimulated but treated with active JNKi exhibited significantly less lung histopathology.

DISCUSSION
Naturally occurring CD4 ϩ CD25 ϩ Foxp3 ؉ T cells (nTregs), although comprising only a small subset of T cells derived in the thymus (37), appear essential to the maintenance of immunological tolerance. In the absence of functional Foxp3, the key transcription regulator for Treg development and function (38), severe and life-threatening autoimmune and allergic diseases develop (17, 18). These regulatory T cells have also been implicated in the maintenance of immune homeostasis in the airways as they have been shown to regulate allergen-induced AHR and inflammation, at least in part, through the actions of IL-10 and TGF-␤ (12), and in an antigen-nonspecific manner (15). In the lungs of both BALB/c and C57BL/6 mice, the activation and expression of this suppressive phenotype appeared dependent on the interaction of MHC class I on nTregs with CD8; inhibition or interference with this interaction led to the loss of nTreg suppressive activity (13,15). A role for CD8 in maintaining suppressive activity in the periphery and regulating the production of endogenous IL-6 in Tregs was recently demonstrated (19). Similar to other reports (6,7), in the absence of CD8-expressing cells, activation of nTregs through GITR in the lungs of recipient mice was shown to be sufficient to abrogate suppression and convert these cells to pathogenic effector cells resulting in the enhancement of lung allergic responses (8). Significantly, GITRL expression in recipients appeared to provide the necessary signals to attenuate suppression, as administration of anti-GITRL antibody prevented rather than enhanced lung allergic responses in association with little increase in levels of IL-13 and maintenance of basal levels of IL-10 and TGF-␤ known to be essential for suppressive activity (12,39).
In this study, we investigated the molecular events following stimulation of nTregs through GITR. Although the roles of p38 (27), ERK (28), and TAK1 (29) have been implicated in the development and function of Tregs, their involvement in the  stimulatory activity of GITR in Tregs has not been defined. In this study, we defined a signaling pathway following ligation of GITR, a cascade that was associated with the loss of suppressive activity and phenotypic conversion. In vitro stimulation of nTregs with GITRL increased phosphorylation of JNK but not ERK or p38. The activation of JNK was linked to changes in the phenotype, capacity to produce immunosuppressive cytokines, and in vitro and in vivo suppressive activities. The expression levels of the surface receptors CD25, CD152 (CTLA-4), and GITR were decreased following GITR stimulation, rendering nTregs with an effector phenotype. Loss of suppression was associated with a decrease in expression of these surface molecules and levels of Foxp3 mRNA and protein. Corresponding with the effector phenotype, lower levels of IL-10 and TGF-␤ and higher levels of IL-13 were detected in the supernatants of in vitro cultures. Similar to previous studies (6,7,38), following GITR ligation nTregs failed to suppress the in vitro proliferation of CD4 ϩ CD25 Ϫ T cells activated with anti-CD3 and anti-CD28. In the absence of additional stimulation and unlike a previous study (40), the loss of suppression was not associated with GITR-induced proliferation of nTregs.
The importance of JNK activation in the spectrum of GITRmediated effects on nTregs was confirmed using SP600125, a known inhibitor of JNK (31), and genetically deficient mice. Phosphorylation of JNK in GITRL-treated nTregs was prevented by the inhibitor. The link between JNK activation and GITR stimulation was also demonstrated by increases in the phosphorylation of JNK and corresponding activity, as indicated by levels of p-c-Jun, detected only in the immunoprecipitates from ligated nTregs from WT but not JNK Ϫ/Ϫ or GITR Ϫ/Ϫ mice. Furthermore, treatment with the inhibitor abolished GITRL-mediated phosphorylation and activity of JNK in the immunoprecipitates of nTregs from WT mice. The GITR signaling cascade was further defined both upstream and downstream of JNK phosphorylation. Upstream, activation of MKK7 but not MKK4 was demonstrated. Both MKK7 and MKK4 have been reported to activate JNK (26,33,34), but only MKK4 has additional activity phosphorylating p38 MAPK in vitro (9,26). Our data are consistent with this notion because little or no increase in the activation of p38 following GITR stimulation was detected and only MKK7 was identified in the activation of nTregs through GITR. Downstream, phosphory- lation of JNK was associated with increases in total c-Jun and p-c-Jun, a known downstream substrate of JNK (30,31). Corresponding with the increase in p-c-Jun, greater amounts of c-Jun were also detected in the nucleus.
The loss of nTreg-mediated suppression following GITR ligation has been shown to be dependent on the activation of NF-B (9). We confirmed that GITR ligation increased the activation of subunits of NF-B, including c-rel, p65, and to a lesser extent p50 in cytoplasmic and nuclear cell extracts. Interestingly, the activation of NF-B coincided with divergent effects on the levels of proinflammatory and immunosuppressive cytokines. Multiple factors may be involved in these transcriptional responses, including selective phosphorylation and subsequent degradation of NF-B inhibitors or the result of differential subunit distribution, affinity, or number of binding sites engaged in these reactions.
The importance of JNK activation in mediating the abrogation of nTreg suppressive activity through GITR was also demonstrated in vivo in sensitized and challenged mice. As in previous studies (12,13,15,19), following sensitization and allergen challenge, mice developed a significant increase in airway responsiveness to inhaled methacholine, eosinophilic inflammation, and Th2 skewing in cytokine production. These findings were accompanied by changes in lung pathology, especially eosinophil accumulation in the lung parenchyma and goblet cell metaplasia and mucus hyperproduction. Consistent with our previous report (8), GITR ligation of nTregs prior to transfer into sensitized and challenged mice eliminated the suppression of lung allergic responses. However, the full suppression of all lung allergic responses and lung pathology could be restored when the GITR-ligated nTregs were treated with the JNKi prior to transfer into sensitized recipients prior to airway allergen challenge.
Taken together, the results demonstrate that stimulation of nTregs through GITR initiates a signaling cascade that involves MKK7, JNK phosphorylation, c-Jun activation, and the activation of NF-B. Associated with the phosphorylation of JNK were changes in nTreg surface marker expression, conversion of the cytokine profile from IL-10/TGF-␤ to IL-13 production, attenuation of in vitro suppressive activities, and in an experimental model of allergic asthma, elimination of the nTreg regulatory activities on development of altered airway responsiveness, eosinophilic airway inflammation, and Th2 cytokine production. Incubation of the GITRL-stimulated nTregs with an inhibitor of JNK activation resulted in the restoration of nTreg activities and phenotype in vitro and in vivo. These findings demonstrate that targeting JNK phosphorylation can have a major influence on nTreg suppressive function.