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T follicular regulatory (Tfr) cells control the magnitude and specificity of the germinal centre reaction, but how regulation is contained to ensure generation of high-affinity antibody is unknown. Here we show that this balance is maintained by the reciprocal influence of interleukin (IL)-2 and IL-21. The number of IL-2-dependent FoxP3+ regulatory T cells is increased in the peripheral blood of human patients with loss-of-function mutations in the IL-21 receptor (IL-21R). In mice, IL-21:IL-21R interactions influence the phenotype of T follicular cells, reducing the expression of CXCR4 and inhibiting the expansion of Tfr cells after T-cell-dependent immunization. The negative effect of IL-21 on Tfr cells in mice is cell intrinsic and associated with decreased expression of the high affinity IL-2 receptor (CD25). Bcl-6, expressed in abundance in Tfr cells, inhibits CD25 expression and IL-21-mediated inhibition of CD25 is Bcl-6 dependent. These findings identify a mechanism by which IL-21 reinforces humoral immunity by restricting Tfr cell proliferation.
Cytokines provide cues that influence the growth, survival and differentiation of immune cells. The cytokines interleukin (IL)-2 and IL-21 are the products of neighbouring genes on chromosome 3 in mice and chromosome 4 in humans. The Il2/Il21 locus has been associated with risk for several autoimmune and inflammatory diseases in genome-wide association studies1,2. Il2 and Il21 have similar intron and exon structures, suggesting that these two genes arose by gene duplication3,4. However, despite structural similarities, the gene products IL-2 and IL-21 are growth and differentiation factors for CD4+ T-cell subsets with distinct functions.
IL-2 is secreted by activated/effector T cells and is a survival factor for Forkhead Box P3 (Foxp3)-expressing regulatory T (Treg) cells, which are vital for regulating immune responses in mice5,6,7. In humans, a severe autoimmune disease immunodysregulation polyendocrinopathy enteropathy X-linked syndrome results from inactivating mutations in FOXP3, leading to dysfunction or deficiency in Treg cells8. The utilization of IL-2 by Treg cells is facilitated by binding of IL-2 by the cell surface expressed α-chain of the heterotrimeric high-affinity IL-2 receptor, comprising the IL-2Rα chain (CD25), the IL-2Rβ chain (CD122) and the common γ-chain (CD132)9.
The production of IL-21, in turn, is mostly restricted to T follicular helper (Tfh) cells that provide help to B cells for the generation of affinity-matured antibody during the germinal centre (GC) reaction10,11. The receptor for IL-21 is closely related to the IL-2Rβ3,12 and is broadly expressed on haematopoietic cells, where IL-21 imparts both autocrine and paracrine effects on lymphocytes that influence survival and differentiation13,14,15. In humans, loss-of-function mutations in IL21 or IL21R cause a primary immunodeficiency syndrome associated with an increased susceptibility to chronic infections and gastrointestinal inflammation16,17,18,19. In addition to its roles in immunity, IL-21 contributes to the development of inflammatory and autoimmune diseases13.
Studies have revealed that IL-21-producing Tfh cells are controlled by a subset of IL-2-dependent FoxP3-expressing follicular Treg (Tfr) cells, a specialized subset of Foxp3+ Treg cells that co-localize during GC reactions within B-cell follicles20,21,22. FoxP3+ Tfr cells originate from natural (thymus-derived) Treg cells and acquire features of Tfh cells, such as expression of the B-follicular homing chemokine receptor CXCR5 (refs 20, 23) and high expression of the co-inhibitory molecule PD-1 (ref. 24). However, unlike Tfh cells, they lack expression of CD40L, IL-4 and IL-21 (refs 20, 21, 22). Tfr cells are suppressive and abrogating either Tfr cell development or their follicular localization enhances the GC reaction and antibody production20,21,22.
We have previously shown that Treg cells expand to a greater extent in Il21−/− mice than in IL-21-sufficient mice after immunization and co-administration of anti-CD28 monoclonal antibodies11 and more recent studies have shown that IL-21:IL-21R signalling inhibits Treg expansion both in vitro25 and after lymphocytic choriomeningitis virus (LCMV) infection26. IL-21 has been shown to reduce FoxP3 expression, inhibit Treg suppressor function and influence Treg homeostasis by decreasing IL-2 production from effector T cells in vitro25,27,28,29,30,31. By contrast, IL-2 inhibits Tfh cell differentiation through activation of STAT5 and the subsequent repression of Bcl-6 (refs 32, 33, 34, 35).
In this study, we provide evidence that IL-21 has the capacity to reinforce the generation of a robust humoral immune response by inhibiting the proliferation of Tfr cells.
We have previously shown that Treg cell populations undergo greater expansion in Il21−/− mice than in IL-21-sufficient mice following administration of anti-CD28 monoclonal antibodies in conjunction with immunization with the polyvalent antigen sheep red blood cells (SRBC)11. To further analyse the influence of IL-21 on Treg cells, we used intracellular immunostaining to distinguish total Foxp3+ CD4+ Treg and FoxP3+ Tfr cells in Il21r−/− and wild-type (WT) mice following immunization with SRBC.
The percentages of Tfh cells, defined as CXCR5hiPD-1hi CD4+ T cells, in the spleen were similar in Il21r−/− and WT mice 7 days after immunization with SRBC (Fig. 1a,b and Supplementary Fig. 1). By contrast, Il21r−/− Foxp3+ Tfr cells within the CXCR5hiPD-1hi T follicular population were increased in the spleen compared with WT Tfr cells in terms of both the percentage (Fig. 1a,c) and absolute number of Tfr cells (Fig. 1d). The effect of IL-21R on the T follicular cell populations resulted in a significant (twofold) decrease in the Tfh:Tfr cell ratio (Fig. 1e). Tfr cells derive from Treg cells20 and both subsets were observed to express comparable amounts of the receptor for IL-21 (Supplementary Fig. 2). We similarly observed an increased fraction of Il21r−/− total Foxp3+ Treg cells compared with WT Treg cells following SRBC immunization (Fig. 1f). In contrast to SRBC-immunized mice, the percentages of Treg cells in the spleen of unmaniplated Il21r−/− and Il21r+/+ mice were similar (Fig. 1g). Thus, IL-21:IL-21R interactions, limit the expansion of both total Treg cells and Tfrs following immunization.
To determine whether the increased fraction of Il21r−/− Tfr cells and Treg cells was associated with increased proliferation of these subsets, we immunostained for Ki67, which is a nuclear protein associated with cellular proliferation. A greater percentage of both Il21r−/− Treg cells (Fig. 1h) and Il21r−/− Tfr cells (Fig. 1i) were observed to express Ki67 than their WT counterparts on day 7 of SRBC immunization. The populations of FoxP3+ Treg cells and Tfr cells comprise both cells that express the high-affinity receptor for IL-2 (identified by expression of the α-chain of the IL-2R, CD25) and cells that lack CD25 (Fig. 1a). In this regard, it was of interest to note that the Il21r−/− Ki67+ proliferating Treg population contained a greater fraction of CD25+ Treg cells relative to CD25− Treg cells than the WT Ki67+ proliferating Treg population (Fig. 1j). This bias was more evident in the proliferating Tfr cell population, where CD25+ and CD25− Ki67+ Tfr cells were present in equal ratios in Il21r−/− mice, whereas in WT mice, CD25+ Tfr cells represented a minority of the Ki67+ population (Fig. 1k).
Previous studies have demonstrated that the expression of CXCR5 on Treg cells depends upon the transcriptional repressor Bcl-6 (ref. 21). Further analyses of the Tfr populations identified increased expression of Bcl-6 in Tfr cells that lack CD25 when compared with CD25+ Tfr cells (Fig. 1l,m). Furthermore, CD25+ Tfr cells from Il21r−/− mice, despite exhibiting increased proliferation, exhibited lower expression of Bcl-6 than WT CD25+ Tfr cells (Fig. 1m). Collectively, these findings demonstrate that IL-21:IL-21R signalling reduces the proliferation of CD25-expressing Treg cells and Tfr cells, and indicate that responsiveness to IL-2 is associated with reduced expression of Bcl-6.
We next tested whether IL-21 had an influence on Treg expansion in vitro. In the presence of anti-CD3 and anti-CD28 monoclonal antibodies alone, Il21r−/− CD4+ T-cell cultures exhibited a greater fraction of FoxP3+ Treg cells compared with WT CD4+ T-cell cultures (Fig. 1n and Supplementary Fig. 3). Moreover, Il21r−/− CD4+ T cells cultured under polarizing (transforming growth factor-β) conditions exhibited an approximately twofold greater expansion of Foxp3+ Treg cells when compared with WT Treg cells cultured under the same conditions (Fig. 1o). Taken together, these findings indicate that IL-21 inhibits Treg expansion both in vivo and in vitro.
In humans, loss-of-function mutations in the IL21R gene cause a primary immunodeficiency syndrome associated with recurrent and chronic infections16,19. To determine whether Treg cells were affected by IL-21R deficiency in humans, we analysed Treg cells and Tfr-phenotype cells in the blood of three patients P1 (B.II-1, a 13-year-old boy) and P2 (B.II-2, an 8-year-old boy), whose lymphocytes have previously been shown to exhibit a loss of IL-21-mediated signalling due to a homozygous deletion in exon 4 of the IL21R gene16, and P3 (a 5-month-old sister of a previously reported patient with the homozygous point mutation c.G602A)19. Treg cells in the peripheral blood of the IL-21R-deficient patients were compared with those in five age-matched healthy control subjects.
Treg cells can be defined based on expression of CD4, CD25 and Foxp3. In humans, CD127 (IL-7Rα) is downregulated on Foxp3+ CD4+ T cells, including those that express medium levels of CD25 (refs 35, 36). Treg cells, identified as CD3+CD4+Foxp3+CD127lo were markedly increased in the peripheral blood of all three IL-21R-deficient patients relative to healthy control patients, shown as a percentage of CD4+ T cells (Fig. 2a,b and Supplementary Fig. 4) and as a percentage of peripheral blood lymphocytes (Fig. 2c). Similarly, CD25+FoxP3+CD3+CD4+ Treg cells were increased within CD4+ T-cell populations (Fig. 2d) and total lymphocyte populations (Fig. 2e) of all three IL-21R-deficient patients compared with healthy controls.
FoxP3-expressing CD4+ T cells that exhibit a Tfr phenotype have previously been detected in the peripheral blood of mice37. Circulating and lymph node resident Tfr cells shared properties of memory cells, but blood Tfr cells were found to exhibit a relatively reduced suppressive capacity compared with lymphoid tissue-derived Tfr cells38. When we analysed follicular T-cell populations in the peripheral blood of the three IL-21R-deficient patients, we observed that the fractions of circulating CD4+CXCR5hiPD-1hiFoxp3− Tfh phenotype cells were within the broad range of healthy controls (Fig. 2f), which is consistent with previous observations19,39. By contrast, the percentages of CD4+CXCR5hiPD-1hiCD127loFoxp3+ Tfr phenotype cells in the peripheral blood of IL-21R-deficient patients were elevated relative to healthy controls (Fig. 2g). Thus, FoxP3+ total Treg cells and Tfr cells are increased in the blood of humans with loss-of-function mutations in the IL-21R and the expansion or increase in Treg cells occurs very early in life.
Tfh cells were observed in similar percentages in the presence and absence of IL-21R in humans and in mice following T-dependent immunization. Previous studies have shown that IL-6 can act redundantly to support Tfh cell differentiation in Il21r−/− mice40,41. However, whether Il21r−/− and WT Tfh cell populations are phenotypically distinct remains largely unexplored. C-X-C chemokine receptor type 4 (CXCR4) is a chemokine receptor expressed on T-extrafollicular helper cells42 and is also expressed on a fraction of Tfh cells43,44. Analyses of CXCR4+ PD-1hi CD4+ Th cells on day 7 of SRBC-immunized Il21r−/− and WT mice demonstrated that IL-21 significantly limits the expression of CXCR4 and the expansion of CXCR4+ PD-1hi T cells (Fig. 3a). The percentages of Il21r−/− CXCR4+ CXCR5− PD-1hi FoxP3− Tfh cells were notably increased relative to WT extrafollicular T-helper cells (Fig. 3a,b). Interestingly, we also observed a fraction of previously undescribed CXCR4+ extrafollicular Treg cells (CXCR4+ CXCR5− PD-1hi FoxP3+ CD4+ T cells) in both Il21r−/− and WT mice (Fig. 3a,c).
When we focused on Tfh cells, we observed that CXCR4 distinguished Il21r−/− Tfh cells from WT Tfh cells. Il21r−/− Tfh cells had an increased propensity to co-express CXCR4 (Fig. 3d) and IL-21:IL-21R interactions significantly reduced the expression of CXCR4 on Tfh cells (Fig. 3e,f). Interestingly, we observed a similar theme for Tfr cells 7 days after SRBC immunization, with increased percentages of CXCR4 expressing Il21r−/− Tfr cells compared with WT Tfr cells (Fig. 3g). The intensity of CXCR4 expressed on the surface of Il21r−/− Tfr was also significantly increased (Fig. 3h,i). These findings demonstrate that IL-21:IL-21R interactions influence the phenotype of follicular T-cell populations by restricting CXCR4-expressing Tfh and Tfr cells, and the intensity of expression of CXCR4.
In stark contrast to Th cells, CXCR4-expressing GC B cells were decreased in the absence of IL-21:IL-21R interactions. CXCR4-expressing GC B cells, a phenotype consistent with centroblasts45, were reduced in Il21r−/− mice on day 7 following SRBC immunization and the intensity of CXCR4 expression was similarly decreased on Il21r−/− GC B cells (Supplementary Fig. 5). Moreover, the reduced fraction of CXCR4 expressing cells and intensity of CXCR4 expression was specific to GC B cells, since the percentage of CXCR4+ cells and the intensity of CXCR4 were similar on the total Il21r−/− and WT B cell populations (Supplementary Fig. 5).
The above findings indicated that IL-21 alters the phenotype of T follicular cells, but did not explain the marked expansion of Tfr cells in Il21r−/− mice. To determine whether IL-21:IL-21R interactions had a cell intrinsic contribution to Treg cell subsets, we examined total Treg cells and Tfr cells during GC reactions that form following immunization in mixed bone marrow (BM) chimeras in mice consisting of WT BM expressing the congenic marker Thy1.1 and either Il21r−/− Thy1.2 BM or control WT Thy1.2 BM delivered at 1:1 ratios into irradiated WT CD45.1 recipients. The host CD45.1 congenic marker enabled exclusion of host radioresistant T cells, which typically constitute 10% of the total T cells. Eight weeks later, and after checking chimerism following reconstitution, mice were immunized with SRBC and the relative contribution of WT and Il21r−/− T cells to the percentages of follicular T cells and Treg cells were determined.
Control chimeras consisting of 50% WT Thy1.1 BM and 50% WT Thy1.2 BM exhibited similar contributions of each congenic marker to the total CD4+ T cell (Fig. 4a–c and Supplementary Fig. 6), Tfh cell (Fig. 4a), Treg (Fig. 4b) and Tfr cell (Fig. 4c) populations. For chimeras consisting of 50% WT Thy1.1 BM and 50% Il21r−/− Thy1.2 BM, equal fractions (50%:50%) of Thy1.1 WT and Thy1.2 Il21r−/− lymphocytes were detected in blood before immunization (Fig. 4d). However, following immunization with SRBC, ~39% of CD4+ T cells in the spleen were derived from Thy1.2 Il21r−/− (Fig. 4e). CXCR5hiPD-1hiFoxp3−CD4+TCRβ+ Tfh cells exhibited similar proportions as total CD4+ T cells, with a slightly decreased fraction of Thy1.2+ Il21r−/− Tfh cells (mean of 34.8% of the total donor CD45.2+ Tfh cells) derived from the Thy1.2+ Il21r−/− CD4+ T-cell donor population (mean of 39% of CD45.2 CD4+ T cells) in each mouse (Fig. 4e). Similarly, there was only a small cell intrinsic contribution of IL-21R expression on Treg cells, with a slightly greater increase in Thy1.2 Il21r−/− Treg cells (44.3%) relative to Thy1.2 Il21r−/− CD4+ T cells (39%) within the total CD45.2+ CD4+ T-cell donor population of each mouse (Fig. 3f). By contrast, ~39% of Il21r−/− CD4+ T cells contributed 54% of the total CD45.2+ Tfr cell population, whereas 61% of WT Thy1.1+CD4+ T cells contributed only 46% of the total Tfr cells, demonstrating an increased conversion of Il21r−/− cells to the Tfr phenotype relative to WT cells (Fig. 4g).
Parallel analyses of the T-cell subsets within each donor population showed that the fractions of Il21r−/− and WT Tfh cells were similar, with a minor decrease in Il21r−/− Tfh cells compared with WT Tfh cells observed (Fig. 4h). Similarly, Il21r−/− Treg cells were observed at slightly higher percentages compared with WT Treg cells (Fig. 4i). By contrast, there was a markedly greater percentage of Il21r−/− Foxp3+ Tfr cells compared with WT Tfr cells (Fig. 4j). The increased fraction of Il21r−/− Tfr cells resulted in a twofold decrease in the overall ratio of Tfh:Tfr Il21r−/− cells compared with WT cells (Fig. 4k). Detection of Foxp3+ cells in histological sections of the spleen in mixed BM chimeras identified both Thy1.1 WT and Thy1.2 Il21r−/− Tfr cells within the IgDlo GC areas (Fig. 4l). Enumeration of Foxp3+ Thy1.1+ and Thy1.2+ GC cells revealed that Il21r−/− Thy1.2+ Tfr cells comprising a significantly greater percentage of the total GC Foxp3+ population (Fig. 4m). Taken together, these findings demonstrated that the cell-intrinsic effect of IL-21R was conspicuous for Tfr cells, but not for total Treg cells.
In addition to the analyses of the relative proportions of WT and Il21r−/− CD4+ T-cell subsets in the SRBC-immunized mixed BM chimeras, we measured expression of IL-2Rα (CD25), which closely aligns with the Foxp3+ Treg population in mice. Treg cells in SRBC-immunized Il21r−/−:WT mixed BM chimeras demonstrated increased percentages of both CD25− Il21r−/− Treg cells (Fig. 5a,b) and CD25+ Il21r−/− Treg cells (Fig. 5a,c) compared with WT Treg cells. However, equivalent high expression levels of CD25 were observed on WT and Il21r−/− Foxp3-expressing (non-follicular) Treg cells (Fig. 5d). By contrast, we observed equivalent percentages of CD25− Tfr cells derived from Il21r−/− and WT BM (Fig. 5e,f), but the percentages of Il21r−/− CD25+ Tfr cells were over twofold greater than WT CD25+ Tfr cells (Fig. 5e,g). These data indicate that within the same recipient mice, IL-21 modulated the expression of CD25 on Tfr cells, but not on the non-follicular Treg population. Furthermore, an expansion of Il21r−/− Treg cells was observed in both the CD25+ and CD25− populations, whereas the increased fraction of Il21r−/− Tfr cells were predominantly those that expressed CD25.
Tfr cells are derived from Treg cells, but exhibited lower expression of CD25 (Fig. 5d,h). It was of interest to observe that in the absence of IL-21R, CD25 expression levels on Tfr cells approximated that of their Treg precursors (Fig. 5h). Given that Tfrs derive from Treg cells, this finding suggested that in mixed BM chimeras with presumably equivalent IL-2 bioavailability, the expression of CD25 on Tfr cells was reduced by IL-21 in a cell intrinsic manner. Taken together, these data show a more marked effect of IL-21 on Tfr cells, and that the relatively mild effect of IL-21 on CD25 expression on non-follicular Treg cells correlates with these cells already having maximum high CD25 expression. Therefore, our findings are consistent with an ability of IL-21:IL-21R signalling to limit responsiveness to IL-2.
As the expression of CD25 influences receptiveness to IL-2, we argued that Il21r−/− Tfr cells should be more responsive to IL-2 than WT Tfr cells. To test this possibility, we administered IL-2:IL-2mAb complexes46 to SRBC-immunized Il21r−/− and WT mice, to drive the expansion of CD25-expressing cells that occurs following SRBC immunization. A greater percentage of Il21r−/− Treg cells than WT Treg cells was observed after IL-2:IL-2mAb administration (Fig. 5i). However, the fold increase in IL-2:IL-2mAb expanded Treg cells relative to Treg cells in control SRBC-immunized mice just reached significance (Fig. 5j). Consistent with the effect of the IL-2:IL-2mAb complexes on expansion of Treg cells, the percentage of Il21r−/− Tfr cells was significantly greater than that of WT Tfr cells after IL-2:IL-2mAb treatment (Fig. 5k). However, in contrast to the Treg population, IL-2:IL-2mAb treatment induced a significantly greater expansion of Il21r−/− Tfr cells, shown as an increase in the fold change above SRBC-immunized mice (Fig. 5l). Thus, Foxp3+CD4+ T cells expanded more efficiently in the absence of IL-21:IL-21R signalling and this was most pronounced in the Tfr population. The increased expansion in response to an excess of exogenous IL-2 by Il21r−/− Tfr cells was associated with increased surface expression of CD25, the high-affinity IL-2 receptor. However, this relationship was not evident in the IL-2-dependent non-follicular Treg population, where CD25 was expressed similarly and at the highest levels on both WT and Il21r−/− Treg cells.
A central function of STAT5 in T cells is to mediate signalling by IL-2. As there was no obvious difference in the level of expression of CD25 on the large non-follicular Treg population, we further tested whether the deficiency of IL-21R influenced Treg responsiveness to IL-2 by measurement of rmIL-2-induced phosphorylation of STAT5 by immunostaining and flow cytometry. Both WT and Il21r−/− CD25+ Foxp3+ Treg cells exhibited increased STAT5 phosphorylation after 15min of stimulation with rmIL-2 (Supplementary Fig. 7). However, Il21r−/− cells exhibited increased pSTAT5 intensity and an increased percentage of Foxp3+ Treg cells containing pSTAT5 compared with WT cells in response to the same titration of rmIL-2 (Supplementary Fig. 2). Inclusion of exogenous rmIL-21 had no effect on rmIL-2-mediated phosphorylation of STAT5 in WT cells (Supplementary Fig. 2). This finding indicated that Il21r−/− Treg cells were preconditioned for heightened signalling in response to IL-2.
We were intrigued that IL-21:IL-21R signalling had a more pronounced cell intrinsic effect on Tfr cells than Treg cells. As discussed earlier, Tfr cells derive from Treg precursors and upregulate Bcl-6 and CXCR5 (which is dependent upon Bcl-6)47, enabling their follicular localization. Therefore, we next determined whether IL-21 influenced CD25 expression directly and whether Bcl-6 mediated the effects of IL-21 on CD25 expression.
We first determined whether blockade of IL-21:IL-21R in vitro could mimic the increased expression of CD25 observed on Il21r−/− CD4+ T cells. Culture of CD4+ T cells stimulated with soluble anti-CD3 monoclonal antibody and decreasing doses of soluble anti-CD28 monoclonal antibody over 3 days in the presence of IL-21-neutralizing IL-21RFc increased CD25 expression on both the total CD4+ T-cell population (Fig. 6a and Supplementary Fig. 7) and the Foxp3− CD4+ T-cell population at lower doses of CD28 (<0.25μgml−1) (Fig. 6b and Supplementary Fig. 7). In contrast to the Foxp3− CD4+ T-cell population, the intensity of CD25 expression on Foxp3+ Treg cells was not changed by IL-21 neutralization (Fig. 6c and Supplementary Fig. 7). The increased intensity of CD25 expression could be accounted for by an increased percentage of cells expressing high levels of CD25 on both the total CD4+ T-cell population (Fig. 6d) and the Foxp3− population (Fig. 6e). By contrast, but consistent with the intensity of CD25 expression of Treg cells, the fraction of CD25-expressing Treg cells did not improve with the addition of IL-21RFc over the 3-day culture (Fig. 6f). Thus, neutralization of IL-21 improved responsiveness to IL-2 in CD4+ T cells and this was particularly evident under conditions of limiting co-stimulation by anti-CD28 monoclonal antibodies.
IL-21 can upregulate the expression of Bcl-6 in CD4+ T cells48. To determine whether Bcl-6 mediated the effects of IL-21 on CD25 expression, we analysed the influence of IL-21 on CD25 expression on both CD4+ T cells and CD4+ T cells deficient in Bcl-6 in vitro. CD4+ T cells lacking Bcl-6 (CD4Cre/WT:BCL6fl/fl) exhibited increased expression of CD25 (Fig. 6g) and increased percentages of CD4+ T cells expressing high amounts of CD25 (Fig. 6h) in response to stimulation with anti-CD3 monoclonal antibody in the presence of anti-CD28 monoclonal antibody. There was a consistent trend of modulation of CD25 by IL-21 on WT (WT/WT:BCL6fl/fl) CD4+ T cells: when shown as fold change relative to the mean of CD3 monoclonal antibody and CD28 monoclonal antibody alone, the intensity of CD25 expression (Fig. 6i) and the percentages of CD25hi CD4+ T cells (Fig. 6j) were reduced in the presence of exogenous rmIL-21 compared with IL-21RFc. However, IL-21RFc did not efficiently upregulate CD25 or increase CD25hi CD4+ T cells in the presence of an excess of exogenous rmIL-21 (Fig. 6i,j, respectively). It was of interest to observe that IL-21 had a greater inhibitory effect on the intensity of CD25 expression and the percentages of CD25hi CD4+ T cells in cultures stimulated with anti-CD3 monoclonal antibodies alone (Fig. 6k,l, respectively). Conversely, in the absence of CD28 costimulation, IL-21RFc neutralization was less effective at modulating CD25 expression (Fig. 6k,l). The ability of IL-21 to modulate CD25 expression was dependent upon expression of Bcl-6 in CD4+ T cells, as neither the intensity of CD25 on Bcl-6-deficient CD4+ (Cre/WT:BCL6fl/fl) T cells (Fig. 6g–i) nor the percentages of CD25hi Bcl-6-deficient CD4+ T cells (Fig. 6j–l) were different either in the presence or absence of IL-21 or IL-21RFc. Taken together, these findings demonstrate that Bcl-6 inhibits CD25 expression on CD4+ T cells, and that IL-21 can limit the magnitude of CD25 expression and CD25-expressing CD4+ T cells through Bcl-6.
To determine whether IL-21R expression on Treg cells had functional consequences in terms of GC output, we performed adoptive transfer of IL-21R-deficient (Il21r−/−) and IL-21R-sufficient (WT) Treg cells into Treg-deficient recipients. FoxP3DTR-recipient mice were treated with diphtheria toxin to remove endogenous Treg cells, before transfer of Il21r−/− or WT Treg cells and immunization with 4-hydroxy-3-nitrophenyl acetyl-hapten (NP)-OVA adsorbed to alum. We immunized with NP-OVA to enable the identification of antigen (NP)-specific B cells. On day 10 of immunization, the spleens of recipient mice were analysed histologically showing localization of both Il21r−/− Tfr cells (Fig. 7a) and WT Tfr cells (Fig. 7b) to the GC of FoxP3DTR recipients.
Immunostaining and flow cytometric analyses on day 10 of NP-OVA immunization demonstrated similar percentages of Treg cells from Il21r−/− and WT donors (Fig. 7c and Supplementary Fig. 7 for gating strategy), as well as efficient depletion of endogenous FoxP3+ CD4+ Treg cells by diphtheria toxin administration in mice that did not receive exogenous Treg cells (Fig. 7c). By contrast, Foxp3DTR recipients of Il21r−/− Treg cells contained a greater fraction of Tfr cells compared with recipients of WT Treg cells (Fig. 7d) and a greater fraction of Il21r−/− Tfr cells expressed CD25 (Fig. 7e). CXCR4 was increased on Tfr cells in the absence of IL-21:IL-21R interactions (Fig. 4), but was not significantly different on Tfr cells from either donor genotype in FoxP3DTR recipients (Fig. 7f). By contrast, the percentages of CXCR5hi Bcl-6hi Tfh cells were slightly decreased in recipients of Il21r−/− Treg cells (Fig. 7g). Thus, Il21r−/− Tfr cells derived from adoptively transferred Il21r−/− Treg cells and expand to a greater extent than WT Tfr cells, and this finding is consistent with our observations of the behaviour of Il21r−/− Tfr cells in mixed BM chimeras (Fig. 4).
Analysis of the effect of Il21r−/− and WT Treg transfer on the GC B-cell population showed equivalent percentages of GC B cells in FoxP3DTR recipients of Il21r−/− and WT Treg cells (Fig. 7h and Supplementary Fig. 8). However, a closer examination of the GC B-cell population revealed that recipients of Il21r−/− Treg cells harboured reduced percentages of IgG1+ GC B cells (Fig. 7i), with a relative reduction of IgG1+ cells within the total GC B-cell population (Fig. 7j). Furthermore, FoxP3DTR recipients of Il21r−/− Treg cells had slightly reduced percentages of NP-specific GC B cells (Fig. 7k,l) and, in keeping with the reduced IgG1+ GC B cell population, reduced percentages of IgG1+ NP-specific GC B cells (Fig. 7m). These data suggest that the increased percentages of Il21r−/− Tfr cells had the functional effect of reducing the percentages of IgG1+ GC B cells.
The discovery of Treg cells that function within the B-cell follicle provided evidence that regulation of antibody production occurs within the GC niche20,21,22. Our study provides insights into how the interplay between two neighboring genes, namely Il2 and Il21, can shape antibody responses. IL-21 activates the Jak–STAT signalling pathway, leading to phosphorylation of STAT1 and STAT3, whereas IL-2 strongly activates STAT5. The ability of different STAT molecules to compete for STAT binding sites and affect gene transcription may underpin the relative influence of IL-2 and IL-21 on Tfh and regulatory subsets31,32,33,34,49. The relative influence of IL-2 and IL-21 on T follicular cells is likely to be dictated by several factors including the localization of cytokine production within the T-cell areas and B-cell follicles of secondary lymphoid organs50,51.
Both total FoxP3+ Treg cells and Tfr-phenotype cells were increased in the blood of IL-21R-deficient humans, suggesting that IL-21:IL-21R signalling has a negative influence on human Treg cells. CD25hi CD4+ T cells in peripheral blood were previously shown to be similar between IL-21R-deficient patients and healthy controls19,39, and our findings are consistent with these observations. By contrast, dual expressing FoxP3+CD25hi Treg cells were increased by IL21R deficiency. We also identified an increase in the fraction of Tfr-phenotype cells in peripheral blood, but the relationship of these cells with Tfr cells described in secondary lymphoid organs remains unknown. The initial study describing immune dysregulation in IL-21R defective patients reported that they exhibit recurrent and chronic infections16. Suppression of the immune response to infection by Treg cells in humans has been suggested previously. For instance, in HIV infection, the Foxp3+CD127lo CD4+ T-cell population may be particularly important in limiting immune activation52. The increase in Treg cells and Tfr-phenotype cells in IL-21R-defective patients is a remarkable finding, but whether the expanded population of Treg cells contributes to the inability to control chronic infection in these patients remains unknown.
In mice, the cell-intrinsic effect of IL-21R was more conspicuous for the follicular subset of Foxp3+ T cells than for the broader Treg population. Previous studies have demonstrated that IL-21 has direct negative effects on Treg cells and can destabilize FoxP3 expression27,28,29,30,53. IL-21 can inhibit both Treg expansion following LCMV infection in a cell intrinsic manner26 and Foxp3+CXCR5+ICOS+CD4+ cells in autoimmune BXD2 mice54. In addition, another recent study demonstrated that IL-21 limits Treg cells in a cell extrinsic manner by inhibiting IL-2 production from conventional T cells in vitro25 and our findings are consistent with IL-2 or other extrinsic factors contributing to the size of the total Treg population. Here we describe a mechanism that may connect previous observations that the inhibition of Tfr cell expansion by IL-21 was associated with a decreased expression of CD25 and responsiveness to IL-2.
IL-21-mediated suppression of the α-chain of the high-affinity IL-2 receptor (CD25) was evident on Tfr cells following SRBC immunization, as Il21r−/− Tfr cells expressed CD25 at the high or maximum levels observed on non-follicular Treg cells. The FoxP3+ Tfr population comprises both CD25+ and CD25− cells, and we observed that the CD25+ Tfr population proliferated to a greater extent in the absence of IL-21:IL-21R interactions. IL-21 reduced and neutralization of IL-21 improved responsiveness to IL-2 in CD4+ T cells in vitro and IL-21 was most effective under conditions of limiting co-stimulation by anti-CD28 monoclonal antibodies. As one of the major functions of CD28 is to augment IL-2 production55, these findings are consistent with IL-21 being less efficient at limiting CD25 expression and Tfr cell expansion where IL-2 is abundant. Previous studies have demonstrated that Cd25 is a target of Bcl-6, binding to an intron within Cd25 (ref. 56). Our findings suggest that other cytokines that can upregulate Bcl-6 may also modulate CD25 expression on Tfr cells. In this regard, adoptively transferred TCR transgenic Smarta (SM) CD4+ T cells and SM Th1 cells retained a notably higher level of CD25 expression in Il6−/− recipient mice compared with SM cells in WT recipients after LCMV infection57. However, our observation that IL-21:IL-21R signalling had a cell intrinsic role in Tfr cells suggests that IL-6 does not fully compensate for IL-21 in this setting. The explanation for this finding remains unknown, but may reflect the kinetics and localization of IL-21 production during Tfr cell differentiation and that IL-21 provides multiple inputs, including the upregulation of Bcl-6 (refs 48, 58, 59), inhibition of CD25 expression and destabilization of Foxp3 (refs 27, 28).
The relative percentages of Tfh cells in WT and Il21r−/− mice reported by our group and others have varied11,60,61, influenced by the redundant roles of IL-21 and IL-6 in Tfh cell differentiation40,41. As shown in this study, a contributing factor to the variations in Tfh cell frequencies in Il21r−/− mice may be Il21r−/− Tfr cells that constitute a greater proportion of the total CXCR5hiPD-1hi T follicular population than WT Tfr cells. Although the percentages of Il21r−/− and WT Tfh cells were similar, the phenotype of Tfh cells was altered by Il21r deficiency with a notable increase in CXCR4 expression. CXCR4 is an α-chemokine receptor specific for stromal-derived-factor-1 (CXCL12), which is important in haematopoietic stem cell homing to the BM62 and for sorting of centroblasts into the GC dark zone45. A previous study has shown that CXCR4+CXCR5+ double-positive Tfh cells arise following influenza infection and could be identified within the GC43. CXCR4+CXCR5+ and CXCR5 single-positive Tfh cells both provided help for B-cell antibody production in vitro, but CXCR5 single-positive Tfh cells were superior at inducing B-cell proliferation43. Within the T-helper populations, IL-21R deficiency resulted in an expansion of CXCR4+ (CXCR5−) extrafollicular helper T cells. Il21r−/− mice harbour increased levels of IgE63, but whether the expanded CXCR4+ extrafollicular subset contributes to this effect remains unknown.
The increased ratio of Il21r−/− Tfr:Tfh cells reinforces the importance of distinguishing FoxP3− follicular helper and FoxP3+ follicular Treg cell populations and may contribute to the important role of IL-21 acting on T cells for humoral immunity64,65. In this context, we provided evidence that the increased expansion or differentiation of Il21r−/− Tfr cells has functional significance and was associated with a reduction in Tfh cells, IgG1+ GC B cells and antigen specific IgG1+ B cells and this finding is in line with previous observations on the influence of adoptively transferred functionally deficient Tfr cells21. The presence or absence of IL-21R on donor Treg cells had little effect on the total GC B cell population and, whilst we observed slightly reduced antigen specific B cells in FoxP3DTR recipients of Il21r−/− Treg cells, the greatest effect was on the broader IgG1+ population, which is consistent with Tfr cells acting to reduce the outgrowth of antigen non-specific B-cell clones20.
The propensity for Il21r−/− T cells to differentiate into Tfr cells reflects the balance between responsiveness to IL-2 and IL-21 and reinforces the important role for IL-21 in humoral immunity. The containment of Tfr cells is important for a productive GC reaction and humoral immune response. Cytokines such as IL-21 that upregulate Bcl-6 have the capacity to reinforce antibody responses within the GC by constraining CD25 expression and the subsequent expansion of Tfr cells.
Peripheral blood samples of patients, their unaffected first-degree relatives and healthy volunteers were obtained upon written (parental) consent. The study protocols were approved by the National Institute of Allergy and Infectious Diseases Intramural Institutional Review Board in Bethesda, MD, the Sydney Children's Hospital Ethics committee and approved according to the Declaration of Helsinki by the local review board and Ministry of Health (0306-10-HMO).
Il21r−/− mice (created on 129 background and backcrossed onto C57BL/6ByJ to N12) were kindly provided by Dr Warren Leonard (NIH) and Ly5.1 C57BL/6 congenic mice were purchased from the Animal Research Centre in Perth, Australia. B6.129(Cg)-Foxp3tm3(DTR/GFP)Ayr/J (Foxp3DTR) mice were kindly provided by Alexander Rudensky65. The Garvan Institute and St Vincent's Hospital Animal Ethics Committee granted permission to perform animal experiments. Animals were housed under specific pathogen-free conditions and handled in accordance with the Australian code of practice for the care and use of animals for scientific purposes. Age-matched littermate mice used for experimental purposes were between 8 and 10 weeks of age. Conditional Bcl6−/− mice on a mixed C57BL/6–129Sv background in which CD4+ T cells were made genetically deficient in Bcl-6 (CD4Cre/WT:BCL6fl/fl) were described previously66.
Mice were immunized (intravenous) with 2 × 108 sheep red blood cells (IMVS, Australia) or (intraperitoneal, i.p.) with 100μg of NP13-OVA absorbed to alum and spleens analysed at timepoints shown. For adoptive transfer experiments: Treg cells were enriched using the mouse CD4+ CD25+ Regulatory T Cell Isolation Kit, according to the manufacturer's instructions (Milentenyi Biotec, catalogue number 130-091-041). Body weight (50μgkg−1) of diphtheria toxin was injected to deplete endogenous Treg cells on days −1 and 4 of immunization. Treg cells (5 × 105) were transferred into FoxP3DTR mice on day 0 of NP-OVA immunization. IL-2:IL-2mAb administration: in addition to SRBC immunization, IL-2:IL-2mAb complexes47,67 were injected i.p. every other day (days 0, 2, 4 and 6) with JES6-1 monoclonal antibody complexed with IL-2 and immunized i.p. with 2 × 108 SRBC on day 0, splenocytes were analysed on day 7 via flow cytometry
Cohorts of B6 mice were lethally irradiated by a 137Cs source (B6: two doses of 0.45Gy 4h apart) and reconstituted the following day by intravenous injection with BM cells isolated from femurs and tibiae obtained by flushing bone with lymphocyte isolation media in sterile conditions. After irradiation, mice were maintained on antibiotic water containing cotrimoxazole (Roche) for 7 days. Irradiated CD45.1 B6 mice were reconstituted with 1 × 107 BM cells from Il21r+/+ mice expressing the congenic markers CD45.2 and CD90.1 (Thy1.1) or CD90.2 (Thy1.2) to allow detection, combined with equal proportions BM from Thy1.2 CD45.2 WT or Il21r−/− mice. Our reconstitution protocol typically resulted in an ~40–60:60–40 ratio of WT:Il21r−/− lymphocytes, and was contaminated with ~10% of endogenous CD45.1+ radio-resistant T cells. Mice were used for immunization protocols as described above at 8 weeks post reconstitution.
For flow cytometric analysis of human peripheral blood; cells were stained with antibodies directed against surface molecules and intracellular Foxp3. Antibodies purchased from BD Biosciences were: anti-CD3-BV786 (SK7, dilution 1/5), anti-CD25-PE (2A3, dilution 1/10), anti-CD127-BV421 (HIL-7R-M21, dilution 1/20), anti-CXCR5-A647 (RF8B2, dilution 1/30) and Strepdavidin-BV605 (dilution 1/100); antibodies purchased from eBioscience were anti-CD4-PE-Cy7 (RPA-T4, dilution 1/20) and anti-PD-1-biotin (eBioJ105, dilution 1/30). Nuclear Foxp3 was detected with anti-Foxp3-A488 (259D/C7, dilution 1/20) antibody using the eBioscience intracellular staining kit (catalogue number 00-5523-00) according to the manufacturer's instructions. For flow cytometric analysis of mouse lymphocytes; red blood cells were removed by hypotonic lysis. Fifty microlitres of a single cell suspension at 2 × 107 cells per ml from the spleen and lymph nodes were stained in FACS buffer containing pre-titred antibodies in 96-well V-bottomed microtitre plates (Nunc, Roskilde, Denmark). Antibodies against surface molecules purchased from BD Bioscience were anti-CD4-PE-Cy7 (RM4–5, dilution 1/300), anti-CD25-APC & BV605 (PC61, dilution 1/100), anti-CD45.1-PE-Cy7 (A20, dilution 1/200), anti-CD45.2-APC-Cy7 (104, dilution 1/200), anti-CD90.1-eF450 (HIS51, dilution 1/200), anti-CD90.2-BV605 (53-2.1, dilution 1/200), anti-CXCR4-PE (2B11/CXCR4, dilution 1/50), anti-CXCR5-biotin (2G8, dilution 1/100), anti-GL7-PE (GL7, dilution 1/300), anti-FAS-FITC (Jo2, dilution 1/200), anti-IgG1-biotin (A85-1, dilution 1/100) and anti-Ki67-A647 (B56, dilution 1/100). Antibodies purchased from eBioscience were anti-CD19-eF450 (1D3, dilution 1/200), anti-ICOS-PE (C398.4A, dilution 1/300), anti-PD-1-FITC (RMP1–30, dilution 1/100), Streptavidin-PerCP-Cy5.5 and APC (dilution 1/300), anti-TCRβ-APC, FITC and PerCP-Cy5.5 (H57–597, dilution 1/300). For intracellular immunostaining of CXCR5+ cells, FoxP3 was detected with the anti-Foxp3-eF450 (FJK-16s, dilution 1/100) antibody purchased from eBioscience, whereas Bcl-6 was detected using the anti-Bcl-6-PE (112-91, dilution 1/50) antibody purchased from BD Bioscience using the BD intracellular staining kit (catalogue number 554714) according to the manufacturer's instructions. Detection of NP specific B cells was carried out by NIP-PE staining (dilution 1/100), to this end NIP-OSu (Biosearch Technologies) was conjugated to phycoerythrin (PE) (Molecular Probes)68. In short, PE was dialysed against 3% NaHCO3 over night at 4°C, NIP-OSu was diluted in dimethylformamide and added to PE at a molar ratio of 20:1. The reaction mixture was rotated for 4h at room temperature and afterwards dialysed against PBS overnight at 4°C to remove unconjugated NIP. Intracellular P-STAT5 was detected with anti-P-STAT5-PerCP-Cy5.5 (47, dilution 1/5) antibody using the BD Phosphlow buffer III (Cat#558050) according to manufacturer's instructions. Cells were acquired using either a FACS Canto II or a LSRII SORP cytometer (BD Biosciences, CA) and analysed using Flowjo (Treestar, CA).
Five-micrometre frozen OCT (Tissue Tek, Australia) spleen sections were fixed in ice-cold acetone for 8min, washed and incubated with blocking reagent (Avidin/biotin (Dako)) at room temperature. Primary biotin or fluorochrome-conjugated antibodies were incubated at room temperature overnight. Antibodies against surface molecules purchased from BD Biosciences were anti-CD4-A488 (RM4–5, dilution 1/100) and anti-CD90.2-A647 (53-2.1, dilution 1/100). CD90.1 was detected using anti-CD90.1-eF450 (HIS51, dilution 1/100) antibody purchased from eBioscience, IgD was detected using anti-IgD-A488 & A647 (11-26c2a, dilution 1/100) antibodies purchased from Biolegend. Detection of FoxP3 was performed using TSA Kit 42, with HRP Streptavidin and Alexa Fluor 555 TyramideT (catalogue number Tx30955, Thermo Fisher) and the anti-FoxP3-biotin (FJK-16s, dilution 1/100) antibody purchased from eBioscience. Sections were analysed using a Leica DM I6000 SP8 confocal microscope (Leica Microsystems, Wetzlar, Germany). The images were processed using the Leica acquisition and analysis software ImageJ (Freeware NIH, Bethesda, USA) or Adobe Photoshop, version 7 (San José, CA).
CD4+ T cells were magnetic activated cell sorting (MACS) enriched from the spleens of WT mice and triplicate samples of 2 × 106 cells per ml were preincubated for 5min with or without 5μgml−1 IL-21RFc and then cultured for 3 days with 0.5μgml−1 soluble anti-CD3 (clone 145-2C11) and anti-CD28 (clone 37.51) monoclonal antibody titrated from a starting concentration of 1μgml−1. IL-21R/Fc chimera used to neutralize IL-21 in vitro was generated in house69. In brief, the DNA encoding the predicted extracellular domain (aa 1–235) of mouse IL-21R with a GSGS linker were amplified by PCR, and linked to mIgG2a Fc. The Fc domain contains four amino acid mutations (L285E, E368A, K370A and K372A) to minimize Fc binding and complement fixation. The resulting construct was subcloned into pEE12.4 (Lonza), a mammalian glutamine synthase expression vector, transfected into Chinese hamster ovary-K1SV cells, and grown in the presence of 25μmoll−1 methionine sulphoximine. Following protein A purification, purity of IL-21R/Fc was checked by SDS–PAGE (Coomassie blue staining and silver stain, Lonza) and tested for presence of endotoxin (Lonza). In vitro BAF-3 proliferation assay measuring biological activity of IL-21R/Fc construct was conducted. For in vitro experiments using Bcl-6-deficient CD4+ T cells; CD4+ T cells were MACS enriched from the spleen of WT (WT/WT:BCL6fl/fl) and Bcl6 conditional knockout mice (CD4Cre/WT:BCL6fl/fl) mice and triplicate samples of 2 × 106 cells per ml were preincubated for 5min with or without 5μgml−1 IL-21RFc and then cultured for 3 days with 0.5μgml−1 soluble anti-CD3 monoclonal antibody with or without 0.031μgml−1 anti-CD28 monoclonal antibody in the presence or absence of rmIL-21 (RnD Systems or made in house70). Following culture, live cells were immunostained and analysed by flow cytometry.
CD4+ cells were isolated from splenocytes by positive selection using magnetic beads. The CD4-negative fractions were irradiated with 3,000rad and used as antigen presenting cells. To induce Treg cell conversion, CD4+ T cells were activated in the presence of 3ngml−1 recombinant human transforming growth factor-β1 with 1 μgml−1 anti-CD3 monoclonal antibody (clone 145-2C11), either soluble in the presence of antigen presenting cells, or plate-bound together with soluble 2μgml−1 anti-CD28 monoclonal antibody (clone 37.51). Conversion efficiency was assessed by flow cytometry on day 3 after surface staining for CD4 and 7-aminoactinomycin D (7-AAD) followed by intracellular staining for Foxp3.
P-values between data sets were determined by two-tailed Student's t-test, assuming equal variance or one-way analysis of variance where indicated. Mixed BM chimeras were analysed in individual mice by pairwise analyses (t-test).
The authors declare that the data supporting the findings of this study are available within the article and its Supplementary Information files.
How to cite this article: Jandl, C. et al. IL-21 restricts T follicular regulatory T cell proliferation through Bcl-6 mediated inhibition of responsiveness to IL-2. Nat. Commun. 8, 14647 doi: 10.1038/ncomms14647 (2017).
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We thank Drs Cindy Ma and Stuart Tangye for their help with human samples. This work was supported by grants from the Diabetes Australia Research Trust and the National Health and Medical Research Council.
The authors declare no competing financial interests.
Author contributions C.J. performed mouse and human experiments and statistical analyses, and edited the manuscript. S.M.L. performed experiments, statistical analyses and edited the manuscript. P.F.C., J.W., W.E.H., A.V. and K.W. performed and assisted experiments. M.E.C., G.U., P.S., B.K. and K.W. prepared and provided human tissues and edited sections of the manuscript. A.D. and J.S. provided reagents. C.K. oversaw analyses, wrote and edited the final manuscript.