Increased frequency of circulating IL-21 producing Th-cells in patients with granulomatosis with polyangiitis (GPA)
© Abdulahad et al.; licensee BioMed Central Ltd. 2013
Received: 16 January 2013
Accepted: 24 June 2013
Published: 24 June 2013
The present study aimed to explore a possible role for IL-21 producing Th-cells in the immunopathogenesis of granulomatosis with polyangiitis (GPA).
Peripheral blood from 42 GPA patients in remission and 29 age-matched healthy controls (HCs) were stimulated in vitro, and the frequencies of IL-21 producing Th-cells were determined by flow cytometry. Since Th17-cells produce a low level of IL-21, IL-17 was also included in the analysis. Given that IL-21 is a hallmark cytokine for T follicular helper cells (TFH), we next evaluated the expression of their key transcription factor BCL-6 by RT-PCR and flow cytometry. To investigate the effect of IL-21 on autoantibody-production, PBMCs from GPA patients were stimulated in vitro with BAFF/IL-21 and total IgG and ANCA levels were measured in supernatants. In addition, the expression of IL-21-receptor on B-cells was analyzed.
Percentages of IL-21 producing Th-cells were significantly elevated in GPA-patients compared to HCs, and were restricted to ANCA-positive patients. The expression of BCL-6 was significantly higher in ANCA-positive GPA-patients, as compared with ANCA-negative patients and HCs. IL-21 enhanced the production of IgG and ANCA in vitro in stimulated PBMCs from GPA patients. No difference was found in the expression of the IL-21-receptor on B-cells between ANCA-negative patients, ANCA-positive patients, and HCs.
The increased frequency of circulating IL-21 producing Th-cells in ANCA-positive GPA patients and the stimulating capacity of IL-21 on ANCA-production suggest a role for these cells in the immunopathogenesis of GPA. Blockade of IL-21 could constitute a new therapeutic strategy for GPA.
Granulomatosis with polyangiitis (GPA) is an autoimmune vasculitis of small- to medium-sized blood vessels, associated with the presence of circulating anti-neutrophil cytoplasmic autoantibodies (ANCA) that are mainly directed against proteinase 3 [1–3]. Histopathologically, GPA is characterized by granulomatous inflammation and pauci-immune vasculitis, including necrotizing crescentic glomerulonephritis.
Although the production of ANCA is directly attributable to autoreactive B-cells, there is extensive evidence that T-cells play a critical role in GPA as well. The immunoglobulin (Ig)G subclass distribution of ANCA, with a preponderance of the IgG1 and IgG4 subclasses, suggests a T-cell-dependent immune response . Infiltrating T-cells in granulomatous lesions and persistent T-cell activation have been observed in GPA patients [5, 6]. In addition, an aberrant T-cell phenotype and impaired regulatory T-cell function are also reported in GPA patients in remission [7–9], suggesting that even during remission, the immune system is dysregulated. Moreover, T-helper (Th) cell polarization with an increase in Th17 cells has been demonstrated [10, 11]. Th17 cells and their cytokine IL-17 have been shown to play a critical role in many inflammatory diseases. In addition to IL-17, Th17 cells can produce IL-21, a cytokine that is largely responsible for B-cell class switching and antibody production, and which induces differentiation of B-cells towards plasma cells by synergizing with B-cell activating factor (BAFF)[12, 13]. Therefore, it is conceivable that IL-21 may contribute to the production of pathogenic autoantibodies in GPA.
Multiple studies in animal models indicate a pivotal role of IL-21 in the pathogenesis of autoimmune diseases. Studies in arthritis models have shown that blockade of IL-21 activity reduces joint inflammation and destruction . Subsequent investigations demonstrated that blocking of the IL-21 pathway reduces levels of anti-dsDNA autoantibodies and prevents renal disease in mouse models of systemic lupus erythematosus (SLE) . In addition, mice deficient in IL-21-receptor expression were found to be protected to a large extent against the development of inflammatory bowel disease (IBD) and type-I diabetes [16, 17]. Interestingly, recent genome-wide association studies have provided convincing evidence that genetic variants in the region on chromosome 4q27 that harbor the IL-21 and IL-2 genes are associated with chronic inflammatory disorders, including SLE, IBD and psoriasis [18–20]. Thus, IL-21 seems to play an important role in autoimmune diseases in general and could constitute a novel target for therapy.
IL-21 is produced mainly by activated CD4+ Th-cells. Recent studies have demonstrated that IL-21, besides its production by Th17 cells, is predominantly secreted by a distinct Th-cell lineage, termed follicular helper T-cells (TFH) that express the transcription factor BCL-6 and are considered to be specialized providers of B-cell help . Expansion of circulating T-cells resembling TFH cells has been reported in patients with SLE and in patients with rheumatoid arthritis [22–24]. To date, no study has investigated the role of IL-21-producing Th-cells in GPA. Therefore, this study aimed to assess the frequency of IL-21-producing Th-cells, and to evaluate whether TFH cells or Th17 cells are the major source of IL-21 in GPA patients. For this purpose, we examined the expression of both IL-21 and IL-17 in circulating CD4+ T-cells of patients with GPA. To improve our understanding of the role of IL-21-producing Th cells in autoantibody production we assessed their frequencies in ANCA-positive and ANCA-negative patients, and studied effects of IL-21 on Ig and ANCA production in vitro.
Clinical and laboratory characteristics of patients with granulomatosis with polyangiitis (GPA) at the time of blood sampling
Age, mean ± SD (range), years
59 ± 14 (28, 81)
Localized/generalized GPA, number
Positive/negative for PR3-ANCA†, number
Receiving/not receiving treatment††, number
Relapses, median (range), number
0 (0, 5)
Disease duration, median (range), months
112 (20, 334)
Measurement of ANCA titres and specificity
ANCA titers were measured by indirect immunofluorescence (IIF) on ethanol-fixed human granulocytes according to standard procedures as previously described . ANCA titers higher than 1:40 were considered positive. ANCA antigenic specificity was determined using an in-house capture ELISA as described before [29, 30]. Briefly, a 96-well plate was coated with goat-anti-mouse Ig for 48 hours. After washing, plates were incubated with mouse monoclonal antibody against human PR3 for 2 hours. After washing, the plate was incubated overnight at 4°C with an extract of human azurophilic granules, which were isolated from neutrophils of healthy donors. Further, serial dilutions of serum (with a starting dilution of 1:100) were incubated for 1 hour. The plate was washed, and the captured antibodies were detected with purified F(ab)2 goat-anti-human IgG conjugated to alkaline phosphatase. P-nitrophenyl-phosphate disodium was used as a substrate, and the optical density was measured at 405 nm.
Antibodies used in flow cytometry
The following conjugated antibodies were used in flow cytometry: allophycocyanin (APC)-conjugated anti-CD3 (clone UCHT1), peridin chlorophyll protein (PerCP)-conjugated anti-CD8 (clone SK1), phycoerythrin (PE)-conjugated anti-IL-21-receptor (clone 17A12), and PerCP-conjugated anti-CD19 (clone 4G7), all purchased from Becton & Dickinson (Amsterdam, The Netherlands); PE-conjugated anti-IL-21 (clone eBio3A3-N2), Alexa Fluor® 488 (A488)-conjugated anti-IL-17 (clone eBio64DEC17), and A488-conjugated anti-FoxP3 (clone PCH101), all purchased from eBioscience (San Diego, CA, USA); and PE-conjugated anti-BCL-6 (clone IC5046P) obtained from R&D Systems (Minneapolis, MN, USA).
Sample preparation and in vitrostimulation
Lithium-heparinized venous blood was obtained from patients and healthy donors. Immediately after sampling, 400 μL blood was mixed with 400 μL RPMI1640 (Cambrex Bio Science, Verviers, Belgium), supplemented with 50 μg/ml gentamycin (Gibco, Scotland, UK), and aliquoted in two 5-mL polypropylene tubes (BD Biosciences, Amsterdam, The Netherlands) (400 μL per tube). Diluted blood samples were stimulated 4 hours with 50 ng/mL phorbol myristate acetate (PMA; Sigma-Aldrich, Steinheim, Germany) and 2 nM calcium ionophore (Ca-Io; Sigma-Aldrich). As a negative control, one sample was kept in medium only without stimulation. For inhibiting cytokine release from the cells, 10 μg/ml of brefeldin A (Sigma-Aldrich) was added to each sample.
Intracellular fluorescence-activated cell sorter (FACS)-staining for cytokines
After stimulation cells were washed in wash buffer (PBS, 5% fetal bovine serum (FBS), 0.1% sodium azide (Merk, Germany)] and stained with PerCP-conjugated anti-CD8 and APC-conjugated anti-CD3 for 15 minutes at room temperature. Cells were fixed with 100 μL Reagent A (Caltag/Invitrogen., Breda, The Netherlands) for 10 minutes. After washing, the pellet was resuspended in 100 μL permeabilization Reagent B (Caltag/Invitrogen) and labeled with A488-conjugated anti-IL-17 and PE-conjugated anti-IL-21 for 20 minutes in the dark. After staining, the cells were washed and immediately analyzed on the FACS-Calibur flow cytometer (Becton & Dickinson). Data were collected for 2 × 105 cells, and plotted using the Win-List software package (Verity Software House Inc, ME, USA) ME, USA). Because stimulation reduces surface expression of CD4 on T-cells, CD4+T-cells were identified indirectly by gating on CD3-positive and CD8-negative lymphocytes. Gated CD4+ T-cells were further displayed as a dot plot for evaluation of intracellular cytokine production. The unstimulated control sample was used as a guide for setting the linear gates to discriminate positive and negative populations.
Intracellular staining for transcription factors
Peripheral blood mononuclear cells (PBMCs) from GPA patients and HCs were prepared from heparinized venous blood by density-gradient centrifugation on Lymphoprep (Axis-Shield PoC AS, Oslo, Norway). Cells recovered from the gradient interface were washed twice in PBS and stained for BCL-6 and FoxP3 according to the manufacturer's instructions (eBioscience staining set for transcription factors). Briefly, PBMCs were adjusted to 1 × 106 cells in 100 μL and incubated with appropriate concentration of APC-conjugated anti-CD3 and PerCP-conjugated anti-CD8 for 30 minutes at 4°C in the dark, followed by fixation and permeabilizaion in Fix/Perm buffer (eBioscience) for 45 minutes. Cells were then washed twice with 1 × permeabilization buffer (eBioscience), and stained with PE-conjugated anti-BCL-6 and A488-conjugated anti-FoxP3. After incubation for 30 minutes in the dark, the cell suspension was washed and immediately analyzed on the FACS-Calibur flow cytometer (Becton & Dickinson). Lymphocytes were gated by forward and side scatter patterns, and plotted using the Win-List software package (Verity Software House Inc). Isotype matched control antibodies of irrelevant specificity were obtained from eBioscience and R&D systems.
Immunofluorescent surface staining for IL-21R on B-cells
Fresh blood samples from GPA patients and HCs were labeled with PE-conjugated anti-IL21R, and PerCP-conjugated anti-CD19 for 15 minutes in the dark. Cells were successively treated with 2 mL diluted FACS lysing solution (BD, Amsterdam, The Netherlands) for 10 minutes and then washed twice in wash buffer and immediately analyzed by flow cytometry.
RNA isolation and real-time reverse transcription (RT)-PCR
Erythrocytes were lysed and leukocytes were fixed and washed twice in 1% BSA. RNA was isolated from total leukocytes with TRIzol reagent (Invitrogen) according to the manufacturer's instructions. DNAse treatment (Ambion, Huntingdon, Cambridgeshire, UK) was performed and subsequently cDNA was synthesized using M-MLV reverse transcriptase and oligo (dT) 14 to 18 as primer. For measurement of mRNA for BCL-6 and glyceraldehyde-3-phosphate dehydrogenase (GAPDH), 1 μL of cDNA in triplicate was used for amplification by the Taqman RT-PCR system (ABI Prism 7900HT Sequence Detection System, Applied Biosystems, Foster City, CA, USA) with specific Taqman primers/probes (BCL-6 (Hs 00153368_m1) and GAPDH (Hs 99999905_m1), Applied Biosystems). Amplification was performed using standard conditions and calculations of fold induction were performed. We normalized gene expression to GAPDH and expressed values relative to control using the ΔΔCT (cycle threshold) method.
Cell stimulation and total IgG production
PBMCs recovered from the gradient interface were washed twice in PBS and adjusted to 106 cells/mL in RPMI 1640 (Lonza, Basel, Switzerland) supplemented with 10% FCS (Lonza, Switzerland) and 50 μg/mL gentamicin (GIBCO, Invitrogen). Cells were cultured in the presence of 100 ng/mL rhIL-21 (ImmunoTools GmbH, Friesoythe, Germany) and/or 100 ng/mL rhBAFF (PeproTech, NJ, USA) for 12 days at 37°C with 5% CO2. After 12 days, culture supernatants were collected and total IgG was measured using an in-house ELISA as described previously . Briefly, Costar 96-well ELISA plates were coated with 2 mg/mL goat anti-human-Ig antibody (Southern Biotech, Birmingham, AL, USA) in carbonate buffer (0.01 M, pH 9.6). Plates were washed with washing buffer (0.025 M Tris-HCl, 0.15 M NaCl, 0.05% Tween-20) and blocked for 1 hour with blocking/incubation-buffer (0.05 M Tris-HCl, 0.3 M NaCl, 0.05% Tween-20, 1% BSA). Cell culture supernatants were diluted in incubation buffer. Purified human IgG with a known concentration was used as a standard sample. The bound IgG was detected with goat-anti-human-IgG antibody conjugated with alkaline phosphatase (Sigma, St Louis, MO, USA). P-nitrophenyl-phosphate disodium was used as substrate and optical density was read at 405 nm using an Emax microplate reader (Molecular Devices, Silicon Valley, CA, USA).
Measurement of in vitroproduction of PR3-ANCA
In vitro PR3-ANCA IgG production in PBMC culture supernatants was measured by Phadia ImmunoCAP® 250 analyzer (Thermo Fisher Scientific, MA, USA) using ELiA™ PR3, and the levels of PR3-ANCA IgG production were expressed in response units (RU).
Data are presented as median values unless stated otherwise. The nonparametric Mann-Whitney U-test was used to compare data from patients with those of HCs. The Wilcoxon matched pairs test was used for intra-individual comparison. Correlations were assessed using Spearman's rank correlation coefficient. Two-tailed P-values lower than 0.05 were considered statistically significant.
Increased percentage of circulating IL-21+IL-17-cells in ANCA-positive GPA patients compared to ANCA-negative patients and healthy controls
To rule out the possibility that the increased proportion of IL-21+IL-17- Th-cells in GPA patients was the result of current treatment, the ANCA-positive patient group was divided into treated and untreated patients, and the percentages of IL-21+IL-17- Th-cells were compared. No significant differences were observed between treated and untreated patients (data not shown). We also compared the percentage of IL-21+IL-17- Th-cells between currently untreated ANCA-positive patients with a history of generalized disease and those with localized disease. No difference was found between these patient groups (data not shown).
Increased frequencies of IL-21+IL-17-Th-cells correlate positively with Th17 response
Increased frequencies of BCL-6+ CD4+T-cells in peripheral blood of ANCA-positive GPA patients
Because in recent studies a new population of FoxP3+ regulatory T-cells has been described that shares features with TFH cells by expressing the transcription factor BCL-6, we also evaluated whether the increase in BCL-6+ T-cells in GPA patients was a result of an increase in FoxP3+BCL-6+ T-cells [36, 37]. This analysis showed that the increase in BCL-6 expression in GPA patients was restricted to TFH cells and although a low percentage of FoxP3+BCL-6+ T-cells was found (< 0.3%), no differences in these cell frequencies were observed between GPA patients and HCs (data not shown).
Proportions of IL-21-receptor expressing B-cells do not differ between GPA patients and healthy controls
IL-21 induces IgG and ANCA production by B-cells from GPA patients
In the present study, we demonstrate an increase in the percentage of circulating IL-21-producing Th-cells in GPA patients. We found that elevated frequencies of IL-21-producing Th-cells were restricted to ANCA-positive GPA patients and that these cells were distinct from Th17-cells. We also confirmed that IL-21 can enhance the production of IgG and ANCA in vitro.
Over the past few years, Th17-cells have challenged the classical Th1/Th2 paradigm, and have been implicated in a growing number of autoimmune and inflammatory diseases . Recently, a distinct Th-cell subset termed TFH and characterized by elevated expression levels of multiple surface proteins and BCL-6 as well as enhanced IL-21 secretion, have been identified as true helper cells for antibody responses. We and others have previously demonstrated that circulating Th17-cells are significantly increased in GPA patients even during quiescent disease [10, 11]. However, data are lacking to support a role of IL-21-producing Th-cells in GPA. Since Th17 cells also produce IL-21, we investigated whether Th17 cells in GPA are a source of IL-21. Strikingly, the majority of circulating CD4 T-cells that produced IL-21 were distinct from Th17 cells, indicating that other Th-cell subsets such as TFH cells are the source of this cytokine. Importantly, the expansion of TFH cells in GPA patients was confirmed by increased BCL-6 expression. To the best of our knowledge, this is the first report demonstrating an increase in the frequency of circulating IL-21-producing Th-cells in GPA, suggesting that TFH cell-derived IL-21 may contribute to disease pathogenesis via stimulation of (auto)antibody production.
TFH cells are considered to be the major source of IL-21 and seem to be an important subset for adaptive immune responses, although there are conflicting reports on their mode of action in vivo. It has been demonstrated that IL-21-producing Th-cells induce Th17 development and proliferation [32, 33], which has been shown to promote germinal center (GC) formation in a BXD2 mouse model of autoimmunity . In agreement with these findings, we demonstrate a significant positive relationship between IL-17+IL-21- Th-cells and IL-17-IL-21+ Th-cells in peripheral blood of GPA patients. It seems likely that increased Th17 cells in GPA-patients are the result of an enhanced TFH response, which in turn may participate in granuloma formation and vascular damage. The role of IL-21 in vasculitis was previously suggested by Chen and coworkers . In their study, mice deficient in interferon regulatory factor-4, a protein that inhibits IL-17A production, rapidly developed large-vessel vasculitis and showed increased IL-21 synthesis in addition to increased IL-17A production . Moreover, a role of IL-21 in recruitment of Th17-cells to inflamed tissues has been reported by Caruso and coworkers  by showing that IL-21 induces gut epithelial cells to secrete macrophage inflammatory protein-3α (MIP-3α), a chemokine that mediates Th17-cell homing to the skin, joints, and mucosal tissues. Given that endothelial cells are known to produce MIP-3α, it is possible that IL-21 in GPA patients enhances the migration and accumulation of Th17-cells into the vascular wall resulting in inflammation. Besides, IL-21 was shown to enhance granzyme B expression  and increase perforin-mediated cytotoxicity by human CD8 T-cells  and natural killer cells . It is therefore conceivable that IL-21 can contribute to vessel injury and disease progression in GPA patients. This is an area worth of further investigation.
In contrast to the pro-inflammatory role of TFH cells, recent studies have identified a distinctive population of TFH cells that displays a regulatory function and suppresses the differentiation of GC B-cells in follicles in vivo. This subset was termed follicular regulatory T-cells (TFR), which express the regulatory transcription factor FoxP3 in addition to their specific lineage transcription factor BCL-6 [36, 37]. As circulating FoxP3+ T-cells are increased in GPA patients , it is conceivable that the observed increase in TFH cells in patients is due to an increase in TFR cells that co-express FoxP3 and BCL-6. We have investigated this possibility but found that the increase in circulating TFH cells in GPA patients cannot be explained by increase in TFR cells (data not shown).
In our study, increased frequencies of TFH cells were observed in patients who were ANCA-positive at the time of inclusion. This suggests the involvement of IL-21 in the process of autoantibody production in GPA. These data are in line with previous reports showing that TFH cells act directly on B-cells through the IL-21/IL-21R pathway, and that IL-21 is a potent inducer of class-switch recombination and plasma cell differentiation [39, 48, 49]. The expression of IL-21R on B-cells from ANCA-positive and ANCA-negative GPA patients was comparable, which suggests that both patient populations have the same ability to respond to IL-21. However, in vitro stimulation with IL-21 enhanced the production of ANCA in cell cultures from ANCA-positive patients only, although enhanced total IgG-production was observed in both patient groups. So it is conceivable that autoreactive B-cells were enriched in the peripheral blood of ANCA-positive patients. This might be clinically relevant as well, because ANCA-positive patients are at increased risk for disease relapse [50, 51].
In this study, patients were evaluated for the distribution of TFH cells during remission. We have previously shown that activated T-cells are present at the time of clinically quiescent disease [9, 10]. Furthermore, during active disease effector T-cells appear to migrate towards inflamed tissue . Therefore, in order to study dysbalance of T-cells in GPA patients using peripheral blood samples, we choose to- select patients without or with low dosages of immunosuppressive medication and at the time of clinically quiescent disease.
In conclusion, the data presented here demonstrate a prominent increase of circulating TFH cells in ANCA-positive GPA patients. The key cytokine of these TFH cells, that is IL-21, contributes to the production of ANCA autoantibodies in vitro. These data support the notion that TFH cells are associated with the pathogenic process in GPA patients and may constitute a novel target for therapeutic intervention.
anti-neutrophil cytoplasmic autoantibodies
B-cell activating factor
Birmingham Vasculitis Activity Score
enzyme-linked immunosorbent assay
fluorescence-activated cell sorter
fetal bovine serum
fetal calf serum
follicular helper T-cells
granulomatosis with polyangiitis
inflammatory bowel disease
macrophage inflammatory protein-3α
mean fluorescence intensity
peripheral blood mononuclear cells
peridin chlorophyll protein
phorbol myristate acetate
reverse transcription-polynerase chain reaction
systemic lupus erythematosus
follicular regulatory T-cells.
We are grateful to the patients and healthy donors for their co-operation and participation in this study. The research leading to these results has received funding from the European Union Seventh Framework Programme (FP7/2007-2013) under grant agreement n° 261382, and from the Groningen University Institute for Drug Exploration (GUIDE).
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