Abstract
Recently, we reported elevated proportions of circulating follicular T helper cells and higher levels of interleukin- (IL-) 21 in primary Sjögren’s syndrome (pSS). Interaction of invariant natural killer T (iNKT) cells with B cells and granzyme B (GrB) production may be also important in pSS. Thirty-two pSS patients and 24 healthy controls were enrolled in our study. We investigated the expression of intracellular GrB and IL-21 receptor (IL-21R) of CD19+CD5+ and CD19+CD5− B cells; furthermore, we determined the IL-21 expression of iNKT cells as well. We also assessed the proportion of transitional (), mature () and primarily memory () B cells. CD5+ but not CD5− B cells showed elevated GrB and IL-21R expression in pSS; additionally IL-21 expression of iNKT cells was also elevated. The ratios of transitional and mature B cells were elevated in pSS, while primarily memory B cell percentages were decreased, which correlated with GrB and IL-21R expression of CD19+ B cells. Our results suggest that enhanced IL-21R expression of CD19+CD5+ B cells and production of IL-21 by iNKT cells may play an important role in the pathogenesis of pSS by regulating CD19+CD5+ B cell functions and increasing GrB production, presumably leading to a counter-regulatory effect in the disease.
1. Introduction
Primary Sjögren’s syndrome (pSS) is a common systemic autoimmune disease characterized by inflammation and consequential destruction of exocrine glands. In the last decades, large amount of studies confirmed that B cell activation plays a crucial role in the pathogenesis of pSS through antigen presentation, autoantibody production, and secretion of several proinflammatory factors. The pathological hallmark of pSS is extensive lymphocytic infiltration in salivary glands. The extension and structural arrangement of the infiltrations vary between wide limits; even ectopic germinal centres may develop. These structures are characterized by in situ autoantibody production and high expression of homing and retentive chemokines and adhesion molecules. It was reported that the number of ectopic GCs in salivary glands correlates with the severity of inflammation and anti-SSA/SSB autoantibody production [1, 2]. Additionally, formation of ectopic GCs in glandular tissues carries a higher risk of developing B cell lymphoma in pSS [3].
The proliferation and differentiation of B cells in GCs highly depend on their collaboration with follicular helper T () cells, which are generated from peripheral naive CD4+ T cells in the T cell zone of lymphoid organs. The appropriate interaction of activated B cells and cells is crucial for the generation of extrafollicular short-lived low-affinity plasma cells, high-affinity memory B cells, and long-lived plasma cells [4]. Recent investigations shed light on altered profiles in various autoimmune conditions, suggesting the important role of cells and IL-21 cytokine secretion in autoreactive B cell activation and autoantibody production [4]. In labial salivary gland biopsies of pSS patients, cell markers (CD84, PD-1, and Bcl-6) were detected in the lymphocytic infiltrations, especially, in more organized lymphoid structures [5]. In peripheral blood, elevated CD4+CXCR5+ICOS+PD-1+-like cell percentages were reported in pSS, which showed strong association with anti-SSA and/or anti-SSB autoantibody positivity. Moreover, patients with higher cell proportions had elevated IL-21 serum levels [6].
As part of immune responses, IL-21 is produced by activated CD4+ T cells and natural killer (NK) T cells. IL-21-activated B cells produce IL-6, which further activates B cells in an autocrine manner and contributes to cell differentiation and autoantibody production [7]. Recently, Lindner et al. revealed that IL-21 induces B cells to produce and secrete the active form of the cytotoxic serine protease granzyme B (GrB) and gain immune regulatory properties by limiting T cell proliferation by a GrB-dependent degradation of T cell receptor ζ-chain [8]. In systemic lupus erythematosus, CD19+CD5+ B cells were reported to be one of the main sources of GrB [9]. These observations raise the possibility that beside the key role of cells in B cell activation, the interaction of IL-21-producing invariant NKT (iNKT) cells with B cells and GrB production may also play a potential role in the pathogenesis of pSS.
In our study, we investigated the expression of IL-21 receptor (IL-21R) and GrB of B cell subsets; we assessed the IL-21 expression of iNKT cells and determined the distribution of transitional, mature, and primarily memory B cell subsets in the peripheral blood of pSS patients.
2. Materials and Methods
2.1. Patients and Healthy Individuals
We enrolled 32 pSS patients in the study, who visited our outpatient clinic for systemic autoimmune diseases in the Division of Clinical Immunology of the University of Debrecen for a regular medical check-up between April and June 2014. Exclusion criteria included other autoimmune, allergic, and malignant diseases, pregnancy, immunosuppressive or immunomodulating medications, and ongoing infections. The diagnosis was based on the European-American consensus criteria [10]. Twenty-four age- and sex-matched healthy individuals served as controls.
Among pSS patients, 18 suffered from extraglandular manifestations (EGMs), while 14 had glandular symptoms only. The distribution of EGMs of pSS patients was as follows: polyarthralgia/polyarthritis , Raynaud’s phenomenon , polyneuropathies , and vasculitis . Vasculitis or other EGMs needing immunosuppressive treatment were newly recognised or in inactive status. Informed written consent was obtained from the subjects, and the study has been approved by the Ethics Committee of the University of Debrecen. All experiments carried out were in compliance with the Declaration of Helsinki. Data on subjects enrolled in the study are summarized in Table 1.
2.2. Analysis of GrB Production and IL-21R Expression of CD19+CD5+ and CD19+CD5− B Cells
For the evaluation of intracellular GrB production of CD19+CD5+ and CD19+CD5− B cell, peripheral blood mononuclear cells (PBMCs) were isolated from heparinized venous blood sample by Ficoll-Histopaque (Sigma-Aldrich, St. Louis, MO, USA) density-gradient centrifugation. Cells were then harvested and washed twice and cultured in modified RPMI 1640 medium with GLUTAMAX-I (Life Technologies Corporation, Carlsbad, CA, USA) supplemented with 100 U/mL penicillin, 100 ng/mL streptomycin, and 10% heat-inactivated fetal calf serum (FCS) (Life Technologies). Cells were stimulated at 1 × 106 cells/mL concentration using 6,5 μg/mL anti-human B cell receptor (BCR) antibody (Jackson ImmunoResearch, West Grove, PA, USA) and 50 ng/mL recombinant human IL-21 (R&D Systems, Inc., Minneapolis, MN, USA) for 18 hours at 37°C in an atmosphere containing 5% CO2, based on the protocol described previously by Hagn et al. [9]. The transport of de novo synthesized cytokines from the Golgi apparatus was inhibited by 10 μg/mL brefeldin-A (Sigma-Aldrich). Unstimulated cells served as controls. Next, cells were stained with fluorescein isothiocyanate- (FITC-) conjugated anti-CD5 and phycoerythrin-cyanine (PC)5-labelled anti-CD19 antibodies (BD Biosciences, San Diego, CA, USA, and Beckman Coulter Inc., Miami, FL, USA) for 30 min at 4°C. The cells then were fixed and permeabilized with Intraprep permeabilization reagent (Beckman Coulter) according to the manufacturer’s instructions, and intracellular GrB were stained with phycoerythrin- (PE-) conjugated anti-GrB antibody (BD Biosciences).
For the evaluation of IL-21R expression, anti-CD5-FITC, anti-CD19-PC5, and anti-IL-21R- (CD360-) PE antibodies were used (BD Biosciences, Beckman Coulter and BioLegend, San Diego, CA, USA), and mean fluorescence intensity (MFI) was determined. Mouse immunoglobulin (Ig) G1 antibodies were used as isotype control throughout the experiments. The measurements were performed on a FACSCalibur flow cytometer (Becton Dickinson, Franklin Lakes, NJ, USA). CD19+, CD19+CD5+, and CD19+CD5− B cells were quantified as their percentage in the entire lymphocyte population. GrB positivity and IL-21R expression levels were quantified within the investigated B cell subpopulations.
2.3. Assessment of Peripheral iNKT Cell Percentages and Their IL-21 Expression
In order to determine iNKT cells from heparinized blood samples, the following monoclonal antibodies to cell surface markers were used: FITC-conjugated anti-CD3 and PE-conjugated 6B11 (BD Biosciences). Samples were processed according to the Coulter Q-PREP protocol and system (Beckman Coulter Inc.). Briefly, cells from 50 μL of whole blood were stained with 10 μL of each monoclonal antibody. After 20 min incubation, red blood cells were haemolysed and leucocytes were washed in phosphate-buffered saline (PBS) supplemented with bovine serum albumin (BSA) (10 mg/L) and sodium-azide (2 mg/L). The cells were fixed subsequently using 500 μL of 1% paraformaldehyde.
The cytoplasmic IL-21 content of circulating iNKT cells was also determined by flow cytometry. Briefly, isolated PBMCs were cultured at a concentration of 2 × 106/mL in modified RPMI 1640 medium with GLUTAMAX-I (Life Technologies) supplemented with 100 U/mL penicillin, 100 ng/mL streptomycin, and 10% heat-inactivated fetal calf serum (Life Technologies). Cells were stimulated using 25 ng/mL phorbol-myristate-acetate (Sigma Aldrich) and 1 μg/mL ionomycin (Sigma Aldrich) for 6 hours at 37°C in an atmosphere containing 5% CO2. The transport of de novo synthesized cytokines from the Golgi apparatus was inhibited by 10 μg/mL brefeldin-A (Sigma Aldrich). After stimulation, cells were stained with anti-CD3-FITC and 6B11-PE antibodies (BD Biosciences) for 30 min at 4°C. The cells then were fixed and permeabilized with Intraprep permeabilization reagent (Beckman Coulter Inc.) according to the manufacturer’s instructions, and intracellular cytokines were stained with allophycocyanin- (APC-) conjugated anti-IL-21 antibody (BioLegend). Mouse IgG1 antibodies were used as isotype control throughout the experiments. The measurements were performed on a FACSCalibur flow cytometer (Becton Dickinson). The CD3+6B11+ iNKT cells were quantified as their percentage in the entire lymphocyte population, while IL-21+ iNKT cells were determined as their proportions in the population of CD3+6B11+ iNKT cells.
2.4. Determination of Transitional, Mature, and Primarily Memory B Cells
PBMCs were isolated from heparinized venous blood sample by Ficoll-Histopaque (Sigma-Aldrich) density-gradient centrifugation. Cells were then harvested and washed twice and stained for 20 min at 4°C using specific antibodies. To identify transitional, mature, and primarily memory B cell subpopulations, cells were stained with the combination of the following monoclonal antibodies: PC5-labelled anti-CD19 (Beckman Coulter), Alexa Fluor 488-labelled anti-CD24 (BioLegend), and PC7-labelled anti-CD38 (BD Biosciences). After 30 min incubation, leucocytes were washed in phosphate-buffered saline (PBS) supplemented with bovine serum albumin (BSA) (10 g/L) and sodium-azide (2 mg/L). The cells were fixed subsequently using 500 μL of 1% paraformaldehyde. Mouse immunoglobulin (Ig) G1 antibodies were used as isotype control throughout the experiments. Samples were processed according to the Coulter Q-PREP protocol and system (Beckman Coulter Inc., Miami, FL, USA). Measurements were performed on a Coulter FC500 flow cytometer (Beckman Coulter Inc.). (transitional), (mature), and (primarily memory) B cells were quantified as their percentage in the CD19+ lymphocyte population.
2.5. Assessment of Anti-dsDNA, Anti-Ro/SSA, and Anti-La/SSB Autoantibodies
Autoantibodies were determined by enzyme-linked immunosorbent assay (ELISA) technique with AUTOSTAT II kits (Hycor Biomedical, Indianapolis, IN, USA), according to the manufacturer’s instructions.
2.6. Statistical Analysis
The SPSS ver. 20.0 (SPSS Inc., Chicago, IL, UDA) was used for statistical analysis. To assess the distribution of the data Kolmogorov-Smirnov test was used. In cases of normal distribution, we determined mean ± standard deviation (SD) values and used two-sample -test for statistical evaluation of the experimental data. In cases of distributions different from normal, median, minimum, and maximum values were calculated, and the Mann-Whitney test was used. When the strength of the linear relationship between two variables was evaluated, Pearson’s correlation coefficient was used, while in cases of nonnormal distribution, Spearman’s correlation coefficient was applied. Differences were considered statistically significant at .
3. Results
3.1. Granzyme B Production Capability of B Cells Is Increased in pSS
We found no significant differences in peripheral blood CD19+, CD19+CD5+, and CD19+CD5− B cell percentages between pSS patients, subgroups of patients, and healthy controls (data not shown). When GrB expressions of these B cell subsets were investigated, in the whole CD19+ B cell population, significantly enhanced GrB expression was observed in the whole group of pSS patients (median (min–max): 5.225 (0.41–28.1)% versus 3.69 (0.04–7.29)%, resp., ) and in all subgroups of patients (pSS glandular: median (min–max): 5.505 (0.41–28.1)% versus 3.69 (0.04–7.29)%, resp., ; pSS EGMs: median (min–max): 4.735 (0.73–22.34)% versus 3.69 (0.04–7.29)%, resp., ), compared to the values measured in the healthy controls (Figure 1).
When we divided CD19+ B cell population on the basis of their CD5 positivity, we found that only CD19+CD5+ B cells expressed GrB significantly higher in each group of pSS patients, compared to control values (pSS: median (min–max): 4.59 (1.04–26.45)% versus 2.8 (0.18–6.13)%, resp., ; pSS glandular: median (min–max): 6.81 (1.6–26.45)% versus 2.8 (0.18–6.13)%, resp., ; pSS EGMs: median (min–max): 4.03 (1.04–23.91)% versus 2.8 (0.18–6.13)%, resp., ) (Figure 1).
3.2. IL-21 Receptor Expression Is Enhanced on CD19+CD5+ B Cells in pSS
We observed significantly enhanced IL-21R expression on CD19+ B cells in the whole group of pSS patients (mean ± SD: MFI versus MFI, resp., ) and in subgroup of patients with EGMs, compared to values measured in healthy individuals (mean ± SD: MFI versus MFI, resp., ) (Figure 2).
When we divided CD19+ B cell population on the basis of their CD5 positivity, we found that only CD19+CD5+ B cells expressed IL-21R significantly higher in the whole group of pSS patients (mean ± SD: MFI versus MFI, resp., ) and in the subgroup of patients with EGMs, compared to control values (mean ± SD: MFI versus MFI, resp., ) (Figure 2).
Moreover, we found positive correlation between the percentages of GrB positivity and the level of IL-21R expression within both CD19+ B cells (, ) and CD19+CD5+ B cells (, ) in pSS (Figures 3(a) and 3(b)).
(a)
(b)
3.3. Elevated Intracellular IL-21 Cytokine Expression of iNKT Cells in pSS Patients
We observed no significant differences in the peripheral blood iNKT percentages between pSS patients and controls (data not shown). However, in the pSS patient population, we found significantly elevated percentages of IL-21-producing iNKT cells within iNKT population, compared to the values determined in healthy individuals (median (min–max): 2.81 (0.1–29.02)% versus 1.16 (0.1–12.1)%, resp., ).
3.4. Transitional, Mature, and Primarily Memory B Cell Proportions and Presence of Autoantibodies in pSS
The distribution of B cells was also evaluated in the study (Figure 4). The percentages of transitional B cells were significantly higher in pSS patients compared to healthy control (median (min–max): 5.21 (1.68–27.83)% versus 3.19 (0.57–13.4)%, resp., ). Regarding the subgroups of patients, subjects suffering from EGMs had also elevated percentages (median (min–max): 5.44 (3.41–27.83)% versus 3.19 (0.57–13.4)%, resp., ), while values of patients with glandular symptoms did not differ significantly from the results of healthy individuals.
The proportions of mature B cells were significantly elevated in the whole group of pSS patients (mean ± SD: % versus %, resp., ) and in both of pSS subgroups (pSS glandular: mean ± SD: % versus %, resp., ; pSS EGMs: mean ± SD: % versus %, resp., ), compared to control values.
On the contrary, the frequency of primarily memory B cells were significantly decreased in all groups of pSS patients, compared to controls (pSS: mean ± SD: % versus %, resp., ; pSS gland: mean ± SD: % versus %, resp., ; pSS EGMs: mean ± SD: % versus %, resp., ).
Additionally, we found a positive correlation between the percentages of GrB positive CD19+ B cells and mature B cells (, ), while a negative correlation between the percentages of GrB positive CD19+ B cells and primarily memory B cells (, ) (Figures 5(a) and 5(b)). Similarly, positive correlation was observed between the levels of IL-21R expression of CD19+ B cells (, ), while negative correlation was revealed between the levels of IL-21R expression of CD19+ B cells and primarily memory B cells (, ) (Figures 5(c) and 5(d)). We observed no further correlations between the other investigated parameters.
(a)
(b)
(c)
(d)
Thirteen individuals were positive for anti-Ro/SSA and/or anti-La/SSB antibody among pSS patients. We observed no association between the presence of autoantibodies and the investigated parameters.
4. Discussion
Formerly, we reported higher level of circulating IL-21 in pSS and found increased circulating cell percentages in the disease [6]. In the present study, we observed elevated IL-21 expression of iNKT cells, which, along with the increased IL-21R expression of B cells, may contribute to the enhanced B cell activation in pSS. Interestingly, B cells expressing enhanced IL-21R on surface were typically positive for surface antigen CD5. Furthermore, when we divided patients into two groups based on the presence or absence of EGMs, significant increase in expression of IL-21R was found only in the group of EGM patients, compared to the control values. This observation is in line with our previous results; namely, significantly elevated ratio of peripheral cells was observed only in pSS patients with EGMs and not in those without EGMs; furthermore, higher IL-21 cytokine concentrations were associated with the presence of EGMs [6]. Regarding the IL-21 overproduction of iNKT cells, we did not find marked difference between the subgroups of patients.
Basically, IL-21 stimulation on B cells may have at least three outcomes. In the absence of both B cell receptor (BCR) engagement and T cell help, it induces B cell apoptosis [11]. In the presence of CD40 ligation and either a BCR or a Toll-like receptor signal, IL-21 stimulation fundamentally promotes B cell activation and differentiation processes into memory and plasma cells. However, the combination of IL-21 stimulation and BCR engagement in the absence of CD40 ligation enables B cells to produce and secrete the active form of GrB [12] (Figure 6). Besides its important and well-known function in antiviral immune responses, GrB secretion plays a potential role in the regulation of autoimmune responses as well, through different mechanisms. The spectrum of functions exhibited by GrB includes antigen processing, matrix degradation, cleavage, and activation of inflammatory cytokines and immunoregulatory effects [13, 14]. Consequently, GrB-producing B cells may acquire a regulatory function and effects on other immune cells; furthermore, leakage of GrB in the cytoplasm may also result in the apoptotic demise of autoreactive B cells [15]. Based on our observations, GrB expression of B cells, especially in CD19+CD5+ ones, is significantly increased in pSS regardless of the presence of EGMs. Importantly, we observed a clear positive correlation between GrB production and IL-21R expression on CD19+ B and CD19+CD5+ B cells as well. Additionally, we also found further associations with the altered distribution of transitional, mature, and primarily memory B cells. Our observations, namely, elevated mature B cell proportions and decreased primarily memory B cell percentages, are in line with former observations [16] pointing at the hyperactivated state of B cells in pSS patients. In our study, we revealed that not only IL-21R expression but also GrB production on CD19+ B cells correlates positively with the frequency of transitional and mature B cell subsets and correlates negatively with primarily memory B cells.
5. Conclusions
Based on our results, we assume that, parallel with the pathologic B cell activation and enhanced autoantibody production driven by the expansion of cells and their pronounced IL-21 expression, GrB production is mainly induced in CD5+ B cell subsets in pSS, which could be part of an increased counter-regulatory reaction, presumably compensating the derailed, disproportional immune responses. We believe that further investigation on the activation and function of GrB-producing regulatory B cells will open new avenues to understand the B cell operation and autoimmune processes in pSS; furthermore, the modulation of these cells could be a potentially powerful element of the novel therapeutic selection in the disease.
Conflict of Interests
The authors declare that there is no conflict of interests regarding the publication of this paper.
Authors’ Contribution
Gábor Papp and Edit Gyimesi contributed equally to this work.
Acknowledgments
This work was supported by the Hungarian National Scientific Research Fund (OTKA Grant no. K101470) and the TÁMOP-4.2.2.A-11/1/KONV-2012-0023 “DEFENSE-NET” project. The project was cofinanced by the European Union and the European Social Fund.