- Research article
- Open Access
T-bet+CD11c+ B cells are critical for antichromatin immunoglobulin G production in the development of lupus
Arthritis Research & Therapyvolume 19, Article number: 225 (2017)
A hallmark of systemic lupus erythematosus is high titers of circulating autoantibodies. Recently, a novel CD11c+ B-cell subset has been identified that is critical for the development of autoimmunity. However, the role of CD11c+ B cells in the development of lupus is unclear. Chronic graft-versus-host disease (cGVHD) is a lupus-like syndrome with high autoantibody production. The purpose of this study was to explore the role of CD11c+ B cells in the pathogenesis of lupus in cGVHD mice.
cGVHD was induced by an intraperitoneal injection of 5 × 107 Bm12 splenocytes into B6 mice. Flow cytometry was used to analyze mice splenocytes and human samples. Magnetic beads were used to isolate mice B cells. Gene expression was determined by real-time quantitative polymerase chain reaction (RT-qPCR). Enzyme-linked immunosorbent assay (ELISA) was used to detect antibodies in serum and supernatants.
The percentage and absolute number of CD11c+ B cells was increased in cGVHD-induced lupus, with elevated levels of antichromatin immunoglobulin (Ig)G and IgG2a in sera. CD11c+ plasma cells from cGVHD mice produced large amounts of antichromatin IgG2a upon stimulation. Depletion of CD11c+ B cells reduced antichromatin IgG and IgG2a production. T-bet was upregulated in CD11c+ B cells. Knockout of T-bet in B cells alleviated cGVHD-induced lupus. Importantly, the percentage of T-bet+CD11c+ B cells increased in lupus patients and positively correlated with serum antichromatin levels.
T-bet+CD11c+ B cells promoted high antichromatin IgG production in the lupus-like disease model cGVHD. In lupus patients, the percentage of T-bet+CD11c+ B cells was elevated and positively correlated with antichromatin antibodies. The findings provide potential therapeutic insight into lupus disease treatment.
Systemic lupus erythematosus (SLE) is a prototypic autoimmune disease characterized by an array of autoantibodies that target multiple normal cellular components [1,2,3]. When encountered by self-antigens, autoantibodies can bind with them to form immunoglobulin complexes (ICs) which deposit in the kidney, activate the complement system, and trigger a series of inflammatory responses. Accumulating evidence has indicated that the presence of certain autoantibodies are highly associated with some symptoms of the disease [4, 5]. For example, antiphospholipid antibodies are critically linked to the development of thrombotic events and obstetric morbidity , antiribonucleoprotein (RNP) antibodies are associated with myositis and Raynaud’s phenomenon , and antidouble-stranded DNA (dsDNA) antibodies are associated with lupus nephritis . However, the characterization of B cells that produce these distinct kinds of pathogenic antibodies is still unclear.
Chromatin, the native complex of histones and DNA found in the cell nucleus of eukaryotes, consists of approximately 40% DNA, 40% histones, 20% nonhistone proteins, RNA, and other macromolecules . Data accumulated over recent years have indicated that antichromatin autoantibody is involved in the pathogenesis of SLE and is associated with disease activity and lupus nephritis [10,11,12]. Several studies of lupus-like murine models have found that genetic loci, such as sle1, are related to antichromatin antibody production . Immunization with active chromatin induces lupus-like syndrome in BALB/c mice . Certain knockout mice, such as C1q, serum amyloid protein (SAP) and Dnase I-deficient mice, have high titers of antichromatin antibodies [15, 16]. However, it is not quite clear how B cells lose tolerance to chromatin in the development of lupus.
Transfer of major histocompatibility complex (MHC) II-mismatched splenocytes from Bm12 mice into B6 mice causes a chronic graft-versus-host disease (cGVHD) [17,18,19]. The majority of autoantibodies in cGVHD are antichromatin and anti-erythrocytes . Recently, a novel B-cell subset, CD19+CD11c+, has been identified in aged female B6 mice that is able to produce large amounts of antichromatin autoantibody in response to the Toll-like receptor (TLR)7 ligand in vitro . However, little is known about the differentiation and function of CD19+CD11c+ B cells in the development of lupus.
In this manuscript, we examined the role of CD19+CD11c+ B cells in the development of lupus induced by cGVHD. Our data showed that CD11c+ B cells were able to produce large amounts of antichromatin autoantibody, in particular the immunoglobulin (Ig)G2a isotype, in cGVHD mice. T-bet was critical for CD11c+ B-cell development and antichromatin autoantibody production. Finally, we analyzed the phenotype of T-bet+CD11c+ B cells in lupus patients, as well as its correlation with circulating levels of autoantibody.
Human study subject samples
Twenty-two patients with SLE and 10 age-matched and sex-matched normal controls were recruited to analyze the percentage of T-bet+CD11c+CD19+ B cells in peripheral blood mononuclear cells (PBMCs). Healthy donors had no history of autoimmune disease or any treatment with immunosuppressive agents. Patients with concurrent infection were excluded from the study. All SLE patients were recruited from the Renji Hospital and fulfilled the American College of Rheumatology (ACR) 1982 revised criteria for SLE , and 14 of these patients met the ACR criteria for lupus nephritis . The Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) score was determined for each patient at the time of blood draw . Additional clinical information about the subjects is listed in Table 1. Informed consent was obtained from all the subjects. The study was approved by the Research Ethics Board of Shanghai Renji Hospital.
B6(C)-H2-Ab1bm12/KhEgJ(Bm12), C57BL/6 J(B6), B6.129P2-Igh-Jtm1Cgn/J (μMT), B6.FVB-Tg(Itgax-DTR/EGFP)57Lan/J(B6.CD11c-DTR), and B6.129S7-Ifngr1tm1Agt/J (B6.IFNGR1–/–) were purchased from The Jackson Laboratory (Bar Harbor, ME). The bm12 strain differs from the B6 by three amino acids in the beta chain of the I-A molecule . Bm12 and B6 were propagated in the animal facility at Cincinnati Children’s Hospital Medical Center (CCHMC; Cincinnati, USA). μMT and B6.CD11c-DTR mice were maintained in the animal facility at the Institute of Health Science (IHS; Shanghai, China). All animals were 10–12 weeks old at the time of experimentation. All animal protocols were approved by the Animal Care and Use Committee of CCHMC and IHS.
A single-cell suspension of Bm12 splenocytes was prepared in 1× phosphate-buffered saline (PBS) and filtered through 0.2-μm sterile nylon mesh; 5 × 107 splenocytes were then intraperitoneally injected into B6 mice. After 2 weeks, the recipient mice were sacrificed for analysis.
Antibodies and flow cytometry
The following monoclonal antibodies (mAbs) used for staining were purchased from BioLegend/BD bioscience: APC-Cy7 anti-CD19, BV421 anti-CD138, APC-eF780 anti-CD11c, Bv605 anti-CD19, FITC anti-CD11c, PE anti-IgG2a, Bv421 anti-CD4, APC anti-IFNγ, and APC anti-T-bet. eF506 Live/Dead dye was obtained from eBioscience. Cells were fixed in BD Cytofix™ buffer (BD bioscience) before FACS analysis. Intracellular staining for T-bet was performed using the BD Cytofix/Cytoperm™ Kit (BD bioscience). Data were collected on Fortessa2 and an LSR-II flow cytometer and analyzed by FlowJo software.
Cell isolation and in vitro culture
Spleen cells from cGVHD mice were pooled together (n = 5). CD19+ B cells were first positively selected using CD19-positive MACS beads. CD11c+CD138+ and CD11c–CD138+ cells were then sorted by FACSDiva. Equal cell numbers were then cultured in RPMI-1640 supplemented with 10% fetal bovine serum (FBS), 2 mM l-glutamine, 100 U/ml penicillin, 100 U/ml streptomycin, and 50 μM 2-mercaptoethanol for 72 h. Lipopolysaccharide (LPS; 1 μg/ml) or R848 (1 μg/ml) were used for cell stimulation. The supernatant was assayed by antichromatin antibody enzyme-linked immunosorbent assay (ELISA). To test for interferon (IFN)γ+ T cells, 2 × 107 spleen cells from cGVHD mice were cultured in the above cell culture medium with 1× cell stimulation cocktail (plus protein transport inhibitors) (eBioscience) for 6 h and then stained with Live/Dead dye, anti-CD4, and anti-IFN-γ mAbs.
ELISA for antichromatin antibodies
Chromatin was prepared as previously described [26, 27]. Plates were coated with chromatin at 3 μg/ml overnight at 4 °C. The plates were then washed and incubated with blocking buffer for 2 h at room temperature (RT). The plates were washed again and then 1/500 diluted serum samples were added in duplicate and incubated for 2 h at RT. Biotin-labeled anti-IgG, anti-IgG1, anti-IgG2a, anti-IgG2b, and IgG3 (BioLegend) were used as capture antibodies, and streptavidin-conjugated horseradish peroxidase (HRP) (Thermo Scientific) was used as the detective antibody. Tretramethylbenzidine (TMB, 1×; eBioscience) was then added and incubated for 30 min at RT. Sulfuric acid (2 N) was used as a stop solution and optical density (OD) values were then measured at 450 nm and 570 nm.
Sera antichromatin and anti-dsDNA antibodies of SLE patients were measured with ELISA kits from Inova Diagnostics Company. The experiments were performed according to the manufacturer’s instructions.
Depletion of CD11c+ B cell in cGVHD mice
CD11c-DTR mice with cGVHD were induced by transferring 5 × 107 splenocytes from Bm12. For depletion of CD11c+ cells, mice were then intraperitoneally injected with 100 ng diphtheria toxin (in PBS; Sigma) at day 7, day 9, and day 11 post-cGVHD induction. The efficiency of depletion was then examined by flow cytometry 14 day post-cGVHD induction.
Data were analyzed using GraphPad Prism (version 5.01). Statistical differences were calculated using one-way analysis of variance (ANOVA) and the Student’s t test. Nonparametric correlation (Spearman) was used for correlation studies. Values are presented as the mean ± standard deviation (SD). A value of p < 0.05 was considered to be statistically significant.
CD11c+ B cells were increased in cGVHD autoimmune mice
Consistent with the results of the earlier study , we found that B6 mice that received splenocytes from Bm12 mice developed a lupus-like syndrome after 14 days of injection. As illustrated in Fig. 1a and b, both the mass and cell number of the spleen in the Bm12 to B6 group were elevated along with higher levels of antichromatin IgG and IgG2a antibodies in the sera compared with the B6 to B6 group. It has been reported that the CD11c+ B-cell population accumulated in both old female mice and humans with autoimmune disease, and might play a direct role in the development of autoimmunity . Thus, we next analyzed the phenotype of CD11c+ B cells by flow cytometry in cGVHD mice. Our data showed that CD19+CD11c+ B cells were dramatically increased during the development of cGVHD (Fig. 1c). Furthermore, the fraction of the CD11c+ population in CD138+ plasma cells was also markedly elevated in cGVHD mice (Fig. 1d). Based on the above evidence, we speculated that CD11c+ B cells were probably involved in the development of lupus by autoantibody production.
CD11c+ plasma cells produced large amounts of antichromatin IgG in vitro
To further investigate the role of CD11c+ cells in cGVHD-induced lupus, we sorted CD11c+CD138+ and CD11c–CD138+ cells from mice that received Bm12 splenocytes and performed an in vitro functional assay. As indicated in Fig. 2a, CD11c+CD138+ cells produced more antichromatin IgG antibodies than did CD11c–CD138+ cells in response to LPS or R848 stimulation, although no statistical significance was observed in the R848 group.
The effector mechanisms of the subclasses of antibodies were distinct due to different constant regions. IgG2a is reported to have the most protective and pathogenic properties among mouse IgG subclasses [28, 29]. Notably, we found that antichromatin IgG2a was exclusively produced by CD11c+CD138+ cells (Fig. 2b).
Depletion of CD11c+ B cells ameliorated antichromatin IgG production in vivo
Next, we wanted to know whether depletion of CD11c+ B cells in cGVHD mice could reduce the level of antichromatin IgG in vivo. To this end, CD11c-DTR mice were transferred with 5 × 107 splenocytes of Bm12. The mice then received an intraperitoneal injection of 100 ng diphtheria toxin at day 7, day 9, and day 11 (Fig. 3a). As expected, the percentage and absolute number of CD11c+ B cells was dramatically reduced by diphtheria treatment in CD11c-DTR mice that received Bm12 splenocytes (Fig. 3b). Moreover, transient depletion of CD11c+ B cells significantly decreased the circulating levels of antichromatin IgG and IgG2a antibodies (Fig. 3c). In general, these results demonstrated that CD11c+ B cells might be critical for antichromatin IgG production, both in vitro and in vivo.
T-bet+CD11c+ B cells were significantly increased after cGVHD induction
IgG2a is known as the most pathogenic antibody in autoimmune disease [30, 31]. Many studies have demonstrated that T-bet is critical for IgG2a class switching [32, 33] and IgG2a memory response . Recently, it has been reported that T-bet drives CD11c+ B-cell activation to secrete a virus-specific IgG2a antibody upon virus infection . Thus, we next investigated the role of T-bet in CD11c+ B-cell differentiation and antichromatin IgG2a production in cGVHD-induced lupus. As shown by quantitative polymerase chain reaction (qPCR), T-bet expression was remarkably upregulated in spleen B cells from B6 mice that received Bm12 splenocytes at 14 days, relative to B6 to B6 mice. However, no significant change was observed in non-B cells (Fig. 4a). Furthermore, the mice that received Bm12 splenocytes showed more T-bet+CD11c+CD19+ B cells than those that received B6 splenocytes (Fig. 4b). As mentioned earlier, CD138+ plasma cells were dramatically expanded in cGVHD mice. Notably, we found that more than 70% of CD138+ cells were IgG2a-positive (Additional file 1: Figure S1A). The fraction of T-bet+ and CD11c+ cells was significantly increased in CD138+ plasma cells (Additional file 1: Figure S1B). Therefore, these results suggested that T-bet expression might contribute to the production of antichromatin IgG2a in the development of cGVHD.
Depletion of T-bet+ B cells ameliorated antichromatin IgG production in vivo
Next, we wondered whether depletion of T-bet+ B cells in cGVHD mice could reduce the level of antichromatin IgG in vivo. We generated B-cell specific T-bet–/– mice by transplanting 20% T-bet-deficient B-cell bone marrow with 80% μMT bone marrow into irradiated μMT mice and then induced cGVHD (Fig. 4c). As expected, depletion of T-bet+ B cells inhibited the expression of CD11c in B cells after cGVHD induction (Fig. 4d). Moreover, the levels of antichromatin IgG and IgG2a were significantly decreased in the absence of T-bet+ B cells (Fig. 4e). Taken together, our data demonstrated that T-bet is critical for CD11c+ B-cell differentiation and antichromatin IgG2a production in cGVHD-induced lupus.
T-bet+CD11c+CD19+ B cells were significantly increased in lupus patients
Next, we investigated the abnormality of T-bet+CD11c+CD19+ B cells in lupus patients. As shown in Fig. 5a, the frequency of T-bet+CD11c+CD19+ B cells was significantly increased in the PBMCs of lupus patients. We then analyzed the relationship between the frequency of T-bet+CD11c+CD19+ B cells and autoantibodies in the same group of SLE patients. No significant correlation was observed between the percentage of T-bet+CD11c+CD19+ B cells and the presence of antinuclear antibodies (ANA) and anti-dsDNA antibodies (Additional file 1: Figure S2). However, the proportion of T-bet+CD11c+CD19+ B cells positively correlated with the serum titer of antichromatin IgG in SLE patients (Fig. 5b). Moreover, the percentage of T-bet+CD11c+CD19+ B cells was relatively higher in patients with nephritis than in those without nephritis (Fig. 5c). Our data indicated that T-bet+CD11c+CD19+ B cells might be responsible for the abnormal levels of antichromatin in SLE patients which might prove helpful in the diagnosis and treatment of SLE.
Bm12-induced cGVHD is initiated with injection of MHC II-incompatible spleen cells and leads to a chronic syndrome which closely resembles SLE . This syndrome is characterized by the production of a spectrum of autoantibodies similar to those seen in human SLE, including autoantibodies to erythrocytes, chromatin, nuclear antigens, and, to a more limited degree, dsDNA . It is also accompanied by some of the pathological manifestations of SLE, such as lymphoid hyperplasia and immune complex glomerulonephritis [18, 20]. This model has been demonstrated to be valuable for elucidating the immunopathophysiology of SLE [17, 37, 38].
The typical feature of immunological defects in SLE is the production of autoantibodies . Although autoantibodies were found in SLE more than 60 years ago, more studies need to be performed to illuminate the specific function of an individual autoantibody in the development of lupus . Accumulating evidence has indicated that the detection of certain autoantibodies is essential for the diagnosis and treatment of SLE [40, 41]. Since an antibody with a unique specificity is produced by the corresponding B-cell clone, it is crucial to identify the phenotype of the B cell that produces the pathogenic autoantibody.
Chromatin, the native histone-DNA complex, is found in the nucleus of eukaryotic cells. In recent years, numerous studies have found that antichromatin antibodies are quite specific for SLE [10, 42]. Studies from mice experiments including (NZB × NZW) F1, MRL/lpr mice, and cGVHD mice revealed that antichromatin antibodies play a key role in the pathogenesis of lupus [16, 43, 44]. Recently, it is reported that CD11c+ B cells could produce antichromatin autoantibody upon TLR7 stimulation . In this study, we found that CD11c+ B cells with a high frequency in cGVHD mice produced huge amounts of antichromatin IgG and IgG2a, implying that these B cells might be involved in the development of lupus. In addition, the percentage and absolute number of CD11c+ B cells and the levels of antichromatin IgG and IgG2a antibodies were dramatically reduced by diphtheria treatment in CD11c-DTR mice induced by cGVHD. Thus, we infer that CD11c+ B cells play an essential role in antichromatin antibody production. Further studies are needed to exclude the contribution of CD11c+ DC to the disease in the DTR experiment.
Early studies have shown that T-bet expression in the B lineage promotes class switching to IgG2a  and is indispensable for IgG2a memory formation . Recently, Rubtsova et al. revealed that T-bet+CD11c+ B cells appear at the peak of the antiviral response, secrete antiviral IgG2a, and are essential for effective viral clearance . IgG2a is the most potent isotype in mediating the development of lupus [46,47,48]. In our study, we demonstrated that T-bet expression was upregulated in splenic B cells and CD11c+ B cells of lupus-like cGVHD mice, with elevated levels of antichromatin IgG and IgG2a in the serum. Interestingly, over 70% of the increased CD138+ cells in cGVHD mice were IgG2a-positive. Moreover, T-bet+CD11c+CD138+ cells were significantly increased. And depletion, T-bet+ B cells reduced the percentage and absolute number of CD11c+ B cells and the levels of antichromatin IgG and IgG2a production. More recently, a report also showed that B cell-specific deletion of T-bet reduced the titers of autoantibodies and the appearance of CD11c+ B cells in SLE mice . These data suggest that T-bet might regulate CD11c+ B-cell differentiation and activation in the development of lupus. However, the underlying mechanism of T-bet in the development and function of CD11c+ B cells is still unclear, and needs to be further explored.
IFNγ has been reported to play a pathogenic role in lupus nephritis. Depletion of IFNγ significantly improved renal disease induced by pristane, with reduction in the production of the anti-DNA/chromatin autoantibody [50,51,52]. Treatment of MRL-Lpr mice with IFNγR/Fc significantly reduced serum levels of IFNγ and autoantibody, consequently improving renal pathology. IFNγ is well known to be able to induce B cell IgG2a class-switching . An in vitro study showed that IFNγ and anti-IgM synergistically induced T-bet expression in B cell in a STAT-1-dependent manner to promote IgG2a production . However, it is still unclear how IFNγ triggers B cells to secrete autoantibodies in vivo. We noted that the expression of IFNγ was dramatically elevated both in the total spleen and in CD4+ T cells at day 14 post-cGVHD induction (Additional file 1: Figure S3A). IFNγ+CD4+ T cells were significantly increased in spleens from mice that received Bm12 splenocytes compared with the control group (Additional file 1: Figure S3B). Notably, the percentage and absolute number of T-bet+CD11c+CD19+ B cells was decreased in IFNGR1–/– mice induced by cGVHD (Additional file 1: Figure S3C). Thus, we suggest that IFNγ might induce the expression of T-bet in B cells leading to their differentiation into CD11c+ B cells in lupus-like cGVHD mice. Further studies are needed to confirm this hypothesis.
A recent study showed that CD11c+ B cells are expanded only in a handful of SLE patients . Others studies have shown that a population of B cells increased in the peripheral blood of rheumatoid arthritis (RA) patients and some autoimmune individuals with common variable immunodeficiency [54,55,56]. We found that the T-bet+CD11c+CD19+ B-cell population was significantly increased in the peripheral blood of SLE patients compared with healthy controls. Interestingly, the percentage of T-bet+CD11c+CD19+ B cells in PBMCs was associated with the sera level of antichromatin autoantibody, and elevated in SLE patients with lupus nephritis. Through further analysis, we found that the percentage of T-bet+CD11c+CD19+ B cells might be higher in patients with moderate or severe disease than in those with inactive disease (data not shown). These data suggest that T-bet+CD11c+CD19+ B cells might serve as a biomarker for clinical diagnosis and treatment for lupus patients. More clinical data are needed to verify this point.
We have demonstrated that a newly discovered population of B cells, T-bet+CD11c+CD19+, is associated with the titer of antichromatin in lupus patients and is directly involved in secretion of autoantibody in cGVHD mice. Targeted depletion of CD11c or T-bet efficiently reduced the production of antichromatin autoantibodies. These findings highlight that T-bet+CD11c+CD19+ B cells might serve as a potential therapeutic target of lupus.
American College of Rheumatology
Cincinnati Children’s Hospital Medical Center
Chronic graft-versus-host disease
- Dnase I:
Enzyme-linked immunosorbent assay
Institute of Health Science
Major histocompatibility complex
Peripheral blood mononuclear cell
Quantitative polymerase chain reaction
Serum amyloid protein
Systemic lupus erythematosus
Systemic Lupus Erythematosus Disease Activity
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This work was supported by the National Basic Research Program of China (973 program, grants 2014CB541901 and 2014CB541902), the National Natural Science Foundation of China (grants 81230072, 31630021, 31370880, 81571576, 81401331, and 81571588), the Key Research Program of Bureau of Frontier Sciences and Education Chinese Academy of Sciences (grant QYZDJ-SSW-SMC006), and the Key Research Program of the Chinese Academy of Sciences (grant KJZD-EW-L01-3).The funders had no role in the study design, data collection or analysis, decision to publish, or preparation of the manuscript.
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Human studies were approved by the Research Ethics Board of Shanghai Renji Hospital, and written informed consent was obtained from all patients. All animal protocols were approved by the Animal Care and Use Committee of Cincinnati Children’s Hospital Medical Center (Cincinnati, USA) and the Institute of Health Science (Shanghai, China).
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T-bet+ CD11c+ B cells are critical for antichromatin immunoglobulin G production in the development of lupus. Figure S1. The fraction of T-bet and CD11c positive population was increased in CD138+ plasma cells. Figure S2. Correlation between the percentage of T-bet+ CD11c+ CD19+ B cells and the titers of anti-ANA antibodies (A), anti-dsDNA antibodies (B) from 22 SLE patients. Figure S3. IFNγ is required for T-bet+ CD11c+ B cell differentiation and activation. 5 × 107 splenocytes from Bm12 mice or B6 mice cells were injected intraperitoneally into B6 mice (n = 5). (PDF 361 kb)