Anti-Jo-1 autoantibodies which recognize histidyl-tRNA synthetase identify patients with the rare rheumatologic disease, anti-histidyl-tRNA synthetase syndrome (Jo-1 ARS), a phenotypically distinct subset of idiopathic inflammatory myopathies (IIM). Jo-1-binding B cells (JBCs) are implicated in disease pathogenesis, yet they have not been studied directly. We therefore aimed to characterize JBCs to better understand how they expand and function in Jo-1 ARS.
We enrolled 10 IIM patients diagnosed with Jo-1 ARS, 4 patients with non-Jo-1 IIM, and 8 age- and sex-matched healthy controls. We phenotypically characterized peripheral blood mononuclear cells (PBMCs) ex vivo using flow cytometry to define the B cell subsets in which JBCs reside. We further tested their ability to differentiate into antibody-secreting cells following stimulation in vitro.
The majority of JBCs were IgM+ (not class-switched). Compared to non-JBCs in the same donors, JBCs contained a higher percentage of autoimmune-prone CD21lo cells and were increased in the CD21lo IgM+ IgD− CD27+ memory subset relative to healthy donor B cells. Whereas non-JBCs were present in the anergic BND B cell subset, JBCs were nearly absent from this compartment. JBCs were detected among plasmablasts in some donors, but a reduced frequency of JBCs differentiated into CD38hi24− plasmablasts compared to non-JBCs present in the same wells following in vitro stimulation.
JBCs are enriched for autoimmune-prone CD21lo B cells, some of which exhibit a memory phenotype in the peripheral repertoire of Jo-1 ARS patients. JBCs undergo limited class switch and show reduced capacity to differentiate into antibody-secreting cells. This suggests complex B cell biology exists beyond class-switched cells that differentiate to secrete anti-Jo-1 autoantibody (i.e., what is captured through serum autoantibody studies). New Jo-1 ARS therapies should thus ideally target non-class-switched JBCs in addition to those that have undergone IgG class-switching to most effectively block cross-talk with autoreactive T cells.
The idiopathic inflammatory myopathies (IIMs) are multi-system rheumatologic disease processes involving inflammation of skeletal muscles that affect 2.4–33.8 per 100,000 persons worldwide . Classically, patients have been categorized as having dermatomyositis or polymyositis based on the presence or absence of cutaneous disease. However, the IIM phenotype can be more precisely characterized by distinct autoantibodies that correlate with clinical manifestations and comorbidities [2,3,4]. One subset of IIMs is known as “anti tRNA synthetase syndrome” (ARS) due to autoantibodies that target specific tRNA synthetases. ARS manifestations frequently include interstitial lung disease, myositis, non-erosive arthritis, Raynaud’s phenomenon, and skin rashes . The most common anti-tRNA autoantibody in ARS patients is anti-histidyl-tRNA synthetase (Jo-1) which defines Jo-1 ARS . Jo-1 autoantibody levels correlate with increased Jo-1 ARS disease severity . Despite the value of anti-Jo-1 humoral responses in guiding clinical management decisions, the characteristics and phenotype of Jo-1-binding B cells (JBCs), anti-Jo-1 autoantibody precursors, have not been defined.
Although histopathologic studies have implicated T cell-mediated tissue destruction in muscle damage , evidence suggests autoreactive B cells play an important role in this process. Serum measurements of B cell activating factor of the tumor necrosis factor family (BAFF) are increased in patients with IIM and correlate with anti-Jo-1 autoantibody titers and disease activity severity [6, 8]. B cell-targeting rituximab is commonly used to treat refractory ARS, and depletion of anti-Jo-1 autoantibodies correlates with clinical response [9, 10]. Clonal analysis of muscle-infiltrating B cells shows evidence of an antigen-driven immune response with somatic hypermutation, further providing evidence for B cell involvement in disease [11, 12].
The mechanism behind the immunologic response against the Jo-1 autoantigen and clinical manifestations of Jo-1 ARS is incompletely understood. Epitope heterogeneity suggests the mechanism is not simple molecular mimicry, but rather is directed against Jo-1 itself [13,14,15]. MHC class II haplotype and specific amino acids at particular positions within MHC class II molecules associate with Jo-1 autoantibody positivity [16, 17]; thus, Jo-1 autoantigen presentation to T cells contributes to Jo-1 ARS pathogenesis. Autoantibodies in patient sera demonstrate affinity maturation over time, further supporting an antigen-driven humoral response against Jo-1 . The membrane-bound B cell receptor (BCR) is not automatically secreted as antibody; thus, Jo-1 autoantibodies may not mirror the full spectrum of JBCs competent to present Jo-1 autoantigen to T cells.
In this study, we established a cohort of Jo-1 ARS patients and developed methods to identify JBCs by high-throughput ELISA and flow cytometry. We phenotypically characterized JBCs and identified specific B cell subsets that serve as reservoirs for antigen-specific B cells. Given the identification of JBCs among both non-class-switched IgM and class-switched IgG populations, these data suggest the functional potential of JBCs as autoantigen-presenting cells should be considered independently of autoantibody production in monitoring expansion of autoreactive clones in disease, or alternatively their contraction as future experimental drug efficacy is assessed.
Patient selection and clinical information
Jo-1 ARS patients were selected from enrollees in the Myositis and Scleroderma Treatment and Investigative Center (MYSTIC) cohort at Vanderbilt University Medical Center as approved by the Vanderbilt Institutional Review Board. To capture all levels of disease severity, patients were recruited from outpatient rheumatology and pulmonology clinics, inpatient rheumatology and pulmonology consult services, and the intensive care unit. IIM patients were eligible for the study if they were 18 years or older and had been diagnosed with dermatomyositis or ARS by a rheumatologist or pulmonologist. Exclusions were pregnancy or HIV positivity. Twelve Jo-1 ARS patients were enrolled. One subject was excluded due to having subsequent negative Jo-1 testing from a commercial source, and one patient was excluded due to recent administration of rituximab. Of the remaining 10 subjects, five had active disease and five were noted to have stable disease. “Active disease” was defined by having immunosuppression increased during their outpatient visit or requiring hospitalization due to life-threatening disease. Subjects were defined as having “stable disease” if no medications were discussed during the encounter and current medications were either continued or de-escalated. Patients with active disease were typically earlier in their disease course with median enrollment 1.0 years after disease onset, while subjects with stable disease tended to have had the disease for a longer duration (median 13.8 years). Patients with active disease were typically being treated with high-dose steroids (80%), while stable subjects were using alternative steroid-sparing treatments including azathioprine, hydroxychloroquine, IVIG, and leflunomide (100%).
Four IIM subjects with alternative antibodies (anti-PL-7, anti-EJ with anti-Ro52, anti-Mi-2, and anti-TIF1-γ) were used as disease controls. Healthy participants recruited from the community were eligible if they were 18 years or older, had no personal history or first-degree relatives with autoimmune disease, and had no history of malignancy treated with immunomodulatory therapy. Healthy controls were age- and sex-matched with stable and active Jo-1 ARS cases. As shown in Table 1, the median age of subjects with active disease and stable disease was similar at 53.8 and 57.1 years, respectively, while the healthy subjects were slightly younger with a median age of 48.2. Our Jo-1 ARS cohort was predominately female (80%) and Caucasian (80%). Clinical, laboratory, medication, and radiologic electronic medical record data were collected. Data were managed using the REDCap software system (Vanderbilt).
Sample collection and processing
Peripheral blood mononuclear cells (PBMCs) were obtained by collecting whole blood into mononuclear cell preparation tubes with sodium heparin (BD) via peripheral venipuncture. Cells were washed twice in PBS and red blood cells were lysed using Ack Lysis Buffer (Gibco). Cells were again washed in PBS and counted. Cells were cooled in 10% dimethyl sulfoxide (DMSO) in fetal bovine serum (FBS) at a rate of − 1 °C/min until they reached a temperature of − 80 °C for 24–72 h. Cryopreserved PBMCs were stored in liquid nitrogen until the time of analysis and thawed with ~ 80% viability. To collect serum samples, peripheral venipuncture was performed and blood was collected into serum collection tubes with silica act clot activator (BD). After complete coagulation, tubes were spun and serum was frozen in aliquots at − 80 °C for future analysis.
Recombinant protein cloning, expression, and purification
Online Supplemental Fig. S1 shows GST-Jo-1 fusion protein and GST-only (control) expression plasmids. Homo sapiens histidyl-tRNA synthetase (Jo-1), transcript variant 1 cDNA sequence (NM_002109.5) was purchased commercially (VB180802-1099xav, VectorBuilder) including an N-terminus GST-tag. The control vector was constructed similarly but only included the GST-tag sequence (VB181211-1124ant, VectorBuilder). Plasmids were transformed into BL21-CodonPlus (DE3)-RIL competent cells (Agilent). GST-Jo-1 and GST were expressed following induction with 0.1 mM IPTG for 16 h at 25 °C and affinity purified by Sepharose Glutathione beads (ThermoFisher). Online Supplemental Fig. S2 shows protein purity.
Three hundred eighty-four-well ELISA plates (Maxisorp) were coated with 1 μg/ml purified GST-Jo-1 or GST protein in 1X PBS overnight at 4 °C. Plates were blocked with 5% FBS in 1X PBS plus 0.5% Tween (1X PBS-T) at 25 °C and washed 5X with 1X PBS-T. Plates were incubated at RT with 1:1000 patient sera or stimulated PBMC culture supernatants diluted 1:2 in blocking buffer. Parallel wells were incubated with 100X soluble GST-Jo-1 competitor during sera binding to measure specific binding. Bound antibody was detected by anti-human IgG Fc-specific-HRP (Sigma), anti-human IgG-HRP, or anti-human IgM-HRP (Southern Biotech) secondary antibodies diluted in 5% FBS/1X PBS-T. Plates were washed, TMB Ultra ELISA substrate (Thermo Fisher) was added, and plates were read at O.D. 370 nm using a microplate reader (SpectraMax M3).
B cell stimulation
Cryopreserved PBMCs were rapidly thawed, washed, and resuspended in ClonaCell-HY Medium A (StemCell). Cells were plated at a density of 0.033 × 106 cells/ml in Medium A with 0.833 μg/ml of CpG + 0.133 μg/ml each of mouse-anti-human kappa and lambda antibodies (Southern Biotech). In addition, 0.033 × 106 cells/ml viable gamma-irradiated NIH3T3 fibroblasts were added that had been genetically engineered to express cell-surface human CD40L and secrete human B cell activating factor (BAFF) and human IL-21. These stimuli drive B cells to secrete BCR as antibody to enable screening for antigen-specific B cells . The mixture was then plated into 384-well flat bottom plates (Corning). Plates were incubated with 5% CO2 at 37 °C and screened for the presence of anti-Jo-1 antibody by ELISA on day 7, as described above.
Cells were stained for flow cytometry analysis using the following reactive antibodies and reagents: CD38-AF700 (HIT2), CD27-APC (O323), CD21-PcP-Cy5.5 (Bu32), CD24-APC-Cy7 (ML5), CD10-PE (HI10a), IgM-Pacific Blue (MHM-88), CD5-BV785 (UCHT2), CD3-BV510 (OKT3), CD14-BV510 (M5E2), CD16-BV510 (3G8), CD19-BUV395 (SJ25C1), IgG-PE-Cy7 (M131G05), and IgD-FITC (Ia6-2) (BioLegend, BD Biosciences, eBioscience, or Tonbo Biosciences). Jo-1 binding cells were identified through staining with GST-Jo-1 followed by detection with anti-GST-Texas Red (Abcam). Samples were acquired using a LSR II flow cytometer (BD Biosciences) and data were analyzed using FlowJo software (Tree Star). Flow cytometry samples identifying less than 20 JBC events were excluded from downstream analysis of B cell subset composition. Non-JBC subset analysis was still performed for these donors.
All statistical analysis was performed using GraphPad Prism software version 8.3.1 (GraphPad Software). The resulting data are expressed as the mean frequency of the parent population ± standard deviation. Differences across B lymphocyte populations for a given phenotype were tested using a Mann-Whitney U test.
High-throughput screening detects JBCs in the peripheral blood of Jo-1 ARS patients with both inactive and active disease
Our ELISA assay detects serum anti-Jo-1 IgG and distinguishes Jo-1+ disease from healthy control donors (A370 mean difference of 1.22 ± 0.25, p < 0.0001, Fig. 1a). One subject did not have sera collected and was thus excluded. To confirm specificity of our ELISA assay, 4 IIM subjects with non-Jo-1 disease were also tested and were negative for anti-Jo-1 autoantibody (Fig. 1a). A GST-only control produced minimal signal compared to GST-Jo-1 (A370 mean difference of 1.20 ± 0.02, p < 0.0001), indicating signal was specific to the Jo-1 portion of the fusion protein. Fluorescence was reduced by a mean of 84% when 200-fold excess competitor Jo-1-GST protein was co-incubated with patient sera, further demonstrating the specificity of the assay to detect anti-Jo-1 IgG (Fig. 1b). Inhibitable, Jo-1-specific IgM was also found in Jo-1 ARS patients, but not in IIM subjects with non-Jo-1 disease (Fig. 1a, b). These data show that Jo-1 autoantibody is produced by class-switched (IgG+), as well as non-class-switched (IgM+) B cells in Jo-1 ARS patients.
To identify JBCs in the peripheral blood of Jo-1 ARS patients, we used a high-throughput method capable of capturing antigen-specific B cells as rare as 1 in 20 million cells . This stimulation protocol drives B cells to secrete the BCR as antibody so that wells containing antigen-specific B cells can be identified using ELISA screening. The majority of wells secreted immunoglobulin (99.9%, Fig. 1c), including both IgG and IgM (99.9%, Fig. 1c and Fig. S3). Figure 1d shows identification of wells that contained JBCs using PBMCs isolated from two representative Jo-1 ARS patients. On average, 20.33% of stimulated wells produced anti-Jo-1 autoantibodies (data not shown). Therefore, JBCs are present in the peripheral blood repertoire of these subjects.
The majority of JBCs are not class-switched but are found in both IgM+ and IgG+ B cell subsets in Jo-1 ARS patients with both stable and active disease
We next sought to measure the frequency of circulating JBCs in Jo-1 ARS patients and phenotypically characterize these cells ex vivo. In order to account for disease progression as a potential driving force behind cell phenotypic variation, we used flow cytometry to analyze PBMCs from Jo-1 ARS donors whose disease was progressing (active disease, n = 5), donors whose disease is not progressing (stable disease, n = 5), and healthy controls (n = 8). These samples were matched according to age and sex. JBCs were readily identified in a subset of Jo-1 ARS patients with active disease and stable disease, but not healthy controls (Fig. 2a, c). The majority of JBCs were IgM+ (Fig. 2a, d; mean ± SD, 66.6 ± 10.7% IgM+ vs 12.8 ± 11.3% IgG+; p = 0.0022). We further measured the frequency of JBCs within IgM+ and IgG+ B cells. IgM+ and IgG class-switched JBCs were observed in both stable and active disease patients (Fig. 2e, f).
JBCs are biased away from the anergic BND subset but towards CD21lo B cells
Peripheral immune tolerance can render autoreactive B cells anergic in both mice and humans [20,21,22,23]. BND B cells (IgD+ IgMlo CD27−, Table 2) were shown previously to be functionally anergic [24, 25]. We therefore investigated whether JBCs were enriched among this subset. JBCs were skewed away from the BND B cell subset compared to non-JBCs or healthy control B cells (Fig. 3a, c; 0.22 ± 0.55% versus 2.76 ± 1.14%; p = 0.0009 (non-JBCs) and 2.083 ± 1.28%; p = 0.0023 (healthy)).
CD21lo B cells are a heterogeneous subset that have been reported to have functional properties of anergic, recently activated, or memory B cells [20, 26,27,28,29]. Previous studies showed increased IgM+ CD21lo B cells in rheumatoid arthritis (RA) and Sjögren’s syndrome (SjS) patients [20, 30]. We therefore investigated whether an increased frequency of CD21lo B cells was present among JBCs and compared Jo-1 ARS patients with healthy controls. Autoreactive-prone CD21lo B cells are typically IgM+; however, IgG+ CD21lo B cells have also been identified [20, 27, 30]. JBCs and non-JBCs were identified in the same donor and the frequencies of B cell phenotypic subsets were compared (Fig. 3b). We found that JBCs contain a higher proportion of CD21lo B cells than non-JBCs (Fig. 3b, d, e; IgM, p < 0.01 and IgG, p < 0.05).
JBCs are skewed towards CD21lo non-switched CD27+ memory B cells
Memory B cells have complex phenotypes. We investigated memory markers among CD21lo B cells as shown in Fig. 4a and b and previously described . Unswitched CD21lo memory (CD21lo IgM+ IgD+ CD27+) B cells were decreased in JBCs when compared to healthy controls (Fig. 4c, p < 0.05), though no difference was found between JBCs and non-JBCs (p = 0.54). CD21lo IgM only memory cells (CD21lo IgM+ IgD− CD27+) were increased in JBCs when relative to non-JBCs (Fig. 4d, p = 0.0312), but not when compared to healthy control B cells (p = 0.18). No difference was observed in the frequency of IgG-switched CD21lo memory between JBCs and non-JBCs or healthy cells (Fig. 4e, p = 0.54 (non-JBCs) and p = 0.32 (healthy controls)).
No difference was observed between JBCs and non-JBCs or healthy donors for unswitched (IgM+ IgD+) memory (Fig. 4f, p = 0.15 (non-JBCs) and p = 0.06 (healthy controls)), IgM+ IgD− CD27+ (Fig. 4g, p = 0.06 (non-JBCs) and p = 0.09 (healthy controls)), IgD− CD27+ IgG+ (Fig. 4h, p = 0.6901 (non-JBCs) and p = 0.55 (healthy)), or IgD- CD27- CD24- CD38- (Figure S4c) subsets. JBCs are therefore enriched for CD21lo IgM+ memory B cells, a phenomenon that depends on autoantigen specificity of the B cell, rather than general differences in donor skewing towards these B cell subsets.
JBCs do not show transitional B cell enrichment
Fifty to 75% of transitional B cells (Table 2) are autoreactive, which are culled by immune checkpoints in healthy individuals . These checkpoints function less efficiently in patients with autoimmunity, resulting in increased transitional B cells in the peripheral blood of patients with other rheumatic diseases [33,34,35,36]. To test whether a higher proportion of JBCs are transitional B cells in Jo-1 ARS, we measured this subset among JBCs and non-JBCs from the same Jo-1 ARS donors as well as healthy controls. While not significant, JBCs from Jo-1 ARS subjects trended towards having a higher frequency of transitional B cells relative to healthy controls (Fig. 5a, b, d, 3.3 ± 5.4% versus 3.0 ± 1.7%; p = 0.41).
JBCs do not show plasmablast enrichment compared to non-JBCs or healthy donors
B cells differentiate into short-lived plasmablasts during acute immune responses; thus, plasmablasts can contain a relatively high proportion of antigen-specific B cells [37, 38]. Given the importance of Jo-1 autoantibody in predicting clinical phenotype , we tested whether JBCs showed an increased frequency of plasmablasts (CD38hiCD24−). Contrary to our expectations, the frequency of CD38hiCD24− plasmablasts was not increased among JBCs relative to non-JBCs from the same donors, or healthy controls (Fig. 5a, c, JBCs versus non-JBCs, p = 0.93 and healthy controls p = 0.39). JBCs were found among IgM and IgG plasmablasts (not shown).
A lower frequency of JBCs acquire a plasmablast phenotype following stimulation in vitro
To test the functional capacity of JBCs, we stimulated PBMCs isolated from Jo-1 ARS patients with active disease as in Fig. 1 to drive their differentiation into antibody-secreting cells. After 6 days of stimulation, we used flow cytometry to determine the phenotype of JBCs versus non-JBCs from the same donors. Both JBCs and non-JBCs expanded following polyclonal BCR stimulation (not shown). We identified JBCs and non-JBCs within wells derived from individual patients and compared the resulting phenotypic subsets across patients. Consistent with our ex vivo findings (Fig. 2), the majority of JBCs were IgM+ following stimulation (p = 0.0079, Fig. 6a, b).
The proportion of CD21lo B cells did not differ between JBC and non-JBC populations (Fig. 6c, d, IgM+ JBCs vs. IgM+ non-JBCs, p = 0.42; IgM− JBCs vs. IgM− non-JBCs, p = 0.84). In vitro stimulation reduced CD21 expression across all B cells, compared to CD21 levels on B cells ex vivo (not shown); thus, CD21lo B cell differences could be masked in this setting. A comparison of relative frequencies for CD19+ CD38hi CD24− cells revealed a smaller proportion of cells with a plasmablast phenotype among JBCs relative to non-JBCs (Fig. 7a, b; IgM+ JBCs vs IgM+ non-JBCs, p < 0.0001), consistent with ex vivo findings (Fig. 55). This was also observed among IgM− (class-switched) cells (IgM− JBCs vs IgM− non-JBCs, p <0.0001). These stimulated populations contained a substantial proportion of CD38hi cells with intermediate CD24 expression, designated CD38hi CD24mid. A significantly larger proportion of IgM+ JBCs expressed this phenotype when compared to IgM+ non-JBCs (Fig. 7a, c; IgM+ JBCs vs IgM+ non-JBCs, p = 0.015), indicating that while JBCs show less downregulation of CD24, most upregulate CD38 following in vitro stimulation (Figs. 6 and 7).
In this study, we developed methods to identify JBCs and show they are present in the peripheral blood of patients with Jo-1 ARS among both IgM+ and IgG+ B cells. We find JBCs are enriched for CD21lo B cells, a subset that is globally elevated among total B cells in other rheumatic diseases [20, 39]. Our samples were collected from patients with differences in disease severity, including patients requiring hospitalization and intensive care that would not be captured by outpatient enrollment. The ability to compare between JBCs and the remaining non-JBC repertoire within the same patient reduces the influence of confounding variables such as sex, age, ethnicity, individual immune variation, and treatment effects. Targeting autoantigen-specific B cells was successfully applied to mice to prevent autoimmune disease and is an attractive strategy to treat human autoimmunity [40, 41]. JBCs are thus putative therapeutic targets in Jo-1 ARS. Overall, these data advance the understanding of antigen-specific B cell biology in Jo-1 ARS by extending their potential autoimmune contributions beyond IgG class-switching and antibody production.
We detect IgM+ JBCs in peripheral blood, which is consistent with ARS/IIM patient muscle biopsy findings that suggest IgG class switch and terminal differentiation of JBCs occurs at the site(s) of attack [11, 12, 42]. The majority of JBCs identified in peripheral blood had not undergone class switch. Tetanus toxoid responses in hyperimmunized individuals also skew towards IgM in the peripheral blood; tetanus toxoid-specific B cell enrichment is primarily observed among IgG+ B cells proximal to vaccination and does not persist . We identified 5/10 Jo-1 ARS patients that had clear IgG+ JBCs in peripheral blood, ranging from 1 to 3% of total IgG+ B cells; this population was found in both stable and active disease patients. This suggests class-switching is likely ongoing in Jo-1 ARS disease and is not restricted to a rare immune tolerance breach event resulting in a clonal burst of IgG-switched JBCs. This finding suggests that IgG class-switching of JBCs is not restricted to tissue and/or that they exit tissues to recirculate after undergoing IgG class switch.
Defective tolerance checkpoints allow increased escape of autoreactive B cells from the bone marrow into the transitional compartment in the periphery in multiple autoimmune diseases, including RA, SjS, type 1 diabetes, and systemic lupus erythematosus (SLE), thereby increasing the probability of developing autoantibodies [33,34,35,36]. In juvenile dermatomyositis, immature transitional B cells are expanded in patients with active disease and have an inflammatory phenotype with high interferon alpha and TLR7-pathway signals . Whereas one patient with severe disease shows an elevated percentage of transitional B cells among JBCs, a larger Jo-1 ARS patient cohort will be required to ascertain the extent to which the developmental block observed in other autoimmune diseases impacts JBCs in Jo-1 ARS.
Autoantigen-binding B cells are absent from the anergic (BND) B cell compartment in pre-diabetic and new-onset type 1 diabetes subjects and autoimmune thyroid disease patients, suggesting escape from this tolerant state is a harbinger of fulminant autoimmunity [45, 46]. Furthermore, loss of BND B cells in type 1 diabetes donors is associated with high-risk MHC class II alleles, suggesting interaction with T cells is involved in this process  and that BND B cells may regain functionality to present antigen to T cells. JBCs are not skewed towards the anergic BND subset, suggesting anergy, a mechanism of peripheral tolerance, is not a major force governing JBCs. The BND compartment is not globally absent in Jo-1 ARS patients; non-JBCs show a similar frequency of BND cells compared to healthy controls. This suggests specific factors, rather than global host defects, are overriding anergic programming for JBCs.
CD21lo B cells have complex biology. In RA patients, CD21lo B cells have anergic properties . In the context of immunization, CD21lo B cells exhibit properties that suggest they recently exited germinal center reactions and have transcriptional programs that indicate they are poised for plasma cell differentiation . Such activated B cells can drive cognate T cell activation and acquisition of effector function. IgM+CD21lo B cells are autoreactive-prone [20, 34] and are increased in the peripheral blood of SLE, RA, and SjS patients [26, 47, 48]. Compared to B cells isolated from healthy individuals, a higher fraction of JBCs from Jo-1 ARS patients had a CD21lo phenotype (Fig. 3). Increased CD21lo B cell frequency correlates with disease severity in SLE and RA [47, 48]. We also found that Jo-1 ARS patients with more severe disease had a trend towards increased frequency of CD21lo cells relative to patients with stable disease, despite the small sample size in these subgroups. Given the contrasting potential functionality of CD21lo B cells (anergy versus plasma cell precursors), we could not infer function from CD21lo phenotype alone in our ex vivo studies. In vitro stimulation drove a lower frequency of JBCs to develop a plasmablast-like phenotype (CD38hiCD24−) relative to non-JBCs from the same patient, suggesting JBCs may show some degree of functional impairment, but not enough to prevent at least a subset of JBCs from undergoing IgG class switch and plasmablast differentiation.
T cells that proliferate to Jo-1 were found in the peripheral blood of both Jo-1 ARS and healthy controls, suggesting the mere presence of Jo-1-reactive T cells is insufficient to explain disease pathology; rather, Ascherman et al. postulated interaction with professional antigen-presenting cells is likely necessary to invoke pathologic T cell responses . IgM-restricted, autoantigen-binding B cells drive disease in type 1 diabetes-prone mice through their role as antigen-presenting cells, despite their inability to secrete IgG autoantibody [22, 50]. Thus, autoreactive B cell differentiation into antibody-secreting cells may not be required for their involvement in promoting pathologic autoimmune responses. Human IgM+ B cells can present antigen to T cells, including IgM+ CD21lo B cells isolated from healthy and autoimmune donors . While enrichment of JBCs is increased among IgG+ B cells, their predominant detection among IgM+ B cells suggests non-class-switched JBCs should be considered when designing new immunomodulatory strategies for Jo-1 ARS, as depletion of plasmablasts or plasma cells would not eliminate antigen presentation and activation of T cells by IgM+ (or IgG+) JBCs.
In previous studies, total peripheral blood B cell immunophenotyping in patients with Jo-1 ARS demonstrated a decreased frequency of CD19+CD27+ memory cells (recapitulated here) and increased frequency of naïve B cells in the peripheral blood . Interestingly, B cells infiltrating the muscle of IIM patients exhibited both memory and plasma cell phenotypes [12, 42] and showed evidence of somatic hypermutation, selection, and clonal diversification of their B cell receptors [11, 12]. Our analyses, focused specifically on JBCs, show a higher frequency of JBCs is CD21lo IgM+ memory B cells compared to non-JBCs from the same Jo-1 ARS patients.
Our findings highlight the propensity of JBCs to enter CD21lo subsets. CD21lo B cells isolated from rheumatic disease patients upregulate costimulatory molecules and drive CD69 upregulation on T cells, suggesting CD21lo B cells are competent to present antigen to T cells . It is possible JBCs identified within CD21lo subsets are competent to present antigen autoreactive T cells, but this will need to be tested in future work. Detection of JBCs in peripheral blood highlights their potential utility as a biomarker in immunomodulatory clinical trials to allow easy measurement of therapy-induced contraction or phenotypic alteration of autoreactive JBCs.
Anti-Jo-1 autoantibodies identify the Jo-1 ARS subset of IIM patients. Clinical responses to rituximab implicate B cells in autoimmune pathogenesis. Serologic testing for class-switched Jo-1 autoantibodies identifies Jo-1 ARS patients, but our studies show they do not fully recapitulate the JBC repertoire, as the majority of JBCs have not undergone class switch. These studies define the functional subsets in which JBCs reside to better understand how they expand in Jo-1 ARS patients and highlight their capacity to enter CD21lo and certain memory subsets that are increased in many autoimmune diseases. Our approach also informs the development of future immune therapies; selectively targeting antigen-specific B cells should limit side effects related to broad immune suppression caused by treatments like rituximab. Achieving this goal in Jo-1 ARS requires improved understanding of JBC biology; an optimal approach depends on which functional subset(s) are enriched for this deleterious population of B cells. Additionally, flow cytometry identification of JBCs in Jo-1 ARS patients suggests JBCs could be tracked as biomarkers to assess the efficacy of experimental drugs.
Availability of data and materials
The datasets during and/or analyzed during the current study are available from the corresponding author upon reasonable request.
Anti tRNA synthetase syndrome
B cell receptor
Glutathione S transferase
- Jo-1 ARS:
Anti-histidyl-tRNA synthetase syndrome
Horse radish peroxidase
Idiopathic inflammatory myopathy
Jo-1-binding B cell
Myositis and Scleroderma Treatment and Investigative Center
Peripheral blood mononuclear cells
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We would like to acknowledge the Vanderbilt Institute for Infection, Immunology, and Inflammation.
National Institutes of Health Grants NIH T32 HL087738, NIH T32 AR059039, and K12 HD 043483, Porter Family Fund for Autoimmunity Research, Vanderbilt Division of Rheumatology and Immunology, Vanderbilt CTSA UL1TR000445, and the Vanderbilt Human Immunology Discovery Initiative supported this work, along with the Vanderbilt Medical Center Flow Cytometry Shared Resource (supported by P30 CA68485, DK058404, P30 EY08126, and G20 RR030956). None of these funding bodies was involved in the design of the study or collection, analysis, and interpretation of data or in writing the manuscript.
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Young-Glazer, J., Cisneros, A., Wilfong, E.M. et al. Jo-1 autoantigen-specific B cells are skewed towards distinct functional B cell subsets in anti-synthetase syndrome patients. Arthritis Res Ther 23, 33 (2021). https://doi.org/10.1186/s13075-020-02412-8
- Autoimmune diseases
- B lymphocytes