Objectives Rheumatoid arthritis (RA) is an immune-mediated inflammatory disease of unknown aetiology. Recent work has shown that systemic autoimmunity precedes synovial inflammation, and animal models have suggested that changes in the lymph nodes may precede those in the synovial tissue. Therefore, we investigated the cellular composition of the lymph node in the earliest phases of inflammatory arthritis.
Methods Thirteen individuals positive for immunoglobulin M (IgM) rheumatoid factor and/or anticitrullinated protein antibodies without arthritis were included. Additionally, we studied 14 early arthritis patients (arthritis duration ≤6 months, naïve for disease-modifying antirheumatic drugs), and eight healthy controls. All subjects underwent ultrasound-guided inguinal lymph node biopsy. Different T- and B-lymphocyte subsets were analysed by multicolour flow cytometry.
Results There was an increase in activated CD69 CD8 T cells and CD19 B cells in early arthritis patients compared with healthy controls. We also observed a trend towards increased CD19 B cells in autoantibody-positive individuals without arthritis compared with healthy controls.
Conclusions This exploratory study suggests that there is increased immune cell activation within lymph nodes of early arthritis patients as well as in autoantibody-positive individuals at risk of developing RA. This method provides a unique tool to investigate immunological changes in the lymph node compartment in the earliest phases of inflammatory arthritis.
- Early Rheumatoid Arthritis
- T Cells
- B cells
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Rheumatoid arthritis (RA) is a prototypic inflammatory autoimmune disease with a poorly understood etiopathogenesis. Given the destructive nature of the disease, early diagnosis and start of treatment is highly important.1–3 Several studies have shown that elevated acute-phase proteins, chemokines, cytokines and RA-specific autoantibodies (rheumatoid factor (RF) and anticitrullinated protein antibodies (ACPA)) can be detected in peripheral blood years before the onset of arthritis.4–9 In prospective cohort studies, these autoantibody-positive individuals can be defined as having systemic autoimmunity associated with RA and being at risk of developing RA.10 A recent study showed that the cellular composition of the primary target of RA, the synovium, is comparable with that of healthy controls during this phase.11 Thus, systemic autoimmunity appears to precede the development of synovial inflammation. Since the RA-specific autoantibodies can be present for years without disease symptoms and without increased synovial cellularity, factors outside the synovial compartment should be responsible for the initial changes leading to RA.
As a general principle, the recruitment of activated immune cells to the site of inflammation is initiated after informing a nearby lymph node of a danger signal. Thus, the immune reaction in lymph nodes generally precedes the influx of effector cells into the target tissue. Indeed, animal models have shown that the onset of arthritis is preceded by phenotypic changes in the cellular compartment of draining lymph nodes, indicating a primary role for lymph nodes in the initiation of arthritis.12–14 However, very little is known about the initial events that occur in lymph nodes before disease onset in patients with arthritis. Recently, we developed core-needle biopsy sampling of inguinal lymph nodes for research in RA, and we have shown that the procedure is generally well tolerated.15 In the current study, we investigated the cellular composition of lymph node biopsies obtained from autoantibody-positive individuals at risk of developing RA, and compared the results with those observed in early arthritis patients and healthy controls.
Study subjects and lymph node biopsy sampling
Individuals with elevated IgM-RF and/or ACPA levels without arthritis were included in the study. These individuals were otherwise healthy and have systemic autoimmunity associated with RA, and are therefore at risk of developing RA (phase c, ref. 10) (further referred to as ‘at risk’ individuals). Additionally, early arthritis patients (arthritis duration ≤6 months, determined from the first clinical signs and symptoms of arthritis as assessed by the rheumatologist; disease-modifying antirheumatic drug naïve) and healthy controls without any joint complaints and without RA-specific antibodies were included. Ultrasound-guided inguinal lymph node biopsies were obtained by a radiologist using a 16G core needle as previously described,15 and immediately processed for flow cytometry analysis. The study was approved by the local ethical committee, and all study subjects gave written informed consent.
Flow cytometry analysis
Lymph node biopsy samples were put through a 70 μm cell strainer (BD Falcon) to obtain a single cell suspension. Subsequently, cells were washed with phosphate buffered saline (PBS) containing 0.01% NaN3 and 0.5% BSA. Cells were stained for 30 min at 4°C and protected from light using the following directly labelled antibodies: CD3 FITC (Sanquin, Amsterdam, The Netherlands), CD45 V500, CD69 PerCP, CD27 PerCP-Cy5.5, IgD FITC (BD Biosciences, Breda, The Netherlands), CD19 eFluor 450, CD4 Pe-Cy7, CD45RO PE, CD45RA eFluor 450 and CD8 APC eFluor 780 (eBioscience). After incubation, cells were washed and measured on a FACS CANTO II (BD Biosciences). Data were analysed using FlowJo software (Tree Star, Ashland, Oregon, USA).
Not normally distributed data were presented as medians (IQR). Differences between study groups were analysed using one-way analysis of variances with post-Bonferroni's multiple comparison tests or unpaired t test where appropriate. Categorical data were presented as numbers (percentages), and differences between groups were analysed using χ2 test. GraphPad Prism Software (V.5, GraphPad Software, La Jolla, California, USA) was used for statistical analysis.
Lymph node biopsies were obtained from 13 IgM-RF and/or ACPA positive individuals without arthritis. Nine of them were referred to the outpatient rheumatology clinic because of joint pain, and four through testing first-degree relatives of RA patients (two of the latter did not have arthralgia, all other individuals did have arthralgia). None of these autoantibody-positive individuals has developed arthritis yet after a follow-up time of median (IQR) 12 (9–14) months. Additional characteristics are given in online supplementary table S1. For comparison, lymph node biopsies were obtained from 14 early arthritis patients (eight RA according to the 2010 ACR/EULAR criteria for RA and six unclassified arthritis (UA) of whom four fulfilled 2010 ACR/EULAR criteria for RA after follow-up; median (IQR) arthritis duration one (0–2) months) and eight autoantibody-negative healthy controls. Table 1 shows the demographic data of the study participants.
To explore the cellular composition of the lymph node compartment, freshly collected lymph node specimens were directly analysed by multicolour flow cytometry for the presence of specific T and B lymphocytes including their activation or differentiation state (figure 1). The frequencies of CD4 and CD8 T cells were within the expected range (∼80% CD4 and ∼20% CD8 within CD3 T cells) and no differences were observed between at risk individuals, early arthritis patients and healthy controls (figure 2A,B). Subsequently, the percentage of activated T cells was determined by analysing coexpression of CD69 (figure 2C,D). Interestingly, the percentage of activated CD8 T cells was different between the three study groups (p=0.012), and specifically increased in early arthritis patients compared with healthy controls (median (IQR) 33.10 (23.60–42.905) vs 22.20 (15.75–26.55), p<0.05)). The increase in percentage of activated T cells was not dependent on the presence of autoantibodies or the presence of arthritis in the lower limb on the ipsilateral side of the biopsied lymph node (data not shown). In addition, there were no differences between UA and RA patients.
Next, we analysed the percentage of CD19 B cells which showed a significant difference between the three study groups (p=0.049). The percentage of CD19 B cells was significantly higher in early arthritis patients compared with healthy controls (median (IQR) 38.45 (21.45–48.90) vs 20.05 (13.03–28.25), p<0.05) (figure 2E). We also observed a trend towards increased CD19 B cells in at risk individuals compared with healthy controls (median (IQR) 29.60 (19.85–39.65) vs 20.05 (13.03–28.25), p>0.05). The increased number of B cells was independent of the presence of autoantibodies (figure 2F). In the group of early arthritis patients, no differences were observed between UA and RA patients, and the increased number of B cells was independent of the presence of arthritis in the lower limb on the ipsilateral side of the biopsied lymph node (data not shown). The percentage of different subsets of B cells, naïve, memory switched and memory non-switched (based on IgD and CD27), was comparable between the different study groups (data not sown).
This explorative study was undertaken to explore for the first time the cellular composition of lymph nodes in at risk individuals having systemic autoimmunity associated with RA, and early arthritis patients compared with healthy controls. First, the results indicate that flow cytometry analysis of lymph node biopsies is a feasible method for studying the cellular composition and activation of lymph node tissue in the earliest phases of arthritis. Second, we observed more CD19 B cells and activated CD8 T cells in early arthritis patients compared with healthy controls. Third, there was a trend towards an increase in CD19 B cells in at risk individuals compared with healthy controls.
During an immune response, the egress of T lymphocytes from lymph nodes is shut down transiently by downregulation of S1P1 and upregulation of CD69 leading to lymphocyte retention, maturation and proliferation.16 The results of this explorative study suggest increased activation of T cells, as shown by coexpression of CD69, within lymph nodes of arthritis patients during the earliest phase of disease. Of interest, the percentage of activated CD8 T cells is increased. These results are in line with animal models of arthritis where a skewed CD4/CD8 ratio is observed in regional lymph nodes before the onset of arthritis.13 ,14 These results support the notion that T cells are intimately involved in the initiation of seropositive RA.17–19 Future research should focus on the identification of T-cell subset(s) and antigen specificity associated with development of RA.
Of interest, an increased percentage of CD19 B cells was observed in lymph nodes of early arthritis patients and autoantibody-positive subjects at risk of developing RA. These results of the lymph node analyses differ from those in a previous study on peripheral blood, in which gene expression profiling of at risk individuals revealed a low B-cell signature especially in those individuals who developed arthritis after follow-up.20 It is tempting to speculate that the B cells are retained in the lymph nodes, to ensure maturation and differentiation during the immune response which would be in line with findings in animal models of arthritis.12 ,13
An obvious limitation of the current study is the small sample size and the short follow-up period of the ‘at risk’ individuals. Of note, it has been challenging to obtain lymph node biopsy samples from these patients and controls. We now have all the tools available to first identify those individuals at risk of developing arthritis and to prospectively analyse the immune cells in lymph node tissues. This will create a framework for studying the molecular events taking place in lymph nodes before the onset of arthritis that can be potentially related to the processes involved in the pathogenic changes in synovial tissues.
We thank our study subjects for participating in the study, the department of radiology for the lymph node sampling, the AMC KIR lab technicians for sample processing and Johan Dobber for his advice on flow cytometry on lymph node needle biopsies.
Review history and Supplementary material
This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.
Files in this Data Supplement:
- Data supplement 1 - Online table
Handling editor Tore K Kvien
LGMvB and MJHdH contributed equally.
Contributors LGMvB and MJHdH were involved in study design, data collection and analysis, interpretation of the results and writing of the manuscript; both contributed equally to the manuscript. THR was involved in data collection and analysis, interpretation of the results and writing of the manuscript. IJAJZ was involved in data collection, interpretation of the results and revising the manuscript. MM was involved in study design, data collection, interpretation of the results and revising the manuscript. DMG was involved in study design, data collection, interpretation of the results and revising the manuscript. PPT was involved in study design, interpretation of the results and revising the manuscript.
Funding This study was sponsored by the Dutch Arthritis Foundation grants 08-1-310 and 11-1-308, The Netherlands Organisation for Health Research and Development (ZonMw) Veni project 916.12.109, and the IMI EU-funded project BeTheCure no. 115142.
Competing interests None.
Ethics approval The medical ethical committee of the Academic Medical Center Amsterdam approved this study.
Provenance and peer review Not commissioned; externally peer reviewed.
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