In rheumatoid arthritis, changes in autoantibody levels reflect intensity of immunosuppression, not subsequent treatment response
Rheumatoid arthritis (RA) is characterized by the presence of autoantibodies like rheumatoid factor (RF), anti-cyclic citrullinated peptide-2 (anti-CCP2), and anti-carbamylated protein (anti-CarP) antibodies. It is currently unclear whether changes in autoantibody levels are associated with disease activity/treatment outcomes and whether they are modified by treatment intensity. Therefore, we determined longitudinal changes in RA-autoantibody levels, the association between these changes and activity score (DAS) and treatment outcomes, and the effect of intensity of immunosuppressive treatment on levels.
In 381 seropositive RA patients from the IMPROVED study, we measured IgG, IgM, and IgA of anti-CCP2 and anti-CarP; IgM and IgA of RF; and IgG against four citrullinated and two acetylated peptides at 4-month intervals over the first year of treatment. Following initial prednisone and methotrexate (MTX), treatment was changed every 4 months aiming for DAS < 1.6. We investigated changes in autoantibody levels following treatment escalation versus tapering, and the association of levels with DAS over time, EULAR response, and drug-free remission (DFR) ≥ 1 year.
For all 14 autoantibodies, levels decreased from 0 to 4 months and then rose until 12 months. Following treatment escalation, autoantibody levels dropped markedly, while they rose following tapering: RF IgM levels, a representative autoantibody, dropped 10% after restarting prednisone and rose 15% aU/mL after tapering MTX (p < 0.0001). There was no association between autoantibody levels and DAS over time or EULAR response. Greater relative changes between 0 and 12 months did not predict DFR (0–12-month relative change RF IgM, − 39% for no DFR (n = 126) and − 16% for DFR (n = 18)).
Changes in RA-autoantibody levels are not associated with DAS or long-term treatment response, but reflect intensity of immunosuppression. This suggests that autoantibody levels are modifiable by current therapies, but that modifying levels is in itself of limited clinical relevance.
ISRCTN11916566. Registered on 7 November 2006
KeywordsRheumatoid arthritis Autoantibodies Ant-CCP2 Rheumatoid factor Anti-carbamylated protein antibodies Disease activity Immunosuppression
Anti-citrullinated protein antibody
Anti-modified protein antibodies
Anti-citrullinated protein 2
Body mass index
Disease activity score
Disease-modifying anti-rheumatic drug
Enzyme-linked immunosorbent assay
Generalized estimating equations
Health Assessment Questionnaire
Induction therapy with Methotrexate and Prednisone in Rheumatoid Or Very Early arthritic Disease
Sharp/van der Heijde Score
Rheumatoid arthritis (RA) is a chronic inflammatory joint disease characterized by the presence of autoantibodies. Rheumatoid factor (RF) and anti-cyclic citrullinated peptide-2 (anti-CCP2) are the most well-known of these, but other autoantibody systems such as anti-carbamylated protein (anti-CarP) and anti-acetylated peptide antibodies have also been identified [1, 2]. Autoantibody-positive patients have a worse prognosis, more radiographic damage, and a lower chance of achieving drug-free remission [3, 4].
Serum concentrations of these autoantibodies may change over time. Given the link between autoantibodies and disease severity and the value of measuring autoantibodies in other autoimmune diseases, these serological changes in RA may hold promise as an accessible biomarker for the future disease course. A substantial drop in autoantibody levels may, for example, be hypothesized to precede successful drug-free remission. However, studies documenting the relationship between fluctuations in autoantibodies and disease activity have been conflicting [5, 6, 7]. Importantly, most of these studies did not account for factors like intensity of immunosuppressive treatment, which likely influences both level changes and disease activity. It is unknown whether changes in autoantibody levels reflect immunosuppressive therapy or whether changes are indicative of future disease course. Furthermore, most studies investigated a limited number of autoantibodies and did not take “newer” autoantibodies into account, such as anti-CarP, which has been described to be associated with disease activity .
Because of this, the clinical implications of changes in autoantibody levels remain unclear, but are potentially relevant for two reasons. First, if autoantibody levels are a marker of future disease activity, it may be useful to measure pre-treatment values or monitor level changes over time. Second, understanding the changes in autoantibody levels and their association with both immunosuppression and disease activity might shed new light on mechanisms underlying the B cell autoimmune response in RA and its role in disease persistence. To that end, we longitudinally characterized changes in RA-associated autoantibody levels over time and investigated whether levels are affected by intensity of immunosuppressive treatment, how they associate with disease activity over time, and whether level changes associate with both short-term and long-term treatment outcomes.
Study design, patient selection, and outcomes
The Induction therapy with Methotrexate and Prednisone in Rheumatoid Or Very Early arthritic Disease (IMPROVED) study is a multicenter, randomized controlled trial that enrolled 610 patients with early (< 2 years) untreated RA or undifferentiated arthritis. It was steered at disease activity score-remission (DAS44 < 1.6) and for those achieving remission, at drug-free remission (DFR), with treatment adjusted every 4 months according to whether treatment targets had been reached. Initial treatment comprised methotrexate (MTX) and high-dose prednisone .
Subjects selected for this study were all 381 patients fulfilling the 2010 ACR/EULAR RA criteria with serum available at least once within the first year and seropositive by routine clinical testing for anti-CCP2 IgG, RF IgM, or our in-house assay for anti-CarP IgG at baseline or at 1 year (details described in ). Clinical outcomes investigated were DAS, health assessment questionnaire (HAQ), EULAR response at 4 and 12 months, and long-term sustained DFR. Long-term sustained DFR was defined as disease-modifying anti-rheumatic drug (DMARD)-free remission lasting at least 1 year, starting at any time point and continuing until the last moment of that individual’s follow-up (maximum of 5 years follow-up). Radiographic progression at 1 and 5 years was assessed using the Sharp/van der Heijde Score (SHS), as previously described .
Enzyme-linked immunosorbent assays (ELISAs) were used as described previously  to measure at 4-month intervals over the first year of treatment: anti-CCP2 IgG, IgM, and IgA; RF IgM and IgA; anti-CarP IgG, IgM, and IgA; anti-citrullinated-vimentin 59–74 IgG, anti-citrullinated-fibrinogen β 36–52 and α 27–43 IgG, and anti-citrullinated-enolase 5–20 IgG (all in-house assays); and anti-acetylated lysine vimentin IgG and anti-acetylated ornithine vimentin IgG (Orgentec Diagnostika GmbH, Germany) . Samples were considered positive if they fell above a cutoff of the mean arbitrary units (aU) per milliliter plus two standard deviations of 76 sera of healthy controls from the Leiden area.
Composites reflecting the number of autoantibodies present at every time point were constructed: the number of isotypes: anti-CCP2 IgG, IgM, IgA; RF IgM and IgA; anti-CarP IgG, IgM, IgA (range 1–8), and the number of IgG anti-modified peptide antibodies (AMPAs): anti-CCP2, anti-CarP, and the antibodies against citrullinated and acetylated peptides described above (range 1–8).
Longitudinal, repeated measures data (autoantibodies, DAS, HAQ) were modeled using generalized estimating equations (GEE), which allow missing data in the outcome. A model with a Toeplitz (m-dependent) correlation structure and a standard Gaussian distribution was chosen (akin to linear regression). For the number of autoantibodies over time (count data), a negative binomial model was specified.
With repeated measurements of the autoantibody levels/number as the dependent variable, we investigated by GEE whether a certain treatment decision (4 months, no change versus escalation of treatment; 8 months: tapering versus escalation of treatment) was associated with a subsequent change in autoantibody levels/number. An interaction term of treatment decision * time was used to assess whether changes in the autoantibody levels over time were different in patients that tapered/did not change versus those that escalated immunosuppressive therapy. For comparison purposes, a normalization of the different measurement units was applied to the final model estimates (which were in aU/mL) by dividing them by the maximum of the autoantibody’s range.
The association between autoantibody levels and DAS over time was investigated using GEE, with DAS as the outcome. The same was conducted for HAQ over time. Ordinal, logistic, and linear regression was used to investigate the association of relative changes in autoantibody levels/absolute changes in number of autoantibodies with EULAR response, long-term sustained DFR, and SHS radiographic progression scores, respectively.
All models were adjusted for gender and age; clinical outcome analyses were adjusted for treatment decisions. Other covariates (i.e., disease duration, smoking, body mass index (BMI), baseline HAQ/DAS) were only included in final models if they were univariably associated with the outcomes of interest (p < 0.1). Holmes-Bonferroni methods were used to correct all analyses for multiple testing, assuming the same number of tests as autoantibodies investigated (14 tests).
Autoantibody levels decrease upon initiation and escalation of immunosuppressive treatment
Another treatment decision was the one made at 4 months: patients that achieved remission at 4 months continued MTX monotherapy, while those that did not were randomized to one of the two treatment arms, where therapy was escalated by an addition of multiple DMARDs (prednisone, hydroxychloroquine, and sulfasalazine; arm 1) or adalimumab (arm 2). Levels consistently rose between 4 and 8 months during continued treatment with MTX while they either dropped or stayed relatively stable following treatment escalation (Additional file 1: Figure S2). At this moment, the difference in treatment intensity was less pronounced than at 8 months (i.e., no patients tapered to drug-free), as were the differences in autoantibody level changes.
The total autoantibody number changed in a manner similar to the changes in levels, both at treatment initiation (Additional file 1: Figure S1) and for the decision at 4 and at 8 months (not shown).
This indicates that autoantibody levels are responsive to immunosuppression and likely change upon decisions to escalate or taper therapy. The next question was whether these autoantibody changes are associated with treatment outcomes, and thus whether the changes in autoantibody levels in response to treatment might be clinically relevant to monitor over time.
Autoantibody levels are not longitudinally associated with DAS
Association of DAS over time with autoantibody levels over time
Outcome: DAS over time
β (95% CI) in DAS units per aU/mL
Anti-CCP2 IgG (0–1600)
1.1 × 10−4 (9.3 × 10−6 to 2.0 × 10−4)
Anti-CCP2 IgM (0–1400)
3.5 × 10−4 (1.4 × 10−4 to 5.7 × 10−4)
Anti-CCP2 IgA (0–1160)
3.6 × 10−4 (3.8 × 10−5 to 6.7 × 10−4)
RF IgM (0–200)
1.8 × 10−3 (8.2 × 10−4 to 2.8 × 10−3)
RF IgA (0–200)
7.9 × 10−4 (− 8.9 × 10−5 to 1.7 × 10−3)
Anti-CarP IgG (0–5272)
1.1 × 10−4 (4.1 × 10−5 to 1.7 × 10−4)
Anti-CarP IgM (0–3650)
1.7 × 10−4 (8.9 × 10−5 to 2.6 × 10−4)
Anti-CarP IgA (0–3100)
2.7 × 10−4 (1.6 × 10−4 to 3.8 × 10−4)
Anti-acetyl-lysine IgG (0–1000)
2.5 × 10−4 (2.1 × 10−5 to 4.7 × 10−4)
Anti-acetyl-ornithine IgG (0–1000)
2.0 × 10−4 (2.4 × 10−5 to 3.8 × 10−4)
Cit-Vim IgG (0–10,000)
3.7 × 10−5 (1.2 × 10−5 to 6.1 × 10−5)
Cit-Fib α IgG (0–25,000)
1.6 × 10−6 (− 2.0 × 10−5 to 2.3 × 10−5)
Cit-Fib β IgG (0–100,000)
4.2 × 10−6 (2.2 × 10−6 to 6.2 × 10−6)
Cit-Eno IgG (0–70,000)
2.9 × 10−6 (− 8.8 × 10−7 to 6.8 × 10−6)
Autoantibody levels and HAQ were generally not significantly associated, and if they were (significant for only 3/14 autoantibodies), the magnitude of association was similarly minute as found for DAS (not shown).
Changes in autoantibody levels are not associated with EULAR response
Changes in autoantibody levels are not associated with long-term outcomes like sustained DFR or radiographic progression
The next outcome we wished to analyze was long-term sustained DFR, which is the closest approximation of RA cure currently available. Interestingly, relative changes in autoantibody levels or number of isotypes or AMPAs between 0 and 12 months did not significantly differ between patients that did and did not achieve DFR (Fig. 3c; composites not shown). There was also no association between autoantibody levels at 8 months and ability to achieve DFR at 12 months (not shown). This indicates that autoantibody level changes over the first year of treatment are not informative for the ability to become drug-free.
In patients with radiographs available, 19% (67/360) had radiographic progression (≥ 0.5-point change from baseline) at 1 year, and 52% (152/294) had progression at 5 years. There was no association between baseline autoantibody levels or relative changes in autoantibody levels (0–12 months) and radiographic progression points at either 1 or 5 years (not shown).
In RA, it is unknown whether changes in autoantibody levels are associated with disease activity and treatment outcomes, or whether levels are modified by intensity of immunosuppressive therapy. Most studies have shown that RF (IgM, IgA, and IgG) levels decrease after treatment initiation with different DMARD classes [5, 6, 7, 10, 11], while anti-CCP2 (IgG) levels decrease only marginally, rebound after decreasing, or do not decrease at all [5, 6, 7, 10, 11, 12, 13]. Our results support this notion, as multiple forms and combinations of immunosuppressive medication in the IMPROVED led to reduction of autoantibody levels. Our results also showed that RF IgM decreases somewhat more than anti-CCP2 IgG, in line with previous reports .
Although the diagnostic and prognostic value of testing for autoantibody positivity in RA is well-established, reports are conflicting regarding the potential association of level fluctuations with disease activity in seropositive patients [5, 6, 7]. In the current study, there was no relevant association between autoantibody changes and disease activity. Moreover, we also found no association with functional status, treatment response, or long-term outcomes such as DFR and radiographic progression. Instead, autoantibody level changes seem to be largely a reflection of immunosuppressive therapy, rather than an indication of disease-specific clinically relevant processes. Therefore, their monitoring over time seems of limited value.
Autoantibody stability in different autoimmune diseases varies substantially, with some autoantibodies fluctuating with flares of disease, while others remain stable. These differences may be due to differences in longevity and place of residence of the autoantibody-producing cells. In RA, the synovial compartment appears to function as an inflammatory niche that promotes long-term survival of anti-citrullinated protein antibody (ACPA)-producing plasma cells . ACPA-producing plasmablasts also home to the bone marrow and differentiate to long-lived plasma cells there [14, 15]. As RA disease activity subsides with anti-inflammatory treatment, the survival niches in inflamed joints may be eliminated and plasma cells residing there could be displaced and die . Meanwhile, it appears plausible that bone marrow plasma cells remain unaffected by resolution of peripheral inflammation and continue to stably secrete RA-associated autoantibodies. This could explain why circulating autoantibodies show an initial decrease when treatment is initiated or intensified (elimination of joint survival niches) but are never fully eradicated (persistence of bone marrow niches), even in the absence of clinical symptoms. Whether the surviving bone marrow B cells/plasma cells contribute to the chronic pathogenic cascade remains to be determined. It is possible that such contributions may occur via pathways independent of autoantibody production, such as antigen presentation to T cells, cytokine secretion, or other immunoregulatory mechanisms. There may also exist autoantibody-specific differences in survival niches that plasma cells utilize that might explain why some autoantibodies change quite substantially upon immunosuppressive treatment while others remain more stable.
The current findings have some limitations. First, we chose not to further dilute serum samples above the highest standard of the ELISA, precluding the detection of level changes in patients with very high concentrations. However, sensitivity analyses excluding these patients yielded the same conclusions (not shown). Second, it is possible that the autoantibody level decreases seen between 0 and 4 months in all patients and between 8 and 12 months for those with treatment intensification are primarily due to the effect of prednisone, as prednisone has been shown to decrease total circulating immunoglobulin levels, especially IgG . The design of this study did not allow us to investigate whether this was the case. Thirdly, we do not have serological data in the timeframe between 12 months and the long-term outcomes investigated. It is possible that antibody changes closer to the outcome are more relevant than those over the first year of treatment. Fourth, only the effect of conventional DMARDs and anti-TNF has been investigated. It may be that DMARDs with other modes of action, such as rituximab, have different effects on autoantibody levels. It is also possible that the same agents applied during a disease state may associate with different level changes than demonstrated here, as our results only apply to early RA. Finally, we recognize that due to the limited radiographic progression that occurred in the IMPROVED study, we lacked sensitivity for finding a relationship with autoantibody levels.
Strengths of this study include the extensive array of autoantibodies measured and the longitudinal nature of the analyses, which allowed analysis of absolute changes in 14 different autoantibodies spanning four autoantibody families in 4-month intervals over the first year of treatment while accounting for missing serum. The nature of the IMPROVED trial and its long follow-up also allowed us to investigate multiple short-term and long-term outcomes not previously linked to autoantibody changes, as well as the effect of immunosuppression on level changes.
We conclude that in early RA, changes in autoantibody levels do not associate DAS over time or with treatment response. Instead, autoantibody level changes seem to be a reflection of treatment intensity. Together, these results suggest that autoantibody levels change over time and are modifiable by commonly used DMARDs, but that autoantibody level changes are in itself of limited clinical relevance and not useful to monitor over time.
We thank Gerrie Stoeken and Linda Herb-van Toorn for their expertise and guidance during the experiments.
This project was funded by the ZonMw (the Netherlands Organisation for Health Research and Development)-consortium MOlecular DIagnostics in RA (MODIRA), project number 436001001.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author upon reasonable request.
EM, VD, and DW designed the research. EM and VD performed the experiments. HB kindly provided assays for anti-acetylated peptide antibodies. GC, LL, and CA were responsible for the design and clinical data collection of the IMPROVED study. EM and VD analyzed the data. EM drafted the manuscript. All authors contributed to the interpretation of the data and preparation of the manuscript. All authors read and approved the final manuscript.
Ethics approval and consent to participate
This study was conducted with the approval of the regional ethics committee at Leiden University Medical Center. The IMPROVED study was approved by the Medical Ethics Committees of all participating hospitals. Informed consent was obtained from all participants.
Consent for publication
R.E.M.T., T.W.J.H., and L.A.T. are among the inventors of a patent on the use of carbamylated antigens for diagnosis. H.B. is an employee of Orgentec Diagnostika, which manufactures diagnostic anti-acetylated peptide antibody assays. All other authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
- 3.van der Kooij SM, Goekoop-Ruiterman YP, de Vries-Bouwstra JK, Guler-Yuksel M, Zwinderman AH, Kerstens PJ, et al. Drug-free remission, functioning and radiographic damage after 4 years of response-driven treatment in patients with recent-onset rheumatoid arthritis. Ann Rheum Dis. 2009;68(6):914–21.CrossRefGoogle Scholar
- 8.Truchetet ME, Dublanc S, Barnetche T, Vittecoq O, Mariette X, Richez C, et al. Association of the presence of anti-carbamylated protein antibodies in early arthritis with a poorer clinical and radiologic outcome: data from the French ESPOIR cohort. Arthritis Rheumatol. 2017;69(12):2292–302.CrossRefGoogle Scholar
- 11.Mikuls TR, O'Dell JR, Stoner JA, Parrish LA, Arend WP, Norris JM, et al. Association of rheumatoid arthritis treatment response and disease duration with declines in serum levels of IgM rheumatoid factor and anti-cyclic citrullinated peptide antibody. Arthritis Rheum. 2004;50(12):3776–82.CrossRefGoogle Scholar
- 12.Jansen D, Emery P, Smolen JS, Westhovens R, Le Bars M, Connolly SE, et al. Conversion to seronegative status after abatacept treatment in patients with early and poor prognostic rheumatoid arthritis is associated with better radiographic outcomes and sustained remission: post hoc analysis of the AGREE study. RMD Open. 2018;4(1):e000564.CrossRefGoogle Scholar
- 14.Kerkman PF, Kempers AC, van der Voort EI, van Oosterhout M, Huizinga TW, Toes RE, et al. Synovial fluid mononuclear cells provide an environment for long-term survival of antibody-secreting cells and promote the spontaneous production of anti-citrullinated protein antibodies. Ann Rheum Dis. 2016;75(12):2201–7.CrossRefGoogle Scholar
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