Article Text


Low circulating soluble interleukin 2 receptor level predicts rapid response in patients with refractory rheumatoid arthritis treated with infliximab
  1. A Kuuliala1,
  2. R Nissinen2,
  3. H Kautiainen3,
  4. H Repo4,
  5. M Leirisalo-Repo5
  1. 1Department of Bacteriology and Immunology, Haartman Institute, University of Helsinki, Helsinki, Finland
  2. 2Department of Molecular Medicine, National Public Health Institute, Helsinki
  3. 3Rheumatism Foundation Hospital, Heinola, Finland
  4. 4Division of Infectious Diseases, Department of Medicine, Helsinki University Central Hospital
  5. 5Division of Rheumatology, Department of Medicine, Helsinki University Central Hospital
  1. Correspondence to:
    Antti Kuuliala
    Haartman Institute, Department of Bacteriology and Immunology, PO Box 21 (Haartmaninkatu 3), FIN-00014 Helsingin Yliopisto, Helsinki, Finland; antti.kuuliala{at}


Background: Treatment with infliximab induces a rapid therapeutic response in most patients with active rheumatoid arthritis. Factors predicting good response are not well known.

Objective: To study the predictive value of baseline level of soluble interleukin 2 receptor (sIL2R), a marker of lymphocyte activation, on the treatment response.

Methods: 24 patients with active rheumatoid arthritis received intravenous infusions of infliximab at study entry, at two weeks, at six weeks, and at eight week intervals thereafter. Outcome was evaluated at six weeks and 22 weeks. Clinical assessment and standard laboratory tests were made and the DAS28 disease activity score was calculated. Serum sIL2R level at entry was measured by automated immunoassay analyser (Immulite®). The mean change in DAS28 score from entry to six weeks and 22 weeks was calculated and related to sIL2R level using baseline adjusted robust regression analysis.

Results: Baseline level of serum sIL2R (mean (SD), 621 (325) U/ml) did not correlate with baseline DAS28 score (r = 0.24 (95% confidence interval, −0.18 to 0.58)). At six weeks DAS28 scores improved, with a mean change of −2.53 (−3.08 to −1.98) (p<0.001). This change was predicted by low baseline sIL2R level (regression coefficient per 100 U/ml: 0.205 (0.003 to 0.407) (p = 0.047)). At 22 weeks the DAS28 scores improved, with a mean change of −2.26 (−2.75 to −1.77) (p<0.001). The change was not predicted by baseline sIL2R level.

Conclusions: Low baseline sIL2R level may predict a rapid clinical response in patients with refractory rheumatoid arthritis treated with infliximab.

  • DAS28, 28 joint disease activity score
  • DMARD, disease modifying antirheumatic drug
  • HAQ, Health Assessment Questionnaire
  • sIL2R, soluble interleukin 2 receptor
  • rheumatoid arthritis
  • infliximab
  • soluble interleukin 2 receptor

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Rheumatoid arthritis is a systemic autoimmune disease characterised by polyarticular joint inflammation. The disease is heterogeneous with respect to clinical features, genetic background, and immunopathogenesis. The pathogenesis of rheumatoid arthritis is incompletely understood. It involves collaboration between dendritic cells, T cells, and monocytes/macrophages, which may initiate and perpetuate immune activation.1,2 Activated CD4+ T cells in the synovium stimulate monocytes and macrophages which produce proinflammatory cytokines, causing synovial inflammation. The synovium can have features of lymphocytic follicles.3 Indeed, T cells are the most abundant cells in the pannus.

Upon activation, T cells express on their surface interleukin 2 receptor (IL2R) which is shed from the cells and can be detected as a soluble form of IL2R (sIL2R) in synovial fluid and in serum. Activation of T lymphocytes can be evaluated by measuring circulating levels of sIL2R.4

A key proinflammatory cytokine in rheumatoid inflammation is tumour necrosis factor (TNF). Monocytes and macrophages are the major source of TNF.1 The blockade of TNF with infliximab, a chimeric monoclonal anti-TNF antibody, results in a rapid clinical response in the majority of rheumatoid patients. However, only 20–40% of the patients achieve a good clinical response (⩾ACR50). In the rest of the patients, the effect is only modest or is not observed at all.5 The reasons for varying responses are largely unknown, but inflammatory and immunological heterogeneity of patients with rheumatoid arthritis might be one explanation.

We have recently presented data suggesting that low baseline serum sIL2R levels may predict early remission in patients with early active DMARD-naive rheumatoid arthritis treated with a single DMARD.6 This prompted us to study whether baseline sIL2R level serves as a predictor of early treatment response to treatment with infliximab in rheumatoid patients refractory to conventional DMARDs. We reasoned that strong lymphocyte activation, as defined by high levels of sIL2R in the circulation, may, by intensifying macrophage TNF production, delay the clinical response to, or even render the patient refractory to, treatment with infliximab. Here we report that low circulating sIL2R level may predict rapid response to infliximab treatment.


This study comprises 24 patients with chronic active rheumatoid arthritis. Treatment with all conventional DMARDs had failed. Nineteen patients (79%) were on low dose prednisolone (⩽15 mg/day). After starting infliximab, DMARD treatment was continued with minor modifications during the study period.

All patients gave their informed consent for participation in the study. The study protocol was approved by the ethics committee of the Helsinki University Central Hospital.

The patients received infliximab infusions (3–4 mg/kg) at entry, and at two weeks, six weeks, 14 weeks, and 22 weeks. The outcome was assessed at six weeks and 22 weeks (one patient died before the 22 week check up visit). Swollen and tender joints were counted. Patient’s assessment of pain, and patient’s and physician’s global assessments were recorded on a 10 cm visual analogue scale. The patients filled in the Finnish version of the Stanford Health Assessment Questionnaire (HAQ)7 and the HAQ score was calculated. Erythrocyte sedimentation rate (ESR) and serum C reactive protein concentrations were measured using standard laboratory methods. The DAS28 disease activity score was calculated.8 Immediately before the first infliximab infusion, blood was collected into EDTA, and plasma was separated by centrifugation and frozen at −20°C. The sIL2R levels were measured by Immulite® automated immunoassay analyser (DPC, Los Angeles, California, USA). The sIL2R measurements were carried out blinded, without knowledge of the clinical data.

Pearson correlation coefficients were calculated for serum sIL2R level and baseline DAS28 score. The changes in DAS28 scores, with 95% confidence intervals (CI) were calculated. Probability (p) values for changes in DAS28 scores were calculated by the t test. The predictive value of baseline sIL2R level for change in DAS28 score at six and 22 weeks was calculated by robust regression analysis. This type of regression analysis, in which the weight given to outliers is reduced, is appropriate for analysis of small datasets because it makes the results less sensitive to the presence of outliers.


Table 1 presents the characteristics of the patients and table 2 the DMARDs used by the patients. The mean (SD) serum sIL2R was 621 (325) U/ml, and the DAS28 score, 6.3 (1.0). The serum sIL2R level did not correlate with the baseline DAS28 score (r = 0.24 (95% CI, −0.18 to 0.58)).

Table 1

 Baseline characteristics of the patients

Table 2

 Disease modifying antirheumatic drugs used by the patients at entry

There was a distinct clinical response to infliximab. At six weeks, DAS28 scores improved (mean (SD) score, 3.7 (1.7)), with a mean change of −2.53 (95% CI, −3.08 to −1.95) (p<0.001). This change was predicted by baseline sIL2R level (table 3; fig 1A) but not by baseline DAS28 score or infliximab dose. At 22 weeks, the mean DAS28 score was 4.0 (1.2)), and the mean change from baseline was −2.26 (−2.75 to −1.77) (p<0.001). This change was predicted by neither the baseline sIL2R level (table 3; fig 1B) nor the baseline DAS28 score or infliximab dose.

Table 3

 Baseline adjusted robust regression for baseline serum soluble interleukin 2 receptor (sIL2R) predicting change in 28 joint disease activity score (DAS28) after six and 22 weeks

Figure 1

 Baseline serum soluble interleukin 2 receptor (sIL2R) versus change in 28 joint disease activity score (ΔDAS28) from baseline to six weeks and baseline to 22 weeks. The filled circles represent the means (with 95% confidence intervals).

In four patients initially receiving a combination of DMARDs the treatment regimen was tapered as their clinical condition improved during the infliximab treatment. One patient had a temporary pause in the methotrexate treatment because of raised liver enzyme levels.


The results show that low serum sIL2R level predicts early (six weeks) response to infliximab treatment. To the best of our knowledge such a predictor for early response has not been described before. Given that the serum sIL2R level serves as a marker to T cell activation,4 our results suggest that enhanced T cell activation is related to delayed response to the infliximab treatment. This suggestion emphasises the impact of lymphocytes on the rheumatic inflammation and is supported by at least two lines of evidence.

First, about one third of patients with rheumatoid arthritis have extensive lymphocytic infiltration in the synovium with T and B cell conglomerates, sometimes forming germinal centres. Such patients have a more active disease and higher levels of sIL2R in their sera.9,10 Consequently, the patients with high baseline sIL2R may have large numbers of activated T cells in the synovium, thus requiring several infliximab infusions before the synovial infiltrate is reduced and disease activity is lowered.

Second, we have previously investigated chemokine receptor expression on circulating lymphocytes in the same patients. The patients responding to infliximab (fulfilling the ACR20 response) had smaller numbers of T cells expressing CCR3 and CCR5 at baseline compared with non-responders.11 The results are in agreement with the present study, indicating that high activation of lymphocytes impairs the efficacy of infliximab treatment. Taken together, these findings raise an intriguing question as to whether the patients with signs of high lymphocyte activation are particularly suitable for treatment with CTLA4Ig12 or other drugs suggested to act through inhibition of T cell activation.13

In the present study, the serum sIL2R level did not predict the later (22 week) response. This finding agrees with the previous studies of patients with refractory rheumatoid arthritis treated with methotrexate for 18 weeks,14 or DMARD naive patients treated with sulfasalazine or parenteral gold for 37 weeks,15 indicating that there is no correlation between initial serum sIL2R level and the response to treatment.

Our patients, being very refractory, had received DMARDs previously and also received them during the whole study period, mostly in combination with prednisolone. A decrease in the sIL2R level may occur during the treatment with methylprednisolone, either as intravenous pulse16 or as intramuscular injections,17 or during the treatment with some of the DMARDs such as methotrexate14,18–23, ciclosporine A,24 and sulfasalazine,15 but may not occur during the treatment with parenteral15,25 or oral26 gold, or with azathioprine.19,20,22 Thus it is possible that the DMARD treatment may have affected the results by decreasing the sIL2R levels measured before starting infliximab. Furthermore, the DMARDs were continued and may have had synergistic effects with infliximab on the treatment response. Finally, the present study has the common weaknesses of an open label study. To address these questions further, randomised controlled studies with sufficient numbers of patients are needed.

We have shown that in the DMARD-naive patients with early active rheumatoid arthritis participating in the FIN-RACo study,27 low sIL2R level at baseline predicted remission at six months in patients treated with a single DMARD, but not in patients treated with a combination strategy.6 With respect to serum sIL2R levels, the patients in the current study—having failed all conventional DMARDs, often used in combinations—were similar to the DMARD-naive patients in the FIN-RACo trial.28 Thus a low sIL2R level can be a feature of early rheumatoid arthritis or of established disease and be a marker of a subtype of rheumatoid arthritis, notoriously known to be heterogeneous, and indicate a more rapid and favourable response to treatment.

In conclusion, low circulating sIL2R level, denoting a low degree of lymphocyte activation, may be predictive of a rapid response to treatment with infliximab in patients with refractory rheumatoid arthritis. However, the marker does not identify the patients in remission after 22 weeks. Further studies are needed to clarify the predictive value of sIL2R in infliximab treatment.


Supported by grants from Finnish Cultural Foundation, Paulo Foundation, and Helsinki University Central Hospital research funds.


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  • Published Online First 7 June 2005

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