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A substantial proportion of patients with rheumatoid arthritis (RA) do not respond, or lose initial response, to adalimumab treatment. One explanation for non‐response is that patients develop anti‐adalimumab antibodies.
To evaluate the incidence of formation of antibody against adalimumab and the association with serum adalimumab concentrations and clinical response.
In a cohort of 121 consecutive patients with RA treated with adalimumab, serum adalimumab concentrations and antibodies against adalimumab were measured together with clinical response variables before and up to 28 weeks after the start of treatment.
Anti‐adalimumab antibodies were detected in 21 patients (17%) during 28 weeks of treatment. EULAR non‐responders had antibodies significantly more often than good responders (34% vs 5%; p=0.032). Patients with antibodies showed less improvement in disease activity (mean (SD) delta DAS28 0.65 (1.35)) than patients without antibodies (mean delta DAS28 1.70 (1.35)) (p=0.001). Patients with antibodies during follow‐up had lower serum adalimumab concentrations at 28 weeks than patients without antibodies (median 1.2 mg/l, range 0.0–5.6 vs median 11.0 mg/l, range 2.0–33.0, respectively; p<0.001). Good responders had higher serum adalimumab concentrations than moderate responders (p=0.021) and non‐responders (p=0.001). Concomitant methotrexate use was lower in the group with anti‐adalimumab antibodies (52%) than in the group without antibodies (84%) (p=0.003).
Serum antibodies against adalimumab are associated with lower serum adalimumab concentrations and non‐response to adalimumab treatment.
A substantial proportion of patients with rheumatoid arthritis (RA) still have persistent disease activity or flare of disease activity despite tumour necrosis factor (TNF)α blocking therapy.1 An explanation may be that antibodies are formed against these therapeutic agents. In patients with RA or Crohn's disease, human anti‐chimeric antibodies (HACAs) to infliximab have been reported. Initially, the clinical significance of these antibodies was uncertain. However, recent data on Crohn's disease indicate that these anti‐infliximab antibodies are associated with allergic reactions and a shorter duration of response.2 In RA, the development of antibodies against infliximab is associated with a reduced response to infliximab after treatment for an extended period of time.3 Simultaneous immunosuppressive therapy has been shown to reduce HACA formation.2,4
Adalimumab is a fully human antibody and therefore thought to be less immunogenic than chimeric antibodies.5 Nevertheless, it has previously been suggested that human anti‐human antibodies against adalimumab may develop as well, although the data are limited. Anti‐adalimumab antibodies were found in 12% of patients with RA receiving adalimumab monotherapy at a dose of 40 mg every other week.6,7 Contradictory results have been reported with regard to the influence of these antibodies on clinical response.6,7 We recently found high anti‐adalimumab concentrations in a patient with RA, which was associated with undetectable serum adalimumab concentrations and a diminished clinical response.8 This case report suggested that human anti‐human antibody formation may play an important role in some patients who do not respond to adalimumab treatment. This emphasises the need for further investigation with standardised analytical techniques into the effect of antibody formation on clinical response. Therefore, we evaluated adalimumab and anti‐adalimumab antibody concentrations in relation to clinical response in a cohort of patients with RA up to 28 weeks after initiation of treatment.
This prospective observational cohort study consisted of 121 consecutive patients with RA treated with adalimumab at the Departments of Rheumatology of the Jan van Breemen Institute and the Academic Medical Center, Amsterdam. All patients fulfilled the American College of Rheumatology 1987 revised criteria for RA and had active disease, indicated by a disease activity score in 28 joints (DAS28) of 3.2 despite earlier treatment with two disease‐modifying anti‐rheumatic drugs (DMARDs) including methotrexate at a dose of 25 mg a week or at the maximal tolerable dose, according to the Dutch consensus statement on the initiation and continuation of TNF blocking therapy in RA.9 Patients were treated with either adalimumab and concomitant DMARD or adalimumab alone. All patients used adalimumab 40 mg subcutaneously every other week. In patients with an inadequate response as judged by the treating rheumatologist, the dosing frequency of adalimumab could be increased to 40 mg a week. The study was approved by the medical ethics committee of the Slotervaart Hospital, BovenIJ Hospital, the Jan van Breemen Institute, and the Academic Medical Center/University of Amsterdam. All patients gave written informed consent.
Disease activity was assessed at baseline and after 4, 16 and 28 weeks of treatment using the DAS28 score.10 Clinical response was assessed by the European League Against Rheumatism (EULAR) criteria and the change in DAS28 score (delta DAS28).11 Serum samples were collected just before an injection with adalimumab at baseline, and after 4, 16 and 28 weeks.
Trough serum adalimumab concentrations were measured by ELISA, based on the principle that adalimumab is captured through its ability to bind TNFα. Adalimumab was quantified as described previously for infliximab measurement with one modification.12 Adalimumab binding was assessed by incubation with biotinylated rabbit IgG directed to the adalimumab idiotype. The detection limit of the assay is about 0.001 mg/l.
Anti‐adalimumab antibodies were detected with a newly developed radioimmunoassay. The assay measures specific high‐avidity IgG antibodies against adalimumab by an antigen‐binding test as described previously for the detection of antibodies against infliximab.3 Serum (1 μl/test) was preincubated with Sepharose‐immobilised protein A (1 mg/test; Pharmacia, Uppsala, Sweden) in Freeze buffer (Sanquin, Amsterdam, the Netherlands). Non‐bound serum components were removed by washing before 50 μl 125I‐labelled F(ab)′2 fragment of adalimumab was added. After overnight incubation, non‐bound radiolabel was washed out and Sepharose‐bound radioactivity was measured. Test results were converted into arbitrary units per millilitre (AU/ml) by comparison with dilutions of a reference serum. The mean cut‐off value was set at 12 AU/ml (mean + 6 SD of the pretreatment values), which was derived from 100 healthy donors. In agreement with this, all sera of patients in this study contained less than 12 AU/ml anti‐adalimumab before they received their first adalimumab injection. Assay specificity was demonstrated by the absence of anti‐adalimumab in 25 sera containing high‐titre anti‐infliximab. Because the presence of adalimumab interferes with the assay, it is to be expected that in patients with high concentrations of adalimumab, anti‐adalimumab is underestimated or undetectable. The antibody test was considered positive when the antibody concentration exceeded 12 AU/ml and the adalimumab concentration was 5 mg/l or less. We occasionally observed patients with anti‐adalimumab concurrent with serum concentrations of adalimumab. Adalimumab and antibody concentrations were measured at baseline and 28 weeks after initiation of treatment. At week 4 and 16, antibody concentrations were determined only in serum of patients with an adalimumab concentration of less than 5 mg/l and in patients with anti‐adalimumab at week 28.
For differences between groups, we used the independent samples t test or Mann‐Whitney U test as appropriate. For differences between paired samples, we used the paired samples t test or Wilcoxon signed rank test. The threshold for significance was set at p<0.05. We used multiple logistic regression analysis to investigate the relationship between EULAR response and adalimumab concentration, as well as the presence of anti‐adalimumab antibodies and the influence of sex, age, methotrexate and prednisone use and dose on this relationship.
To analyse clinical response in patients with and without antibodies after 28 weeks of treatment, we used the last observation carried forward for patients who stopped treatment because of non‐response or adverse events. In a sub‐analysis, the effects of increasing the adalimumab dosing frequency to 40 mg a week were studied using the data obtained after the more frequent dosing.
Most of the 121 patients who entered the study were female (79%), and the mean (SD) age was 53 (13) years (table 11).). At baseline, patients had active disease, as indicated by a mean DAS28 score of 5.3 (1.1). Mean disease duration was 12 (10) years, and, on average, patients had failed 3.6 (1.6) prior DMARDs. Most patients used concomitant methotrexate (79%) with a mean dose of 19.4 (7.4) mg/week, and 34% used prednisone at a mean dose of 7.9 (4.3) mg/day. Fourteen (12%) patients used sulfasalazine and/or hydroxychloroquine in combination with methotrexate, two (2%) patients used concomitant hydroxychloroquine only, and 24 (20%) patients were receiving adalimumab monotherapy.
The percentage of patients with antibodies against adalimumab who used concomitant methotrexate was significantly lower than the percentage of patients without such antibodies (p=0.003). The mean (SD) methotrexate dose did not differ significantly between antibody positive and negative patients.
After 28 weeks follow‐up, 109 of 121 patients were still receiving adalimumab treatment. Dosing frequency was increased in 10 patients. Of the remaining 99 patients, 77 (78%) were classified as responders according to the EULAR response criteria. The responders consisted of 34 (34%) good responders and 43 (43%) moderate responders. The mean improvement in DAS28 was 1.7 (1.3).
Twelve patients stopped treatment before week 28, six because of inefficacy (as concluded by the treating rheumatologist), and four because of side effects (chronic coughing, flu‐like symptoms, palpitations, dysuria, and fever of unknown origin). In one patient, adalimumab was stopped because of a suspected malignancy, and one patient died from an unknown cause after 16 weeks of treatment.
During 28 weeks of follow‐up, antibodies were detected in 21 (17%) patients. Nine (8%) patients were found to be positive for anti‐adalimumab at week 4 after the start of treatment, six (5%) patients at week 16, and another six (5%) at week 28. The serum concentrations of anti‐adalimumab showed two clusters, which could be separated at a cut‐off value of 100 AU/ml. Ten of the 21 patients had antibody concentrations that stayed below 100 AU/ml at all time points (range 13–57 AU/ml), and 11 patients had antibody concentrations above 100 AU/ml (range 115–10344 AU/ml). When antibody concentrations of 100 AU/ml or more were present, these remained high during treatment, and concentrations increased further over time. Antibody concentrations between 12 and 100 AU/ml were less stable over time and were intermittently detectable or undetectable.
The percentage of patients using concomitant methotrexate was significantly lower in patients with antibodies against adalimumab (52%) than in patients without such antibodies (84%) (p=0.003) (table 11).). The mean methotrexate dose did not differ significantly between anti‐adalimumab positive and negative patients. The mean methotrexate dose was 19.7 (7.3) mg/week in the patients without anti‐adalimumab antibodies, 21.9 (6.3) mg/week in the low‐antibody group (12–100 AU/ml), and 14.3 (8.9) mg/week in patients with high anti‐adalimumab antibody concentrations (>100 AU/ml). A trend towards a lower methotrexate dose was seen in the group with high antibody concentrations > 100 AU/ml (p=0.056). Patients receiving concomitant methotrexate had a lower rate of antibody development than patients receiving adalimumab monotherapy (12% vs 38%).
At 28 weeks, median trough adalimumab concentration was 10 mg/l and varied from undetectable to 28 mg/l in patients receiving adalimumab at a dose of 40 mg every other week. In patients who received 40 mg a week, the median trough adalimumab concentration was 12 mg/l and varied from 8 to 43 mg/l.
Figure 11 shows the course of the median trough adalimumab concentrations over 28 weeks of adalimumab. Serum adalimumab concentrations in patients with anti‐adalimumab antibodies were significantly lower than in patients without these antibodies (median 1.2 mg/l, range 0.0–5.6 vs median 11.0 mg/l, range 2.0–33.0; p<0.001).
EULAR non‐responders had anti‐adalimumab antibodies significantly more often than good responders (p=0.006). After adjustment for sex and methotrexate dose, the presence of anti‐adalimumab antibodies remained a significant determinant of EULAR response (p=0.032). EULAR non‐responders had anti‐adalimumab antibodies significantly more often than moderate responders (p=0.039). However, this difference between non‐responders and moderate responders was no longer present after adjustment for methotrexate use (p=0.148). The difference between good and moderate responders did not reach statistical significance.
Of the 11 patients with anti‐adalimumab concentrations above 100 AU/ml, nine (82%) were non‐responders and two were moderate responders (18%). Of patients with anti‐adalimumab concentrations of 12–100 AU/ml (n=10), only three were non‐responders, five were moderate responders, and two were good responders. Mean improvement in DAS28 in these patients was 0.20 (0.98). Of all patients in whom no antibodies against adalimumab were detected during the 28 weeks follow‐up, 23 (23%) were non‐responders, 41 (41%) moderate responsers, and 35 (35%) good responders. Figure 22 shows the relationship between EULAR response and presence or absence of anti‐adalimumab. Patients with anti‐adalimumab showed significantly less improvement in DAS28 (mean delta DAS28 0.65 (1.35)) than patients without anti‐adalimumab (mean delta DAS28 1.70 (1.35)) (p=0.001). Figure 33 shows the relationship between DAS28 and adalimumab and anti‐adalimumab concentrations.
EULAR non‐responders had significantly lower serum adalimumab concentrations than good responders (median 5.4 mg/l, range 0.0–21.2 vs 9.8 mg/l, range 0.0–33.0; p=0.001). Furthermore, non‐responders had lower serum adalimumab concentrations than moderate responders (p=0.043). However, this difference was no longer significant after adjustment for methotrexate use (p=0.098). Figure 44 shows the relationship between EULAR response and adalimumab concentration. Good responders had significantly higher serum adalimumab concentrations than moderate responders (p=0.021).
Prednisone and methotrexate dose remained relatively stable in 17 of 21 patients who tested positive for anti‐adalimumab. In two of the 21 patients, low‐dose prednisone (5.0 and 7.5 mg/day) was stopped. The methotrexate dose (5 mg/week) was discontinued in one of the 21 patients, and in another patient methotrexate (15 mg/week) was started simultaneously with adalimumab.
In 10 patients (8%), the dosing frequency of adalimumab was increased to 40 mg a week, while concomitant methotrexate and prednisone dose remained stable. At the last visit before the dosing frequency was increased, seven patients were non‐responders, one was a moderate responder, and two were good responders (who subjectively perceived inefficacy). In five of the seven non‐responders, anti‐adalimumab antibodies were detectable, with antibody concentrations in the range 39–184 AU/ml. Anti‐adalimumab antibodies were no longer detectable after the increase in dosing frequency, and adalimumab concentrations significantly increased from a mean concentration of 2.0 (1.8) mg/l to 15.0 (8.0) mg/l (p=0.043). Clinical response improved in the non‐responders, with a mean decrease in DAS28 of 1.7 (1.2). Figure 55 shows the effects of increasing the dosing frequency on DAS28 and adalimumab and anti‐adalimumab concentrations.
After 28 weeks of treatment, anti‐adalimumab antibodies were found in 17% of the patients. Our results show that the presence of anti‐adalimumab is associated with diminished adalimumab concentrations and that especially high anti‐adalimumab concentrations are associated with the absence of detectable serum adalimumab. Furthermore, the presence of anti‐adalimumab as well as low serum adalimumab concentrations is associated with a diminished clinical response.
With infliximab treatment, HACAs were found in 29% of the patients during 30 weeks follow‐up.3 Infliximab is a chimeric monoclonal antibody, with a human constant region and murine variable regions. In adalimumab, a “fully human” antibody, the constant and variable regions are both “human”. Therefore, one can expect adalimumab to be less immunogenic. However, when comparing the relative immunogenicity, we have to take into account not only the extent of humanisation but also the differences in dosing schedules and route of administration of these two monoclonal antibodies.13 It is doubtful that any biological treatment will be completely without immunogenicity, but some may be more immunogenic than others.
Anti‐adalimumab antibodies have been previously reported in 12% of patients receiving adalimumab monotherapy 40 mg every other week for 26 weeks.7 In that study, no significant difference in ACR 20 response was found between patients with and without antibodies. In contrast, our data show that the presence of especially high concentrations of antibodies against adalimumab is associated with EULAR non‐response. Other data confirm our finding that a diminished clinical response is seen in patients with detectable antibodies compared with patients without antibodies.6 Differences between studies may be due to the use of different assays. Therefore, to come to an agreement on the immunological and clinical importance of antibody formation, it will be essential to further standardise the assays used for studying immunogenicity. Obviously, this is not only important for adalimumab but for all therapeutic monoclonal antibodies.
During 28 weeks follow‐up, high anti‐adalimumab antibody concentrations (>100 AU/ml) were associated with low serum trough adalimumab concentrations. The reduced adalimumab concentration in these patients is probably due to increased clearance of adalimumab via the formation of adalimumab–anti‐adalimumab immune complexes. This notion is supported by recent observations in patients with RA receiving 99 technetium‐labelled infliximab.14 In one HACA‐positive non‐responder, the formation of small immune complexes could be detected, which coincided with rapid clearance from the blood and high uptake of infliximab in the liver and spleen. Without adalimumab in the circulation, its function would logically be impaired. It is possible that a patient has adalimumab in the circulation in the interval between two dosings, and the concentration falls below the detection limit just before the next adalimumab injection. In this case, it would be possible for a patient to have a good response based on adequate adalimumab concentrations in the 2 week dosing interval despite the presence of antibodies against adalimumab and undetectable trough concentrations before the next injection. However, the fact that most patients with anti‐adalimumab concentrations above 100 AU/ml were non‐responders indicates that, overall, serum adalimumab concentrations were probably too low to have a therapeutic effect.
As there is competition for the assay in the presence of adalimumab, the incidence of anti‐adalimumab antibodies may be underestimated in all patients. Anti‐adalimumab antibodies may cause increased clearance and lower adalimumab concentrations in some patients while not yet detectable. This may be one explanation for the fact that serum adalimumab concentrations were significantly higher in EULAR good responders compared with moderate responders.
The question arises what causes anti‐adalimumab antibody formation in some patients, but not in others, and what could explain the difference between patients with high and low anti‐adalimumab concentrations. It is likely that immunosuppression with methotrexate reduces anti‐adalimumab formation, as shown previously for anti‐infliximab antibodies.4,6 Our data confirm the notion that concomitant methotrexate use reduces the rate of antibody development.
Anti‐adalimumab antibodies were no longer detectable in all five patients with anti‐adalimumab antibodies in whom the dosing frequency was increased. Increasing the dosing frequency might overload the capacity of the immune system to produce anti‐adalimumab, or alternatively induce immunotolerance. Interestingly, the disease activity (mean DAS28) improved considerably in these patients. It can be speculated that continuation of treatment with an increased dosing frequency of adalimumab can be effective in some patients with anti‐adalimumab antibody titres; however, dose escalation is not effective in all patients.8,15 In summary, these results show that anti‐adalimumab antibodies are associated with diminished adalimumab concentrations, which may be related to an increased clearance of serum adalimumab. Furthermore, a clear association was found between the presence of anti‐adalimumab antibodies and a diminished clinical response, indicating that the formation of anti‐adalimumab antibodies may be an explanation for non‐response to adalimumab treatment. Quantification of serum adalimumab and anti‐adalimumab antibody and learning more about the underlying factors that affect these concentrations should lead to more individualised and optimised treatment in the future.
We thank Els de Groot for preparation of the rabbit anti‐idiotype, and Henk de Vrieze and Shirley J. Janssen for performing the assays. We also acknowledge the research nurses, Marga Kammeijer‐Rippen and Margot P Colombijn, for performing clinical assessments.
DAS28 - disease activity score in 28 joints
DMARD - disease‐modifying anti‐rheumatic drug
EULAR - European League Against Rheumatism
HACA - human anti‐chimeric antibody
RA - rheumatoid arthritis
TNF - tumour necrosis factor
Funding: Abbott Laboratories. CAW is supported by a grant (945‐02‐029) from the Netherlands Organization for Health Research and Development (ZonMw). The study sponsors had no involvement in the study design, the collection, analysis, and interpretation of data, the writing of the report, or the decision to submit the paper for publication.
Competing interests: Professor Dijkmans and Professor Tak are members of the advisory board of Abbott and have received honoraria for lectures.