Synovial effusion and synovial fluid biomarkers in psoriatic arthritis to assess intraarticular tumor necrosis factor-α blockade in the knee joint

Introduction The purpose of this study was theevaluation of synovial effusion (SE), synovial fluid (SF) and synovial tissue (ST) biomarkers in relation to disease activity indexes to assess the response to intraarticular (IA) tumor necrosis factor (TNF)-α blockers in psoriatic arthritis (PsA). Methods Systemic and local disease activity indexes (disease activity score (DAS); the Ritchie articular index (mRAI), erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP); Thompson articular (THOMP) and joint articular (KJAI)-Index ) and ST samples were assessed at baseline, throughout treatment, and during the follow-up in 14 patients affected with PsA who underwent IA injections (0.5 ml to 12.5 mg) in the knee joint of etanercept (E) or placebo (P) once every two weeks for a 10-week period. Total SF white blood cell (WBC) counts (WBC/μl) and SF cytokine/chemokine (CK/CCK) levels were measured before IA-E at baseline, after IA-E, and as long as there were adequate amounts of SF for knee aspiration (post). Characterization of synovial mononuclear cell infiltration and synovial vessels was carried out in 8 out of 14 knees by staining serial sections of synovial tissue biopsies for CD45, CD3, CD68, CD31 and CD105. Results At baseline, CRP and/or ESR were significantly correlated with SF-CK (interleukin- (IL-)1β, IL-1Ra, IL-6, IL-8) and CCK (CCL3). Post-IA injections, there was a decrease in SE in the knees in which aspiration following IA-E injection was possible as well as a significant reduction in SF WBC/μl and in SF-CK (IL-1β, IL-1Ra, IL-6 and IL-22). Pre- and post-IA-E injections, there were significant correlations between ST markers and SF-CK (IL-1β with CD45; IL-1β and IL-6 with CD31) and between SF-CCK (CCL4 and CCL3 with CD3). At the end of the study, there was a significant reduction in disease activity indexes (CRP, DAS, RAI, THOMP, KJAI) as well as in the ST markers (CD45; CD3). Conclusions Synovial effusion regression is a reliable indicator of the response to IA TNF-α blockers in PsA patients as it is confirmed by the correlation between SF biomarkers to disease activity and synovial tissue inflammation.


Introduction
Actively inflamed joints in psoriatic arthritis (PsA) patients unresponsive to systemic treatments [1] show comparable levels of functional [2] and radiological disease progression [3] compared to those in rheumatoid arthritis (RA).
Prominent vascular alterations just beneath the lining cell layer, reduced layer lining thickness, and lower CD68 expression are distinctive features of PsA synovitis with respect to RA [4,5]. Tumor necrosis factor-alpha (TNF-α) plays an important role in the chronic inflammation found in PsA patients, and its increased expression together with that of other pro-inflammatory cytokines, including interferon-γ (IFN-γ), interleukin (IL) -12, IL-15, IL-17 and IL-18, and in particular, IL-6 and IL-1β, have been demonstrated in PsA synovium [6,7]. Disease-related cytokines in synovial tissue may also promote osteoclast formation resulting in bone erosion [8].
While the efficacy of TNF-α-blocking agents in reducing disease activity in PsA patients [9,10] has been demonstrated, their actual mechanisms of action are not completely understood [11][12][13]. Recent research has made it possible to identify new genetic factors [14,15] and immunopathological mechanisms common to psoriasis and psoriatic joint inflammation [16,17].
Genetic risk factors have implicated the interleukin (IL)-23 pathway and the induction and regulation of type 17 T-helper (TH-17) cells in the pathogenesis of psoriasis [18,19]. Secretion of cytokines, such as IL-22 and IL-17, could, moreover, induce keratinocyte proliferation and skin inflammation [19,20].
Biomarkers have been used as surrogate treatment endpoints in preliminary, short-term, proof-of-concept studies [21], but only limited data concerning biological biomarkers in psoriasis and psoriatic arthritis are available. It has been seen that histological findings are not correlated with clinical disease parameters [5]. The expressions of RANK ligand and osteoprotegerin (OPG) are similar in non-psoriatic spondyloarthropathy (SpA) as compared to PsA spondyloarthropathy [8], but neither are related to the degree of systemic or local inflammation, nor are they significantly modulated by effective response to TNF-α blockers [16,22]. The need, therefore, of reliable biomarkers to assess disease progression in PsA is clearly indisputable [21].
The aim of this longitudinal study was to investigate synovial effusion (SE), synovial fluid (SF) and synovial tissue (ST) biomarkers in relation to local and systemic disease activity biomarkers to assess the outcome of intra-articular (IA) TNF-α blockade therapy on gonarthritis in PsA patients [23][24][25].

Materials and methods
IA-treatment was assessed by means of a single blind comparison between IA-etanercept (E) and IA-placebo (P), administered once every two weeks for a 10-week period in all those patients not needing to drop-out because of drug inefficacy, with a cross-over after the first IA injection. Those needing to drop-out were included in the open-label extension part of the study during which four IA-E injections were administered once every two weeks. Each 0.5 ml IA-injection (E: 12.5 mg, placebo: NaCl) was administered in individual knee joints after synovial fluid aspiration. The mean cumulative IA-E dosage for all of the patients was 50 mg for both the blind and open-label extension study. The study protocol (Etanercept/TNR-001:n.878P) was approved by the local ethics committee (Padova, 20 September 2004) and all patients signed consent statements after being informed about the intent and the methodology of the study [26].
PsA was defined as the presence of both psoriasis and inflammatory arthritis, regardless of their rheumatoid factor (RF) status. All 14 patients participating in the study fulfilled the CASPAR (CLASsification criteria for Psoriatic ARthritis) classification criteria for PsA [27]. The psoriasis area and severity index (PASI) was less than 10 in these patients. Affected with active gonarthritis, which was characterized by pain, tenderness, and effusion, all of the patients were being treated with stable DMARD, steroid, and/or E systemic therapy.

Assessment
Patients' responses to therapy were blindly assessed by the same investigator (LC).
SF cell counts (C/μl) were performed on all of the samples aspirated before IA-E injection throughout the entire study.
The primary efficacy endpoint utilized was the knee Thompson Articular Index (THOMP) [28], a sum of scores for each knee joint concerning pain on movement (0 to 3), soft tissue swelling (0 to 3) and warmth (0 to 3); (range 0 to 9). The secondary efficacy endpoint was: the Knee Joint Articular Index (KJAI), already validated in RA, PsA, and SpA-Knee Joint Synovitis (KJS) patients, likewise a sum of scores (0 to 14) for tenderness (0 to 3), joint swelling (0 to 3), the ballottement of patella or the bulge sign (0 to 2), the range of knee joint flexion (0 to 3) and extension (0 to 3) [29].
The systemic secondary endpoints were: (i) The modified Ritchie Articular Index (mRAI), a sum of scores assessing 30 joints for tenderness (0 to 3) including hand and foot Distal Interphalangeal Joints (DIP) with each side considered as a group score (DIP involvement is often observed in oligo-and poli-PsA patients) [30] and the Disease Activity Score (DAS). (ii) Erythrocyte Sedimentation Rate (ESR) (≤ 28 mm/h) and serum C-reactive Protein (CRP) values (≤ 0.5 mg/dl) were assessed at baseline and at the end of the study.

Synovial fluid biomarkers
SF samples, aspirated from knee joints before the first IA-E injection, at baseline, and before each IA-E injection, were collected and frozen at -80°.
The post-treatment synovial effusion was defined as the last SF sample available for aspiration after one or more IA-E injections in each knee. The last SF sample available from each knee (post-treatment) underwent synovial effusion analysis. The SF samples were analysed for total white blood cell (WBC) counts (WBC/μl). The cytokines: IL-1β, IL-1 receptor antagonist (IL-1Ra), IL-6, IL-17, TNF-α, IFN-γ, the CXC chemokine IL-8, the CC chemokines, CCL2, the monocyte chemoattractant protein-1 (MCP-1), CCL3, the macrophage inflammatory protein (MIP-1α) and CCL4, the macrophage inflammatory protein-1β (MIP-1β), were measured using a commercially available multiplex bead immunoassay, based on the Luminex platform (Fluorokine MAP Multiplex Human Cytokine Panel A, R&D Systems, Minneapolis, MN, USA) following the manufacturer's instructions. Normal serum values were those established in 50 healthy blood donors. IL-22 was measured using a commercially available ELISA kit (Quantikine Human IL-22, R&D Systems). SF was centrifuged before determinations were made at 1,000 g to remove cells and debris.

Synovial biopsy
Synovial biopsies were carried out during arthroscopy while patients were under the effect of anaesthesia, no earlier than two weeks before the first IA-E injection and no later than two to four weeks after the last one. Synovial specimens were obtained targeting the areas of intense synovial hyperemic proliferation. Multiple biopsy samples from each patient were stored in paraformaldehyde and embedded en bloc in paraffin.

Immunohistochemistry
Characterization of synovial mononuclear cell infiltration and synovial vessels was carried out in consecutive serial sections of synovial biopsies obtained from eight patients before the first and after the last IA-E injection. In particular they were immunostained by using the following antibodies: CD3 (Novocastra, Newcastle Upon Tyne, UK), CD68, CD45 (clone 2B11), CD31 (clone JC70A), CD105 (SN6h) (Dako Cytomation, Glostrup, Denmark). All the parameters were measured by computer-assisted morphometric analysis (Image Proplus version 5) and a 2 mm square area was evaluated.

Statistical analysis
Mean and standard deviations were used as descriptive statistics. Changes over time of selected outcomes and biological markers after IA-E treatment were evaluated using the non-parametric Wilcoxon Signed Rank test. All analyses were performed using SPSS software (SPSS 15.0 (SPSS Inc., Chicago, IL, USA). The Spearman Rank test was used for correlation analysis.

Results
The main clinical details as well as systemic disease activity indexes of all patients are listed in Table 1. Four PsA patients were being treated with parenteral E from the time of screening to the end of the IA treatment period.
SF samples were aspirated immediately before the first IA injection from all 14 knees. There was a decrease in SE in the knees in which aspiration following IA-E injection was possible. In 10 knees the effusion disappeared before the fifth IA-E injection (Figure 1). There was a statistically significant reduction in synovial fluid WBC/μl when pre and post IA-E values were compared. (Figure 2a).
The Thompson Articular Knee Index values were significantly reduced (Figure 2b) in the 14 knees at the post-treatment assessment (at the time the last SF sample was available) as well as at the end of the study (two weeks after the last IA-E injection), and there were no differences in the results between these two points in time. A statistically significant reduction in the systemic biological (CRP: 0.86 ± 0.95 and 031 ± 0.26, P = 0.019) and clinical (DAS: 2.93 ± 0.43 and 2.24 ± 0.90, P = 0.002, mRAI: 7.50 ± 4.88 and 4.71 ± 5.37, P = 0.011) disease activity indexes was observed at the end of the study, as well as statistically significant reduction of local composite (THOMP; KJAI) disease activity indexes at the post-treatment assessment (Figure 2b, c) and the end of the study.

Discussion
The aim of this longitudinal study was to evaluate SE, SF and ST biomarkers to assess the response to intra-articular TNF-α blockade therapy in PsA patients. The study's most striking finding was that synovial effusion disappeared in the knees of PsA patients, indicating that the therapy was effective. Its regression in the   The delay in the response of several knees of PsA patients after IA TNF-α blockade, may indicate that drug dosage was insufficient to control local knee disease activity.
The expression of proinflammatory cytokine/chemokine at baseline in the SF of the PsA patients is consistent with previous findings in the SF [31,32] and in the ST [5][6][7]11,33] of these patients. IL-6 concentrations were similar in the SF of RA and SpA to PsA [34] while higher IL-17 levels were observed in the SF of SpA to PsA [35][36][37]. At baseline, IL-1β was correlated to IL-6 levels in SF as well as to CD45 expression in ST and MIP-1 β/ CCL4 was correlated to post CD3 expression in ST.
High circulating [38] and SF levels of (MCP-1)/CCL2 have been observed in RA, PsA and SpA patients [34,39,40] and were also associated to the response to etanercept in RA patients [41]. In PsA, localized CCL2 production was correlated to the T cell infiltration of PsA synovium [42]. In accordance with previous reports, our findings in the SF of PsA patients support the hypothesis that (MCP-1)/CCL2, MIP-1α/CCL3 and MIP-1β/CCL4 chemokines play an important role in PsA development [43].
Elevated IL-22 expression in the SF of PsA patients, a novel finding in our patients, suggests that the Th17   system may have an underlying role in both skin [20] and joint involvement. The potential proinflammatory function in joints of IL-22, a cytokine of the IL-10 family, has been suggested by IL-22 mRNA expression by macrophages and fibroblasts, by MCP-1/CCL2 production and fibroblast proliferation of RA patients [44] and by the promotion of osteoclastogenesis in collagen induced arthritis [45]. Alterations in CD45 and CD3 ST expressions are in agreement with the decrease in the global cellular infiltration and T-lymphocytes, already found to be associated with active systemic anti TNF-α treatment in both Ra and PsA [46][47][48].
With regard to serum biological biomarkers, IL-6, ILra, IL-10 and ESR have been studied in PsA, but only IL-1ra and ESR have been found to reflect disease activity [49,50]. ESR and C-reactive protein were found to be closely correlated to TNF-α blockade response [51,52], but not to cytokine levels [21].
No previous study has evaluated the correlation between SF biomarkers and systemic and local composite disease activity indexes in PsA patients [53,54]. Synovial fluid analysis carried out in our patients during this study indicates that SF biomarkers are correlated to ST inflammation markers and to local and systemic indexes of disease activity in PsA.
Serum IL-17 does not seem to be influenced by TNF-α blockade following etanercept and infliximab both in SpA and in RA [35,55]. According to experimental data, TNF-α may lead to an increased activity of other proinflammatory pathways [56][57][58]. The fact that IL-22 and IL-17 do not react in the same way in the SF of PsA would seem to indicate that they have distinct regulatory pathways [59,37] and different cellular sources [60][61][62].
This study has important limitations: use of monovariate statistical methods, the limited number of patients studied, the concomitant DMARD treatment, the differences in the drug doses utilized, and the number of injections administered. Larger, controlled studies are, therefore, clearly warranted to further assess their clinical relevance.

Conclusions
Regression of synovial effusion is a reliable indicator of the response to intra-articular TNF-α blockade therapy in PsA patients as it is confirmed by the correlation of SF biomarkers to disease activity and synovial tissue inflammation.