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Arthritis Research & Therapy

Research article
Open Access

Protection against cartilage and bone destruction by systemic interleukin-4 treatment in established murine type II collagen-induced arthritis

  • Leo AB Joosten1,
  • Erik Lubberts1,
  • Monique MA Helsen1,
  • Tore Saxne1, 2,
  • Christina JJ Coenen-de Roo1, 3,
  • Dick Heinegård1, 2 and
  • Wim B van den Berg1
Arthritis Research & Therapy19991:81

https://doi.org/10.1186/ar14

©  Current Science Ltd 1999

Received: 26 August 1999

Accepted: 8 October 1999

Published: 26 October 1999

Statement of findings

Destruction of cartilage and bone are hallmarks of human rheumatoid arthritis (RA), and controlling these erosive processes is the most challenging objective in the treatment of RA. Systemic interleukin-4 treatment of established murine collagen-induced arthritis suppressed disease activity and protected against cartilage and bone destruction. Reduced cartilage pathology was confirmed by both decreased serum cartilage oligomeric matrix protein (COMP) and histological examination. In addition, radiological analysis revealed that bone destruction was also partially prevented. Improved suppression of joint swelling was achieved when interleukin-4 treatment was combined with low-dose prednisolone treatment. Interestingly, synergistic reduction of both serum COMP and inflammatory parameters was noted when low-dose interleukin-4 was combined with prednisolone. Systemic treatment with interleukin-4 appeared to be a protective therapy for cartilage and bone in arthritis, and in combination with prednisolone at low dosages may offer an alternative therapy in RA.

Keywords

bone destructioncartilage oligomeric matrix protein levelscollagen-induced arthritisinterleukin-4prednisolone

Abstract

Introduction

Rheumatoid arthritis (RA) is associated with an increasedproduction of a range of cytokines including tumour necrosis factor(TNF)-α and interleukin (IL)-1, which display potent proinflammatoryactions that are thought to contribute to the pathogenesis of the disease.Although TNF-α seems to be the major cytokine in the inflammatory process,IL-1 is the key mediator with regard to cartilage and bone destruction. Apartfrom direct blockade of IL-1/TNF, regulation can be exerted at the level ofmodulatory cytokines such as IL-4 and IL-10. IL-4 is a pleiotropic T-cellderived cytokine that can exert either suppressive or stimulatory effects ondifferent cell types, and was originally identified as a B-cell growth factorand regulator of humoral immune pathways. IL-4 is produced by activatedCD4+ T cells and it promotes the maturation of Th2 cells. IL-4stimulates proliferation, differentiation and activation of several cell types,including fibroblasts, endothelial cells and epithelial cells. IL-4 is alsoknown to be a potent anti-inflammatory cytokine that acts by inhibiting thesynthesis of proinflammatory cytokines such as IL-1, TNF-α, IL-6, IL-8 andIL-12 by macrophages and monocytes. Moreover, IL-4 stimulates the synthesis ofseveral cytokine inhibitors such as interleukin-1 receptor antagonist (IL-1Ra),soluble IL-1-receptor type II and TNF receptors IL-4 suppressesmetalloproteinase production and stimulates tissue inhibitor ofmetalloproteinase-1 production in human mononuclear phagocytes and cartilageexplants, indicating a protective effect of IL-4 towards extracellular matrixdegradation. Furthermore, IL-4 inhibits both osteoclast activity and survival,and thereby blocks bone resorption in vitro. Of great importance isthat IL-4 could not be detected in synovial fluid or in tissues. This absenceof IL-4 in the joint probably contributes to the disturbance in the Th1/Th2balance in chronic RA.

Collagen-induced arthritis (CIA) is a widely used model ofarthritis that displays several features of human RA. Recently it wasdemonstrated that the onset of CIA is under stringent control of IL-4 andIL-10. Furthermore, it was demonstrated that exposure to IL-4 during theimmunization stage reduced onset and severity of CIA. However, after cessationof IL-4 treatment disease expression increased to control values.

Aims

Because it was reported that IL-4 suppresses severalproinflammatory cytokines and matrix degrading enzymes and upregulatesinhibitors of both cytokines and catabolic enzymes, we investigated the tissueprotective effect of systemic IL-4 treatment using established murine CIA as amodel. Potential synergy of low dosages of anti-inflammatoryglucocorticosteroids and IL-4 was also evaluated.

Methods

DBA-1J/Bom mice were immunized with bovine type II collagen andboosted at day 21. Mice with established CIA were selected at day 28 afterimmunization and treated for days with IL-4, prednisolone, or combinations ofprednisolone and IL-4. Arthritis score was monitored visually. Joint pathologywas evaluated by histology, radiology and serum cartilage oligomeric matrixprotein (COMP). In addition, serum levels of IL-1Ra and anticollagen antibodieswere determined.

Results

Treatment of established CIA with IL-4 (1 μg/day) resultedin suppression of disease activity as depicted in Figure 1. Of great interest is that, although 1 μg/day IL-4 hadonly a moderate effect on the inflammatory component of the disease activity,it strongly reduced cartilage pathology, as determined by histologicalexamination (Fig. 1). Moreover, serum COMP levels weresignificantly reduced, confirming decreased cartilage involvement. In addition,both histological and radiological analysis showed that bone destruction wasprevented (Fig. 1). Systemic IL-4 administrationincreased serum IL-1Ra levels and reduced anticollagen type II antibody levels.Treatment with low-dose IL-4 (0.1 μg/day) was ineffective in suppressingdisease score, serum COMP or joint destruction. Synergistic suppression of botharthritis severity and COMP levels was noted when low-dose IL-4 was combinedwith prednisolone (0.05 mg/kg/day), however, which in itself was noteffective.

Discussion

In the present study, we demonstrate that systemic IL-4 treatmentameliorates disease progression of established CIA. Although clinical diseaseprogression was only arrested and not reversed, clear protection againstcartilage and bone destruction was noted. This is in accord with findings inboth human RA and animal models of RA that show that inflammation and tissuedestruction sometimes are uncoupled processes. Of great importance is that,although inflammation was still present, strong reduction in serum COMP wasfound after exposure to IL-4. This indicated that serum COMP levels reflectedcartilage damage, although a limited contribution of the inflamed synoviumcannot be excluded.

Increased serum IL-1Ra level (twofold) was found after systemictreatment with IL-4, but it is not likely that this could explain thesuppression of CIA. We and others have reported that high dosages of IL-1Ra areneeded for marked suppression of CIA. As reported previously, lower dosages ofIL-4 did not reduce clinical disease severity of established CIA. Of importanceis that combined treatment of low dosages of IL-4 and IL-10 appeared to havemore potent anti-inflammatory effects, and markedly protected against cartilagedestruction. Improved anti-inflammatory effect was achieved withIL-4/prednisolone treatment. In addition, synergistic effects were found forthe reduction of cartilage and bone destruction. This indicates that systemicIL-4/prednisolone treatment may provide a cartilage and bone protective therapyfor human RA.

Figure 1
Figure 1

Effects in mice of treatment with interleukin-4 or control ondisease activity, cartilage damage and bone destruction. Mice were treatedintraperitoneally for 7 days with either vehicle (control) or 1 μg/dayinterleukin-4 (IL-4). CIA, collagen-induced arthritis. *P< 0.05, versus control, by Mann-Whitney U test.

Introduction

Interleukin (IL)-4 is a pleiotropic T-cell-derived cytokine that can exert either suppressive or stimulatory effects on different cell types. It was originally identified as a B-cell growth factor and regulator of humoral immune pathways [1,2]. IL-4 is produced by activated CD4+ T cells and it promotes the maturation of Th2 cells. IL-4 inhibits the differentiation of naïve T cells to Th1 and cytokine (ie IL-2 and interferon-γ) production by Th1 cells [3]. IL-4 stimulates proliferation, differentiation or activation of several cell types, including fibroblasts, endothelium cells and epithelium cells [4]. IL-4 is also known to be a potent anti-inflammatory cytokine that acts by inhibiting the synthesis of proinflammatory cytokines such as IL-1, tumour necrosis factor (TNF)-α, IL-6, IL-8 and IL-12 by macrophages and monocytes [5,6,7]. Moreover, IL-4 stimulates the synthesis of several cytokine inhibitors such as interleukin-1 receptor antagonist (IL-1Ra), IL-1-receptor type II and TNF receptors [8,9,10]. IL-4 suppresses metalloproteinase production and stimulates tissue inhibitor of metalloproteinase-1 production in human mononuclear phagocytes and cartilage explants, indicating a protective effect of IL-4 towards extracellular matrix degradation [11,12]. Furthermore, IL-4 inhibits both osteoclast activity and survival, and thereby blocks bone resorption in vitro [13,14].

RA is associated with an increased production of a range of cytokines including TNFα and IL-1, which display potent proinflammatory actions that are thought to contribute to the pathogenesis of rheumatoid arthritis (RA) [15,16]. Although TNF-α seems to be the major cytokine involved in the inflammatory process, IL-1 is the key mediator with regard to cartilage and bone destruction [17,18]. Apart from direct blockade of IL-1/TNF, regulation can be exerted at the level of modulatory cytokines such as IL-4 and IL-10. Of great importance is that IL-4 could not be detected in synovial fluid and tissues [19,20], and this lack of IL-4 is likely to contribute to the uneven Th1/Th2 balance in chronic RA.

Although having a number of side effects, including osteoporosis and reduced adrenal function, glucocorticoids are potent and commonly used anti-inflammatory agents in human RA. Glucocorticoids downregulate proinflammatory cytokine production, such as IL-1 and TNF-α, by macrophages and monocytes via several mechanisms. One mechanism is through enhanced IκBα protein synthesis. IκBα forms inactive cytoplasmic complexes with nuclear factor-κB, which itself activates many immunoregulatory genes in response to proinflammatory cytokines [21,22]. Other mechanisms of action that have been reported recently [23] are downmodulation of histone acetyltransferase and upregulation of histone deacetyltransferase, which both affected messenger RNA transcription negatively.

Murine collagen-induced arthritis (CIA) is a widely used experimental model of arthritis. Neutralization of the monokines IL-1 and TNF-α before or during onset of arthritis arrested the development of CIA [24,25]. Expression of CIA is also under particularly stringent control by IL-4 and IL-10. Treatment with anti-IL-4/anti-IL-10 shortly before onset accelerated the disease expression [26]. Furthermore, it was demonstrated that IL-12 plays a crucial role in the development of CIA, because blockade of endogenous IL-12 completely prevented onset of the disease [27]. In accord with these findings, during onset of CIA predominantly Th1 responses towards collagen type II were found [28,29]. It has been claimed [30,31] that IL-4 exposure could induce immune deviation by enhanced development of Th2-like primary CD4 effector cells. Several animal studies indicated that IL-4 administration, starting just after immunization with the disease-inducing agent, ameliorated Th1-mediated models of autoimmune diseases such as diabetes in nonobese diabetic mice and experimental arthritis [32,33,34].

In the present study the effects of systemic high dose IL-4 therapy in established CIA were investigated. Furthermore, the potential synergy of combined prednisolone and IL-4 treatment were examined. We investigated the protective effect of IL-4 alone or in combination with prednisolone on disease activity as well as cartilage and bone destruction as determined histologically, radiologically and by serum measurements of cartilage oligomeric matrix protein (COMP). Anticollagen type II specific antibodies and serum IL-1Ra levels were assessed, in order to obtain an insight into the mechanism of action. The findings suggest that IL-4 treatment protects against cartilage and bone destruction, and that combined IL-4/steroid treatment may provide a safe, anti-inflammatory and anti-destructive therapy in human RA.

Materials and methods

Animals

Male DBA-1/Bom mice were purchased from Bomholdgård (Ry, Denmark). The mice were housed in filter top cages, and were given free access to water and food. The mice were immunized at the age of 10–12 weeks.

Materials

Complete Freund's adjuvant and Mycobacterium tuberculosis (strain H37Ra) were obtained from Difco Laboratories (Detroit, MI, USA). Bovine serum albumin and prednisolone 21-sodium succinate (P-4153) were purchased from Sigma Chemicals (St Louis, MO, USA). Antimurine IL-1Ra antibodies (capture MAP-480, detection BAF-480) were obtained from R&D Systems (Minneapolis, MN, USA). PolyHRP-streptavidine (M2032) and Caseine colloid buffer (M2052) was from CLB (Amsterdam, The Netherlands). Recombinant murine IL-1Ra was purchased from R&D systems. Recombinant murine IL-4 (6.5 × 107 U/mg) was kindly provided by Dr S Smith (Schering-Plough, Kenilworth, NJ, USA).

Collagen preparation

Articular cartilage was obtained from metacarpophalangeal joints of 1–2 year old cows. Bovine type II collagen was prepared according to the method of Miller and Rhodes [35]. It was dissolved in 0.05 mol/l acetic acid (5 mg/ml) and stored at -70ºC.

Immunization

Bovine type II collagen was diluted with 0.05 mol/l acetic acid to a concentration of 2 mg/ml and was emulsified in an equal volume of complete Freund's adjuvant (2 mg/ml MT H37Ra). The mice were immunized intradermally at the base of the tail with 100 μl emulsion (100 μg collagen). At day 21 the animals were boosted with an intra-peritoneal injection of 100 μg collagen type II, diluted in phosphate-buffered saline (pH 7.4).

Assessment of arthritis

Mice were examined for visual appearance of arthritis in peripheral joints, and scores for severity were given (arthritis score) as previously described [17,18,25,26,27]. Mice were considered arthritic when significant changes in redness and/or swelling were noted in digits or in other parts of the paws. At later time points ankylosis was also included in the arthritis score. Clinical severity of arthritis was graded on a scale of 0–2 for each paw, according to changes in redness and swelling: 0, no changes; 0.5, significant; 1.0, moderate; 1.5, marked; and 2.0, maximal swelling and redness, and later on ankylosis. Arthritis score (mean± stan-dard deviation) was expressed as cumulative value for all paws, with a maximum of eight and expressed as percentage of the initial score at the beginning of treatment.

Treatment of collagen-induced arthritis with interleukin-4,prednisolone or interleukin-4/prednisolone

To evaluate the effect of IL-4, prednisolone or the combination IL-4/prednisolone on established CIA, mice with CIA were selected at day 28 and divided into groups of at least 10 mice with similar arthritis scores. Thereafter, mice were treated twice a day intraperitoneally with IL-4 (0.1 or 1μg/day), prednisolone (0.05 mg/kg/day), or with IL-4 and prednisolone (at the same doses for the noncombined regimens) for each of several days as indicated in the results.

Determination of interleukin-1 receptor antagonist levels

IL-1Ra was measured using enzyme-linked immunosorbent assay (ELISA). Briefly, Nunc Maxisorb ELISA plates (Nunc, Rostilde, Denmark) were coated with capture antibodies (5 μg/ml, carbonate buffer, pH 9.6, 24 h at 4°C), and thereafter nonspecific binding sites were blocked with 1% bovine serum albumin/phosphate-buffered saline-Tween. Standards and unknown samples were diluted in normal DBA-1 serum and incubated for 3 h at room temperature. Biotinylated detection antibodies were added at concentrations of 0.2–0.4 μg/ml in 0.5% bovine serum albumin in phosphate-buffered slaine-Tween for 1.5 h at room temperature. Thereafter plates were incubated with PolyHRP (0.1 μg/ml in 1% caseine colloid buffer) for 45 min and orthophenylenediamine (0.8 mg/ml) was used as substrate. Plates were read at 495 nm.

Measurement of cartilage oligomeric matrix protein

At the end of the experiments, serum samples were taken and murine cartilage oligomeric matrix protein (COMP) levels were determinated using ELISA under similar conditions as those described for the assay for human COMP [36]. The assay was modified by using rat COMP for coating the microtitre plates, the standard curve included in each plate and by using the polyclonal antiserum raised against rat COMP to detect the antibody [37,38]. A high cross-reactivity was found to murine COMP [39]. This was shown by parallel dilution curves of murine sera to the standard curve prepared with rat COMP, as well as in experiments in which a dilution of murine serum was added to the standard curve.

Determination of anticollagen antibodies

Antibodies against bovine type II collagen were examined by using an ELISA. Titres of total IgG, IgG1 and IgG2a were measured. Briefly, plates were coated with 10 μg bovine type II, and thereafter nonspecific bindings sites were blocked with 0.1 mol/l ethanolamin (Sigma Chemicals). Serial 1 : 2 dilutions of the sera were added, followed by incubation with isotype-specific goat antimouse peroxidase (Southern Biotechnology Associates, Birmingham, AL, USA) and substrate (5-aminosalicyclic acid; Sigma Chemicals). Plates were read at 492 nm. Titres were expressed as means ± standard deviation dilution, which gives the half maximal value.

Radiological analysis of bone destruction

At the end of the experiments, knee joints were removed and used for radiological analysis as a measure of bone destruction. Radiographs were carefully examined using a stereo microscope, and joint destruction was graded on a scale from 0 to 5, ranging from no damage, minor bone destruction observed as one enlightened spot, moderate changes, two to four spots observed in one area, marked changes, two to four spots observed in more areas, severe erosions afflicting the joint, complete destruction of joint and/or new bone formations. Bone destruction was scored on the femoral head, tibia and patella as described previously [17].

Histology

Mice were killed by ether anaesthesia. Knee joints were removed and fixed for 4 days in 4% formaldehyde. After decalcification in 5% formic acid, the specimens were processed for paraffin embedding [17,18,25,26,27]. Tissue sections (7 μm thick) were stained with haematoxylin and eosin, or safranin O. Histopathological changes were scored using the following parameters.

Infiltration of cells was scored on a scale from 0 to 3, depending on the amount of inflammatory cells in the synovial tissues. Inflammatory cells in the joint cavity were graded on a scale from 0 to 3 and expressed as exudate. Cartilage proteoglycan depletion was determined using safranin O staining. The loss of proteoglycans was scored on a scale from 0 to 3, ranging from fully stained cartilage to destained cartilage or complete loss of articular cartilage. A characteristic parameter in CIA is the progressive loss of articular cartilage. This destruction was separately graded on a scale from 0 to 3, ranging from the appearance of dead chondrocytes (empty lacunae) to complete loss of the articular cartilage. Bone erosion was scored on a scale ranging from 0 to 3, ranging from no abnormalities to complete loss of cortical and trabecular bone of the femoral head and patella. Histopathological changes in the knee joints were scored in the patella/femur region on 5 semiserial sections of the joint, spaced 70 μm apart. Scoring was performed on decoded slides by two observers, as described earlier [17,18,25,26,27].

Statistical analysis

Differences between experimental groups were tested using the Mann-Whitney U test, unless otherwise stated.

Results

Amelioration of arthritis score in collagen-induced arthritis byin vivo treatment of interleukin-4

To investigate effects of in vivo treatment of established CIA with IL-4, mice that expressed CIA at day 28 after immunization were injected intraperitoneally with vehicle, 0.1 or 1 μg IL-4 per day. Figure 2 shows that administration of 1 μg/day IL-4 results in significant amelioration of the arthritis score, but a lower dosage of 0.1 μg/day IL-4 was without effect. The anti-inflammatory effect of 1 μg/day IL-4 was further illustrated in Figure 3, in which disease progression is expressed as change in (Δ) disease activity of all individual mice. Increased severity of CIA score can be seen in animals treated either with vehicle or 0.1 μg/day IL-4, whereas significantly decreased disease activity was noted after treatment with 1 μg/day IL-4. Histology revealed that no effect was found on the influx of inflammatory cells in joint tissues of IL-4-treated animals when compared with the vehicle-treated animals (Table 1).

Interleukin-4 protects against cartilage destruction

Systemic treatment with high-dose IL-4 (1μg/day) significantly decreased cartilage destruction, determined as chondrocyte death and cartilage erosions (Fig. 4,Table 1). It did not result in a significantly reduced loss of matrix proteoglycans, as determined by safranin O staining (Fig. 5, Table 1). It has been demonstrated (data not shown) that there is a strong correlation between severe cartilage damage and increased serum COMP levels during murine CIA. In naïve DBA-1 mice, serum COMP levels are approximately 4.0 μg/ml and COMP levels increased up to 8–12 μg/ml in mice with fully established CIA. Serum COMP levels were determined in the various groups to identify the protection against severe cartilage destruction by IL-4. Figure 6 shows that elevated COMP in CIA were not reduced by treatment with low-dose IL-4. It is of particular interest, that treatment with high-dose IL-4 (1 μg/day) significantly reduced serum COMP levels to values found in nonarthritic control animals.

Interleukin-4 protects against bone destruction

Bone destruction, which is a common feature of murine collagen arthritis, was examined by radiological analysis. Radiographs of knee joints were taken at the end of the treatment period. Figure 7 showed that treatment with 1 μg/day IL-4 was sufficient to prevent bone destruction, determined as bone erosions on the head of the femur, the patella and the tibia. Little or no effect was noted after treatment with low-dose IL-4. Histological analysis of knee joints corroborated the protective effect of IL-4 (Table 1). Figure 8 (a, c) depicts degradation of patellar and femural cortical bone by osteoclasts in the vehicle-treated group, whereas almost no osteoclasts were seen in the IL-4-treated group (Fig. 8d).

Combined interleukin-4/prednisolone treatment

We examined potential synergistic effects of IL-4 and prednisolone, using low-dose prednisolone (0.05 mg/kg/day) and 0.1 or 1μg/day IL-4. Treatment of CIA with IL-4/prednisolone completely arrested the development of inflammatory signs of CIA (Figs 2 and 3). Both combinations tested revealed full suppression of disease progression. In accord with previous observations, mice treated with 0.05 mg/kg/day prednisolone alone did not show significant suppression of arthritis. Histology taken after 7 days of treatment showed enhanced safranin O staining only in animals treated with IL-4/prednisolone (1 μg per kg/0.05 kg daily), indicating reduced depletion of matrix proteoglycans (Table 1, Fig. 5d). This was in accord with the marked reduction in joint inflammation, as can be seen in Figure 4d. Both combinations of IL-4 and prednisolone reduced serum COMP to values found in naïve DBA-1 mice. Interestingly, synergistic suppression of serum COMP was noted after exposure to low-dose IL-4 and prednisolone (Fig. 6). In contrast to serum COMP levels, combined IL-4/prednisolone treatment did not result in synergistic protection against bone destruction. High-dose IL-4 alone was already highly effective, and the combination of IL-4 with prednisolone did not improve the effect further, or was there an adverse effect of prednisolone (Table 1, Figs 7 and 8b). Treatment of CIA with 1 μg/day IL-4 alone and in combination with prednisolone (0.05 mg/kg/day) for 7 days caused similar reduction in osteoclast numbers (data not shown).

Effect of interleukin-4, or interleukin-4/prednisolone treatmenton interleukin-1 receptor antagonist and anticollagen antibody levels

Serum IL-1Ra levels were determined at the end of the experiments and Table 2 shows a twofold increase after IL-4 treatment (1μg/day dose). Treatment with 0.1μg/day IL-4 showed no significant effects on serum IL-1Ra levels. Prednisolone reduced IL-1Ra levels when compared with vehicle-treated animals. In accord with these findings, combined IL-4/prednisolone (1 μg per day/ 0.05 mg per kg per day) treatment resulted in lower IL-1Ra levels than found with IL-4 alone.

Anticollagen antibodies were assayed at the end of treatment period at day 35. The antibody levels increased rapidly after clinical expression of CIA around day 28 after immunization. After IL-4 (1μg/day) treatment for 7 days, total IgGs levels as well as IgG1 and IgG2a anticollagen type II antibody levels were lower compared with vehicle treated animals (Fig. 9). Although all anticollagen type II antibodies were reduced, IgG2a levels showed the most prominent reduction, indicating an effect on the Th1 rather than on the Th2 immune response. No decreased anticollagen type II antibody levels were found after treatment with low-dose IL-4. The high-dose IL-4/prednisolone regimen reduced anticollagen type II antibodies to levels similar to those found after treatment with 1μg/day IL-4.
Figure 2
Figure 2

Dose dependent suppression of disease activity of collagen-inducedarthritis (CIA) by interleukin (IL)-4 and the combination of IL-4/prednisolone(Pred). Mice with established CIA were divided into separate groups of at least10 mice. Groups were treated intraperitoneally twice a day with vehicle, IL-4,prednisolone, or combined IL-4/prednisolone for 8 consecutive days. The datarepresent the mean arthritis score, expressed as percentage of initial value atday 28. Experiments were repeated once with approximately the same outcome.*P < 0.05, versus vehicle, by Mann-Whitney U test.

Figure 3
Figure 3

Dose-dependent arrest of disease activity by treatment withinterleukin (IL)-4 and IL-4/prednisolone (Pred). The enhanced disease activitybetween days 28 and 35 of each individual mouse is expressed as change in(Δ) disease activity. For treatment protocol, see Fig. 2. P < 0.05, versus vehicle, by Mann-Whitney Utest.

Figure 4
Figure 4

Interleukin (IL)-4 treatment reduced cartilage destruction,whereas IL-4/prednisolone treatment additionally decreased cell influx.(a) Knee joint from vehicle-treated mouse. Severe cartilage destructioncan be seen. Empty lacunae reflects chondrocyte death as marker of cartilagedestruction, indicated by arrows. (b) Knee joint of a mouse treated withIL-4 1 μg/kg/day for eight consecutive days. Note the reduced cartilagedestruction and chondrocyte death. (c) Knee joint of vehicle-treatedanimal. Note the severe cell influx in synovial tissues and joint cavity.(d) Knee joint of a mouse treated with IL-4/prednisolone (1 μg perday/0.05 mg per kg). Note the marked reduction of cell influx. All specimenswere sampled at day 35. P, patella; F, femur; JS, joint space; C, cartilage; S,synovium. Haematoxylin and eosin staining was used. Original magnifications:× 200 (a, b) and × 100 (c, d).

Figure 5
Figure 5

Effect of IL-4 or IL-4/prednisolone treatment on matrixproteoglycan loss. (a) Knee joint of a control naïve mouse. Thefully stained cartilage layers indicate no loss of proteoglycans. (b) Knee joint of an arthritic mouse treated with vehicle. Note the severe jointinflammation and complete loss of safranin O staining of the cartilage layers(indicated by arrows). (c) Mouse treated with IL-4 (1 μg/day).Loss of matrix proteoglycan can still be seen. (d) Knee joint of a mousetreated with IL-4/prednisolone (1 μg per day/0.05 mg per kg). Markedreduction in matrix proteoglycan depletion after combined treatment. Fordetails see Fig. 4. Safranin O staining, originalmagnification × 100.

Figure 6
Figure 6

Serum cartilage oligomeric matrix protein (COMP) level as a markerof cartilage turnover. Suppression of serum COMP was found after treatment withinterleukin (IL)-4 and IL-4/prednisolone (Pred). IL-4(1 μg/day) and bothdoses (0.1 μg per day/0.05 mg per kg per day; and 1 μg perday/0.05 mg per kg per day) of IL-4/prednisolone reduced serum COMP levels tobasic levels as found in nonimmunized animals (4.2 ± 0.2 μg/ml). Thedata represent the mean± standard deviation COMP level of at least sixsera per group. *P < 0.01, versus vehicle, byMann-Whitney U test.

Figure 7
Figure 7

Protection of interleukin (IL)-4 and IL-4/prednisolone (Pred)treatment on bone destruction. Knee joints were isolated at day 35 and bonedestruction was examined by radiographic analysis. For treatment scheme seeFig. 2. Erosions were scored on a scale ranging from 0 to5 on the femur head, tibia and patella. Each group consists of at least nineknee joints per group. *P < 0.01, versus vehicle, byMann-Whitney U test.

Figure 8
Figure 8

Bone destruction is prevented by interleukin (IL)-4 andIL-4/prednisolone treatment. (a) Severe bone destruction in patella andfemur in knee joint of vehicle-treated animal. (b) Almost no bonedegradation was noted after treatment with IL-4/prednisolone (1 μg perday/0.05 mg per kg). (c) Bone destruction in femur of a vehicle-treatedanimal at higher magnification. Osteoclasts, large multinuclear cells, locatedat the site of bone destruction (arrows). (d) No osteoclast-like cellswere found in IL-4 (1 μg/day) treated animals. For treatment details seeFig. 4. S, synovium; B, bone; BM, bone marrow. Originalmagnifications × 200 (a, b), × 400 (c, d).

Figure 9
Figure 9

Interleukin (IL)-4 or IL-4/prednisolone (Pred) treatment isassociated with reduced anticollagen type II (CII) antibody levels. Treatmentwith 1 μg/day IL-4 resulted in lower anticollagen type II antibodies.Total Immunoglobulins (Ig tot), IgG1 and IgG2a levelswere reduced. Similar effects were found after treatment with IL-4/prednisolone(1 μg per day/0.05 mg per kg). Anticollagen type II levels were determinedin at least six mice per group. Data are expressed as means ± standarddeviation dilution, which gives the half maximal value.

Table 1

Effect of prednisolone, interleukin (IL)-4 or IL-4/prednisolone treatment on the joint pathology of collagen-induced arthritis in Mice

   

Cartilage

Proteoglycan

Bone

 

Treatment

Dose

Infiltrate

destruction

loss

erosin

n

Vehicle

-

2.3 ± 0.9

2.2 ± 0.9

2.7 ± 1.0

1.9 ± 0.9

20

Prednisolone

0.05

2.1 ± 0.8

2.1 ± 1.2

2.6 ± 0.6

1.7 ± 1.1

20

IL-4

0.1

2.5 ± 0.7

2.5 ± 0.8

2.9 ± 0.3

2.0 ± 0.8

10

IL-4

1

2.0 ± 1.0

1.2 ± 0.8*

2.0 ± 0.7

0.6 ± 0.6*

20

IL-4/prednisolone

0.1/0.05

2.1 ± 0.4

1.6 ± 0.7

2.5 ± 0.8

2.1 ± 0.6

10

IL-4/prednisolone

1/0.05

1.2 ± 0.5*

1.1 ± 0.9*

1.4 ± 0.7*

0.4 ± 0.5*

10

Histopathology scores of arthritic knee joints after treatmentwith vehicle, IL-4, prednisolone or the combination of IL-4/prednisolone. Micewere sacrified and knee joints were used for histology. Histology was scored asindicated in the Materials and methods section. Mice were treated twice a dayintraperitoneally with either prednisolone (0.05 mg/kg), or IL-4 (0.1 or 1μg/day], or IL-4 (at both dosages) combined with prednisolone(0.05 mg/kg). *P <0.05, versus vehicle, by Mann-Whitney Utest.

Table 2

Serum interleukin-1 receptor antagonist (IL-1Ra levels) after treatment with either interleukin (IL)-4, prednisolone, or IL-4/prednisolone

Treatment

Dose

IL-1Ra (pg/ml)

Vehicle

-

414 ± 155

IL-4

0.1

386 ± 213

IL-4

1

838 ± 187*

Prednisolone

0.05

326 ± 165

IL-4/prednisolone

0.1/0.05

422 ± 129

 

1/0.05

499 ± 187

Serum IL-1Ra was determined using enzyme-linked immunosorbentassay at day 35 after immunization. Mice were treated as indicated in Table1. The data represent the mean± standard deviationof at least eight mice per group. The sensitivity of the IL-1Ra assay was towithin 160 pg/ml. *P < 0.05, versus vehicle, byMann-Whitney U test.

Discussion

The present study demonstrates clear tissue-protective effects of IL-4, although IL-4 did not prove to be a very potent anti-inflammatory cytokine. Both cartilage and bone erosion were prevented by IL-4 treatment of established CIA. Combination with low-dose prednisolone enhanced the anti-inflammatory capacity of IL-4. This might offer an attractive alternative to the use of high-dose prednisolone, because it can circumvent the unwanted side effects of the drug, including steroid-induced osteoporosis.

In previous studies of murine collagen arthritis [17,18,25] it was shown that TNF-α is important at onset of the disease, whereas IL-1 is the dominant cytokine, not only at the onset, but also in the progression of the arthritis and the concomitant cartilage destruction. Further support for the critical role of IL-1 is provided by the absence of collagen arthritis in IL-1β-deficient mice, and the marked reduction of this arthritis in ICE-deficient mice as well as in normal mice treated with IL-1β-converting enzyme inhibitors [40,41]. Moreover, reduced onset of arthritis was noted in TNF-receptor-deficient mice, but once a joint was afflicted the arthritis progressed to full-blown expression and cartilage destruction, again emphasizing that TNF is important in onset, but is not the dominant cytokine in progression and tissue destruction [42].

In recent studies, it was clearly demonstrated that onset of CIA is under stringent control of IL-4 and IL-10, because blockade of both IL-4 and IL-10 by the use of antibodies accelerated disease onset [26]. Furthermore, treatment of established murine CIA with low-dose IL-4 showed no suppressive effect on disease activity and joint pathology. Interestingly, combination of low-dose IL-4 and IL-10 appeared to have more potent anti-inflammatory effects, and resulted in protection against cartilage pathology [26]. Systemic treatment of murine CIA with high-dose IL-4 (3 μg/day) during the immunization stage delays onset as well as reduces severity. When IL-4 administration was terminated, however, disease expression and activity rapidly accelerated and was indistinguishable from that in the vehicle-treated control group [34]. Systemic IL-4 treatment of streptococcal cell wall arthritis in rats resulted in suppression of disease activity, and ameliorated the chronic destructive process leading to decreased lesions [33]. This was associated with enhanced levels of IL-1Ra, the natural inhibitor of IL-1, which is in accord with observations in the present study and with studies in humans systemically treated with IL-4 [43]. However, it is not likely that the twofold increment in serum IL-1Ra levels, found after IL-4 exposure, is sufficient to suppress CIA. As previously mentioned, blockade of IL-1 by anti-IL-1 antibodies or very high-dose IL-1Ra completely suppressed CIA and lead to full protection against joint pathology [17,18,25]. Whether IL-4 acts locally or systemically is at present unknown. Further experiments on biodistribution of IL-4 are needed to resolve this issue.

IL-4 levels are virtually undetectable in arthritic tissue of RA patients, suggesting that the disease is either a selective Th1 process or is not driven at all by T cells. An alternative explanation could be the fact that IL-1α and IL-1β specifically inhibit IL-4 synthesis by T cells [44]. Other proinflammatory cytokines, such as TNF-α, IL-6 and IL-12 did not decrease IL-4 production, indicating the pivotal role of IL-1 in RA. It is known that IL-4 has a suppressive effect on Th1 activity and is a crucial factor in differentiation of naïve T cells into the Th2 phenotype. This suppression has been suggested to be due to the inhibitory effect of IL-4 on IL-12 generation by antigen-presenting cells and macrophages [7]. IL-12, on the other hand, is a potent stimulator of the generation of Th1 cells. Analysis of anticollagen type II antibodies revealed that systemic IL-4 treatment did not alter the balance of IgG2a/IgG1 antibodies, indicating no suppressive effect on the Th1 immune response. Total anticollagen type II antibody levels were lower in both IL-4 (1 μg/day) and IL-4/prednisolone treated animals when compared with the vehicle group. We have previously found that anticollagen type II antibody levels rapidly increased after onset of CIA and reached the highest levels after 7 days (Joosten LAB, unpublished data). IL-4 treatment arrested the development of high anticollagen type II antibody levels after onset and did not alter IgG2a/IgG1 balance.

Cartilage alterations were screened for by histology as well as COMP levels in sera of mice at the end of the experiments. COMP is a prominent component of articular cartilage. In a process affecting cartilage turnover, fragments are released and eventually reach the circulation. Thus, serum levels may be used as a marker of generalized cartilage turnover [44,45]. More recent studies [46,47] have demonstrated the production of COMP by activated synovial cells and synovial tissue of RA and osteoarthritis patients. Although the relative contribution to serum levels is not firmly established, important information has been obtained from studies of collagen arthritis in rats. Thus, increased serum COMP levels are seen at time points when erosive changes appear in cartilage, whereas in early stages with marked inflammation in the synovium no increased COMP levels are seen [37,38] (Larsson E, Saxne T, unpublished data). Furthermore, serum COMP levels are reduced to normal in murine CIA after treatment with IL-1-blocking antibodies, in correspondence with a marked suppression of the cartilage lesion as viewed histologically [17]. Thus, evidence so far indicates that changes in serum COMP relate to changes in the cartilage turnover. In accord with these findings, low-dose IL-4/prednisolone treatment did not suppress disease activity, largely reflecting synovitis, but clearly reduced serum COMP levels. Histology interestingly revealed that serum COMP levels correlated more with cartilage erosions than with loss of matrix proteoglycans, which is a reversible process.

Recently, it was shown that expression of neo-epitope VDIPEN correlated with marked cartilage erosions during experimental arthritis. This neoepitope is formed by proteolytic cleavage of aggrecan by matrix metalloproteinases (MMPs). VDIPEN expression reflects MMP-3 (eg stromelysin) activity and it colocalized with collagen breakdown epitopes, indicating severe cartilage damage by MMPs [48,49]. It was demonstrated that IL-4 down-regulates both stromelysin and collagenase synthesis and thereby contributed to inhibition of cartilage destruction [11,12,50]. Thus, reduction of cartilage destruction found after IL-4 treatment may well be due to a lower production of MMPs and/or inhibition of their activity. The fact that IL-4 treatment did not protect against proteoglycan loss does suggest that IL-4 has no major suppressive effect on aggrecanase. In a previous study [51] we showed that early proteoglycan loss is mediated by aggrecanase, whereas erosive, late destruction is linked to stromelysin.

Control of bone destruction is a most challenging objective in treatment of RA. In areas of tumour-like synovial tissue, erosion of subchondral and cortical bone is common, leading to the characteristic erosions seen on radiography. Osteoclasts can be seen in the areas of bone destruction during CIA. It has been reported that IL-4 inhibits bone resorption by inhibition of osteoclast development and activity in vitro [13,14]. Here, we report for the first time that systemic IL-4 treatment of established CIA markedly reduced bone erosions, examined by radiographic analysis and histopathology. Neither bone destruction nor osteoclasts were noted in arthritic knee joints of animals treated with high-dose IL-4, indicating decreased formation of these cells. IL-4 furthermore downregulates IL-1, IL-6, TNF-α and prostaglandin E2 production in several cell types that play a role in the resorption process of the bone. Interestingly, blocking studies with neutralizing antibodies directed against IL-4 in CIA indicated that the endogenous cytokine inhibited bone destruction. In animals treated with anti-IL-4, bone destruction determined by radiographic analysis was aggravated compared with that in vehicle-treated animals (data not shown).

Glucocorticoids are potent and commonly accepted anti-inflammatory agents, but the major drawback on continued usage in arthritis is the severe negative effect on the bone. More recent studies on the mechanism of action revealed strong downregulation of macrophage production of the proinflammatory cytokines TNF-α and IL-1, related to enhanced IκBα synthesis. Intriguingly, over a large dose range steroids not only inhibit TNF and IL-1, but also reduce the production of IL-1Ra and regulatory cytokines such as IL-4 and IL-10 [52]. This suggests that the net effect in joint inflammation is impaired by the lack of the protective cytokines, which inhibit TNF/IL-1 production as well as induce potent upregulators of scavengers such as soluble receptors for TNF and IL-1, and IL-1Ra [8,9,53]. Moreover, IL-4 powerfully reduces inducible nitric oxide synthase expression, thereby counteracting the suppressive effect of IL-1 on chondrocyte proteoglycan synthesis, which is mainly nitric oxide mediated. Evidence for the latter was provided in in vitro studies with nitric oxide inhibitors. In further support of a role in vivo, we recently demonstrated that IL-1 failed to inhibit chondrocyte proteoglycan synthesis in inducible nitric oxide synthase deficient mice [54].

The present data clearly demonstrates the synergistic effect of combination therapy of low-dose prednisolone and IL-4. Low-dose IL-4 was without suppressive effect on clinical disease activity, which is in accord with previous studies [39]. However, when combined with prednisolone the progression of CIA was completely arrested. Furthermore, synergistic suppression of cartilage destruction was demonstrated by lowered serum COMP levels, which was also reflected by histology. Only combined therapy with high-dose IL-4 and prednisolone was able to suppress the influx of inflammatory cells in joint tissues and reduce the loss of matrix proteoglycans.

In conclusion, IL-4 might offer an alternative cartilage-and bone-protective therapy that is complementary to TNF/IL-1 inhibitors. Its limited effect on the inflammatory process warrants combination with other therapeutic modalities. The present data suggest that combination with prednisolone at low dosages provides an intriguing option. In accord with earlier observations of both IL-10/prednisolone and IL-4/IL-10 synergy [26,39], it must be considered that a cocktail of IL-4, IL-10 and low-dose glucocorticosteroids or glucocorticoids might be an even more efficacious therapy for human RA.

Authors’ Affiliations

(1)
University Hospital Nijmegen, Nijmegen, The Netherlands
(2)
Lund University, Lund, Sweden
(3)
NV Organon, Oss, The Netherlands

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