Background: Monosodium urate (MSU) and calcium pyrophosphate dihydrate (CPPD) crystal-induced interleukin 1 β (IL1β) release contributes to inflammation in subcutaneous air pouch and peritoneal models of acute gout and pseudogout. However, consequences of IL1 inhibition have not been explored in more clinically relevant models of crystal-induced arthritis.
Objective: To develop a novel mouse model of acute gouty ankle arthritis and use it to assess the effects of genetic deletion of IL1 receptor type (IL1R1) and of exogenous mIL1 Trap (a high-affinity blocker of mouse IL1α and IL1β) on pain, synovitis and systemic inflammatory biomarkers.
Methods: MSU crystals were injected into the mouse ankle joint and pain and ankle swelling were measured over 4 days. The effects of IL1 inhibition were determined in this model, and in the comparator models of crystal-induced peritonitis and subcutaneous air pouch inflammation.
Results: Both IL1R1-null mice and mice pretreated with mIL1 Trap showed reduced neutrophil influx in MSU and CPPD crystal-induced peritonitis and air pouch models (p<0.05). In the ankle joint model, both IL1R1 knockout mice and pretreatment with mIL1 Trap were associated with significant reductions in MSU crystal-induced elevations in hyperalgesia, inflammation, serum amyloid A and the levels of multiple inflammatory cytokines and chemokines (p<0.05). Additionally, it was found that administration of mIL1 Trap after MSU crystal injection reduced established hyperalgesia and ankle swelling.
Conclusions: IL1 inhibition both prevented and relieved pain and ankle joint inflammation in response to intra-articular MSU crystals in mice. Results suggested that IL1 Trap has the potential to both prevent and treat gouty arthritis.
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Acute gouty arthritis, an extremely painful condition,1 is provoked by activation of multiple inflammatory mediators by uric acid crystals.2 This process is driven by neutrophil influx into the joint and is associated with systemic manifestations such as fever, leukocytosis and elevated acute phase reactants.3 4 5
Monosodium urate (MSU) crystal-induced release of interleukin 1β (IL1β),6 7 mediated by NLRP3 inflammasome activation,8 is central to experimental gouty inflammation.9 The NLRP3 inflammasome acts as an activating scaffold for caspase-1, which cleaves and activates pro-IL1β into mature IL1β.10 Macrophages from mice deficient in inflammasome components cryopyrin, ASC, or caspase-1, or in the IL1 receptor IL1R1, have reduced neutrophil influx in response to MSU crystals in vivo.9 11 Additionally, pharmacological blockade of the IL1 pathway reduces neutrophil influx in response to MSU using either recombinant IL1 receptor antagonist (IL1ra; anakinra) or blocking antibodies to IL1 and IL1R1.11 12
Consequences of IL1 blockade have not been explored in the joint in gout animal models. In this study we developed a mouse model of gout-like joint hyperalgesia and inflammation in response to MSU crystals in the ankle. Systemic IL1 inhibition, using IL1R1 knockouts or mIL1 Trap, prevented and suppressed ankle hyperalgesia and synovitis.
Male IL1R1 knockouts on a C57BL/6 background and C57BL/6 age-matched control mice were obtained from the Jackson Laboratory (stock no 003245; Bar Harbor, Maine, USA) and used between the ages of 12 and 16 weeks. For mIL1 Trap and colchicine studies, male C57BL/6 mice were obtained from the Jackson Laboratory or Taconic Laboratories (Hudson, New York, USA). Mice were individually housed for at least 1 week before study on a standard 12:12 h light–dark cycle (lights on 07:00). Food and water were freely available. All experiments were approved by the Regeneron Institutional Animal Care and Use Committee.
MSU crystals were prepared as described previously.13 Monoclinic calcium pyrophosphate dihydrate (CPPD) crystals were kindly provided by Dr Kenneth Pritzker and incubated for 2 h at 200°C. Both MSU and CPPD crystals were suspended at 25 mg/ml in sterile endotoxin-free phosphate-buffered saline (PBS; Gibco, Carlsbad, California, USA) and verified to be free of detectable lipopolysaccharide contamination by Limulus amebocyte lysate assay (Cambrex, East Rutherford, New Jersey, USA).
Murine IL1 Trap (5–35 mg/kg) was used for pharmacological IL1 inhibition because the high affinity human IL1 Trap (rilonacept) cross-reacts poorly with rodent IL1β.14 mIL1 Trap was dissolved in 10 mM phosphate, 100 mM NaCl, 0.004% polysorbate 20, pH 6.5. Mouse Fc control protein was dissolved in 10 mM Tris, 150 mM NaCl, 5% glycerol, pH 7.5. Colchicine (Sigma-Aldrich, St Louis, Missouri, USA) was suspended in saline at 1 mg/ml and diluted into working solutions.
Crystal-induced peritonitis and subcutaneous (SC) air pouch models
Mice were intraperitoneally injected with 1 mg MSU or CPPD crystals resuspended in 0.5 ml endotoxin-free PBS (Cambrex, East Rutherford, New Jersey, USA). After 6 h, mice were killed and their peritoneal cavities washed and harvested with 10 ml stain buffer (BD Pharmingen, San Jose, California, USA). The air pouch model was developed as previously described.13 Six hours after crystal injection, air pouches of these mice were harvested with 5 ml stain buffer. Isolated cells were incubated with the monoclonal antibody CD16/CD32 (mouse BD Fc Block, BD Pharmingen) to block FcγRII/III receptors. Cells were then stained with a neutrophil-specific monoclonal antibody (PE-Ly-6G (R-phycoerythrin (R-PE)-conjugated rat anti-mouse Ly-6G monoclonal antibody); BD Pharmingen) and sorted (MoFlo high-speed cell sorter; Beckman Coulter, Fullerton, California, USA). The total number of lavage neutrophils was determined by dividing the number of cells counted by the percentage lavage recovery. This number was multiplied by the percentage Ly-6G-positive cells from the FACS count.
Crystal-induced ankle arthritis model and behavioural testing
MSU crystals (0.5 mg) suspended in 20 μl endotoxin-free PBS or PBS control were injected intra-articularly into the tibio-tarsal joint (ankle) of mice anaesthetised with 2.5% isoflurane. Mice were assessed for nociceptive threshold and inflammation for up to 4 days. Before behavioural testing, mice were acclimatised to the testing room for at least 1 h. All behavioural measures were taken by experimenters blind to genotype or treatment. Baseline readings were obtained for each measure before injections.
To study thermal hyperalgesia after ankle injections, the Hargreaves’ test was performed as previously described.15 Briefly, a radiant heat source was applied to the heel and the latency for the animal to withdraw its foot was recorded. For each mouse, three readings were obtained and the median latency was used. The results are presented as the percentage change from the baseline readings.
To test willingness to bear weight on injected ankles, the weightbearing test was performed using an Incapacitance meter (model 600, IITC Life Sciences, Woodland Hills, California, USA). Each hind paw was placed on a transducer pad and the weight distribution, in grams, was recorded over 4 s. The results are presented as percentage weight distributed to the affected limb.
The diameter of ankle joints was measured with callipers while mice were anaesthetised under 2.5% isoflurane. The results are presented as percentage change from baseline diameter.
For histological analyses, at least 10 mice per group were killed 1 day after ankle injection. The ankle region was isolated and fixed in buffered neutral 10% formalin (VWR, West Chester, Pennsylvania, USA), embedded in paraffin and sectioned at 5 μm for staining with haematoxylin and eosin (Histoserv, Germantown, Maryland, USA).
Mouse serum amyloid A (SAA) and cytokine profiling
Mice were killed one day after ankle injection and blood was collected by cardiac puncture. Whole blood (100 μl) was transferred to a serum separator tube (Microtainer Brand SST, Becton Dickinson, Franklin Lanes, New Jersey, USA) and SAA levels were measured using a mouse SAA ELISA kit (Biosource, Carlsbad, California, USA), according to manufacturer’s instructions. Injected ankles were dissected and homogenised in a protease inhibitor cocktail (1 tablet/50 ml, Boehringer Manheim, Indianapolis, Indiana, USA) using a Mixer Mill MM 300 (Qiagen, Valencia, California, USA). Homogenates were centrifuged and supernatants analysed according to the manufacturer’s instructions with a Luminex instrument (Luminex, Austin, Texas, USA) and a mouse cytokine/chemokine multiplex panel that detected 22 different proteins (mIL1α, mIL1β, mIL2, mIL4, mIL5, mIL6, mIL7, mIL9, mIL10, mIL12 (p70), mIL13, mIL15, mIL17, mIFNγ, mIP10, mG-CSF, mGM-CSF, mTNFα, mKC, mMCP1, mMIP-1α and mRantes) (Millipore, Billerica, Massachusetts, USA).
Data are expressed as means (SEM) and were analysed using analysis of variance (ANOVA) and post hoc tests to probe significant effects (Bonferroni tests for one- or two-way ANOVAs; Tukey HSD tests for three-way ANOVAs).
IL1 signalling mediates crystal-induced inflammation in the peritoneum and synovium-like air pouch
We confirmed9 11 a marked decrease in neutrophil ingress in the IL1R1 knockout (KO) mice compared with wild-type (WT) mice in the MSU-induced peritonitis model (fig 1A). Next, prophylactic subcutaneous (SC) injections of mIL1 Trap were administered on alternate days for three treatments, with the last given the day before MSU crystal injections. mIL1 Trap produced a significant dose-dependent decrease in neutrophil ingress (fig 1B). Similar decreases were seen using the CPPD crystal-induced peritonitis model of pseudogout9 (online supplementary figure 1). In contrast, intraperitoneal injection of 0.2 mg zymosan caused comparable neutrophil influx in IL1 R1 KOs and WTs (data not shown). Hence, IL1R1 KOs did not exhibit a general deficiency in neutrophil recruitment.
To investigate the effects of IL1 inhibition on MSU and CPPD crystal-induced inflammation in a synovitis model, we used SC air pouches.13 16 In response to either MSU or CPPD, significant reductions in neutrophil influx were detected in IL1R1 KOs compared with WTs (fig 1C) and in mIL1 Trap-treated versus vehicle-treated mice (fig 1D).
IL1 inhibition prevented hyperalgesia in a murine model of acute gouty arthritis
Animals exhibited thermal hyperalgesia for 2 days after an intra-articular ankle injection of MSU crystals, peaking 1 day after injection (fig 2A). This thermal hyperalgesia was significantly reduced in IL1R1 KOs compared with WTs. No hyperalgesia was detected in mice of either genotype with ankle injection of PBS (fig 2A).
Ankle injections of MSU, but not PBS, induced a significant shift in weight bearing away from the affected limb in WTs, peaking one day after injection (fig 2B). In contrast, IL1R1 KOs showed significantly less weight redistribution. In the same model, mIL1 Trap treatment significantly reduced both thermal hyperalgesia in the Hargreaves’ test (fig 2C) and weight redistribution in the weightbearing test (fig 2D).
Inhibition of IL1 reduced inflammation in a murine model of acute gout
Control injections of PBS into the ankle did not cause inflammation as assessed histologically in any of the groups (data not shown). Both WTs (fig 3C) and mice injected with vehicle (fig 3D) exhibited a dramatic cellular infiltrate in the ankle after MSU injection. In contrast, IL1R1 KOs (fig 3C) and mice treated with mIL1 Trap (fig 3D) showed marked reduction in this infiltrate.
The acute phase protein SAA rises during acute gout flares in patients and subsequently decreases with treatment.17 MSU crystal injections significantly increased SAA (figs 3E and F). IL1R1 KOs developed less SAA elevation than WTs (fig 3E) and mIL1 Trap blunted SAA induction (fig 3F).
mIL1 Trap is as effective as high doses of colchicine in preventing pain and inflammation
Colchicine dose-dependently decreased neutrophil influx in crystal-induced peritonitis (fig 4A). mIL1Trap was as effective as the two highest doses of colchicine in preventing influx in both MSU- and CPPD crystal-induced peritonitis (fig 4B; data not shown). To test colchicine in the ankle model, we injected 1 mg/kg colchicine SC concurrent with the ankle injection and then administered an additional 0.5 mg/kg on days 1–4 after MSU. This dosing schedule was the highest colchicine regimen tolerated without causing weight loss and lethargy (data not shown). Mice were treated with mIL1 Trap, colchicine, or both and then injected with MSU crystals into the ankle. Thermal hyperalgesia was significantly reduced by mIL1 Trap, but not colchicine, and no synergistic effect was detected with co-treatment (fig 4C). Ankle swelling was decreased by both mIL1 Trap and colchicine in the first 3 days after ankle injection; the combination therapy did not lead to any greater reduction (fig 4D).
mIL1 Trap provides relief of established pain and inflammation similar to colchicine
To study efficacy in relieving established pain and inflammation, mice were injected with a single tail vein intravenous injection of mIL1 Trap (5 or 35 mg/kg) or colchicine (1 mg/kg) 1 day after ankle injection of MSU. Significant relief of thermal hyperalgesia was achieved with both doses of mIL1 Trap and with colchicine (fig 5A). In the weightbearing test, a significant reduction of weightbearing redistribution was seen in mice treated with 35 mg/kg mIL1 Trap or colchicine (fig 5B). Both mIL1 Trap and colchicine significantly decreased ankle swelling (fig 5C). Therefore, mIL1 Trap reduced hyperalgesia and inflammation as effectively as colchicine even when administered after the pain and inflammation were established.
IL1 inhibition attenuates cytokine and chemokine upregulation in the ankle model
To identify cytokines and chemokines altered by ankle injection of MSU crystals, as well as to study the role of IL1 in their regulation, we performed cytokine and chemokine profiling on ankles and serum samples collected 24 h after ankle injection. Luminex profiling confirmed increased IL1β in MSU crystal-injected ankles (table 1). Additionally, six other cytokines, IL6, monocyte chemotactic protein-1 (MCP-1; CCL2), macrophage inhibitory protein-1 (MIP-1α; CCL3), KC (CXCL1), tumour necrosis factor α (TNFα) and granulocyte-colony stimulating factor (G-CSF) were upregulated in the injected ankles and three others, IL6, KC and G-CSF, in the serum. In contrast, IL1α was significantly decreased with MSU treatment (online supplementary fig 2). A significant attenuation of MSU-induced increases in cytokines and chemokines was seen with genetic deletion of IL1R1 and treatment with mIL1 Trap (table 1), though normalisation of IL1α was not observed.
This study reinforced the hypothesis that IL1 signalling plays a critical role in MSU and CPPD crystal-induced inflammation,9 11 12 including joint inflammation.2 3 18 19 Furthermore, we described a novel mouse model of crystal-induced synovitis and associated hyperalgesia. As previously reported in rat studies of intra-articular injections of MSU crystals,20 21 we observed a reluctance to place full weight on the injected hind leg and ankle swelling. Additionally, as observed in rats,20 21 hyperalgesic responses were fully developed within 1 day and subsided after several days.
mIL1 Trap was generally as effective as genetic deletion of IL1R1 against both inflammation and hyperalgesia in our model. Colchicine was previously established to inhibit MSU-induced neutrophil influx in rats,22 23 and here we showed that mIL1 Trap worked as well as 1 or 2 mg/kg of colchicine. However, these colchicine doses are near the mouse LD50 of 3 mg/kg intraperitoneally22 and identical to the 2 mg/kg dose which reduced oedema by 71% but resulted in the death of 75% of the animals in a rat study.23 Our finding that both mIL1 Trap and maximum tolerated doses of colchicine relieve MSU crystal-induced hyperalgesia does not necessarily indicate a commonality of mechanism. High-dose colchicine does, however, suppress IL1β maturation and release.9
Luminex-based cytokine assays revealed upregulation of multiple cytokine mediators of gouty inflammation, including IL1β, at the injection site.18 24 25 26 27 28 29 Our observation that MSU injection decreased IL1α was unexpected and strengthens the argument that it is IL1β which mediates MSU-induced pain and inflammation. Furthermore, it suggests that it is inhibition of IL1β, not IL1α, which underlies the therapeutic effects of mIL1 Trap and genetic deletion of IL1R1. IL1 inhibition caused significant reduction in multiple inflammatory cytokines, including IL6, MCP-1 and KC,11 24 25 30 but did not completely normalise the levels of these cytokines, suggesting contributions from IL1-independent pathways. IL1R1 KOs showed more attenuation than mice treated with mIL1 Trap, suggesting potentially better inhibition with genetic deletion of the IL1 receptor than with pharmacological inhibition of IL1.
IL1 modulates other pain mediators such as nerve growth factor, prostaglandin, substance-P and matrix metalloproteinase-9,26 and also modulates neuronal excitability directly via TRPV1, sodium channels, γ-aminobutyric acid (GABA) receptors and N-methyl d-aspartate (NMDA) receptors.27 The beneficial effect of IL1β inhibition on gout-related pain could therefore operate via a number of candidate mechanisms. Our newly characterised mouse model could serve as a platform to assess the relative contributions of these pathways.
In summary, IL1β drives both hyperalgesia and inflammation in a mouse model of gout, and mIL1 Trap both prevents and treats crystal-induced hyperalgesia and inflammation. The long-acting IL1 blocker rilonacept, the human version of IL1 Trap, was recently approved by the FDA for treatment of cryopyrin-associated periodic syndromes.28 29 Our data suggest that IL1 Trap has therapeutic potential for both the prophylaxis and treatment of acute gouty arthritis.
We thank Regeneron colleagues for advice and assistance.
Funding RAT received support from the VA Research Service. RL-B received support from NIH AR1067966.
Competing interests Regeneron Pharmaceuticals employed most authors, funded the work and holds a proprietary interest in the IL1 Trap reagent.
Provenance and Peer review Not commissioned; externally peer reviewed.
▸ Additional figures are published online only at http://ard.bmj.com/content/vol68/issue10
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