Skip to main content


Enhanced activity of NLRP3 inflammasome in peripheral blood cells of patients with active rheumatoid arthritis



Interleukin-1β (IL-1β) is a major inflammatory cytokine, produced predominantly by innate immune cells through NLRP3-inflammasome activation. Both intrinsic and extrinsic danger signals may activate NLRP3. Genetic variations in NLRP3-inflammasome components have been reported to influence rheumatoid arthritis (RA) susceptibility and severity. We sought to assess the activity of NLRP3-inflammasome in patients with active RA compared to healthy individuals.


Intracellular protein expression of NLRP3, ASC, pro- and active caspase-1, pro- and active IL-1β was assessed by immunoblotting both at baseline and upon inflammasome activation. NLRP3 function (IL-1β secretion) was assessed upon priming of TLR2 (Pam(3)CysSK(4), TLR3 (poly(I:C)) or TLR4 (LPS) and ATP sequential treatment. We used caspase inhibitors (casp-1, 3/7 and 8) to assess their contribution to IL-1β maturation. All experiments were performed in whole blood cells.


Active RA patients (n = 11) expressed higher basal intracellular levels of NLRP3 (p < 0.008), ASC (p < 0.003), active caspase-1 (p < 0.02) and pro-IL-1β (p < 0.001). Upon priming with TLR4 (LPS) and ATP, RA-derived cell extracts (n = 7) displayed increased expression of NLRP3 (p < 0.01) and active caspase-1 (p < 0.001). Secreted IL-1β in culture supernatants from whole blood cells activated with TLR4 (LPS) or TLR3 agonist (poly(I:C)) plus ATP was higher in RA patients (n = 20) versus controls (n = 18) (p < 0.02 for both). Caspase-1 inhibition significantly reduced IL-1β secretion induced by all stimuli, whereas caspase-8 inhibition affected only TLR4 and TLR3 cell priming.


Patients with active RA have increased expression of NLRP3 and NLRP3-mediated IL-1β secretion in whole blood cells upon stimulation via TLR3 and TLR4 but not TLR2. In these patients, IL-1β secretion seems to be predominately driven by caspase-1 and caspase-8. Targeting NLRP3 or downstream caspases may be of benefit in suppressing IL-1β production in RA.


Inflammasomes are cytosolic multiprotein complexes that drive the production of inflammatory cytokines, mainly interleukin-1β (IL-1β) and IL-18, in response to pathogens or danger signals [1]. Inflammasomes are composed of a danger sensor, an adaptor protein that is mainly the apoptosis-associated speck-like protein containing a CARD (ASC protein), and caspase-1. There is remarkable diversity in the sensor proteins that form the inflammasomes, thus leading to the assembly of distinct complexes specialized to sense various signals. The nucleotide binding domain and leucine-rich repeat pyrin 3 domain (NLRP3 or cryopyrin) sensor protein, organizes the assembly of the best-characterized inflammasome, the NLRP3-inflammasome. A diverse set of signals has been shown to activate NLRP3, including pathogens, danger signals from damaged/stressed cells and environmental microparticles [2]. NALP3-inflammasome assembly results in ASC polymerization, procaspase-1 self-activation to the active protease, which then catalyzes pro-IL1β maturation [3]. Mutations in the gene encoding for NLRP3 have been linked to autoinflammatory syndromes (cryopyrinopathies) associated with aberrant IL-1β production [4], which have been further characterized by mouse models of mutant NLRP3 [5, 6].

Rheumatoid arthritis (RA) is a chronic inflammatory arthritis, which may be caused by various combinations of genetic and environmental triggers. IL-1β drives cartilage destruction, while its role in disease pathogenesis is further supported by the efficacy of IL-1β blockade in mouse and humans [7]. Interestingly, mutations in NLRP3-inflammasome proteins (NLRP3 and CARD8) have been associated with RA susceptibility and severity in some but not all ethnic backgrounds [810]. Animal studies have revisited the role of NLRP3 in the evolution of arthritis. Although earlier studies in the collagen- and antigen-induced arthritis models suggest that disease pathology is ASC-related but independent of NLRP3 [11, 12], more recent studies in a novel spontaneous arthritis model (A20myel-KO mice) show that arthritis pathology critically relies on the NLRP3 inflammasome/IL-1β axis [13]. P2X7 purinergic receptor (P2X7R) an ATP-gated ion channel is an important cell surface inducer of key inflammatory cytokines mainly through NLRP3 activation [14]. Its role in inflammatory responses of RA has been shown in the animal model of arthritis [15] and recently, a P2X7R antagonist has been evaluated in a clinical study [16].

Although there is emerging evidence for involvement of the NLRP3-inflammasome/IL-1β axis in the inflammatory responses of RA, studies in humans are scarce [17, 18]. We therefore sought to investigate in peripheral blood cells the expression of NLRP3-related proteins, their potential to promote IL-1β maturation and secretion upon stimulation. Our results demonstrate enhanced expression and function of NLRP3-iflammasome in the peripheral blood of active RA patients.


Patients and treatment

Peripheral blood samples were obtained from patients diagnosed with RA according to the 1987 American College of Rheumatology (ACR) criteria [19], who were followed by the Rheumatology Clinic of the University Hospital of Crete. At the time of sampling all patients had high disease activity according to the disease activity score based on the 28 joint counts (DAS28) [20]. The study was approved by the Ethics Committee of the University Hospital of Heraklion, University of Crete School of Medicine, and all participants gave informed consent.

Ex vivo activation of NLRP3-inflammasome in whole blood cells

Although human innate and adaptive immune responses are typically studied in vitro in isolated peripheral blood mononuclear cells (PBMCs), this approach has intrinsic limitations and therefore assays based on whole blood have been proposed [21] and lately better standardized to assess immune function in humans [22]. Moreover, although the NLRP3-inflammasome is expressed predominantly in monocytes/macrophages and dendritic cells, neutrophils, the most abundant cells in peripheral blood, also express functional NLRP3-inflammasome [23]. Thus, we performed all experiments in whole blood cells.

Heparin-anticoagulated whole blood from RA patients and healthy controls was collected and immediately processed. Cell viability assessed by trypan blue staining was >90 % and did not differ between patients and healthy individuals. After red blood cell (RBC) lysis in ammonium persulfate buffer (NH4Cl 0.15 M/KHCO3 10 mM/Na2EDTA 0.1 mM, pH 7.2 − 7.4) baseline expression of NLRP3, IL-1β, caspase-1 was assessed by immunoblotting in cell lysates.

NLRP3-inflammasome function (activation) was assessed in cultures (1.5 × 106/mL) at 37 °C (5 % CO2) in RMPI-1640 (Gibco Thermofisher Scientific, Waltham, MA. USA) medium supplemented with 10 % heat-inactivated FBS (Gibco Thermofisher Scientific Waltham, MA. USA) with or without pre-treatment with various Toll-like receptor (TLR) ligands, followed by ATP pulse to activate NLRP3-inflammasome (ATP 5 mM, 20 min) (Sigma-Aldrich Chemie GmbH, Buchs, Switzerland, #A1852). In detail, TLR ligands that were applied were for TLR4 (lipopolysaccharide (LPS), 250 pg/mL, 2 h) (Calbiochem Billerica, MA, USA, #437627), TLR3 (Polyinosinic-polycytidylic acid, 50 μg/mL, 2 h) (Sigma-Aldrich Chemie GmbH, Buchs, Switzerland, #P0913) and TLR2 (pam3CysSK 200 ng/mL, 2 h) (EMC microcollections Tübingen, Germany, #L2000). Caspase-1 inhibitor Ac-YVAD-CHO (10 μM, 15 min) (Calbiochem Billerica, MA, USA #400010), or caspase-8 inhibitor (Calbiochem Billerica, MA, USA #218840)  or caspase-3/7 inhibitor (Calbiochem Billerica, MA, USA, #218832), were applied for 15 min prior to ATP pulse. Cell culture supernatants were collected prior to and following ATP treatment to measure levels of TNFα and IL-1β by ELISA (e Bioscience San Diego, CA, USA, #88-7346-22 and 88-7010-88 respectively)  and cell extracts were collected to assess intracellular NLRP3-inflammasome activation.

Western blot analysis

Intracellular expression of NLRP3, caspase-1, and IL-1β was assessed by immunoblotting in lysates from freshly isolated whole blood cells and also from whole blood cells cultured in medium alone or in the presence of TLR ligands/ATP as described above. Cells were lysed in 10 mM Tris–HCl pH 8.0, 150 mM NaCl, 1 mM EGTA, 1 % Triton-X 100 in the presence of complete mini EDTA-Free Protease Inhibitor Cocktail (Roche, Basel, Switzerland, #04693124001). Protein concentration was determined by the Bradford method using the Bio-Rad protein assay solution (Bio-Rad Laboratories GmbH Hercules CA, USA, #500-006) Lysates were subjected to SDS-PAGE using 12 % polyacrylamide gels, and were subsequently transferred to 0.2 μm nitrocellulose membrane. The membrane was blocked for 1 h at room temperature followed by incubation overnight at 4 °C with antibodies against human NALP3 (Alexis Biocehmicals Enzo Life Sciences, Inc Farmingdale, NY, USA, #ALX-804-819), caspase-1 (Cell Signaling technologies Danvers, MA, USA, #2225), anti-IL-1β (Cell Signaling technologies Danvers, MA, USA, #2022), anti-ASC (Santa Cruz biotechnology Dallas, Texas U.S.A., #sc-271054)  and β-actin (Merck-Milipore Billerica, MA, USA, #MAB1501). Afterwards, the blots were washed and incubated with horseradish peroxidase-conjugated secondary antibodies for 1 h at room temperature. The blots were developed with electro-chemiluminescence using ECL plus (Pierce-Thermofisher Scientific Waltham, MA, USA). Protein densitometry was assessed using Image J and the intensity of the protein of interest was normalized to β-actin expression.

Enzyme-linked immunosorbent assay (ELISA)

IL1-β and TNFα content in supernatants was determined by ELISA (Ebioscience-, San Diego, CA, #88-7010-88 and #88-7346-22 respectively) according to the manufacturer’s instructions.

Statistical analysis

Results are shown as mean ± standard error (SEM). Differences between groups were analyzed by independent or paired samples t test as appropriate, using the Statistical Package for Social Sciences software version 20.0 (SPSS, Inc.). P value ≤0.05 (two-tailed) were considered statistically significant.


Patients’ clinical characteristics at baseline

At the time of sampling, all patients had highly active disease (mean (SEM) DAS28 5.2 (0.2)) with high inflammatory serum markers (erythrocyte sedimentation rate (ESR) 39.8 (7.3) mm/h, C-reactive protein (CRP) 2.4 (1.3) mg/dL), irrespective of background treatment (Table 1).

Table 1 Baseline demographics and clinical characteristics of the RA patients included in the study

Freshly isolated peripheral blood from active RA expresses increased levels of NLRP3-inflammasome proteins

First we assessed the baseline expression of NLRP3-inflammasome-related proteins in RA patients compared to healthy controls. To this end we performed immunoblotting in freshly isolated unstimulated whole blood cells and found that patients with active RA (n = 11) expressed higher intracellular levels of NLRP3 (p <0.008), ASC (p <0.003) and active caspase-1 (p <0.02) as compared to controls (n = 11) (Fig. 1a, b). Accordingly, RA patients expressed higher intracellular levels of pro-IL-1β (p <0.0001), while levels of active IL-1β were lower compared to controls (p <0.001) (Fig. 1c-h). As expected, mature IL-1β levels in cell culture supernatants were minimal and comparable between patients and controls (data not shown).

Fig. 1

Baseline expression of nucleotide binding domain and leucine-rich repeat pyrin 3 domain (NLRP3) inflammasome-related proteins in controls (a) as compared to patients with rheumatoid arthritis (RA) (b). Western blots were performed in cell lysates of freshly isolated whole blood cells for CASP 1, NLRP3, IL1β and ASC, from healthy controls (a) (n = 11) and patients with active RA (b) (n = 11). Protein densitometry was assessed by the use of Image J program and the intensity of the protein of interest was normalized to β-actin expression (c-h). HC healthy controls, CTL control

Activation of NLRP3-inflammasome in a whole blood cell assay

Optimal NLRP3-inflammasome activation requires two signals. The first one is an inflammatory stimulus that signals through the TLRs or cytokine receptors, to upregulate gene products required for activation of the caspase-1, and the second is an NLRP3-specific trigger, typically ATP [24]. In preliminary experiments performed in blood drawn from healthy individuals (n = 15), we assessed the efficiency and specificity of sequential TLR4 and ATP activation to induce NLRP3. TLR4 priming (ultra-pure LPS, 250 pg/mL, 2 h) followed by pulse ATP stimulation (5 mM, 20 min) efficiently activated NLRP3-inflammasome, assessed by IL-1β secretion in supernatants, as compared to either stimulus alone (p <0.001) (Fig. 2a). IL-1Ra belongs to the IL-1 family of cytokines, and is also produced upon LPS stimulation [25]. LPS and ATP sequential treatment effectively induced secreted IL-1Ra (p = 0.0001 vs unstimulated cells, data not shown). In contrast, we observed no increase in TNFα secretion upon combined LPS and ATP treatment, supporting the specificity of the assay for NLRP3-inflammasome induction (Fig. 2b). Addition of a caspase-1 inhibitor effectively inhibited IL-1β secretion (Fig. 2a).

Fig. 2

Specificity for nucleotide binding domain and leucine-rich repeat pyrin 3 domain (NLRP3) stimulation of the method applied. a Toll-like receptor (TLR)4 priming (ultra-pure lipolysaccharide (LPS) (250 pg/mL, 2 h)) followed by ATP pulse (5 mM, 20 min) efficiently activates NLRP3-inflammasome, assessed by IL-1β secretion in supernatants of whole blood cells of healthy controls (n = 15). b No increase in TNFα secreted by peripheral whole blood cells stimulated by the same triggers (n = 12). HC healthy controls, RA rheumatoid arthritis, Casp1Inh caspase1 inhibitor

Activation of NLRP3-inflammasome results in higher IL-1β secretion by peripheral blood cells in active RA

We have shown that NLRP3-inflammasome-related proteins are overexpressed in freshly, unstimulated peripheral blood cells from RA patients with active disease. Next we sought to assess whether upon its activation, NLRP3-inflammasome has differential expression and function in RA. For this, we applied sequential treatment with TLR4 ligand (LPS) and ATP on whole blood cells from healthy controls (n = 7, Fig. 3a) and patients with active RA (n = 7, Fig. 3b) and quantified intracellular expression of NLRP3-inflammasome-related proteins. The expression of both NLRP3 and active caspase-1 (p20) was induced upon NLRP3 induction in whole blood cells of patients as compared to controls (Fig. 3). Of interest, active IL-1β intracellular expression was comparable between the two groups.

Fig. 3

Induction of nucleotide binding domain and leucine-rich repeat pyrin 3 domain (NLRP3)-inflammasome related proteins in peripheral whole blood cells, upon sequential stimulation with lipolysaccharide (LPS) (250 pg/mL, 2 h) and ATP (5 mM, 20 min), in healthy individuals and patients with rheumatoid arthritis (RA). Western blots were performed in freshly isolated whole blood cells without (−) or with (+) LPS + ATP treatment from healthy controls (a) (n = 7) and patients with active RA (b) (n = 7). Protein densitometry was assessed using Image J program and the intensity of the protein of interest was normalized to that of β-actin (c-h). HC healthy controls

Besides TLR4 triggering, investigators have applied other TLR ligands as the first signal for NLRP3-inflammasome activation [26]. In addition to TLR4 [27], signaling through TLR2 [28] and TLR3 [29] may participate in inflammatory responses in RA. To assess NLRP3-inflammasome function upon activation with stimuli relevant to RA, we applied sequential treatment of whole blood cells with TLR2, TLR3 or TLR4 ligands followed by ATP [26] and measured IL-1β.

We found that upon TLR2, TLR3 or TLR4 cell priming and sequential ATP-pulse, high levels of IL-1β were secreted as compared to either stimulus alone (Fig. 4). Interestingly, cells from RA patients (n = 20) secreted significantly larger amounts of IL-1β compared to controls (n = 18) upon cell priming with TLR3 or TLR4 ligands (Fig. 4a, b), while IL1-β secretion was comparable when TLR2 ligand was applied (Fig. 4c). These data, together with the findings of higher intracellular NLRP3 and active caspase-1 upon NLRP3-inflammasome induction in whole blood cells in RA, indicate increased function of NLRP3-inflammasome in RA patients.

Fig. 4

Functional assessment of nucleotide binding domain and leucine-rich repeat pyrin 3 domain (NLRP3)-inflammasome upon activation. Whole blood from patients (n = 20) or healthy individuals (n = 18) were primed with Toll-like receptor (TLR)4 (lipopolysaccharide (LPS), 250 pg/mL, 2 h) (a), TLR3 (poly IC, 50 μg/mL, 2 h) (b) or TLR2 (pam3CysSK 200 ng/mL, 2 h) (c) ligands and sequentially pulsed with ATP (ATP 5 mM, 20 min). IL-1β secretion in cell supernatants was quantified by ELISA (pg/mL). HC healthy controls, RA rheumatoid arthritis, pIC polyinosinic-polycytidylic acid, Pam pam3CysSK

Different caspases are involved in pro-IL1β maturation

Upon NLRP3 activation, pro-caspase-1 is auto-cleaved to its active form to induce proteolysis of pro-IL-1β. Nevertheless, there is evidence that inflammatory caspases other than caspase-1 may also contribute to IL-1β activation [3032]. Thus, we sought to assess the contribution of other caspases (caspase-3/7, caspase-8) in NLRP3-mediated IL-1β production in RA. To this end, we applied caspase-1, caspase-3/7 and caspase-8 inhibitors prior to ATP pulse and measured secreted IL-1β (see “Methods”). All three caspase inhibitors inhibited IL-1β secretion (Fig. 5). Interestingly, only caspase-1 inhibition significantly reduced IL-1β secretion by whole blood cells from patients and across all three TLR agonists used for cell priming (p <0.05). On the other hand, both caspase-3/7 and caspase-8 inhibition reduced IL-1β secretion, only upon TLR4 cell priming, while caspase-8 inhibited IL-1β secretion upon TLR3 priming as well.

Fig. 5

Assessment of the effect of inhibition of various caspases in IL-1β maturation upon nucleotide binding domain and leucine-rich repeat pyrin 3 domain (NLRP3) activation. Whole blood cells from patients with rheumatoid arthritis (RA) (n = 20) were primed with Toll-like receptor (TLR)4 (lipopolysaccharide (LPS), 250 pg/mL, 2 h) (a), TLR3 (poly IC, 50 μg/mL, 2 h) (b) or TLR2 (pam3CysSK 200 ng/mL, 2 h) (c) ligands and sequentially pulsed with ATP (ATP 5 mM, 20 min). Inhibitors of caspase-1 (a) or caspase-3/7 (b) or caspase-8 (c) were applied. IL-1β secretion in cell supernatants was quantified by ELISA (pg/mL). pIC polyinosinic-polycytidylic acid, Pam pam3CysSK, Casp1Inh caspase1 inhibitor, Casp3/7Inh caspase3 and 7 inhibitor, Casp8Inh caspase8 inhibitor


Herein we sought to characterize the expression and function of NLRP3-inflammasome in RA. Compared to healthy individuals, whole blood cells from RA patients express higher basal amounts of NLRP3-related proteins and they demonstrate even higher expression following NLRP3 activation. Importantly, RA whole blood cells were found to secrete larger amounts of IL-1β upon NLRP3 activation, supporting that the overexpressed NLRP3-inflammasome is also overactive. These findings support a role of this intracellular complex in the systemic inflammation of RA.

In the context of sterile inflammation such as in the case of RA, multiple endogenous signals have been shown to induce NLRP3-inflammasome expression and activation. Inflammatory cytokines like TNFα and IL-1β [33, 34], several danger-associated molecular patterns (DAMPs) like ATP released by mitochondria of damaged cells [35], HMGB1 [36] and S100A proteins [37]. Interestingly, many of these DAMPs are upregulated in peripheral blood in RA [38, 39]; they may participate through inflammasome activation in the systemic inflammation of the disease and some have been assessed as therapeutic targets for inflammatory arthritis [40]. Our data corroborate recently reported data suggesting upregulation of NLRP3-inflammasome-related gene expression in mononuclear cells (PBMCs) in peripheral blood from patients with active RA [17] and earlier data showing increased NALP3 mRNA levels in the synovium in RA compared with osteoarthritis (OA) [18]. Clinicians are familiar with the limited efficacy of IL-1Ra (anakinra) in RA patients. This has been attributed to factors such as limited bioavailability (due to rapid renal clearance) and the need to block the majority of cellular IL-1R in order to effectively inhibit the effects of IL-1β [41]. Thus, elucidating the molecular components and intracellular cascades that control IL-1β production, are an alternative for interfering with IL-1β-mediated effects aiming to inhibit its production. Several small-molecule inhibitors of NLRP3-inflammasome have been described and already tested in vitro or in animal models of systemic inflammatory disease [42]. Whether this approach will have better clinical results as compared to IL-1Ra remains to be seen.

In the collagen- and antigen-induced arthritis mouse models, pathology has been shown to be independent of NLRP3 but dependent on ASC [11, 12]. Recently, Vande Walle et al. have shown that arthritis pathology is critically related to the NLRP3 inflammasome/IL-1 signaling axis, in the arthritis model A20 myel-KO mice, in which the A20/Tnfaip3 RA susceptibility gene is deleted in myeloid cells [13]. This new model A20 myel-KO might be suitable for validation of therapies targeting NLRP3-inflammasome or IL-1 signaling. Animal models of inbred mice have not, in most cases, been a reliable guide to developing treatments for human immunological diseases and there is also significant reservation about their relevance to the initiation of RA and the chronic inflammatory processes of RA.

Addressing the involvement of inflammasome in human disease has been challenging. Demonstrating IL-1β cleavage by caspase-1 in biologic specimens is difficult, while demonstrating increased activity of the inflammasome is even more challenging [43]. We applied immunoblotting for NLRP3-inflammasome-related protein assessment intracellularly and we quantified IL-1β secretion in peripheral blood. Although both have limitations, mainly when addressing inflammasome function, nevertheless they have been applied in most of the human studies so far [44]. Recently, it has been shown that in mouse bone-marrow-derived macrophages (BMDMs), the activation of inflammasomes resulted in the extracellular release of active inflammasome oligomers as particles that acted extracellularly as danger signals to amplify the inflammatory response by activating caspase-1 [45]. Thus, our method of assessment of intracellular inflammasome-related proteins may underestimate its presence and function.

Although monocytes, macrophages and dendritic cells are the major NLRP3-expressing cells, human and mouse neutrophils have been also shown to have functional NLRP3-inflammasome [23]. Neutrophils are the most abundant cells in peripheral blood. Although human immune responses are usually studied in vitro in isolated PBMCs, assays based on whole blood cells have been proposed and lately have been better standardized, to assess immune function in humans [22]. Notably, direct measurements made in whole blood have the advantage of minimizing contamination and sample handling. Moreover, maintaining total leukocytes (e.g., polymorphonuclear cells) and platelets in a plasma matrix may provide a more accurate reflection of in vivo responsiveness to immune stimuli [22]. In preliminary experiments, we applied the same triggers in peripheral blood isolated monocytes and we found comparable results to those of whole blood. For these reasons, we performed our experiments in whole blood after red cell lysis.

Caspase-1 is an inflammatory caspase activated by the assembly of inflammasomes [46]. It is a protease that controls the release of various leader-less proteins, as well as its own release [47]. Interestingly, this is not the only protease involved in IL-1β maturation [3032]. Caspase-4 has been shown to participate in IL-1β maturation probably through caspase-1 activation [32]. Moreover, a role in canonical and noncanonical NLRP3-inflammasome priming and activation through TLRs has been attributed to caspase-8 [30, 31]. In our functional studies we applied selective caspase inhibitors to assess their importance in IL-1β secretion. Although all caspase inhibitors applied could downregulate IL-1β secretion upon TLR priming and ATP pulse, only caspase-1 inhibitor resulted in significant downregulation of IL-1β with all three different stimuli (TLR2, TLR3 and TLR4) applied. Caspase-8 inhibitor significantly downregulated IL-1β secretion only upon TLR4 and TLR3 cell priming. These data support the role of caspase-1 but also of caspase-8 in inflammatory responses through NLRP3 in humans with inflammatory arthritis, as it has been shown in the aforementioned studies in mouse-derived cells and keratinocytes. The role of caspase-3 and caspase-7 in inflammatory response has not yet been established as it has been for apoptosis [48].


In summary we found increased expression and function of NLRP3-inflammasome in patients with RA by applying whole blood cell analysis. These data support a role of NLRP3 in mediating systemic inflammatory responses in the context of RA. Caspase-1, and also caspase-8, may be important mediators for IL-1β release, and hence potential therapeutic targets.



American College of Rheumatology


apoptosis-associated speck-like protein containing a CARD


adenosine triphosphate


Caspase recruitment domain family, member 8


C-reactive protein


danger-associated molecular pattern


disease activity score in 28 joints


enzyme-linked immunosorbent assay


erythrocyte sedimentation rate


fetal bovine serum


High-mobility group protein B1




IL-1 receptor antagonist




nucleotide binding domain and leucine-rich repeat pyrin 3 domain


P2X7 receptor


peripheral blood mononuclear cell


polyinosinic:polycytidylic acid


rheumatoid arthritis


Roswell Park Memorial Institute


Toll-like receptor


tumor necrosis factor α


  1. 1.

    Schroder K, Tschopp J. The inflammasomes. Cell. 2010;140:821–32.

  2. 2.

    Latz E, Xiao TS, Stutz A. Activation and regulation of the inflammasomes. Nat Rev Immunol. 2013;13:397–411.

  3. 3.

    Lopez-Castejon G, Brough D. Understanding the mechanism of IL-1beta secretion. Cytokine Growth Factor Rev. 2011;22:189–95.

  4. 4.

    Martinon F, Mayor A, Tschopp J. The inflammasomes: guardians of the body. Annu Rev Immunol. 2009;27:229–65.

  5. 5.

    Brydges SD, Mueller JL, McGeough MD, Pena CA, Misaghi A, Gandhi C, et al. Inflammasome-mediated disease animal models reveal roles for innate but not adaptive immunity. Immunity. 2009;30:875–87.

  6. 6.

    Meng G, Zhang F, Fuss I, Kitani A, Strober W. A mutation in the Nlrp3 gene causing inflammasome hyperactivation potentiates Th17 cell-dominant immune responses. Immunity. 2009;30:860–74.

  7. 7.

    van den Berg WB. Arguments for interleukin 1 as a target in chronic arthritis. Ann Rheum Dis. 2000;59:i81–4.

  8. 8.

    Fontalba A, Martinez-Taboada V, Gutierrez O, Pipaon C, Benito N, Balsa A, et al. Deficiency of the NF-kappaB inhibitor caspase activating and recruitment domain 8 in patients with rheumatoid arthritis is associated with disease severity. J Immunol. 2007;179:4867–73.

  9. 9.

    Kastbom A, Verma D, Eriksson P, Skogh T, Wingren G, Soderkvist P. Genetic variation in proteins of the cryopyrin inflammasome influences susceptibility and severity of rheumatoid arthritis (the Swedish TIRA project). Rheumatology (Oxford). 2008;47:415–7.

  10. 10.

    Ben Hamad M, Cornelis F, Marzouk S, Chabchoub G, Bahloul Z, Rebai A, et al. Association study of CARD8 (p.C10X) and NLRP3 (p.Q705K) variants with rheumatoid arthritis in French and Tunisian populations. Int J Immunogenet. 2012;39:131–6.

  11. 11.

    Kolly L, Karababa M, Joosten LA, Narayan S, Salvi R, Petrilli V, et al. Inflammatory role of ASC in antigen-induced arthritis is independent of caspase-1, NALP-3, and IPAF. J Immunol. 2009;183:4003–12.

  12. 12.

    Ippagunta SK, Brand DD, Luo J, Boyd KL, Calabrese C, Stienstra R, et al. Inflammasome-independent role of apoptosis-associated speck-like protein containing a CARD (ASC) in T cell priming is critical for collagen-induced arthritis. J Biol Chem. 2010;285:12454–62.

  13. 13.

    Vande Walle L, Van Opdenbosch N, Jacques P, Fossoul A, Verheugen E, Vogel P, et al. Negative regulation of the NLRP3 inflammasome by A20 protects against arthritis. Nature. 2014;512:69–73.

  14. 14.

    Ferrari D, Pizzirani C, Adinolfi E, Lemoli RM, Curti A, Idzko M, et al. The P2X7 receptor: a key player in IL-1 processing and release. J Immunol. 2006;176:3877–83.

  15. 15.

    Labasi JM, Petrushova N, Donovan C, McCurdy S, Lira P, Payette MM, et al. Absence of the P2X7 receptor alters leukocyte function and attenuates an inflammatory response. J Immunol. 2002;168:6436–45.

  16. 16.

    Keystone EC, Wang MM, Layton M, Hollis S, McInnes IB, Team DCS. Clinical evaluation of the efficacy of the P2X7 purinergic receptor antagonist AZD9056 on the signs and symptoms of rheumatoid arthritis in patients with active disease despite treatment with methotrexate or sulphasalazine. Ann Rheum Dis. 2012;71:1630–5.

  17. 17.

    Mathews RJ, Robinson JI, Battellino M, Wong C, Taylor JC, Biologics in Rheumatoid Arthritis G, Genomics Study S, et al. Evidence of NLRP3-inflammasome activation in rheumatoid arthritis (RA); genetic variants within the NLRP3-inflammasome complex in relation to susceptibility to RA and response to anti-TNF treatment. Ann Rheum Dis. 2014;73:1202–10.

  18. 18.

    Rosengren S, Hoffman HM, Bugbee W, Boyle DL. Expression and regulation of cryopyrin and related proteins in rheumatoid arthritis synovium. Ann Rheum Dis. 2005;64:708–14.

  19. 19.

    Arnett FC, Edworthy SM, Bloch DA, McShane DJ, Fries JF, Cooper NS, et al. The American Rheumatism Association 1987 revised criteria for the classification of rheumatoid arthritis. Arthritis Rheum. 1988;31:315–24.

  20. 20.

    Prevoo ML, van’t Hof MA, Kuper HH, van Leeuwen MA, van de Putte LB, van Riel PL. Modified disease activity scores that include twenty-eight-joint counts. Development and validation in a prospective longitudinal study of patients with rheumatoid arthritis. Arthritis Rheum. 1995;38:44–8.

  21. 21.

    Eskola J, Soppi E, Viljanen M, Ruuskanen O. A new micromethod for lymphocyte stimulation using whole blood. Immunol Commun. 1975;4:297–307.

  22. 22.

    Duffy D, Rouilly V, Libri V, Hasan M, Beitz B, David M, et al. Functional analysis via standardized whole-blood stimulation systems defines the boundaries of a healthy immune response to complex stimuli. Immunity. 2014;40:436–50.

  23. 23.

    Bakele M, Joos M, Burdi S, Allgaier N, Poschel S, Fehrenbacher B, et al. Localization and functionality of the inflammasome in neutrophils. J Biol Chem. 2014;289:5320–9.

  24. 24.

    Kahlenberg JM, Lundberg KC, Kertesy SB, Qu Y, Dubyak GR. Potentiation of caspase-1 activation by the P2X7 receptor is dependent on TLR signals and requires NF-kappaB-driven protein synthesis. J Immunol. 2005;175:7611–22.

  25. 25.

    Dinarello CA. Biologic basis for interleukin-1 in disease. Blood. 1996;87:2095–147.

  26. 26.

    Mariathasan S, Weiss DS, Newton K, McBride J, O’Rourke K, Roose-Girma M, et al. Cryopyrin activates the inflammasome in response to toxins and ATP. Nature. 2006;440:228–32.

  27. 27.

    Abdollahi-Roodsaz S, Joosten LA, Roelofs MF, Radstake TR, Matera G, Popa C, et al. Inhibition of Toll-like receptor 4 breaks the inflammatory loop in autoimmune destructive arthritis. Arthritis Rheum. 2007;56:2957–67.

  28. 28.

    Huang QQ, Sobkoviak R, Jockheck-Clark AR, Shi B, Mandelin 2nd AM, Tak PP, et al. Heat shock protein 96 is elevated in rheumatoid arthritis and activates macrophages primarily via TLR2 signaling. J Immunol. 2009;182:4965–73.

  29. 29.

    Meng L, Zhu W, Jiang C, He X, Hou W, Zheng F, et al. Toll-like receptor 3 upregulation in macrophages participates in the initiation and maintenance of pristane-induced arthritis in rats. Arthritis Res Ther. 2010;12:R103.

  30. 30.

    Allam R, Lawlor KE, Yu EC, Mildenhall AL, Moujalled DM, Lewis RS, et al. Mitochondrial apoptosis is dispensable for NLRP3 inflammasome activation but non-apoptotic caspase-8 is required for inflammasome priming. EMBO Rep. 2014;15:982–90.

  31. 31.

    Gurung P, Anand PK, Malireddi RK, Vande Walle L, Van Opdenbosch N, Dillon CP, et al. FADD and caspase-8 mediate priming and activation of the canonical and noncanonical Nlrp3 inflammasomes. J Immunol. 2014;192:1835–46.

  32. 32.

    Sollberger G, Strittmatter GE, Kistowska M, French LE, Beer HD. Caspase-4 is required for activation of inflammasomes. J Immunol. 2012;188:1992–2000.

  33. 33.

    Franchi L, Eigenbrod T, Nunez G. Cutting edge: TNF-alpha mediates sensitization to ATP and silica via the NLRP3 inflammasome in the absence of microbial stimulation. J Immunol. 2009;183:792–6.

  34. 34.

    Bauernfeind FG, Horvath G, Stutz A, Alnemri ES, MacDonald K, Speert D, et al. Cutting edge: NF-kappaB activating pattern recognition and cytokine receptors license NLRP3 inflammasome activation by regulating NLRP3 expression. J Immunol. 2009;183:787–91.

  35. 35.

    Iyer SS, Pulskens WP, Sadler JJ, Butter LM, Teske GJ, Ulland TK, et al. Necrotic cells trigger a sterile inflammatory response through the Nlrp3 inflammasome. Proc Natl Acad Sci U S A. 2009;106:20388–93.

  36. 36.

    Andersson U, Wang H, Palmblad K, Aveberger AC, Bloom O, Erlandsson-Harris H, et al. High mobility group 1 protein (HMG-1) stimulates proinflammatory cytokine synthesis in human monocytes. J Exp Med. 2000;192:565–70.

  37. 37.

    Simard JC, Cesaro A, Chapeton-Montes J, Tardif M, Antoine F, Girard D, et al. S100A8 and S100A9 induce cytokine expression and regulate the NLRP3 inflammasome via ROS-dependent activation of NF-kappaB(1.). PLoS One. 2013;8:e72138.

  38. 38.

    Chen YS, Yan W, Geczy CL, Brown MA, Thomas R. Serum levels of soluble receptor for advanced glycation end products and of S100 proteins are associated with inflammatory, autoantibody, and classical risk markers of joint and vascular damage in rheumatoid arthritis. Arthritis Res Ther. 2009;11:R39.

  39. 39.

    Hamada T, Torikai M, Kuwazuru A, Tanaka M, Horai N, Fukuda T, et al. Extracellular high mobility group box chromosomal protein 1 is a coupling factor for hypoxia and inflammation in arthritis. Arthritis Rheum. 2008;58:2675–85.

  40. 40.

    Ostberg T, Kawane K, Nagata S, Yang H, Chavan S, Klevenvall L, et al. Protective targeting of high mobility group box chromosomal protein 1 in a spontaneous arthritis model. Arthritis Rheum. 2010;62:2963–72.

  41. 41.

    Dinarello CA. The many worlds of reducing interleukin-1. Arthritis Rheum. 2005;52:1960–7.

  42. 42.

    Guo H, Callaway JB, Ting JP. Inflammasomes: mechanism of action, role in disease, and therapeutics. Nat Med. 2015;21:677–87.

  43. 43.

    Netea MG, van de Veerdonk FL, van der Meer JW, Dinarello CA, Joosten LA. Inflammasome-independent regulation of IL-1-family cytokines. Annu Rev Immunol. 2014;33:49-77.

  44. 44.

    Gattorno M, Tassi S, Carta S, Delfino L, Ferlito F, Pelagatti MA, et al. Pattern of interleukin-1beta secretion in response to lipopolysaccharide and ATP before and after interleukin-1 blockade in patients with CIAS1 mutations. Arthritis Rheum. 2007;56:3138–48.

  45. 45.

    Baroja-Mazo A, Martin-Sanchez F, Gomez AI, Martinez CM, Amores-Iniesta J, Compan V, et al. The NLRP3 inflammasome is released as a particulate danger signal that amplifies the inflammatory response. Nat Immunol. 2014;15:738–48.

  46. 46.

    Martinon F, Burns K, Tschopp J. The inflammasome: a molecular platform triggering activation of inflammatory caspases and processing of proIL-beta. Mol Cell. 2002;10:417–26.

  47. 47.

    Keller M, Ruegg A, Werner S, Beer HD. Active caspase-1 is a regulator of unconventional protein secretion. Cell. 2008;132:818–31.

  48. 48.

    Lakhani SA, Masud A, Kuida K, Porter Jr GA, Booth CJ, Mehal WZ, et al. Caspases 3 and 7: key mediators of mitochondrial events of apoptosis. Science. 2006;311:847–51.

Download references


We would like to thank nurses (P. Rapsomaniki, M. Terizaki) and clinicians (A. Fanouriakis, A. Raptopoulou) from the Rheumatology Clinic of the University Hospital of Heraklion.

The work was funded by the “Synergasia” Action “Investigation of new inflammatory mechanisms in chronic autoinflammatory & autoimmune diseases” of the Operational Programme “Education and Lifelong Learning” (co-funded by the European Social Fund (ESF) and National Resources), the Greek General Secretariat of Research and Technology (Aristeia I 2344 to DB), the Hellenic Society of Rheumatology and the Pancretan Health Association. George Bertsias received support from the FP7–2011-REGPOT-1 (TransPOT: ‘Enhancing University of Crete Medical School Scientific Excellence and Translational Research Potential in Human Diseases’).

Author information

Correspondence to Prodromos Sidiropoulos.

Additional information

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

CC contributed to study design, performed the experiments, and drafted and reviewed the manuscript. GP performed part of the experiments and reviewed the manuscript. AR and EK performed patient data acquisition, took care of the patients, and reviewed the manuscript. KK, KR, GB and DTB contributed to study design and reviewed the manuscript. PS contributed to study design and statistical analysis, and drafted and reviewed the manuscript. All authors read and approved the final manuscript.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Choulaki, C., Papadaki, G., Repa, A. et al. Enhanced activity of NLRP3 inflammasome in peripheral blood cells of patients with active rheumatoid arthritis. Arthritis Res Ther 17, 257 (2015).

Download citation


  • Rheumatoid Arthritis
  • Rheumatoid Arthritis Patient
  • Active Rheumatoid Arthritis
  • Rheumatoid Arthritis Susceptibility
  • NLRP3 Activation