Effector mechanisms of interleukin-17 in collagen-induced arthritis in the absence of interferon-γ and counteraction by interferon-γ
© Kelchtermans et al.; licensee BioMed Central Ltd. 2009
Received: 3 March 2009
Accepted: 17 August 2009
Published: 17 August 2009
Interleukin (IL)-17 is a pro-inflammatory cytokine in rheumatoid arthritis (RA) and collagen-induced arthritis (CIA). Since interferon (IFN)-γ inhibits Th17 cell development, IFN-γ receptor knockout (IFN-γR KO) mice develop CIA more readily. We took advantage of this model to analyse the mechanisms of action of IL-17 in arthritis. The role of IFN-γ on the effector mechanisms of IL-17 in an in vitro system was also investigated.
IFN-γR KO mice induced for CIA were treated with anti-IL-17 or control antibody. The collagen type II (CII)-specific humoral and cellular autoimmune responses, myelopoiesis, osteoclastogenesis, and systemic cytokine production were determined. Mouse embryo fibroblasts (MEF) were stimulated with IL-17, tumor necrosis factor (TNF)-α and the expression of cytokines and chemokines were determined.
A preventive anti-IL-17 antibody treatment inhibited CIA in IFNγR KO mice. In the joints of anti-IL-17-treated mice, neutrophil influx and bone destruction were absent. Treatment reduced the cellular autoimmune response as well as the splenic expansion of CD11b+ cells, and production of myelopoietic cytokines such as granulocyte macrophage colony-stimulating factor (GM-CSF) and IL-6. IL-17 and TNF-α synergistically induced granulocyte chemotactic protein-2 (GCP-2), IL-6 and receptor activator of NFκB ligand (RANKL) in MEF. This induction was profoundly inhibited by IFN-γ in a STAT-1 (signal transducer and activator of transcription-1)-dependent way.
In the absence of IFN-γ, IL-17 mediates its pro-inflammatory effects mainly through stimulatory effects on granulopoiesis, neutrophil infiltration and bone destruction. In vitro IFN-γ profoundly inhibits the effector function of IL-17. Thus, aside from the well-known inhibition of the development of Th17 cells by IFN-γ, this may be an additional mechanism through which IFN-γ attenuates autoimmune diseases.
IL-17 is a pro-inflammatory cytokine produced by activated CD4+ T cells distinct from Th1 or Th2 cells, designated as Th17 cells [1–3]. IL-17 promotes inflammation by enhancing production of cytokines such as IL-1β, TNF-α, IL-6 and receptor activator of nuclear factor-κB ligand (RANKL), as well as chemokines such as macrophage inflammatory protein (MIP)-2 and IL-8 [4–6]. Factors that promote Th17 cell differentiation and/or expansion are transforming growth factor (TGF)-β, IL-6 and IL-23 . Interferon (IFN)-γ, as a contrast, strongly inhibits development of Th17 cells both in vitro and in vivo [1, 3, 8]. Anti-IFN-γ added during in vitro Th17 differentiation causes increased IL-17 expression, and treated cells display increased expression of the IL-23 receptor (R) . This, together with the observation that IFN-γ decreases the expression of IL-23R in IFN-γ-deficient CD4+ T cells differentiated towards a Th17 phenotype, indicates that IFN-γ is able to inhibit expression of the IL-23R. Additionally, IFN-γ-deficient mice have increased numbers of IL-17-producing T cells following mycobacterial infection as compared with wild-type mice, and exogenous IFN-γ reduces the frequency of IL-17-producing T cells in IFN-γ-deficient mice .
There is considerable evidence that IL-17 contributes to the inflammation associated with rheumatoid arthritis (RA). IL-17 is spontaneously produced by RA synovial membrane cultures and high levels of IL-17 were detected in the synovial fluid of patients with RA [10, 11]. In collagen-induced arthritis (CIA), an animal model reminiscent in several aspects to RA, treatment with neutralizing anti-IL-17 antibody after the onset of arthritis reduces joint inflammation, cartilage destruction and bone erosion . Authors proposed that the mechanisms responsible for slowing the disease are suppression of pro-inflammatory cytokines, such as IL-1β, TNF-α and IL-6, and elimination of the additive/synergistic effects between IL-17 and these pro-inflammatory cytokines. In addition, mice genetically deficient in IL-17 or IL-17R were found to be less susceptible for induction of CIA . In contrast, local IL-17 overexpression accelerates the onset of CIA and aggravates synovial inflammation . Evidence that IFN-γ regulates susceptibility to CIA through suppression of IL-17 comes from the observation that mice of the prototypical CIA-susceptible strain DBA/1 demonstrate a high IL-17 and low IFN-γ cytokine profile as compared with CIA-resistant C57BL/6 mice . In addition, knocking out the IFN-γ gene renders the C57BL/6 mice susceptible to disease and switched their CD4+ T cell differentiation towards Th17.
Despite the exciting new knowledge about Th17 cells and IL-17, their mechanisms of action in the pathogenesis of arthritis are still unclear. In the present study we investigated pro-inflammatory characteristics of IL-17 using the CIA model. As IFN-γ is counteracting the development of Th17 cells, we chose to induce CIA in IFN-γR knock out (KO) mice. Through neutralization of IL-17 using monoclonal anti-IL-17 antibody, we tested the effect of endogenous IL-17 on various potential effector targets of CIA, such as autoimmune cellular and humoral responses, production of cytokines and chemokines, stimulation of hematopoiesis and osteoclastogenesis. We found a clear-cut inhibition of CIA by treatment with anti-IL-17 antibody and the protection was associated with profound inhibition of myelopoiesis and production of myelopoietic cytokines. Extensive myelopoiesis is a well-described phenomenom in IFN-γR KO mice challenged with (auto)antigen in complete Freund's adjuvant (CFA; reviewed in [16, 17]), so in an in vitro system using murine embryo fibroblast (MEF) cells we verified whether IL-17 may directly be involved in the induction of myelopoietic cytokines and/or chemokines and whether IFN-γ may influence this process.
Materials and methods
Antibodies and cytokines
Recombinant mouse IFN-γ was derived from the supernatant fluid of Mick cells, a Chinese hamster ovary (CHO) cell line developed in our laboratory . IFN-γ was purified by affinity chromatography to a specific activity of 108.5units/mg as described .
Anti-IL-17A antibody MM17F3 (IgG1-K) was derived from C57Bl/6 mice immunized with IL-17A-ovalbumin complexes as described . Murine IgG1 monoclonal antibody (9E10), that recognizes part of the human c-myc protein, and is produced by the MYC1-9E10.2 (ATCC CRL 1729) hybridoma, was used as control antibody .
Mice, induction, evaluation and treatment of CIA
Generation and basic characteristics of the mutant mouse strain (129/Sv/Ev) with a disruption in the gene encoding for the α-chain of the IFN-γ R (IFN-γR KO) have been described . These IFN-γR KO mice were backcrossed with wild-type DBA/1 mice for 10 generations to obtain IFN-γR KO DBA/1 mice. Homozygous IFN-γR KO mice were identified by PCR as described . Wild-type and IFN-γR KO DBA/1 mice were bred in the Experimental Animal Centre of the Rega Institute for Medical Research at Leuven.
The generation and basic characterization of IFN-γ-deficient mice of the 129 × BALB/c strain have been described . These mice were backcrossed for eight generations to the parental BALB/c strain. The signal transducer and activator of transcription (STAT)-1-/- and interferon regulatory factor (IRF)-1-/- mice, on a C57BL/6 background, were from Dr. David E. Levy of the New York University School of Medicine (New York, USA) and from Dr. Tak Mak of the Ontario Cancer Institute (Ontario, Canada), respectively. The generation and characteristics of these mice have been described [25, 26]. C57BL/6 mice (Harlan, Zeist, the Netherlands) were used as wild-type controls.
Chicken collagen type II (CII; Sigma-Aldrich, St Louis, MO, USA) was dissolved at 2 mg/ml in PBS containing 0.1 M acetic acid by stirring overnight at 6°C and emulsified in an equal volume of CFA (Difco Laboratories, Detroit, MI, USA) with added heat-killed Mycobacterium butyricum (1.5 mg/ml). Mice were sensitized with a single intradermal injection at the base of the tail with 100 μl of the emulsion on day 0, and treated with 0.2 mg of neutralizing anti-IL-17 or control antibody (in 250 μl PBS) once a week. Clinical and histological severity of arthritis were recorded following a scoring system as described [27, 28].
All animal experiments were approved by the local ethical committee (University of Leuven).
Measurement of total and anti-CII IgG antibodies and delayed-type hypersensitivity to CII
Blood samples were taken from the orbital sinus and were allowed to clot at room temperature for one hour and at 4°C overnight. Individual sera were tested for antibodies directed to chicken CII by ELISA as described . For the determination of CII-specific IgG1, IgG2a and IgG2b antibody, plates were incubated for two hours with biotinylated rat antibody to mouse IgG1, IgG2a or IgG2b (Zymed Laboratories, San Francisco, CA, USA), followed by a one-hour incubation with streptavidin-conjugated peroxidase. For measurement of total IgG antibody, plates were coated with goat anti-mouse IgG (Jackson Immunoresearch Laboratories, West Grove, PA, USA; 10 μg/ml; 100 μl/well), followed by the same procedure as described in .
For evaluation of delayed-type hypersensitivity (DTH) reactivity, CII/CFA-immunized mice were subcutaneously injected with 20 μg of CII/20 μl PBS in the left ear and with 20 μl PBS in the right ear. DTH response was calculated as the percentage swelling (the difference between the increase of thickness of the left ear and the right ear, divided by the thickness of the right ear, multiplied by 100).
Isolation of splenocytes and mouse embryo fibroblasts
Spleens were harvested, gently cut into small pieces and passed through cell strainers (Becton Dickinson Labware, Franklin Lakes, NJ, USA). Red blood cells were lysed by two consecutive incubations (5 and 3 minutes at 37°C) of the suspension in NH4Cl (0.83% in 0.01 M Tris-HCl, pH 7.2). Remaining cells were washed and counted.
To exclude any interference from endogenous IFN-γ, MEF were from IFN-γ KO BALB/c origin (unless otherwise mentioned). MEF were isolated from mouse embryos between 16 and 18 days of gestation, as described . Two times 105 MEF in a total volume of 300 μl Eagle's minimal essential medium (EMEM) containing 2% heat-inactivated FCS were seeded in chamber slides (LAB-TEK Brand Products, Nalge Nunc International, Naperville, IL, USA). After an incubation of 48 hours, cells were stimulated with IL-17 (20 ng/ml) (R&D systems, Abingdon UK) and/or TNF-α (20 ng/ml) (R&D systems, Abingdon UK) in the presence or absence of IFN-γ (100 units/ml) for 48 hours. Supernatants were collected and cells were harvested using a cell scraper (LAB-TEK Brand Products, Nalge Nunc International, Naperville, IL, USA). Cells were washed and pellets were used for PCR.
Single-cell splenocyte suspensions (0.5 × 106 cells) were incubated for 15 minutes with the Fc-receptor-blocking antibodies anti-CD16/anti-CD32 (BD Biosciences Pharmingen, San Diego, CA, USA). Cells were washed with PBS (2% FCS) and stained with the indicated fluorescein isothiocyanate (FITC)-conjugated antibodies (0.5 μg) for 30 minutes, washed and incubated with the indicated phycoerythrin (PE)-conjugated antibodies for 30 minutes. FITC-conjugated anti-CD25 (7D4) and FITC-conjugated anti-B220 were purchased from BD Biosciences Pharmingen, San Diego, CA, USA). FITC-conjugated anti-CD11b (M1/70), FITC-conjugated anti-CD8 (53-6.7), PE conjugated anti-CD4 (L3T4), and PE-conjugated anti-Gr-1 (RB6-8C5) were from eBioscience (ImmunoSource, Halle-Zoersel, Belgium). Cells were washed, fixed with 0.37% formaldehyde in PBS and flowcytometric analysis was performed on a FACScan flow cytometer with Cell Quest® software (Becton Dickinson, San Jose, CA, USA).
Detection of cytokines by quantitative PCR and ELISA
MEF were obtained as described above. RNA was extracted using the Micro-to-Midi Total RNA Purification System (Invitrogen Life Technologies, Carlsbad, CA, USA) in accordance with the manufacturer's instructions. cDNA was obtained by reverse transcription using Superscript II Reverse Transcriptase and random primers (Invitrogen Life Technologies, Carlsbad, CA, USA), in accordance with the manufacturer's instructions. For real-time PCR we used a TaqMan® Assays-on-Demand™ Gene expression Product from Applied Biosystems (Foster City, CA, USA). Expression levels of granulocyte chemotactic protein-2 (GCP-2) (assay ID Mm00436451_g1, Applied Biosystems, Foster City, CA, USA), IL-6 (assay ID Mm00446190_m1, Applied Biosystems, Foster City, CA, USA), RANKL (assay ID Mm00441908_m1, Applied Biosystems, Foster City, CA, USA), IP-10 (assay ID Mm99999072_m1) and granulocyte macrophage colony-stimulating factor (GM-CSF; assay ID Mm99999059_m1) were normalized for 18S RNA (Cat. No. 4319413E, Applied Biosystems, Foster City, CA, USA) expression. Analysis was performed in an ABI Prism 7000 apparatus (Applied Biosystems, Foster City, CA, USA) under the following conditions: inactivation of possible contaminating amplicons by AmpErase uracil-N-glycosylase at 50°C for two minutes, initial denaturation at 95°C for 10 minutes, followed by 40 thermal cycles of 15 seconds at 95°C and 90 seconds at 60°C. The relative gene expression was assessed using the 2-ΔΔCT method .
Expression of cytokines (i.e. IL-1β, IL-2, IL-4, IL-5, IL-6, IL-10, GM-CSF, IFN-γ and TNF-α) was determined by the Bio-Plex 200 system, Bio-plex Mouse Cytokine 8-plex assay and Bio-plex Mouse IL-6 Assay (Bio-Rad, Hercules, CA). IL-17, IP-10 and GM-CSF levels were measured by ELISA (R&D systems, Abingdon UK). GCP-2 was detected by an ELISA developed in our laboratory, as described .
Increased levels of IL-17 in CII/CFA-immunized IFN-γR KO mice
Neutralization of IL-17 inhibits arthritis development in IFN-γR KO mice
Reduced humoral and cellular auto-immune responses in IFN-γR KO mice treated with anti-IL-17 antibodies
Inhibition of arthritis in IFN-γR KO mice is associated with reduced expansion of CD11b+ cells
Anti-IL-17 treatment in IFN-γR KO mice decreases the production of hemopoietic cytokines
The reduced expansion of the CD11b+ cell population following treatment with anti-IL-17 antibodies might result from inhibition of the production of hemopoietic cytokines. Therefore, sera of anti-CD3-challenged IFN-γR KO mice treated with anti-IL-17 or control antibodies were collected on day 21 and tested for the presence of cytokines. Levels of GM-CSF, IL-6 and IL-12, known to stimulate hemopoiesis, were significantly reduced in the sera of mice treated with anti-IL-17 antibodies as compared with control-treated mice (Figure 4d), possibly providing an explanation for the reduced expansion of CD11b+ cells in the spleen of anti-IL-17-treated mice. Expression of IFN-γ, known to inhibit the CFA-induced expansion of CD11b+ cells, was also found to be significantly reduced upon treatment with anti-IL-17. However, as IFN-γR KO mice were used, levels of IFN-γ have no effect in our model. With regard to the expression of other cytokines, levels of the pro-inflammatory cytokine TNF-α were slightly reduced upon treatment with anti-IL-17 antibodies (1133.3 ± 658.6 and 721.9 ± 562.3 pg/ml for the control- and anti-IL-17-treated mice, respectively), and expression of all other tested cytokines (IL-2, IL-4, IL-5 and IL-10) were comparable in the sera of both groups of mice (data not shown).
IL-17 induces the production of IL-6, RANKL and GCP-2 in mouse embryo fibroblasts, and this induction is potently inhibited by IFN-γ
Inhibition of the effector function of IL-17 by IFN-γ is STAT-1- but not IRF-1-dependent
IL-17 plays a key inflammatory role in the propagation of RA and CIA [11, 34, 35]. IL-17 promotes inflammation through enhancing the production of inflammatory cytokines, such as IL-1β, TNF-α and RANKL, as well as neutrophil-specific chemokines such as MIP-2 and IL-8 [4, 5, 36]. Inhibition of the IFN-γ signaling enhances development of pathogenic Th17 cells that can exacerbate autoimmunity [3, 9]. IFN-γR KO mice have been found to experience an accelerated and more severe form of CIA . Events contributing to this protective effect of IFN-γ in CIA are inhibition of the CFA-induced myelopoiesis and osteoclastogenesis, inhibition of the production of GCP-2 and thus neutrophil infiltration, and stimulation of Treg cell activity [23, 27, 28, 31]. Recently, IFN-γ was found to regulate susceptibility to arthritis through suppression of IL-17 [15, 37]. Although Th17 cells and IL-17 have been studied extensively in previous years, much of their effector functions remain unknown. To observe maximal effects of IL-17 neutralization in CIA, we chose to start from IFN-γR KO mice for the induction of CIA. A preventive treatment with the anti-IL-17 antibodies (starting from the day of the immunization), almost completely abrogated arthritis development in IFN-γR KO mice and inhibited the influx of immunocompetent cells (predominantly neutrophils), hyperplasia of the synovial membrane and bone destruction. Lubberts and colleagues found that treatment with anti-IL-17 antibody after the onset of CIA significantly reduces the severity of CIA in wild-type mice . In line with our results, lower numbers of multinucleated cells were present in the joints of the anti-IL-17-treated mice as compared with control mice.
IL-17 is known to be a potent stimulator of osteoclastogenesis through induction of RANKL [10, 38]. Nonetheless, if splenocytes from immunized anti-IL-17-treated and control mice were stimulated ex vivo with RANKL and M-CSF for induction of osteoclastogenesis, in the absence or presence of exogenously added neutralizing anti-IL-17 antibody, no differences could be observed in the numbers or activity of osteoclasts (data not shown). More recently, however, Sato and colleagues have demonstrated that IL-17 has no effect on osteoclastogenesis in the RANKL-M-CSF system, but promotes osteoclast differentiation in the co-culture system through the induction of RANKL on osteoblastic cells .
Joint inflammation in CIA is assumed to depend in part on collagen-specific humoral and cellular immune reactivity. Treatment with anti-IL-17 antibody resulted in reduced, although not significantly, titers of total anti-CII IgG antibodies. No differences in anti-CII IgG1 and IgG2b could be detected, but significantly lower levels of anti-CII IgG2a in sera of anti-IL-17-treated IFN-γR KO mice were established. As IgG2a and IgG1 kinetics indirectly reflect Th1/Th2 responses, these data are suggestive for a lower Th1 response after treatment with anti-IL-17 antibodies. IL-17 was previously shown to be important in the induction of autoreactive humoral immune responses because a deficiency in this cytokine is associated with a decline in the autoantibody response in CIA and experimental autoimmune encephalomyelitis [13, 40]. Recently, IL-17 was found to drive autoimmune responses by promoting the formation of spontaneous germinal centers . With regard to the cellular immune responses, we found significantly impaired DTH to CII in IFN-γR KO mice treated with anti-IL-17 antibody. In IL-17 KO mice, Nakae and colleagues have established significantly reduced proliferative responses of lymph node cells against CII in comparison with that of wild-type mice . Taken together, these results demonstrate a crucial role for IL-17 in the activation of CII-specific cellular responses.
As we reported earlier , the increased severity of CIA in IFN-γR KO mice is associated with an increased CFA-induced extramedullary expansion of immature CD11b+ macrophages and neutrophils. In the present study we showed that anti-IL-17 antibodies inhibit the expansion of this CD11b+ cell population. Characterization of these CD11b+ splenocytes indicated a significant reduction in the numbers of (immature) neutrophils. The lower numbers of neutrophils present in the spleen may provide an explanation for the reduced influx of neutrophils in the joints of the anti-IL-17-treated mice. IL-17 has been found to act as a stimulatory hematopoietic cytokine by expanding myeloid progenitors and initiating proliferation of mature neutrophils . It has been described to induce the secretion of hematopoietic cytokines such as IL-6 and G-CSF in fibroblasts, through which these stimulated fibroblasts can sustain the proliferation of hematopoietic progenitors and their preferential maturation into neutrophils . In the same line, IL-17R KO mice have impaired hemopoietic recovery following gamma irradiation; hemopoietic precursors are reduced by 50% and neutrophils by 43% . In the present study, the reduced granulopoiesis observed in anti-IL-17-treated mice probably resulted from reduced production of GM-CSF, IL-6 and IL-12. Treatment with neutralizing anti-IL-17 antibodies after the onset of arthritis has also been demonstrated to result in significantly reduced systemic IL-6 levels in wild-type mice . Along the same line, stimulation of various cell types with IL-17 has been found to induce production of pro-inflammatory mediators such as IL-6 and GM-CSF [4, 44, 45].
In a previous set of experiments we tested whether the observed reduced influx of neutrophils in the joints, bone destruction and hematopoiesis directly result from neutralization of IL-17, or were a reflexion of the reduced inflammation present in the anti-IL-17-treated mice. In mice, IL-8, the prototype of human CXC chemokines that mainly affect neutrophil migration, has not been described, but the only neutrophil-attracting chemokine recognizing CXCR1 and 2 is GCP-2, generally considered as the functional equivalent of IL-8 in humans [46, 47]. We found that IL-17 and TNF-α synergistically induce the production of GCP-2, RANKL, IL-6 and GM-CSF in MEF, thereby providing an explanation for the observed phenomena upon neutralization of IL-17. The induction of IL-6 and RANKL by IL-17 has been described [4, 48, 49]. In addition, studies have already linked IL-17 to induction of neutrophil-specific chemokines such as IL-8 and MIP-2 and the consequent effects on neutrophil recruitment [5, 6, 49]. More recently, IL-17 was shown to promote the selective expression of ELR+ CXC chemokines in RA synoviocytes, especially in the presence of TNF-α, highlighting its role in neutrophil recruitment into the joint . Furthermore, IL-17 induces the production of GCP-2 in a preosteoblast cell line and normal mesenchymal cells [50, 51]. Shen and colleagues have shown that the CXC family chemokines, including KC, MIP-2 and GCP-2, were dramatically induced by IL-17 and/or TNF-α . Recently, IL-17 was found to enhance cartilage destruction by increasing the production of KC and MIP-2, and thereby the influx of Fcγ R-bearing neutrophils . Importantly, we established an inhibition of this production of GCP-2, RANKL and IL-6 upon addition of IFN-γ. Levels of other tested cytokines induced by TNF-α/IL-17 were upregulated or not affected by IFN-γ, indicating that inhibition was specific. Although IFN-γ has been described to regulate neutrophil influx through inhibition of the IL-1β-, TNF-α-driven or mycobacteria-driven production of IL-8 and/or GCP-2 [28, 51, 53, 54], its effect on IL-17-induced gene expression was so far not investigated. Using STAT-1-/- and IRF-1-/- MEF, we found that the observed inhibition by IFN-γ is IRF-1-independent, but STAT-1-dependent. Taken together, aside from the well-known inhibition of the development of Th17 cells by IFN-γ, we demonstrate that IFN-γ profoundly inhibits the effector function of IL-17 in a STAT-1-dependent way.
As levels of IL-17 were found to be significantly lower in wild-type mice as compared with IFN-γR KO mice and because IFN-γ profoundly inhibits the effector function of IL-17, we expected the protective effect of anti-IL-17 in wild-type mice to be less pronounced. However, a preventive anti-IL-17 antibody treatment significantly inhibited the clinical and histological symptoms of arthritis in wild-type mice (with a total of 16 mice in each group, an incidence was reached of 54% and 13% respectively in control-treated and anti-IL-17-treated wild-type mice). In an attempt to unravel the mechanism of protection, we analysed the effect of anti-IL-17 treatment on different effector targets. Whereas the CII cellular autoimmune response (i.e. DTH) was found to be reduced by half upon treatment with anti-IL-17 antibody, the production of anti-CII autoantibodies and the splenic expansion of CD11b+ cells were not affected (data not shown). Thus, although anti-IL-17 antibody is effective in reducing the clinical symptoms of arthritis in both IFN-γR KO and wild-type mice, the mechanism of endogenous IL-17 in the pathogenesis of CIA appears to be somewhat different between the two groups of mice.
It is generally accepted that different pathways, such as humoral and cellular immune responses, myelopoiesis and osteoclastogenesis are all required to develop CIA. Depending on the presence or absence of IFN-γ, IL-17 mediated several of these processes and it can be speculated that blocking just one of these pathways, for example DTH, may be sufficient to prevent symptoms of arthritis. Alternatively, there may exist a profound effector mechanism of IL-17 in both IFN-γR KO and wild-type mice that has not been investigated in our study and still needs to be discovered.
In conclusion, our experiments underscore that IL-17 mediates its pro-inflammatory role in CIA in IFN-γR KO mice mainly through stimulatory effects on granulopoiesis, neutrophil infiltration and bone destruction. Importantly, our data reveal also an additional mechanism through which IFN-γ can attenuate some autoimmune diseases and autoimmune arthritis in particular. Apart from the inhibition of the production of IL-17, IFN-γ also abrogates some of the effector functions of IL-17. Thus, through its inhibition of the IL-17-induced production of IL-6, GCP-2 and RANKL, IFN-γ can profoundly limit granulopoiesis, mobilisation of neutrophils, and bone destruction, which are all important in joint inflammation.
complete Freund's adjuvant
Chinese hamster ovary
collagen type II
delayed type hypersensitivity
enzyme-linked immunosorbent assay
Eagle's minimal essential medium
fetal calf serum
granulocyte chemotactic protein-2
granulocyte colony-stimulating factor
granulocyte macrophage colony-stimulating factor
- IFN-γR KO:
interferon-γ receptor knock-out
interferon regulatory factor
interferon-inducible T cell alpha chemoattractant
monocyte chemotactic protein
macrophage colony-stimulating factor
mouse embryo fibroblasts
monokine induced by gamma interferon
macrophage inflammatory protein
phosphate buffered saline
polymerase chain reaction
receptor activator of nuclear factor-κB ligand
Regulated upon Activation, Normal T-cell Expressed, and Secreted
signal transducer and activator of transcription
transforming growth factor-β
tumor necrosis factor-α.
We thank Chris Dillen and Willy Put for excellent assistance. We are grateful to Prof. Dr. Ghislain Opdenakker for critical review of the manuscript. This study was supported by grants from the Fund of Scientific Research Flanders (FWO Vlaanderen), and from the Regional Government of Flanders (GOA program). HK is a postdoctoral research fellow of the FWO Vlaanderen, and LG holds a fellowship from the FWO Vlaanderen.
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