Skip to main content
Top
Published in: Drugs & Aging 2/2010

01-02-2010 | Review Article

Anticytokine Therapy for Osteoarthritis

Evidence to Date

Author: Professor Charles J. Malemud

Published in: Drugs & Aging | Issue 2/2010

Login to get access

Abstract

Several recent in vitro investigations and experimental studies performed in animal models of osteoarthritis (OA) sustained the previously held view that interleukin (IL)-1 or tumour necrosis factor-α (TNFα) disrupt the metabolism of synovial joint tissues. The evidence to date indicates that, in addition to IL-1 and TNFα, other pro-inflammatory cytokines, including IL-6, members of the IL-6 protein superfamily, IL-7, IL-17 and IL-18, can also promote articular cartilage extracellular matrix protein degradation or synergize with other cytokines to amplify and accelerate cartilage destruction. Most importantly, many of these cytokines have been implicated in causing synovial tissue activation and damage to subchondral bone as well as altering cartilage homeostasis in spontaneously occurring or surgically induced animal models of OA and in transgenic mice genetically primed to develop OA. In this regard, these pro-inflammatory cytokines may also play a significant role in the pathogenesis of human OA. However, attempts to modify the progression of human OA in well designed, controlled clinical trials with an IL-1 receptor antagonist protein (IRAP) have not been successful. Several anabolic cytokines (also termed growth factors), including transforming growth factor-β (TGF-β), insulin-like growth factor-1 (IGF-1), fibroblast growth factor-2 (FGF-2), platelet-derived growth factor (PDGF) and connective tissue growth factor (CTGF), have also been proposed as regulators of skeletal long bone growth and development as well as cartilage and bone homeostasis. TGF-β, IGF-1 and FGF-2, in particular, have been characterized as potential chondroprotective agents. Thus, enzymatic disruption and removal of these growth factors from cartilage extracellular matrix proteins, as in the case of TGF-β and FGF-2, or disruption of their function, as in the case of the enhanced binding of free IGF-1 with IGF binding proteins in OA joint synovial fluid, may compromise and ultimately be responsible for the inadequate repair of articular cartilage in OA. An improved understanding of the cellular and molecular mechanisms by which pro-inflammatory and/or anabolic cytokines alter both the structure and function of synovial joints may eventually result in the commercial development of disease-modifying OA drugs (DMOADs). Since the prevalence of OA is high in the elderly population, future development of DMOADs must also take into account potential differences in the way DMOADs would be metabolized in the older individual compared with younger people.
Literature
1.
2.
go back to reference Fernandes JC, Martel-Pelletier J, Pelletier J-P. The role of cytokines in osteoarthritis pathophysiology. Biorheology 2002; 39(1–2): 237–46PubMed Fernandes JC, Martel-Pelletier J, Pelletier J-P. The role of cytokines in osteoarthritis pathophysiology. Biorheology 2002; 39(1–2): 237–46PubMed
3.
4.
go back to reference Blom AB, van der Kraan PM, van den Berg WB. Cytokine targeting in osteoarthritis. Curr Drug Targets 2007; 8(2): 283–92PubMedCrossRef Blom AB, van der Kraan PM, van den Berg WB. Cytokine targeting in osteoarthritis. Curr Drug Targets 2007; 8(2): 283–92PubMedCrossRef
5.
go back to reference Martel-Pelletier J, Pelletier J-P. Inflammatory factors involved in osteoarthritis. In: Buckwalter JA, Lotz M, Stoltz J-F, editors. Osteoarthritis, inflammation and degradation: a continuum. Amsterdam: IOS Press, 2007: 3–13 Martel-Pelletier J, Pelletier J-P. Inflammatory factors involved in osteoarthritis. In: Buckwalter JA, Lotz M, Stoltz J-F, editors. Osteoarthritis, inflammation and degradation: a continuum. Amsterdam: IOS Press, 2007: 3–13
6.
go back to reference Otero M, Lago R, Gómez R, et al. Leptin, a metabolic hormone that functions as a proinflammatory adipokine. Drug New Prospect 2006; 19(1): 21–6CrossRef Otero M, Lago R, Gómez R, et al. Leptin, a metabolic hormone that functions as a proinflammatory adipokine. Drug New Prospect 2006; 19(1): 21–6CrossRef
7.
go back to reference Saklatvala J. Inflammatory signalling in cartilage: MAPK and NF-κB pathways in chondrocytes and the use of inhibitors for research into the pathogenesis and therapy of osteoarthritis. Curr Drug Targets 2007; 8(2): 305–13PubMedCrossRef Saklatvala J. Inflammatory signalling in cartilage: MAPK and NF-κB pathways in chondrocytes and the use of inhibitors for research into the pathogenesis and therapy of osteoarthritis. Curr Drug Targets 2007; 8(2): 305–13PubMedCrossRef
8.
go back to reference Fan Z, Söder S, Oehler S, et al. Activation of interleukin-1 signaling cascades and osteoarthritic cartilage. Am J Pathol 2007; 171(3): 938–46PubMedCrossRef Fan Z, Söder S, Oehler S, et al. Activation of interleukin-1 signaling cascades and osteoarthritic cartilage. Am J Pathol 2007; 171(3): 938–46PubMedCrossRef
9.
go back to reference Pujol J-P, Chadjichristos C, Legendre F, et al. Interleukin-1 and transforming growth factor-β1 as crucial factors in osteoarthritic cartilage metabolism. Connect Tissue Res 2008; 49(3): 293–7PubMedCrossRef Pujol J-P, Chadjichristos C, Legendre F, et al. Interleukin-1 and transforming growth factor-β1 as crucial factors in osteoarthritic cartilage metabolism. Connect Tissue Res 2008; 49(3): 293–7PubMedCrossRef
10.
go back to reference Corr M. Wnt-beta-catenin signaling in the pathogenesis of osteoarthritis. Nat Clin Pract Rheumatol 2008; 4(10): 550–6PubMedCrossRef Corr M. Wnt-beta-catenin signaling in the pathogenesis of osteoarthritis. Nat Clin Pract Rheumatol 2008; 4(10): 550–6PubMedCrossRef
11.
go back to reference Morales TI. The quantitative and functional relation between insulin-like growth factor-1 (IGF) and IGF-binding proteins during human osteoarthritis. J Orthop Res 2008; 26(4): 465–74PubMedCrossRef Morales TI. The quantitative and functional relation between insulin-like growth factor-1 (IGF) and IGF-binding proteins during human osteoarthritis. J Orthop Res 2008; 26(4): 465–74PubMedCrossRef
12.
go back to reference Goldring MB, Otero M, Tsuchimochi K, et al. Defining the roles of inflammatory and anabolic cytokines in cartilage metabolism. Ann Rheum Dis 2008; 67Suppl. 3: iii75-82PubMedCrossRef Goldring MB, Otero M, Tsuchimochi K, et al. Defining the roles of inflammatory and anabolic cytokines in cartilage metabolism. Ann Rheum Dis 2008; 67Suppl. 3: iii75-82PubMedCrossRef
13.
go back to reference Verbruggen G. Chondroprotective drugs in degenerative joint diseases. Rheumatology (Oxford) 2006; 45(2): 129–38CrossRef Verbruggen G. Chondroprotective drugs in degenerative joint diseases. Rheumatology (Oxford) 2006; 45(2): 129–38CrossRef
14.
go back to reference Tincani A, Andreoli L, Bazzani C, et al. Inflammatory molecules: a target for treatment in systemic autoimmune diseases. Autoimmun Rev 2007; 7(1): 1–7PubMedCrossRef Tincani A, Andreoli L, Bazzani C, et al. Inflammatory molecules: a target for treatment in systemic autoimmune diseases. Autoimmun Rev 2007; 7(1): 1–7PubMedCrossRef
15.
go back to reference Sizova L. Approaches to the treatment of early rheumatoid arthritis with disease-modifying antirheumatic drugs. Br J Clin Pharmacol 2008; 66(2): 173–8PubMedCrossRef Sizova L. Approaches to the treatment of early rheumatoid arthritis with disease-modifying antirheumatic drugs. Br J Clin Pharmacol 2008; 66(2): 173–8PubMedCrossRef
16.
go back to reference Alonso-Ruiz A, Pijoan JI, Ansuategui E, et al. Tumor necrosis factor alpha drugs in rheumatoid arthritis: systemic review and metaanalysis of efficacy and safety. BMC Musculoskel Disord 2008; 9: 52CrossRef Alonso-Ruiz A, Pijoan JI, Ansuategui E, et al. Tumor necrosis factor alpha drugs in rheumatoid arthritis: systemic review and metaanalysis of efficacy and safety. BMC Musculoskel Disord 2008; 9: 52CrossRef
17.
go back to reference Tayal V, Kaira BS. Cytokines and anti-cytokines as therapeutics: an update. Eur J Pharmacol 2008; 579(1–3): 1–12PubMedCrossRef Tayal V, Kaira BS. Cytokines and anti-cytokines as therapeutics: an update. Eur J Pharmacol 2008; 579(1–3): 1–12PubMedCrossRef
18.
go back to reference Daheshia M, Yao JQ. The interleukin 1b pathway in the pathogenesis of osteoarthritis. J Rheumatol 2008; 35(12): 2306–12PubMedCrossRef Daheshia M, Yao JQ. The interleukin 1b pathway in the pathogenesis of osteoarthritis. J Rheumatol 2008; 35(12): 2306–12PubMedCrossRef
19.
go back to reference Glasson SS. In vivo osteoarthritis target validation using genetically-modified mice. Curr Drug Targets 2007; 8(2): 367–76PubMedCrossRef Glasson SS. In vivo osteoarthritis target validation using genetically-modified mice. Curr Drug Targets 2007; 8(2): 367–76PubMedCrossRef
20.
go back to reference Chen LX, Lin X, Wang HJ, et al. Suppression of early experimental osteoarthritis by in vivo delivery of the adenoviral vector-mediated NF-κB65-specific siRNA. Osteoarthritis Cartilage 2008; 16(2): 174–84PubMedCrossRef Chen LX, Lin X, Wang HJ, et al. Suppression of early experimental osteoarthritis by in vivo delivery of the adenoviral vector-mediated NF-κB65-specific siRNA. Osteoarthritis Cartilage 2008; 16(2): 174–84PubMedCrossRef
21.
go back to reference Huebner JL, Selfer DR, Kraus VB. A longitudinal analysis of serum cytokines in the Hartley guinea pig model of osteoarthritis. Osteoarthritis Cartilage 2007; 15(3): 354–6PubMedCrossRef Huebner JL, Selfer DR, Kraus VB. A longitudinal analysis of serum cytokines in the Hartley guinea pig model of osteoarthritis. Osteoarthritis Cartilage 2007; 15(3): 354–6PubMedCrossRef
22.
go back to reference Ley C, Ekman S, Elmén A, et al. Interleukin-6 and tumour necrosis factor in synovial fluid from horses with carpal joint pathology. J Vet Med A Physiol Pathol Clin Med 2007; 54(7): 346–51PubMedCrossRef Ley C, Ekman S, Elmén A, et al. Interleukin-6 and tumour necrosis factor in synovial fluid from horses with carpal joint pathology. J Vet Med A Physiol Pathol Clin Med 2007; 54(7): 346–51PubMedCrossRef
23.
go back to reference Maccoux LJ, Salway F, Day PJ, et al. Expression profiling of select cytokines in canine osteoarthritis tissues. Vet Immunol Immunopathol 2007; 118(1–2): 59–67PubMedCrossRef Maccoux LJ, Salway F, Day PJ, et al. Expression profiling of select cytokines in canine osteoarthritis tissues. Vet Immunol Immunopathol 2007; 118(1–2): 59–67PubMedCrossRef
24.
go back to reference Bondeson J, Wainwright SD, Lauder S, et al. The role of synovial macrophages and macrophage-produced cytokines in driving aggrecanases, matrix metalloproteinases, and other destructive and inflammatory responses in osteoarthritis. Arthritis Res Ther 2006; 8(6): R187PubMedCrossRef Bondeson J, Wainwright SD, Lauder S, et al. The role of synovial macrophages and macrophage-produced cytokines in driving aggrecanases, matrix metalloproteinases, and other destructive and inflammatory responses in osteoarthritis. Arthritis Res Ther 2006; 8(6): R187PubMedCrossRef
25.
go back to reference Doss F, Menard J, Hauschild N, et al. Elevated IL-6 levels in the synovial fluid of osteoarthritis patients stem from plasma cells. Scand J Rheumatol 2007; 36(2): 136–9PubMedCrossRef Doss F, Menard J, Hauschild N, et al. Elevated IL-6 levels in the synovial fluid of osteoarthritis patients stem from plasma cells. Scand J Rheumatol 2007; 36(2): 136–9PubMedCrossRef
26.
go back to reference Kobayashi M, Squires GR, Mousa A, et al. Role of interleukin-1 and tumor necrosis factor α in matrix degradation of human osteoarthritic cartilage. Arthritis Rheum 2005; 52(1): 128–35PubMedCrossRef Kobayashi M, Squires GR, Mousa A, et al. Role of interleukin-1 and tumor necrosis factor α in matrix degradation of human osteoarthritic cartilage. Arthritis Rheum 2005; 52(1): 128–35PubMedCrossRef
27.
go back to reference Burger D, Dayer J-M, Palmer G, et al. Is IL-1 a good therapeutic target in the treatment of arthritis? Best Pract Res Clin Rheumatol 2006; 20(5): 879–96PubMedCrossRef Burger D, Dayer J-M, Palmer G, et al. Is IL-1 a good therapeutic target in the treatment of arthritis? Best Pract Res Clin Rheumatol 2006; 20(5): 879–96PubMedCrossRef
28.
go back to reference Goupille P, Mulleman D, Chevalier X. Is interleukin 1 a good target for therapeutic intervention in intervertebral disc degeneration: lessons for the osteoarthritic experience. Arthritis Res Ther 2007; 9(6): 110PubMedCrossRef Goupille P, Mulleman D, Chevalier X. Is interleukin 1 a good target for therapeutic intervention in intervertebral disc degeneration: lessons for the osteoarthritic experience. Arthritis Res Ther 2007; 9(6): 110PubMedCrossRef
29.
go back to reference Iqbal I, Fleischmann R. Treatment of osteoarthritis with anakinra. Curr Rheumatol Rep 2007; 9(1): 31–5PubMedCrossRef Iqbal I, Fleischmann R. Treatment of osteoarthritis with anakinra. Curr Rheumatol Rep 2007; 9(1): 31–5PubMedCrossRef
30.
go back to reference Chevalier X, Giraudeau B, Conrozier T, et al. Safety study of intraarticular injection of interleukin 1 receptor antagonist in patients with painful knee osteoarthritis: a multicenter study. J Rheumatol 2005; 32(7): 1317–23PubMed Chevalier X, Giraudeau B, Conrozier T, et al. Safety study of intraarticular injection of interleukin 1 receptor antagonist in patients with painful knee osteoarthritis: a multicenter study. J Rheumatol 2005; 32(7): 1317–23PubMed
31.
go back to reference Chevalier X, Goupille P, Beaulieu AD, et al. Intraarticular injection of anakinra in osteoarthritis of the knee: a multicenter, randomized, double-blind placebo-controlled trial. Arthritis Rheum 2009; 61(3): 344–52PubMedCrossRef Chevalier X, Goupille P, Beaulieu AD, et al. Intraarticular injection of anakinra in osteoarthritis of the knee: a multicenter, randomized, double-blind placebo-controlled trial. Arthritis Rheum 2009; 61(3): 344–52PubMedCrossRef
32.
go back to reference Yang KG, Raijmakers NJ, van Arkel ER, et al. Autologous interleukin-1 receptor antagonist improves function and symptoms in osteoarthritis when compared to placebo in a prospective randomized controlled trial. Osteoarthritis Cartilage 2008; 16(4): 498–505PubMedCrossRef Yang KG, Raijmakers NJ, van Arkel ER, et al. Autologous interleukin-1 receptor antagonist improves function and symptoms in osteoarthritis when compared to placebo in a prospective randomized controlled trial. Osteoarthritis Cartilage 2008; 16(4): 498–505PubMedCrossRef
33.
go back to reference Richette P, François M, Vicaut E, et al. A high interleukin 1 receptor anatagonist/IL-1b ratio occurs naturally in knee osteoarthritis. J Rheumatol 2008; 35(8): 1650–4PubMed Richette P, François M, Vicaut E, et al. A high interleukin 1 receptor anatagonist/IL-1b ratio occurs naturally in knee osteoarthritis. J Rheumatol 2008; 35(8): 1650–4PubMed
34.
go back to reference Lequesne MG. The algofunctional indices for hip and knee osteoarthritis. J Rheumatol 1997; 24(4): 779–81PubMed Lequesne MG. The algofunctional indices for hip and knee osteoarthritis. J Rheumatol 1997; 24(4): 779–81PubMed
35.
go back to reference Miyaki S, Nakasa T, Otsuki S, et al. MicroRNA-140 is expressed in differentiated human articular chondrocytes and modulates interleukin-1 responses. Arthritis Rheum 2009; 60(9): 2723–30PubMedCrossRef Miyaki S, Nakasa T, Otsuki S, et al. MicroRNA-140 is expressed in differentiated human articular chondrocytes and modulates interleukin-1 responses. Arthritis Rheum 2009; 60(9): 2723–30PubMedCrossRef
36.
go back to reference Tetlow LC, Adlam DJ, Woolley DE. Matrix metalloproteinase and proinflammatory cytokine production by chondrocytes of human osteoarthritis cartilage: associations with degenerative changes. Arthritis Rheum 2001; 44(3): 585–94PubMedCrossRef Tetlow LC, Adlam DJ, Woolley DE. Matrix metalloproteinase and proinflammatory cytokine production by chondrocytes of human osteoarthritis cartilage: associations with degenerative changes. Arthritis Rheum 2001; 44(3): 585–94PubMedCrossRef
37.
go back to reference Wu W, Billinghurst RC, Pidoux I, et al. Sites of collagenase cleavage and denaturation of type II collagen in aging and osteoarthritic articular cartilage and their relationship to the distribution of matrix metalloproteinase 1 and matrix metalloproteinase 13. Arthritis Rheum 2002; 46(8): 2087–94PubMedCrossRef Wu W, Billinghurst RC, Pidoux I, et al. Sites of collagenase cleavage and denaturation of type II collagen in aging and osteoarthritic articular cartilage and their relationship to the distribution of matrix metalloproteinase 1 and matrix metalloproteinase 13. Arthritis Rheum 2002; 46(8): 2087–94PubMedCrossRef
38.
go back to reference Brandt KD, Dieppe P, Radin E. Etiopathogenesis of osteoarthritis. Med Clin North Am 2009; 93(1): 1–24, xvPubMedCrossRef Brandt KD, Dieppe P, Radin E. Etiopathogenesis of osteoarthritis. Med Clin North Am 2009; 93(1): 1–24, xvPubMedCrossRef
39.
go back to reference Denko CW, Malemud CJ. Metabolic disturbances and synovial membrane responses in osteoarthritis. Front Biosci 1999; 4: D686–93PubMed Denko CW, Malemud CJ. Metabolic disturbances and synovial membrane responses in osteoarthritis. Front Biosci 1999; 4: D686–93PubMed
40.
go back to reference Denko CW, Malemud CJ. Role of the growth hormone/insulin-like growth factor-1 paracrine axis in rheumatic diseases. Semin Arthritis Rheum 2005; 35(1): 24–34PubMedCrossRef Denko CW, Malemud CJ. Role of the growth hormone/insulin-like growth factor-1 paracrine axis in rheumatic diseases. Semin Arthritis Rheum 2005; 35(1): 24–34PubMedCrossRef
41.
go back to reference Patel IR, Attur MG, Patel RN, et al. TNF-α convertase enzyme from human arthritis-affected cartilage: isolation of cDNA by differential display, expression of the active enzyme, and regulation of TNF-α. J Immunol 1998; 160(9): 4570–9PubMed Patel IR, Attur MG, Patel RN, et al. TNF-α convertase enzyme from human arthritis-affected cartilage: isolation of cDNA by differential display, expression of the active enzyme, and regulation of TNF-α. J Immunol 1998; 160(9): 4570–9PubMed
42.
go back to reference Skotnicki JS, DiGrandi MJ, Levin JI. Design strategies for the identification of MMP-13 and TACE inhibitors. Curr Opin Drug Discov Devel 2003; 6(5): 742–59PubMed Skotnicki JS, DiGrandi MJ, Levin JI. Design strategies for the identification of MMP-13 and TACE inhibitors. Curr Opin Drug Discov Devel 2003; 6(5): 742–59PubMed
43.
go back to reference Levin JI. The design and synthesis of aryl hydroxamic acid inhibitors of MMPs and TACE. Curr Top Med Chem 2004; 4(12): 1289–310PubMedCrossRef Levin JI. The design and synthesis of aryl hydroxamic acid inhibitors of MMPs and TACE. Curr Top Med Chem 2004; 4(12): 1289–310PubMedCrossRef
44.
go back to reference Pelletier J-P, Martel-Pelletier J, Malemud CJ. Effects of non-steroidal anti-inflammatory drugs and corticosteroids on cartilage metabolism in rheumatoid arthritis and osteoarthritis. In: Lewis AJ, Furst DE, editors. Non-steroidal anti-inflammatory drugs: mechanisms and clinical uses. 2nd ed. New York: Marcel Dekker, 1994: 5–25 Pelletier J-P, Martel-Pelletier J, Malemud CJ. Effects of non-steroidal anti-inflammatory drugs and corticosteroids on cartilage metabolism in rheumatoid arthritis and osteoarthritis. In: Lewis AJ, Furst DE, editors. Non-steroidal anti-inflammatory drugs: mechanisms and clinical uses. 2nd ed. New York: Marcel Dekker, 1994: 5–25
45.
go back to reference Hochberg MC, Dougados M. Pharmacological therapy of osteoarthritis. Best Pract Res Clin Rheumatol 2001; 15(4) 583–93PubMedCrossRef Hochberg MC, Dougados M. Pharmacological therapy of osteoarthritis. Best Pract Res Clin Rheumatol 2001; 15(4) 583–93PubMedCrossRef
46.
go back to reference Petrella RJ, Petrella M. A prospective, randomized, double-blind, placebo controlled study to evaluate the efficacy of intraarticular hyaluronic acid for osteoarthritis of the knee. J Rheumatol 2006; 33(5): 951–6PubMed Petrella RJ, Petrella M. A prospective, randomized, double-blind, placebo controlled study to evaluate the efficacy of intraarticular hyaluronic acid for osteoarthritis of the knee. J Rheumatol 2006; 33(5): 951–6PubMed
47.
go back to reference Brzusek D, Petron D. Treating knee osteoarthritis with intra-articular hyaluronans. Curr Med Res Opin 2008; 24(12): 3307–22PubMedCrossRef Brzusek D, Petron D. Treating knee osteoarthritis with intra-articular hyaluronans. Curr Med Res Opin 2008; 24(12): 3307–22PubMedCrossRef
48.
go back to reference Schnitzer TJ, Weaver AL, Polis AB, et al. Efficacy of rofecoxib, celecoxib, and acetaminophen in patients with osteoarthritis of the knee: a combined analysis of the VACT studies. J Rheumatol 2005; 32(6): 1093–105PubMed Schnitzer TJ, Weaver AL, Polis AB, et al. Efficacy of rofecoxib, celecoxib, and acetaminophen in patients with osteoarthritis of the knee: a combined analysis of the VACT studies. J Rheumatol 2005; 32(6): 1093–105PubMed
49.
go back to reference Singh G, Fort JG, Goldstein JL, et al. Celecoxib versus naproxen and diclofenac in osteoarthritis patients: SUCCESS-I study. Am J Med 2006; 1993(3): 255–66CrossRef Singh G, Fort JG, Goldstein JL, et al. Celecoxib versus naproxen and diclofenac in osteoarthritis patients: SUCCESS-I study. Am J Med 2006; 1993(3): 255–66CrossRef
50.
go back to reference Becker MC, Wang TH, Wisniewski L, et al. Rationale, design and governance of Prospective Randomized Evaluation of Celecoxib Integrated Safety versus Ibuprofen or Naproxen (PRECISION), a cardiovascular end point trial of nonsteroidal anti-inflammatory agents in patients with arthritis. Am Heart J 2009; 157(4): 606–12PubMedCrossRef Becker MC, Wang TH, Wisniewski L, et al. Rationale, design and governance of Prospective Randomized Evaluation of Celecoxib Integrated Safety versus Ibuprofen or Naproxen (PRECISION), a cardiovascular end point trial of nonsteroidal anti-inflammatory agents in patients with arthritis. Am Heart J 2009; 157(4): 606–12PubMedCrossRef
51.
go back to reference Curtis SP, Bockow B, Fisher C, et al. Etoricoxib in the treatment of osteoarthritis over 52-weeks: a double blind, active comparator controlled trial [NCT00242489]. BMC Musculoskelet Disord 2005; 6: 58PubMedCrossRef Curtis SP, Bockow B, Fisher C, et al. Etoricoxib in the treatment of osteoarthritis over 52-weeks: a double blind, active comparator controlled trial [NCT00242489]. BMC Musculoskelet Disord 2005; 6: 58PubMedCrossRef
52.
go back to reference Reginster JY, Malmstrom K, Mehta A, et al. Evaluation of the efficacy and safety of etoricoxib compared with naproxen in 2, 138-week randomised studies of patients with osteoarthritis. Ann Rheum Dis 2007; 66(7): 945–51PubMedCrossRef Reginster JY, Malmstrom K, Mehta A, et al. Evaluation of the efficacy and safety of etoricoxib compared with naproxen in 2, 138-week randomised studies of patients with osteoarthritis. Ann Rheum Dis 2007; 66(7): 945–51PubMedCrossRef
53.
go back to reference Dahlberg LE, Holme I, Høye K, et al. A randomised, multicentre, double-blind, parallel-group study to assess adverse event-related discontinuation rate with celecoxib and diclofenac in elderly patients with osteoarthritis. Scand J Rheumatol 2009; 38(2): 133–43PubMedCrossRef Dahlberg LE, Holme I, Høye K, et al. A randomised, multicentre, double-blind, parallel-group study to assess adverse event-related discontinuation rate with celecoxib and diclofenac in elderly patients with osteoarthritis. Scand J Rheumatol 2009; 38(2): 133–43PubMedCrossRef
54.
go back to reference Mastbergen SC, Bijlsma JW, Lafeber FP. Selective COX-2 inhibition is favorable to human early and late-stage osteoarthritic cartilage: a human in vitro study. Osteoarthritis Cartilage 2005; 13(6): 519–26PubMedCrossRef Mastbergen SC, Bijlsma JW, Lafeber FP. Selective COX-2 inhibition is favorable to human early and late-stage osteoarthritic cartilage: a human in vitro study. Osteoarthritis Cartilage 2005; 13(6): 519–26PubMedCrossRef
55.
go back to reference Mastbergen SC, Marijnissen AC, Vianen ME, et al. Inhibition by celecoxib in the canine groove model of osteoarthritis. Rheumatology (Oxford) 2006; 45(4): 405–13CrossRef Mastbergen SC, Marijnissen AC, Vianen ME, et al. Inhibition by celecoxib in the canine groove model of osteoarthritis. Rheumatology (Oxford) 2006; 45(4): 405–13CrossRef
56.
go back to reference Bottone FG, Barry WT. Postmarketing surveillance of serious adverse events associated with the use of rofecoxib from 1999–2002. Curr Med Res Opin 2009; 25(6): 1535–50PubMedCrossRef Bottone FG, Barry WT. Postmarketing surveillance of serious adverse events associated with the use of rofecoxib from 1999–2002. Curr Med Res Opin 2009; 25(6): 1535–50PubMedCrossRef
57.
go back to reference Jeffrey JE, Aspden RM. Cyclooxygenase inhibition lowers prostaglandin E2 release from articular cartilage and reduces apoptosis but not proteoglycan degradation following an impact load in vitro. Arthritis Res Ther 2007; 9(6): R129PubMedCrossRef Jeffrey JE, Aspden RM. Cyclooxygenase inhibition lowers prostaglandin E2 release from articular cartilage and reduces apoptosis but not proteoglycan degradation following an impact load in vitro. Arthritis Res Ther 2007; 9(6): R129PubMedCrossRef
58.
go back to reference Malemud CJ, Gillespie HJ. The role of apoptosis in arthritis. Curr Rheum Rev 2005; 1(2): 131–42CrossRef Malemud CJ, Gillespie HJ. The role of apoptosis in arthritis. Curr Rheum Rev 2005; 1(2): 131–42CrossRef
59.
60.
go back to reference Weng LH, Wang CJ, Ko JY, et al. Inflammation induction of Dickkopf-1 mediates chondrocyte apoptosis in osteoarthritic joint. Osteoarthritis Cartilage 2009; 17(7): 919–29CrossRef Weng LH, Wang CJ, Ko JY, et al. Inflammation induction of Dickkopf-1 mediates chondrocyte apoptosis in osteoarthritic joint. Osteoarthritis Cartilage 2009; 17(7): 919–29CrossRef
61.
go back to reference Burrage PS, Mix KS, Brinckerhoff CE. Matrix metalloproteinases: role in arthritis. Front Biosci 2006; 11: 529–43PubMedCrossRef Burrage PS, Mix KS, Brinckerhoff CE. Matrix metalloproteinases: role in arthritis. Front Biosci 2006; 11: 529–43PubMedCrossRef
62.
go back to reference Gupta K, Shukla M, Cowland JB, et al. Neutrophil-gela-tinase-associated lipocalin is expressed in osteoarthritis and forms a complex with matrix metalloproteinase-9. Arthritis Rheum 2007; 56(10): 3326–35PubMedCrossRef Gupta K, Shukla M, Cowland JB, et al. Neutrophil-gela-tinase-associated lipocalin is expressed in osteoarthritis and forms a complex with matrix metalloproteinase-9. Arthritis Rheum 2007; 56(10): 3326–35PubMedCrossRef
63.
go back to reference Jackson MT, Smith MM, Smith SM, et al. Activation of cartilage matrix metalloproteinases by activated protein C. Arthritis Rheum 2009; 60(3): 780–91PubMedCrossRef Jackson MT, Smith MM, Smith SM, et al. Activation of cartilage matrix metalloproteinases by activated protein C. Arthritis Rheum 2009; 60(3): 780–91PubMedCrossRef
64.
go back to reference Fosang AJ, Little CB. Drug insight: aggrecanases as therapeutic targets for osteoarthritis. Nat Clin Pract Rheumatol 2008; 4(8): 420–7PubMedCrossRef Fosang AJ, Little CB. Drug insight: aggrecanases as therapeutic targets for osteoarthritis. Nat Clin Pract Rheumatol 2008; 4(8): 420–7PubMedCrossRef
65.
go back to reference Bondeson J, Wainwright S, Hughes C, et al. The regulation of ADAMTS4 and ADAMTS5 aggrecanases in osteoarthritis: a review. Clin Exp Rheumatol 2008; 26(1): 139–45PubMed Bondeson J, Wainwright S, Hughes C, et al. The regulation of ADAMTS4 and ADAMTS5 aggrecanases in osteoarthritis: a review. Clin Exp Rheumatol 2008; 26(1): 139–45PubMed
66.
go back to reference Malemud CJ, Islam N, Haqqi TM. Pathophysiological mechanisms in osteoarthritis lead to novel therapeutic strategies. Cells Tissues Organs 2003; 174(1–2): 34–48PubMedCrossRef Malemud CJ, Islam N, Haqqi TM. Pathophysiological mechanisms in osteoarthritis lead to novel therapeutic strategies. Cells Tissues Organs 2003; 174(1–2): 34–48PubMedCrossRef
67.
go back to reference Aigner T, Sachse A, Gebhard A, et al. Osteoarthritis: pathobiology-targets and ways for therapeutic intervention. Adv Drug Deliv Rev 2006; 58(2): 128–49PubMedCrossRef Aigner T, Sachse A, Gebhard A, et al. Osteoarthritis: pathobiology-targets and ways for therapeutic intervention. Adv Drug Deliv Rev 2006; 58(2): 128–49PubMedCrossRef
68.
go back to reference Malemud CJ, Schulte ME. Is there a final common pathway for arthritis? Future Rheumatol 2008; 3(3): 253–68CrossRef Malemud CJ, Schulte ME. Is there a final common pathway for arthritis? Future Rheumatol 2008; 3(3): 253–68CrossRef
69.
go back to reference Chen FH, Tuan RS. Mesenchymal stem cells in arthritic diseases. Arthritis Res Ther 2008; 10(5): 223PubMedCrossRef Chen FH, Tuan RS. Mesenchymal stem cells in arthritic diseases. Arthritis Res Ther 2008; 10(5): 223PubMedCrossRef
70.
go back to reference Abramson SB, Attur M. Developments in the scientific understanding of osteoarthritis. Arthritis Res Ther 2009; 11(3): 227PubMedCrossRef Abramson SB, Attur M. Developments in the scientific understanding of osteoarthritis. Arthritis Res Ther 2009; 11(3): 227PubMedCrossRef
71.
go back to reference Koelling S, Kruegel J, Irmer M, et al. Migratory chondrogenic progenitor cells from repair tissue during the later stages of human osteoarthritis. Cell Stem Cell 2009; 4(4): 324–35PubMedCrossRef Koelling S, Kruegel J, Irmer M, et al. Migratory chondrogenic progenitor cells from repair tissue during the later stages of human osteoarthritis. Cell Stem Cell 2009; 4(4): 324–35PubMedCrossRef
72.
go back to reference Zaslav K, Cole B, Brewster R, et al. A prospective study of autologous chondrocyte implantation in patients with failed prior treatment for articular cartilage defect of the knee: results of the Study of the Treatment of Articular Repair (STAR) clinical trial. Am J Sports Med 2009; 37(1): 42–55PubMedCrossRef Zaslav K, Cole B, Brewster R, et al. A prospective study of autologous chondrocyte implantation in patients with failed prior treatment for articular cartilage defect of the knee: results of the Study of the Treatment of Articular Repair (STAR) clinical trial. Am J Sports Med 2009; 37(1): 42–55PubMedCrossRef
73.
go back to reference Goldring SR. Role of bone in osteoarthritis pathogenesis. Med Clin North Am 2009; 93(1): 25–35, xvPubMedCrossRef Goldring SR. Role of bone in osteoarthritis pathogenesis. Med Clin North Am 2009; 93(1): 25–35, xvPubMedCrossRef
74.
go back to reference Sawitzke AD, Shi H, Finco MF, et al. The effect of glucosamine and/or chondroitin sulfate on the progression of knee osteoarthritis: a report from the Glucosamine/Chondroitin Arthritis Intervention Trial. Arthritis Rheum 2008; 58(10): 3183–91PubMedCrossRef Sawitzke AD, Shi H, Finco MF, et al. The effect of glucosamine and/or chondroitin sulfate on the progression of knee osteoarthritis: a report from the Glucosamine/Chondroitin Arthritis Intervention Trial. Arthritis Rheum 2008; 58(10): 3183–91PubMedCrossRef
75.
go back to reference Bruyere O, Reginster JY. Glucosamine and chondroitin sulfate as therapeutic agents for knee and hip osteoarthritis. Drugs Aging 2007; 24(7): 573–80PubMedCrossRef Bruyere O, Reginster JY. Glucosamine and chondroitin sulfate as therapeutic agents for knee and hip osteoarthritis. Drugs Aging 2007; 24(7): 573–80PubMedCrossRef
76.
go back to reference Huskison EC. Glucosamine and chondroitin for osteoarthritis. J Int Med Res 2008; 36(6): 1161–79 Huskison EC. Glucosamine and chondroitin for osteoarthritis. J Int Med Res 2008; 36(6): 1161–79
77.
go back to reference Uebelhart D. Clinical review of chondroitin sulfate in osteoarthritis. Osteoarthritis Cartilage 2008; 16Suppl. 3: S19–21PubMedCrossRef Uebelhart D. Clinical review of chondroitin sulfate in osteoarthritis. Osteoarthritis Cartilage 2008; 16Suppl. 3: S19–21PubMedCrossRef
78.
go back to reference Martin JA, Buckwalter JA. Aging, articular cartilage chondrocyte senescence and osteoarthritis. Biogerontology 2002; 3(5): 257–64PubMedCrossRef Martin JA, Buckwalter JA. Aging, articular cartilage chondrocyte senescence and osteoarthritis. Biogerontology 2002; 3(5): 257–64PubMedCrossRef
79.
go back to reference Valdes AM, Spector TD. The contribution of genes to osteoarthritis. Med Clin North Am 2009; 93(1): 45–66, xPubMedCrossRef Valdes AM, Spector TD. The contribution of genes to osteoarthritis. Med Clin North Am 2009; 93(1): 45–66, xPubMedCrossRef
80.
go back to reference Yasuda T. Cartilage destruction by matrix degradation products. Mod Rheumatol 2006; 16(4): 197–205PubMedCrossRef Yasuda T. Cartilage destruction by matrix degradation products. Mod Rheumatol 2006; 16(4): 197–205PubMedCrossRef
81.
go back to reference Sakao K, Takahashi KA, Mazda O, et al. Enhanced expression of interleukin-6, matrix metalloproteinase-13, and receptor activator of NF-KB ligand in cells derived from osteoarthritic subchondral bone. J Orthop Sci 2008; 13(3): 202–10PubMedCrossRef Sakao K, Takahashi KA, Mazda O, et al. Enhanced expression of interleukin-6, matrix metalloproteinase-13, and receptor activator of NF-KB ligand in cells derived from osteoarthritic subchondral bone. J Orthop Sci 2008; 13(3): 202–10PubMedCrossRef
82.
go back to reference Livshits G, Zhai G, Hart DJ, et al. Interleukin-6 is a significant predictor of radiographic knee osteoarthritis: the Chingford study. Arthritis Rheum 2009; 60(7): 2037–45PubMedCrossRef Livshits G, Zhai G, Hart DJ, et al. Interleukin-6 is a significant predictor of radiographic knee osteoarthritis: the Chingford study. Arthritis Rheum 2009; 60(7): 2037–45PubMedCrossRef
83.
go back to reference Pola E, Papaleo P, Pola R, et al. Interleukin-6 gene polymorphism and risk of osteoarthritis of the hip: a case-control study. Osteoarthritis Cartilage 2005; 13(11): 1025–8PubMedCrossRef Pola E, Papaleo P, Pola R, et al. Interleukin-6 gene polymorphism and risk of osteoarthritis of the hip: a case-control study. Osteoarthritis Cartilage 2005; 13(11): 1025–8PubMedCrossRef
84.
go back to reference de Hooge AS, van de Loo FA, Bennink MB, et al. Male IL-6 gene knock out mice developed more advanced osteoarthritis upon aging. Osteoarthritis Cartilage 2005; 13(1): 66–73PubMedCrossRef de Hooge AS, van de Loo FA, Bennink MB, et al. Male IL-6 gene knock out mice developed more advanced osteoarthritis upon aging. Osteoarthritis Cartilage 2005; 13(1): 66–73PubMedCrossRef
85.
go back to reference Nile CJ, Read RC, Akil M, et al. Methylation status of a single CpG site in the IL6 promoter is related to IL6 messenger RNA levels and rheumatoid arthritis. Arthritis Rheum 2008; 58(9): 2686–93PubMedCrossRef Nile CJ, Read RC, Akil M, et al. Methylation status of a single CpG site in the IL6 promoter is related to IL6 messenger RNA levels and rheumatoid arthritis. Arthritis Rheum 2008; 58(9): 2686–93PubMedCrossRef
86.
go back to reference Pretzel D, Pohlers D, Weinert S, et al. In vitro model for the analysis of synovial fibroblast-mediated degradation of intact cartilage. Arthritis Res Ther 2009; 11(1): R25PubMedCrossRef Pretzel D, Pohlers D, Weinert S, et al. In vitro model for the analysis of synovial fibroblast-mediated degradation of intact cartilage. Arthritis Res Ther 2009; 11(1): R25PubMedCrossRef
87.
go back to reference Pulai JI, Chen H, Im HJ, et al. NF-κB mediates the stimulation of cytokine and chemokine expression by human articular chondrocytes in response to fibronectin fragments. J Immunol 2005; 174(9): 5781–8PubMed Pulai JI, Chen H, Im HJ, et al. NF-κB mediates the stimulation of cytokine and chemokine expression by human articular chondrocytes in response to fibronectin fragments. J Immunol 2005; 174(9): 5781–8PubMed
88.
go back to reference Stanton H, Ung L, Fosang AJ. The 45 kDa collagen-binding fragment of fibronectin induces matrix metalloproteinase-13 synthesis by chondrocytes and aggrecan degradation by aggrecanases. Biochem J 2002; 364 (Pt 1): 181–90PubMed Stanton H, Ung L, Fosang AJ. The 45 kDa collagen-binding fragment of fibronectin induces matrix metalloproteinase-13 synthesis by chondrocytes and aggrecan degradation by aggrecanases. Biochem J 2002; 364 (Pt 1): 181–90PubMed
89.
go back to reference Klatt AR, Paul-Klausch B, Klinger G, et al. A critical role for collagen II in cartilage matrix degradation: collagen II induces pro-inflammatory cytokines and MMPs in primary human chondrocytes. J Orthop Res 2009; 27(1): 65–70PubMedCrossRef Klatt AR, Paul-Klausch B, Klinger G, et al. A critical role for collagen II in cartilage matrix degradation: collagen II induces pro-inflammatory cytokines and MMPs in primary human chondrocytes. J Orthop Res 2009; 27(1): 65–70PubMedCrossRef
90.
go back to reference Klatt AR, Zech D, Kühn G, et al. Discoidin domain receptor 2 mediates the collagen II-dependent release of interleukin-6 in primary human chondrocytes. J Pathol 2009; 218(2): 241–7PubMedCrossRef Klatt AR, Zech D, Kühn G, et al. Discoidin domain receptor 2 mediates the collagen II-dependent release of interleukin-6 in primary human chondrocytes. J Pathol 2009; 218(2): 241–7PubMedCrossRef
91.
go back to reference Porée B, Kypriotou M, Chadjichristos C, et al. Interleukin-6 (IL-6) and soluble IL-6 receptor down-regulation of human type II collagen gene expression in articular chondrocytes requires a decrease of Sp1.Sp3 ratio and of the binding activity of both factors to the COL2A1 promoter. J Biol Chem 2008; 283(8): 4850–65PubMedCrossRef Porée B, Kypriotou M, Chadjichristos C, et al. Interleukin-6 (IL-6) and soluble IL-6 receptor down-regulation of human type II collagen gene expression in articular chondrocytes requires a decrease of Sp1.Sp3 ratio and of the binding activity of both factors to the COL2A1 promoter. J Biol Chem 2008; 283(8): 4850–65PubMedCrossRef
92.
go back to reference Mathy-Hartert M, Hogge L, Sanchez C, et al. Interleukin-1β and interleukin-6 disturb the anti-oxidant enzyme system in bovine chondrocytes: a possible explanation for oxidative stress generation. Osteoarthritis Cartilage 2008; 16(7): 756–63PubMedCrossRef Mathy-Hartert M, Hogge L, Sanchez C, et al. Interleukin-1β and interleukin-6 disturb the anti-oxidant enzyme system in bovine chondrocytes: a possible explanation for oxidative stress generation. Osteoarthritis Cartilage 2008; 16(7): 756–63PubMedCrossRef
93.
go back to reference Roach HI. The complex pathology of osteoarthritis: even mitochondria are involved. Arthritis Rheum 2008; 58(8): 2217–8PubMedCrossRef Roach HI. The complex pathology of osteoarthritis: even mitochondria are involved. Arthritis Rheum 2008; 58(8): 2217–8PubMedCrossRef
94.
go back to reference Guillén MI, Megías J, Clérigues V, et al. The CO-releasing molecule CORM-2 is a novel regulator of the inflammatory process in osteoarthritic chondrocytes. Rheumatology (Oxford) 2008; 47(9): 1323–8CrossRef Guillén MI, Megías J, Clérigues V, et al. The CO-releasing molecule CORM-2 is a novel regulator of the inflammatory process in osteoarthritic chondrocytes. Rheumatology (Oxford) 2008; 47(9): 1323–8CrossRef
95.
go back to reference Tanaka M, Miyajima A. Oncostatin M, a multifunctional cytokine. Rev Physiol Biochem Pharmacol 2003; 149: 39–52PubMedCrossRef Tanaka M, Miyajima A. Oncostatin M, a multifunctional cytokine. Rev Physiol Biochem Pharmacol 2003; 149: 39–52PubMedCrossRef
96.
go back to reference Hui W, Rowan AD, Richards CD, et al. Oncostatin M in combination with tumor necrosis factor α induces cartilage damage and matrix metalloproteinases expression in vitro and in vivo. Arthritis Rheum 2003; 48(12): 3404–18PubMedCrossRef Hui W, Rowan AD, Richards CD, et al. Oncostatin M in combination with tumor necrosis factor α induces cartilage damage and matrix metalloproteinases expression in vitro and in vivo. Arthritis Rheum 2003; 48(12): 3404–18PubMedCrossRef
97.
go back to reference Hui W, Barksby HE, Young DA, et al. Oncostatin M in combination with tumour necrosis factor α induces a chondrocyte membrane associated aggrecanase that is distinct from ADAMTS aggrecanase-1 or -2. Ann Rheum Dis 2005; 64(11): 1624–32PubMedCrossRef Hui W, Barksby HE, Young DA, et al. Oncostatin M in combination with tumour necrosis factor α induces a chondrocyte membrane associated aggrecanase that is distinct from ADAMTS aggrecanase-1 or -2. Ann Rheum Dis 2005; 64(11): 1624–32PubMedCrossRef
98.
go back to reference El Mabrouk M, Qureshi HY, Li WQ, et al. Interleukin-4 antagonizes oncostatin M and transforming growth β-induced responses in articular chondrocytes. J Cell Biochem 2008; 103(2): 588–97PubMedCrossRef El Mabrouk M, Qureshi HY, Li WQ, et al. Interleukin-4 antagonizes oncostatin M and transforming growth β-induced responses in articular chondrocytes. J Cell Biochem 2008; 103(2): 588–97PubMedCrossRef
99.
go back to reference Durigova M, Roughley PJ, Mort JS. Mechanism of proteoglycan aggregate degradation in cartilage stimulated by oncostatin M. Osteoarthritis Cartilage 2008; 16(1): 98–104PubMedCrossRef Durigova M, Roughley PJ, Mort JS. Mechanism of proteoglycan aggregate degradation in cartilage stimulated by oncostatin M. Osteoarthritis Cartilage 2008; 16(1): 98–104PubMedCrossRef
100.
go back to reference Durigova M, Soucy P, Fushimi K, et al. Characterization of an ADAMTS-5-mediated cleavage site in aggrecan in OSM-stimulated bovine cartilage. Osteoarthritis Cartilage 2008; 16(10): 1245–52PubMedCrossRef Durigova M, Soucy P, Fushimi K, et al. Characterization of an ADAMTS-5-mediated cleavage site in aggrecan in OSM-stimulated bovine cartilage. Osteoarthritis Cartilage 2008; 16(10): 1245–52PubMedCrossRef
101.
go back to reference Barksby HE, Hui W, Wappler I, et al. Interleukin-1 in combination with oncostatin M up-regulates multiple genes in chondrocytes: implications for cartilage destruction and repair. Arthritis Rheum 2006; 54(2): 540–50PubMedCrossRef Barksby HE, Hui W, Wappler I, et al. Interleukin-1 in combination with oncostatin M up-regulates multiple genes in chondrocytes: implications for cartilage destruction and repair. Arthritis Rheum 2006; 54(2): 540–50PubMedCrossRef
102.
go back to reference El Mabrouk M, Sylvester J, Zafarullah M. Signaling pathways in oncostatin M-induced aggrecanase-1 and matrix metalloproteinase-13 expression in human articular chondrocytes. Biochim Biophys Acta 2007; 1773(3): 309–20PubMedCrossRef El Mabrouk M, Sylvester J, Zafarullah M. Signaling pathways in oncostatin M-induced aggrecanase-1 and matrix metalloproteinase-13 expression in human articular chondrocytes. Biochim Biophys Acta 2007; 1773(3): 309–20PubMedCrossRef
103.
go back to reference Malemud CJ, Pearlman E. Targeting JAK/STAT signaling pathway in inflammatory diseases. Curr Signal Transduct Ther 2009; 4(3): 201–21CrossRef Malemud CJ, Pearlman E. Targeting JAK/STAT signaling pathway in inflammatory diseases. Curr Signal Transduct Ther 2009; 4(3): 201–21CrossRef
104.
go back to reference Little CB, Flannery CR, Hughes CE, et al. Cytokine induced matrix metalloproteinase expression and activity does not correlate with focal susceptibility of articular cartilage to degeneration. Osteoarthritis Cartilage 2005; 13(2): 162–70PubMedCrossRef Little CB, Flannery CR, Hughes CE, et al. Cytokine induced matrix metalloproteinase expression and activity does not correlate with focal susceptibility of articular cartilage to degeneration. Osteoarthritis Cartilage 2005; 13(2): 162–70PubMedCrossRef
105.
go back to reference Sanchez C, Deberg MA, Piccardi N, et al. Osteoblasts from the sclerotic subchondral bone downregulate aggrecan but upregulate metalloproteinase expression by chondrocytes. This effect is mimicked by interleukin-6, -1β and oncostatin M pre-treated non-sclerotic osteoblasts. Osteoarthritis Cartilage 2005; 13(11): 979–87PubMedCrossRef Sanchez C, Deberg MA, Piccardi N, et al. Osteoblasts from the sclerotic subchondral bone downregulate aggrecan but upregulate metalloproteinase expression by chondrocytes. This effect is mimicked by interleukin-6, -1β and oncostatin M pre-treated non-sclerotic osteoblasts. Osteoarthritis Cartilage 2005; 13(11): 979–87PubMedCrossRef
106.
go back to reference Manicourt DH, Poilvache P, Van Egeren A, et al. Synovial fluid levels of tumor necrosis factor α and oncostatin M correlate with levels of markers of the degradation of crosslinked collagen and cartilage aggrecan in rheumatoid arthritis but not in osteoarthritis. Arthritis Rheum 2000; 43(2): 281–8PubMedCrossRef Manicourt DH, Poilvache P, Van Egeren A, et al. Synovial fluid levels of tumor necrosis factor α and oncostatin M correlate with levels of markers of the degradation of crosslinked collagen and cartilage aggrecan in rheumatoid arthritis but not in osteoarthritis. Arthritis Rheum 2000; 43(2): 281–8PubMedCrossRef
107.
go back to reference Moreau JF, Donaldson DD, Bennett F, et al. Leukaemia inhibitory factor is identical to the myeloid growth factor human interleukin for DA cells. Nature 1988; 336(6200): 690–2PubMedCrossRef Moreau JF, Donaldson DD, Bennett F, et al. Leukaemia inhibitory factor is identical to the myeloid growth factor human interleukin for DA cells. Nature 1988; 336(6200): 690–2PubMedCrossRef
108.
go back to reference Auernhammer CJ, Melmed S. Leukemia-inhibitory factor-neuroendocrine modulator of endocrine function. Endocr Rev 2000; 21(3): 313–45PubMedCrossRef Auernhammer CJ, Melmed S. Leukemia-inhibitory factor-neuroendocrine modulator of endocrine function. Endocr Rev 2000; 21(3): 313–45PubMedCrossRef
109.
go back to reference Linker R, Gold R, Luhder F. Function of neutrotrophic factors beyond the nervous system: inflammation and autoimmune demyelination. Crit Rev Immunol 2009; 29(1): 43–68PubMedCrossRef Linker R, Gold R, Luhder F. Function of neutrotrophic factors beyond the nervous system: inflammation and autoimmune demyelination. Crit Rev Immunol 2009; 29(1): 43–68PubMedCrossRef
110.
go back to reference Starr R, Novak U, Willson TA, et al. Distinct roles for leukemia inhibitory factor α-chain and gp 130 in cell type-specific signal transduction. J Biol Chem 1997; 272(32): 19982–86PubMedCrossRef Starr R, Novak U, Willson TA, et al. Distinct roles for leukemia inhibitory factor α-chain and gp 130 in cell type-specific signal transduction. J Biol Chem 1997; 272(32): 19982–86PubMedCrossRef
111.
go back to reference Malemud CJ. Small molecular weight inhibitors of stress-activated and mitogen-activated protein kinases. Mini Rev Med Chem 2006; 6(6): 689–98PubMedCrossRef Malemud CJ. Small molecular weight inhibitors of stress-activated and mitogen-activated protein kinases. Mini Rev Med Chem 2006; 6(6): 689–98PubMedCrossRef
112.
go back to reference Malemud CJ. Inhibitors of stress-activated and mitogen-activated protein kinase pathways. Curr Opin Pharmacol 2007; 7(3): 339–43PubMedCrossRef Malemud CJ. Inhibitors of stress-activated and mitogen-activated protein kinase pathways. Curr Opin Pharmacol 2007; 7(3): 339–43PubMedCrossRef
113.
go back to reference Malemud CJ, Miller AH. Pro-inflammatory cytokine-induced SAP/MAPK and JAK/STAT in rheumatoid arthritis and the new anti-depression drugs. Expert Opin Ther Targets 2008; 12(2): 171–83PubMedCrossRef Malemud CJ, Miller AH. Pro-inflammatory cytokine-induced SAP/MAPK and JAK/STAT in rheumatoid arthritis and the new anti-depression drugs. Expert Opin Ther Targets 2008; 12(2): 171–83PubMedCrossRef
114.
go back to reference Lotz M, Moats T, Villiger PM. Leukemia inhibitory factor is expressed in cartilage and synovium and can contribute to the pathogenesis of arthritis. J Clin Invest 1992; 90(3): 888–96PubMedCrossRef Lotz M, Moats T, Villiger PM. Leukemia inhibitory factor is expressed in cartilage and synovium and can contribute to the pathogenesis of arthritis. J Clin Invest 1992; 90(3): 888–96PubMedCrossRef
115.
go back to reference Alaaeddine N, Di Battista JA, Pelleter J-P, et al. Differential effects of IL-8, LIF (pro-inflammatory) and IL-11 (anti-inflammatory) on TNF-α-induced PGE2 release and on signalling pathways in human OA synovial fibroblasts. Cytokine 1999; 11(12): 1020–30PubMedCrossRef Alaaeddine N, Di Battista JA, Pelleter J-P, et al. Differential effects of IL-8, LIF (pro-inflammatory) and IL-11 (anti-inflammatory) on TNF-α-induced PGE2 release and on signalling pathways in human OA synovial fibroblasts. Cytokine 1999; 11(12): 1020–30PubMedCrossRef
116.
go back to reference Lisignoli G, Piacentini A, Toneguzzi S, et al. Osteoblasts and stromal cells isolated from femora in rheumatoid arthritis (RA) and osteoarthritis (OA) patients express IL-11, leukaemia inhibitory factor and oncostatin M. Clin Exp Immunol 2000; 119(2) 346–53PubMedCrossRef Lisignoli G, Piacentini A, Toneguzzi S, et al. Osteoblasts and stromal cells isolated from femora in rheumatoid arthritis (RA) and osteoarthritis (OA) patients express IL-11, leukaemia inhibitory factor and oncostatin M. Clin Exp Immunol 2000; 119(2) 346–53PubMedCrossRef
117.
go back to reference Fan Z, Bau B, Yang H, et al. IL-1β induction of IL-6 and LIF in normal articular human chondrocytes involves the ERK, p38 and NFκB signaling pathways. Cytokine 2004; 28(1): 17–24PubMedCrossRef Fan Z, Bau B, Yang H, et al. IL-1β induction of IL-6 and LIF in normal articular human chondrocytes involves the ERK, p38 and NFκB signaling pathways. Cytokine 2004; 28(1): 17–24PubMedCrossRef
118.
go back to reference Sandell LJ, Xing X, Franz C, et al. Exuberant expression of chemokine genes by adult human articular chondrocytes in response to IL-1β. Osteoarthritis Cartilage 2008; 16(12): 1560–71PubMedCrossRef Sandell LJ, Xing X, Franz C, et al. Exuberant expression of chemokine genes by adult human articular chondrocytes in response to IL-1β. Osteoarthritis Cartilage 2008; 16(12): 1560–71PubMedCrossRef
119.
go back to reference Malemud CJ, Reddy SK. Targeting cytokines, chemokines and adhesion molecules in rheumatoid arthritis. Curr Rheum Rev 2008; 4(4): 219–34CrossRef Malemud CJ, Reddy SK. Targeting cytokines, chemokines and adhesion molecules in rheumatoid arthritis. Curr Rheum Rev 2008; 4(4): 219–34CrossRef
120.
121.
122.
go back to reference Sakkas LI, Scanzello C, Johanson N, et al. T-cells and T-cell transcripts in the synovial membrane in patients with osteoarthritis. Clin Diagn Lab Immunol 1998; 5(4): 430–7PubMed Sakkas LI, Scanzello C, Johanson N, et al. T-cells and T-cell transcripts in the synovial membrane in patients with osteoarthritis. Clin Diagn Lab Immunol 1998; 5(4): 430–7PubMed
123.
go back to reference Haynes MK, Hume EL, Smith JB. Phenotypic characterization of inflammatory cells from osteoarthritic synovial fluids. Clin Immunol 2002; 105(3): 315–25PubMedCrossRef Haynes MK, Hume EL, Smith JB. Phenotypic characterization of inflammatory cells from osteoarthritic synovial fluids. Clin Immunol 2002; 105(3): 315–25PubMedCrossRef
124.
go back to reference Nakamura H, Tanaka M, Masuko-Hongo K, et al. Enhanced production of MMP-1, MMP-3, MMP-13, and Rantes by interaction of chondrocytes with autologous T cells. Rheumatol Int 2006; 26(11): 984–90PubMedCrossRef Nakamura H, Tanaka M, Masuko-Hongo K, et al. Enhanced production of MMP-1, MMP-3, MMP-13, and Rantes by interaction of chondrocytes with autologous T cells. Rheumatol Int 2006; 26(11): 984–90PubMedCrossRef
125.
go back to reference Sakkas LI, Platsoucas CD. The role of T cells in the pathogenesis of osteoarthritis. Arthritis Rheum 2007; 56(2): 409–24PubMedCrossRef Sakkas LI, Platsoucas CD. The role of T cells in the pathogenesis of osteoarthritis. Arthritis Rheum 2007; 56(2): 409–24PubMedCrossRef
126.
go back to reference Rollin R, Marco F, Jover JA, et al. Early lymphocyte activation in the synovial microenvironment in patients with osteoarthritis: comparison with rheumatoid arthritis patients and healthy controls. Rheumatol Int 2008; 28(8): 757–64PubMedCrossRef Rollin R, Marco F, Jover JA, et al. Early lymphocyte activation in the synovial microenvironment in patients with osteoarthritis: comparison with rheumatoid arthritis patients and healthy controls. Rheumatol Int 2008; 28(8): 757–64PubMedCrossRef
127.
go back to reference Van Roon JA, Lafeber FP. Role of interleukin-7 in degenerative and inflammatory joint diseases. Arthritis Res Ther 2008; 10(2): 107PubMedCrossRef Van Roon JA, Lafeber FP. Role of interleukin-7 in degenerative and inflammatory joint diseases. Arthritis Res Ther 2008; 10(2): 107PubMedCrossRef
128.
go back to reference Long D, Blake S, Song XY, et al. Human articular chondrocytes produce IL-7 and respond to IL-7 with increased production of matrix metalloproteinase-13. Arthritis Res Ther 2008; 10(1): R23PubMedCrossRef Long D, Blake S, Song XY, et al. Human articular chondrocytes produce IL-7 and respond to IL-7 with increased production of matrix metalloproteinase-13. Arthritis Res Ther 2008; 10(1): R23PubMedCrossRef
129.
go back to reference Yammani RR, Long DD, Loeser RF. Interleukin-7 stimulates secretion of S100A by activating the JAK/STAT signaling pathway in human articular chondrocytes. Arthritis Rheum 2009; 60(3): 792–800PubMedCrossRef Yammani RR, Long DD, Loeser RF. Interleukin-7 stimulates secretion of S100A by activating the JAK/STAT signaling pathway in human articular chondrocytes. Arthritis Rheum 2009; 60(3): 792–800PubMedCrossRef
130.
go back to reference Geginat J, Campagnaro S, Sallusto F, et al. TCR-in-dependent proliferation and differentiation of human CD4+ cell subsets induced by cytokines. Adv Exp Med Biol 2002; 512: 107–12PubMedCrossRef Geginat J, Campagnaro S, Sallusto F, et al. TCR-in-dependent proliferation and differentiation of human CD4+ cell subsets induced by cytokines. Adv Exp Med Biol 2002; 512: 107–12PubMedCrossRef
131.
go back to reference van Roon JAG, Hartgring SAY, Wenting-van Wijk M, et al. Persistence of interleukin-7 activity and levels on tumor necrosis factor α blockade in patients with rheumatoid arthritis. Ann Rheum Dis 2007; 66(5): 664–9PubMedCrossRef van Roon JAG, Hartgring SAY, Wenting-van Wijk M, et al. Persistence of interleukin-7 activity and levels on tumor necrosis factor α blockade in patients with rheumatoid arthritis. Ann Rheum Dis 2007; 66(5): 664–9PubMedCrossRef
132.
go back to reference Dinarello CA. The IL-1 family and inflammatory diseases. Clin Exp Rheumatol 2002; 20(5 Suppl. 27): S1–13PubMed Dinarello CA. The IL-1 family and inflammatory diseases. Clin Exp Rheumatol 2002; 20(5 Suppl. 27): S1–13PubMed
133.
go back to reference Nakanishi K, Yoshimoto T, Tsutsui T, et al. Interleukin-18 regulates both TH1 and TH2 responses. Annu Rev Immunol 2001; 19:423–74PubMedCrossRef Nakanishi K, Yoshimoto T, Tsutsui T, et al. Interleukin-18 regulates both TH1 and TH2 responses. Annu Rev Immunol 2001; 19:423–74PubMedCrossRef
134.
go back to reference Singh R, Ahmed S, Malemud CJ, et al. Epigallocatechin-3-gallate selectively inhibits interleukin-1 b-induced activation of mitogen activated protein kinase subgroup c-Jun-N-terminal kinase in human osteoarthritis chondrocytes. J Orthop Res 2003; 21(1): 102–9PubMedCrossRef Singh R, Ahmed S, Malemud CJ, et al. Epigallocatechin-3-gallate selectively inhibits interleukin-1 b-induced activation of mitogen activated protein kinase subgroup c-Jun-N-terminal kinase in human osteoarthritis chondrocytes. J Orthop Res 2003; 21(1): 102–9PubMedCrossRef
135.
go back to reference Notoya K, Jovanovic DV, Reboul P, et al. The induction of cell death in human osteoarthritis chondrocytes by nitric oxide is related to the production of prostaglandin E2 via the induction of cyclooxygenase-2. J Immunol 2000; 165(6): 3402–10PubMed Notoya K, Jovanovic DV, Reboul P, et al. The induction of cell death in human osteoarthritis chondrocytes by nitric oxide is related to the production of prostaglandin E2 via the induction of cyclooxygenase-2. J Immunol 2000; 165(6): 3402–10PubMed
136.
go back to reference Matsui K, Tsutsui H, Nakanishi K. Pathophysiological roles for IL-18 in inflammatory arthritis. Expert Opin Ther Targets 2003; 7(6): 701–24PubMedCrossRef Matsui K, Tsutsui H, Nakanishi K. Pathophysiological roles for IL-18 in inflammatory arthritis. Expert Opin Ther Targets 2003; 7(6): 701–24PubMedCrossRef
137.
go back to reference Lee JK, Kim SH, Lewis EC, et al. Differences in signaling pathways by IL-1β and IL-18. Proc Natl Acad Sci U S A 2004; 101(23): 8815–20PubMedCrossRef Lee JK, Kim SH, Lewis EC, et al. Differences in signaling pathways by IL-1β and IL-18. Proc Natl Acad Sci U S A 2004; 101(23): 8815–20PubMedCrossRef
138.
go back to reference Wannamaker W, Davies R, Namchuk M, et al. (S)-1-((S)-2-{[1-(4-amino-3-chloro-phenyl)-methanoyl]-amino}-3, 3-dimethyl-butanoyl)-pyrrolidine-2-carboxylic acid ((2R,3S)-2-ethoxy-5-oxo-tetrahydro-furan-3-yl)-amide (VX–765), an orally available selective interleukin (IL)-converting enzyme/caspase-1 inhibitor, exhibits potent anti-inflammatory activities by inhibiting the release of IL-1β and IL-18. J Pharmacol Exp Ther 2007; 321(2): 509–16PubMedCrossRef Wannamaker W, Davies R, Namchuk M, et al. (S)-1-((S)-2-{[1-(4-amino-3-chloro-phenyl)-methanoyl]-amino}-3, 3-dimethyl-butanoyl)-pyrrolidine-2-carboxylic acid ((2R,3S)-2-ethoxy-5-oxo-tetrahydro-furan-3-yl)-amide (VX–765), an orally available selective interleukin (IL)-converting enzyme/caspase-1 inhibitor, exhibits potent anti-inflammatory activities by inhibiting the release of IL-1β and IL-18. J Pharmacol Exp Ther 2007; 321(2): 509–16PubMedCrossRef
139.
go back to reference Gracie JA, Forsey RJ, Chan WL, et al. A proinflammatory role for IL-18 in rheumatoid arthritis. J Clin Invest 1999; 104(10): 1393–401PubMedCrossRef Gracie JA, Forsey RJ, Chan WL, et al. A proinflammatory role for IL-18 in rheumatoid arthritis. J Clin Invest 1999; 104(10): 1393–401PubMedCrossRef
140.
go back to reference Wei XQ, Leung BP, Arthur HM, et al. Reduced incidence and severity of collagen-induced arthritis in mice lacking IL-18. J Immunol 2001; 166(1): 517–21PubMed Wei XQ, Leung BP, Arthur HM, et al. Reduced incidence and severity of collagen-induced arthritis in mice lacking IL-18. J Immunol 2001; 166(1): 517–21PubMed
141.
go back to reference Ye XJ, Tang B, Ma Z, et al. The role of interleukin-18 in collagen-induced arthritis in the BB rat. Clin Exp Immunol 2004; 136(3): 440–7PubMedCrossRef Ye XJ, Tang B, Ma Z, et al. The role of interleukin-18 in collagen-induced arthritis in the BB rat. Clin Exp Immunol 2004; 136(3): 440–7PubMedCrossRef
142.
go back to reference Futani H, Okayama A, Matsui K, et al. Relationship between interleukin-18 and PGE2 in synovial fluid of osteoarthritis: a potential therapeutic target of cartilage degradation. J Immunother 2002; 25Suppl. 1: S61–4PubMedCrossRef Futani H, Okayama A, Matsui K, et al. Relationship between interleukin-18 and PGE2 in synovial fluid of osteoarthritis: a potential therapeutic target of cartilage degradation. J Immunother 2002; 25Suppl. 1: S61–4PubMedCrossRef
143.
go back to reference Dai SM, Shan ZZ, Nishioka K, et al. Implication of interleukin 18 in production of matrix metalloproteinases in articular chondrocytes in arthritis: direct effect on chondrocytes may not be pivotal. Ann Rheum Dis 2005; 64(5): 735–42PubMedCrossRef Dai SM, Shan ZZ, Nishioka K, et al. Implication of interleukin 18 in production of matrix metalloproteinases in articular chondrocytes in arthritis: direct effect on chondrocytes may not be pivotal. Ann Rheum Dis 2005; 64(5): 735–42PubMedCrossRef
144.
go back to reference John T, Kohl B, Mobasheri A, et al. Interleukin-18 induces apoptosis in human articular chondrocytes. Histol Histopathol 2007; 22(5): 469–82PubMed John T, Kohl B, Mobasheri A, et al. Interleukin-18 induces apoptosis in human articular chondrocytes. Histol Histopathol 2007; 22(5): 469–82PubMed
145.
go back to reference Verri Jr WA, Cunha TM, Parada CA, et al. Antigen-induced inflammatory mechanical hypernocioception in mice is mediated by IL-18. Brain Behav Immun 2007; 21(5): 535–43PubMedCrossRef Verri Jr WA, Cunha TM, Parada CA, et al. Antigen-induced inflammatory mechanical hypernocioception in mice is mediated by IL-18. Brain Behav Immun 2007; 21(5): 535–43PubMedCrossRef
146.
go back to reference Honorati MC, Neri S, Cattini L, et al. Interleukin-17, a regulator of angiogenic factor release by synovial fibroblasts. Osteoarthritis Cartilage 2006; 14(4): 345–52PubMedCrossRef Honorati MC, Neri S, Cattini L, et al. Interleukin-17, a regulator of angiogenic factor release by synovial fibroblasts. Osteoarthritis Cartilage 2006; 14(4): 345–52PubMedCrossRef
147.
go back to reference Van Bezooijen RL, Van Der Wee-Pals L, Papapoulos SE, et al. Interleukin 17 synergizes with tumour necrosis factor alpha to induce cartilage destruction in vitro. Ann Rheum Dis 2002; 61(10): 870–6PubMedCrossRef Van Bezooijen RL, Van Der Wee-Pals L, Papapoulos SE, et al. Interleukin 17 synergizes with tumour necrosis factor alpha to induce cartilage destruction in vitro. Ann Rheum Dis 2002; 61(10): 870–6PubMedCrossRef
148.
go back to reference Miljkovic D, Trajkovic V. Inducible nitric oxide synthase activation by interleukin-17. Cytokine Growth Factor Rev 2004; 15(1): 21–32PubMedCrossRef Miljkovic D, Trajkovic V. Inducible nitric oxide synthase activation by interleukin-17. Cytokine Growth Factor Rev 2004; 15(1): 21–32PubMedCrossRef
149.
go back to reference Honorati MC, Bovara M, Cattini L, et al. Contribution of IL-17 to human cartilage degradation and synovial inflammation in osteoarthritis. Osteoarthritis Cartilage 2002; 10(10): 799–807PubMedCrossRef Honorati MC, Bovara M, Cattini L, et al. Contribution of IL-17 to human cartilage degradation and synovial inflammation in osteoarthritis. Osteoarthritis Cartilage 2002; 10(10): 799–807PubMedCrossRef
150.
go back to reference Honorati MC, Cattini L, Facchini A. VEGF production by osteoarthritic chondrocytes cultured in micromass stimulated by IL-17 and TNF-α. Connect Tissue Res 2007; 48(5): 239–45PubMedCrossRef Honorati MC, Cattini L, Facchini A. VEGF production by osteoarthritic chondrocytes cultured in micromass stimulated by IL-17 and TNF-α. Connect Tissue Res 2007; 48(5): 239–45PubMedCrossRef
151.
go back to reference Lubberts E, Koenders MI, van den Berg WB. The role of T-cell interleukin-17 in conducting destructive arthritis: lessons from animal models. Arthritis Res Ther 2005; 7(1): 29–37PubMedCrossRef Lubberts E, Koenders MI, van den Berg WB. The role of T-cell interleukin-17 in conducting destructive arthritis: lessons from animal models. Arthritis Res Ther 2005; 7(1): 29–37PubMedCrossRef
152.
go back to reference Aigner T, Van der Kraan P, Van den Berg WB. Osteoarthritis and inflammation: inflammatory changes in osteoarthritic synoviopathy. In: Buckwalter JA, Lotz M, Stoltz J-F, editors. Osteoarthritis, inflammation and degradation: a continuum. Amsterdam: IOS Press, 2007: 219–35 Aigner T, Van der Kraan P, Van den Berg WB. Osteoarthritis and inflammation: inflammatory changes in osteoarthritic synoviopathy. In: Buckwalter JA, Lotz M, Stoltz J-F, editors. Osteoarthritis, inflammation and degradation: a continuum. Amsterdam: IOS Press, 2007: 219–35
153.
go back to reference Wang G, Matsuura I, He D, et al. Transforming growth factor-β-inducible phosphorylation of Smad3. J Biol Chem 2009; 284(15): 9663–73PubMedCrossRef Wang G, Matsuura I, He D, et al. Transforming growth factor-β-inducible phosphorylation of Smad3. J Biol Chem 2009; 284(15): 9663–73PubMedCrossRef
154.
go back to reference Scharstuhl A, Vitters EL, van der Kraan PM, et al. Reduction of osteophyte formation and synovial thickening by adenoviral overexpression of transforming growth factor β/bone morphogenetic protein inhibitors during experimental osteoarthritis. Arthritis Rheum 2003; 48(12): 3442–51PubMedCrossRef Scharstuhl A, Vitters EL, van der Kraan PM, et al. Reduction of osteophyte formation and synovial thickening by adenoviral overexpression of transforming growth factor β/bone morphogenetic protein inhibitors during experimental osteoarthritis. Arthritis Rheum 2003; 48(12): 3442–51PubMedCrossRef
155.
go back to reference Roman-Blas JA, Stokes DG, Jimenez SA. Modulation of TGF-β signaling by proinflammatory cytokines in articular chondrocytes. Osteoarthritis Cartilage 2007; 15(12): 1367–77PubMedCrossRef Roman-Blas JA, Stokes DG, Jimenez SA. Modulation of TGF-β signaling by proinflammatory cytokines in articular chondrocytes. Osteoarthritis Cartilage 2007; 15(12): 1367–77PubMedCrossRef
156.
go back to reference Blaney Davidson EN, Vitters EL, van den Berg WB, et al. TGF β-induced cartilage repair is maintained but fibrosis is blocked in the presence of Smad7. Arthritis Res Ther 2006; 8(3): R65PubMedCrossRef Blaney Davidson EN, Vitters EL, van den Berg WB, et al. TGF β-induced cartilage repair is maintained but fibrosis is blocked in the presence of Smad7. Arthritis Res Ther 2006; 8(3): R65PubMedCrossRef
157.
go back to reference Blaney Davidson EN, Scharstuhl A, Vitters EL, et al. Reduced transforming growth factor-beta signaling in cartilage of old mice: role in impaired repair capacity. Arthritis Res Ther 2005; 7(6): R1338–47PubMedCrossRef Blaney Davidson EN, Scharstuhl A, Vitters EL, et al. Reduced transforming growth factor-beta signaling in cartilage of old mice: role in impaired repair capacity. Arthritis Res Ther 2005; 7(6): R1338–47PubMedCrossRef
158.
go back to reference Wu Q, Kim KO, Sampson ER, et al. Induction of an osteoarthritis-like phenotype and degradation of phosphorylated Smad3 by Smurf2 in transgenic mice. Arthritis Rheum 2008; 58(10): 3132–44PubMedCrossRef Wu Q, Kim KO, Sampson ER, et al. Induction of an osteoarthritis-like phenotype and degradation of phosphorylated Smad3 by Smurf2 in transgenic mice. Arthritis Rheum 2008; 58(10): 3132–44PubMedCrossRef
159.
go back to reference Nakajima M, Kizawa H, Saitoh M, et al. Mechanisms for asporin function and regulation in articular cartilage. J Biol Chem 2007; 282(44): 32185–92PubMedCrossRef Nakajima M, Kizawa H, Saitoh M, et al. Mechanisms for asporin function and regulation in articular cartilage. J Biol Chem 2007; 282(44): 32185–92PubMedCrossRef
160.
go back to reference Kizawa H, Kou I, Iida A, et al. An aspartic acid repeat polymorphism in asporin inhibits chondrogenesis and increases susceptibility to osteoarthritis. Nat Genet 2005; 37(2): 138–44PubMedCrossRef Kizawa H, Kou I, Iida A, et al. An aspartic acid repeat polymorphism in asporin inhibits chondrogenesis and increases susceptibility to osteoarthritis. Nat Genet 2005; 37(2): 138–44PubMedCrossRef
161.
go back to reference Kou I, Nakajima M, Ikegawa S. Expression and regulation of the osteoarthritis-associated protein asporin. J Biol Chem 2007; 282(44): 32193–9PubMedCrossRef Kou I, Nakajima M, Ikegawa S. Expression and regulation of the osteoarthritis-associated protein asporin. J Biol Chem 2007; 282(44): 32193–9PubMedCrossRef
162.
go back to reference Lires-Deän M, Caramés B, Cillero-Pastor B, et al. Anti-apoptotic effect of transforming growth factor-β1 on human articular chondrocytes: role of protein phosphatase 2A. Osteoarthritis Cartilage 2008; 16(11): 1370–8PubMedCrossRef Lires-Deän M, Caramés B, Cillero-Pastor B, et al. Anti-apoptotic effect of transforming growth factor-β1 on human articular chondrocytes: role of protein phosphatase 2A. Osteoarthritis Cartilage 2008; 16(11): 1370–8PubMedCrossRef
163.
go back to reference Rollín R, Alvarez-Lafuente R, Marco F, et al. Abnormal transforming growth factor-β expression in mesenchymal stem cells from patients with osteoarthritis. J Rheumatol 2008; 35(5): 904–6PubMed Rollín R, Alvarez-Lafuente R, Marco F, et al. Abnormal transforming growth factor-β expression in mesenchymal stem cells from patients with osteoarthritis. J Rheumatol 2008; 35(5): 904–6PubMed
164.
go back to reference Nelson AE, Fang F, Shi XA, et al. Failure of transforming growth factor-beta (TGF-β) as a biomarker of radiographic osteoarthritis of the knee and hip: a cross-sectional analysis in the Johnston County Osteoarthritis Project. Osteoarthritis Cartilage 2009; 17(6): 772–6PubMedCrossRef Nelson AE, Fang F, Shi XA, et al. Failure of transforming growth factor-beta (TGF-β) as a biomarker of radiographic osteoarthritis of the knee and hip: a cross-sectional analysis in the Johnston County Osteoarthritis Project. Osteoarthritis Cartilage 2009; 17(6): 772–6PubMedCrossRef
165.
go back to reference Schmidt MB, Chen EH, Lynch SE. A review of the effects of insulin-like growth factor and platelet derived growth factor on in vivo cartilage healing and repair. Osteoarthritis Cartilage 2006; 14(5): 403–12PubMedCrossRef Schmidt MB, Chen EH, Lynch SE. A review of the effects of insulin-like growth factor and platelet derived growth factor on in vivo cartilage healing and repair. Osteoarthritis Cartilage 2006; 14(5): 403–12PubMedCrossRef
166.
go back to reference Loeser RF, Shanker G, Carlson CS, et al. Reduction in the chondrocyte response to insulin-like growth factor 1 in aging and osteoarthritis: studies in a non-human primate model of naturally occurring disease. Arthritis Rheum 2000; 43(9): 2110–20PubMedCrossRef Loeser RF, Shanker G, Carlson CS, et al. Reduction in the chondrocyte response to insulin-like growth factor 1 in aging and osteoarthritis: studies in a non-human primate model of naturally occurring disease. Arthritis Rheum 2000; 43(9): 2110–20PubMedCrossRef
167.
go back to reference Okada A, Mochizuki S, Yatabe T, et al. ADAM-12 (meltrin-α) is involved in chondrocyte proliferation via cleavage of insulin-like growth factor binding protein 5 in osteoarthritic cartilage. Arthritis Rheum 2008; 58(3): 778–9PubMedCrossRef Okada A, Mochizuki S, Yatabe T, et al. ADAM-12 (meltrin-α) is involved in chondrocyte proliferation via cleavage of insulin-like growth factor binding protein 5 in osteoarthritic cartilage. Arthritis Rheum 2008; 58(3): 778–9PubMedCrossRef
168.
go back to reference Cravero JD, Carlson CS, Im HJ, et al. Increased expression of the Akt/PKB inhibitor TRB3 in osteoarthritic chondrocytes inhibits insulin-like growth factor 1-mediated cell survival and proteoglycan synthesis. Arthritis Rheum 2009; 60(2): 492–500PubMedCrossRef Cravero JD, Carlson CS, Im HJ, et al. Increased expression of the Akt/PKB inhibitor TRB3 in osteoarthritic chondrocytes inhibits insulin-like growth factor 1-mediated cell survival and proteoglycan synthesis. Arthritis Rheum 2009; 60(2): 492–500PubMedCrossRef
169.
go back to reference Du K, Herzig S, Kulkarni RN, et al. TRB3: a tribbles homolog that inhibits Akt/PKB activation by insulin in liver. Science 2003; 300(5625): 1574–7PubMedCrossRef Du K, Herzig S, Kulkarni RN, et al. TRB3: a tribbles homolog that inhibits Akt/PKB activation by insulin in liver. Science 2003; 300(5625): 1574–7PubMedCrossRef
170.
go back to reference Massicotte F, Aubry I, Martel-Pelletier J, et al. Abnormal insulin-like growth factor 1 signaling in human osteoarthritic subchondral bone osteoblasts. Arthritis Res Ther 2006; 8(6): R177PubMedCrossRef Massicotte F, Aubry I, Martel-Pelletier J, et al. Abnormal insulin-like growth factor 1 signaling in human osteoarthritic subchondral bone osteoblasts. Arthritis Res Ther 2006; 8(6): R177PubMedCrossRef
171.
go back to reference Sawaji Y, Hynes J, Vincent T, et al. Fibroblast growth factor 2 inhibits induction of aggrecanase activity in human articular cartilage. Arthritis Rheum 2008; 58(11): 3498–509PubMedCrossRef Sawaji Y, Hynes J, Vincent T, et al. Fibroblast growth factor 2 inhibits induction of aggrecanase activity in human articular cartilage. Arthritis Rheum 2008; 58(11): 3498–509PubMedCrossRef
172.
go back to reference Chia SL, Sawaji Y, Burleigh A, et al. Fibroblast growth factor 2 is an intrinsic chondroprotective agent that suppresses ADAMT-5 and delays cartilage degradation in murine osteoarthritis. Arthritis Rheum 2009; 60(7): 2019–27PubMedCrossRef Chia SL, Sawaji Y, Burleigh A, et al. Fibroblast growth factor 2 is an intrinsic chondroprotective agent that suppresses ADAMT-5 and delays cartilage degradation in murine osteoarthritis. Arthritis Rheum 2009; 60(7): 2019–27PubMedCrossRef
173.
go back to reference Vincent TL, McLean CJ, Full LE, et al. FGF-2 is bound to perlecan in the pericellular matrix of articular cartilage where it acts as a chondrocyte mechanotransducer. Osteoarthritis Cartilage 2007; 15(7): 752–63PubMedCrossRef Vincent TL, McLean CJ, Full LE, et al. FGF-2 is bound to perlecan in the pericellular matrix of articular cartilage where it acts as a chondrocyte mechanotransducer. Osteoarthritis Cartilage 2007; 15(7): 752–63PubMedCrossRef
174.
go back to reference Huang K, Wu LD. Aggrecanase and aggrecan degradation in osteoarthritis: a review. J Int Med Res 2008; 36(6): 1149–60PubMed Huang K, Wu LD. Aggrecanase and aggrecan degradation in osteoarthritis: a review. J Int Med Res 2008; 36(6): 1149–60PubMed
175.
go back to reference Daouti S, Latario B, Nagulapalli S, et al. Development of comprehensive functional genomic screens to identify novel mediators of osteoarthritis. Osteoarthritis Cartilage 2005; 13(6): 508–18PubMedCrossRef Daouti S, Latario B, Nagulapalli S, et al. Development of comprehensive functional genomic screens to identify novel mediators of osteoarthritis. Osteoarthritis Cartilage 2005; 13(6): 508–18PubMedCrossRef
176.
go back to reference Pohlers D, Huber R, Ukena B, et al. Expression of platelet-derived growth factors C and D in the synovial membrane of patients with rheumatoid arthritis and osteoarthritis. Arthritis Rheum 2006; 54(3): 788–94PubMedCrossRef Pohlers D, Huber R, Ukena B, et al. Expression of platelet-derived growth factors C and D in the synovial membrane of patients with rheumatoid arthritis and osteoarthritis. Arthritis Rheum 2006; 54(3): 788–94PubMedCrossRef
177.
178.
go back to reference Tardif G, Reboul P, Pelletier J-P, et al. Ten years in the life of an enzyme: the story of human MMP-13 (collagenase-3). Mod Rheumatol 2004; 14(3): 197–204PubMedCrossRef Tardif G, Reboul P, Pelletier J-P, et al. Ten years in the life of an enzyme: the story of human MMP-13 (collagenase-3). Mod Rheumatol 2004; 14(3): 197–204PubMedCrossRef
179.
go back to reference Omoto S, Nishida K, Yamaai Y, et al. Expression and localization of connective tissue growth factor (CTGF/Hcs24/CCN2) in osteoarthritic cartilage. Osteoarthritis Cartilage 2004; 12(10): 771–8PubMedCrossRef Omoto S, Nishida K, Yamaai Y, et al. Expression and localization of connective tissue growth factor (CTGF/Hcs24/CCN2) in osteoarthritic cartilage. Osteoarthritis Cartilage 2004; 12(10): 771–8PubMedCrossRef
180.
go back to reference Nishida T, Kubota S, Kojima S, et al. Regeneration of defects in articular cartilage in rat knee joints by CCN2 (connective tissue growth factor). J Bone Miner Res 2004; 19(8): 1308–19PubMedCrossRef Nishida T, Kubota S, Kojima S, et al. Regeneration of defects in articular cartilage in rat knee joints by CCN2 (connective tissue growth factor). J Bone Miner Res 2004; 19(8): 1308–19PubMedCrossRef
181.
go back to reference Blaney Davidson EN, Vitters EL, Mooren FM, et al. Connective tissue growth factor/CCN2 overexpression in mouse synovial lining results in transient fibrosis and cartilage damage. Arthritis Rheum 2006; 54(5): 1653–61PubMedCrossRef Blaney Davidson EN, Vitters EL, Mooren FM, et al. Connective tissue growth factor/CCN2 overexpression in mouse synovial lining results in transient fibrosis and cartilage damage. Arthritis Rheum 2006; 54(5): 1653–61PubMedCrossRef
182.
go back to reference Woods A, Pala D, Kennedy L, et al. Rac1 signaling regulates CTGF/CCN2 gene expression via TGFβ/Smad signaling in chondrocytes. Osteoarthritis Cartilage 2009; 17(3): 406–13PubMedCrossRef Woods A, Pala D, Kennedy L, et al. Rac1 signaling regulates CTGF/CCN2 gene expression via TGFβ/Smad signaling in chondrocytes. Osteoarthritis Cartilage 2009; 17(3): 406–13PubMedCrossRef
183.
go back to reference Genovese MC, McKay JD, Nasonov EL, et al. Interleukin-6 receptor inhibition with tocilizumab reduces disease activity in rheumatoid arthritis with inadequate response to disease-modifying antirheumatic drugs: the Tocilizumab in Combination with Traditional Disease-modifying Antirheumatic Drug Therapy Study. Arthritis Rheum 2008; 58(10): 2968–80PubMedCrossRef Genovese MC, McKay JD, Nasonov EL, et al. Interleukin-6 receptor inhibition with tocilizumab reduces disease activity in rheumatoid arthritis with inadequate response to disease-modifying antirheumatic drugs: the Tocilizumab in Combination with Traditional Disease-modifying Antirheumatic Drug Therapy Study. Arthritis Rheum 2008; 58(10): 2968–80PubMedCrossRef
184.
go back to reference Bliddal H, Terslev L, Qvistgaard E, et al. A randomized, controlled study of a single intra-articular injection of etanercept or glucocorticoids in patients with rheumatoid arthritis. Scand J Rheumatol 2006; 35(5): 341–5PubMedCrossRef Bliddal H, Terslev L, Qvistgaard E, et al. A randomized, controlled study of a single intra-articular injection of etanercept or glucocorticoids in patients with rheumatoid arthritis. Scand J Rheumatol 2006; 35(5): 341–5PubMedCrossRef
185.
go back to reference van der Bijl AE, Teng YKO, van Oosterhout M, et al. Efficacy of intraarticular infliximab in patients with chronic or recurrent gonarthritis: a clinical randomized trial. Arthritis Care Res 2009; 61(7): 974–8CrossRef van der Bijl AE, Teng YKO, van Oosterhout M, et al. Efficacy of intraarticular infliximab in patients with chronic or recurrent gonarthritis: a clinical randomized trial. Arthritis Care Res 2009; 61(7): 974–8CrossRef
186.
go back to reference Kim HA, Cho M-L, Choi HY, et al. The catabolic pathway mediated by Toll-like receptors in human osteoarthritic chondrocytes. Arthritis Rheum 2006; 54(7): 2152–63PubMedCrossRef Kim HA, Cho M-L, Choi HY, et al. The catabolic pathway mediated by Toll-like receptors in human osteoarthritic chondrocytes. Arthritis Rheum 2006; 54(7): 2152–63PubMedCrossRef
187.
go back to reference Zhang Q, Hui W, Litherland GJ, et al. Differential Toll-like receptor-dependent collagenase expression in chondrocytes. Ann Rheum Dis 2008; 67(11): 1633–41PubMedCrossRef Zhang Q, Hui W, Litherland GJ, et al. Differential Toll-like receptor-dependent collagenase expression in chondrocytes. Ann Rheum Dis 2008; 67(11): 1633–41PubMedCrossRef
188.
go back to reference Scanzello CR, Plaas A, Crow MK. Innate immune system activation in osteoarthritis: is osteoarthritis a chronic wound? Curr Opin Rheumatol 2008; 20(5): 565–72PubMedCrossRef Scanzello CR, Plaas A, Crow MK. Innate immune system activation in osteoarthritis: is osteoarthritis a chronic wound? Curr Opin Rheumatol 2008; 20(5): 565–72PubMedCrossRef
189.
go back to reference Yudoh K, Nguyen T, Nakamura H, et al. Potential involvement of oxidative stress in cartilage senescence and development of osteoarthritis: oxidative stress induces chondrocyte telomere instability and downregulation of chondrocyte function. Arthritis Res Ther 2005; 7(2): R380–91PubMedCrossRef Yudoh K, Nguyen T, Nakamura H, et al. Potential involvement of oxidative stress in cartilage senescence and development of osteoarthritis: oxidative stress induces chondrocyte telomere instability and downregulation of chondrocyte function. Arthritis Res Ther 2005; 7(2): R380–91PubMedCrossRef
190.
go back to reference Vicini P, Incerti M, Cardile V, et al. Benzo[d]isothiazol-3-yl-benzamidines: a class of protective agents on culture of human cartilage and chondrocytes stimulated by IL-1β. ChemMedChem 2007; 2(1): 113–9PubMedCrossRef Vicini P, Incerti M, Cardile V, et al. Benzo[d]isothiazol-3-yl-benzamidines: a class of protective agents on culture of human cartilage and chondrocytes stimulated by IL-1β. ChemMedChem 2007; 2(1): 113–9PubMedCrossRef
191.
go back to reference Cillero-Pastor B, Caramés B, Lires-Deàn M, et al. Mitochondrial dysfunction activates cyclooxygenase 2 expression in cultured normal human chondrocytes. Arthritis Rheum 2008; 58(8): 2409–19PubMedCrossRef Cillero-Pastor B, Caramés B, Lires-Deàn M, et al. Mitochondrial dysfunction activates cyclooxygenase 2 expression in cultured normal human chondrocytes. Arthritis Rheum 2008; 58(8): 2409–19PubMedCrossRef
192.
go back to reference Kim HA, Blanco FJ. Cell death and apoptosis in osteoarthritic cartilage. Curr Drug Targets 2007; 8(2): 333–45PubMedCrossRef Kim HA, Blanco FJ. Cell death and apoptosis in osteoarthritic cartilage. Curr Drug Targets 2007; 8(2): 333–45PubMedCrossRef
193.
go back to reference Lago R, Gomez R, Otero M, et al. A new player in cartilage homeostasis: adiponectin induces nitric oxide synthase II and pro-inflammatory cytokines in chondrocytes. Osteoarthritis Cartilage 2008; 16(9): 1101–9PubMedCrossRef Lago R, Gomez R, Otero M, et al. A new player in cartilage homeostasis: adiponectin induces nitric oxide synthase II and pro-inflammatory cytokines in chondrocytes. Osteoarthritis Cartilage 2008; 16(9): 1101–9PubMedCrossRef
194.
go back to reference Giatromanolaki A, Sivridis E, Athanassou N, et al. The angiogenic pathway ‘vascular endothelial growth factor/flk-1 (KDR) receptor’ in rheumatoid arthritis and osteoarthritis. J Pathol 2001; 194(1): 101–8PubMedCrossRef Giatromanolaki A, Sivridis E, Athanassou N, et al. The angiogenic pathway ‘vascular endothelial growth factor/flk-1 (KDR) receptor’ in rheumatoid arthritis and osteoarthritis. J Pathol 2001; 194(1): 101–8PubMedCrossRef
195.
go back to reference Giatromanolaki A, Sivridis E, Maltezos E, et al. Upregulated hypoxia-inducible factor-1α and -2α in rheumatoid arthritis and osteoarthritis. Arthritis Res Ther 2003; 5(4): R193–201PubMedCrossRef Giatromanolaki A, Sivridis E, Maltezos E, et al. Upregulated hypoxia-inducible factor-1α and -2α in rheumatoid arthritis and osteoarthritis. Arthritis Res Ther 2003; 5(4): R193–201PubMedCrossRef
196.
go back to reference Valdes AM, Lories RJ, van Meurs JB, et al. Variation at the ANP32a gene is associated with risk of hip osteoarthritis in women. Arthritis Rheum 2009; 60(7): 2046–54PubMedCrossRef Valdes AM, Lories RJ, van Meurs JB, et al. Variation at the ANP32a gene is associated with risk of hip osteoarthritis in women. Arthritis Rheum 2009; 60(7): 2046–54PubMedCrossRef
197.
go back to reference Egli RJ, Southam L, Wilkins JM, et al. Functional analysis of the osteoarthritis susceptibility-associated GDF5 regulatory polymorphism. Arthritis Rheum 2009; 60(7): 2055–64PubMedCrossRef Egli RJ, Southam L, Wilkins JM, et al. Functional analysis of the osteoarthritis susceptibility-associated GDF5 regulatory polymorphism. Arthritis Rheum 2009; 60(7): 2055–64PubMedCrossRef
198.
go back to reference Nixon AJ, Haupt L, Frisbie DD, et al. Gene-mediated restoration of cartilage matrix by combination insulin-like growth factor-I/interleukin receptor antagonist therapy. Gen Ther 2005; 12(2): 177–86CrossRef Nixon AJ, Haupt L, Frisbie DD, et al. Gene-mediated restoration of cartilage matrix by combination insulin-like growth factor-I/interleukin receptor antagonist therapy. Gen Ther 2005; 12(2): 177–86CrossRef
199.
go back to reference Malemud CJ. Gene therapy for arthritis: defining novel gene targets. Gen Ther Mol Biol 2007; 11: 27–36 Malemud CJ. Gene therapy for arthritis: defining novel gene targets. Gen Ther Mol Biol 2007; 11: 27–36
Metadata
Title
Anticytokine Therapy for Osteoarthritis
Evidence to Date
Author
Professor Charles J. Malemud
Publication date
01-02-2010
Publisher
Springer International Publishing
Published in
Drugs & Aging / Issue 2/2010
Print ISSN: 1170-229X
Electronic ISSN: 1179-1969
DOI
https://doi.org/10.2165/11319950-000000000-00000

Other articles of this Issue 2/2010

Drugs & Aging 2/2010 Go to the issue

Adis Drug Evaluation

Zoster Vaccine (Zostavax®)

Live Webinar | 27-06-2024 | 18:00 (CEST)

Keynote webinar | Spotlight on medication adherence

Live: Thursday 27th June 2024, 18:00-19:30 (CEST)

WHO estimates that half of all patients worldwide are non-adherent to their prescribed medication. The consequences of poor adherence can be catastrophic, on both the individual and population level.

Join our expert panel to discover why you need to understand the drivers of non-adherence in your patients, and how you can optimize medication adherence in your clinics to drastically improve patient outcomes.

Prof. Kevin Dolgin
Prof. Florian Limbourg
Prof. Anoop Chauhan
Developed by: Springer Medicine
Obesity Clinical Trial Summary

At a glance: The STEP trials

A round-up of the STEP phase 3 clinical trials evaluating semaglutide for weight loss in people with overweight or obesity.

Developed by: Springer Medicine

Highlights from the ACC 2024 Congress

Year in Review: Pediatric cardiology

Watch Dr. Anne Marie Valente present the last year's highlights in pediatric and congenital heart disease in the official ACC.24 Year in Review session.

Year in Review: Pulmonary vascular disease

The last year's highlights in pulmonary vascular disease are presented by Dr. Jane Leopold in this official video from ACC.24.

Year in Review: Valvular heart disease

Watch Prof. William Zoghbi present the last year's highlights in valvular heart disease from the official ACC.24 Year in Review session.

Year in Review: Heart failure and cardiomyopathies

Watch this official video from ACC.24. Dr. Biykem Bozkurt discusses last year's major advances in heart failure and cardiomyopathies.