Prophylactic treatment with S100A9 inhibitor paquinimod reduces pathology in experimental collagenase-induced osteoarthritis

被引:90
作者
Schelbergen, R. F. [1 ]
Geven, E. J. [1 ]
van den Bosch, M. H. J. [1 ]
Eriksson, H. [2 ]
Leanderson, T. [3 ]
Vogl, T. [4 ]
Roth, J. [4 ]
van de Loo, F. A. J. [1 ]
Koenders, M. I. [1 ]
van der Kraan, P. M. [1 ]
van den Berg, W. B. [1 ]
Blom, A. B. [1 ]
van Lent, P. L. E. M. [1 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Dept Rheumatol, Expt Rheumatol, NL-6500 HB Nijmegen, Netherlands
[2] Act Biotech AB, Lund, Sweden
[3] Lund Univ, Immunol Grp, Lund, Sweden
[4] Univ Munster, Inst Immunol, D-48149 Munster, Germany
关键词
SERUM-LEVELS; CELLS; MICE; INFLAMMATION; MACROPHAGES; SYNOVITIS; ARTHRITIS; PROTEINS; EFFICACY; LESIONS;
D O I
10.1136/annrheumdis-2014-206517
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Objectives Alarmins S100A8/A9 regulate pathology in experimental osteoarthritis (OA). Paquinimod is an immunomodulatory compound preventing S100A9 binding to TLR-4. We investigated the effect of paquinimod on experimental OA and human OA synovium. Materials and methods Two OA mouse models differing in level of synovial activation were treated prophylactic with paquinimod. Synovial thickening, osteophyte size and cartilage damage were measured histologically, using an arbitrary score, adapted Pritzker OARSI score or imaging software, respectively. Human OA synovia were stimulated with S100A9, with or without paquinimod. Results Paquinimod treatment of collagenase-induced OA (CIOA) resulted in significantly reduced synovial thickening (57%), osteophyte size at the medial femur (66%) and cruciate ligaments (67%) and cartilage damage at the medial tibia (47%) and femur (75%; n=7, untreated n=6). In contrast, paquinimod did not reduce osteophyte size and reduced cartilage damage at one location only in destabilised medial meniscus, an OA model with considerably lower synovial activation compared with CIOA. In human OA synovium, paquinimod blocked proinflammatory (interleukin (IL)-6, IL-8, tumour necrosis factor-alpha) and catabolic (matrix metalloproteinases 1 and 3) factors induced by S100A9 (n=5). Conclusions Prophylactic treatment of paquinimod reduces synovial activation, osteophyte formation and cartilage damage in experimental OA with high synovial activation (CIOA) and ameliorates pathological effects of S100A9 in OA synovium ex vivo.
引用
收藏
页码:2254 / 2258
页数:5
相关论文
共 23 条
[1]
Synovitis: a potential predictive factor of structural progression of medial tibiofemoral knee osteoarthritis - results of a 1 year longitudinal arthroscopic study in 422 patients [J].
Ayral, X ;
Pickering, EH ;
Woodworth, TG ;
Mackillop, N ;
Dougados, M .
OSTEOARTHRITIS AND CARTILAGE, 2005, 13 (05) :361-367
[2]
Pharmacokinetics, tolerability, and preliminary efficacy of paquinimod (ABR-215757), a new quinoline-3-carboxamide derivative: Studies in lupus-prone mice and a multicenter, randomized, double-blind, placebo-controlled, repeat-dose, dose-ranging study in patients with systemic lupus erythematosus [J].
Bengtsson, Anders A. ;
Sturfelt, Gunnar ;
Lood, Christian ;
Ronnblom, Lars ;
van Vollenhoven, Ronald F. ;
Axelsson, Bengt ;
Sparre, Birgitta ;
Tuvesson, Helen ;
Ohman, Marie Wallen ;
Leanderson, Tomas .
ARTHRITIS AND RHEUMATISM, 2012, 64 (05) :1579-1588
[4]
Identification of Human S100A9 as a Novel Target for Treatment of Autoimmune Disease via Binding to Quinoline-3-Carboxamides [J].
Bjork, Per ;
Bjork, Anders ;
Vogl, Thomas ;
Stenstrom, Martin ;
Liberg, David ;
Olsson, Anders ;
Roth, Johannes ;
Ivars, Fredrik ;
Leanderson, Tomas .
PLOS BIOLOGY, 2009, 7 (04) :800-812
[5]
Synovial lining macrophages mediate osteophyte formation during experimental osteoarthritis [J].
Blom, AB ;
van Lent, PLEM ;
Holthuysen, AEM ;
van der Kraan, PM ;
Roth, J ;
van Rooijen, N ;
van den Berg, WB .
OSTEOARTHRITIS AND CARTILAGE, 2004, 12 (08) :627-635
[6]
Crucial role of macrophages in matrix metalloproteinase-mediated cartilage destruction during experimental osteoarthritis - Involvement of matrix metalloproteinase 3 [J].
Blom, Arjen B. ;
van Lent, Peter L. ;
Libregts, Sten ;
Holthuysen, Astrid E. ;
van der Kraan, Peter M. ;
van Rooijen, Nico ;
van den Berg, Wim B. .
ARTHRITIS AND RHEUMATISM, 2007, 56 (01) :147-157
[7]
MRP8/14 serum levels as a strong predictor of response to biological treatments in patients with rheumatoid arthritis [J].
Choi, Ivy Y. ;
Gerlag, Danielle M. ;
Herenius, Marieke J. ;
Thurlings, Rogier M. ;
Wijbrandts, Carla A. ;
Foell, Dirk ;
Vogl, Thomas ;
Roth, Johannes ;
Tak, Paul P. ;
Holzinger, Dirk .
ANNALS OF THE RHEUMATIC DISEASES, 2015, 74 (03) :499-505
[8]
Parallel evolution of OA phenotypes and therapies [J].
Conaghan, Philip G. .
NATURE REVIEWS RHEUMATOLOGY, 2013, 9 (02) :68-70
[9]
Synovial inflammation, immune cells and their cytokines in osteoarthritis: a review [J].
de Lange-Brokaar, B. J. E. ;
Ioan-Facsinay, A. ;
van Osch, G. J. V. M. ;
Zuurmond, A. -M. ;
Schoones, J. ;
Toes, R. E. M. ;
Huizinga, T. W. J. ;
Kloppenburg, M. .
OSTEOARTHRITIS AND CARTILAGE, 2012, 20 (12) :1484-1499
[10]
Phagocyte-specific S100 proteins and high-sensitivity C reactive protein as biomarkers for a risk-adapted treatment to maintain remission in juvenile idiopathic arthritis: a comparative study [J].
Gerss, Joachim ;
Roth, Johannes ;
Holzinger, Dirk ;
Ruperto, Nicolino ;
Wittkowski, Helmut ;
Frosch, Michael ;
Wulffraat, Nico ;
Wedderburn, Lucy ;
Stanevicha, Valda ;
Mihaylova, Dimitrina ;
Harjacek, Miroslav ;
Len, Claudio ;
Toppino, Claudia ;
Masi, Massimo ;
Minden, Kirsten ;
Saurenmann, Traudel ;
Uziel, Yosef ;
Vesely, Richard ;
Teresa Apaz, Maria ;
Kuester, Rolf-Michael ;
Rua Elorduy, Maria Jesus ;
Burgos-Vargas, Ruben ;
Ioseliani, Maka ;
Magni-Manzoni, Silvia ;
Unsal, Erbil ;
Anton, Jordi ;
Balogh, Zsolt ;
Hagelberg, Stefan ;
Mazur-Zielinska, Henryka ;
Tauber, Tsivia ;
Martini, Alberto ;
Foell, Dirk .
ANNALS OF THE RHEUMATIC DISEASES, 2012, 71 (12) :1991-1997