Early anti-inflammatory intervention ameliorates axial disease in the proteoglycan-induced spondylitis mouse model of ankylosing spondylitis

被引:9
作者
Tseng, Hsu-Wen [1 ,2 ]
Glant, Tibor T. [3 ]
Brown, Matthew A. [1 ,4 ]
Kenna, Tony J. [1 ,4 ]
Thomas, Gethin P. [1 ,5 ]
Pettit, Allison R. [2 ]
机构
[1] Univ Queensland, Diamantina Inst, Translat Res Inst, 37 Kent St, Woolloongabba, Qld 4102, Australia
[2] Univ Queensland, Fac Med, Mater Res Inst, Translat Res Inst, 37 Kent St, Woolloongabba, Qld 4102, Australia
[3] Rush Univ, Med Ctr, Dept Orthoped Surg, Sect Mol Med, 1735 W Harrison Str,Cohn Res Bldg, Chicago, IL 60612 USA
[4] Queensland Univ Technol, Inst Hlth & Biomed Innovat, Translat Res Inst, 37 Kent St, Woolloongabba, Qld 4102, Australia
[5] Charles Sturt Univ, Boorooma St, Wagga Wagga, NSW 2678, Australia
来源
BMC MUSCULOSKELETAL DISORDERS | 2017年 / 18卷
基金
澳大利亚国家健康与医学研究理事会;
关键词
Ankylosing spondylitis; Spondyloarthropathy; Osteoproliferation; Early intervention; Proteoglycan-induced; spondylitis mouse model; BONE-FORMATION; INFLAMMATION; SPONDYLOARTHRITIS;
D O I
10.1186/s12891-017-1600-7
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Background: Ankylosing spondylitis (AS) is characterised by immune-mediated arthritis and osteoproliferation, ultimately leading to joint ankylosis. Whether inflammation is necessary for osteoproliferation is controversial, fuelled by the unclear efficacy of anti-inflammatory treatments on radiographic progression. In proteoglycan-induced spondylitis (PGISp), a mouse model of AS, inflammation is the prerequisite for osteoproliferation as osteoproliferation was only observed following inflammation-driven intervertebral disc (IVD) destruction. We hypothesised that early intervention with a potent anti-inflammatory therapy would protect IVD integrity and consequently alter disease progression. Methods: PGISp mice received vehicle or a combination of etanercept (ETN) plus prednisolone (PRD) therapy for 2 or 6 weeks initiated at an early disease stage. Peripheral arthritis was scored longitudinally. Spinal disease was assessed using a semi-quantitative histological scoring regimen including inflammation, joint destruction and excessive tissue formation. Results: ETN + PRD therapy significantly delayed the onset of peripheral arthritis. IVD integrity was significantly protected when treatment was commenced in early disease. Six-weeks of treatment resulted in trends towards reductions in intervertebral joint damage and excessive tissue formation. IVD score distribution was dichotomized, likely reflecting the extent of axial disease at initiation of therapy. In the sub-group of mice with high IVD destruction scores, ETN + PRD treatment significantly reduced IVD destruction severity, inflammation and bone erosion and reduced cartilage damage and excessive tissue formation. Conclusions: Early intervention with anti-inflammatory treatment not only improved inflammatory symptoms but also ameliorated structural damage of spine in PGISp mice. This preclinical observation suggests that early anti-inflammatory intervention may slow radiographic progression in AS patients.
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页数:9
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