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早期抗炎干预可改善强直性脊柱炎蛋白聚糖诱导的脊柱炎小鼠模型中的轴性疾病。

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

作者信息

Tseng Hsu-Wen, Glant Tibor T, Brown Matthew A, Kenna Tony J, Thomas Gethin P, Pettit Allison R

机构信息

The University of Queensland Diamantina Institute, Translational Research Institute, 37 Kent Street, Woolloongabba, QLD, 4102, Australia.

Mater Research Institute-The University of Queensland, Faculty of Medicine, Translational Research Institute, 37 Kent St, Woolloongabba, QLD, 4102, Australia.

出版信息

BMC Musculoskelet Disord. 2017 May 30;18(1):228. doi: 10.1186/s12891-017-1600-7.

Abstract

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.

摘要

背景

强直性脊柱炎(AS)的特征是免疫介导的关节炎和骨质增生,最终导致关节强直。由于抗炎治疗对影像学进展的疗效不明确,炎症对于骨质增生是否必要存在争议。在蛋白聚糖诱导的脊柱炎(PGISp)这一AS小鼠模型中,炎症是骨质增生的前提条件,因为骨质增生仅在炎症驱动的椎间盘(IVD)破坏后才会出现。我们推测,早期使用强效抗炎疗法进行干预可保护IVD完整性,从而改变疾病进程。

方法

PGISp小鼠在疾病早期开始接受载体或依那西普(ETN)加泼尼松龙(PRD)联合治疗2周或6周。纵向评估外周关节炎。使用包括炎症、关节破坏和过度组织形成的半定量组织学评分方案评估脊柱疾病。

结果

ETN + PRD治疗显著延迟了外周关节炎的发作。在疾病早期开始治疗时,IVD完整性得到显著保护。六周的治疗导致椎间关节损伤和过度组织形成有减少的趋势。IVD评分分布呈二分法,可能反映了治疗开始时轴向疾病的程度。在IVD破坏评分高的小鼠亚组中,ETN + PRD治疗显著降低了IVD破坏的严重程度、炎症和骨侵蚀,并减少了软骨损伤和过度组织形成。

结论

早期抗炎治疗干预不仅改善了炎症症状,还减轻了PGISp小鼠脊柱的结构损伤。这一临床前观察结果表明,早期抗炎干预可能会减缓AS患者的影像学进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/035c/5450150/2858809e2a6b/12891_2017_1600_Fig1_HTML.jpg

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