Effects of Ab501 (certolizumab mice equivalent) in arthritis induced bone loss.

IF 1.4 4区 医学 Q3 RHEUMATOLOGY ARP Rheumatology Pub Date : 2024-10-01
Bruno Vidal, Mikko Finnilä, Inês Lopes, Rita Cascão, João Eurico Fonseca
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Abstract

Introduction - Rheumatoid arthritis (RA) is a chronic immune-mediated inflammatory disease, which causes local and systemic bone damage. The main goal of this work was to analyze, how treatment intervention with Ab501 (certolizumab mice equivalent) prevents the disturbances on bone structure and mechanics induced by arthritis. Methods - Thirty DBA/1 collagen-induced arthritis (CIA) mice were randomly housed in experimental groups, as follows: arthritic untreated (N=9), preventive intervention (N=10) and treatment intervention (N=11). A non-induced group (N=5) was used as a control. Mice were monitored during 70 days after disease induction for the inflammatory score, ankle perimeter and body weight. After 70 days of disease progression mice were sacrificed and bone samples were collected for histology, micro-computed tomography (µCT) and 3-point bending analysis. In addition, blood samples were also collected for bone turnover markers quantification. Results - Results showed that Ab501 administration was able to control and abrogate disease development both in preventive and early therapeutic intervention. µCT results revealed that Ab501 was able to preserve trabecular bone structure when delivered before arthritis induction. Conclusion - Ab501 preventive administration was able to control inflammation and prevent the degradative effects of arthritis on trabecular bone structure in a CIA DBA/1 mice model.

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Ab501 (certolizumab小鼠当量)在关节炎诱导的骨质流失中的作用。
类风湿关节炎(RA)是一种慢性免疫介导的炎症性疾病,可引起局部和全身骨损伤。这项工作的主要目的是分析Ab501 (certolizumab小鼠等效物)的治疗干预如何防止关节炎引起的骨结构和力学紊乱。方法:将30只DBA/1胶原诱导关节炎(CIA)小鼠随机分为3组,分别为未治疗组(N=9)、预防干预组(N=10)和治疗干预组(N=11)。非诱导组(N=5)作为对照组。在疾病诱导后70天内监测小鼠的炎症评分、踝关节周长和体重。疾病进展70天后,处死小鼠,收集骨样本进行组织学、微计算机断层扫描(µCT)和三点弯曲分析。此外,还采集血液样本进行骨转换标志物定量分析。结果-结果表明,在预防和早期治疗干预中,给药Ab501能够控制和消除疾病的发展。µCT结果显示,在关节炎诱导前给药时,Ab501能够保留骨小梁结构。结论-在CIA DBA/1小鼠模型中,Ab501预防给药能够控制炎症并阻止关节炎对骨小梁结构的降解作用。
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