Pasztorek Markus, Fischer Johanna, Otahal Alexander, de Luna Andrea, Nehrer Stefan, Rosser Julie
Pregenerate GmbH, Vienna, Austria.
Center for Regenerative Medicine, Department for Health Sciences, Medicine and Research, University for Continuing Education Krems, Krems an der Donau, Austria.
Cartilage. 2024 Sep 5:19476035241277654. doi: 10.1177/19476035241277654.
This study aims to tackle the existing challenges associated with the prediction and optimization of pharmaceutical interventions for osteoarthritis (OA). The primary objective is to develop an innovative tool that provides objective and patient-specific information regarding the most affected tissue in OA, articular cartilage.
We employed an organ-on-a-chip (OoC) approach to replicate the 3D structure of cartilage in an setup. The study focused on assessing the individual drug responses of common medications using this innovative platform. Additionally, we conducted a biomarker analysis to gain insights into the variability of drug responses across patients.
Our findings reveal that OA articular cartilage demonstrates an individualized response to pharmaceutical interventions. Despite the diverse nature of patient responses, our study indicates that Triamcinolone, a standard-of-care medication, consistently exhibits a robust anti-inflammatory response across patient tests. However, as seen in clinical studies, Triamcinolone was concurrently associated with degeneration. The biomarker analysis further underscores the importance of considering individual drug responses in developing effective treatment plans.
In conclusion, this study introduces a valuable tool that not only mimics the 3D structure of cartilage but also provides crucial insights into the individualized responses of patients to various OA treatments. The application of an OoC approach may allow for a more accurate assessment of treatment efficacy. This objective biomarker analysis on patient-specific tissue offers clinicians a means to tailor treatment plans, thereby minimizing joint damage and advancing toward a more personalized approach in OA management.
本研究旨在应对与骨关节炎(OA)药物干预的预测和优化相关的现有挑战。主要目标是开发一种创新工具,该工具可提供有关OA中受影响最严重的组织——关节软骨的客观且针对患者的信息。
我们采用芯片器官(OoC)方法在一种装置中复制软骨的三维结构。该研究专注于使用这个创新平台评估常用药物的个体药物反应。此外,我们进行了生物标志物分析,以深入了解不同患者之间药物反应的变异性。
我们的研究结果表明,OA关节软骨对药物干预表现出个体化反应。尽管患者反应具有多样性,但我们的研究表明,曲安奈德作为一种标准治疗药物,在所有患者测试中始终表现出强烈的抗炎反应。然而,正如临床研究中所见,曲安奈德同时与退变有关。生物标志物分析进一步强调了在制定有效治疗方案时考虑个体药物反应的重要性。
总之,本研究引入了一种有价值的工具,该工具不仅模拟了软骨的三维结构,还提供了关于患者对各种OA治疗的个体化反应的关键见解。OoC方法的应用可能使治疗效果评估更加准确。这种针对患者特定组织的客观生物标志物分析为临床医生提供了一种定制治疗方案的方法,从而将关节损伤降至最低,并朝着OA管理中更个性化的方法迈进。