Lim Maria A, Louie Brenton, Ford Daniel, Heath Kyle, Cha Paulyn, Betts-Lacroix Joe, Lum Pek Yee, Robertson Timothy L, Schaevitz Laura
Vium Inc., San Mateo, CA, United States.
Capella Biosciences Inc., Palo Alto, CA, United States.
Front Pharmacol. 2017 Nov 14;8:818. doi: 10.3389/fphar.2017.00818. eCollection 2017.
Despite a broad spectrum of anti-arthritic drugs currently on the market, there is a constant demand to develop improved therapeutic agents. Efficient compound screening and rapid evaluation of treatment efficacy in animal models of rheumatoid arthritis (RA) can accelerate the development of clinical candidates. Compound screening by evaluation of disease phenotypes in animal models facilitates preclinical research by enhancing understanding of human pathophysiology; however, there is still a continuous need to improve methods for evaluating disease. Current clinical assessment methods are challenged by the subjective nature of scoring-based methods, time-consuming longitudinal experiments, and the requirement for better functional readouts with relevance to human disease. To address these needs, we developed a low-touch, digital platform for phenotyping preclinical rodent models of disease. As a proof-of-concept, we utilized the rat collagen-induced arthritis (CIA) model of RA and developed the Digital Arthritis Index (DAI), an objective and automated behavioral metric that does not require human-animal interaction during the measurement and calculation of disease parameters. The DAI detected the development of arthritis similar to standard methods, including ankle joint measurements and arthritis scores, as well as demonstrated a positive correlation to ankle joint histopathology. The DAI also determined responses to multiple standard-of-care (SOC) treatments and nine repurposed compounds predicted by the SMarTR Engine to have varying degrees of impact on RA. The disease profiles generated by the DAI complemented those generated by standard methods. The DAI is a highly reproducible and automated approach that can be used in-conjunction with standard methods for detecting RA disease progression and conducting phenotypic drug screens.
尽管目前市场上有多种抗关节炎药物,但人们对开发更有效的治疗药物的需求一直存在。在类风湿性关节炎(RA)动物模型中进行高效的化合物筛选和快速评估治疗效果,可以加速临床候选药物的开发。通过评估动物模型中的疾病表型进行化合物筛选,有助于通过增强对人类病理生理学的理解来促进临床前研究;然而,仍需要不断改进疾病评估方法。当前的临床评估方法受到基于评分方法的主观性、耗时的纵向实验以及对与人类疾病相关的更好功能读数的要求的挑战。为了满足这些需求,我们开发了一个低接触的数字平台,用于对临床前啮齿动物疾病模型进行表型分析。作为概念验证,我们利用大鼠胶原诱导性关节炎(CIA)模型开发了数字关节炎指数(DAI),这是一种客观的自动化行为指标,在测量和计算疾病参数时不需要人与动物互动。DAI检测到的关节炎发展情况与标准方法相似,包括踝关节测量和关节炎评分,并且与踝关节组织病理学呈正相关。DAI还确定了对多种标准治疗(SOC)的反应以及SMarTR引擎预测的九种具有不同程度RA影响的重新利用化合物。DAI生成的疾病概况补充了标准方法生成的概况。DAI是一种高度可重复的自动化方法,可与标准方法结合使用,以检测RA疾病进展并进行表型药物筛选。