High-Throughput Assay for Predicting Diarrhea Risk Using a 2D Human Intestinal Stem Cell-Derived Model

Colleen M Pike, James A Levi, Lauren A Boone, Swetha Peddibhotla, Jacob Johnson, Bailey Zwarycz, Maureen K Bunger, William Thelin, Elizabeth M Boazak
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Abstract

Gastrointestinal toxicities (GITs) are the most prevalent adverse events (AE) reported in clinical trials, often resulting in dose-limitations that reduce drug efficacy and delay development and treatment optimization. Preclinical animal models do not accurately replicate human GI physiology, leaving few options for early detection of GI side effects prior to human studies. Development of an accurate model that predicts GIT earlier in drug discovery programs would better support successful clinical trial outcomes. Chemotherapeutics, which exhibit high rates of clinical GIT, frequently target mitotic cells. Therefore, we hypothesized that a model utilizing proliferative cell populations derived from human intestinal crypts would predict the occurrence of clinical GITs with high accuracy. Here, we describe the development of a multiparametric assay utilizing the RepliGut Planar system, an intestinal stem cell-derived platform cultured in an accessible high throughput Transwell format. This assay addresses key physiological elements of GIT by assessing cell proliferation (EdU incorporation), cell abundance (DAPI quantification), and barrier function (TEER). Using this approach, we demonstrate that primary proliferative cell populations reproducibly respond to marketed chemotherapeutics at physiologic concentrations. To determine the ability of this model to predict clinical diarrhea risk, we evaluated a set of 30 drugs with known clinical diarrhea incidence in three human donors, comparing results to known plasma drug concentrations. This resulted in highly accurate predictions of diarrhea potential for each endpoint (balanced accuracy of 91% for DAPI, 90% for EdU, 88% for TEER) with minimal variation across human donors. In vitro toxicity screening using primary proliferative cells may enable improved safety evaluations, reducing the risk of AEs in clinical trials and ultimately lead to safer and more effective treatments for patients.
利用二维人类肠干细胞衍生模型预测腹泻风险的高通量检测方法
胃肠道毒性(GIT)是临床试验中报告的最常见的不良事件(AE),通常会导致剂量限制,从而降低药物疗效,延误研发和治疗优化。临床前动物模型并不能准确复制人体消化道生理机能,因此在人体研究之前几乎没有早期检测消化道副作用的选择。开发一种能在药物发现项目早期预测胃肠道副作用的精确模型,将能更好地支持临床试验取得成功。临床 GIT 发生率较高的化疗药物经常以有丝分裂细胞为靶点。因此,我们假设,利用来自人体肠隐窝的增殖细胞群建立的模型将能高精度地预测临床 GIT 的发生。在此,我们介绍了利用 RepliGut Planar 系统开发的多参数检测方法,该系统是一个肠道干细胞衍生平台,以易于使用的高通量 Transwell 格式进行培养。该检测法通过评估细胞增殖(EdU掺入)、细胞丰度(DAPI定量)和屏障功能(TEER)来解决胃肠道的关键生理要素。利用这种方法,我们证明了原代增殖细胞群对生理浓度的市售化疗药物的反应是可重复的。为了确定该模型预测临床腹泻风险的能力,我们评估了已知临床腹泻发生率的 30 种药物,并将结果与已知血浆药物浓度进行了比较。这使得对每个终点的腹泻可能性预测都非常准确(DAPI 的平衡准确率为 91%,EdU 为 90%,TEER 为 88%),而且不同人体供体之间的差异极小。利用原代增殖细胞进行体外毒性筛选可改进安全性评估,降低临床试验中的AEs风险,最终为患者提供更安全、更有效的治疗。
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