Cypre, Inc., South San Francisco, CA 94080, USA.
Charles River Discovery Research Services Germany GmbH, 79108 Freiburg, Germany.
Cells. 2023 Apr 13;12(8):1145. doi: 10.3390/cells12081145.
Human-relevant systems that mimic the 3D tumor microenvironment (TME), particularly the complex mechanisms of immuno-modulation in the tumor stroma, in a reproducible and scalable format are of high interest for the drug discovery industry. Here, we describe a novel 3D in vitro tumor panel comprising 30 distinct PDX models covering a range of histotypes and molecular subtypes and cocultured with fibroblasts and PBMCs in planar (flat) extracellular matrix hydrogels to reflect the three compartments of the TME-tumor, stroma, and immune cells. The panel was constructed in a 96-well plate format and assayed tumor size, tumor killing, and T-cell infiltration using high-content image analysis after 4 days of treatment. We screened the panel first against the chemotherapy drug Cisplatin to demonstrate feasibility and robustness, and subsequently assayed immuno-oncology agents Solitomab (CD3/EpCAM bispecific T-cell engager) and the immune checkpoint inhibitors (ICIs) Atezolizumab (anti-PDL1), Nivolumab (anti-PD1) and Ipilimumab (anti-CTLA4). Solitomab displayed a strong response across many PDX models in terms of tumor reduction and killing, allowing for its subsequent use as a positive control for ICIs. Interestingly, Atezolizumab and Nivolumab demonstrated a mild response compared to Ipilimumab in a subset of models from the panel. We later determined that PBMC spatial proximity in the assay setup was important for the PD1 inhibitor, hypothesizing that both duration and concentration of antigen exposure may be critical. The described 30-model panel represents a significant advancement toward screening in vitro models of the tumor microenvironment that include tumor, fibroblast, and immune cell populations in an extracellular matrix hydrogel, with robust and standardized high content image analysis in a planar hydrogel. The platform is aimed at rapidly screening various combinations and novel agents and forming a critical conduit to the clinic, thus accelerating drug discovery for the next generation of therapeutics.
对药物发现行业而言,人们非常关注能够以可重复且可扩展的方式模拟与人类相关的 3D 肿瘤微环境(TME),尤其是肿瘤基质中复杂免疫调节机制的系统。在这里,我们描述了一种新颖的 30 种不同 PDX 模型组成的 3D 体外肿瘤模型组,涵盖了多种组织类型和分子亚型,并与成纤维细胞和 PBMC 共培养于平面(平)细胞外基质水凝胶中,以反映 TME-肿瘤、基质和免疫细胞的三个隔室。该模型组构建于 96 孔板格式中,并在 4 天的治疗后使用高内涵图像分析检测肿瘤大小、肿瘤杀伤和 T 细胞浸润。我们首先用化疗药物顺铂对该模型组进行筛选,以证明其可行性和稳健性,然后检测免疫肿瘤学药物 Solitomab(CD3/EpCAM 双特异性 T 细胞衔接器)和免疫检查点抑制剂(ICI)Atezolizumab(抗 PD-L1)、Nivolumab(抗 PD-1)和 Ipilimumab(抗 CTLA4)。Solitomab 在许多 PDX 模型中表现出强烈的反应,在肿瘤减少和杀伤方面表现出色,因此可将其作为 ICI 的阳性对照。有趣的是,与该模型组中的部分模型相比,Atezolizumab 和 Nivolumab 对 Ipilimumab 的反应较为温和。我们后来确定,在实验设置中,PBMC 空间接近度对于 PD1 抑制剂非常重要,我们假设抗原暴露的持续时间和浓度可能是关键因素。所描述的 30 种模型组代表了在细胞外基质水凝胶中包含肿瘤、成纤维细胞和免疫细胞群体的肿瘤微环境体外模型筛选方面的重大进展,该模型组具有强大且标准化的平面水凝胶高内涵图像分析。该平台旨在快速筛选各种组合和新型药物,并与临床建立重要联系,从而加速下一代治疗药物的药物发现。