Hirschhaeuser Franziska, Leidig Tobias, Rodday Bjoern, Lindemann Carsten, Mueller-Klieser Wolfgang
Institute of Physiology and Pathophysiology, University of Mainz, Mainz, Germany.
J Biomol Screen. 2009 Sep;14(8):980-90. doi: 10.1177/1087057109341766. Epub 2009 Aug 12.
The aim of the present study was to assess the feasibility of a 3D tumor cell culture model, that is, multicellular tumor spheroids (MCTSs) as an adequate model for micrometastases and therefore as a pharmacological model for efficacy testing of trifunctional therapeutic antibodies. Unlike conventional monolayer cultures, spheroids allow researchers to study parameters, such as 3D cell shape, 3D cell arrangement and microenvironment, and penetration efficiency of defense cells that may largely influence the efficacy of antibody treatment in vivo. The authors established a long-term coculture of human MCTSs with peripheral blood mononuclear cells (PBMCs) to test the anticancer effect of the trifunctional, bispecific antibody catumaxomab (anti-EpCAM x anti-CD3) or similar therapeutic molecules. The test system is accessible to various analytical methods and thus allows for characterizing multiple parameters, which can help elucidate the mode of action of immunotherapeutic anticancer treatment. For example, the novel approach enables precise, reproducible volume growth analysis of MCTSs under immunotherapeutic treatments. For evaluation of changes within individual spheroids, cryosections can be stained (e.g., for proliferating or apoptotic cells as well as infiltrating PBMCs). Molecular PCR-based assays or flow cytometric analyses allow for discrimination between different cell types, particularly leukocyte subtypes. Furthermore, MCTSs can be disaggregated to form standard monolayers for cell viability or plating efficiency experiments. For these reasons, the MCTS model is a powerful tool to analyze drug efficacy with various endpoints under highly reproducible, standardized conditions.
本研究的目的是评估一种3D肿瘤细胞培养模型,即多细胞肿瘤球体(MCTS)作为微转移合适模型的可行性,因此也作为三功能治疗性抗体疗效测试的药理学模型。与传统的单层培养不同,球体使研究人员能够研究一些参数,如3D细胞形状、3D细胞排列和微环境,以及防御细胞的穿透效率,这些参数可能在很大程度上影响抗体治疗在体内的疗效。作者建立了人MCTS与外周血单核细胞(PBMC)的长期共培养体系,以测试三功能双特异性抗体卡妥索单抗(抗EpCAM×抗CD3)或类似治疗分子的抗癌效果。该测试系统适用于各种分析方法,因此可以表征多个参数,这有助于阐明免疫治疗性抗癌治疗的作用方式。例如,这种新方法能够在免疫治疗下对MCTS进行精确、可重复的体积生长分析。为了评估单个球体内部的变化,可以对冷冻切片进行染色(例如,用于增殖或凋亡细胞以及浸润的PBMC)。基于分子PCR的检测或流式细胞术分析能够区分不同的细胞类型,特别是白细胞亚型。此外,MCTS可以解离形成标准单层用于细胞活力或接种效率实验。基于这些原因,MCTS模型是一种强大的工具,可在高度可重复、标准化的条件下分析具有各种终点的药物疗效。