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用于鉴定原药治疗原发性白血病反应的微生理药物测试平台。

Microphysiological Drug-Testing Platform for Identifying Responses to Prodrug Treatment in Primary Leukemia.

机构信息

Department of Biosystems Science and Engineering, ETH Zurich, Basel, BS, 4058, Switzerland.

Children's Research Center, University Children's Hospital Zurich, Zurich, ZH, 8008, Switzerland.

出版信息

Adv Healthc Mater. 2023 Jan;12(6):e2202506. doi: 10.1002/adhm.202202506. Epub 2023 Jan 27.

Abstract

Despite increasing survival rates of pediatric leukemia patients over the past decades, the outcome of some leukemia subtypes has remained dismal. Drug sensitivity and resistance testing on patient-derived leukemia samples provide important information to tailor treatments for high-risk patients. However, currently used well-based drug screening platforms have limitations in predicting the effects of prodrugs, a class of therapeutics that require metabolic activation to become effective. To address this issue, a microphysiological drug-testing platform is developed that enables co-culturing of patient-derived leukemia cells, human bone marrow mesenchymal stromal cells, and human liver microtissues within the same microfluidic platform. This platform also enables to control the physical interaction between the diverse cell types. Herein, it is made possible to recapitulate hepatic prodrug activation of ifosfamide in their platform, which is very difficult in traditional well-based assays. By testing the susceptibility of primary patient-derived leukemia samples to the prodrug ifosfamide, sample-specific sensitivities to ifosfamide in primary leukemia samples are identified. The microfluidic platform is found to enable the recapitulation of physiologically relevant conditions and the testing of prodrugs including short-lived and unstable metabolites. The platform holds great potential for clinical translation and precision chemotherapy selection.

摘要

尽管过去几十年来儿科白血病患者的生存率有所提高,但某些白血病亚型的预后仍然不容乐观。对患者来源的白血病样本进行药物敏感性和耐药性测试,可以为高危患者提供重要的治疗方案。然而,目前使用的基于培养的药物筛选平台在预测前药的效果方面存在局限性,前药是一类需要代谢激活才能发挥作用的治疗药物。为了解决这个问题,开发了一种微生理药物测试平台,该平台能够在同一个微流控平台中共同培养患者来源的白血病细胞、人骨髓间充质基质细胞和人肝微组织。该平台还能够控制不同细胞类型之间的物理相互作用。在此,可以在平台中重现异环磷酰胺的肝前药激活,这在传统的基于培养的测定中是非常困难的。通过测试原发性患者来源的白血病样本对前药异环磷酰胺的敏感性,可以确定原发性白血病样本中对异环磷酰胺的特异性敏感性。研究发现,该微流控平台能够再现生理相关条件,并测试包括短寿命和不稳定代谢物在内的前药。该平台具有很大的临床转化和精准化疗选择的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fc9/11469234/20473097d8c4/ADHM-12-2202506-g003.jpg

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