Maulana Tengku Ibrahim, Wevers Nienke R, Kristoforus Theodora, Chandler Morgan, Lanz Henriette L, Joore Jos, Vulto Paul, Villenave Remi, Kustermann Stefan, Loskill Peter, Bircsak Kristin M
Department for Microphysiological Systems, Institute of Biomedical Engineering, Faculty of Medicine, Eberhard Karls University Tübingen, Tübingen, Germany.
NMI Natural and Medical Sciences Institute at the University of Tübingen, Reutlingen, Germany.
Annu Rev Pharmacol Toxicol. 2025 Jan;65(1):47-69. doi: 10.1146/annurev-pharmtox-061724-080621. Epub 2024 Dec 17.
New drug modalities offer life-saving benefits for patients through access to previously undruggable targets. Yet these modalities pose a challenge for the pharmaceutical industry, as side effects are complex, unpredictable, and often uniquely human. With animal studies having limited predictive value due to translatability challenges, the pharmaceutical industry seeks out new approach methodologies. Microphysiological systems (MPS) offer important features that enable complex toxicological processes to be modeled in vitro such as () an adjustable complexity of cellular components, including immune components; () a modifiable tissue architecture; () integration and monitoring of dynamic mechanisms; and () a multiorgan connection. Here we review MPS studies in the context of four clinical adverse events triggered by new drug modalities: peripheral neuropathy, thrombocytopenia, immune-mediated hepatotoxicity, and cytokine release syndrome. We conclude that while the use of MPS for testing new drug modality-induced toxicities is still in its infancy, we see strong potential going forward.
新的药物形式通过作用于以前难以成药的靶点为患者带来救命的益处。然而,这些药物形式给制药行业带来了挑战,因为副作用复杂、不可预测,而且往往是人类所特有的。由于可转化性挑战,动物研究的预测价值有限,制药行业正在寻找新的方法学。微生理系统(MPS)具有重要特性,能够在体外模拟复杂的毒理学过程,例如:(1)细胞成分(包括免疫成分)的复杂性可调节;(2)组织结构可修改;(3)动态机制的整合与监测;(4)多器官连接。在此,我们结合新药物形式引发的四种临床不良事件——周围神经病变、血小板减少症、免疫介导的肝毒性和细胞因子释放综合征,对微生理系统的研究进行综述。我们得出结论,虽然将微生理系统用于测试新药物形式诱导的毒性仍处于起步阶段,但我们认为其未来潜力巨大。