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工程化心肌模型在表型药物筛选中的应用。

Engineered Heart Muscle Models in Phenotypic Drug Screens.

机构信息

Institute of Pharmacology and Toxicology, University Medical Center, Georg-August-University, Göttingen, Germany.

DZHK (German Center for Cardiovascular Research), Göttingen, Germany.

出版信息

Handb Exp Pharmacol. 2021;265:143-156. doi: 10.1007/164_2020_385.

Abstract

Classical drug development is compromised by considerable clinical failure of promising drug candidates after decades of costly preclinical work. Failure can be because of previously unrecognized safety concerns or more commonly lack of clinical efficacy. Classical drug discovery and safety pharmacology programs rely heavily on well-established in vitro and preclinical animal models. The availability of human pluripotent stem cells and the possibility to direct them into any somatic cell type suggest that a paradigm shift in drug development may be possible and timely, with the opportunity to test safety and efficacy of candidate drugs on the human target cells and tissue. However, there is considerable uncertainty as to whether human models would only qualify as replacement for well-established tools or add substantially more information to the preclinical data package, to facilitate translation of more promising drug candidates into clinical practice. This chapter provides an overview of tissue-engineered macro-scale heart muscle models for applications in drug discovery and safety pharmacology.

摘要

经典的药物开发受到严重影响,有前途的候选药物在经过几十年的昂贵的临床前工作后,临床效果并不理想。失败的原因可能是之前未被认识到的安全问题,或者更常见的是缺乏临床疗效。经典的药物发现和安全药理学计划严重依赖于成熟的体外和临床前动物模型。人类多能干细胞的可用性和将其定向分化为任何体细胞类型的可能性表明,药物开发可能会发生范式转变,而且时机恰到好处,有机会在人类靶细胞和组织上测试候选药物的安全性和疗效。然而,人们对于人类模型是否只能作为成熟工具的替代品,或者是否会为临床前数据提供更多实质性的信息,从而促进更有前途的候选药物转化为临床实践,存在相当大的不确定性。本章概述了用于药物发现和安全药理学的组织工程化宏观心脏肌肉模型。

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