Loewa Anna, Feng James J, Hedtrich Sarah
Department of Infectious Diseases and Respiratory Medicine, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt Universität zu Berlin, Berlin, Germany.
Department of Chemical and Biological Engineering, University of British Columbia, Vancouver, BC Canada.
Nat Rev Bioeng. 2023 May 11:1-15. doi: 10.1038/s44222-023-00063-3.
Biomedical research is undergoing a paradigm shift towards approaches centred on human disease models owing to the notoriously high failure rates of the current drug development process. Major drivers for this transition are the limitations of animal models, which, despite remaining the gold standard in basic and preclinical research, suffer from interspecies differences and poor prediction of human physiological and pathological conditions. To bridge this translational gap, bioengineered human disease models with high clinical mimicry are being developed. In this Review, we discuss preclinical and clinical studies that benefited from these models, focusing on organoids, bioengineered tissue models and organs-on-chips. Furthermore, we provide a high-level design framework to facilitate clinical translation and accelerate drug development using bioengineered human disease models.
由于当前药物开发过程的失败率极高,生物医学研究正在经历一场范式转变,转向以人类疾病模型为中心的方法。这种转变的主要驱动因素是动物模型的局限性,尽管动物模型在基础研究和临床前研究中仍然是金标准,但存在种间差异,且对人类生理和病理状况的预测能力较差。为了弥合这一转化差距,正在开发具有高度临床模拟性的生物工程人类疾病模型。在这篇综述中,我们讨论了受益于这些模型的临床前和临床研究,重点是类器官、生物工程组织模型和芯片器官。此外,我们提供了一个高层次的设计框架,以促进临床转化,并利用生物工程人类疾病模型加速药物开发。