开发免疫肿瘤疗法的临床前模型。

Immuno-oncology insights Pub Date : 2022-01-01 Epub Date: 2022-09-26 DOI:10.18609/ioi.2022.41
Yufei Wang, Sarah E Shelton, Gabriella Kastrunes, David A Barbie, Gordon J Freeman, Wayne A Marasco
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引用次数: 0

摘要

免疫疗法在临床治疗中取得了巨大成功,尤其是在癌症治疗方面。在此,我们回顾了临床前模型,包括细胞系、三维(3D)培养物和小鼠模型,以支持开发新型免疫肿瘤(I-O)疗法所需的工具。与体内模型相比,体外研究具有相对简单、快速和高通量的优势,但必须精心设计,以再现影响药物疗效的生物条件。三维体外和体内模型的日益普及使筛选和机理研究得以在更复杂、包含多种相互作用细胞类型的类组织环境中进行。另一方面,合成小鼠模型在免疫疗法的历史发展中发挥了重要作用,尽管与人体生理和病理的某些方面不够逼真,但仍然是药物开发的重要工具。异种移植和人源化小鼠模型解决了其中一些难题,但也存在自身的局限性。成功开发和转化新的 I-O 疗法可能需要周到地将上述几种临床前模型结合起来,我们的目标是帮助研发科学家利用适当的工具和技术,促进从临床前评估到临床试验的快速过渡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Preclinical models for development of immune-oncology therapies.

Immunotherapy has demonstrated great success in clinical treatment, especially for cancer care. Here we review preclinical models, including cell lines, three dimensional (3D) cultures, and mouse models to support the need for tools enabling the development of novel immune-oncology (I-O) therapies. While in vitro studies have the advantage of being relatively simpler, faster, and higher throughput than in vivo models, they must be designed carefully to recapitulate the biological conditions that influence drug efficacy. The growing prevalence of 3D in vitro and ex vivo models has enabled screening and mechanistic studies in more complex, tissue-like environments containing multiple interacting cell types. On the other hand, syngeneic mouse models have been instrumental in the historical development of immunotherapies and remain an important tool in drug development, despite lacking fidelity to certain aspects of human physiology and pathology. Xenograft and humanized mouse models address some of these challenges, yet present limitations of their own. Successful development and translation of new I-O therapies will likely require thoughtful combination of several of these preclinical models, and we aim to help research and development scientists utilize the appropriate tools and technologies to facilitate rapid transition from preclinical evaluation to clinical trials.

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