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球状体和类器官作为无支架 3D 人源化工程组织用于 SARS-CoV-2 病毒感染和药物筛选。

Spheroids and organoids as humanized 3D scaffold-free engineered tissues for SARS-CoV-2 viral infection and drug screening.

机构信息

Nucleus of Multidisciplinary Research in Biology (Numpex-Bio), Federal University of Rio de Janeiro (UFRJ), Campus Duque de Caxias, Rio de Janeiro, Brazil.

Postgraduation Program of Translational Biomedicine (Biotrans), Unigranrio, Campus I, Duque de Caxias, Brazil.

出版信息

Artif Organs. 2021 Jun;45(6):548-558. doi: 10.1111/aor.13880. Epub 2021 Jan 10.

Abstract

The new coronavirus (2019-nCoV) or the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was officially declared by the World Health Organization (WHO) as a pandemic in March 2020. To date, there are no specific antiviral drugs proven to be effective in treating SARS-CoV-2, requiring joint efforts from different research fronts to discover the best route of treatment. The first decisions in drug discovery are based on 2D cell culture using high-throughput screening. In this context, spheroids and organoids emerge as a reliable alternative. Both are scaffold-free 3D engineered constructs that recapitulate key cellular and molecular events of tissue physiology. Different studies have already shown their advantages as a model for different infectious diseases, including SARS-CoV-2 and for drug screening. The use of these 3D engineered tissues as an in vitro model can fill the gap between 2D cell culture and in vivo preclinical assays (animal models) as they could recapitulate the entire viral life cycle. The main objective of this review is to understand spheroid and organoid biology, highlighting their advantages and disadvantages, and how these scaffold-free engineered tissues can contribute to a better comprehension of viral infection by SARS-CoV-2 and to the development of in vitro high-throughput models for drug screening.

摘要

新型冠状病毒(2019-nCoV)或严重急性呼吸系统综合症冠状病毒 2 型(SARS-CoV-2)于 2020 年 3 月被世界卫生组织(WHO)正式宣布为大流行。迄今为止,尚无经证实可有效治疗 SARS-CoV-2 的特定抗病毒药物,需要不同研究领域共同努力寻找最佳治疗途径。药物发现的首要决策是基于使用高通量筛选的 2D 细胞培养。在这种情况下,球体和类器官成为可靠的替代方案。两者都是无支架的 3D 工程构建体,可重现组织生理学的关键细胞和分子事件。已有多项研究表明,它们作为包括 SARS-CoV-2 在内的不同传染病和药物筛选模型的优势。将这些 3D 工程组织用作体外模型可以填补 2D 细胞培养和体内临床前测定(动物模型)之间的空白,因为它们可以重现整个病毒生命周期。本综述的主要目的是了解球体和类器官生物学,突出它们的优缺点,以及这些无支架工程组织如何有助于更好地理解 SARS-CoV-2 病毒感染,并开发用于药物筛选的体外高通量模型。

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