为 COVID-19 建立不良后果途径网络

P. Nymark, Laure-Alix Clerbaux, Maria-João Amorim, Christos Andronis, Francesca de Bernardi, Gillina F. G. Bezemer, Sandra Coecke, Felicity N. E. Gavins, Daniel Jacobson, E. Lekka, Luigi Margiotta-Casaluci, Marvin Martens, S. Mayasich, Holly M. Mortensen, Young Jun Kim, M. Sachana, Shihori Tanabe, V. Virvilis, Steve W. Edwards, Sabina Halappanavar
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摘要

COVID-19 大流行产生了大量有关该疾病发病机制的数据,因此需要以简洁的方式整理大量知识。2020 年 4 月至 2023 年 2 月期间,CIAO 联盟利用不良后果途径(AOP)框架,全面收集和系统整理已发表的有关 COVID-19 病理学的科学文献。该项目通过确定导致在患者身上观察到的 19 种不良结果的基本关键事件 (KE),考虑了与 COVID-19 相关的 24 种途径。虽然单个 AOP 定义了导致结果的因果关系,但建立 AOP 网络可直观地反映出各种途径和结果之间的相互关联性。在本研究中,根据质量标准从 COVID-19 的 AOP 中选择了 17 个,通过计算得出了 AOP 网络。该初级网络强调了考虑组织特异性的必要性,并有助于识别缺失或冗余的元素,然后在最终网络中手动实现这些元素。这样一个网络使导致 COVID-19 多方面不同结果的关键基因之间复杂的相互作用可视化,并证实了炎症反应在疾病中的核心作用。此外,这项研究还揭示了术语统一和组织/器官特异性对网络构建的重要性。此外,AOP 中所含信息的完整性和质量参差不齐,这突出表明需要更严格地执行 FAIR 原则,以提高 AOP 的可查找性、可访问性、互操作性和可重用性。最后,研究强调,描述 SARS-CoV-2 复制的特定关键关键因子以及区分生理性和病理性炎症是必要的,但需要对框架进行调整。因此,基于所遇到的挑战,我们为正在进行的和未来的AOP联盟提出了相关建议,这些联盟的目标是在病毒性疾病(但不仅限于病毒性疾病)的背景下建立具有计算生物学意义的AOP网络。
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Building an Adverse Outcome Pathway network for COVID-19
The COVID-19 pandemic generated large amounts of data on the disease pathogenesis leading to a need for organizing the vast knowledge in a succinct manner. Between April 2020 and February 2023, the CIAO consortium exploited the Adverse Outcome Pathway (AOP) framework to comprehensively gather and systematically organize published scientific literature on COVID-19 pathology. The project considered 24 pathways relevant for COVID-19 by identifying essential key events (KEs) leading to 19 adverse outcomes observed in patients. While an individual AOP defines causally linked perturbed KEs towards an outcome, building an AOP network visually reflect the interrelatedness of the various pathways and outcomes. In this study, 17 of those COVID-19 AOPs were selected based on quality criteria to computationally derive an AOP network. This primary network highlighted the need to consider tissue specificity and helped to identify missing or redundant elements which were then manually implemented in the final network. Such a network enabled visualization of the complex interactions of the KEs leading to the various outcomes of the multifaceted COVID-19 and confirmed the central role of the inflammatory response in the disease. In addition, this study disclosed the importance of terminology harmonization and of tissue/organ specificity for network building. Furthermore the unequal completeness and quality of information contained in the AOPs highlighted the need for tighter implementation of the FAIR principles to improve AOP findability, accessibility, interoperability and re-usability. Finally, the study underlined that describing KEs specific to SARS-CoV-2 replication and discriminating physiological from pathological inflammation is necessary but requires adaptations to the framework. Hence, based on the challenges encountered, we proposed recommendations relevant for ongoing and future AOP-aligned consortia aiming to build computationally biologically meaningful AOP networks in the context of, but not limited to, viral diseases.
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