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Harnessing the power of novel animal-free test methods for the development of COVID-19 drugs and vaccines

机译:利用新型无动物的试验方法的力量,用于开发Covid-19药物和疫苗

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The COVID-19-inducing virus, SARS-CoV2, is likely to remain a threat to human health unless efficient drugs or vaccines become available. Given the extent of the current pandemic (people in over one hundred countries infected) and its disastrous effect on world economy (associated with limitations of human rights), speedy drug discovery is critical. In this situation, past investments into the development of new (animal-free) approach methods (NAM) for drug safety, efficacy, and quality evaluation can be leveraged. For this, we provide an overview of repurposing ideas to shortcut drug development times. Animal-based testing would be too lengthy, and it largely fails, when a pathogen is species-specific or if the desired drug is based on specific features of human biology. Fortunately, industry has already largely shifted to NAM, and some public funding programs have advanced the development of animal-free technologies. For instance, NAM can predict genotoxicity (a major aspect of carcinogenicity) within days, human antibodies targeting virus epitopes can be generated in molecular biology laboratories within weeks, and various human cell-based organoids are available to test virus infectivity and the biological processes controlling them. The European Medicines Agency (EMA) has formed an expert group to pave the way for the use of such approaches for accelerated drug development. This situation illustrates the importance of diversification in drug discovery strategies and clearly shows the shortcomings of an approach that invests 95% of resources into a single technology (animal experimentation) in the face of challenges that require alternative approaches.
机译:除非有效的药物或疫苗可用,否则Covid-19诱导病毒SARS-COV2可能仍然是对人类健康的威胁。鉴于目前大流行(在一百多个国家的人民感染者)及其对世界经济的灾难性影响(与人权局限性相关),快速的药物发现至关重要。在这种情况下,过去的投资进入新(无动物)方法方法(NAM)的药物安全,疗效和质量评估。为此,我们概述了对快捷药物发展时代的重新扫描思想。当病原体是特异性或所需的药物是基于人体生物学的特定特征时,基于动物的测试将过于冗长,并且当病原体是特异性的或如果所需的药物是基于人类生物学的特定特征,它在很大程度上。幸运的是,行业已经在很大程度上转移到了NAM,一些公共融资计划推进了无动物技术的发展。例如,NAM可以在几天内预测遗传毒性(致癌性的主要方面),靶向病毒表位的人抗体可以在几周内在分子生物学实验室中产生,并且可以在分子生物学实验室中产生各种人细胞的有机体测试病毒感染性和生物过程控制他们。欧洲药物局(EMA)已形成一个专家组,为使用此类药物开发方式铺平使用这些方法。这种情况说明了在药物发现策略中多样化的重要性,并清楚地表明,面对需要替代方法的挑战,将95%的资源投入单一技术(动物实验)的方法中的缺点。

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