Department of Genetics and Pharmacogenomics, Merck & Co., Inc., Kenilworth, New Jersey, United States of America.
Exploratory Science Center, Merck & Co., Inc., Cambridge, Massachusetts, United States of America.
PLoS Pathog. 2021 Feb 17;17(2):e1009225. doi: 10.1371/journal.ppat.1009225. eCollection 2021 Feb.
Since the initial report of the novel Coronavirus Disease 2019 (COVID-19) emanating from Wuhan, China, Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) has spread globally. While the effects of SARS-CoV-2 infection are not completely understood, there appears to be a wide spectrum of disease ranging from mild symptoms to severe respiratory distress, hospitalization, and mortality. There are no Food and Drug Administration (FDA)-approved treatments for COVID-19 aside from remdesivir; early efforts to identify efficacious therapeutics for COVID-19 have mainly focused on drug repurposing screens to identify compounds with antiviral activity against SARS-CoV-2 in cellular infection systems. These screens have yielded intriguing hits, but the use of nonhuman immortalized cell lines derived from non-pulmonary or gastrointestinal origins poses any number of questions in predicting the physiological and pathological relevance of these potential interventions. While our knowledge of this novel virus continues to evolve, our current understanding of the key molecular and cellular interactions involved in SARS-CoV-2 infection is discussed in order to provide a framework for developing the most appropriate in vitro toolbox to support current and future drug discovery efforts.
自新型冠状病毒病 2019(COVID-19)最初从中国武汉报告以来,严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)已在全球范围内传播。虽然 SARS-CoV-2 感染的影响尚不完全清楚,但疾病的范围似乎很广,从轻微症状到严重呼吸窘迫、住院和死亡。除了瑞德西韦,目前还没有获得美国食品和药物管理局(FDA)批准的 COVID-19 治疗方法;早期努力确定 COVID-19 的有效治疗方法主要集中在药物再利用筛选上,以确定在细胞感染系统中对 SARS-CoV-2 具有抗病毒活性的化合物。这些筛选产生了有趣的发现,但使用源自非肺部或胃肠道来源的非永生化细胞系来预测这些潜在干预措施的生理和病理相关性存在许多问题。虽然我们对这种新型病毒的了解还在不断发展,但我们目前对 SARS-CoV-2 感染涉及的关键分子和细胞相互作用的理解,是为了提供一个框架,以开发最合适的体外工具包来支持当前和未来的药物发现工作。