Department of Pharmacology and Therapeutics, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool L7 3NY, UK.
Centre of Excellence in Long-acting Therapeutics (CELT), University of Liverpool, Liverpool L7 3NY, UK.
J Antimicrob Chemother. 2024 Jan 3;79(1):172-178. doi: 10.1093/jac/dkad362.
Antiviral interventions are required to complement vaccination programmes and reduce the global burden of COVID-19. Prior to initiation of large-scale clinical trials, robust preclinical data to support candidate plausibility are required. This work sought to further investigate the putative antiviral activity of probenecid against SARS-CoV-2.
Vero E6 cells were preincubated with probenecid, or control media for 2 h before infection (SARS-CoV-2/Human/Liverpool/REMRQ0001/2020). Probenecid or control media was reapplied, plates reincubated and cytopathic activity quantified by spectrophotometry after 48 h. In vitro human airway epithelial cell (HAEC) assays were performed for probenecid against SARS-CoV-2-VoC-B.1.1.7 (hCoV-19/Belgium/rega-12211513/2020; EPI_ISL_791333, 2020-12-21) using an optimized cell model for antiviral testing. Syrian golden hamsters were intranasally inoculated (SARS-CoV-2 Delta B.1.617.2) 24 h prior to treatment with probenecid or vehicle for four twice-daily doses.
No observable antiviral activity for probenecid was evident in Vero E6 or HAEC assays. No reduction in total or subgenomic RNA was observed in terminal lung samples (P > 0.05) from hamsters. Body weight of uninfected hamsters remained stable whereas both probenecid- and vehicle-treated infected hamsters lost body weight (P > 0.5).
These data do not support probenecid as a SARS-CoV-2 antiviral drug.
需要抗病毒干预措施来补充疫苗接种计划,以减轻 COVID-19 的全球负担。在启动大规模临床试验之前,需要有强有力的临床前数据来支持候选药物的合理性。这项工作旨在进一步研究丙磺舒对 SARS-CoV-2 的潜在抗病毒活性。
在感染前 2 小时,将丙磺舒或对照培养基预孵育到vero E6 细胞中(SARS-CoV-2/Human/Liverpool/REMRQ0001/2020)。然后重新应用丙磺舒或对照培养基,48 小时后通过分光光度法测定细胞病变活性来重新孵育平板。针对 SARS-CoV-2-VoC-B.1.1.7(hCoV-19/Belgium/rega-12211513/2020;EPI_ISL_791333,2020-12-21),在经过优化的抗病毒检测细胞模型中进行针对丙磺舒的体外人呼吸道上皮细胞(HAEC)测定。在感染前 24 小时,用丙磺舒或载体对叙利亚金黄仓鼠进行鼻内接种(SARS-CoV-2 Delta B.1.617.2),然后进行 4 次每日两次的给药。
在 Vero E6 或 HAEC 测定中,未观察到丙磺舒的明显抗病毒活性。在来自仓鼠的终末肺样本中,未观察到总或亚基因组 RNA 的减少(P>0.05)。未感染的仓鼠的体重保持稳定,而接受丙磺舒和载体处理的感染仓鼠的体重减轻(P>0.5)。
这些数据不支持丙磺舒作为 SARS-CoV-2 抗病毒药物。