Neary Megan, Gallardo-Toledo Eduardo, Sharp Joanne, Herriott Joanne, Kijak Edyta, Bramwell Chloe, Cox Helen, Tatham Lee, Box Helen, Curley Paul, Arshad Usman, Rajoli Rajith K R, Pertinez Henry, Valentijn Anthony, Pennington Shaun H, Caygill Claire H, Lopeman Rose C, Biagini Giancarlo A, Kipar Anja, Stewart James P, Owen Andrew
Department of Pharmacology and Therapeutics, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool L69 3BX, UK.
Centre of Excellence in Long-Acting Therapeutics (CELT), University of Liverpool, Liverpool L69 3BX, UK.
Viruses. 2024 Nov 27;16(12):1838. doi: 10.3390/v16121838.
Favipiravir (FVP) and remdesivir (RDV) have demonstrable antiviral activity against SARS-CoV-2. Here, the efficacy of FVP, RDV, and FVP with RDV (FVP + RDV) in combination was assessed in Syrian golden hamsters challenged with SARS-CoV- 2 (B.1.1.7) following intraperitoneal administration. At day 4 post infection, viral RNA and viral antigen expression were significantly lower in lungs for all three treatment groups compared to the sham treatment. Similarly, viral titres in the lungs were lower in all treatment groups compared to the sham treatment. The FVP + RDV combination was the only treatment group where viral RNA in nasal turbinate and lung, virus titres in lung, and viral antigen expression (lung) were all lower than those for the sham treatment group. Moreover, lower viral titre values were observed in the FVP + RDV group compared to other treatment groups, albeit only significantly lower in comparison to those in the RDV-only-treated group. Further assessment of the potential utility of FVP in combination with RDV may be warranted. Future studies should also consider whether the combination of these two drugs may reduce the speed at which drug resistance mutations are selected.
法匹拉韦(FVP)和瑞德西韦(RDV)对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)具有明显的抗病毒活性。在此,评估了腹腔注射后,法匹拉韦、瑞德西韦以及法匹拉韦与瑞德西韦联合用药(FVP+RDV)对感染SARS-CoV-2(B.1.1.7)的叙利亚金黄地鼠的疗效。感染后第4天,与假处理组相比,所有三个治疗组肺中的病毒RNA和病毒抗原表达均显著降低。同样,与假处理组相比,所有治疗组肺中的病毒滴度均较低。FVP+RDV联合用药组是唯一鼻甲和肺中的病毒RNA、肺中的病毒滴度以及病毒抗原表达(肺)均低于假处理组的治疗组。此外,与其他治疗组相比,FVP+RDV组的病毒滴度值更低,尽管仅与仅用瑞德西韦治疗的组相比有显著降低。可能有必要进一步评估法匹拉韦与瑞德西韦联合用药的潜在效用。未来的研究还应考虑这两种药物的联合使用是否可以降低耐药性突变产生的速度。