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In vitro evaluation of the activity of teriflunomide against SARS-CoV-2 and the human coronaviruses 229E and OC43
Biochem Biophys Rep ; 33:101395.0, 2023.
Article in English | PubMed | ID: covidwho-2242472
ABSTRACT
Previous data have suggested an antiviral effect of teriflunomide, including against severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), the agent underlying the ongoing COVID-19 pandemic. We undertook an in vitro investigation to evaluate the inhibitory activity of teriflunomide against SARS-CoV-2 in a cell-based assay. Teriflunomide was added to Vero (kidney epithelial) cells that had been infected with SARS-CoV-2. A nucleocapsid immunofluorescence assay was performed to examine viral inhibition with teriflunomide and any potential cytotoxic effect. The 50% effective concentration (EC(50)) for teriflunomide against SARS-CoV-2 was 15.22 μM. No cytotoxicity was evident for teriflunomide in the Vero cells (i.e., the 50% cytotoxic concentration [CC(50)] was greater than the highest test concentration of 100 μM). The data were supported by additional experiments using other coronaviruses and human cell lines. In the SARS-CoV-2-infected Vero cells, the prodrug leflunomide had an EC(50) of 16.49 μM and a CC(50) of 54.80 μM. Our finding of teriflunomide-mediated inhibition of SARS-CoV-2 infection at double-digit micromolar potency adds to a growing body of evidence for a broad-ranging antiviral effect of teriflunomide.
Keywords
Antiviral; CC50, 50% cytotoxic concentration; Covid-19; COVID-19, coronavirus disease 2019; CPE, cytopathic effect; Coronavirus; EC50, 50% effective concentration; HCoV, human coronavirus; Human cell line; MS, multiple sclerosis; SARS-CoV-2; SARS-CoV-2, severe acute respiratory syndrome coronavirus-2; TCID50, 50% tissue culture infective dose; Teriflunomide; qPCR, quantitative real-time polymerase chain reaction; personal relationships that could have appeared to influence the work reported in; this paper. The authors declare the following financial interests/personal; relationships which may be considered as potential competing interests: Paul; Lang, PhD reports writing assistance was provided by Elevate Scientific Affairs,; Envision Pharma Group. Paul Lang, PhD reports a relationship with Sanofi that; includes: employment. Svend S. Geertsen, PhD reports writing assistance was; provided by Elevate Scientific Affairs, Envision Pharma Group. Svend S. Geertsen,; PhD reports a relationship with Sanofi that includes: employment. Alex L. Lublin,; PhD reports writing assistance was provided by Elevate Scientific Affairs,; Envision Pharma Group. Alex L. Lublin, PhD reports a relationship with Sanofi; that includes: employment. Michelle C. Potter, PhD reports writing assistance was; provided by Elevate Scientific Affairs, Envision Pharma Group. Michelle C.; Potter, PhD reports a relationship with Sanofi that includes: employment. Tatiana; Gladysheva reports writing assistance was provided by Elevate Scientific Affairs,; Envision Pharma Group. Tatiana Gladysheva reports a relationship with Sanofi that; includes: employment. Jill S. Gregory reports writing assistance was provided by; Elevate Scientific Affairs, Envision Pharma Group. Jill S. Gregory reports a; relationship with Sanofi that includes: employment. Pascal Rufi, MD reports; writing assistance was provided by Elevate Scientific Affairs, Envision Pharma; Group. Pascal Rufi, MD reports a relationship with Sanofi that includes:; employment.

Full text: Available Collection: Databases of international organizations Database: PubMed Type of study: Experimental Studies Language: English Journal: Biochem Biophys Rep Year: 2023 Document Type: Article

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Full text: Available Collection: Databases of international organizations Database: PubMed Type of study: Experimental Studies Language: English Journal: Biochem Biophys Rep Year: 2023 Document Type: Article