Cardoso Nancy Patricia, Mansilla Florencia Celeste, Benedetti Estefanía, Turco Cecilia Soledad, Barone Lucas José, Iserte Javier Alonso, Soria Ivana, Baumeister Elsa, Capozzo Alejandra Victoria
Instituto de Virología e Innovaciones Tecnológicas IVIT, Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET) - Instituto Nacional de Tecnología Agropecuaria (INTA), Hurlingham, Argentina.
Servicio Virosis Respiratorias, Instituto Nacional de Enfermedades Infecciosas, INEI-ANLIS "Dr. Carlos G. Malbrán," Buenos Aires, Argentina.
Front Vet Sci. 2020 Nov 6;7:603622. doi: 10.3389/fvets.2020.603622. eCollection 2020.
Interferon lambda (IFN-λ) is an antiviral naturally produced in response to viral infections, with activity on cells of epithelial origin and located in the mucosal surfaces. This localized activity results in reduced toxicity compared to type I IFNs, whose receptors are ubiquitously expressed. IFN-λ has been effective in the therapy of respiratory viral infections, playing a crucial role in potentiating adaptive immune responses that initiate at mucosal surfaces. Human IFN-λ has polymorphisms that may cause differences in the interaction with the specific receptor in the human population. Interestingly, bovine IFN-λ3 has an -predicted higher affinity for the human receptor than its human counterparts, with high identity with different human IFN-λ variants, making it a suitable antiviral therapeutic candidate for human health. Here, we demonstrate that a recombinant bovine IFN-λ (rbIFN-λ) produced in HEK-293 cells is effective in preventing SARS-CoV-2 infection of VERO cells, with an inhibitory concentration 50% (IC50) between 30 and 50 times lower than that of human type I IFN tested here (α2b and β1a). We also demonstrated the absence of toxicity of rbIFN-λ in human PBMCs and the lack of proinflammatory activity on these cells. Altogether, our results show that rbIFN-λ is as an effective antiviral potentially suitable for COVID-19 therapy. Among other potential applications, rbIFN-λ could be useful to preclude virus dispersion to the lungs and/or to reduce transmission from infected people. Moreover, and due to the non-specific activity of this IFN, it can be potentially effective against other respiratory viruses that may be circulating together with SARS-CoV-2.
干扰素λ(IFN-λ)是一种在病毒感染时自然产生的抗病毒物质,对上皮来源的细胞有活性,位于粘膜表面。与I型干扰素相比,这种局部活性导致毒性降低,I型干扰素的受体在全身广泛表达。IFN-λ在呼吸道病毒感染的治疗中已显示出有效性,在增强始于粘膜表面的适应性免疫反应中发挥关键作用。人类IFN-λ存在多态性,这可能导致其在人群中与特定受体的相互作用存在差异。有趣的是,牛IFN-λ3对人类受体的预测亲和力高于其人类同类物,与不同的人类IFN-λ变体具有高度同源性,使其成为人类健康的合适抗病毒治疗候选物。在此,我们证明在HEK-293细胞中产生的重组牛IFN-λ(rbIFN-λ)可有效预防VERO细胞感染SARS-CoV-2,其半数抑制浓度(IC50)比此处测试的人类I型干扰素(α2b和β1a)低30至50倍。我们还证明了rbIFN-λ在人外周血单核细胞中无毒性,且对这些细胞无促炎活性。总之,我们的结果表明rbIFN-λ是一种可能适用于COVID-19治疗的有效抗病毒药物。在其他潜在应用中,rbIFN-λ可能有助于防止病毒扩散到肺部和/或减少感染者的传播。此外,由于这种干扰素的非特异性活性,它可能对其他可能与SARS-CoV-2一起传播的呼吸道病毒有效。