Bortot Barbara, Romani Arianna, Ricci Giuseppe, Biffi Stefania
Institute for Maternal and Child Health, IRCCS Burlo Garofolo, Trieste, Italy.
Department of Translational Medicine and LTTA Centre, University of Ferrara, Ferrara, Italy.
Front Pharmacol. 2022 May 20;13:877422. doi: 10.3389/fphar.2022.877422. eCollection 2022.
The coronavirus disease (COVID-19) is responsible for more than 5 million deaths worldwide, with respiratory failure being the most common clinical presentation. COVID-19 complications still present a considerable burden on healthcare systems, and signs of the post-COVID syndrome are concerns for potential long-term damages. An increasing body of evidence highlights extracellular vesicles' (EVs) relevance in modulating inflammation and cell death in the diseases related to these processes. Several types of EVs-based investigational new drugs against COVID-19 have been approved by the US Food and Drug Administration to initiate a Phase I/II trial under an Investigational New Drug protocol. EVs can be employed as natural drug delivery nanoparticle-based systems due to their inherent potential in transferring material between cells, their natural origin, and their capability to encapsulate various biological molecules, offering an exciting alternative for administering drugs acting on the cell cycle control. In this context, small-molecule inhibitors of Mouse Double Minute 2 (MDM2) such as Nutlin-3 and Idasanutlin by promoting p53 survival and its antiviral activity might be helpful to modulate the IFN signalling pathway and reduce the overall pro-inflammatory burden.
冠状病毒病(COVID-19)在全球造成了超过500万人死亡,呼吸衰竭是最常见的临床表现。COVID-19并发症仍然给医疗系统带来相当大的负担,而新冠后遗症的迹象令人担忧其可能造成的长期损害。越来越多的证据表明,细胞外囊泡(EVs)在调节与这些过程相关疾病中的炎症和细胞死亡方面具有相关性。几种基于细胞外囊泡的抗COVID-19研究性新药已获得美国食品药品监督管理局批准,可根据研究性新药方案启动I/II期试验。由于细胞外囊泡在细胞间传递物质的内在潜力、其天然来源以及封装各种生物分子的能力,它们可以用作基于纳米颗粒的天然药物递送系统,为施用作用于细胞周期控制的药物提供了令人兴奋的替代方案。在这种情况下,诸如Nutlin-3和Idasanutlin等小鼠双微体2(MDM2)的小分子抑制剂通过促进p53存活及其抗病毒活性,可能有助于调节干扰素信号通路并减轻整体促炎负担。